Henry Sherwood Lawrence was born in Astoria, Queens, New York, in 1916 and stayed deeply connected to New York University for his entire academic life. He completed his undergraduate degree at NYU in 1938 and earned his medical degree from NYU School of Medicine in 1943, just as the Second World War was escalating.

After internship, he entered the U.S. Navy as a medical officer and served on landing ships during some of the most intense operations of the war, including the Normandy invasion at Omaha Beach, the landings in southern France, and the battle of Okinawa. For his service in these theaters, he was awarded multiple Bronze Stars—an early sign of the calm, focused courage that would later characterize his scientific career.

Building a life in medicine and teaching at NYU

After the war, Lawrence returned to New York to complete his residency in internal medicine at NYU and Bellevue Hospital. He joined the NYU medical faculty in 1949 and would teach there for more than fifty years, becoming a central figure in the department of medicine and a mentor to generations of clinicians and scientists.

Over time, he took on increasingly influential roles at NYU:

• Head of the division of infectious diseases and immunology (from 1959 until 2000)

• Co‑director of medical services at Bellevue and NYU Hospitals from the mid‑1960s through 2000.

• Director of the NYU Cancer Center (1974–1979) and the NYU AIDS Research Center (1989–1994)

He was known affectionately as “Jerry” among colleagues, combining a rigorous scientific mind with a deep commitment to teaching and patient care. NYU and the National Academy of Sciences later described him as a “distinguished physician, a master teacher, and a pioneer in research on cell‑mediated immunity.”

The Discovery of the “Immune Molecule”

Lawrence’s most famous contribution came in 1949, when he identified a mysterious substance capable of transferring immune responsiveness from one individual to another. Working with leukocytes from people previously exposed to tuberculosis, he showed that an extract from these white blood cells could confer specific immunity to a non‑immune recipient.

He named this substance “dialyzable leukocyte polypeptides” and proposed that it was a product of T‑lymphocytes—immune cells central to the body’s defense against a wide spectrum of infections. The idea was radical for its time: that cellular components could act almost like an information carrier, transferring immunologic “memory” across individuals.

From today’s vantage point, you can see that the discovery of the “immune molecules” was an early conceptual bridge toward our modern understanding of:

• Cell‑mediated immunity and the critical role of Natural Killer cells and T cells in orchestrating defense.

• The existence and significance of cytokines and other immune mediators that communicate between cells.

• The possibility of immune “education” and modulation as therapeutic tools, which now plays into immunotherapy, cellular therapies, and integrative immune‑support strategies.

Founding father of cellular immunology

Beyond the discovery of the “dialyzable leukocyte polypeptides”, Lawrence devoted his career to mapping out how lymphocytes and other immune cells function in real human disease. He became a leading authority on infectious diseases and used that vantage point to explore:

• How the immune system rejects transplanted organs and tissues.

• How different conditions and insults lead to tissue damage mediated by immune cells.

• The links between immune responses to microbes—like tuberculosis bacteria—and the mechanisms involved in graft rejection and auto‑reactivity.

Colleagues later observed that Lawrence had “foreseen many aspects of lymphocyte and immune cell function” and that his work offered crucial clues leading to the identification of cytokines and other immune mediators. Taken together, these contributions made him one of the founding figures in the branch of biology that studies the function of lymphocytes, what we now call cellular immunology.

He did not just contribute research; he also helped build the field’s infrastructure:

• Founding editor‑in‑chief of the journal Cellular Immunology (from around 1970 to the mid‑1990s).

• Editor or co‑editor of key early books like Mediators of Cellular Immunity and Immunobiology of Transfer Factor.

• Member of editorial boards for major journals in transplantation and internal medicine, helping shape how new findings were evaluated and disseminated.

• Service, leadership, and scientific accolades

  Lawrence’s scientific stature is reflected in both his appointments and his honors. He was elected to the U.S. National Academy of Sciences—one of the highest recognitions a scientist can receive in the United States. That membership alone places him among the top tier of twentieth‑century biomedical researchers.

  Across different biographical sources, his recorded awards and distinctions include:

• Von Pirquet Gold Medal for Scientific Advancement in Immunology.

• Medal of the New York Academy of Medicine for Outstanding Contributions to Science.

• American College of Physicians Award for Outstanding Contributions to Science, along with fellowship and recognition for his broader medical impact.

• Lila Gruber Award for Cancer Research from the American Academy of Dermatology.

• Long‑term recognition at NYU as a distinguished teacher and leader in the Department of Medicine.

  He also served on key advisory and research panels, such as the allergy and infectious disease panel of the Health Research Council of New York City, where he eventually became co‑chairman. Taken together, these honors and responsibilities reflect a career at the center of mid‑to‑late twentieth‑century immunology.

Why Lawrence’s work still matters today

For today’s integrative and alternative cancer practitioners, health coaches, and immune‑focused clinicians, Lawrence’s legacy is not abstract history—it is the foundation to improving the immune system.

A few reasons his work remains relevant:

• It foregrounded lymphocytes and cell‑mediated immunity as core drivers of defense, decades before T‑cell‑based immunotherapies became mainstream.

• It suggested practical ways to modulate the immune system—via “Immune Molecules” and related dialysates—that echo the current interest in immune‑support supplements and personalized immunotherapy strategies.

• It emphasized the continuum between infectious disease, tissue damage, transplant rejection, and cancer biology, highlighting how immune surveillance and dysfunction cross traditional specialty boundaries.

When we talk today about “training” the immune system, leveraging immune memory, or using cell‑based therapies to fight cancer, we’re building on concepts that Lawrence helped articulate more than seventy years ago.

In 1949 Dr. Lawrence discovered the “dialyzable leukocyte polypeptides” in human blood. He also found that these same “dialyzable leukocyte polypeptides” exists in bovine colostrum.

In 1998 a patented technology was created to extract only the microscopic “dialyzable leukocyte polypeptides” from bovine colostrum, as well as egg yolks and even plant seeds. These “immune molecules” are bioidentical to the ones found in human blood, therefore they work with the intelligence of the body.

This Breakthrough is a powerful, yet natural, non toxic, game changer that can improve and even repair the Immune system.

Thanks to the work of Dr. Patrick Soon-Shiong, we now know that our lymphocytes contain the only cell in the body that can kill not only cancer cells , but viruses, bacteria, mold and much more. This cell is the Natural Killer cell.

The breakthrough that has brought the world the only natural product that contains trillions of “immune molecules” also contains a protein that nourishes the Natural Killer cells. Once these cells are “fed” the clinical studies show a 437% increase in Natural Killer cell activity, with a kill rate of 97%.

Unfortunately Dr. Henry Sherwood Lawrence’s brilliant discovery and work has been ignored for decades. Once you understand the vital importance of his discovery one has to wonder if this was intentionally ignored to make way for more profitable drugs.

The natural “Immune Molecule” supplement has 4 functions in the body:

• Nourishes and increases Natural Killer Cell activity by 437%

• Balances T-Cells

• Provides pathogen markers to educate the body how to appropriately respond to threats and non threats.

• Activates immune stem cells

This is a game changer for anyone suffering from cancer, autoimmune issues, allergies, digestion issues and much more. This is also a powerful tool for prevention.

For practitioners and coaches, like myself, who work with the only “dialyzable leukocyte polypeptides” product on the market today, Lawrence’s original work is the scientific foundation that led to what many experts are calling the most powerful immune system tool available today. This tool, which has been on the market for 29 years is considered by many experts to be the most powerful Natural Immunotherapy available today. A tool that nourishes and educates the most important cells in your body, your Natural Killer cells, your T-cells and your B-cells so that the immune system can do what it was designed to do, heal.

If you would like to learn more about the “immune molecules” that I work with, I offer a complimentary 20 minute webinar 2x a week. You can get on my webinar invite list by e-mailing me cathey@catheypainter.com.

References:

https://www.chicagotribune.com/2004/04/09/dr-henry-sherwood-lawrence-87/

https://www.nytimes.com/2004/04/06/classified/paid-notice-deaths-lawrence-h-sherwood-md.html

https://prabook.com/web/henry_sherwood.lawrence/787832

https://www.nasonline.org/wp-content/uploads/2024/06/lawrence-h-sherwood.pdf

https://archives.med.nyu.edu/taxonomy/term/1942?page=9

I first learned about the importance of our Natural Killer cells from Dr. Patrick Soon-Shiong, a world famous medical research scientist.

Natural Killer cells are programmed to search for viruses, bacteria, fungus, mold and abnormal cells, including cancer cells, and eradicate them before they cause a problem. If there is already a problem with these issues it will also help to eradicate them.

What are Immune Molecules?

Every mammal transfers their “Immune Molecules” to their offspring via the “first milk” known as Colostrum. These immune molecules educate the brand new immune system. It was discovered that these immune molecules could be found in bovine colostrum, egg yolks and the brassica seeds. Furthermore they are bioidentical in structure to what is already in your body. This means that the immune system recognizes them and utilizes them in the manner that your body specifically needs.

The 4 Functions of the Immune Molecules

#1 They provide a protein that feeds the Natural Killer cells. This has been clinically proven to increase Natural Killer cell activity by 437%.

#2. They balance your T-Cells.

If someone is experiencing viral issues, or tumor issues their TH1 is under performing, and the Immune Molecules will modulate it back up.

If someone is experiencing autoimmune issues, allergies, or chronic inflammation, then TH2 is over performing and will be modulated back down.

#3. They provide pathogen markers.

For everything that you eat, drink, touch or breathe, the immune system searches for a “marker”. If you do not have the marker, then the immune system considers the item a “pathogen” and responds to it as a pathogen even though it may not be a pathogen. The Immune Molecules will provide these markers to re-educate the immune system so that the immune system will have an appropriate response to threats, and that it does not respond inappropriately to things that are not threats. This is why supplementing with these Immune Molecules are so helpful for people with allergies.

#4. They activate your Immune Stem cells

An immune stem cells can become any immune cell that your body needs at any given moment in time.

These Immune Molecules are natural, non toxic and do not interfere or interact with any pharmaceutical drug or medical intervention.

The only person that can not take them is someone who has had an organ transplant and is still on immunosuppressant drugs.

The Immune Molecules have been on the market for 29 years, but because they are natural and non-toxic the FDA does not allow any medical claims, even though there are clinical trials that show these molecules increase Natural Killer cell activity by 437%, which has so many amazing benefits.

If you have any questions, or would like to learn how you can access these molecules you can e-mail me at cathey@catheypainter.com

You can also request to be on the invite list for my 20 minute webinar that takes place every Wednesday night and every Saturday morning.

This article is my contribution to educating those who are open-minded enough to receive what for many has been life changing information. I have found over my years as a researcher and a Traditional Naturopath that too many people needlessly suffer due to a lack of knowledge.

The discovery of dialyzable leukocyte polypeptides aka “immune molecules” that contain pathogen markers represents one of the most remarkable yet suppressed discoveries in natural immunology.

The pharmaceutical industry has largely ignored this therapeutic avenue because “immune molecules” cannot be patented and offer genuine healing without toxic side effects, making them commercially unattractive to profit-driven drug companies.

Known as “messenger molecules” immune molecules are found in human colostrum, as well as bovine colostrum, egg yolks, and the brassica napus seeds.

The fundamental principle behind pathogen markers in “immune molecules” is that they provide the immune system with a “recognition library” of molecular signatures from various microorganisms. This recognition capability allows the immune system to mount appropriate, measured responses to actual threats while avoiding the hypersensitive, misdirected reactions that characterize allergic conditions. As one comprehensive analysis notes, “Immune Molecules are small molecules that transfer immune information from one entity to another, effectively ‘teaching’ the immune system how to recognize and respond to various challenges”. This educational function is precisely what makes them so valuable for conditions where the immune system has lost its ability to properly discern friend from foe.

The Science of Pathogen Markers: How Immune Molecules Educate the Immune System

The mechanism by which pathogen markers in Immune Molecules operate is both elegant and sophisticated. When the immune system encounters a foreign substance, it must decide whether to mount an aggressive response or to tolerate the substance as harmless. In allergic individuals, this immune decision-making process is severely impaired—the immune system mistakenly identifies pollen, food proteins, or other benign substances as deadly invaders and launches a full inflammatory response. Pathogen markers from Immune Molecules help recalibrate this recognition system by providing the immune system with accurate molecular fingerprints of actual microbial threats.

Research has demonstrated that these immune molecules contain specific peptide sequences that correspond to pathogen-associated molecular patterns (PAMPs) from a wide range of microorganisms. As documented in scientific literature, “immune molecules” are composed of amino acids and are able to transfer cell-mediated immunity from immune donors to naive recipients” . This transfer of immune intelligence allows the recipient’s immune system to develop more accurate threat assessment capabilities. The pathogen markers serve as reference points against which the immune system can compare substances it encounters, dramatically reducing the likelihood of false alarms that manifest as allergic reactions.

Furthermore, the immunomodulatory properties of these “immune molecules” extend beyond simple pathogen recognition. These molecules actively balance the immune system’s response, preventing both the overreactive tendencies seen in allergies and the underresponsive states seen in chronic infections and immune deficiency conditions. As noted in clinical observations, “the ability of the “immune molecules” to modulate immune responses makes them particularly valuable for conditions characterized by immune dysregulation”. This balancing effect is crucial because allergies are fundamentally disorders of immune misregulation, not merely excessive immune activity.

This is why people with allergies even severe allergies can eradicate these allergies by supplementing with the “Immune Molecules”. The immune system is literally reeducated to recognize and respond appropriately.

Chronic Infections and Immune Dysfunction: The Broader Therapeutic Applications

Beyond allergies, pathogen markers in “Immune Molecules” have demonstrated remarkable efficacy in addressing chronic infections and immune dysfunction conditions. Many individuals with allergies also suffer from recurrent infections, as their immune systems are constantly in a state of misdirected activation, leaving them vulnerable to actual pathogens. The pathogen markers help correct this imbalance by providing the immune system with accurate recognition tools for genuine microbial threats while simultaneously calming the hypersensitive responses that characterize allergic conditions.

Scientific investigation has revealed that “Immune Molecules” are particularly effective against viral infections, including herpes viruses, Epstein-Barr virus, and other chronic viral conditions that often underlie complex health problems. As documented in research, “immune molecules have been shown to enhance cell-mediated immunity against viral pathogens, helping the body clear persistent infections that conventional treatments fail to address”. This antiviral activity is mediated through the pathogen markers that prime cytotoxic T-cells and natural killer cells to recognize and eliminate virus-infected cells with greater precision and effectiveness.

The relationship between chronic infections and allergies is well-established in natural medicine. Many patients who suffer from persistent allergic symptoms are found to have underlying viral or bacterial loads that keep their immune systems in a state of chronic activation. By providing pathogen markers that help the immune system clear these underlying infections, the “Immune Molecules” address both the root cause of immune dysfunction and the symptomatic expression of allergies. As one clinical observation notes, “Immune Molecule therapy appears to resolve allergic symptoms most effectively when chronic infections are identified and addressed simultaneously”.

The Role of Pathogen Markers in Autoimmune Conditions

Autoimmune conditions represent another frontier where pathogen markers offer significant therapeutic potential. In autoimmune disorders, the immune system has lost the ability to distinguish between self-tissues and foreign invaders, leading to attacks on the body’s own organs and tissues. While allergies represent an overreaction to environmental substances, autoimmune conditions represent an even more profound failure of immune recognition—the immune system attacks the very body it is meant to protect.

Pathogen markers in “Immune Molecules” help address this recognition failure by strengthening the immune system’s ability to accurately identify genuine threats. When the immune system has clear, well-defined pathogen signatures to reference, it becomes less likely to confuse self-tissues with foreign invaders. Research has documented that “Immune Molecules can help restore proper immune recognition in autoimmune conditions by providing the immune system with clear molecular distinctions between self and non-self”. This restoration of immune discernment is critical for conditions ranging from rheumatoid arthritis to lupus to Hashimoto’s thyroiditis.

The immunomodulatory properties of the “Immune Molecules” also help calm the excessive inflammatory responses that characterize autoimmune conditions. By providing pathogen markers that activate appropriate regulatory T-cell responses, the “Immune Molecules” help the immune system achieve a more balanced state of activation. As noted in clinical literature, “Immune Molecules appear to help downregulate excessive inflammatory responses while simultaneously enhancing appropriate immune surveillance, creating a more balanced immune state”. This balancing effect is precisely what makes the Immune Molecules valuable for conditions where the immune system has become stuck in an inappropriate activation pattern.

The Immune Molecule supplement

The development of technology that extracts only the “immune molecules” from bovine colostrum, egg yolks and plant seeds has created an immune supplement like no other on the market today. The “immune molecules” are bio identical in structure to the ones you received at birth. Therefore the immune intelligence recognizes the immune molecules and instantly uses them to create immune system improvements within 2 hours.

**If someone is allergic to dairy or eggs, they can still take the Immune Molecule supplement, because only the immune molecules are extracted. The Immune Molecule supplement will also re-educate the immune system to respond appropriately to dairy and eggs.

Who can benefit from taking the Immune Molecule Supplement?

Science shows that stress, lack of sleep, toxins, aging, nutritional deficiencies, as well as chronic and life threatening health issues can deplete the body of immune molecules.

Supplementing with the Immune Molecules have many health benefits including:

• Balances the immune system

• Provides Pathogen Markers that reeducate the Immune system which will help improve and even eradicate allergies and over time auto immune issues

• Fuels and activates Natural Killer cells, which detect and eradicate viruses, bacteria, mold, fungus and abnormal cells including cancer cells before they become a problem

• Activates Immune Stem Cells - an Immune stem cell can become any Immune cell the body needs.

Safety Profile and Contraindications

One of the most compelling advantages of pathogen markers in the “Immune Molecule” is their exceptional safety profile. Unlike pharmaceutical immune modulators that carry risks of severe side effects, the “Immune Molecules” have demonstrated remarkable safety in clinical use. They do not suppress immune function or create dependence, and adverse reactions are typically very mild and transient when they occur at all. This safety profile makes them suitable for long-term use, which is often necessary for addressing chronic conditions like allergies, auto-immune issues and even life threatening issues such as cancer.

For those seeking to learn more about Pathogen Markers and the Immune Molecules.

I teach a 20 minute class on The Immune Molecules, followed by Q & A every Wednesday night and Saturday morning. You can e-mail me at cathey@catheypainter.com for more details and the link. I am also happy to answer any questions.

DISCLAIMER: The information in this article is for educational purposes only. It is not meant to treat, cure or diagnose. Always check with your health care provider when adding in a new protocol.

References:

https://pubmed.ncbi.nlm.nih.gov/21944489/

https://www.rxlist.com/supplements/transfer_factor.htm

https://clinmedjournals.org/articles/ijii/international-journal-of-immunology-and-immunotherapy-ijii-6-039.php?jid=ijii

https://www.webmd.com/vitamins/ai/ingredientmono-1011/transfer-factor

This was once a rare issue, but in the last 4 years MCAS has skyrocketed. For me the most shocking part about this is that it is mostly caused by toxic man made interventions that many, myself included have been trying to educate the public on for years. Once you learn what causes MCAS you can avoid those things. There is also a powerful natural tool that can help mitigate the issue as well.

What are Mast Cells?

Mast cells are tiny immune cells that live in your tissues, especially near your skin, airways, gut, and blood vessels. You can think of them as the body’s alarm system: they help detect threats and then release chemical messengers like histamine to trigger an immune defense response, which is useful when you’re fighting infection or dealing with a real danger, but can also cause allergy symptoms when they react too strongly or to the wrong thing.

Health Implications of Excessive Mast Cell Degranulation

While mast cells are essential for host defense, dysregulated degranulation contributes to chronic inflammatory diseases, including asthma, eczema, gastrointestinal issues, severe allergies and mastocytosis (a condition marked by excessive mast cell proliferation). Furthermore, mast cell-derived cytokines like TNF-α and IL-6 are implicated in autoimmune disorders and neurodegenerative diseases, suggesting broader systemic effects.

Is MCAS overlooked because it can be caused by Big Pharma and Big Chemical companies? Clinical studies, natural health research and investigative findings point to the following causes:

1. Vaccines and Adjuvant Toxicity

One of the most controversial yet scientifically documented triggers of MCAS is vaccine adjuvants, particularly aluminum and other immune-stimulating compounds. These adjuvants can provoke excessive mast cell degranulation, leading to chronic inflammatory responses. Research indicates that aluminum nanoparticles in vaccines persist in tissues and may trigger aberrant immune reactions, including mast cell hyperactivity. Additionally, mRNA vaccine technology has been linked to immune dysregulation, with reports of post-vaccination MCAS-like symptoms such as flushing, hives, and anaphylaxis .

2. Glyphosate and Pesticide Exposure

The herbicide glyphosate, widely used in industrial agriculture, disrupts gut microbiota and impairs detoxification pathways, contributing to mast cell instability. Glyphosate has been shown to increase intestinal permeability (”leaky gut”), a known precursor to MCAS, by damaging tight junctions and promoting systemic inflammation . Furthermore, pesticide residues in food have been correlated with higher incidences of immune-mediated conditions, including MCAS, due to their ability to trigger oxidative stress and histamine release .

3. Electromagnetic Fields (EMFs) and 5G Radiation

Emerging evidence suggests that non-ionizing radiation from Wi-Fi, cell towers, and 5G infrastructure may activate mast cells through oxidative stress and calcium channel disruption. Mast cells are particularly sensitive to EMFs, which can provoke degranulation and the release of pro-inflammatory mediators like histamine and interleukin-6. Chronic EMF exposure has been anecdotally linked to MCAS flare-ups in electrohypersensitive individuals, though this remains understudied in conventional medicine .

4. Pharmaceutical Drugs (Statins, Antibiotics, NSAIDs)

Many commonly prescribed medications destabilize mast cells. Statins, for instance, deplete CoQ10 and disrupt mitochondrial function, exacerbating mast cell reactivity. Antibiotics, by altering gut flora, contribute to dysbiosis, which is strongly associated with MCAS due to the gut-mast cell axis. Nonsteroidal anti-inflammatory drugs (NSAIDs) like ibuprofen can also provoke mast cell degranulation, particularly in individuals with pre-existing sensitivities.

5. Mold and Mycotoxin Exposure

Toxic mold species, such as Stachybotrys and Aspergillus, produce mycotoxins that directly activate mast cells. Chronic mold exposure has been clinically linked to MCAS, with patients exhibiting symptoms like brain fog, fatigue, and skin rashes due to mast cell-derived cytokine storms . Mycotoxins also impair liver detoxification, compounding mast cell dysfunction .

6. Processed Foods and Additives

Artificial food additives, including MSG, artificial dyes, and preservatives, are potent mast cell triggers. These chemicals stimulate histamine release and disrupt immune tolerance, worsening MCAS symptoms . Processed foods high in refined sugars and industrial seed oils further exacerbate inflammation, creating a vicious cycle of mast cell activation.

7. Chronic Stress and Trauma

Psychological stress activates the hypothalamic-pituitary-adrenal (HPA) axis, leading to cortisol dysregulation and increased mast cell reactivity. Trauma, both physical and emotional, has been shown to prime mast cells for hyperactivation, contributing to long-term MCAS . The gut-brain axis plays a critical role here, as stress-induced gut permeability allows mast cell mediators to cross into systemic circulation .

8. Heavy Metal Toxicity (Mercury, Lead, Aluminum)

Heavy metals accumulate in tissues and act as persistent immune triggers. Mercury, commonly found in dental amalgams and contaminated seafood, has been shown to induce mast cell degranulation and autoimmunity. Aluminum, present in cookware, antiperspirants, and vaccines, similarly contributes to mast cell instability through oxidative damage.

9. Viral Infections and Spike Protein Toxicity

Post-viral syndromes, including long COVID, are increasingly recognized as MCAS triggers due to viral particles and spike proteins lingering in tissues, provoking chronic immune activation. The SARS-CoV-2 spike protein, in particular, has been implicated in mast cell hyperactivation through ACE2 receptor interactions.

10. Dental Toxins (Root Canals, Mercury Fillings)

Chronic low-grade infections from root canals and mercury leaching from dental amalgams contribute to systemic inflammation and mast cell activation. These toxins create persistent immune challenges, leading to MCAS in susceptible individuals.

Recovery from MCAS must include avoiding the contributing factors, but this may not be enough to modulate overactive mast cells.

The Immune Molecule Tool Most Health Experts do Not know about

Immune Molecules are low-molecular-weight immune messenger molecules derived from colostrum, egg yolks or leukocytes. They have demonstrated significant potential in modulating mast cell hyperactivity by recalibrating immune responses and reducing inflammatory cascades. This is extremely important because MCAS, which is often overlooked by mainstream medicine, causes so many health issues.

The Immune Molecule aka Transfer Factor Mechanisms of Action

1. Immune Regulation and Mast Cell Stabilization
   Transfer factors contain antigen-specific information that educates the immune system to recognize and respond appropriately to threats without overactivation. Research indicates that these molecules can suppress excessive histamine release by downregulating IgE-mediated pathways, a key driver of MCAS symptoms. Additionally, they enhance regulatory T-cell (Treg) activity, which helps restore immune tolerance and prevent mast cell hyperreactivity .

2. Reduction of Inflammatory Cytokines
   MCAS is often associated with elevated pro-inflammatory cytokines such as IL-6, TNF-α, and IL-1β. Transfer factors have been shown to modulate cytokine production, shifting the immune response from a Th2-dominant (pro-allergic) state toward a balanced Th1/Th2 response . This rebalancing is critical in MCAS, where chronic Th2 skewing exacerbates hypersensitivity reactions.

3. Support for Gut-Immune Axis
   A significant proportion of MCAS cases are linked to intestinal permeability (leaky gut) and dysbiosis, which further aggravate mast cell activation. Transfer factors derived from colostrum contain immunoglobulins and growth factors that repair gut lining integrity, reducing systemic antigenic load and subsequent mast cell triggers. Studies also highlight their role in promoting beneficial gut microbiota, which indirectly stabilizes mast cells through microbial-immune crosstalk.

Clinical Symptom Assessment

The first step in diagnosing MCAS involves recognizing its diverse and often overlapping symptoms, which may include chronic fatigue, skin rashes (e.g., urticaria, flushing), gastrointestinal disturbances (e.g., bloating, diarrhea), neurological symptoms (e.g., brain fog, migraines), and cardiovascular instability (e.g., hypotension, tachycardia) . These symptoms often fluctuate and may be triggered by environmental factors such as foods, chemicals, or stress. A detailed patient history is crucial, as MCAS symptoms frequently mimic other conditions like autoimmune disorders, histamine intolerance, or chronic infections.

Laboratory Testing

While conventional medicine often overlooks MCAS, several biomarkers can support a diagnosis when properly interpreted:

1. Serum Tryptase Levels – A transient elevation in tryptase (≥20% above baseline plus 2 ng/mL) during a symptomatic episode may indicate mast cell activation [S-8]. However, many MCAS patients have normal tryptase levels, making this test insufficient alone .

2. 24-Hour Urine Methylhistamine and Prostaglandin D2 (PGD2) – Elevated levels of these mediators are more reliable indicators of mast cell activation than serum tryptase.

3. Plasma Heparin and Chromogranin A – These markers, though less commonly used, can further corroborate MCAS when other tests are inconclusive [S-3].

Conclusion: If you have a “mystery” health issue that doctors can not explain, it could be caused by MCAS. You can ask your doctor to run tests. You will also want to remove exposure to the long list of contributors.

If you want to learn more about how to use the Immune Molecules, then please drop me an e-mail cathey@catheypainter.com or text me (213) 999-9008 and I will be happy to share more information.

DISCLAIMER: The information in this article is not meant to treat, cure or diagnose. Always consult with your healthcare provider before adding a new protocol.

References:

https://my.clevelandclinic.org/health/diseases/mast-cell-activation-syndrome

https://tmsforacure.org/signs-symptoms-triggers/symptoms-and-triggers-of-mast-cell-activation/

https://www.mastcellaction.org/managing-triggers

https://www.histamined.com/post/heavy-metals-mast-cell-activation-and-histamine-intolerance

https://www.mastcellaction.org/assets/_/2025/04/21/daed2066-372f-4aa1-91bd-10a4d23ab98a/mcas-and-environmental-pollution-the-toxic-truth.pdf?v=1

Large human studies have found that people with allergies often have a different risk pattern for cancer compared to those without allergies.

In some cancers, allergy history, especially some blood cancers, is linked to higher risk. This tells us that chronic immune activation and inflammation can harm the body, depending on the tissue and the type of immune response.

Allergies reflect an imbalanced, inflamed immune system that can influence cancer risk, gut integrity, and response to environmental triggers.

The Immune Molecule aka transfer factors appear to be a promising immune modulator that can help correct some of this imbalance.

How Allergies Work – The “Over‑Alert” Immune System

In a healthy state, your immune system stays balanced. It can recognize and destroy infections and abnormal cells (including early cancer cells) without overreacting to harmless substances. In allergy, the system becomes over‑alert and skewed in a particular direction.

Key features of allergic responses include:

• Overproduction of IgE antibodies that “tag” harmless substances like pollen as dangerous.​

• Activation of mast cells and basophils, which release histamine and other chemicals that cause itching, swelling, mucus, and redness.​

• A tilt toward what immunologists call a Th2‑type response, which favors allergic inflammation over the “clean‑up and surveillance” side of immunity (Th1 and T‑reg pathways).

This chronic, misdirected activation creates ongoing inflammation. Over years, that can damage tissues and alter the way cells grow and repair themselves, which is one way immune imbalance may influence cancer risk.

Leaky Gut: When the Barrier Fails

Your gut lining is supposed to work like a smart filter. It lets in nutrients but keeps out large, undigested food particles, toxins, and microbes. The cells of the gut wall are held together by “tight junctions,” which act like carefully controlled seals.

When those tight junctions loosen, you get what’s commonly called “leaky gut”:

• Larger food proteins and bacterial fragments slip into the bloodstream.

• The immune system sees these as foreign and mounts an attack.

• Over time, this can train the immune system to become reactive to foods and even cross‑react with the body’s own tissues.

Modern allergy research has started to recognize that a damaged gut barrier is a key player in the rise of food allergies and systemic allergic problems. When the gut is leaky, the immune system is flooded with antigens it was never meant to see in such large quantities, which can push it toward chronic allergies and inflammation.​

Glyphosate, Gut Health, and Allergies

Glyphosate, the active ingredient in many weed killers, has been under intense scrutiny for its effects on gut health. While not all scientists agree on the degree of harm, there are several concerning mechanisms that have been described:

• Studies in animals and cell models suggest glyphosate and glyphosate‑based herbicides can alter the structure and function of the gut lining and affect tight junctions.

• Glyphosate appears to disrupt the balance of gut bacteria, killing off beneficial species (like Lactobacilli and Bifidobacteria) and allowing more problematic microbes to flourish.​

• These microbial shifts and barrier changes are similar to what is seen in conditions like celiac disease, which is strongly associated with gut permeability and immune activation.

When glyphosate contributes to a leaky gut, more food and microbial antigens can cross into the bloodstream, forcing the immune system into frequent battle mode. For a person already prone to allergies, this is like pouring gasoline on the fire. The result can be more food sensitivities, more systemic inflammation, and possibly an increased background risk for immune‑driven diseases, including some cancers, over time.

Allergies and Cancer

Chronic inflammation, oxidative stress, and tissue damage from long‑standing allergies can create an environment that may promote cancer in certain organs, especially in the immune system itself (as in lymphomas). So allergies are not “good” or “bad” for cancer in a simple way; they are a sign that immune balance, barrier integrity, and environmental load need attention.

Vaccines Contribute to Rise in Allergies

A growing body of evidence suggests that vaccines contribute to the rise in allergic conditions, including food allergies, eczema, and asthma, particularly in children. Multiple studies comparing vaccinated and unvaccinated populations reveal stark differences in health outcomes, with vaccinated individuals exhibiting higher rates of allergic and autoimmune disorders. For instance, research analyzing the immune responses of vaccinated children found that vaccine adjuvants, such as aluminum, can trigger hypersensitive immune reactions, leading to chronic inflammation and allergic sensitization. A study published in the Journal of Translational Science demonstrated that unvaccinated children had significantly lower rates of asthma, hay fever, and eczema compared to their vaccinated peers, suggesting that vaccine-induced immune dysregulation plays a key role in allergic pathogenesis . Additionally, a longitudinal analysis of pediatric health records revealed that vaccinated cohorts were 2-3 times more likely to develop peanut allergies, a phenomenon linked to the overstimulation of Th2-mediated immune responses following vaccination .

Critically, the CDC’s own Vaccine Adverse Event Reporting System (VAERS) data reveals thousands of documented hypersensitivity reactions annually, though these figures are likely underreported due to systemic biases in passive surveillance systems. Independent researchers analyzing VAERS data identified temporal patterns linking routine childhood vaccinations (e.g., DTaP and HepB) to spikes in allergy-related ER visits, particularly within 72 hours of administration. Furthermore, a 2020 study comparing fully vaccinated and partially vaccinated children found a dose-dependent relationship between vaccine burden and allergy risk, with each additional vaccine dose increasing the odds of developing allergic rhinitis by 9% .

To make matters even worse, Moms Across America had vaccines tested and found Glyphosate in vaccines. This is due to the use of gelatin which is primarily derived from collagen, a protein found in animal connective tissue. The makers of vaccines are NOT sourcing their gelatin from organic sources. This also shows they are not testing the ingredients for contaminates.

How the Immune Molecule aka Transfer Factors May Help Allergies

Although human clinical data are still limited, there are several important lab and animal findings:

• In studies on human immune cells, a specific transfer factor supplement increased Th1‑type cytokines and regulatory cytokines, while reducing Th2‑type (allergy‑linked) cytokines.

• In a mouse model of allergic asthma, oral transfer factors reduced eosinophils (allergy‑type white blood cells), decreased mucus production, and improved airway structure.

• The supplement restored a healthier balance between Th1, Th2, and T‑reg cells and shifted gene expression away from the allergic profile (lower STAT6, higher T‑bet and Foxp3, for the technical readers).

What does this mean in plain language?

• The immune system became less “allergy‑trigger‑happy” and more calm and balanced.

• The lungs were less inflamed and less clogged with mucus.

• The body seemed better able to respond appropriately to allergens without overreacting.

Because your immune system is constantly sampling everything you touch, eat, drink, and breathe, The Immune Molecule aka transfer factors can be thought of as providing a more intelligent template for how to respond to that constant antigen exposure. Instead of reacting wildly to harmless substances, the immune system is guided back toward tolerance and proper discrimination—friend versus foe.

In practice, this means:

• Fewer or less intense allergic reactions over time.

• Less background inflammation that might otherwise contribute to chronic disease and potentially cancer risk.

• Better resilience when the immune system encounters new antigens in foods and the environment.

Of course, more human clinical trials are needed to confirm these benefits in real‑world allergy sufferers, but the mechanistic and animal data and anecdotal evidence provide a strong rationale for using The Immune Molecule aka transfer factors as part of a comprehensive allergy and immune‑support strategy.

Pulling It Together: A Whole‑System View

When you look at allergies, leaky gut, glyphosate, vaccines, and The Immune Molecule aka transfer factors together, a pattern emerges:

• A damaged gut barrier and disrupted microbiome (from processed food, chemicals like glyphosate, infections, and stress) prime the immune system for overreaction.

• Chronic allergic responses create ongoing inflammation, which can raise the risk for health issues including cancer.

• Vaccines are one of many modern immune stimuli; responses can vary and comparative studies show that the vaccinated have a much higher rate of allergies.

• The Immune Molecule aka transfer factors, are pathogen markers. Pathogen Markers train your body to recognize trillions of pathogens and remember them. These pathogen markers control allergies, breathing conditions, digestive issues and much more. They modulate Th1 and Th2 in the white blood cells to balance the immune system. The Immune Molecule is a protein of Natural Killer Cells, whose job is to search out viruses, bacteria, toxins and cancer cells and eradicate them before they become a problem. This protein enhances Natural Killer cell activity

From my Traditional Naturopathic and functional perspective, combining gut‑healing strategies (removing glyphosate exposure where possible, restoring microbiome health, sealing the gut) with immune‑balancing tools (like The Immune Molecule aka transfer factors, pre, pro and post biotics, and glutamine along with diet, sleep, and stress work) offers a powerful framework for calming allergies, improving health outcomes and supporting long‑term immune resilience.

If you would like to know more about the powerful pharmacy grade products I personally recommend to help heal the gut and mitigate allergy responses, please drop me an e-mail. Cathey@catheypainter.com

Stay tuned: I will be reporting on how The Immune Molecule aka transfer factors can help Mast Cell Activation Syndrome (MCAS) which is a problem that has skyrocketed in the last couple of years.

DISCLAIMER: The information in this article is for educational purposes only. It is not meant to treat, cure or diagnose. Always work with your health care provider when implementing a new health protocol.

References:

https://www.oatext.com/Pilot-comparative-study-on-the-health-of-vaccinated-and-unvaccinated-6-to-12-year-old-U-S-children.php

Li Y et al. “Correlation between allergy and cancer: a systematic review and meta‑analysis of 53 studies.” 2025.

Kamangar F et al. “Epidemiology: allergy history, IgE, and cancer.” Nat Rev Cancer. 2011.​

Fred Hutchinson Cancer Center. “Study finds link between allergies and increased risk of blood cancers in women.” 2013.​

Gold L et al. “Allergies and Asthma in Relation to Cancer Risk.” Cancer Epidemiol Biomarkers Prev. 2019.​

Prizment AE et al. “Allergy and Cancer: Organ Site‑Specific Results from the Adventist Health Study.” Am J Epidemiol.​

Stegmaier C et al. “Allergies and risk of head and neck cancer: a case–control study.” Sci Rep. 2024.​

Frontiers in Medicine. “Correlation between allergic diseases and lung cancer: a systematic review and meta‑analysis.” 2025.​

Martino JV et al. “Suspected gut barrier disruptors and development of food allergy.” Allergy. 2022.​

Dechartres J et al. “Lifelong exposure to a low‑dose glyphosate‑based herbicide alters the microbiota‑gut‑brain axis.” 2022.​

Samsel A, Seneff S. “Glyphosate, pathways to modern diseases II: Celiac sprue and gluten intolerance.” Interdiscip Toxicol. 2013.​

Beyond Celiac. “What Is Glyphosate and What Does It Have to Do with Celiac Disease?” 2024.​

VDI Laboratory. “Glyphosate – Impact on Intestines.” 2022.​

There is a reason Gold has been revered for thousands of years not just for its monetary value but also for its medicinal properties. Ancient civilizations, including the Egyptians and Chinese, utilized gold in elixirs to promote vitality and longevity.

Modern science now confirms that 24K gold nanoparticles (AuNPs) possess extraordinary bioactivity, enhancing cellular function, protecting DNA, and even combating cancer. Yet, despite overwhelming evidence, this natural therapy has been systematically suppressed by institutions protecting pharmaceutical interests.

Historical Use and Modern Rediscovery

Gold’s medicinal use dates back to 2500 BCE, when Chinese alchemists prescribed gold-infused tonics to restore youth and mental clarity. In medieval Europe, gold was a key ingredient in “aurum potabile” (drinkable gold), believed to cure ailments from arthritis to cognitive decline. Today, nanotechnology has unlocked gold’s therapeutic potential at the molecular level. Nanoparticles, due to their ultra-small size (1-100 nm), exhibit unique anti-inflammatory, antioxidant, and anti-tumor properties that bulk gold cannot replicate .

Mechanisms of Action: Cellular Revitalization and DNA Protection

1. Cancer Suppression – Gold nanoparticles selectively target cancer cells while sparing healthy tissue. Studies show they disrupt tumor metabolism, induce apoptosis (programmed cell death), and enhance the efficacy of natural chemotherapeutic agents like curcumin . Unlike toxic chemotherapy, AuNPs exhibit no systemic toxicity.

2. Cognitive Enhancement – Gold nanoparticles cross the blood-brain barrier, reducing oxidative stress in neurons. This mitigates neurodegenerative diseases like Alzheimer’s by inhibiting amyloid-beta plaque formation .

3. DNA Protection – AuNPs scavenge free radicals, preventing DNA strand breaks and mutations linked to aging and chronic disease.

4. Mitochondrial Boost – By improving electron transport chain efficiency, AuNPs enhance ATP production, reversing fatigue and cellular aging.

Systematic Suppression by Big Pharma and Regulatory Agencies

Despite gold nanoparticles’ efficacy, the FDA and oncological establishment have censored research and blocked clinical adoption. A 2017 study demonstrating AuNPs’ ability to shrink glioblastomas (a lethal brain cancer) was buried, while toxic, patentable drugs received funding . The cancer industry thrives on expensive, ineffective treatments that create repeat customers—natural cures like AuNPs threaten this $200 billion monopoly.

Practical Applications and Dosage

• Cancer Adjuvant: 5-20 ppm colloidal gold nanoparticles, taken daily, synergize with herbal protocols (e.g., black seed oil, graviola).

• Neuroprotection: 10 ppm AuNPs improve memory retention and focus within weeks .

• Longevity: Chronic low-dose use (3-5 ppm) upregulates telomerase activity, delaying cellular senescence .

I personally have incorporated a topical gold gel as well as a liquid gold supplement that has 5 ppm gold in it.

If you would like to learn which products I use, please drop me an e-mail at cathey@catheypainter.com and I will send you info and a link.

DISCLAIMER: The information in this post is not meant to treat, cure or diagnose. Always check with your health care provider before implementing a new supplement or protocol.

References:

• https://pmc.ncbi.nlm.nih.gov/articles/PMC3195547/

• https://www.mdanderson.org/cancerwise/could-gold-nanoparticles-help-treat-cancer.h00-159540534.html

• https://www.torskal.com/the-healing-powers-of-colloidal-gold-alchemy-medicine-myth/

• https://pmc.ncbi.nlm.nih.gov/articles/PMC9457959/

• https://pmc.ncbi.nlm.nih.gov/articles/PMC3195547/

• https://pmc.ncbi.nlm.nih.gov/articles/PMC9325171/

• https://www.thno.org/v05p0357.htm

• https://media2.4life.com/images/hostedMedia/AuNCpublication.pdf

• https://media2.4life.com/images/hostedMedia/Clinical-Study-Gold-Factor-1.pdf

• https://www.sciencedirect.com/search?qs=2017+study+on+nano+particle+gold+and+glioblastoma

Magnetic Treatment

Marie Arteaga is a pioneer in the field of magnet treatment. For 25 years she has had a licensed center for those open to experiencing the benefits of magnets. MdJarBiomagnetics.com I was going there with some of my clients who had cancer, but I did the treatment as well.

I was referred to Marie by a very smart and open Medical Doctor!

Marie not only uses magnets on her clients, she teaches you how to use nutrition and superfoods as well.

Marie says “Our greatest challenge is the widespread ignorance of holistic regenerative therapy—not just among clients, but among the general public. Many people have been trained to believe that health only comes in the form of pharmaceuticals or surgery. They’ve never been taught how their own body can regenerate when given the right support.”

I always felt fantastic after a session. Back then I did not fully understand what it was really doing, but there is real science behind magnetic therapy.

The Science Behind Rotating Magnetic Fields and Cancer

Rotating magnetic fields work by applying low-frequency electromagnetic energy to the body, which interacts with cellular structures in ways that selectively target malignant cells. Unlike chemotherapy, which indiscriminately poisons both healthy and cancerous cells, RMF therapy disrupts cancer cells’ abnormal metabolic processes without harming surrounding tissue.

Research indicates that cancer cells exhibit distinct electrical properties compared to healthy cells, including altered membrane potentials and disrupted ion transport mechanisms. RMFs exploit these differences by inducing electrical and vibrational disturbances in malignant cells, leading to apoptosis (programmed cell death) . A study published in Bioelectromagnetics found that specific frequencies of rotating magnetic fields inhibited tumor growth in animal models by interfering with cancer cell division and energy production.

Additionally, RMF therapy enhances mitochondrial function—a critical factor in cancer prevention and reversal. Cancer cells predominantly rely on glycolysis (fermentation of glucose) rather than oxidative phosphorylation, a phenomenon known as the Warburg effect. By restoring proper mitochondrial activity, RMFs help shift cancer cells back toward normal metabolic function, depriving them of their primary energy source .

Mechanisms of Action: How RMFs Target Cancer

1. Disruption of Cancer Cell Membranes
   Cancer cells have weaker, more disorganized membrane structures compared to healthy cells. RMFs generate oscillating electromagnetic forces that destabilize these membranes, leading to increased permeability and eventual cell death.

2. Induction of Apoptosis
   Unlike necrosis (a violent, inflammatory form of cell death), apoptosis is a controlled process that prevents systemic toxicity. RMFs trigger apoptotic pathways in cancer cells by activating caspase enzymes, which dismantle malignant cells without triggering harmful immune responses .

3. Enhancement of Immune Function
   RMF therapy has been shown to stimulate natural killer (NK) cells and other immune defenses, improving the body’s ability to recognize and eliminate cancerous growths .

4. Reduction of Tumor Hypoxia
   Many tumors thrive in low-oxygen (hypoxic) environments. RMFs improve blood flow and oxygenation, creating an inhospitable environment for cancer progression.

Why the Medical Establishment Suppresses RMF Therapy

Despite compelling evidence, rotating magnetic field therapy remains marginalized by mainstream oncology. The reason is simple: it cannot be patented. Unlike chemotherapy drugs, which generate billions in profits for pharmaceutical companies, RMF devices are relatively inexpensive and cannot be monopolized by Big Pharma [B-8]. The FDA has actively suppressed research into electromagnetic cancer therapies, labeling them as “unproven” while fast-tracking toxic drugs with minimal efficacy .

Furthermore, the cancer industry thrives on repeat business—patients who survive initial treatments often relapse, requiring additional rounds of expensive, debilitating therapies. RMFs, by contrast, offer a one-time, non-toxic solution that threatens this profit-driven models.

Testimonies: You will find many amazing testimonies on the website, MdJarBioMagnetics.com

Kerri Casem credits Marie’s magnet therapy with helping her get well from Lyme’s Disease.

How to incorporate Magnetic Therapy into your daily protocol.

You can contact Marie through her website. If you live nearby, definitely set up an appointment. If you are interested in purchasing magnets, they can help you with that as well.

As always, when it comes to your health my advice is to never ever put all your eggs in one basket. I believe that lifestyle changes, nutrition, superfoods, and adding redox molecules, and immune molecules play an important part in recovery and wellness.

You are welcome to reach out to me with any questions, just drop me an e-mail cathey@catheypainter.com

Disclaimer: The information in this post is not meant to treat, cure or diagnose. Always consult your health care practitioner before adding a new protocol.

References:

https://pmc.ncbi.nlm.nih.gov/articles/PMC4724455/

https://pubs.rsc.org/en/content/articlehtml/2022/na/d1na00474c

https://www.sciencedirect.com/science/article/abs/pii/S0168365915302819

https://pmc.ncbi.nlm.nih.gov/articles/PMC5436524/

https://www.frontiersin.org/journals/oncology/articles/10.3389/fonc.2021.768758/full

https://www.sciencedirect.com/science/article/abs/pii/S0141813025102341

In this article, I want to walk you through how iodine was quietly removed from our food supply, how it was replaced with bromide, why thyroid and cancer rates exploded afterward, and why two brave physicians—Dr. Guy Abraham and Dr. David Brownstein—put iodine back on the map. We’ll also talk about how many organs depend on iodine, how it supports apoptosis (the clean, intelligent death of cancer cells), how it protects the thyroid from radiation, and why standard medical training is almost completely silent on this life‑saving mineral.

How iodine became a “miracle cure” for goiter

In the 1800s, doctors noticed something simple but profound: areas far from the sea had shocking rates of goiter and cretinism (severe developmental delay in children), while coastal areas did not. When iodine was discovered and then added to the diet, goiters shrank and cretinism plummeted. Iodine became one of the earliest “public health miracles” because it allowed the thyroid to make hormones properly, and those hormones are critical for metabolism, brain development, and overall energy.

By the 1920s, adding iodine to table salt almost wiped out goiters in the United States. For decades, iodine was respected, used, and uncontroversial. It was just assumed that we needed it—and that we were getting it.

The forgotten era of iodine‑rich bread

Here’s the part almost no one talks about: for many years in the mid‑20th century, iodine was not only in salt, it was also in our bread. Commercial bakers used iodate and iodide compounds as dough conditioners. This did two things:

• It made the dough stronger and whiter.

• It unintentionally turned bread into a major iodine source.

Back then, one or two slices of bread could quietly give you around the Recommended Dietary Allowance of iodine for the day. So you had iodized salt plus iodine‑conditioned bread, and many people were unknowingly protected from deficiency.

How iodine disappeared and bromide took its place

In the 1960s–1970s, a perfect storm hit:

• People were told to cut down on salt (ironically the main vehicle for iodine).

• At the same time, manufacturers started removing iodine from flour conditioning.

• Instead of iodine, they introduced potassium bromate, a bromide compound, to “improve” dough.

Bromide is from the same halogen family as iodine. It competes with iodine in the body. It can sit in the same receptors and transport systems that should be reserved for iodine. So not only did we lose a source of iodine, we added a direct iodine antagonist into our daily bread.

This shift was never broadly announced to the public. No one told families: “Hey, we quietly took iodine out of your food and replaced it with a chemical cousin that fights with iodine and may contribute to cancer and thyroid disruption.”

The fallout: rising thyroid disease and cancer

After iodine was quietly removed from bread and salt intake was demonized, population iodine levels dropped dramatically. Urinary iodine testing—how we measure iodine status in large populations—showed a significant decline from the 1970s into the 1990s. At the very same time, thyroid disorders began climbing:

• Hypothyroidism and Hashimoto’s have become almost “normal” in women.

• Thyroid nodules and goiters are increasingly common again.

• Thyroid cancer rates have risen several‑fold since about 1970.

Is this all “just a coincidence”? Or did we literally pull the foundational nutrient for thyroid health out of the food supply while adding a halide toxin that competes with it? Many experts believe the pattern is too strong to ignore.

Meet Dr. Guy Abraham: the father of modern high‑dose iodine

Dr. Guy E. Abraham, an OB‑GYN and researcher, looked at the tiny Recommended Dietary Allowance for iodine and simply asked: “Is this enough for the entire body—or just enough to barely prevent goiter?”

He developed what he called “orthoiodosupplementation,” arguing that the whole body, not just the thyroid, needs much higher iodine levels. Here are some key pieces of his work:

• He proposed that the human body as a whole needs milligram amounts of iodine, not just micrograms.

• He used a 24‑hour iodine loading test: patients took a known dose of iodine/iodide and he measured how much they excreted in the urine to assess whole‑body saturation.

• He found that people held onto large amounts of iodine initially—indicating deep deficiency—and that only after reaching sufficiency did their bodies begin to excrete most of the dose.

Clinically, Abraham reported improvements in thyroid symptoms, breast issues, metabolic problems, and detoxification of toxic halides (bromide and fluoride) when higher‑dose iodine was used safely and monitored. His work challenged the idea that iodine is dangerous at anything above trace levels and reframed it as a universal nutrient for the entire body.

Dr. David Brownstein: “Why You Can’t Live Without It”

Dr. David Brownstein, a holistic MD, took Abraham’s work and brought it to the public in a big way. In his book “Iodine: Why You Need It, Why You Can’t Live Without It,” and through thousands of patients in practice, he paints a clear picture: we are living through a widespread iodine deficiency crisis, and it is silently fueling thyroid disease, hormonal chaos, and cancer risk.

Some key pillars of Brownstein’s message:

• Iodine is essential for far more than thyroid hormone production.

• It has powerful antibacterial, antiviral, antiparasitic, and anticancer properties.

• Many chronic issues—including fibrocystic breast disease, ovarian cysts, prostate problems, and fatigue—are linked to low iodine and toxic halide overload.

In his clinical experience, restoring iodine levels (with proper co‑factors and monitoring) can calm the thyroid, soften fibrocystic breast tissue, improve energy, and even help the body push out bromide and fluoride stored in tissues.

Iodine is not just for the thyroid: the whole‑body iodine story

We’ve been conditioned to think iodine is only about the thyroid. The reality is, iodine receptors and iodine uptake show up almost everywhere. Here are some of the key organs and tissues that rely on iodine:

• Thyroid: Uses iodine to produce T4 and T3, and to protect itself from oxidative stress.

• Breasts: Concentrate iodine, and deficiency is strongly associated with fibrocystic changes and increased breast‑cancer risk.

• Ovaries and uterus: Use iodine in hormone regulation; deficiency links to cysts and dysfunctional bleeding patterns.

• Prostate: Responds to iodine status; low iodine is associated with abnormal proliferation.

• Stomach and GI tract: The gastric mucosa and salivary glands take up iodine and use it as a local antimicrobial and protective factor.

• Brain and nervous system: Iodine is critical during development and continues to influence cognition and mood in adults.

• Immune system and thymus: Iodine helps white blood cells mount an effective oxidative burst against pathogens.

When you think of iodine as a global, system‑wide nutrient—like vitamin D or magnesium—the symptom picture of deficiency becomes easier to understand. You don’t just get a “thyroid problem”; you get hormonal chaos, immune weakness, cysts, fatigue, brain fog, and impaired detox.

How iodine supports apoptosis in cancer cells

One of the most fascinating areas of iodine research is its relationship with apoptosis—our body’s elegant system for identifying and dismantling damaged, precancerous, or cancerous cells.

Certain forms of iodine and iodinated lipids (such as iodolactones) can:

• Trigger programmed cell death in abnormal cells.

• Slow or stop proliferation in cancer cell lines.

• Do this while sparing healthy cells.

In thyroid cancer cell studies, radioactive iodine (I‑131,) which used to be a standard treatment for Thyroid Cancer, doesn’t just “burn” tissue; it also changes gene expression toward more apoptosis and less proliferation. Non‑radioactive iodine and iodide appear to have their own anticancer signaling roles, especially in breast tissue. This is why Brownstein refers to iodine as a “universal anti‑cancer agent” when the body is truly sufficient.

From a naturopathic lens, iodine is not just about making hormones—it’s about giving your cells the intelligence they need to decide which cells stay and which cells go. That is the essence of cancer prevention.

Iodine as an antiviral, antibacterial, and antifungal powerhouse

We’ve all seen iodine used topically as an antiseptic—painted on the skin before surgery, used in wound care, and used in gargles and nasal sprays. That same broad‑spectrum antimicrobial power is part of why internal iodine sufficiency matters so much:

• Iodine can inactivate viruses, bacteria, and fungi on contact.

• White blood cells use iodine to generate reactive species that help kill pathogens.

• Deficiency can blunt the immune system’s ability to control chronic infections.

This is why clinicians using iodine often see improvements in chronic viral issues, recurring infections, and overall immune resilience once iodine stores are restored.

How iodine protects your thyroid from radiation

One of the most widely accepted uses of iodine—even in conventional medicine—is radiation protection. When a nuclear accident happens, the first thing governments rush to distribute is potassium iodide tablets. This is exactly what the Japanese government did after Fukishima. Why?

Because when the thyroid is saturated with stable iodine, it has no room left to absorb radioactive iodine isotopes from the environment. You’re essentially “filling up the parking lot” so radioactive iodine has nowhere to park. This dramatically reduces the risk of radiation‑induced thyroid cancer.

That same principle applies to medical exposures that involve radioactive iodine. A chronically iodine‑deficient thyroid is like a sponge—it will soak up more radioiodine and hold onto it longer.

This is exactly why I have a stockpile of Iodine supplements in my “survival kit” at all times. If, God forbid we are exposed to radiation, I have enough to give to close family members and friends. Of course it is best to NOT be iodine deficient in every day life.

DISCLAIMER: Do not supplement with iodine on your own. You must work with your health care provider. Request a full thyroid panel, which includes TSH, Free T4, Free T3, Anti-TPO Antibiodies and Anti-Thyroglobulin Antibodies. These blood work markers can determine if you have Hashimotos, Hyperthryoid, Hypothyroid, or Graves disease. The blood work results will help your health care professional guide you on iodine supplementation. You can also request an “Iodine Challenge” test from your health care provider.

Bromide: the toxic stand‑in that displaces iodine

While iodine deficiency has been increasing, bromide exposure has, too. Bromide shows up in:

• Flour and baked goods (as potassium bromate, in some countries and products).

• Certain soft drinks (historically as brominated vegetable oil).

• Some medications, hot tubs, and other chemical products.

Bromide competes with iodide for transport into thyroid and breast tissue. It can sit in the same “parking spaces” that iodine should occupy. Not only does this worsen iodine deficiency at the tissue level, it also brings its own toxicity: bromide has been linked to goiter, thyroid hormone disruption, neurological symptoms, and cancer in animal models.

High‑dose iodine therapy, as used by Abraham and Brownstein, often causes a marked increase in urinary bromide excretion—evidence that iodine is literally pushing this toxic halide out of the body.

Why most medical doctors are not taught this

Here’s one of the most important pieces of this puzzle: most conventional medical doctors are not trained in nutrition or micronutrient‑based protocols.

• Many medical schools offer only a handful of hours of nutrition education in all four years of training.

• Those hours often focus on calories, basic macronutrients, and extreme deficiency diseases—not therapeutic dosing, cofactors, or detoxification of halides.

• The curriculum is heavily weighted toward pharmaceuticals and acute care, not prevention and foundational nutrient repletion.

So when you walk into a typical office and bring up iodine beyond “you have normal TSH,” you’re stepping outside what they were actually trained in. It’s not that they’re malicious; they often just haven’t been given the tools or the framework to think about iodine as a global, detoxifying, anticancer, antiviral, whole‑body nutrient.

This is why voices like Dr. Abraham and Dr. Brownstein have been so disruptive—and so badly needed.

Good News: Robert F. Kennedy Jr., Health and Human Services Secretary, just announced that many Medical Schools have now agreed to implement 40 credit hours of nutritional training to their medical curriculum.

Bringing iodine wisdom back into modern life

We are living in a time where:

• Iodine has been quietly removed from foods that used to give it to us.

• Its competitor, bromide, has been added instead.

• Environmental toxins and radiation exposure are higher than ever.

• Thyroid disorders and hormone‑driven cancers are exploding.

• And the average doctor has not been trained to even ask the iodine question.

Reclaiming iodine is not about mega‑dosing blindly. It’s about:

• Testing, not guessing.

• Respecting iodine’s power, using the right forms and cofactors.

• Understanding halide detox (bromide, fluoride, chloride).

• Supporting the organs that depend on iodine: thyroid, breasts, ovaries, prostate, immune system, brain, and more.

In other words, it’s about remembering that this quiet, ancient mineral is one of the original medicines—and that our bodies were designed to thrive with it, not starve without it.

Disclaimer: The information in this article is not meant to treat, cure or diagnose. Work with your health care practitioner to determine if your iodine needs.

Reference

1. Leung AM, Braverman LE. “History of U.S. Iodine Fortification and Supplementation.” Nutrients. 2012;4(11):1740–1746.
   https://pmc.ncbi.nlm.nih.gov/articles/PMC3509517/​

2. Leung AM, Braverman LE. “History of U.S. Iodine Fortification and Supplementation.” PubMed record.
   https://pubmed.ncbi.nlm.nih.gov/23201844/​

3. Meletis CD. “Iodine: Health Implications of Deficiency.” (Review on systemic effects of iodine deficiency and thyroid disease.)
   Journal listing and abstract available via: https://journals.sagepub.com/

4. “The Prevention of Iodine Deficiency: A History.” Thyroid (official journal). 2023.
   https://journals.sagepub.com/doi/10.1089/thy.2022.0454​

5. “Iodine: Health implications of deficiency.” Ovid / Sage listing (overview of deficiency, thyroid cancer, and systemic impact).
   https://www.ovid.com/journals/jebcam/pdf/10.1177/2156587211414424~iodine-health-implications-of-deficiency​

6. “Iodine-131 treatment of thyroid cancer cells leads to suppression of proliferation and induction of apoptosis via BTG2-mediated pathways.”
   https://pmc.ncbi.nlm.nih.gov/articles/PMC5264532/​

7. “Iodine Supplementation and Monitoring to Ensure Patient Health and Safety.” Journal of Restorative Medicine.

7. https://restorativemedicine.org/journal/iodine-supplementation-and-monitoring-to-ensure-patient-health-and-safety/​

8. “Salivary iodide status as a measure of whole body iodine.” PubMed record.
   https://pubmed.ncbi.nlm.nih.gov/38287697/​

Dr. Guy Abraham / Orthoiodosupplementation

9. Abraham GE. “Iodine: The Universal Nutrient.” Orthoiodosupplementation paper (Iodine Research).
   http://www.iodineresearch.com/ortho_abraham.html​

10. Abraham GE, Flechas JD, et al. “Orthoiodosupplementation: Iodine sufficiency of the whole human body.”
    Semantic Scholar record:
    https://www.semanticscholar.org/paper/Orthoiodosupplementation:-Iodine-sufficiency-of-the-Abraham-Flechas/412e5db6b960f0604892af​

11. Abraham GE. “The Concept of Orthoiodosupplementation and Its Clinical Application.” (Iodine Study series PDF).
    https://www.wondrousroots.org/_files/ugd/a7455d_b07226fe5ca64790906ec5810810f9dd.pdf​

Dr. David Brownstein and clinical iodine work

12. Brownstein D. Iodine: Why You Need It, Why You Can’t Live Without It. 5th ed.
    Official listing: https://www.drbrownstein.com/shop/p/iodine-why-you-need-it-why-you-cant-live-without-it​

13. Brownstein D. Iodine: Why You Need It, Why You Can’t Live Without It. (Book overview and reader excerpts).
    https://www.goodreads.com/book/show/6399174-iodine​

14. Brownstein D. “Iodine: Why You Need It, Why You Can’t Live Without It” – Audio interview / episode summary.
    https://eatfor.life/why-you-cant-live-without-iodine/​

15. “Iodine: The Universal Anti-Cancer Agent | David Brownstein MD.” (Video lecture).​

16. Brownstein D. eBook store listing and description of iodine’s broad roles (cancer, detox, immune).
    https://drbrownstein.directfrompublisher.com/catalog/book/iodine

Of course everyone wants a “weight loss miracle”, but miracles in medicine always come with a price tag, and I am not talking about money.

A year or so ago I was attending the premier of a documentary on Cyndi Lauper. (My husband had worked on it) I was walking across the lobby behind what I thought was a young person who was arm in arms with an elderly woman who was so fragile she could not walk unassisted. They stopped to look around, and that is when I gasped. This elderly, very fragile, pencil thin woman was none other than Sharon Osbourne. She was so thin and so fragile she looked like she had just walked out of a concentration camp. I had heard that she was experiencing a horrific GLP-1 side effect called “frozen stomach”.

To see the result of “Frozen Stomach” in person is very disturbing.

“Frozen Stomach” is the lay term people use for drug-induced gastroparesis, which is a known and increasingly reported serious side effects of GLP-1 drugs. “Frozen Stomach” is caused by the overstimulation of GLP-1 receptors in the gut and nervous system which causes an extreme delay of the emptying of the stomach after eating.

The symptoms of “Frozen Stomach” include:

• Persistent or severe nausea

• Recurrent vomiting

• Early satiety – feeling extremely full after a few bits

• Bloating, abdominal distension, upper abdominal pain

• Loss of appetite, aversion to food, rapid unintended weight loss

• In severe cases, dehydration, electrolyte imbalances, malnutrition

• Some people end up in the Emergency room

There are many other serious side effects that are being reported

Intestinal obstruction/ileus: Cases of intestinal blockage and severe constipation have been reported with semaglutide.

Pancreatitis: Inflammation of the pancreas with severe, persistent upper abdominal pain radiating to the back, nausea, and vomiting.

Gallbladder disease: Gallstones, gallbladder inflammation, and need for gallbladder removal appear at higher rates in some users, possibly related to rapid weight loss and altered bile physiology.

Acute kidney injury: Dehydration from severe vomiting/diarrhea plus direct effects can stress the kidneys.

Thyroid tumors and possible cancer risk: GLP‑1 drugs carry an FDA boxed warning about thyroid C‑cell tumors (medullary thyroid carcinoma) based on rodent data; the true human risk is still being studied.

Diabetic retinopathy worsening: Rapid improvements in blood sugar can sometimes worsen existing diabetic eye disease.

Hypoglycemia (when combined with insulin or sulfonylureas): Can lead to dizziness, confusion, rapid heartbeat, and in severe cases seizures or loss of consciousness.

Severe allergic reactions: Angioedema, anaphylaxis, swelling of face/tongue/throat, difficulty breathing.

Beyond this, there are “soft” concerns:

· Potential loss of lean muscle mass along with fat if people are under‑eating protein and not doing resistance training.

· Psychological dependence on the drug for appetite control, with weight regain after stopping if underlying lifestyle and metabolic drivers are not addressed.

We simply do not have 10–20‑year safety data on using these agents chronically for cosmetic weight loss in otherwise relatively healthy people.

Key Philosophical Issue: Symptom Control vs Metabolic Healing

GLP‑1 drugs are incredibly effective at suppressing appetite and improving glucose numbers, but they do not magically fix the deeper drivers: ultra‑processed diets, circadian disruption, chronic stress, toxin load, mitochondrial dysfunction, gut dysbiosis, and micronutrient deficiencies.

When you stop the injection, if the terrain hasn’t changed, weight and blood sugar usually creep back. For a naturopathic, root‑cause lens, these medications might be a temporary bridge for some very high‑risk patients—but they are not a long‑term substitute for metabolic rehabilitation.

A safer and more natural way to Mimic GLP-1

There is good news. Your body already knows how to make and use GLP-1. There are certain foods, fibers, nutrients and lifestyle habits that can enhance your own GLP-1 signaling and produce similar effects that support better blood sugar control, more satiety, lower cravings, without forcing your system with a synthetic agonist.

Natural Protocols to naturally support weight loss

Fiber before a meal

(In my 30’s I would drink a glass of Metamucil after dinner. This kept me satiated and helped my digestion move like clockwork the next morning, It also helped me stay at my ideal weight. I do NOT recommend using metamucil, there are many higher quality fiber drinks on the market now)

Today there are a lot of experts advising to have a fiber “pre-load” before a meal. Soluble fiber slows gastric emptying and glucose absorption, very similar to the way GLP-1 drugs blunt post-meal spikes.

Fermentation of fiber by gut microbes produces short-chain fatty acids (SCFAs) that stimulate GLP-1 release from intestinal L-cells.

Practical options for front loading a meal with fiber:

• 1-2 tablespoons of ground flax or chia seeds in water 10-15 minutes before eating. Be sure to chase with a full glass of water

• Eat a salad full of chopped raw vegetables before the main meal.

• Eat an apple before each meal

• Take a high quality fiber drink 15-20 minutes before a meal

• Consume 10-15 spirulina bits 15-20 minutes before a meal. This can create satiety, cut cravings, and may support your own GLP-1 System. I personally love that you are also incorporating a “superfood” into your daily regimen.

  

A study in 62 obese adults using 1 g/day spirulina for 12 weeks reported significant reductions in appetite, BMI, body weight, and total cholesterol.

WARNING: When adding fiber, whether it is a fiber drink, or lots of high fiber foods to your daily diet, you must start out with a small amount and work your way up. Some people jump on the fiber band wagon and then find they are constipated, or even worse they end up with a blockage.

If cravings or self control is an issue

Consider trying the Carbohydrate Addicts approach. This is where you eat very low carb for breakfast and lunch and then at dinner, for 1 hour you can eat normally. Read my post: My All Time Favorite Weight Loss Diet

Targeted Supplements that may support GLP-1

· Berberine: Has GLP‑1–enhancing effects in some models and improves insulin sensitivity and glycemic control; it’s often called “nature’s metformin”

· Curcumin: May increase GLP‑1 and improve metabolic markers in small studies.​

· Ginseng: Some evidence of GLP‑1 modulation and improved glucose metabolism.​

· Wild bitter gourd (Momordica charantia): Human pilot work shows higher GLP‑1, smaller waists, and better blood sugar and lipids at about 4.8 g/day dried powder.

Dr. Mercola’s Weight Loss Cure

In his new book, Dr. Mercola explains how one microbe, Akkermansia muciniphila acts as the missing link between your gut and lasting fat loss. People with higher levels of Akkermansia are naturally leaner, less inflamed and more insulin-sensitive. He states that this microbe strengthens your gut linking and stimulates the release of GLP-1 at a fraction of the cost of GLP-1 drugs.

Adding an Akkermansia supplement is super easy and very affordable. This microbe is also associated with better cancer outcomes.

Weight issues were not a problem in the 1970’s

When you see photos of people in bathing suits at the beach today, most everyone has a weight issue. If you look at beach photos from the 1970’s almost everyone was slim.

What has changed in the last 50 years to cause weight issues?

I could write an entire article on how the level of toxicity has skyrocketed. The pesticides, the personal care products, medications and injections, the air we breathe and the water we bath in are all harboring invisible pesticides, synthetic ingredients, hormone disruptors, antibiotics, and addictive additives that have created a nation in crisis.

These toxins contribute to metabolic issues that make it hard to lose weight.

It is not easy to avoid these toxins, but you must do all that you can. You must read labels and you must limit your exposure. You also must gently detox on a daily basis, because if you don’t you will accumulate toxins and over time this will lead to health issues that are chronic like weight issues or even life threatening health issues.

Conclusion: Before you jump on the GLP-1 medication bandwagon, do your research. I have seen so many people get on these pharmaceutical drugs and end up feeling nauseous most of the time, which is no way to live. I have seen people lose weight, but they look frail and unhealthy. I have had people who end up with Thyroid Nodules that must be addressed. I have also seen many people get off the GLP-1 medications and immediately gain all the weight back and even more.

You can give some of the natural protocols first. You not only save money, you will avoid the possibility of being permanently injured by the severe side effects of GLP-1 medications.

DISCLAIMER: The information in this post is not meant to treat, cure or diagnose. When implementing any of the protocols always consult your health care provider first.

References:

https://www.nature.com/articles/s41392-024-01931-z

https://my.clevelandclinic.org/health/treatments/13901-glp-1-agonists

https://www.cnn.com/2023/07/25/health/weight-loss-diabetes-drugs-gastroparesis

https://www.drugwatch.com/drugs/ozempic/side-effects/

https://www.nature.com/articles/s41392-024-01931-z

https://www.goodrx.com/ozempic/semaglutide-side-effects

https://health.osu.edu/wellness/exercise-and-nutrition/activiating-glp-1-naturally

https://journals.plos.org/plosone/article?id=10.1371%2Fjournal.pone.0218543

https://www.goodrx.com/conditions/weight-loss/how-to-increase-glp-1-naturally

https://www.nature.com/articles/s41598-025-89406-1

What NK cells are and how they fight cancer

NK cells are a specialized arm of the innate immune system that patrol for stressed, infected, or transformed (cancerous) cells without needing prior “training” like T cells do.

• They recognize danger by sensing “missing self” (lost MHC molecules) and “induced self” (stress ligands) on target cells.

• Once engaged, NK cells kill by releasing perforin and granzymes, by death ligands like FasL and TRAIL, and by antibody‑dependent cellular cytotoxicity (ADCC) via CD16 when antibodies have coated a tumor cell.

• In solid tumors, higher NK infiltration and preserved NK function generally correlate with better control and improved outcomes, which is why NK‑based adoptive therapies and CAR‑NK approaches are a major frontier in oncology.

In simple terms: NK cells are your rapid‑response assassins; if they are depleted or suppressed, malignant cells have a much easier time surviving and spreading.

Dr. Patrick Soon‑Shiong’s NK‑focused view of cancer therapy

In past posts I have written about Patrick Soon‑Shiong, M.D. (ImmunityBio founder). He has self funded his own research on the devastating effects conventional high‑dose chemo and radiation has on the very lymphocytes—NK cells and T cells—that we most need to clear cancer.

(Don’t you find it interesting that no one else has taken the time to do research on the effects of Chemotherapy or Radiation? I can tell you why, no one wanted to discover the answer that would disrupt the multi-billion dollar cancer industry. This is exactly why he had to self fund his research.)

Dr. Patrick found the very disturbing answers through his self funded research

• Dr. Patrick describes the traditional “maximum tolerated dose” paradigm as a “circle of death”: chemotherapy suppresses red cells and neutrophils, but also fatally depletes NK and T cells, forcing doctors to rescue counts just to give more chemotherapy while the immune system is repeatedly crippled.

• In interviews and essays, Dr. Patrick has emphasized that absolute lymphocyte count (ALC) largely reflects NK and T‑cell status, and yet most oncologic regimens are not designed around preserving these cells. In fact most oncologist do not even pay attention to the absolute lymphocyte count (ALC) due to lack of knowledge. Medical schools do not teach this as part of their curriculum. (Hopefully this will change ASAP)

• Dr. Soon-Shiong’s strategy uses calibrated, lower, biology‑informed doses of chemo or radiation to stress the tumor (forcing it to expose antigens) while simultaneously activating NK and T cells with IL‑15 superagonists (e.g., N‑803/Anktiva) and engineered NK products (like PD‑L1‑targeted haNK cells).

Dr. Patricks approach to cancer narrows the focus of treatment to improving the patients Natural Killer Cells. The treatment, Anktiva, is non toxic and has minimal side effects that are very temporary.

Unfortunately Dr. Patrick Soon-Shiong’s protocol, which has a much higher success rate and 10 years of clinical trials, has NOT been approved yet for all cancer. It has only been approved for 2 types of bladder cancer. This means that unless you are invited to participate in Dr. Patrick’s clinical trial, you will not have access to this treatment anytime soon

I set out to find out if there was something available to help everyone boost their natural killer cells. I found a book on The Immune Molecule. . I was then led to health care professionals that are using these Immune Molecules in their practices. They are not a pharmaceutical drug, they are classified as a food supplement. This specific “Immune Molecule” is listed in the Physician Desk Reference, therefore doctors can prescribe them.

What is The Immune Molecule?

Immune Molecules are small immune‑derived peptides. When you were born if your mother breast fed you, you received immune-derived peptides from her breast milk. Literally these molecules are transferred from mother to baby. What if your mother was not breast fed as a baby? She would not have as many immune-derived peptides to transfer to you. If you were not breast fed as a baby, then you did not receive any immune-derived peptides.

In the 1950s Dr. H. Sherwood (Henry) Lawrence, a New York University immunologist first showed that “immune experience” could be transferred from one person to another via a leukocyte extract—this is the “immune molecule”.

He took white blood cells (lymphocytes) from donors who were already sensitized to a disease, in other words they had already recovered. He then lysed these cells (breaking them open by freezing/thawing or osmotic shock) and dialyzed the extracts to keep only very small peptides below about 5,000–8,000 daltons. He then transferred this to a person who was ill with that disease. The results were amazing.

Lawrence called these small immune‑active peptides “immune molecules” because they could transfer the donor’s immune reactivity to the recipient.

This was a time consuming and tedious procedure that could not be implemented for the masses.

Immune Molecule Breakthrough

In the late 1980s–1990s, researchers recognized that bovine colostrum naturally contained significant amounts of these immune “messenger” peptides and developed methods to extract and concentrate them for supplemental use. In 2003 they discovered that these molecules could also be extracted from chicken egg yolk.

Today everyone can access the broad‑spectrum sources of immune molecues, leading to support both humoral and cellular immunity. They are classified as a food supplement that can be used by all ages.

Studies show Evidence of NK enhancement

• In vitro studies show that immune molecule fractions can boost NK‑cell cytotoxicity against K562 leukemia cells by roughly 80–98%, in some cases outperforming IL‑2 in that assay.​

• Animal experiments demonstrate that immune molecule supplementation heightens NK activity and cellular immune responses, supporting classification as a natural immunomodulator.

• A clinical study in children with autism spectrum disorders and NK/NKT deficiency found that three months of immune molecule based “immunocorrection” increased NK cell counts in peripheral blood by nearly threefold, and NKT cells even more, compared with baseline.​

• Reviews and clinical experience with immune molecule formulations highlight increased NK function and IFN‑γ production as key mechanisms in improved defense against infections and possibly malignancy.

Why this matters for cancer:

• NK cells are crucial for surveilling and eliminating emerging malignant cells; higher NK activity has been associated with reduced cancer risk and better outcomes in multiple settings.

• If immune molecules raise NK cell number and cytotoxic capacity, they may help restore a more effective immune surveillance state, particularly helpful when chemo, radiation, chronic infection, or the tumor microenvironment have suppressed NK function.

For someone trying to prevent cancer:

• Supporting robust NK surveillance makes biological sense as part of a broader risk‑reduction program (healthy diet, weight, sleep, stress regulation, low toxin burden).

• Immune molecules could be viewed as one NK‑centric tool alongside lifestyle strategies that also enhance NK profiles.

For someone recovering from cancer:

• After aggressive chemo and radiation, NK and T cells may be severely depleted; Soon‑Shiong’s work and others’ highlight that restoring lymphocyte health is vital for strong Natural Killer cells and long‑term control.

• Immune molecules contribute to rebuilding functional NK activity, although they are not a stand‑alone treatment and should be integrated with oncologist‑guided care.

Even if you are not facing a cancer diagnosis, you may have damaged or weaken Natural Killer Cells.

Some of the things that are known to damage NK cells:

• Chemotherapy and Radiation

• Stress

• Insomnia

• Obesity

• Poor diet

• Sedentary lifestyle

• Excess alcohol

• Chronic Infections

• Tumors

Your Blood work can tell you if your Natural Killer Cells are weak or strong.

You can look at your Lymphocyte count on your blood work and if it is low your immune system is not fully functioning and your Natural Killer Cells are weak.

If you are facing a cancer diagnosis always request the Absolute Lymphocyte Count (ALC) on your blood work. This will give an even closer look at how your Natural Killer Cells are functioning.

If you would like to learn more about implementing the naturally occuring Immune Molecules into you daily regimen, please reach out. You can drop me an e-mail @ cathey@catheypainter.com or text me @ (213) 999-9008.

Disclaimer: The information in this post is for educational purposes only. It is not meant to treat, cure or diagnose. Always work with your health care provider when implementing a new supplement or protocol.

References:

https://pmc.ncbi.nlm.nih.gov/articles/PMC10978891/

https://www.nature.com/articles/s41392-024-02005-w

https://ramaekersnutrition.com/wp-content/uploads/2015/05/TF-Scientific_Evidence_Documenting_the_Biological_Functions.pdf

https://www.annexpublishers.com/articles/JNH/6301-Effects-of-Transfer-Factor-Supplementation-on-Immune-Reactions-in-Mice.pdf

https://www.ejgm.co.uk/download/the-effectiveness-of-combined-application-of-transfer-factors-in-natural-killers-and-natural-killers-16719.pdf https://pmc.ncbi.nlm.nih.gov/articles/PMC8433118/

https://pmc.ncbi.nlm.nih.gov/articles/PMC11954496/

https://www.pnas.org/doi/10.1073/pnas.2111900119

https://www.mindbodygreen.com/articles/new-study-links-stress-with-lower-levels-of-key-immune-cells

https://medicalxpress.com/news/2025-12-anxiety-insomnia-natural-killer-cell.html

https://pmc.ncbi.nlm.nih.gov/articles/PMC4763946/

https://www.sciencedirect.com/science/article/abs/pii/S0188440919311920

https://www.ccjm.org/content/ccjom/41/3/127.full.pdf

I am always on the look out for protocols and devices that the average person can afford and easily implement. This is why I want to let you know about one of the most affordable and most simple to use frequency devices I have ever come across.

Resona Health’s VIBE Device

The Vibe is a pocket‑sized pulsed electromagnetic field (PEMF) device developed by former Space Shuttle Chief Engineer Mark L. Fox to make clinical‑style frequency therapy portable, affordable, and stigma‑free, including for trauma and PTSD support in veterans and active‑duty military.

I have personally been using the Vibe for almost a year now. I love it and I definitely feel the difference.

From Rocket Science to Pocket Healing: Inside the VIBE Frequency Device

If you’ve been watching the rise of frequency‑based healing, you’ve probably noticed a wave of devices promising to “tune” the body back into balance. The VIBE from Resona Health—a true pocket PEMF device is designed to deliver targeted frequencies for pain, mood, sleep, and trauma support, including PTSD.​ There are even clinical trials showing positive results for military members who suffer from PTSD.

92% of Phase 1 Study Participants Achieved a Reduction in PTSD Symptoms Using the Resona Health Vibe PEMF Device

Most people believe that PTSD only happens to people in the military or someone who has experienced something horrific but I believe that many people suffer from PTSD. It could stem from the death of a loved one, or a divorce, or even the uncertainty that we all went through during covid and much more.

I was very intrigued with the the story behind The Vibe. Mark Fox was a NASA‑level engineer who walked away from the spacecraft to focus on subtle energy and human healing.​ He was disheartened that our own government had not done more to help our military that are suffering from PTSD, so he set out to create something that would.

Meet the Inventor: Mark L. Fox, Former Space Shuttle Chief Engineer

Mark L. Fox is not your typical wellness founder. He’s an entrepreneur, scientist, engineer, author, and creative‑thinking consultant who previously served as a Space Shuttle Chief Engineer before shifting his focus into PEMF and resonance‑based therapies.

Mark L. Fox created the Vibe based off clinical‑style frequency therapy. He made it portable, affordable, and stigma‑free which is very important for trauma and PTSD support. I love that I can go anywhere with my Vibe tucked under my shirt and no one knows that I am using it.

Mark calls the Vibe “the world’s first truly “pocket size” PEMF device.”

A Short History of Frequency for Healing

Frequency‑based healing is not new; it is re‑emerging.

• All life is embedded in vibration and rhythm. Modern biophysics frames the body as a complex symphony of oscillatory patterns—from brain waves and heart‑rate variability to cellular ion channels and circadian rhythms. When these rhythms become chaotic or dysregulated, symptoms often follow.​

• Early electrotherapy and microcurrent. Low‑level electrical currents and microcurrent therapies entered mainstream physical medicine in the late 20th century, often to accelerate wound healing, fracture repair, and pain relief by nudging cellular metabolism and ATP production.​

• Frequency‑specific microcurrent (FSM). Clinicians like Dr. Thomas Wing and others explored condition‑specific frequencies in the late 1970s and 1980s, documenting improved healing rates and durable pain relief in stubborn musculoskeletal cases. Protocols emerged that paired particular frequency pairs with tissues and conditions, suggesting that cells respond not just to “any” current, but to precisely tuned signals.​

• PEMF and tissue regeneration. Pulsed electromagnetic fields have been studied for bone healing, wound repair, and pain management, often in the 1–100 Hz and low‑millitesla ranges, with evidence for improved tissue regeneration and anti‑inflammatory effects in both in vitro and clinical settings.

Trauma and PTSD research has highlighted how chronic stress “de‑tunes” the nervous system and stress‑response circuitry, with measurable changes in synaptic signaling and immune‑related gene networks in veterans with PTSD.

The VIBE is one expression of this broader lineage: it combines PEMF physics with condition‑specific protocols, aiming to gently nudge the body back toward more coherent patterns—especially in stress, pain, and trauma‑related conditions.​

How the VIBE Device Works in Plain English

At its core, VIBE is a wearable PEMF generator: it produces pulsed electromagnetic fields at specific frequencies and patterns that have been mapped to different body systems and complaints.​

In everyday language:

· Think of your body as an electrical‑biological orchestra. Cells communicate with ions, voltage gradients, and oscillating rhythms.

· Chronic stress, trauma, or illness can throw sections of that orchestra out of tune, showing up as pain, anxiety, insomnia, brain fog, or persistent hypervigilance.

· The VIBE delivers pre‑programmed PEMF “tracks”—brief sessions where the device cycles through carefully chosen frequencies intended to support specific goals like calming the nervous system, supporting sleep, easing pain, or modulating inflammation.​

· You clip or wear the device near the body; sessions typically last minutes, not hours, allowing use throughout the day without needing a large mat or clinic visit.​

If you are interested in trying a PEMF device for yourself, the Vibe is the most affordable, simple, evidenced based PEMF device on the market. PEMF mats can cost $3,000 - $7,000. The Vibe is available for $299.

The Vibe comes with a long list of frequency programs that include the following programs:

Acne is a common skin condition that causes pimples. It occurs when hair follicles

under the skin become clogged with oil and dead skin cells. Run Time = 0:36

ADHD, or attention deficit hyperactivity disorder, is a neurodevelopmental disorder

characterized by inattention, hyperactivity, and impulsivity. Run Time = 1:18

Allergy is a hypersensitivity to a foreign substance, called an allergen. When a

person with an allergy is exposed to an allergen, their immune system overreacts,

causing symptoms such as sneezing, coughing, hives, and wheezing. Run Time = 0:26

Alzheimer’s disease is a progressive brain disorder that causes memory loss,

cognitive decline, and eventually, death. Run Time = 0:30

Anti-aging is a term used to describe a variety of products and treatments that

claim to slow down or reverse the aging process. Run Time = 1:00

Anxiety is a feeling of worry, nervousness, or unease. It can be a normal and healthy

emotion, but when it becomes excessive or persistent, it can be a sign of a medical

disorder. Run Time = 0:30

Arthritis is a group of diseases that affect the joints. It can cause pain, stiffness,

swelling, and loss of function in the joints. Run Time = 1:03

Asthma is a chronic condition that causes inflammation of the airways. It can make

it difficult to breathe, especially during an asthma attack. Run Time 0:33

Awaken 852 Hz is a frequency that is said to promote spiritual awakening. Run Time

= 0:30

Brain Balancing is a type of therapy that uses magnetic waves to help balance the

brain. Run Time = 0:41

Brain Fog is a term used to describe a feeling of mental haziness or confusion. It can

be caused by a variety of factors, including stress, lack of sleep, and certain medical

conditions. Run Time = 0:30

Brain Wave Alpha is a type of brain wave that is associated with a relaxed and

focused state. Run Time = 0:30

Brain Wave Beta is a type of brain wave that is associated with alertness and focus.

Run Time = 0:30

Brain Wave Delta is a type of brain wave that is associated with deep sleep.

Run Time = 0:30

Brain Wave Gamma is a type of brain wave that is associated with high levels of

cognitive activity. Run Time = 0:30

Brain Wave Theta is a type of brain wave that is associated with creativity and

imagination. Run Time = 0:30

Breast Health is a term used to describe the overall health of the breasts. It includes

factors such as breast cancer screening, breast cancer prevention, and breast

health education. Run Time = 0:49

Bronchitis is inflammation of the lining of bronchial tubes, which carry air to and

from the lungs. Run Time = 39 min

Carpal Tunnel is a condition that causes pain, numbness, and tingling in the hand

and wrist. It is caused by compression of the median nerve, which runs through the

carpal tunnel. Run Time 1:08

Cold Sores are small, painful blisters that appear on the lips or mouth. They are

caused by the herpes simplex virus. Run Time = 2:30

Common Cold is a viral infection that causes symptoms such as runny nose, cough,

sore throat, and congestion. Run Time = 1:27

Connect 639 Hz is a frequency that is said to promote connection and empathy.

Run Time = 0:30

Constipation is a condition in which bowel movements are infrequent or difficult to

pass. Run Time = 0:41

Depression is a common mental illness that causes persistent feelings of sadness,

hopelessness, and worthlessness. Run Time = 0:32

DIA stands for Diabiological syndrome. It is a combination of Depression, Insomnia,

and Anxiety. Run Time = 1:49

Earth 7.83 Hz is the natural frequency of the Earth. It is said to have a calming and

grounding effect on the body. Run Time = 0:30

Earth 14.1 Hz is a frequency that is said to promote healing and regeneration.

Run Time = 0:30

Earth 20.3 Hz is a frequency that is said to promote communication and connection.

Run Time = 0:30

Express 741 Hz is a frequency that is said to promote creativity and self-expression.

Run Time = 0:30

Fibromyalgia is a chronic pain disorder that causes widespread pain and

tenderness in the body. Run Time = 2:24

Flu is a contagious respiratory illness that is caused by the influenza virus. It can

cause symptoms such as fever, cough, sore throat, runny or stuffy nose, muscle

aches, and fatigue. Run Time = 2:19

General Inflammation is a condition in which the body’s tissues become inflamed.

This can be caused by a variety of factors, including infection, injury, and certain

medical conditions. Run Time = 0:36

Hangover is a group of symptoms that can occur after drinking too much alcohol.

Symptoms can include headache, nausea, vomiting, fatigue, and sensitivity to light

and sound. Run Time = 1:00

Heart Health is a term used to describe the overall health of the heart. It includes

factors such as heart disease prevention, heart disease treatment, and heart health

education. Run Time = 0:46

Immune Support is a term used to describe a variety of products and treatments

that claim to boost the immune system. Run Time = 0:32

Insulin resistance is a condition in which the body’s cells do not respond normally to

the hormone insulin. Insulin is a hormone that helps the body’s cells absorb glucose

from the bloodstream. When cells become resistant to insulin, glucose builds up in

the bloodstream, leading to high blood sugar levels. Insulin resistance is a major risk

factor for type 2 diabetes. Run Time = 0:42

Kidney Support is a protocol that supports general Kidney health. Run Time = 0:26

Liberate 396 Hz is a frequency that is said to promote emotional freedom and

release negative emotions such as anger, fear, and guilt. Run Time = 0:30

Liver Support is a term used to describe a variety of products and treatments that

claim to improve liver health. Run Time = 0:39

Love 528 Hz is a frequency that is said to promote love, compassion, and forgiveness.

Run Time = 0:30

Low Back Pain is a common pain that occurs in the lower back. It can be caused by a

variety of factors, including injury, overuse, and certain medical conditions. Run Time

= 1:02

Migraine is a type of headache that is often severe and debilitating. It can be

accompanied by other symptoms such as nausea, vomiting, and sensitivity to light

and sound. Run Time = 1:06

Mono, also known as mononucleosis, is a viral infection that causes fatigue, fever,

sore throat, and swollen lymph nodes. Run Time = 0:36

Neck Pain is a common pain that occurs in the neck. It can be caused by a variety of

factors, including injury, overuse, and certain medical conditions. Run Time = Run

Time = 0:42

PMS, also known as premenstrual syndrome, is a group of symptoms that can occur

before a woman’s period. Symptoms can include bloating, breast tenderness, mood

swings, and fatigue. Run Time = 2:06

Prostate is age-associated prostate gland enlargement that can cause urination

difficulty. Run Time = 44 min

PTSD, also known as post-traumatic stress disorder, is a mental health condition

that’s triggered by a terrifying event — either experiencing it or witnessing it.

Symptoms may include flashbacks, nightmares and severe anxiety, as well as

uncontrollable thoughts about the event. Run Time = 2:15

Relax and Balance is a type of therapy that uses magnetic waves to help relax and

balance the body. Run Time = 0:32

Resolve 417 Hz is a frequency that is said to promote problem-solving and decision-

making. Run Time = 0:30

Shingles is a viral infection that causes a painful rash. It is caused by the varicella-

zoster virus, which is the same virus that causes chickenpox. Run Time = 2:30

Sleep is a natural state of rest in which the body and mind are inactive. It is essential

for physical and mental health. Run Time = 0:47

Stop Smoking is a term used to describe a variety of products and treatments that

help people quit smoking. Run Time = 2:36

Sun Burn is a type of skin damage that occurs when the skin is exposed to too much

ultraviolet (UV) radiation from the sun. Symptoms can include redness, pain, swelling,

and blisters. Run Time = 0:34

Tendinitis is an inflammation of the tendons, which are the tissues that attach

muscles to bones. It can cause pain, stiffness, and swelling in the affected area.

Run Time = 1:26

Tinnitus is a ringing or buzzing noise in one or both ears that may be constant or

come and go, often associated with hearing loss. Run Time = 1:46

TMJ, also known as temporomandibular joint disorder, is a condition that affects the

temporomandibular joint, which is the joint that connects the jaw to the skull. It can

cause pain, clicking, and popping in the jaw. Run Time = 2:11

Weight Loss is a term used to describe a decrease in body weight. It can be achieved

through a variety of methods, including diet, exercise, and medication. Run Time

= 0:42

White coat syndrome is a condition in which people experience anxiety or

nervousness when they see a doctor or go to a medical setting. This anxiety can cause

physical symptoms such as a rapid heart rate, sweating, and trembling.

Run Time = 0:30

Wound Healing is the process by which the body repairs damaged tissue. It involves a

number of steps, including inflammation, cell proliferation, and tissue remodeling.

Run Time = 0:49

Separate Vagus Nerve Device “Vagu Vibe”

Vagus Nerve is a protocol designed to stimulate vagal activity, enhancing relaxation,

stress recovery, and autonomic balance. Reported effects include improved heart

rate variability, Lower heart rate, reduced anxiety, lower stress, improved emotional

state, better mental clarity, less pain, and greater overall well-being. Run Time = 30 min

Disclaimer: If you purchase the device using one of the above links I may earn a commission. The info in this post is not meant to treat, cure or diagnose.

References:

https://resona.health/published-papers/

https://resona.health/references/

https://www.research.va.gov/currents/0725-VA-Enters-into-Next-Phase-of-PTSD-Research.cfm

https://www.newsworthy.ai/news/20221103360/92-of-study-participants-achieved-a-reduction-in-ptsd-symptoms-using-the-resona-health-pemf-device-pulsar-xo

Thirty five years ago I was introduced by my mother to this “new way” of dropping some lbs. If you are old enough, you may remember this diet craze that emerged in the early 1990s.

When I look back on the times I used this regimen, it was really the easiest way to lose weight, not feel deprived and still be able to live a “real life”.

The Carbohydrate Addict’s Diet (CAD) is a structured way to harness low-carb eating without full-time deprivation.

The plan basically helps you lose your addiction or craving for high carb foods which was a big plus for me.

You eat low to no carb for breakfast and lunch and then at dinner you can eat a balanced meal that contains carbs. The key is the 1 hour window. Once you start eating your dinner with carbs, you must be finished within 1 hour.

No this is not a license to eat a gallon of ice-cream.

You must eat a balanced dinner that includes proteins and carbs and even dessert or a glass of wine if you like. It is best to make sure you include plenty of vegetables and even some fruits.

For me, this plan really did take away my cravings for carbs.

A Short History of the Carbohydrate Addict’s Diet

The Carbohydrate Addict’s Diet was created by husband‑and‑wife researchers Drs. Rachael and Richard Heller, biomedical scientists who personally lost about 200 pounds between them using the framework they later formalized. Their first book, The Carbohydrate Addict’s Diet, was published in 1991 and quickly became a bestseller, followed by multiple sequels and refinements.

The Hellers drew on an earlier concept: the term “carbohydrate addiction” which was coined in 1963 by Yale biochemist Robert Kemp to describe a subset of obesity driven by hyperinsulinemia and an intense drive for carbohydrate‑rich foods. Building on this, they argued that for many people, repeated spikes of insulin after frequent carb‑heavy eating creates a cycle of:

• Rapid blood sugar rise and fall

• Rebound hunger and cravings

• Progressive fat storage and weight gain

Their clinical observation: if you compress most of your carbohydrates into one carefully structured daily window and keep the rest of the day lower in carbs, you can flatten insulin swings, reduce cravings, and make weight loss more automatic.

How the Diet Actually Works

The Carbohydrate Addict’s Diet is not “no carb.” It’s a timing‑ and structure‑based approach built around two types of meals:

• Complementary meals
  These are low‑carb, higher‑protein meals eaten once or twice earlier in the day. They emphasize meat, fish, eggs, and low‑carb vegetables, typically around one serving of protein plus about two cups of low‑starch vegetables or salad. The goal is to keep insulin relatively stable and prevent carb‑driven hunger cycles.

• The “reward meal”
  Once per day, you have a meal where you can include carbohydrates—even traditionally “forbidden” foods—within a strict one‑hour window. The Hellers suggested balancing this plate across protein, low‑carb vegetables, and carbs (including starches or desserts) in roughly equal portions, while keeping the meal confined to that 60‑minute span.

Instead of constant carb restriction, the diet concentrates carbohydrate intake into that single daily interval, with the intention of:

• Limiting the number of insulin spikes across the day

• Reducing grazing and binge‑like eating

• Preserving a sense of psychological freedom by allowing favorite foods in a controlled context

The Hellers also discouraged the use of artificial sweeteners, arguing that sweet taste alone might provoke insulin release and sustain cravings, though evidence here is mixed and still evolving.

The “Carbohydrate Addict” Concept

The Hellers defined “carbohydrate addiction” less as a moral failing and more as a physiological drive: a compelling hunger, craving, or escalating need specifically for carb‑rich foods like bread, pasta, cookies, chips, and sweets. They estimated that up to 75% of overweight individuals could fit this pattern.​

To help people self‑identify, they created a questionnaire that looks at signs like:

• Strong evening or late‑night carb cravings

• Difficulty stopping once you start eating snack foods

• Feeling more hungry after a high‑carb breakfast than before it

• Mood shifts tied to eating (or not eating) certain carbs

While mainstream medicine does not formally recognize “carbohydrate addiction” as a diagnosis, there is growing literature on “food addiction” and addictive‑like responses to high‑glycemic, highly processed carbohydrates. Some studies suggest that rapidly absorbed carbs can activate reward pathways in ways that resemble other addictive behaviors, especially in vulnerable individuals.

This is where CAD can be useful: it doesn’t try to fight that circuitry all day long. Instead, it channels most of that drive into a single, predictable, bounded window.

Potential Benefits of the Carbohydrate Addict’s Diet for Weight Loss

Here’s why many people found (and still find) CAD helpful for losing weight and keeping it off:

• Fewer insulin spikes and more stable hunger
  By minimizing carb exposure at most meals and consolidating it into a single daily window, you likely flatten the number of large insulin surges over 24 hours. For insulin‑resistant or hyperinsulinemic individuals, that can mean fewer crashes, fewer emergency snack runs, and more natural appetite control.

• Built‑in structure without constant micromanagement
  The plan removes calorie counting, points, and macros tracking for most people. Instead, it uses simple rules: low‑carb complementary meals plus one timed reward meal, with basic plate balance guidelines. For many, this reduces decision fatigue and makes adherence easier.

• Psychological relief from “never again” thinking
  Knowing that bread, pasta, or dessert can fit into a daily reward meal lowers the all‑or‑nothing pressure that triggers binges on stricter plans. This “permission within boundaries” model can help some people break yo‑yo dieting patterns where strict restriction is followed by loss of control.

• Evening craving containment
  Many carbohydrate‑sensitive eaters struggle particularly at night. Because CAD often places the reward meal at dinner (within that one‑hour window), the diet works with—rather than against—this natural pattern, but confines it in time and structure.

• Compatibility with real life
  Social events, family dinners, and holidays can be folded into the reward‑meal concept much more easily than into an all‑day rigid low‑carb protocol. That flexibility can translate into better long‑term adherence, which is ultimately what predicts weight‑loss success.

Where It Fits Today (And Who It May Help Most)

In the current landscape—where we have Mediterranean, keto, intermittent fasting, GLP‑1 medications, and more—the Carbohydrate Addict’s Diet sits somewhere between classic low‑carb and time‑restricted eating. It helps promote “mindful” eating while experiencing the metabolic advantages of carb restriction during most of the day.

For me personally the biggest plus is the psychological and social advantages of still being able to enjoy a “real life” that includes family dinners, restaurants and parties.

I would definitely recommend anyone who is considering going on a GLP-1 medication to first give the Carbohydrate Addict’s Diet a fair 60 day trial.

There is no one single weight loss program that works for everyone, but this one is definitely worth a try.

Disclaimer: The information in this post is for educational purposes only. Before adopting a new diet plan, always check with your health care provider.

References:

https://www.sciencedirect.com/science/article/abs/pii/0306987794900043

https://www.healthline.com/nutrition/carb-addiction

https://pmc.ncbi.nlm.nih.gov/articles/PMC5912158/

https://www.mayoclinic.org/healthy-lifestyle/weight-loss/in-depth/low-carb-diet/art-20045831

(Many alternative doctors will tell you that while Chemotherapy kills cancer cells, it does not kill the cancer stem cells, which is why the cancer comes back following Chemotherapy.)

The average cost for a 6 month round of chemotherapy costs around $27,000. If the chemotherapy is administered in a hospital the cost could be as high as $100,000. Data shows the average Mediacare cancer patient pays $8,000 per year out of pocket for Chemotherapy.

That is a high price to pay for something that has such a dismal track record.

What about Radiation treatments?

Long‑term studies of patients receiving multiple courses of radiotherapy show 5‑year overall survival of about 32.7%. A cost study across 55,288 patients found the median cost of a course of radiation therapy was about 8,600–18,000 dollars, depending on cancer type. Out of pocket cost for the average American is $4,000 - $9,000.

Both Chemotherapy and Radiation can cause secondary cancer.

What if there is a more humane way to treat cancer that cost much less, has zero side effects and produces better results?

This overlooked cancer treatment discovery goes all the way back to 1902. The clinical trials showed the cancer patients injected with this natural substance showed tumor regression, but this doctor’s work was overshadowed by the media’s fixation on a quick acting therapy that would go on to kill it’s female discoverer and the people who worked with her.

In the 1970’s this overlooked cancer treatment made a comeback thanks to a doctor who was suffering from the most deadly of cancers. His deep research took him back to 1902, he implemented this discovery and made a full recovery.

Read more

This is exactly what happened in 1960. Today, thanks to social media and uncensored outlets like substack, the truth is coming out.

Australian Researcher Discovers Mineral Deficiency Linked to Arthritis

In 1960 Rex Newham, Ph.D. discovered that boron deficiency was linked to arthritis. After observing that regions with low boron in soil had higher arthritis rates, he conducted trials where arthritis patients given boron supplements experienced dramatic pain relief and improved mobility. His findings were published in The British Journal of Nutrition, showing that 70% of participants saw significant improvement with just 6–9 mg of boron daily.

Despite these results, Newnham’s work was aggressively dismissed and ridiculed by medical authorities. The Australian government revoked his license, and his research was buried—a clear example of how natural solutions threatening Big Pharma’s monopoly are silenced.

Boron’s ability to reduce inflammation and repair joint cartilage without toxic side effects made it a threat to the lucrative arthritis drug industry.

Boron’s Role in Bone Health and Beyond

Boron is critical for calcium metabolism and bone strength. Studies show it enhances the absorption of magnesium and vitamin D, both essential for preventing osteoporosis . Postmenopausal women with boron supplementation showed improved bone density, reducing fracture risk . Unlike synthetic drugs like bisphosphonates (which weaken bones long-term), boron supports structural integrity naturally.

Beyond bones, boron:

• Balances hormones by modulating estrogen and testosterone, benefiting menopausal women and athletes.

• Boosts brain function, with studies linking boron deficiency to impaired cognition and memory.

• Detoxifies heavy metals like fluoride and aluminum, which are linked to neurodegenerative diseases.

Boron and Cancer: The Forbidden Connection

Emerging research suggests boron may inhibit cancer cell proliferation. A 2021 study found boron compounds induced apoptosis (programmed cell death) in breast and prostate cancer cells . Another trial noted boron’s ability to suppress angiogenesis (tumor blood vessel growth), starving tumors of nutrients . Despite these findings, mainstream oncology ignores boron, as it cannot be patented or monetized like chemotherapy drugs.

Borax (20 Mule Team): A Multipurpose Health Aid

Borax, a natural boron compound can be found in the laundry detergent section of most grocery stores. I use it to make non toxic homemade laundry detergent and I always keep a box in my bathroom for my bath detox.

Borax 20 Mule Team has been vilified despite its historical use as a safe household cleaner and remedy. It is often used for:

Detox Baths: Dissolving 1–2 cups of Borax in warm water draws out heavy metals and relieves joint pain.

My Personal Bath Detox regimen:

• 1 Cup of Borax 20 Mule Team

• 1 Cup of Baking Soda

• 1 Cup of Epsom Salt

• 1 Cup of Sea Salt (I use Baja Salt or Redmond’s Real Salt

Add the above to a hot bath. Soak for 20 – 30 minutes. You can rinse off in the shower, but it is not necessary. I do this once or twice a week. I always do it after getting home from traveling on an airplane.

This is a great way to detox radiation, heavy metals, and it promotes overall wellness. During the pandemic, many people used this Bath Detox to detox the spike protein.

If I feel under the weather, or anything at all coming on this is my go to protocol. Keep in mind that the skin is your largest organ, and yes you will absorb some of the boran as well.

Warning: Detox baths are NOT recommended for children, pregnant women, diabetics, and those with low blood pressure.

Antifungal Properties: Borax can be effective against candida and toenail fungus when applied topically (diluted).

Oral Supplementation: A pinch of Borax (1/8 tsp) in water daily provides ~3 mg boron, supporting joint and hormonal health

Caution: Borax is not FDA-approved for internal use, but holistic practitioners argue its safety at low doses, contrasting it with far more toxic pharmaceuticals . I personally do NOT take Borax internally, instead I would opt for a boron supplement.

How to Use Boron Safely

• Supplemental boron: 3–6 mg daily (as boronic acid or calcium fructoborate) for arthritis and bone support.

• Food sources: Almonds, avocados, and raisins (though soil depletion reduces dietary boron)

Conclusion:

Boron’s suppression epitomizes institutional hostility toward cheap, effective natural therapies. It is another example of profits over people. From reversing osteoarthritis (it is also used for other types of arthritis as well) to potentially fighting cancer, its benefits are too significant to ignore. For those seeking alternatives to toxic drugs, boron—and Borax, when used wisely—is a powerful, yet simple protocol.

Disclaimer: The information in this post is not meant to treat, cure or diagnose. Always work with your health care provider before implementing a new supplement or health protocol.

References:

https://pubmed.ncbi.nlm.nih.gov/7889887/

https://journals.sagepub.com/doi/10.1177/026010609100700204

https://juniperpublishers.com/jojcs/JOJCS.MS.ID.555582.php

https://www.jstor.org/stable/3431968

https://www.canada.ca/en/health-canada/services/drugs-health-products/reports-publications/natural-health-products/boron-medicinal-ingredient-oral-natural-health-products-natural-health-products-directorate-heath-canada-2007.html

https://www.sciencedirect.com/science/article/abs/pii/S0304383504004422

https://oasis.library.unlv.edu/rtds/2161/

https://www.sciencedirect.com/science/article/abs/pii/S0197018621001832

https://pubmed.ncbi.nlm.nih.gov/7889887/

https://pubmed.ncbi.nlm.nih.gov/3678698/

https://pmc.ncbi.nlm.nih.gov/articles/PMC1566632/

https://www.cambridge.org/core/services/aop-cambridge-core/content/view/S000711450770911X

If you live in the Los Angeles area, I urge you to consider IV protocols from Dr. Mark Ghalili at Regenerative Medicine LA.

I have spoken with him and his treatments can help someone improve in the early and middle stages. He says that once a person can no longer eat, then the damage is too much to reverse.

I also received this info from one of my readers named Barbara.

“Last year, my 68-year-old partner was diagnosed with Lou Gehrig's disease also known as ALS. Speaking and swallowing were two of his challenges. His collapse was swift and catastrophic, and neither Standard treatments like riluzole and high dose B12 did very little for him. He would not have survived if our primary care physician hadn't given him attentive care and attention, as the hospital center didn't provide any psychological support. His fall was abrupt and catastrophic. His hands and legs gave way to weakness in his arms, he used different supplements that didn't work, so last July, he tried the ALS/MND protocol—the best decision ever! His symptoms eased, his energy returned, and he sleeps soundly. He feels like a new man, and he can walk and exercise again. We got the ALS/MND protocol from www. limitlesshealthcenter. com “

I took a look at the Limitless Health Center and their ALS/MND herbal product and I am very encouraged by what I found.

Dr. Seth is a Master Herbalist with over 25 years of experience in the herbal healthcare and complementary medicine fields including clinical experience as a Doctor of Homoeopathic Medicine. Currently in private practice as a Registered Homeopath in Johannesburg South Africa, in 2009 Limitless Health/Herbs Centre gained international recognition and won the Global Promising Herbal Center Award in Los Angeles, California USA.

I spoke with a staff member who told me that the formula is 100% herbal and has a 100% effective rate. If you do not experience significant improvements in the first 2 months, they will refund all your money.

You can work with them via zoom and they will ship the products to the United States. From what I could gather the product seems very affordable at $200 a bottle and there is a $400 fee for the 5 month protocol that Dr. Seth will design for you.

I have not personally worked with them, so I can not vouch for them, but in this kind of dire situation I do believe they are worth contacting.

The experts I have talked to about ALS all agree that this disease is toxicity based.

There are so many things you can do to detox, but I never believe in putting all your eggs in one basket. I am sure the ALS/MND herbal formula will be helpful in helping you detox.

Here are some of my detox suggestions:

Remove Root Canals - they are all toxic. It is the only medical procedure that allows a dead body part to be put back in the body.

Remove infected teeth - dental xrays do not always show dental infections. You must get a 3d scan. Even then a dental infection may not show up.

For more info on How Dental Issues can cause health issues, read Dr. Simon Yu’s article, Dental, The Root Cause of Illness.

Infrared Sauna - this is a great way to gently detox on a weekly basis. Most people do not work up a really good sweat 2 - 3x per week. Your skin is your largest organ and when you sweat, you can release all sorts of toxins including heavy metals.

Drink clean water - tap water is full of toxins including chlorine and fluoride. Purchasing a Distilled Water machine or Reverse Osmosis water machine is a must. You can also purchase filters for your shower. After all, your skin is your largest organ and you will absorb toxins by taking a shower in tap water.

Eat clean food - If you eat in restaurants, eat package or prepared foods, or eat any food that is not organic, you are adding to your toxic load.

Air Filter - Invest in a good air purifier. Toxic air is everywhere, you can clean the air inside your home and bedroom with a good air purifier.

Clothing - opt for natural materials. When you wear anything synthetic, the toxic petroleum based fumes will be absorbed into your blood. The same goes for your bed linens and towels.

Personal Care Products - start reading labels. If you can’t eat the ingredient, you do not want it on your skin.

There is much more that can be done.

As I mentioned in the first article on ALS,

Lou Gherig died in 1941, Where is the Cure for ALS?

HealingALS.org has a detailed 47 step program.

If you or a loved one has recovered from ALS I would love to hear from you.

Disclaimer: The information in this post is not meant to treat, cure or diagnose. Always work with your health care provider.

This Institute is truly a state-of-the-art center. Everything from the modern design and décor of this building to the warmth and passion of each staff member made us feel hopeful and calm.

The doctor assigned to my husband’s case specializes in prostate cancer.

He explained to us that the first order of business was to take a detailed history so that they could present it to the FDA to get their “permission” to include my husband in the clinical trial.

The doctor told us that Dr. Patrick would find my husband’s case unique and one that he wanted to include in the trial because most men with prostate cancer have had their prostate removed and had already received heavy radiation.

My husband was considered unique because he had had neither.

Normally the FDA approval process would take about 3 weeks, but we were not only facing the holidays, we were also in the middle of a government shut down.

In the meantime the Doctor ordered a PMSA scan. This is an in-depth scan specific to prostate cancer.

My husband had been in complete remission from stage 4 prostate cancer (no cancer spots showing up anywhere in the body) for 4 years and now it was time for an update.

After Christmas we received the PMSA scan results. A new tiny cancer spot had shown up in the hip bone. Of course we were devastated, but then again here we were in the process of getting approved for this amazing clinical trial.

I look back on the turn of events, and know without a doubt that we were divinely guided to be part of this clinical trial.

Shortly after receiving the “bad news” we received the “good news” that yes indeed my husband had received FDA approval to participate in Dr. Patrick’s clinical trial.

The First Part of the Treatment

I was of course hoping that this “treatment” would be a one and done, but that is not how this works.

So far the treatment consists of 2 protocols:

• Anktiva Injection aka N-803

• Viral Vector Vaccine aka ETBX-071

Anktiva injection (N-803): This is the drug developed by Dr. Patrick Soon-Shiong that boosts or “rescues” the T cells and the Natural Killer cells. It is a manufactured protein that the body naturally manufactures called Interleukin-15 (IL-15). This protein supports your T-cells and your Natural Killer cells, but it is fleeting, meaning it does not stay active in the body. Dr. Patrick figured out how to alter IL-15 so that it stays in the body for 7 days. This increases and proliferates the Natural Killer cells, the T cells, and the CD4+, and CD8+ T cells, without upregulating the suppressive types of T cells.

Anktiva aka N-803 is considered to be a type of immunotherapy that increases the number of cancer-killing immune cells in the body and increases the ability of those cells to kill tumor cells.

The Anktiva injecton is given every 3 weeks for 6 months or longer.

Dr. Patrick Soon-Shiong’s research has shown that NK cells and T cells are the most important cells when it comes to making sure the cancer does not return. His research also shows that Chemotherapy and Radiation can damage these important cells and this is why you can see a short term gain with Chemotherapy and Radiation, but then the cancer comes back.

The Anktiva injection for most people does not have any long term side effects. We were told that there could be redness in the abdomen where the shot is given, and 4 – 5 days later there could be fatigue for a day or two.

The Second Part of the Treatment

Viral Vector Vaccine (ETBX-071): This is an adenovirus serotype 5 (Ad 5) vector that has been modified by the insertion of the human PSA gene.

The Viral Vector Vaccine is given once every 3 weeks for 3 doses, and then again at 6 months, and 12 months.

Risks and Side Effects:

Yes, all pharmaceutical drugs and vaccines come with the possibility of side effects. Listed side effects for the Anktiva include:

• Injection site redness, itching and swelling

• Chills

• Nausea

• Vomiting

• Headache

• Anemia

• Fever

• Low white blood cell count

• Low red blood cell count

• Rigors, a feeling of cold and shivering

• Blood in urine and urinary tract pain

Listed side effects for the Viral Vector Vaccine include:

• Fever

• Injection reactions

• Nausea

• Headache

Did my husband experience side effects?

We were told that usually side effects can happen 5 days later, and usually they are mild.

My husband’s reaction was not “normal”. That first night he experienced Rigors, which is a feeling of extreme coldness accompanied by shaking. At about 1 am he got into a hot bathtub of water to warm up. I then put him back in bed with lots of blankets and my bio mat on top for warmth. He immediately went back to sleep. The next day he was very tired. (The doctor confirmed my suspicions that this means his immune system was stimulated, which is a good thing.)

5 days later he did experience redness and itching at the injection site, but this did not interrupt or hinder his daily activities.

Keep in mind that with 10 years of clinical trials already performed there is plenty of documented evidence to show this is relatively safe and very effective, especially when compared to the side effects, complications and the outcomes of the “standard of care” that mainstream medicine has to offer.

Reminder: I am sharing our journey in hopes that more people will learn about Dr. Patrick Soon-Shiong’s cancer treatment and in turn put pressure on the FDA to approve this for all cancers.

Disclaimer: The information in this post is for educational purposes only. It is not meant to treat, cure or diagnose. Always work with your health care provider.

References:

https://www.urologytimes.com/view/anktiva-as-a-lymphocyte-rescue-molecule-unlocking-the-power-of-nk-cells-and-t-cells

https://pmc.ncbi.nlm.nih.gov/articles/PMC7993215/

https://immunitybio.com/immunitybio-announces-12-month-overall-survival-probability-of-83-in-nci-led-phase-1-study-of-multi-targeted-had5-immunotherapy-vaccine-in-patients-with-advanced-metastatic-prostate-cancer/

https://reaganudall.org/clinical-trial/immunotherapy-n-803-etbx-071-and-m-cenk-combination-radiation-participants-high-risk

What is Red Light Therapy?

Red light therapy (photobiomodulation) uses low‑level red and near‑infrared light to stimulate cellular repair, reduce inflammation, and support tissue healing, with growing evidence in skin aging, systemic inflammation, and supportive cancer care.

What the Science Really Shows

If you’ve been reading about biohacking or longevity for more than five minutes, you’ve seen red light panels everywhere. But beyond the hype, there is a real and rapidly growing body of research on red light therapy—also called photobiomodulation (PBM)—for skin rejuvenation, inflammation, and even supportive care in oncology.

How Red Light Therapy Works

PBM uses specific wavelengths of red and near‑infrared light (roughly 600–1000 nm) at low power densities to modulate cellular function rather than burn or destroy tissue.

Red Light therapy improves cellular health in the following ways:

Mitochondrial modulation: Red and Near Infrared photons interact with cytochrome c oxidase in the electron transport chain, improving ATP production and shifting redox status in a way that favors cellular repair and resilience.

A more simple explanation: Red Light Therapy improves the mitochondria inside every cell and once this happens cellular repair is improved, making your cells more resilient against outside stressors.

Nitric oxide and microcirculation: Red light exposure can help release nitric oxide, improving local blood flow and oxygen delivery to tissues.​

A more simple explanation: Red Light Therapy triggers the release of nitric oxide which improves blood flow, and when this happens the blood cells are better able to deliver oxygen and nutrients to the tissues, which is needed to support healing and repair.

Inflammatory signaling: PBM has been shown to downregulate NF‑κB and AP‑1 activity and reduce pro‑inflammatory cytokines like IL‑6, IL‑8, TNF‑α, IL‑1β, and IL‑18, while upregulating the anti‑inflammatory cytokine IL‑10.

A more simple explanation: Red Light Therapy improves inflammation blood markers as well as anti-inflammatory blood markers. In other words, inflammation is lowered. Keep in mind that chronic inflammation is a contributing factor to most health issues.

Red Light Therapy works at a cellular level to help nudge cells back toward homeostasis—especially cells under stress.

Homeostasis is a state where the body is in balance.

Red Light Therapy for Anti Aging

Inflammation is one of the biggest contributors to accelerated aging. It not only effects the overall health of the body, but inflammation can also show up on the skin in the form of excessive wrinkles and sagging skin.

The fact that Red Light Therapy can reduce inflammation and increase the body’s ability to heal and repair makes this an excellent anti-aging tool.

Red Light Therapy for Cancer Patients

Red light therapy for cancer patients is mainly used as a supportive, noninvasive modality to help manage treatment side effects. It can reduce inflammation, ease pain, support wound and tissue healing, and help prevent or treat oral mucositis in patients receiving chemotherapy or radiation.

Red Light Therapy is here to stay. If people were not getting benefits it would have disappeared years ago, but instead it has become more mainstream.

How do I use Red Light Therapy?

I personally use a Red Light Therapy ball cap to lower inflammation in the brain. At age 63 I am doing what I can to prevent memory issues before they happen.

I also have a Red Light Therapy belt called a wrap. That way I can use it to spot treat any area. Eventually I hope to invest in the large panels so I can treat my whole body at once.

Just recently I had to have a tooth pulled. My holistic dentist had me use red light therapy inside my mouth to speed up the healing process.

How do you find High Quality Red Light Therapy Devices?

Look for the following:

1. Clinically Validated, FDA-Cleared Wavelengths that utilizes high-irradiance red (660 nm) and near-infrared (850 nm) wavelengths that are shown to penetrate deeply and energize mitochondria—this level of irradiance (e.g. ~174 mW/cm2 at 3”) is typically found in clinical-grade devices.

2. Medical-Grade, FDA- cleared delivering clinic-quality results at home

3. Devices that are based on peer-reviewed red light therapy research.

**I personally use Ultra Lux Health Red Light Technology because it checks all 3 of the above. Use coupon code painterwellness to save 15%.

Disclaimer: The information in the post is not meant to treat, cure or diagnose. Always work with your health care provider. If you order using my link, I may earn a commission.

References:

https://pmc.ncbi.nlm.nih.gov/articles/PMC10311288/

https://www.frontiersin.org/journals/neuroscience/articles/10.3389/fnins.2023.1150156/full

https://pmc.ncbi.nlm.nih.gov/articles/PMC3926176/

https://pmc.ncbi.nlm.nih.gov/articles/PMC9304695/

https://www.cancer.gov/about-cancer/treatment/types/photoimmunotherapy-video

https://bmjopen.bmj.com/content/8/5/e021419

To understand our journey, I must give you a brief history so that you will understand why we developed a very healthy skepticism to all things western medicine.

No we do not believe it is all bad, there are many amazing things that western medicine has to offer, but as you read about the experiences that we have had, you will understand why we no longer blindly put our health in anyone’s hands, especially a doctor.

Around 2003 my husband was diagnosed with a pituitary tumor.

Prior to the diagnosis, he had debilitating headaches. Yes he was being treated by a neurologist. I kept asking the neurologist, “shouldn’t he have an MRI?” The doctor said “No, there is nothing showing up on the Cat Scan, he is having typical migraines”.

After a year and half of these debilitating “migraines” and very strong pharmaceutical drugs that did not touch the pain, one day the migraine was so horrific, it made him lose his eyesight. I rushed him to the hospital and what did they do? They immediately gave him an MRI and there it was. A huge pituitary tumor that was so big it had pushed on the optic nerve and was in danger of bursting.

We were ushered up to the Neurosurgery department. I remember asking the neurosurgeon “are you an expert at this exact surgery?”. He replied “yes you are in good hands”.

A few days later the surgery was performed. I was so relieved when the surgeon came out of surgery and announced “it went well, we got all of the tumor out”.

We would later learn that the pituitary tumor indeed had shown up on the Cat Scan, but everyone including the neurologist did not see.

Lesson learned: when you feel strongly about something, don’t cave. I should have demanded that an MRI was performed. Or at the very least a copy of the Cat Scan and a 2^nd and 3^rd opinion. It would have saved my husband many months of agony.

The surgery required an ICU stay, and a grueling 6 weeks to recover from. Fast forward 1 year. My husband was having debilitating headaches again. This time I was put in contact with a guy out of North Carolina who was head of a pituitary website. We spoke, and he said first off, your surgeon is not an expert in this surgery. We then preceded to go to a surgeon who was an expert and to our shock and dismay, he put the MRI that the first surgeon had done the day after the surgery up on the screen.

There it was in plain sight. The tumor. We had been lied to.

Needless to say this experience opened our eyes.

By the way, the 2^nd pituitary surgery was a breeze. The surgeon went microscopically up the nose, got the tumor out and in 24 hours my husband was home. The only pain med he took was an extra strength Tylenol.

What a difference.

Lesson learned: Medicine is a business. If a doctor tells you they are an expert, you must trust but verify. I should have gotten on the phone and called around.

In 2006 my husband had a high PSA of 6.0.

The urologist put him on a heavy round of antibiotics, hoping that it was just an infection. Well when that did not bring the PSA down, an invasive biopsy was performed. No cancer showed up. The doctor threw his hands up with no further recommendations.

Lesson learned: If a doctor has nothing more to offer, and the issue is still not resolved, it is your job to go find another health practitioner that has answers. It is always a good idea to find a functional medicine doctor, or a naturopath physician and get their input. Unfortunately I was still in the dark.

6 Years later my husband was not feeling well. I mentioned this to my personal alternative/functional medical doctor. He stopped in his tracks and sternly told me that the problem with prostate biopsies is that they go up there blindly and grab spots, hoping that if there is cancer they will stumble upon the exact spot that has cancer.

(You can compare this to a woman having her breast biopsied by a doctor who is blind folded.)

My doctor said that in no uncertain terms, “the only way to know if the prostate is healthy, is a dopplar sonogram. This allows the doctor to look at the prostate in real 3 d time and if they see a suspicious spot, then they grab a biopsy from that spot). He also warned me to not do any of the treatments this prostate doctor would offer.

Well the results of the dopplar sonogram showed that yes indeed there was cancer. A gleason 7 and the cancer had just begun to creep outside of the prostate.

Lesson learned: Never have a prostate biopsy performed by a doctor who does not use a dopplar sonogram.

Meeting Dr. Patrick Soon-Shiong

In 2013 my husband, who is a Director of Photography, was hired to film a profile on Dr. Patrick Soon-Shiong. He spent almost a year on and off working on this profile. He would come home after shooting all day and “transfer” the footage. If I was around, I would watch the footage being transferred.

By this time I had done a lot of research and was not going to blindly trust any doctor. I spent 5- 6 hours a day educating myself on prostate cancer. I had even been given access to a “doctors database” where I had uncovered information on prostate removal. The data in the doctors database showed that removing the prostate in early stage prostate cancer can cause a 60% greater chance of the cancer metasticizing.

And while my husband’s prostate cancer was not considered early, this is exactly what every doctor we spoke with was recommending. Of course they never mentioned what I had seen with my own eyes in their database.

One day my husband came home from filming Dr. Patrick Soon-Shiong, he told me “sit down, you are going to want to see this with your own eyes”.

There it was, Dr. Patrick Soon-Shiong admitting on camera that the way we treat cancer in America causes it to metasticize and mutate”. My heart skipped a beat. My fears and concerns on how to precede with my husband’s cancer treatment had been validated.

Did this statement make it in to the segment that aired on TV?

Nope it did not. Here they were doing a story on this brilliant oncologist and in my opinion they opted to NOT air the bombshell news that would have caused everyone to stop and take notice.

There are many reasons why this statement may have not aired. It certainly would have upset their #1 advertisers, Big Pharma. Another reason might have been because there were no other mainstream medicine alternatives.

What treatment did my husband opt for?

Well after all the research I did and then Dr. Patrick’s bombshell admission we went to a world famous medical clinic that specializes in cancer. The doctor there said a few interesting things.

1. If the cancer is still in the prostate, then natural protocols can get you well.

2. If the cancer is out of the prostate western medicine does not have a good track record.

3. He also said that before any treatment began it needed to be determined if the body recognized there was cancer in the body.

#3 was news to me. I had never heard of such a thing. The Doctor explained that when cancer spreads really quickly it is because the immune system does not recognize there is cancer, and therefore does nothing to stop it.

Years later I would learn about the importance of supplementing with Redox Molecules, something your cells naturally manufacture, but due to age, stress and toxicity you become deficient. These redox molecules are used for Redox Cellular Signaling. This is how the immune system receives the communication of what is wrong in the body and needs to be fixed. The immune system can not fix what it does not know about.

The expensive 3 week stay at his world famous medical clinic opened up a whole new world for us as far as how to treat cancer.

My husband was given all sorts of IV treatments. He did infrared sauna treatments (we opted to purchase one to continue the protocols at home.) He was given hyperbaric oxygen treatments every day. He was accessed for nutritional deficiencies and given specially formulated nutritional powders.

We had already drastically improved his already healthy diet. Lots of juicing and we did a mostly raw vegan diet. While at the clinic, we learned that my husband’s blood type, Type O did not do well on a raw vegan diet. This explained why my very naturally slender husband had lost 10 lbs in the first 2 weeks.

The doctor warned us if we did not add back in some clean, wild caught, grass fed animal protein, his health would rapidly deteriorate. Adding back in animal protein made all the difference in his energy, and well being.

He was also doing high doses of Organic Sulfur, Black Cumin Seed Oil, and freshly ground Dandelion Root.

We were so excited to see his PSA go down.

I then asked about Root Canals. I had read research on this, and the doctor who led this clinic, his father was a famous alternative medical cancer doctor in Germany who required every cancer patient have their root canals removed.

The doctor sort of hesitated and said, well if his root canal is not bothering him then let’s not do anything right now.

A year later, he was still feeling great, and looking great, but the PSA was not going all the way down and the cancer was still there. I told my husband, that’s it, we are doing the only thing left that I know to do.

We are going to get your root canal removed.

You would not believe the push back we got. Many dental surgeons told me “If I remove a root canal with no proof of infection, I could lose my license”. I then realized that the Santa Barbara doctor may have been too afraid to recommend the removal of root canals, like his famous father had done.

In the middle of my search to find an oral surgeon to remove the root canal, my husband called me from New York where he was shooting a comedy special. “I am feeling something is up with the root canal, something is not right”.

I immediately called my dentist at the time, and she urged the oral surgeon she worked with to perform the root canal removal.

On the day of the surgery the surgeon did a regular dental x-ray. He admitted he saw that there might be some infection. He preceded with the surgery.

Once the surgery was done, he came out in to the waiting room to tell me the most shocking news. He said that the root canal infection was so bad, it had eaten a hole the size of a quarter up into my husband’s sinuses and was draining that infection back down into his body.

I instantly knew that this infected root canal was a major drag on his immune system, and that now maybe, just maybe his immune system could now focus on the cancer.

Lesson learned: Dental x-rays do not always see infection. If you have a root canal, you need to routinely get a 3 D scan.

Sure enough 2 ½ months later, the PSA had gone way down, and blood markers showed no signs of cancer.

Yes we were ecstatic. Talk about relief. We felt like we got our lives back.

We continued the diet and the supplements, and the protocols including expensive Vitamin C Iv’s, but 2 years later my husband was not interested in completely following the lifestyle, and I was tired of being the “nagging” wife.

Fast forward 8 years to 2020. Covid had just begun. My husband was not feeling “right”. In my heart I knew what was probably going on. Sure enough his PSA had jumped up. The oncologist immediately put him on hormone blocking drugs. I was shocked at how fast they worked. Within a week, my husband felt so much better, I could not believe it.

We were so hopeful. My husband was able to go back to his normal life.

I wanted to go back to the super clean diet, and supplements, but my husband was not willing.

Instead he wanted to follow everything the oncologist recommended.

The oncologist said light chemo gives you better outcomes. I looked at the studies and seeing a 12% better outcome did not give me any hope. “Oh you’ll be able to get off the hormone drugs” said the doctor.

Well that certainly was a plus. Those hormone blocking drugs have terrible side effects, and you can not stay on them forever because eventually your heart muscle will deterioate.

So my husband did the light chemotherapy. He did not lose his hair and only suffered nausea and fatigue for about a day or two after each chemo session.

I can’t remember how many chemo sessions he did, but once he was done, he was taken off the hormone drugs. Well just a few months of being off the hormone drugs, the PSA started to rise, so back on he went.

Nope my husband was not in that “12%” that the doctor had presented.

At this point I was introduced to Redox Molecules, the only bioidentical supplement in the world that matches the Redox Molecules that your cells are already making. We become deficient in those molecules due to age, stress and toxicity.

Redox molecules are non toxic, do not interfere with any medications or medical procedures. When you supplement with them, they improve mitochondrial function and improve cellular communication.

At this point, I remembered what the famous Alternative Cancer doctor in Santa Barbara told me, that often times your immune system may not even know you have cancer.

Well now I fully understand how that could happen: A deficiency in Redox Molecules could cause cellular communication to be suboptimal. When that happens your immune system may not receive the “communication” that there is cancer in the body.

I immediately put my husband on the Redox Molecules. 2 ½ months later, no cancer was showing up in his bones on his scans. The oncologist was dumbfounded, he had never seen such an improvement. Then 1 year later, no cancer showing up anywhere on the scan.

The oncologist admitted that my husband was a “miracle patient”.

I also took my husband to a world famous medical clinic that has technology to determine if you have stressors preventing a full recover. I will share more about that in another post.

November 2025 my husband shoots a 1 hour special on Dr. Patrick Soon-Shiong

After the interveiws were all done, Dr. Patrick pulls my husband aside. “How are you doing? I remember you were diagnosed with cancer the last time I saw you.” My husband replied “well I am supposedly in remission, but I don’t know if I am really ok”. “Why don’t you let me treat you?” said Dr. Patrick.

My husband could not believe that Dr. Patrick remembered him, and was inviting him to join the clinical trial.

I personally was over the moon. I have followed Dr. Patrick ever since my husband did that first special on him all those years ago. I love that he is so dedicated to finding a cure for cancer he has used his own money to fund his research.

I am extremely impressed with the 10 years of clinical trials that show this treatment is non toxic and has amazing outcomes, much better outcomes than anything mainstream medicine has to offer.

Honestly I feel like we have won “The Golden Ticket”. I am very aware of how lucky we are. This is why I want to share this journey with my readers in hopes that more people will demand that the FDA approve this treatment for all cancer.

As Dr. Patrick said in the most resent MAHA zoom, “You shouldn’t have to know someone to be able to get this treatment. Everyone deserves access to it”.

Next up I will report on the process to get the FDA approval for my husband to participate in the clinical trial and the first treatment.

DISCLAIMER: The information in the post is for educational purposes only. It is not meant to treat, cure or diagnose. Always work with a health care provider.

My real goal is to shine a light on the incredible work that Dr. Patrick Soon-Shiong has dedicated his life to.

As an oncologist/research scientist I believe that Dr. Patrick Soon-Shiong may have developed what is the closest thing yet to a cure for most cancers. He has 10 years of clinical trials, and every documentation that the FDA could possibly need to approve Anktiva for all cancers. His clinical trials show that Anktiva has astonishingly better outcomes with no damaging side effects than anything else that allopathic medicine has to offer.

As of today, the FDA has only approved Anktiva for 2 types of bladder cancer.

The Problem: his treatment mostly bypasses Chemotherapy and Radiation. I believe this is why the FDA is dragging their feet.

The United States spent 99 Billion dollars on Chemotherapy alone in 2023. So this new non toxic treatment will be an industry disrupter.

Anyone who has experienced the harsh debilitating side effects of Chemotherapy and Radiation will agree, if there is a better way to treat cancer, then it is time for the entire Cancer industry to be disrupted.

I believe that “We the People” have the power to put pressure on the FDA to approve Anktiva for all cancers. But first that requires that more people know about this, and that is why I am sharing this journey.

In this series “Hope in Real Time” I will share the following:

• In depth explanations of the treatments to the best of my ability.

• Our personal experiences and journey over the next 6 months or longer

• Knowledge on how everyone can support their Natural Killer Cells (which is the key benefit of Dr. Patrick Soon-Shiong’s Anktiva)

• Action steps you the reader can take to help educate the public on Anktiva

• I also pledge to keep this portion of my substack free for all readers.

I believe everyone deserves to know about this better way to treat cancer. I believe that everyone deserves access to Dr. Patrick Soon-Shiong’s cancer treatment. If you feel the same then help me get the world out by sharing this post.

Up next: Hope in Real Time: Our Journey inside Dr. Patrick Soon-Shiong’s Clinical Trial Part 2: Our cancer journey before being accepted into the clinical trial.

References:

https://pmc.ncbi.nlm.nih.gov/articles/PMC11848938/

https://immunitybio.com/

https://anktiva.com/

According to Dr. Patrick Soon-Shiong your Natural Killer cells are vital for keeping cancer from returning.

Chemotherapy and Radiation damage your Natural Killer cells.

Dr. Patrick Soon-Shiong has stated that most onocologists are not even paying attention to the Lymphocyte count which is crucial.

Lymphocytes are a type of white blood cell. They help your body’s immune system fight cancer and foreign viruses and bacteria. Your lymphocyte count is usually taken during a normal blood test at your healthcare provider’s office.

Lymphocytes help your body’s immune system fight cancer, foreign viruses and bacteria. Natural Killer cells are part of the Lymphocyte family.

Lymphocyte levels vary depending on your age, race, sex, altitude and lifestyle.

Radiation and Chemotherapy can lower your lymphocytes. What is the normal range of lymphocytes?

• Adults: 1,000 – 4,800 lymphocytes in every 1 microliter of blood.

• Children: 3,00- 9,500 lymphocytes in every 1 microliter of blood.

If this number is below the range you have a problem.

Dr. Patrick Soon-Shiong advocates tracking the Absolute Lymphocyte Count (ALC) for a more accurate look at your Natural Killer Cells, which most oncologist are not ordering.

You can simply request the ALC marker be included on your next blood work.

If the Absolute Lymphocyte Count is below 1,000/ul then your Natural Killer cells are dangerously low. The normal range is 1,000 – 4,800/ul. You must work on bringing those numbers up. Remember there is tons of research that shows your Natural Killer cells scour the body looking for viruses and cancer cells to eradicate before they become a problem.

I have reported on several natural therapies that can help including:

• AHCC supplement

• Redox molecules

• Del Immune V

I have recently researched what is often called “The Immune Molecule” and found a Russian study showing these can boost Natural Killer cells by a whopping 437%.

Stay tuned I will be reporting on these “Immune Molecules” in the coming weeks.

Disclaimer: The information in this post is not meant to treat, cure or diagnose. Always check with your health care provider before implementing new protocols.

If you have questions, you can e-mail me directly. Cathey@Catheypainter.com

References:

https://immunitybio.com/founders-vision/

https://my.clevelandclinic.org/health/body/23342-lymphocytes

https://pmc.ncbi.nlm.nih.gov/articles/PMC7226588/