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DMSO Transforms The Treatment of Infectious Diseases

https://www.midwesterndoctor.com/p/dmso-transforms-the-treatment-of?

DMSO Transforms The Treatment of Infectious Diseases

How DMSO can treat many challenging infections

A Midwestern Doctor
Dec 29, 2024

Story at a Glance:

•Dimethyl Sulfoxide (DMSO) is a remarkably safe naturally occurring substance that has a variety of remarkable properties that make it well suited to treating a variety of challenging medical conditions (e.g., pain, injuries, wounds, strokes, spine injuries, autoimmune conditions, cancer, and internal organ diseases).

•DMSO has broad antimicrobial properties, protects the body from microbial toxins (e.g., from C. diff), eliminates antibiotic resistance, and serves as a vehicle that can bring antimicrobials deep into the body and treat otherwise inaccessible infections.

•DMSO significantly enhances the treatment of many common bacterial infections (e.g., of the head, mouth, and skin) and many severe bacterial infections that require hospitalization (e.g., tuberculosis, sepsis, peritonitis, severe lung infections, osteomyelitis). In many cases, this has allowed an individual requiring an amputation of a chronically infected area to instead fully recover.

•DMSO has significant antiviral properties, which have most extensively been studied for herpes and shingles (both of which it excels in treating), but also in a variety of other conditions (e.g., feline panleukopenia, one of the most deadly conditions cats face.

•DMSO has significant value in treating challenging fungal and parasitic infections. Additionally, evidence suggests its utility in treating cancer and autoimmune disorders arise from DMSO’s unique antimicrobial properties.

•In this article, we will review the body of evidence showing DMSO’s remarkable contributions to the treatment of infectious diseases and provide guidance on how DMSO can be used to treat many of the conditions listed in this article.

Introduction

DMSO is a remarkably safe and naturally occurring substance (provided you use it correctly) that rapidly improves a variety of conditions medicine struggles with — particularly chronic pain. For reference, those conditions included:

  • Strokes, paralysis, a wide range of neurological disorders (e.g., Down Syndrome and dementia), and many circulatory disorders (e.g., Raynaud’s, varicose veins, hemorrhoids), which I discussed here.
  • A wide range of tissue injuries such as sprains, concussions, burns, surgical incisions, and spinal cord injuries (discussed here).
  • Chronic pain (e.g., from a bad disc, bursitis, arthritis, or complex regional pain syndrome), which I discussed here.
  • A wide range of autoimmune, protein, and contractile disorders such as scleroderma, amyloidosis, and interstitial cystitis (discussed here).
  • A variety of head conditions, such as tinnitus, vision loss, dental problems, and sinusitis (discussed here).
  • A wide range of internal organ diseases such as pancreatitis, infertility, liver cirrhosis, and endometriosis (discussed here).
  • A wide range of skin conditions such as burns, varicose veins, acne, hair loss, ulcers, skin cancer, and many autoimmune dermatologic diseases (discussed here).

In turn, since I started this series, it struck a cord and has now been seen by millions of people, and I have received over 1400 reports of remarkable responses to DMSO many readers have had (which can be read here).

This begs an obvious question — if a substance capable of doing all of that exists, why does almost no one know about it? Simply put, like many other promising therapies, it fell victim to a pernicious campaign by the FDA which kept it away from America despite decades of scientific research, Congressional protest, and thousands of people pleading for the FDA to reconsider their actions. Consider for example, this 60 Minutes program about DMSO that aired on March 23, 1980.  (Go to top link to watch program)

DMSO and Infectious Diseases

DMSO has a variety of unique properties that make it incredibly well suited to addressing microbial infections (e.g., bacteria, fungi, viruses, and parasites).

These include:

  • While non-toxic, it has an antiseptic effect that is harmful to microorganisms, especially the smallest ones (mycobacteria, cell wall deficient bacteria, and viruses). This property appears to be the most beneficial for herpes, shingles, and other complex conditions, which I believe have a microbiological component (e.g., cancer and autoimmunity).
  • It can remove the antibiotic resistance of bacteria. This is particularly helpful in widespread problematic infections that have gradually developed a resistance to many existing antibiotics (e.g., tuberculosis) and challenging infections that are not responding to antibiotics (e.g., ones that would otherwise require an amputation).
  • It can further increase the sensitivity of already susceptible microorganisms to antimicrobial agents.
  • It can deliver antimicrobial agents to areas that are typically difficult to reach (e.g., deep in a bone) and also directly to regions that would otherwise require a systemic application of the medication.
  • It can increase circulation to many parts of the body, something which is often critical for resolving illnesses (as a healthy blood supply allows the immune system to enter and heal diseased areas). Likewise, pretreatment with DMSO has been shown to increase the immune system’s ability to resist a subsequent infection.
  • Much in the same way DMSO protects cells from a wide variety of lethal stressors, it can also protect them from the harmful effects of bacterial toxins (e.g., with the most pertinent applications studied being for sepsis and clostridium difficile). Likewise, it can also mitigate the toxicity of antimicrobial agents taken for a prolonged period.

DMSO and Bacterial Infections

DMSO has six properties that make it useful in treating bacterial infections.

  1. Data suggests DMSO increases bacterial cell membrane permeability and concurrently creates changes in the cell indicative of damage to its membrane. In addition to directly eliminating bacteria, it also reduces their ability to prevent antibiotics from entering them. In turn, existing data shows DMSO has a much greater ability to increase the potency of antibiotics that target structures inside bacteria rather than ones that target their cell wall (e.g., penicillin).
    Note: this property is particularly important for tuberculosis as it has a robust external barrier that impairs antibiotic entry.
  2. By increasing membrane permeability, it can also make bacteria more susceptible to taking up the nucleic acids of lethal bacteriophages (viruses that kill bacteria and have been extensively researched outside of America due to their efficacy in treating a wide range of bacterial infections).
  3. DMSO can often simply dissolve bacteria and cause their contents to leak out.
  4. DMSO can interfere with the normal functioning of bacteria. A 1977 study, for instance, found that it interferes with the production of membrane proteins that E. coli (and other bacteria) need for metabolism.
  5. As discussed throughout a previous article, DMSO greatly improves circulation (which, when impaired often leads to chronic infections).
  6. In the same way DMSO can protect cells from various lethal stressors (discussed here), DMSO effectively mitigates the harmful effects of many bacterial toxins.

Cancer and Autoimmunity

One of DMSO’s widely recognized properties is that it causes cancerous cells to revert to normal. In researching that, I came across a fascinating study that tested cancer patients for pleomorphic bacteria (something many previous pioneers of successful but suppressed alternative cancer therapies like Rife and Naessens also believed caused many cancers). While difficult to culture, pleomorphic bacteria were eventually isolated from the blood of some of them, in the blood of some of those who had been around those who had recently died from cancer for a prolonged period.

Note: the morphology of the bacteria is extensively described in the paper, but essentially matches what many other pleomorphic researchers have found over the years.

The pleomorphic model of bacteria (discussed further here) essentially states that bacteria can significantly change their morphology (to the point they are almost unrecognizable from their original form), that these changes are often done in response to their environment, and that some forms are relatively harmless to the body, while others cause disease. In turn, since things that kill bacteria often transform them into ones that are more pathogenic, a longtime belief within certain schools of natural medicine is that the goal should be to change the terrain of the body to encourage a benign morphology of bacteria rather than trying to kill them all off.

A large group of modern researchers studied this subject for decades (e.g., hundreds of research studies they conducted are summarized in this wonderful textbook by Lida Mattman). Five of their key observations were:

  1. Antibiotics will often fail to kill every bacteria present and then trigger those that survive to enter a primitive survival state known as a “cell wall deficient” (CWD) form resembling a mycoplasma. This process in turn, was most commonly triggered by antibiotics that attack bacterial cell walls (which characterizes many commonly used antibiotics).
  2. CWD bacteria are very hard to detect (most standard microbial methods will determine that no organisms are there when CWDs are present).
  3. When conditions are more optimal for survival, CWD organisms can revert to the active form and cause an infection that had been eliminated with antibiotics to suddenly and inexplicably recur (which, for example, we frequently see with urinary tract infections).
  4. Once present, CWD bacteria will often enter cells and cause chronic inflammation because the immune system will attack cells with the CWD bacteria.
  5. Many different unexplained autoimmune disorders (e.g., sarcoidosis) have characteristic CWD bacteria present that can be repeatedly identified from their inflamed tissue (the textbook cites an exhaustive amount of data substantiating this).

While standard antibiotics are ineffective in treating CWD infections, non-standard ones (e.g., erythromycin or minocycline) often are, but the sensitivity to those antibiotics is highly variable depending on the causative organism.

In practice, we find 10-15% of chronic illnesses (including blood clots and cancers) have a pleomorphic etiology, but rather than try to eliminate those organisms with antibiotics (which always have side effects), we instead give signaling products derived from healthy bacteria that cause the pathologic bacteria to transform into a non-harmful form, which in those applicable cases, frequently yields remarkable results (e.g., this approach is very useful for lupus and many cancers). Likewise, I believe this model explains a longstanding belief within natural medicine that giving antibiotics for an acute infection often transforms it into a chronic illness down the road.

Note: ultraviolet blood irradiation is also quite effective at eliminating these organisms and the diseases they cause. 

Lastly, Individuals with chronic fatigue syndrome often find relief from DMSO, which some have attributed to its antiviral properties (e.g., towards Epstein Barr). This for example, is a letter Stanley. Jacob received from a patient.

Note: Readers have also reported to me (e.g., here, here, and here) that DMSO helped their chronic fatigue.  (See link for article)

______________

**Comment**

Please note that DMSO did best when it was coupled with antibiotics or other antimicrobials.

For more:

  • https://madisonarealymesupportgroup.com/2018/03/02/dmso-msm-for-lyme-msids/
  • https://madisonarealymesupportgroup.com/2024/11/01/how-dmso-cures-eye-ear-nose-throat-and-dental-disease/
  • https://madisonarealymesupportgroup.com/2024/10/25/how-dmso-treats-incurable-autoimmune-and-contractile-disorders/
  • https://madisonarealymesupportgroup.com/2024/09/16/dmso-its-remarkable-properties/
  • https://madisonarealymesupportgroup.com/2024/12/18/dmso-protects-heals-organs-and-revolutionizes-the-skin/

Category:

C-diff, Cancer, Dentistry, Eye Issues, Inflammation, Lyme, Pain Management, Parasites, research, Treatment, Viruses

Holistic Healing From Lyme Disease

https://open.spotify.com/episode/6NrQSPu2G1mLXey82vETIY?si=38cLPjQXSsOvDcijvgNqcw&nd=1&dlsi=060f76815c2e45d7  Go here to listen on Spotify (Approx. 1 hour)

https://podcasts.apple.com/us/podcast/holistic-healing-from-lyme-disease-with-theresa/id1771868024?i=1000681031732  Go here to listen on Apple Podcasts

Holistic Healing From Lyme Disease

Theresa Haselmayer/Foundations Wellness

12/19/24

Co-host Dan Wagner sits down with the founder of Foundations Wellness, Theresa Haselmayer, R.N., to discuss her journey from patient to healer.  With over 33 years of varied clinical experience, Theresa trained for 4 years at the Uprooting Lyme Clinic in Hudson Valley NY, a hotbed of Lyme Disease.  She is currently one of dozens of highly knowledgable certified Uprooting Lyme practitioners nationwide.  Theresa is also a member of ILADS, the International 
Lyme and Associated Diseases Society, as well as ISEAI – The International Society of Environmentally Acquired Illness.  

For more:

  • https://madisonarealymesupportgroup.com/2016/02/13/lyme-disease-treatment/

Category:

Herbs, Lyme, Treatment

Advances in Lyme & Babesiosis Research

https://www.globallymealliance.org/news/from-diagnostics-to-disease-mechanisms-advances-in-lyme-and-babesiosis-research?

From Diagnostics to Disease Mechanisms: Advances in Lyme and Babesiosis Research

by Cara DeAngelis, Ph.D. on January 3, 2025

<span id="hs_cos_wrapper_name" class="hs_cos_wrapper hs_cos_wrapper_meta_field hs_cos_wrapper_type_text" style="" data-hs-cos-general-type="meta_field" data-hs-cos-type="text" >From Diagnostics to Disease Mechanisms: Advances in Lyme and Babesiosis Research</span>
Cutting-edge research funded by GLA advances diagnostics and insights into Lyme disease and babesiosis, identifying key biomarkers and genetic risk factors.

Three GLA-funded investigators have been making exciting progress. Dr. Rafal Tokarz’s team has been uncovering key insights into the immune response to specific proteins of Lyme bacteria, paving the way for more accurate diagnostics. Dr. Ben Mamoun has achieved an important milestone by developing the first diagnostic tests for detecting active Babesia duncani infections.  Dr. Klemen Strle’s research suggests that specific genetic factors may increase the risk of developing chronic Lyme arthritis. Meanwhile, Dr. Strle’s new findings are shedding light on how certain genetic factors may heighten the risk of developing chronic Lyme arthritis. 

Summary: 

GLA-funded research continues to shed light on key aspects of Lyme and tick-borne diseases, from diagnostic biomarkers to genetic factors influencing disease outcomes. 

Dr. Rafal Tokarz and his team at Columbia University used peptide arrays and machine learning to identify immune reactive proteins in Borrelia burgdorferi to differentiate between phases of Lyme disease. These insights could enhance the accuracy of antibody-based diagnostic tests by improving their sensitivity and specificity (Tokarz et al., 2024). 

At Yale University, Dr. Choukri Ben Mamoun and his team developed the first antigen detection tests for Babesia duncani, a parasite often responsible for severe babesiosis. These assays, validated with over 1,700 samples, can detect active infections with high sensitivity and specificity, paving the way for early diagnosis, reservoir animal screening, and improved blood safety (Chand et al., 2024).  

Research by Dr. Klemen Strle and his group at Tufts University identified genetic variations associated with chronic Lyme arthritis. These variations are linked to increased inflammation and autoantibody responses, suggesting that some patients may have a genetic predisposition to persistent arthritis in Lyme disease. These findings may guide future biomarker development to predict disease risk (Ehrbar et al., 2024). 

These studies reflect GLA’s unwavering commitment to support research that addresses critical challenges in diagnosing and managing tick-borne diseases. 

Publications: 

Tokarz, R., Guo, C., Sanchez-Vicente, S., Horn, E., Eschman, A., Turk, S. P., Lipkin, W. I., & Marques, A. (2024). Identification of reactive Borrelia burgdorferi peptides associated with Lyme disease. mBio, 15(10). https://doi.org/10.1128/mbio.02360-24   

Chand, M., Vydyam, P., Pal, A. C., Thekkiniath, J., Darif, D., Li, Z., Choi, J. Y., Magni, R., Luchini, A., Tonnetti, L., Horn, E. J., Tufts, D. M., & Ben Mamoun, C. (2024). A set of diagnostic tests for detection of active Babesia duncani infection. International Journal of Infectious Diseases, 147, 107178. https://doi.org/10.1016/j.ijid.2024.107178  

Ehrbar, D., Arvikar, S. L., Sulka, K. B., Chiumento, G., Nelson, N. L. J., Hernandez, S. A., Williams, M. A., Strle, F., Steere, A. C., & Strle, K. (2024). Variants in the late cornified envelope gene locus are associated with elevated T-helper 17 responses in patients with postinfectious Lyme arthritis. The Journal of Infectious Diseases, 230(Supplement_1), S40–S50. https://doi.org/10.1093/infdis/jiae164  

https://www.globallymealliance.org/news/decoding-chronic-lyme-investigating-epigenetic-signatures?

Decoding Chronic Lyme: Investigating Epigenetic Signatures

by Admin at Global Lyme Alliance on January 3, 2025

<span id="hs_cos_wrapper_name" class="hs_cos_wrapper hs_cos_wrapper_meta_field hs_cos_wrapper_type_text" style="" data-hs-cos-general-type="meta_field" data-hs-cos-type="text" >Decoding Chronic Lyme: Investigating Epigenetic Signatures</span>
Pictured: Tanja Petnicki-Ocwieja, PhD, courtesy of Tufts University School of Medicine
Tufts University, with support from GLA, is leading research to uncover epigenetic mechanisms behind chronic Lyme disease. Dr. Tanja Petnicki-Ocwieja’s work could improve treatments and reveal commonalities with other post-infectious syndromes like long COVID.

By Mase Peterson

In the fight against Lyme disease, cutting-edge research is essential for advancing treatment and prevention strategies. Tanja Petnicki-Ocwieja, PhD, a research assistant professor at Tufts University School of Medicine, is a key contributor to this effort through her work with the Tufts Lyme Disease Initiative. This collaborative group of faculty, staff, and students is dedicated to eliminating the public health threat of Lyme disease by 2030.

Tufts is home to one of the world’s most comprehensive groups of tick-borne disease researchers. Led by co-directors Linden Hu, Paul and Elaine Chervinsky Professor of Immunology, and Robert P. Smith, a physician at Maine Medical Center and professor of medicine, the team recently secured a $20.7 million federal grant, further solidifying Tufts’ position as a global leader in Lyme disease research.

In this Q&A, part of a feature series spotlighting members of the Initiative, Professor Petnicki-Ocwieja discusses her research on the immunological and epigenetic mechanisms underlying chronic Lyme disease and its potential to transform patient outcomes…

Read the rest from Tufts School of Medicine

_____________

**Comment**

I’d love to be hopeful, but when the moniker PTLDS continues to be used it shows an inherent bias that ongoing infections aren’t to blame for people’s ongoing symptoms.  This must change.

For more:

  • https://madisonarealymesupportgroup.com/2020/08/13/slyme-an-interview-we-need-to-drop-the-term-ptld-like-a-bad-habit/
  • https://madisonarealymesupportgroup.com/2020/08/16/70-post-treatment-lyme-disease-syndrome-publications-ignore-infection/
  • https://madisonarealymesupportgroup.com/2023/08/02/nih-funds-ptlds-research-more-deception/
  • https://madisonarealymesupportgroup.com/2019/03/25/the-shortfalls-of-h-r-220-national-lyme-and-tick-borne-diseases-control-and-accountability-act-of-2019-the-devil-is-in-the-details/  Very important article laying out the sordid details controlling Lymeland that are imperative to know.
  • https://madisonarealymesupportgroup.com/2023/03/17/iv-antibiotics-helpful-for-ptlds/
  • https://madisonarealymesupportgroup.com/2022/06/22/efficacy-of-short-term-high-dose-pulsed-dapsone-combination-therapy-in-the-treatment-of-chronic-lyme-disease-post-treatment-lyme-disease-syndrome-ptlds-associated-coinfections-a-report-of-3-c/
  • https://madisonarealymesupportgroup.com/2021/03/10/how-ptlds-aca-affect-lyme-patients/
  • https://madisonarealymesupportgroup.com/2021/03/15/part-2-ptld-insurance-coverage/
  • https://madisonarealymesupportgroup.com/2021/03/18/part-3-ptld-insurance-coverage/

Category:

Babesia, Lyme, research, Uncategorized

First Reported U.S. H5N1 Death, COVID Shot Brain Damage & Hundreds of Operational Biolabs

https://petermcculloughmd.substack.com/p/first-reported-us-h5n1-bird-flu-death?

First Reported U.S. H5N1 Bird Flu Death, COVID-19 ‘Vaccine’ Brain Damage, and Hundreds of Operational Biolabs

Epidemiologist Nicolas Hulscher on Brannon Howse Live
 
Nicolas Hulscher, MPH
Jan 07, 2025

Please enjoy my interview on Worldview Tube with Brannon Howse, where we discuss breaking public health developments:

  1. The first H5N1 bird flu death ever reported in the United States: The Louisiana Department of Health should release more details — This patient was over 65 years old with multiple underlying health conditions. It’s entirely possible that these pre-existing conditions were the primary cause of death, rather than H5N1 itself. A few weeks ago, Labcorp launched an H5N1 bird flu PCR test in the U.S., now available for order through physicians. As a result, we can expect the Biopharmaceutical Complex to soon use falsely inflated PCR ‘case counts’ and the first reported death as tools to increase public fear of bird flu, driving higher demand for bird flu vaccinations.

  2. Catastrophic Neurological and Psychiatric Damage from COVID-19 ‘Vaccines’: Increased risks of ischemic stroke, hemorrhagic stroke, transient ischemic attack, myelitis, myasthenia gravis, Alzheimer’s disease, cognitive impairment, depression, anxiety, and sleep disorders.

  3. Biolabs: We need a clean sweep of the hundreds of operational BSL3/BSL4 biolabs that possess modified pathogens with pandemic potential, most of which are located in dense population centers. Since 2001, there have been ~300 confirmed biolab pathogen leaks globally, with the vast majority (78.6%) occurring in the United States. State-sponsored bio-terrorism must be SHUT DOWN to prevent another man-made pandemic.

_______________

For More:

  • https://madisonarealymesupportgroup.com/2025/01/07/despite-mounting-evidence-data-covid-shots-continue-to-kill-maim/
  • https://madisonarealymesupportgroup.com/2024/12/31/wisconsin-dhs-reports-presumptive-positive-human-case-of-h5n1-meanwhile-congress-looks-to-bankroll-more-biolabs-to-experiment-on-dangerous-pathogens/
  • https://madisonarealymesupportgroup.com/2023/02/08/more-on-u-s-funding-of-biolabs-in-ukraine-a-jobs-program-for-foreign-scientists/
  • https://madisonarealymesupportgroup.com/2024/04/09/here-we-go-again-the-great-bird-flu-scare-is-back-cdc-sends-alert/
  • https://madisonarealymesupportgroup.com/2024/12/09/unidentified-flu-like-illness-h5n1-more-fear-porn/
  • https://madisonarealymesupportgroup.com/2020/05/05/2009-h1n1-vaccine-caused-brain-damage-in-children-dont-let-it-happen-again/
  • https://madisonarealymesupportgroup.com/2018/12/11/ny-senator-passes-away-at-47-after-linking-illness-to-flu-shot-symptoms/
  • https://madisonarealymesupportgroup.com/2018/12/14/man-blames-flu-shot-for-blindness-partial-paralysis/
  • https://madisonarealymesupportgroup.com/2019/01/29/awkward-flu-jabs-attempted-at-golden-globes/
  • https://madisonarealymesupportgroup.com/2021/03/02/60-minutes-1979-swine-flu-investigation-has-uncanny-resemblance-to-covid-19/

Category:

Activism, vaccines, Viruses

Despite Mounting Evidence & Data, COVID Shots Continue to Kill & Maim

Despite all common sense, repeated warnings, and:

  • censored evidence that the mRNA injections are neither effective nor safe but actually have negative efficacy
  • causing more adverse reactions and death than any other vaccine historically
  • an FDA study showing DNA levels exceeding safety limits by 6-470 times
  • 63 peer-reviewed studies linking COVID shots to ‘vaccine’ resistant viral variants
  • studies showing surges in deadly neurological, psychiatric, and endothelial damage
  • proof there are at least 55 undeclared chemical elements
  • proof nanoparticles are “microchips” that emit signals known as “MAC address” phenomenon that persist in the body for at least two years
  • proof they are a biological weapon delivery system
  • delayed media admissions
they still have not been removed! 

And now world leaders in 10 countries have received ‘notice of extreme concern’ from a team of experts who are calling for the shots to be banned from public use.

https://lionessofjudah.substack.com/p/global-covid-vaccine-damage-estimates?

Global COVID ‘Vaccine’ Damage Estimates by Edward Dowd

“Killed: 7.5 – 15 million people, Disabled: 29 – 60 million people, Injured: 500 – 900 million people….Arrests made: ZERO”

Lioness of Judah Ministry
Dec 29, 2024
Global COVID ‘vaccine’ damage estimates by ex-BlackRock executive, whistleblower, Ed Dowd:

Killed: 7.5 – 15 million people

Disabled: 29 – 60 million people

Injured: 500 – 900 million people

5 billion people received mRNA shot(s)

Arrests made: ZERO

Notice that the world appears to be in a constant wars, but in a matter of months every country magically agreed to use an untested, experimental ‘vaccine’ with lipid nanoparticles.

Source: EDWARD DOWD

https://petermcculloughmd.substack.com/p/vast-mrna-vaccine-biodistribution?

Vast mRNA ‘Vaccine’ Biodistribution, Persistence, and Adjuvant Toxicity Research Library Published

Over 100 peer-reviewed studies demonstrate serious safety concerns.

Nicolas Hulscher, MPH
Dec 28, 2024

A comprehensive research library that contains over 100 peer-reviewed studies (n=130) documenting mRNA “vaccine” biodistribution, persistence, and adjuvant toxicity has just been published (Compiled by Dr. Martin Wucher, MSC Dent Sc (eq DDS), Dr. Byram Bridle, PhD, Erik Sass, et al). You can read it here.

Be sure to also check out their massive Spike protein Pathogenicity Research Library, which has now been updated to include 320 peer reviewed studies.

For those who still believe COVID-19 injections are safe, I encourage you to carefully review the over 400 peer-reviewed studies available in both libraries and then reassess your position.

Nicolas Hulscher, MPH

Epidemiologist and Foundation Administrator, McCullough Foundation

http://www.mcculloughfnd.org

_______________


Recently Steve Kirsch gave the following information:
There is no Autism in the Amish community as well as any of the other newer diseases such as ADD, autoimmune disease, PANDAS, PANS, epilepsy, etc.  The U.S. has been studying the Amish for decades, but there’s never been a public report.  The reason is it would show that if you don’t follow government guidelines you’re going to end up healthier.

Category:

Activism, vaccines, Viruses

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  • Mycoplasma Treatment
  • Pain Management
  • PANS
  • Parasite Treatment
  • Parasites
  • Pregnancy
  • Prevention
  • Psychological Aspects
  • Q Fever
  • research
  • Rickettsia
  • Rocky Mountain Spotted Fever
  • Sleep
  • Supplements
  • Support Group Presentations
  • Syphilis
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  • thyroid
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  • Ticks
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  • Tularemia
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  • vaccines
  • Viruses
  • Zika

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