Author Archive

Abyssinian in Crisis – Cured By MMS

https://pierrekorymedicalmusings.com/p/report-a-case-of-persistent-feline?

Abyssinian in Crisis: How One Cat’s Mysterious Illness and an Unconventional Therapy Transformed a Family — A Physician-Patient Case Report

One of my favorite cancer patients shared her increasing anxiety over Pearl, her new Abyssinian cat that was dying of viral infections. An offhand suggestion led to a complete recovery.

Pierre Kory, MD, MPA
Sep 02, 2025

This is the third report in a growing series of cases successfully treated with chlorine dioxide therapy. The first two were of my own personal illnesses (infectious colitis and paronychial abscess), and this third one is of… a cat named Pearl.

The following case report is co-authored by me and my patient, who has requested anonymity (I will refer to her as Laura).

In a recent follow-up visit with Laura, whom I treat for the prevention of recurrence of breast cancer (which she has had 4 separate times), one of the many topics we covered was her glowing update on the condition of her cat Pearl. Meet Pearl:

SUMMARY:

Dr. Kory’s case report written for an academic journal (AI-assisted).

Title

Clinical Report: A Case of Persistent Feline Calicivirus and Mycoplasma felis Infection in an Abyssinian Kitten and the Use of Chlorine Dioxide (MMS) Therapy

Abstract

We report the clinical course and management of a blue-ticked Abyssinian kitten (“Pearl”) presenting with chronic gastrointestinal, respiratory, and ocular disease following adoption from a multiple-cat household and a recent vaccination for FVRCP. Diagnostic workup established infections with Feline Calicivirus and Mycoplasma felis. Despite conventional therapy, the patient’s symptoms persisted. Off-label use of chlorine dioxide (MMS) was initiated by the parents, along with nutritional support and adjunct therapies. Clinical improvements were observed, including resolution of gastrointestinal symptoms and improved activity. This case highlights the complex interplay between vaccination, pathogen persistence, and adjunctive therapies in feline medicine.

Clinical Outcome

Within days of initiating MMS and supportive nutrition, Pearl demonstrated improved appetite, resolution of diarrhea and vomiting, normalization of respiratory effort, and increased mobility. No serious adverse effects were reported, save for transient gastrointestinal upset during dosage increases (interpreted as Herxheimer reaction by parents). By ten months, Pearl exhibited vigorous activity and weight gain (7 lbs 10 oz), with persistent ocular sight impairment but otherwise full return to health. Co-housed littermate Clio remained asymptomatic following similar supportive care. (See link for full article)

______________

**COMMENT**

Cats AND humans can be infected with Mycoplasma felis, the smallest known organism capable of free existence that does not possess a cell wall.  It can cause pneumonia, UT issues, conjunctivitis, bite wound abscesses, and other diseases. Mycoplasma can cause mycoplasmosis, which can lead to inflammation of several joints, such as knees, ankles, hips, or shoulders. Other symptoms include long-term lethargy, difficulty moving, fever, discomfort, and respiratory issues like sneezing and coughing.

Antibiotic treatment for mycoplasma infections can last a long time, so it is important to remain patient and follow the veterinarian’s or doctor’s instructions. Source

For more:

Category:

Activism, Mycoplasma, research, Transmission, Treatment

Petition: Repeal the PREP Act

https://jamesroguski.substack.com/p/sign-the-petition-to-repeal-the-prep

Sign the Petition to REPEAL the PREP Act

The purpose of this petition is to help ORGANIZE a nationwide effort to convince Congress to REPEAL the PREP Act. Activists are needed in all 50 states and in all 435 Congressional Districts.

James Roguski
Aug 11, 2025
This PETITION is different than any other “petition” you have ever seen before.

Please read this entire article in order to comprehend how THIS IS MUCH MORE THAN JUST A PETITION. This is an organizing tool to create a permanent and inter-connected network of activists across the United States.

GET THE DETAILS: REPEALThePREPAct.com
SIGN THE PETITION: REPEALThePREPAct.ORG
Please watch the videos and listen to the audio below:

https://rumble.com/v6xau3s-repeal-the-prep-act-with-james-roguski-noor-bin-ladin-calls…-s02e18.html

Invite other people to sign the petition:

Invite everyone you possibly can to visit this page and encourage them to sign the petition to REPEAL The PREP Act.

If you feel that there are not yet enough signatures on the petition from your Congressional District and/or your state for the petition to be as effective as you would like it to be, THEN GO OUT AND GET MORE SIGNATURES IN YOUR AREA!!!

GET THE DETAILS: REPEALThePREPAct.com
SIGN THE PETITION: REPEALThePREPAct.ORG

The text of the petition that you are encouraged to sign is below:

I strongly encourage you to support legislation to REPEAL THE PREP ACT.

The PREP Act clearly violates the United States Constitution and the unalienable rights of the people that are supposed to be guaranteed by the Bill of Rights in many, many ways.

All of the existing PREP Act declarations providing lawsuit and liability protection for “covered persons” who manufacture, distribute, promote and administer “covered countermeasures” must be REVOKED.

The PREP Act was attached to the end of H.R. 2863, the “Department of Defense, Emergency Supplemental Appropriations to Address Hurricanes in the Gulf of Mexico, and Pandemic Influenza Act, 2006” at the last minute, under very questionable circumstances, and over the objections of many prominent members of Congress.

The PREP Act was signed into law by President George W. Bush on December 30, 2005.

The PREP Act does not provide adequate compensation for the harms that have been caused by “covered countermeasures.”

The PREP Act has led to a state of lawlessness in which those who manufacture, distribute, promote and administer “covered countermeasures” have been literally able to get away with murder and have received an enormous profit with absolutely no accountability for their actions.

The only solution to the problems that have been caused by the PREP Act is for Congress to pass legislation to REPEAL THE PREP ACT.

I strongly encourage you to support legislation to REPEAL THE PREP ACT.

Use the links below to identify your Congressional District:

https://www.congress.gov/members/find-your-member

https://ziplook.house.gov/htbin/findrep_house

Please enter your Congressional district in the format OH-14, TN-03, etc.

Category:

Activism

Upcoming 2025 ILADS Conference

2025 ILADS Annual Scientific Conference

Join us in San Antonio for the 2025 ILADS Scientific Conference, October 9-12, 2025!

This year’s theme, From Terrain to Treatment: Advances in Vector-Borne Illness will highlight the latest breakthroughs in research and innovative therapies for vector-borne illnesses. Don’t miss out on impactful sessions, valuable networking, and CME opportunities.

Register now to be part of shaping the future of Lyme and complex inflammatory disease treatment!

#ILADS2025 #LymeDisease #VectorBorneIllness #MedicalConference #CME

What’s New:

  • IV Therapies Workshop – Build practical skills with expert guidance
  • Small Group Deep Dives – Engage in focused, intensive learning with topic experts
  • Breakout Tracks including:
    • Pregnancy & Tick-Borne Illness
    • Pediatric Lyme
    • Integrative Therapies
    • Neuromodulation & Brain Health

Register today– see you in San Antonio! 

Category:

Activism, Lyme

Highlights: How Fenben and Meben Disrupt Cancer Pathways

https://drturner.substack.com/p/cancer-fighters-fenbendazole-and?

Cancer Fighters: Fenbendazole and Mebendazole

Repurposing Parasite Drugs to Target Tumors and Disrupt Cancer Pathways

 
Michael Turner M.D.
Aug 26, 2025
Article Excerpts:

Mebendazole, Fenbendazole and Albendazole all belong to a class of medications called “benzimidazoles” which were originally developed as treatment for parasites. Turns out they also do nasty things to cancer cells. (What follows is not an exhaustive list, but rather highlights some of the most prominent mechanisms.)

1. Induce Apoptosis (Programmed Cell Death)

Did you know that all cells have the ability to eliminate themselves by entering a process called “apoptosis”? Apoptosis is a form of guided, programmed cell death that allows the body to remove damaged, unnecessary, or potentially harmful cells in a controlled and orderly way.

For example, during embryonic development, it helps sculpt structures like fingers and toes by removing unneeded cells. In the immune system, apoptosis eliminates infected or malfunctioning cells, such as those with DNA damage, preventing them from becoming cancerous.

Turns out that these medications trigger apoptosis in cancer cells by activating pathways such as p53 and BAX.

Apoptosis gets rid of cells by breaking them into bits your body recycles or destroys

2. Prevent cancer cells from dividing.

A cell is a 3-dimensional object that has an internal skeleton (think of it as a “scaffold”) around which the parts of the cell are attached. In order for a cell to divide, the genetic material replicates, a scaffolding system forms on the opposite end of the cell, and the the scaffold from each side reaches out and pulls the genetic material apart equally.

These pieces of scaffolding are called “microtubules” and if they can’t replicate and move properly, the cell is frozen — unable to divide.

Guess what?

These medications disrupt cancer cell microtubule function!

What about normal cells?

Cancer cells divide rapidly, depending heavily on microtubules for mitosis. Interruption of microtubule function thus has a disproportionately higher impact on these cells.

3. Kill cancer stem cells.

Cancer stem cells are the “seeds” that spawn further cancer growth — but they are not typically targeted by traditional approaches including radiation, surgery or chemotherapy; hence their failure rates.

Watch the video in the link above for more.

What this means, practically, is that measures should be taken to destroy cancer stem cells wherever they may be hiding.

Turns out these medications directly kill cancer stem cells.

(Extra credit: so do Ivermectin, doxycycline, metformin, atorvastatin, green tea extract (EGCG), melatonin, vitamin D3, curcumin, berberine, omega-3 fatty acid, resveratrol, aspirin, diclofenac, and phosphodiesterase 5-inhibitors)

For more reading: https://imahealth.org/cancer-stem-cells/

4. Interfere with the tumor’s ability to form new blood vessels.

In order for a tumor to grow, two essentials are needed: blood supply and energy supply (typically as glucose or glutamine; more on that next..)

So the tumor can only grow to the extent to which it can surround itself with new blood vessels. This process of recruiting blood vessels is called “angiogenesis”.

Guess what?

These medications inhibit angiogenesis (particularly by inhibiting a molecule called vascular endothelial growth factor (VEGF). So by cutting off the nutrient supply, these medications induce tumor starvation and shrinkage.

5. Inhibit Glucose Metabolism (Warburg Effect).

Normal cells have a choice of three main sources of biochemical energy: glucose, fatty acids and ketones. Cancer cells predominately rely on glucose (aka blood sugar) and glutamine—which is a vulnerability that can be exploited.

What if we interfered with the cancer cell’s ability to absorb and utilize glucose as a fuel?

Exactly.

These medications interfere with glucose uptake and utilization by “downregulating”glucose transporters such as GLUT1 and possibly hexokinase; the result is the cell is starved of energy.

Normal cells, which are less dependent on glucose as a fuel source, are less affected by these metabolic disruptions.

Here is Dr. Seyfried talking about the importance of glucose and glutamine for cancer growth:

And finally…

6. Disrupt cancer signaling pathways.

Imagine your body as a city with a traffic light system. Imagine that traffic light system operates during rush hour in a newly developing city (youth). Once the city is built (adulthood), the system mostly shuts down. But in certain rogue neighborhoods (tumors), this traffic controller comes back online and starts creating bypasses, shortcuts, and green lights for dangerous drivers (cancer cells), allowing them to speed through red zones, avoid checkpoints, and grow unchecked.

One of these traffic control systems is called the “Hedgehog (Hh) Pathway”.

Now you already know what I’m going to tell you next, right? 🙂

These medications decrease the activity of the Hedgehog pathway. (Extra credit: so does Ivermectin, Doxycycline, Vitamin D, Curcumin, and Sulforaphane.)

Treatment:

  • These medications should only be obtained from a licensed pharmacy (quality assurance) and taken under the supervision of a healthcare professional, as they are very bioactive, the dosing for cancer is different than for parasites, they interact with other medications and supplements, and require lab monitoring.

  • Mebendazole is the human form (pricey and difficult to find), while Fenbendazole is the veterinary form (a bit harder on the liver but much more affordable and accessible).  (See link for article and references)

Further Reading:

IMA cancer protocol, page 94

http://

The Metabolic Theory of Cancer: Glucose, Glutamine & Anti-Parasitics, Fenbendazole — Thomas Seyfried

The Moss Report
Aug. 30, 2025
 
In this groundbreaking conversation, Professor Thomas N. Seyfried, PhD (Boston College), author of Cancer as a Metabolic Disease, joins Ralph W. Moss, PhD and Ben Moss to discuss the Mitochondrial and Metabolic Theory of Cancer — and why it challenges decades of conventional thinking. Dr. Seyfried explains how cancer cells depend on glucose and glutamine as their dual fuel supply — and how cutting off both pathways may be the key to shutting cancer down.
 
He details the role of the Glucose Ketone Index (GKI), nutritional ketosis, and new interest in anti-parasitic drugs like fenbendazole and mebendazole, which appear to target cancer’s energy metabolism.
 
The full article with links, resources and full transcript can be found here: https://themossreport.com/s5-e13-prof…
 
This episode explores: 
  • Why the somatic mutation theory no longer explains cancer’s true origin
  • How mitochondrial dysfunction drives tumor growth
  • The critical role of glucose and glutamine fermentation in sustaining cancer cells • Why targeting both fuels together is essential for effective therapy
  • Emerging research on fenbendazole, mebendazole, and DON as tools in metabolic therapy
  • The potential of a paradigm shift in oncology — from genes to metabolism
 

For more:

 

Category:

Cancer, research, Treatment

Vaccines: Danish Mercury & Autism Paper is Shamwizardry

https://anthonycolpo.substack.com/p/vaccines-mercury-and-autism-cdc-and

Vaccines, Mercury & Autism: CDC & Danish Researchers Involved in Fraudulent Cover-Up

The time when everyone dumped on Andrew Wakefield, but looked the other way while pro-vaccine researchers & officials engaged in blatant shitefookery.

 
Anthony Colpo
Aug 26, 2025
 
Important Article Excerpts
 
Regarding the author’s conclusion that autism actually increased when thimerosal was removed:

According to Dr Brian Hooker, “This paper has two severe methodological flaws. First, the Denmark NCRR database changed diagnostic criteria for autism diagnoses in 1994 from ICD8 to ICD10. This led to a greater number of autism diagnoses overall.”

“Second, the Denmark NCRR database changed the accounting of autism based on outpatient visits in 1995, whereas up to 1995, only inpatient (i.e., Hospital) visits were accounted. This led to a significant increase in autism cases counted beyond 1994.”

“These two data artifacts … show a misleading jump in the prevalence of autism after 1995. However, when these are corrected for, the actual autism rates in Denmark decreased by as much as 4 times upon the phase out of thimerosal-containing vaccines (Trelka et al. 2004).”

“Although the raw data from the Madsen et al. 2003 publication has been requested, the authors chose not to release it, creating significant difficulty in confirming this decrease.”

What are you hiding, Kreesten?

Despite this, the CDC endorsed the article and, in a December 10, 2002  recommendation letter to the editor of Pediatrics, encouraged expedited review and publication of the article.

How Madsen et al Hid the Inconvenient Truth

We know that in 1992, thimerosal was removed from childhood vaccines in Denmark.

We also know that in 1994 Denmark adopted the ICD-10 criteria for diagnosing autism (“ICD”, by the way, stands for the WHO’s International Classification of Diseases, which are periodically updated).

Denmark previously used ICD-8, and never adopted ICD-9.

This is critical because there was no actual mention of “autism” in ICD-8. Instead, the category of “299 Unspecified psychosis“ was used.

It wasn’t until ICD-9 that “299 Infantile autism” was added.

ICD-10 expanded the criteria and added further diagnoses like “Asperger syndrome”, “childhood autism”, “atypical autism” etc.

This meant far more children were eligible to be diagnosed with autism and related disorders.

Which, of course, would have served to mask a decline in actual autism rates. (See link for article)

______________

**Comment**

Must read article.  

‘The powers that be’ simply can not admit a link between vaccines and autism despite evidence to the contrary and the opinion of a top government vaccine expert.

Numerous studies have shown a significant link between heavy metals like mercury and autism.

These powers will mislead, destroy evidence, ignore and manipulate their own data, lie,  destroy dissenting researchers and doctors, recommend 72 doses of vaccines to children without any safety studies to examine health effects, and accept money from Big Pharma to fast track vaccines.

 

Category:

Activism, vaccines