https://www.si.com/golf/news/back-from-lyme-disease-and-career-abyss-jimmy-walker-grabs-lead-at-heritage

Back From Lyme Disease and Career Abyss, Jimmy Walker Grabs Lead at Heritage

Jimmy Walker, who won the PGA Championship in 2016, is back on tour thanks to a one-year exemption. He’s looking to make the most of it.

HILTON HEAD, S.C. – Jimmy Walker is like Kodak, an iconic brand name that was known by everyone until the world passed it by and film morphed into digital.

Walker may not have been as iconic as Kodak or Blackberry, but for a stretch from 2014 to 2016, Walker had six wins, including the 2016 PGA Championship. He was a force.

As time went on, instead of contending on the weekend he was back home, at first wondering where his game had gone and then eventually resigned to the fact that it was over.

A bout with Lyme disease near the end of 2016 caused irreparable harm and from there his confidence and to some extend his ability ebbed away.

And like Kodak, the golfing world passed him by.  (See link for article)

________________

**Comment**

The article points out that the pro golfer was also infected with EBV, West Nile virus, two different types of bacterial pneumonia, as well as Lyme disease.  He suffered “brain to body disconnects” and lack of energy which caused depression.

Now he’s back playing golf.

‘’I’m still a competitor, I still want to win, I still want to have all those feels and have all that built inside me,” Walker said. “And I mean, that doesn’t change, right?

“I want it bad. So that’s the bottom line.”

And we out here in Lymeland are all rooting for him to win as well, but winning in golf pales in comparison to overcoming Lyme/MSIDS!

For more:

https://api.theepochtimes.com/health/rna-based-vaccine-technology-the-trojan-horse-did-not-contain-mrna_5195804.html

RNA-Based Vaccine Technology: The Trojan Horse Did Not Contain mRNA

It Contains modRNA That Genetically Manipulates Healthy Cells
Apr 21 2023

A few years ago, the term “mRNA” was primarily confined to scientific circles and research papers. Then, the use of messenger RNA seemed promising: It would teach cells to create a protein that would initiate an immune response against a specific pathogen.

Today, many more of us have heard of mRNA, as both the Pfizer-BioNTech and Moderna COVID-19 vaccines use messenger ribonucleic acid, or mRNA, as the active ingredient. At least, that’s what we’ve been told.

In fact, RNA-based vaccine technology utilizes modified RNA (“modRNA”), not mRNA. This applies to the COVID-19 vaccines and all vaccines currently in the research and development stages. Because mRNA is so fragile that the human immune system will destroy it within a few minutes, mRNA cannot be effective on its own. Therefore, the current technology was made possible only after stabilizing mRNA; the result is modified RNA.

Furthermore, modified RNA-based “vaccines” are not vaccines but gene-based injections that force healthy cells to produce a viral protein. In this article, we will look at the uses and dangers of modRNA.

Natural Infection and Conventional Vaccination

When you are infected naturally by a virus or have received a conventional vaccine, your immune system identifies virus-specific antigens from active or inactivated virus particles, respectively.

The two main types of immune cells, T and B cells, behave differently. T cells identify infected cells and initiate apoptosis (the cell-killing process), while B cells produce antibodies that bind to the virus and thus prevent infection of other cells.

There are various “proteins”—called antigens—on the surface of each virus. Your immune system can memorize more than one of them. When the virus mutates and some proteins change, your immune system can still recognize and kill them. This is referred to as cross-immunity.  (See link for article)

_______________

SUMMARY:

  • modified RNA (modRNA) is packaged in lipid nanoparticles (LNPs), to protect against destruction by the immune system and which, due to their nano size can easily overcome biological barriers and cross the blood, brain, barrier.
  • the spike protein is the antigen which is a target for the generation of neutralizing antibodies as well as non-neutralizing antibodies which can lead to antibody-dependent enhancemen (ADE), weakening the immune system and making it more susceptible to illness.  This spike protein also transforms the recipient cell from friend to foe causing autoimmunity.
  • the COVID shots only deliver genetic info for the Wuhan sequence and will be worthless against variants/mutations.
  • natural immunity will ALWAYS be more effective.
  • modRNAs are different from mRNA which is short lived. ModRNAs are developed for longevity and maximal efficiency, so they will disrupt and block the machinery of cell metabolism due to three problems:
    • It can increase errors while making spike proteins
    • Active ingredients vary greatly by different batches
    • modRNA may be incorporated into the human genome as shown by two studies
  • both Pfizer and Moderna RNA-based “vaccines” contain DNA impurities in addition to modRNA.  Nearly one-quarter of the nucleic acids in analyzed vials are DNA impurities while modRNA represents the remaining three-quarters
  • DNA concentration is several orders of magnitude over the EMA limit and implies that billions or DNA molecules are transferred with each injection which increases the risk of developing multi-resistant germs, aberrant gene expression, and synthesis of imperfect spike proteins.

For more:

https://www.theepochtimes.com/in-depth-controversial-gene-and-mrna-technologies-now-targeting-livestock

Controversial mRNA Technology Now Targeting Livestock

by Allan Stein

April 19, 2023

At least five states have introduced bills restricting the use of controversial mRNA technology or gene therapies in livestock or demand full disclosure to consumers on product packaging.

The states considering legislation include North Dakota, Tennessee, Arizona, Idaho, and Missouri.

Idaho House Bill 154 would make it a misdemeanor offense for anyone who provides or administers a vaccine using mRNA technology “for use in an individual or any other mammal in this state.”

Arizona House Bill 2762 requires conspicuous labeling of all aquatic, livestock, or poultry products that received mRNA vaccines, and prohibits these products from being labeled as organic.

Tennessee House Bill 0099 amends an existing law to prohibit the manufacture or sale of livestock or meat that contains mRNA “vaccine of vaccines materials” without a conspicuous label that there are such ingredients in the product.

In North Dakota, state lawmakers filed SB2384, which seeks to ban the use of mRNA vaccines in humans and to introduce a penalty for anyone breaking the prohibition.

Missouri State Rep. Holly Jones, a Republican, is the lead sponsor of a bill requiring product labeling of all livestock meat containing “potential gene therapy products.

“We label everything around the world. We label non-GMO. We label GMO. We label grass-fed. We label no antibiotics used. We label manufactured in a plant that has nuts,” Jones said.

“We should label anything that has not been proven safe and effective. As we’ve seen with the COVID vaccines, they’re neither safe nor effective. Even the CDC has come out with that.”

While HB1169 does not mention mRNA by name, the proposed ban would include all “potential gene therapy products.”

(See link for article)

________________

**Comment**

Contact your reps and ask them to introduce similar legislation in your state to protect our food source for adulteration without consent.

Important excerpt:

In 2016, the U.S. Congress removed a labeling law requiring the country of origin on meat products.

“That means we could take beef from Argentina, Australia, China—anywhere around the world—and this gets mixed in because we no longer have to label it as country of origin.

https://weather.com/health/video/tick-disease-now-endemic-in-10-states-heres-what-that-means  News Video Here (Approx. 1 Min)

Tick Disease Endemic In 10 States; What That Means

The Weather Channel

April 1, 2023

Some tick diseases are at record highs and one in particular is Babesiosis which is now endemic in 10 states.  Pets can be infected with it as well.

For more:

https://www.change.org/p/the-us-senate-calling-for-a-congressional-investigation-of-the-cdc-idsa-and-aldf/u/31520021

To: The FDA… What shenanigans are taking place here?

Carl Tuttle

Hudson, NH, United States

APR 23, 2023 — 

Please see the following inquiry/complaint sent to the FDA.

Dr. Gary Wormser has developed diagnostics for Pfizer’s Lyme vaccine trial?

What shenanigans are taking place here? This is a huge red flag! Controlling the Lyme disease narrative for the past 30yrs and now the outcome of a vaccine trial?

I believe the FDA will refuse to respond to my complaint so PLEASE demand an answer to this citizens complaint by sending an email to  the Center for Biologics Evaluation and Research at ocod@fda.hhs.gov referencing my letter below. Everyone has permission to cut and paste my correspondence.

Complaint sent to the Center for Biologics Evaluation and Research at the FDA:

———- Original Message ———-
From: CARL TUTTLE <runagain@comcast.net>
To: ocod@fda.hhs.gov
Cc: Brennan, Patti (NIH/NLM) [E], Schor, Nina (NIH/OD) [E], Gregurick, Susan (NIH/OD) [E], michael.lauer@nih.gov, lyric.jorgenson@nih.gov
Date: 04/18/2023 11:34 AM
Subject: Clinical Trial of a 6-Valent OspA-Based Lyme Disease Vaccine (VLA15)

An Efficacy, Safety, Tolerability, Immunogenicity, and Lot-Consistency Clinical Trial of a 6-Valent OspA-Based Lyme Disease Vaccine (VLA15) (VALOR)
https://clinicaltrials.gov/ct2/show/NCT05477524

Apr 18, 2023

Food and Drug Administration
Center for Biologics Evaluation and Research (CBER)
10903 New Hampshire Avenue
Silver Spring, MD 20993-0002

Re: ClinicalTrials.gov Identifier: NCT05477524

To whom it may concern,

For the past thirty years there has been a handful of academics controlling the Lyme disease narrative who have a vested interest in bringing an “OspA-Based” Lyme disease vaccine to market. Most of these individuals hold patents on technology that would pay out handsomely in royalties.  It would be a flagrant conflict of interest if these individuals reside on Pfizer’s Endpoint Adjudication Committee deciding who has or does not have Lyme disease.

There is another concern here as discovered through the Open Payments Search Tool.

“The Open Payments Search Tool is used to search payments made by drug and medical device companies to physicians, physician assistants, advanced practice nurses and teaching hospitals.”

Dr. Gary Wormser received $156,000 in 2021 and in one of his recent publications he claims to have developed “Lyme diagnostics for a Lyme vaccine trial” for Pfizer:

Lack of Convincing Evidence that Borrelia burgdorferi Infection Causes Either Alzheimer’s Disease or Lewy Body Dementia
https://doi.org/10.1093/cid/ciab993
Gary P Wormser, Adriana Marques, Charles S Pavia, Ira Schwartz, Henry M Feder, Jr, Andrew R Pachner

COI Statement….

Disclosures: Dr. Wormser reports receiving research grants from the Institute for Systems Biology for exploring biomarkers for outcome of Lyme disease, Pfizer, Inc for developing Lyme diagnostics for a Lyme vaccine trial, NIH/Tufts for Xenodiagnosis to assess persistence of Borrelia, and CSU/NIH. He has been an expert witness in malpractice cases involving Lyme disease and was an expert witness regarding babesiosis; employed by New York Medical College; and is an unpaid board member of the non-profit American Lyme Disease Foundation. He reports no money paid to anyone for U.S. Patent No. 10,669,567 B2 ( HIGH SENSITIVITY METHOD FOR EARLY LYME DISEASE DETECTION Issue Date: June 2, 2020 Inventors: John T. Belisle, Claudia R. Mollins, Gary P. Wormser).

Dr. Marques has a patent US 8,926,989 B2 and 9310367 for compositions and methods for screening for Lyme disease; and is an unpaid Scientific Advisor to the Global Lyme Alliance and to the American Lyme Disease Foundation. Dr. Schwartz has been on the External Advisory Committee for Oklahoma InBRE. Other None

End of COI statement

______________________________

The CDC requires “new tests” to be cleared by the FDA. Is Wormser’s Lyme diagnostics for this clinical trial FDA approved? What behind the scenes shenanigans are going on here?

From the CDC website:

CDC supports the development of new tests
https://www.cdc.gov/lyme/diagnosistesting/index.html

“New tests may be developed as alternatives to one or both steps of the two-step process. Before CDC will recommend new tests, they must be cleared by the Food and Drug Administration (FDA).”

Additional concerns:

There were neurological complications with the previous “OspA-Based” Lyme vaccine (LYMErix) as published in the International Journal of Risk & Safety in Medicine. Reports of cerebral ischemia, transient Ischemic attacks, demyelinating events, optic neuritis, transverse myelitis, and non-specific demyelinating conditions are evaluated in this paper. To my knowledge, there were no studies to determine why LYMErix caused these serious complications.

Neurological complications of vaccination with outer surface protein A (OspA).
Marks DH.
http://www.ncbi.nlm.nih.gov/pubmed/21673416

REPORT ON LYMErix prepared for the 2001 Advisary Committee Meeting:(personal Dropbox storage area)
https://www.dropbox.com/s/sodqs3pdeeesktf/Sheller%20Lymerix.pdf?dl=0

Excerpt

“The people who have contacted us were, prior to vaccination with LYMErix, healthy, active and energetic. Indeed, the very reason they sought the LYMErix vaccine was their desire to preserve their healthy, active lifestyle. However, what they experienced was a dramatic degradation of their health and quality of life. As will be described below, these previously healthy individuals are now afflicted with painful, at times debilitating arthritic symptoms, including joint pain and swelling, as well as extremely severe Lyme-disease-like symptoms which have persisted to this day.”

Below is the link to the Final Judgement and Approval of the class action against SmithKline Beecham as a settlement was awarded to these individuals.

JUDGEMENT, FINAL ORDER AND DECREE GRANTING FINAL APPROVAL OF THE CLASS ACTION SETTLEMENT: (personal Dropbox storage area)
https://www.dropbox.com/s/v3gyw4fv8nst9bz/2003_Vaccine_Judgement_Final_Sttle_Apprvl..pdf?dl=0

Summary of this inquiry:

  1. Who are the individuals residing on the Endpoint Adjudication Committee in North America?
  2. Is Wormser’s “Lyme diagnostics for a Lyme vaccine trial” FDA approved?
  3. Through informed consent have the study participants been advised of Neurological Complications from the previous “OspA-Based” Lyme vaccine and are they made aware of the class action settlement?

Let us not forget that Pfizer paid the largest fine for health care fraud in 2009:

Justice Department Announces Largest Health Care Fraud Settlement in Its History Pfizer to Pay $2.3 Billion for Fraudulent Marketing  https://www.justice.gov/opa/pr/justice-department-announces-largest-health-care-fraud-settlement-its-history

Please provide a prompt reply to this inquiry/complaint and answer all three questions.

Respectfully submitted,

Carl Tuttle
Hudson, NH

Cc: Patricia Flatley Brennan, RN, PhD Director National Library of Medicine

Nina F. Schor, MD, PhD, NIH Deputy Director for Intramural Research
Susan K. Gregurick, PhD, NIH Associate Director for Data Science
Michael Lauer, MD, NIH Deputy Director for Extramural Research
Lyric Jorgenson, PhD, Acting NIH Associate Director for Science Policy

________________

**Comment**

It’s all right here in purple crayon, and is yet more proof the government uses people, social media, mainstream media, and “vaccine” manufacturing companies as subsidiaries for their own nefarious purposes.

For more on Wormser:

  • Immunetics, Inc. (the developer of the insensitive C6 Lyme test, which he promotes).
  • Abbott, Institute for Systems Biology
  • Rarecyte, Inc.
  • Quidel Corporation
  • Insurance companies, by serving as an expert witness in court cases against doctors for treating outside IDSA guidelines
  • NIH: by receiving large shares of grants for Lyme-related research and by being influential in the selection of grant recipients.
  • IDSA – by being chairman of the Lyme guidelines revision panel which is opposed toand biased against chronic/persistent Lyme
Wormser serves the commercial interests of profit-making companies, and trivializes the effects of Lyme on patients as proven by his appearance in Under Our Skin, a documentary on the ravages of chronic Lyme disease