Archive for the ‘Uncategorized’ Category

PR Firm Representing Pfizer & Moderna Also Sits on CDC “Vaccine” Division

Since Youtube censored McCullough, you can read an article at Dailymail on the same subject matter.

http://  Approx. 30 Min

Nov. 18, 2022

Dr. Peter McCullough on Zoom

  • New York-based firm Weber Shandwick has been responsible for elevating Pfizer’s profile for decades. In 2003 it assisted with marketing Viagra and other treatments

  • In 2020 Weber Shandwick also won an up to $50 million contract from the US Government to promote flu vaccines to the public
    • Its responsibilities included distributing social media posts and articles promoting vaccines, and sending press releases to the media
    • It was also involved in ‘paid media placement’, a common euphemism for advertising

  • It also partnered with Moderna in June this year

  • The company was hired by the CDC to create PR campaigns pushing COVID shots

  • Now Weber Schandwick is working with American Board of Internal Medicine (ABIM), despite their charter stating they need to be free of conflicts of interest, & with an artificial intelligence firm called Blackbird AI, and will be co-presenting at a conference called South By Southwest in Austin, TX
    • The title of their presentation: “When Doctors Present Misinformation”
  • This clearly demonstrates that Pfizer and Moderna infiltrated the CDC and the medical boards long ago
  • Predictably, Dr. McCullough has been attacked by the medical board for “misinformation,” and wasn’t even allowed to attend the disciplinary meeting. They recommended that he be decertified (stripped of his credentials) after 4 decades of perfect service
  • McCullough points out that prior to COVID, the National certification of levels of training is done by the American Boards of the American the Colleges was only concerned with medical knowledge, practice-based learning, and competence.
    • Since COVID the group has adopted a “misinformation” policy
  • This again proves that Big Pharma is using medical boards to promote their products, including “vaccines”
  • This is happening globally
  • McCullough speaks here about his new book that he co-authored with true-crime author John Leake: “Courage to Face COVID-19: Preventing Hospitalization and Death While Battling the Bio-Pharmaceutical Complex”
    • McCullough and his colleagues developed an early treatment protocol of generic, repurposed drugs and supplements that saved millions of COVID-19 patients from hospitalization and death
    • In spite of their success, their early treatment protocol was not welcomed by public health officials
    • Fraudulent papers maligning the protocol’s repurposed drugs were published in academic medical journals
    • Other acts of fraud revealed a coordinated smear campaign against early treatment and doctors
    • During this same time of suppression and censorship, the US government and mainstream media proclaimed that the cure to COVID-19 lay in a new generation of “vaccines” that were being developed at warp speed. 
    • The Bio-Pharmaceutical Complex of multinational drug companies, the NIH and other federal agencies, research and virology labs, and the Gates Foundation have become the threat of misplaced power he warned about in his 1961 fare-well address.
    • The book recounts how McCullough and his colleagues began by fighting a virus, but then were forced to fight the tyrannical regime that threatens life on planet earth.

For more:

Category:

Uncategorized

N.S. Mother Says Health-Care System Won’t Treat Her Daughter’s Lyme Disease

https://atlantic.ctvnews.ca/n-s-mother-says-health-care-system-won-t-treat-her-daughter-s-lyme-disease-

Category:

Activism, Lyme, Uncategorized

Could A Major Chronic Infection Be Underlying ME/CFS?

https://www.healthrising.org/blog/2022/10/18/borrelia-miyamotoi-chronic-fatigue-syndrome/

Could a Major Chronic Infection be Underlying ME/CFS? The IACFS/ME Conference Pt. V

by | Oct 18, 2022 |

“B. miyamotoi is a prime candidate to be the major chronic infection underlying ME/CFS”

The fifth in a series of blogs reporting on the 2022 IACFS/ME Conference focuses on an intriguing possibility: that heretofore unknown infection is present in most people with chronic fatigue syndrome (ME/CFS).

Talk about a jaw-dropping statement. With the exception of Dr. Chia’s work on enteroviruses and Ariza’s work on the Epstein-Barr virus, most researchers have pretty much given up on finding “the chronic infection” underlying ME/CFS. Repeated failures to find evidence of a pathogen have led to the conclusion that while ME/CFS can be triggered by a variety of infection, the pathogen is likely long gone. With the emergence of long COVID, though, the idea of viral persistence has caught hold and the question is back – could a persistent pathogen or bits of a pathogen be causing ME/CFS?

It got a bit more interesting when De Meirleir looked where no one has looked before –  at tick-borne pathogens and at ones other than the Lyme disease-causing bug (Borrelia) at that. Plus, he used a new testing approach using bacteriophages to find them.

My numbers may not be correct, but the gist is that in this rather large study, a very large percentage of ME/CFS patients tested positive for B. miyamotoi while few of the healthy controls did. My jumbled notes stated that 81% of people with ME/CFS tested positive while 20% of the healthy controls did.  (See link for article)

________________

**Comment**

Very interesting article.  Important gold nugget:

…he focused on the ileocecal valve that separates the small intestine from the large intestine. I didn’t write down the possible connection between B. miyamotoi and the ileocecal valve, but the last time I remember hearing about it was decades ago from Dr. Cheney who pointed to a spot on my lower right abdomen which he said was almost always painful in ME/CFS. (Mine is).

Category:

Activism, Borrelia Miyamotoi (Relapsing Fever Group), Uncategorized

When Alpha-Gal Syndrome is NOT Related to a Tick Bite

https://www.lymedisease.org/alpha-gal-syndrome-no-tick-bite/

When alpha-gal syndrome is NOT related to a tick bite

Oct. 27, 2022

Typically, alpha-gal syndrome is associated with the bite of a lone star tick, and can result in a life-threatening allergy to red meat. But, according to Pamela Traina, the picture can be more complicated than that. She delivered the following public comments at the Oct. 25 meeting of the federal Tick-Borne Disease Working Group.

Good morning. My name is Pamela Traina. I am 55 years old and live in Los Angeles, California.

My alpha-gal diagnosis came three years ago after spending several years in and out of hospitals due to idiopathic anaphylactic reactions.

I was lucky to have an allergist who never discounted my unusual symptoms, negative allergy tests, and numerous anaphylactic reactions. It still took over two years to pinpoint the cause.

Alpha-gal is virtually unheard of in California because most people who have received an alpha-gal diagnosis live in the southeastern United States and have been infected due to being bitten by the lone star tick. The lone star tick is not found in California. I have not been to the southeastern United States and do not remember ever being bitten by a tick. Yet, I have alpha-gal syndrome. More research is required to pinpoint other possible vectors of how this condition is contracted.

Since my alpha-gal diagnosis, I have been diagnosed with multiple other food and medication allergies, including an uncommon allergy to PEG (polyethylene glycol) and polysorbate. Neither one has a diagnostic test. In addition, my Alpha-Gal test is now negative, but my sensitivity and reactions are still severe.

We need better testing, more education

Current testing is inadequate. We need more accurate testing for Alpha-Gal and other food allergies. We need answers as to why other allergies and conditions emerge after an alpha-gal diagnosis and what are the possible long-term effects of alpha-gal. We also need transparency on all medication and product labels to include inert ingredients.

Finally, hospitals and emergency staff must be educated to treat alpha-gal patients adequately. The hospital and emergency room are extremely dangerous for me due to a lack of awareness of alpha-gal.

I have had eight significant reactions since my alpha-gal diagnosis requiring er visits and hospital stays. I have endured numerous invasive and expensive tests while they search for the cause, discounting my alpha-gal diagnosis.

I have been asked if I was taking drugs and denied breathing treatments and Benadryl during a reaction because they were going to “observe” me since my symptoms didn’t present like typical anaphylaxis.

Education is required for all healthcare providers in the United States, including pharmacists, dieticians, doctors, dentists, and EMS providers, so they are aware of this condition and know how to treat it safely. It is so much more than an allergy to red meat.

Thank you for your time and the work you’re doing for the alpha-gal community.

_______________

For more:

Category:

Alpha Gal Meat Allergy, Uncategorized

9 EpiPens in a Month: The Burden of Lyme, AGS, & More

https://www.lymedisease.org/9-epi-pen-a-month-mccord/

“Nine EpiPens in a month.” The burdens of Lyme, AGS, and more.

Cortney McCord delivered the following public comment at the Oct. 25 meeting of the federal Tick-Borne Disease Working Group.

I’m Cortney McCord, a registered nurse from Tupelo, Mississippi. Since May 8, 2021, I have been in a battle for my life against alpha-gal syndrome, Lyme borreliosis, bartonellosis, babesiosis, and mast cell activation syndrome.

I developed the most severe clinical presentation of alpha-gal syndrome: I react to airborne and contact exposures as well as dietary exposures to alpha-gal.

For me, it’s way more than just a meat allergy.

In January 2022, my infectious burden grew after I contracted COVID. COVID sent me into full-blown mast cell activation syndrome and made asthma and chronic urticaria a part of my daily life.

After being gaslighted by a local allergist who was ignorant of mast cell activation syndrome and airborne alpha-gal reactions, I made an appointment with expert allergist and former Working Group member Dr. Scott Commins. I am thankful to have him in my corner even if it takes a 12-hour drive to see him..

Patients like me do not have the luxury of time to sift through a myriad of ignorant doctors to find someone familiar with their condition. Because symptoms of tick-borne infections, alpha-gal syndrome, and mast cell activation syndrome are manifested in every organ system, physicians in every medical discipline should be literate in these conditions. Nobody deserves to be gaslighted because of a lack of physician education.

Another tick bite

I was bitten by another larval lone star tick at the end of this past August. In September alone, I had to use nine EpiPens. All of this from a tick the size of a speck of dirt.

In addition to long Lyme, I believe I have long COVID complicating my clinical picture.

Long COVID and long Lyme are very similar. Both Sars-CoV-2 and Borrelia burgdorferi are persistent in tissues. Both affect the host’s immune system. Both can cause mast cell activation syndrome. The medical world has no problem saying that COVID is a persistent “long” disease. Why is that not the case for persistent ‘long” Lyme borreliosis? There are stacks of good science supporting persistent “long” Lyme infection–some of which was done by current working group member Dr. Monica Embers.

I refuse to believe that this is the best that our medical and scientific community can do. Testing for both mast cell activation syndrome and tick-borne diseases is abysmal. That has to change. There should be a law requiring alpha-gal to be listed as a major allergen on every medicine, food, and consumable product that Americans have contact with. We need the Tick-borne Disease Working Group to continue in perpetuity because tick-borne conditions will affect more and more Americans as our planet warms.

Please help me. Ask Congress to address these needs. Thank you.

_________________

**Comment**

This is truly a complicated case, but most are in my experience.

While all patients deserve to be heard and treated properly, throwing yet more money at the TBDWG which is filled with people who do not believe in chronic infection, and which has done ZERO to help  patients is not helpful.  IF, and I mean IF any money is appropriated to study this, IMO – whoever is doing the work needs needs to be independently funded.  Researchers can not be the regular cast of characters – receiving grants from corrupt public health agencies, that is literally a Cabal regurgitating old, outdated, highly myopic work which is designed for a pre-determined outcome and completely ignores a huge subset of people.

Unfortunately many patients and even advocates are oblivious to the sordid backstory of the corrupt agencies controlling research and funding.  Insanity truly is doing the same thing over and over and expecting different results.  Time to ditch the public health monopoly and public health agencies controlling research, funding, doctors, testing, treatments, and “vaccines.”

For more:

Category:

Activism, Alpha Gal Meat Allergy, Babesia, Bartonella, Lyme, Mast Cell Activation Syndrome (MCAS), Uncategorized