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Archive for the ‘Treatment’ Category

Lyme Disease Rash: What Does It Really Look Like?

https://danielcameronmd.com/lyme-disease-rash/

Lyme Disease Rash: What Does It Really Look Like?

lyme-disease-rash

Learn all about Lyme disease and rashes in this informative video. In this video, I discuss the various appearances of a Lyme Disease rash, also known as an erythema migrans (EM) rash.

By Dr. Daniel Cameron

Many people assume that a Bull’s-eye or erythema migrans (EM) rash is a common manifestation of Lyme disease. And that the lack of a rash confirms a person does not have the disease. This is far from the truth.

EM rash identification remains a challenge because it often takes on a variety of appearances, according to a study by Burlina and colleagues.

“Only 20% of patients with an EM [rash] in the United States present with lesions that have the central clearing of a classic target lesion (“ring-within-a-ring” or “bull’s eye”).¹

Instead, “the majority of EM lesions appear uniformly red or bluish-red in color and lack central clearing.”

Unfortunately, a Lyme disease rash may look like lesions found in other disorders. For instance, patients with Lyme disease may be misdiagnosed as having a cellulitis rash. The treatment for cellulitis is not necessarily effective for Lyme disease.

Furthermore, between 4% and 8% of Lyme disease rashes present with a central blistering. These cases can be misdiagnosed as shingles, a viral infection that causes blistering and is treated with anti-viral medications. Shingles treatment is not effective in treating Lyme disease.

READ MORE: It wasn’t shingles. It was Lyme disease.

Lastly, about 20% of patients have multiple EM rashes at the time of diagnosis due to the Lyme spirochete disseminating to other areas of the body. This presentation can be confused with erythema multiforme or other skin disorders.

In practice, I treat with an antibiotic if there is uncertainty, as the consequences of missing a diagnosis of Lyme disease can be serious. If the rash is questionable, I often treat with antibiotics that would be effective for either Lyme disease or another possible condition. For example, I might treat a patient with a rash that could be cellulitis or Lyme disease with an antibiotic that works for both such as cefuroxime rather than Keflex.

I typically treat these cases longer if Lyme disease is a possibility. Finally, I have also treated patients with a combination of an anti-viral medication (Valtrex) and cefuroxime if I am unsure whether the rash is related to shingles or Lyme disease.

References:
  1. Burlina PM, Joshi NJ, Mathew PA, Paul W, Rebman AW, Aucott JN. AI-based detection of erythema migrans and disambiguation against other skin lesions. Comput Biol Med. 2020;125:103977.

For more:

  • https://madisonarealymesupportgroup.com/2023/01/26/the-many-presentations-of-the-lyme-disease-rash/
  • https://madisonarealymesupportgroup.com/2019/07/09/not-all-lyme-rashes-are-created-equal/
  • https://madisonarealymesupportgroup.com/2021/07/20/lyme-disease-skin-rash-puzzles-doctors-leads-to-misdiagnoses/
  • https://madisonarealymesupportgroup.com/2019/03/26/formally-challenging-cdc-advice-on-lyme-disease-rashes/
  • https://madisonarealymesupportgroup.com/2020/07/18/misdiagnosis-of-lyme-caused-rash-can-have-potentially-fatal-consequences/
  • https://pmc.ncbi.nlm.nih.gov/articles/PMC7566400/
  • https://madisonarealymesupportgroup.com/2019/02/21/lyme-disease-dont-wait-for-blood-tests-where-patients-have-bullseye-rash/

Category:

Lyme, research, Treatment, Viruses

Part 2: Symptoms After Lyme Disease – What’s Past is Prologue

https://www.change.org/p/the-us-senate-calling-for-a-congressional-investigation-of-the-cdc-idsa-and-aldf/u/33160256?

Symptoms after Lyme disease: What’s past is prologue (Adriana Marques, M.D.) Part 2

Carl Tuttle
Hudson, NH, United States
Jan 12, 2025

As a follow-up to my previous update regarding my letter-to-the-editor of SCIENCE TRANSLATIONAL MEDICINE, the editor refuses to publish my eLetter.

Previous update:

Symptoms after Lyme disease: What’s past is prologue (Adriana Marques, M.D.)
https://www.change.org/p/the-us-senate-calling-for-a-congressional-investigation-of-the-cdc-idsa-and-aldf/u/33044899

I have sent multiple inquiries to Editor Dr. Orla Smith with evidence of antibiotic resistance that has been suppressed/concealed by those who have colluded to deny chronic Lyme disease and here is just one of those letters for your review…

Photo of Marques was found on the following NIH site:
https://www.niaid.nih.gov/research/adriana-marques-md

———- Original Message ———-
From: CARL TUTTLE <runagain@comcast.net>
To: Orla Smith <osmith@aaas.org>
Cc: Courtney Malo <cmalo@aaas.org>, “cope_assistant@publicationethics.org” <cope_assistant@publicationethics.org>, Melissa Norton <mnorton@aaas.org>, Catherine Charneski <ccharneski@aaas.org>, Brandon Berry <bberry@aaas.org>, Dorothy Hallberg <dhallberg@aaas.org>, Daniela Neuhofer <dneuhofer@aaas.org>, Molly Ogle <mogle@aaas.org>, “marybethpf@aol.com” <marybethpf@aol.com>, “aaron@sirillp.com” <aaron@sirillp.com>
Date: 01/12/2025 8:58 AM EST
Subject: Re: Symptoms after Lyme disease: What’s past is prologue

Dr Smith,

For additional evidence of antibiotic resistance, please see the following letter addressed to Dr. Raymond Dattwyler who owns 24 patents for Lyme disease that include diagnostic testing and vaccines both live bacteria and oral.

Guideline signatory Raymond Dattwyler endorses the categorical assertion that chronic Lyme disease does not exist yet his patent for novel chimeric nucleic acids and protein antigens which could serve as a basis for a vaccine or for improved immunodiagnostic reagents for Lyme disease, issuing almost contemporaneously with the 2006 IDSA Lyme Disease Guidelines seems to say exactly the opposite:

“Currently, Lyme Disease is treated with a range of antibiotics, e.g. tetracycline, penicillin and cephalosporins. However, such treatment is not always successful in clearing the infection. Treatment is often delayed due to improper diagnosis with the deleterious effect that the infection proceeds to a chronic condition, where treatment with antibiotics is often not useful. One of the factors contributing to delayed treatment is the lack of effective diagnostic tools.” (Dattwyler, et.al. United States Patent 7,179,448)

Letter to Dattwyler: (It should be noted there was no response)

Important Note!: My letter to Dattwylwyler includes a 1995 study from Stony Brook Lyme clinic. I understand the patient received thirteen spinal taps, multiple courses of IV and oral meds, and relapsed after each one, proven by CSF antigens and/or PCR. The only way this patient (said to be a physician) remained in remission was to keep her on open ended clarithromycin which she was taking for 22 months by the time of publication.

———- Original Message ———-
From: CARL TUTTLE <runagain@comcast.net>
To: “Raymond_Dattwyler@nymc.edu” <Raymond_Dattwyler@nymc.edu>
Cc: “npjvaccines@nature.com” <npjvaccines@nature.com>, “abarrett@utmb.edu” <abarrett@utmb.edu>, “R.W.Titball@exeter.ac.uk” <R.W.Titball@exeter.ac.uk>, “mgomesso@uthsc.edu” <mgomesso@uthsc.edu>
Date: 01/06/2023 2:46 PM EST
Subject: The year that shaped the outcome of the OspA vaccine for human Lyme disease

npj Vaccines Jan 2022

The year that shaped the outcome of the OspA vaccine for human Lyme disease
https://www.nature.com/articles/s41541-022-00429-5
Raymond J. Dattwyler & Maria Gomes-Solecki

Department of Microbiology and Immunology

New York Medical College

Valhalla, NY

Raymond J. Dattwyler, Corresponding Author

Dear Dr. Dattwyler,

I read your manuscript with great interest as you call attention to a treatment-resistant Lyme arthritis with “no evidence of DNA” found in the joints of patients after antibiotic treatment.

For some strange reason however, I could not find the following 1995 publication within your paper identifying treatment-resistant neuroborreliosis:

European Neurology 1995

Seronegative Chronic Relapsing Neuroborreliosis
https://www.karger.com/Article/Abstract/117104

Lawrence C., Lipton R.B., Lowy F.D., Coyle P.K.d

Abstract

We report an unusual patient with evidence of Borrelia burgdorferi infection who experienced repeated neurologic relapses despite aggressive antibiotic therapy. Each course of therapy was associated with a Jarisch-Herxheimer-like reaction. Although the patient never had detectable free antibodies to B. burgdorferi in serum or spinal fluid, the CSF was positive on multiple occasions for complexed anti-B. burgdorferi antibodies, B. burgdorferi nucleic acids and free antigen.

In fact, Dr. Dattwyler there seems to be a great deal of “treatment-resistant” evidence published in multiple journals over the past three decades:

Peer Reviewed Evidence of Persistence of Lyme Disease Spirochete Borrelia burgdorferi and Tick-Borne Diseases (700 References)
https://www.dropbox.com/s/n09sk90eo6xz7ua/700%20articles%20LYME%20EvidenceofPersistence-V2.pdf?dl=0

So that brings me to the reason for this email…

Question:

Does a chronic relapsing seronegative disease fit the vaccine model? If not, would that, in and of itself, be the hidden reason for denying chronic (treatment-resistant) Lyme disease for almost three decades?  In other words, patent royalties and pharmaceutical profits over lifesaving care?

A response to this inquiry is requested.

Carl Tuttle
Hudson, NH

Cc: Alan D.T. Barrett, PhD Editor-in-Chief

Rick Titball, PhD, DSc, Deputy Editor

Letter to the Editor of the BMJ published June 2020
https://www.bmj.com/content/369/bmj.m1041/rr-1

_______________

**Comment**

BOOM!  Another mic drop from Tuttle.

Seriously, the lunacy is breath-taking.

Category:

Activism, Lyme, Treatment, vaccines

Lyme & Herxheimer Reaction in Newborn

https://danielcameronmd.com/lyme-disease-herxheimer-reaction-newborn/

Lyme disease and herxheimer reaction in newborn

Newborn with lyme disease and herxheimer reaction being examined by doctor.

The Herxheimer reaction, also referred to as a Jarisch-Herxheimer reaction, is “a transient clinical phenomenon that occurs in patients infected by spirochetes who undergo antibiotic treatment.”¹ It was first described in patients with syphilis but has also been associated with other spirochetal infections including leptospirosis, Lyme disease, and relapsing fever. The reaction is associated with the onset of new symptoms or a worsening of existing symptoms in patients receiving antibiotic treatment.

By Dr. Daniel Cameron

In 2020, investigators published a case involving a 13-year-old boy with Lyme arthritis, a common manifestation of Lyme disease, who developed a Herxheimer reaction when treated with doxycycline. On the 7th day of treatment, the boy developed a low-grade fever and severe arthralgias with intense hip, ankle and cervical spine pain and myalgias.

You can read more about the 13-year-old boy’s case in an earlier blog “Herxheimer reaction in a 13-year-old boy with Lyme disease.” 

Newborn with herxheimer reaction

In their article “Lyme disease in a neonate complicated by the Jarisch–Herxheimer reaction,”  Prodanuk and colleagues² describe the case of a 21-day-old infant who was admitted to the hospital with decreased activity, poor feeding and abdominal distension.

The parents removed an engorged tick from the infant’s forearm 5 days earlier. An EM rash was present at the site of the tick bite.

“Given the erythema migrans lesion at the site from which the engorged tick was removed, we made a presumptive diagnosis of Lyme disease and administered IV ceftriaxone,” the authors write.

Two hours after treatment began, the infant developed a fever, tachycardia and other symptoms consistent with the Jarisch–Herxheimer reaction.

Testing for Lyme disease was negative.

Clinicians should also “be aware of the possibility of the Jarisch–Herxheimer reaction during the initial phase of treatment.”²

Several studies, they warn, indicate “newborns with findings consistent with early localized disease may also be at higher risk for disseminated disease.”

“Given the limited data for neonates and the possible predisposition of this population to disseminated Lyme disease, clinicians should strongly consider administering IV antibiotics to target Lyme disease,” the authors suggest.

Patients can experience a broad range of symptoms resulting from a herxheimer reaction, explains Nykytyuk and colleagues, including fever, severe polyarthralgias, myalgias, chills, hypotension, nonpruritic, nonpalpable rash, tachycardia, nausea, headache, strengthening of existing or occurrence of new symptoms of the underlying disease.¹

The exact cause of Jarisch-Herxheimer reactions is still unknown. “At first, the role of an endotoxin in the development of JHR was suggested, but later experimental studies showed that spirochetes do not have biologically active endotoxins,” the authors explained.¹

References:
  1. Dhakal A, Sbar E. Jarisch Herxheimer Reaction. [Updated 2022 Apr 28]. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2022 Jan-. Available from: https://www.ncbi.nlm.nih.gov/books/NBK557820/
  2. Prodanuk M, Groves H, Arje D, Bitnun A. Lyme disease in a neonate complicated by the Jarisch-Herxheimer reaction. CMAJ. 2022 Jul 18;194(27):E939-E941. doi: 10.1503/cmaj.220112. PMID: 35851530; PMCID: PMC9299745.

______________

For more:

  • https://madisonarealymesupportgroup.com/2023/11/14/its-crucial-to-acknowledge-treat-congenital-lyme-disease/
  • https://madisonarealymesupportgroup.com/2022/09/16/congenital-lyme-part-1-2/
  • https://madisonarealymesupportgroup.com/2022/03/22/congenital-lyme-the-nih/
  • https://madisonarealymesupportgroup.com/2018/06/19/33-years-of-documentation-of-maternal-child-transmission-of-lyme-disease-and-congenital-lyme-borreliosis-a-review/
  • https://madisonarealymesupportgroup.com/2018/11/17/young-boy-infected-congenitally-with-lyme-speaks-in-ottawa-house-of-commons/
  • https://madisonarealymesupportgroup.com/2021/01/14/mothers-children-panel-5th-annual-lymemind-conference-2020/
  • https://madisonarealymesupportgroup.com/2019/01/28/who-removes-congenital-lyme-from-diagnostic-reference/
  • https://madisonarealymesupportgroup.com/2018/11/11/gestational-lyme-other-tick-borne-diseases-dr-jones/
  • https://madisonarealymesupportgroup.com/2018/02/26/transplacental-transmission-fetal-damage-with-lyme-disease/
  • https://madisonarealymesupportgroup.com/2018/12/12/systematic-review-on-gestational-lyme/

Category:

Lyme, Pregnancy, research, Testing, Ticks, Transmission, Treatment

Chlorine Dioxide: Yet Another Safe, Cheap Treatment Attacked by the FDA

Similarly with DMSO, I’ve sat on the topic of Chlorine Dioxide for years hoping someone  more educated and experienced than I would write about it.  That day has come!

Regarding Lyme disease and CI02, I highly recommend a $7 book written by a patient who used it successfully.  In short, you mix up a daily bottle and drink a specified amount that gives you 3 drops an hour for 8 hours a day after titrating up from one drop.  It’s cheap and safe.  Other than the inconvenience of hourly dosing, it does taste like bleach even though it isn’t bleach.  For those looking for a cheap treatment – it doesn’t get any cheaper than this.  Write and tell me your results.

Even Dr. Pierre Kory has written about how Bolivia’s use of CI02 led to the best outcomes for COVID in South America as well as the fact it is a broad and powerful anti-microbial and disinfectant. Over 500 U.S public water treatment plants add chlorine dioxide to the water full time and as many as 900 use it either part time or seasonally (Leister 2021). Safety levels of orally ingested doses have been well established and are far above therapeutic dosing ranges, period. Numerous oral care and dental products on the market contain chlorine dioxide and a number of trials using intravenous chlorine dioxide have been done safely.

To demonstrate how “dangerous” chlorine dioxide is to the powers that be, know that chlorine dioxide was attacked as a proposed treatment for Covid -19 even before HCQ and ivermectin. It literally was one of the first therapeutics “they” tried to discredit as physicians across the world were searching for effective therapeutics for our patients. We were simply told to stay away from “bleach” (which seemed reasonable to me at the time).

Dr. Kory explains the reason it is not listed as a COVID treatment is due to being under a ‘seemingly impenetrable global research blockade by the FDA and other regulatory authorities.’  Source

The studies that have been done with oral ingestion of chlorine dioxide are beyond compelling, like this one done in Cameroon where they treated 500 people with malaria and all became asymptomatic in two days while the blood became completely free of parasites by Day 6.

It is a documented fact that in 2012, the local Red Cross in Uganda did a highly successful study of orally administered chlorine dioxide to treat malaria. Like in the later Cameroon study of 500 patients, the Ugandan Red Cross treated 154 malaria patients with chlorine dioxide and reported that all became asymptomatic within 2 days (which, if you know anything about malaria, is a shockingly positive result).  The Red Cross erased this from history by never publishing or publicizing it.  Go here to watch a 3 minute video on it.

Go here for more resources.

https://robertyoho.substack.com/p/3395-curious-outlier-repost-how-to?

Curious Outlier Repost: How to Use Chlorine Dioxide, Part 1

Curious is the author of TheUniversalAntidote.com and a world authority on CD with 60,000 people on his Telegram channel.
Robert Yoho, MD
Dec 31, 2024
Yoho resources: For new readers: HERE are links to download my CV, ebooks, the best recent posts, and instructions on searching my archives. Also, HERE are links to purchase OSR, DMSO, and chlorine dioxide products, where to find them, and links to my posts.

If you have not watched The Universal Antidote Documentary, I encourage you to do that. It will give you a solid background on chlorine dioxide (ClO2) and what it can do. In the documentary, I share what I learned from a three-year investigation into this substance and answer questions like: Is ClO2 safe? How effective is ClO2? And what kinds of conditions can ClO2 treat?

I will release a Substack series for those who want to dive deep into chlorine dioxide and become experts. For now, I know what most people are thinking: “Where can I buy it, and how do I take it?” That’s what this fast-track series is for. See the supplier listing at the bottom of this article if you want to order the two-part solution kit.

Curious’s Substack is a reader-supported publication. To receive new posts and support his work, consider becoming a free or paid subscriber.

In this series, you will learn three protocols: the Starting Procedure, Protocol 1000, and Protocol 1000-F. You will also learn about several rules to follow when using ClO2.

Taking Chlorine Dioxide is simple. For a single dose, you simply activate Part A (sodium chlorite solution/MMS) and Part B (acid solution) by adding an equal number of drops of each to a small cup or shot glass. Let this mixture (MMS1) sit for 30 seconds, and then add at least 150 mL of water and drink. If the taste is too strong, you can add more water. The image below provides a simplified illustration of this process.  (See link for article, review of principles and rules and the audio podcast)

https://robertyoho.substack.com/p/3405-part-2-of-curious-outliers-how

PART 2 OF CURIOUS OUTLIER’S HOW TO USE CHLORINE DIOXIDE SERIES

I describe Protocol 1000, which was designed to treat acute illness.

Robert Yoho, MD
Jan 08, 2025

Yoho resources: HERE are links to download my CV, ebooks, the best recent posts, and instructions on searching my archives. Also, HERE are links to purchase OSR, DMSO, and chlorine dioxide products, where to find them, and more. Please review Judas Dentistry; the direct link is HERE. I need your help because a passel of mercury-intoxicated dentists are giving me one-star reviews. Finally, if you have a good story or are an expert who wants to be interviewed, don’t hesitate to contact me at RobertYohoAuthor@gmail.com. I am also available for podcasts anytime for my subscribers; email me by replying to a post. I will repost the session on my platform if we do well.

This series is from his website, TheUniversalAntidote.com. To master CD, download his two summary documents and study them in your spare time:

V1
3.12MB ∙ PDF file

Download

The Universal Antidote Interactive Reference Guidebook 2nd Ed 2022
2.21MB ∙ PDF file

Download

Note: This is for educational purposes. This is not medical advice, and I am not telling you what you should do. Every person is or should be in control of their health despite what the current medical establishment would like you to believe.

Protocol 1000 is the general protocol used for most illness situations after completing the Starting Procedure.

This protocol has an MMS1 starting regimen of 1 drop every hour for 8 hours daily. As with the Starting Procedure, a daily bottle can be made up beforehand.  (See link for article, audio, review of principles, rules, and Jim Humble’s basic info on when to best take it and ‘dos and don’ts)

https://robertyoho.substack.com/p/330-if-you-do-not-understand-the?

By Robert Yoho, MD

10/27/24

Article excerpts:

Chlorine Dioxide Therapy

The heavy-hitter alternative medicine therapies below lie outside Pharma’s tentacles, and each is a kind of miracle. Review their uses (and the original posts from the links if needed) as you go through this. They are all cheap except OSR; those you can afford should already be in your medicine chest.

Each treatment works through electron effects. I had hoped to conclude that all these drugs donated electrons, but after studying them, I concluded that the story was more about electron flow. It is not true that all the “good guys” donate electrons while the “bad guys” remove them.

1. Chlorine dioxide (CD)

Clinical uses: Cures for AIDS, cancer, autism, Lyme disease, viruses, bacteria, inflammatory arthritis, and more have been reported thousands of times. It treats neurological diseases and diabetes effectively and destroys glyphosate. It is the king of human disease care and is heavily suppressed. Ten million people are using CD worldwide.

Mechanisms: CD is a powerful but gentle oxidizer that can accept up to five electrons and interact with various biological molecules, including proteins, lipids, and DNA. It is also a type of reactive oxygen species (ROS). While not all ROS are free radicals, CD can act as one due to its unpaired electron. In biological systems, CD can induce the production of other ROS, which amplifies its effects.

Caution: Antioxidants and CD potentially neutralize each other. Vitamins A, C, E, and B12, copper, zinc, selenium, and methylene blue are all antioxidants. This category includes many foods, including coffee, blueberries, dark chocolate, artichokes, pecans, strawberries, and more. Some consider magnesium the most critical antioxidant because of its effects on glutathione production. DMSO also has antioxidant properties.

Chlorine dioxide can be altered by steel or copper containers through corrosion (oxidation) reactions while simultaneously degrading the container materials over time. Opaque glass is best. Other ideas:

  • CD works better if you eat lightly.
  • Since it vanishes from the body within two hours, wait until this time elapses before taking supplements. (This information comes from experts. Rat studies of CD show half-lives approaching 24 hours.)
  • I use CD and supplements on alternate days, but if you have to take large doses of chlorine dioxide to cure a major disease, stop most supplements.
  • I take magnesium, DMSO, melatonin, and OSR at night, so they hopefully will not interfere. This does not cause me stomach upset.

(See link for insights on more important therapies)

Category:

Lyme, Malaria, Treatment

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/

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