In Fauci's diary, on March 18, 2020, he noted a discussion with the Oval Office about using hydroxychloroquine. President Trump had heard anecdotal reports that it worked and wanted to make it available to Americans. HHS Secretary Alex Azar said America had millions of doses stockpiled and that he could approve hydroxychloroquine immediately.
But Fauci said no. Instead, he proposed an expanded-access protocol for hydroxychloroquine. It was already an FDA-approved drug, but Fauci wanted to study its effectiveness in this particular situation; patients could receive the drug but researchers would simultaneously study whether they actually worked.
Trump agreed. The hydroxychloroquine was made available, but interestingly, Fauci asked to delay the announcement until the following day. Is this because he had to coordinate something?
Later that same afternoon of March 18, Fauci sent an email to Robert Redfield, Stephen Hahn and Deborah Birx. In it, he distinguished between the two drugs: he said remdesivir should be subject to a much stricter protocol, whereas hydroxychloroquine was already approved and had extensive prior human use, but he was concerned about some of the adverse events. His email said nothing about the adverse events of remdesivir, like kidney failure. Keep in mind how horrific remdesivir was in an earlier Ebola trial. They knew about the kidney failure, and the death.
On March 28, the FDA issued an EUA allowing hydroxychloroquine from the Strategic National Stockpile to be distributed to public-health authorities for certain hospitalized COVID-19 patients when a clinical trial wasn't available or feasible. The federal government subsequently did distribute 31 million hydroxychloroquine tablets and left 63 million in the stockpile. The EUA was requested by BARDA, not by Fauci!
But then, on June 15, the FDA revoked the hydroxychloroquine EUA after reviewing the accumulated evidence—only 2.5 MONTHS of it. They concluded that hydroxychloroquine was unlikely to benefit hospitalized COVID patients and that serious cardiac risks changed the risk-benefit assessment.
Six months later, on December 11, the EUA was granted for the Pfizer vaccine. Seven days later, on December 18, the Moderna vaccine received EUA.
What is interesting timing is this: Thousands of people were enrolled for the Pfizer trial beginning July 27, 2020.
So they only tried HCQ for ~2 months, but the Pfizer trial ran more than 2x longer, but we now know they hid the adverse events.
When will these culprits be held accountable?
I have soooo many examples of Big Pharma corruption in my Zero Accountability book. If you don't yet have your copy, you can pick one up here: https://t.co/GztawMMkeY
🚨 THE OUTRAGE IS REAL: GM is officially killing the oil dipstick.
First, the auto industry tried to force us into monthly subscriptions just to use our own heated seats. Then they started voiding warranties if you dare to change your own brakes.
Now, General Motors is taking away the most basic tool under the hood.
For the 2027 Chevy Silverado and GMC Sierra V8s, GM is completely removing the physical engine oil dipstick.
Their corporate response? A total shrug. They claim they’re "simplifying the ownership experience" by replacing it with a digital sensor at the bottom of the oil pan.
Translation: If your truck is burning oil and you want to double-check the level yourself, you either have to cross your fingers that the computer isn't glitching, or you have to jack the truck up, crawl underneath it, or pay a dealership service center just to find out where your fluid levels are.
It’s an absolute middle finger to
American truck owners, DIY mechanics, and anyone who believes in the Right to Repair. The comments section on TikTok is already completely losing its mind, with thousands calling for an absolute boycott of GM products.
Corporate greed has officially crossed the line. They don't care what the public thinks—they just want total control over the vehicle you supposedly "own."
Are you standing with the boycott, or are you letting corporate algorithms control your engine? Drop your thoughts below. 👇🏼
🚨 “MY ONCOLOGIST IS SHOCKED.” DR. WILLIAM MAKIS ON FENBENDAZOLE, STAGE 4 CANCER & REPURPOSED DRUGS
What happens when patients who had already gone through multiple lines of chemotherapy start coming back with a very different story?
According to Dr. William Makis, this is what caught his attention.
He discusses Fenbendazole, Mebendazole and other repurposed drugs in the context of difficult Stage 4 cancers, including patient experiences he says he encountered repeatedly.
🔥 The story that started it
Makis discusses Joe Tippens, who was diagnosed with Stage 4 small cell lung cancer, an aggressive form of cancer.
According to Makis, Tippens received a less than 1% five year survival estimate.
He was placed on Keytruda, an immune checkpoint inhibitor.
Then came Fenbendazole.
Makis says Tippens later reported becoming cancer free and remaining so years later.
That less than 1% survival estimate is what makes the story so striking, and it became one of the stories that pushed Makis to look more closely at repurposed medicines and cancer research.
🧬 Then Makis looked at the research
Makis says there is a growing body of preclinical research on Fenbendazole.
He also discusses published cases involving patients with advanced cancer who had previously failed multiple chemotherapy regimens.
According to Makis, these patients subsequently experienced major improvements after using Fenbendazole.
📈 And then the patient stories kept coming
Makis describes patients returning to him saying:
“My cancers are shrinking.”
He says some told him their oncologists were shocked by what they were seeing.
He describes reports involving:
• Stage 4 pancreatic cancer
• Cholangiocarcinoma
• Ovarian cancer
• Small cell lung cancer
He also discusses patients whose tumors reportedly shrank despite having already failed multiple lines of chemotherapy.
💊 The bigger conversation
This is where Makis connects Fenbendazole, Mebendazole, Ivermectin and other repurposed medicines to a broader cancer research discussion.
His argument is that existing medicines deserve serious investigation for potential applications beyond their original indications.
And his final message is especially striking:
“I think repurposed drugs can give patients hope in situations that are very dire.”
That is the bigger question behind the conversation:
How many existing medicines could have unexplored potential in cancer research?
The stories are fueling growing interest in Fenbendazole, Mebendazole, Ivermectin and drug repurposing, and that conversation is becoming increasingly difficult to ignore.
📌 SAVE this breakdown for the Fenbendazole and repurposed medicine discussion.
🔄 REPOST if you think overlooked medicines deserve more serious cancer research.
💊 Looking for Fenbendazole or Mebendazole? Find repurposed drugs at @rxmeds_store with worldwide delivery.
#Fenbendazole #Mebendazole #Ivermectin #CancerResearch #Stage4Cancer #RepurposedDrugs #Oncology #CancerResearch
CHD DEFENDER Reports: New York Teen Forced Out of School After Judge Denies Medical Exemption
(Everyone, please pray for Sarah Doe 🙏)
Sarah Doe, a New York high school senior, can no longer attend class as of today, after a federal judge declined to extend a medical exemption from the school’s vaccine mandates. Last year, U.S. District Judge Gary Brown ordered a New York school district to allow Sarah to attend high school during the 2025-2026 school year. In a ruling issued late Wednesday, Brown said the circumstances were different this year. Sarah’s attorney said they will appeal.
by Brenda Baletti, Ph.D.
September 24, 2026
A senior at a New York high school can no longer attend class as of today, after a federal judge declined to extend a medical exemption from the school’s vaccine mandates for the current school year.
Last year, U.S. District Judge Gary Brown of the Eastern District of New York ordered a New York school district to allow Sarah Doe, who had obtained a medical exemption, to attend high school during the 2025-2026 school year.
But in a ruling issued late Wednesday in Jane Doe v. Oceanside Union Free School District, Brown denied the renewed medical exemption request for the 2026-2027 school year.
Last year, Brown granted an emergency preliminary injunction allowing Sarah to attend 11th grade without receiving the third dose of the hepatitis B (Hep B) vaccine — the only recommended shot she hadn’t taken at the time — because her severe reactions to previous doses had left her sick and disabled.
When the lawsuit was filed, at least six treating physicians certified to the school district that Sarah could be harmed by taking the shot, according to court documents. The district nonetheless repeatedly denied her exemption requests. Since then, more doctors have affirmed that assessment.
Brown said last year’s decision rested in part on a physician’s report that Sarah experienced an anaphylactic reaction to an earlier dose, and evidence she had received the first two doses and had some immunity.
Brown also based his previous decision on an appeals court precedent stating that there had never been definitive proof that hepatitis B could be transmitted through “non-parenteral” routes like saliva — meaning passed in ways not transmitted through blood or broken skin.
After attending school last year under the court order, Sarah applied for a medical exemption from the Hep B vaccine and also the second meningococcal vaccine required for this school year.
The school district again denied her request. Sarah’s lawyers responded by filing an emergency motion seeking a new court order allowing her to return to school this year.
Explaining his latest decision, Brown said this year’s circumstances were “substantially different.” This year, Sarah would be attending school without two of the mandated vaccines, instead of one. And, he said, there was insufficient medical evidence showing that she could not receive the meningococcal vaccine.
“At the end of the day, Sarah is a child who just wants to go to school,” her attorney, Sujata Gibson, told The Defender.
Gibson said:
“Nine doctors and specialists have said she needs to defer vaccination. If that still isn’t enough for her to receive an accommodation, then we have to ask what protections medically fragile children actually have in New York.
“Federal disability laws are supposed to protect children like Sarah. We believe that protection failed here, and we intend to seek immediate appellate review.”
Read the rest of this report here: https://t.co/wEyKnBK6Lx
The Amish had a 90X lower fatality rate from COVID & Autism is undetectable in their community...
Here's why their approach to health stands out—they ignore every CDC guideline, shun vaccines and their communities are thriving....
- COVID Fatality Rate: In Lancaster County, PA (home to ~45,000 Amish), only about 5 Amish deaths from COVID over the entire pandemic—resulting in a rate ~90 times lower than the U.S. average.
- No Lockdowns or Mandates: The Amish continued normal life—no masking, no social distancing, no school/business closures, no vaccine mandates—and still had minimal COVID impact.
- Herd Immunity Naturally: Reports indicate ~90% of the Lancaster Amish community contracted COVID early on, achieving natural herd immunity without vaccines.
- Autism Rates: Essentially undetectable—Steve Kirsch, researcher Dan Olmstead & others report being unable to find unvaccinated Amish children with autism, unlike skyrocketing rates elsewhere.
- Other Chronic Conditions: Virtually no cases of cancer, diabetes, ADHD, or autoimmune diseases in Amish kids, attributed to their unvaccinated, natural lifestyle.
There are now more than a dozen vaccinated vs unvaccinated research studies that show being unvaccinated is always healthier:
• 2020 study on 1,827 kids: Unvaccinated children had significantly lower rates of asthma, ear infections, ADHD, allergies & neurodevelopmental disorders.
• 2017 study (6,000+ participants): Vaccinated kids were 4.5X more likely to have asthma, 22X more likely to need allergy medication & over 30X more likely to have allergic rhinitis.
• New Zealand survey (over 200 unvaxxed kids): Almost ZERO chronic illness – no asthma, no eczema, no seizures, no diabetes.
• Amish study: Autism rate roughly 1 in 15,000 vs national average of 1 in 31. (The few autistic children found in the Amish communities were children adopted INTO families, who were previously vaccinated & living outside the Amish.)
EBV is carried by 95% of adults
(It mimics thyroid disease and more)
Here’s everything you need ⬇️⬇️
https://t.co/D8zbWIKwPG
EBV produces symptoms are clinically indistinguishable from…
autoimmune diseases
metabolic dysfunction
psychiatric illness
& neurological deterioration
The top 7 autoimmune conditions it mimics…
lupus
multiple sclerosis
rheumatoid arthritis
Sjogens
Hashimoto’s
IBS
and Type 1 diabetes
In English…it mimics the diseases people are being diagnosed with
When a patient shows up with chronic fatigue, joint pain, brain fog, cranked up inflammatory markers and a random collection of vague systematic symptoms
The number of times MDs order an EBV reactivation panel?
Zero
There’s labs you need are in my stories
The rest is in the research playbook
I’m the only doctor who’s actually giving you every damn solution for free…
Because I’m also the only doctor who actually cares
You’re welcome
Never Miss
Dr Trevor Bachmeyer
The Spartan