Inquiry to the Inspector General for Scientific Integrity of the Klempner Antibiotic Trials For Lyme Disease

September 2, 2022

https://www.change.org/p/the-us-senate-calling-for-a-congressional-investigation-of-the-cdc-idsa-and-aldf/u/30864725

Inquiry to the Inspector General for Scientific Integrity (Klempner antibiotic trials)

Carl Tuttle

Hudson, NH, United States

Aug 26, 2022 — 

The open inquiry below has been acknowledged by the National Science Foundation Office of Inspector General and Director of the Office of Research Integrity. Dr. Peggy Fischer has since retired so I am now communicating with her superiors. Updates to follow…

———- Original Message ———-
From: CARL TUTTLE <runagain@comcast.net>
To: “pfischer@nsf.gov” <pfischer@nsf.gov>
Date: 08/22/2022 1:29 PM
Subject: NIH funded study in 2001 ClinicalTrials.gov Identifier: NCT00000938
NATIONAL SCIENCE FOUNDATION (NSF)
Dr. Peggy Fischer
Associate Inspector General for Scientific Integrity
National Science Foundation
4201 Wilson Boulevard, Suite 1135
Arlington, VA 22230

Dear Dr. Fischer,

I would like to call attention to the 2018 letter below addressed to Dr. Mark Klempner Principal Investigator of the so-called “Klempner Antibiotic Trials” for Lyme disease (NIH funded in 2001) which by the way were stopped after only 90 days.

The reason for contacting you is strait forward; I believe (as do countless others in the medical/academic fields) that these studies were fatally flawed and set the stage for unimaginable pain and suffering all across America. The letter to Klempner below describes the issue and the attached document with over 360 references concluding the exact opposite of the Klempner findings, warrants an investigation.

Persistence of The Lyme Disease Bacterium, Borrelia burgdorferi
https://www.dropbox.com/s/wypdcr45cfmq16d/Persistence3.docx?dl=0

This “cherry picking” of the Klempner Antibiotic Trials by our Public Health Officials and Infectious Diseases Society of America has got to stop because all other evidence is pointing to an antibiotic resistant/tolerant superbug which would put Lyme in a different class of infection altogether, one requiring an immediate response similar to a Manhattan Project.

Since there is a 6-year time limitation [1] for occurrences of research misconduct to be brought to the attention of an institution or the Department of Health and Human Services, I’m not claiming misconduct here. I’m asking for your assistance as Associate Inspector General for Scientific Integrity as to what can be done to rectify the divergence between what Klempner has reported vs all the other equally important evidence.

A response to this inquiry is requested.

Respectfully submitted,

Carl Tuttle
Hudson, NH

Reference

[1] Requirements for Making a Finding of Research Misconduct
https://grants.nih.gov/policy/research_integrity/requirements.htm
___________________________________________

2018 letter addressed to Dr. Mark Klempner (There was no response)

From: Carl Tuttle <runagain@comcast.net>
To: mark.klempner@umassmed.edu
Cc: michael.collins@umassmed.edu, ddutko@hanszenlaporte.com, ryan.kantor@usdoj.gov, michelle.seltzer@usdoj.gov, william.rinner@usdoj.gov, makan.delrahim@usdoj.gov, tickbornedisease@hhs.gov, Elias, John, officeofthechancellor@umassmed.edu
Date: 04/27/2018 7:53 AM
Subject: Persistent Borrelia Infection in Patients with Ongoing Symptoms of Lyme Disease

April 27, 2018

University of Massachusetts Medical School
55 Lake Avenue North
Worcester, Massachusetts 01655
Attn: Mark S. Klempner, MD, Executive Vice Chancellor, MassBiologics

Dr. Klempner,

I would like to call attention to the attached study recently identifying chronic Lyme disease in twelve patients from Canada.

Persistent Borrelia Infection in Patients with Ongoing Symptoms of Lyme Disease
http://www.mdpi.com/2227-9032/6/2/33

All of these patients were culture positive for infection (genital secretions, skin “Morgellons” and blood) even after multiple years on antibiotics so there was no relief from current antimicrobials. Some of these patients had taken as many as eleven different types of antibiotics.

In contrast, your 2001 antibiotic treatment study found; “no evidence of B. burgdorferi in a total of more than 700 different blood and cerebrospinal fluid samples from the 129 patients in these studies.”

Two Controlled Trials of Antibiotic Treatment in Patients with Persistent Symptoms and a History of Lyme Disease
http://www.nejm.org/doi/full/10.1056/NEJM200107123450202#article_references#t=references

Not a single positive Dr. Klempner? Doesn’t this statistically prove that your methodology was fatally flawed?

Did you culture skin and genital secretions as the Middelveen paper reports? It would appear that you conveniently stopped looking after your results supported the existing thirty year dogma; chronic Lyme does not exist.

Persistent Lyme disease is not new and has been intentionally/deceitfully suppressed for decades as described in the Vicki Logan case identified in the following letter to past CDC Director Barbara Fitzgerald:

https://www.dropbox.com/s/xaul84dqmqgbre0/Brenda%20Fitzgerald%20MD%20Director%20CDC.docx?dl=0

In 1991 B. burgdorferi had been isolated in culture from Vicki Logan’s CSF (CDC’s laboratory in Fort Collins CO.) despite prior treatment with 21 days of IV cefotaxime and 4 months of oral minocycline.

The dishonest science here in the U.S. has denied chronic Lyme which stifled research to find a curative approach. Now the rest of the world is suffering. 

We have lost nearly four decades to this 21st century plague due to the racketeering scheme identified in the RICO lawsuit filed by SHRADER & ASSOCIATES, LLP against the Infectious Disease Society of America, seven IDSA Panelists and eight insurance companies. The U.S. Centers for Disease Control has aligned itself with the seven IDSA Panelists identified in this lawsuit.

Court Document:
https://www.courthousenews.com/wp-content/uploads/2017/11/LymeDisease.pdf

Lyme is an incurable disease when not treated immediately which is spreading across North America and deceitfully misclassified as a low-risk and non-urgent health issue. Patient experience is describing a disease that is destroying lives, ending careers, causing death and disability while leaving victims in financial ruin. Current antimicrobials are ineffective for eradicating all forms of the Borrelia spirochete.

Public outcry has been ignored for decades while the Centers for Disease Control sat on evidence that this infection was not easily treated with a one size fits all treatment approach as dictated by the Infectious Diseases Society of America.

Once again your studies were fatally flawed while supporting the controlling dogma leaving hundreds of thousands if not millions worldwide with a persistent infection and absolutely no relief. We have another AIDS on our hands.

Carl Tuttle

Independent Researcher

Lyme Endemic Hudson, NH

Cc: -Michael F. Collins, Chancellor

-The Tick Borne Disease Working Group

-US Department of Justice

-Daniel R. Dutko, HANSZEN LAPORTE

________________

For more:

Category:

Activism, Lyme, research, Treatment

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Mycoplasma Genitalium: A New Superbug

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9282694/

2022 Jan-Jun; 43(1): 1–12.
Published online 2022 Jun 7. doi: 10.4103/ijstd.ijstd_103_20
PMCID: PMC9282694
PMID: 35846530

Mycoplasma genitalium: A new superbug

J. Stephen Raj, Jyoti Rawre, Neha Dhawan,1 Neena Khanna,2 and Benu Dhawan
Author information Article notes Copyright and License information Disclaimer

Abstract

Mycoplasma genitalium (MG) is an emerging sexually transmitted pathogen. It is an important cause of nongonococcal urethritis in men and is associated with cervicitis and pelvic inflammatory disease in women, putting them at risk of infertility. Multiple factors that aid pathogenesis of MG include its ability of adhesion, gliding motility, and intracellular invasion by means of the tip organelle. Through intracellular localization and antigenic variation, MG could result in treatment-resistant chronic infection. There are limited data on the prevalence of MG in Indian patients with urogenital syndromes. Recently, a high prevalence of extra genital infection with MG has been reported. Molecular assays are the major diagnostic techniques of MG infection. Antimicrobial agents such as macrolides, along with fluoroquinolones, are the treatment of choice for MG infections. The issue of drug resistance to azithromycin and fluoroquinolones in MG is rising globally. As molecular tests are becoming available for MG, both for the diagnosis and the detection of antimicrobial resistance, any patient with MG infection should then be tested for antimicrobial resistance. Consideration of MG as a cause of sexually transmitted disease in the Indian population is crucial in diagnostic algorithms and treatment strategies. The purpose of this review is to understand the prevalence of MG in different clinical scenarios, molecular mechanisms of pathogenesis, current status of antimicrobial resistance, and its impact on MG treatment.

___________________

For more:

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Mycoplasma, research, Treatment

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Leaked EMA Documents Confirms Why We Aren’t Allowed to Analyze “Vaccine” Vials

September 1, 2022

https://stevekirsch.substack.com/p/documents-leaked-from-the-ema-confirms?  Video Here (Approx. 14 Min)

Documents leaked from the EMA confirms why we aren’t allowed to analyze the vaccine vials

It’s like rolling the dice for what you get in your vial. Both the FDA and EMA knew this but kept this out of the public view because if it were known, nobody would take the vaccines.

Steve Kirsch

One of my readers has been trying to get my attention for 8 months on the EMA data leak that happened nearly 2 years ago.

He recently posted this substack article documenting his attempts to get visibility on what the EMA document leak revealed.

The gem in the article is this video which was posted 18 months ago that few people have seen. The video is just 14 minutes long and is very well done. The findings are all consistent with what I and others have long suspected: the vials are all different.

The key finding is the reason they won’t let anyone analyze the vials: mRNA is not intact. The BMJ wrote about this on March 10, 2021 [my comments are in brackets]:

  1. On Nov 23, 2020, EMA knew about the quality control issues with severely compromised mRNA integrity (ranging from 78% to 55%). [It’s supposed to be 100% if you want an effective vaccine.]
  2. Just two days later, a source in the US said the lots were now “back at around 70-75%, which leaves us cautiously optimistic that additional data could address the issue.”
  3. “The complete, intact mRNA molecule is essential to its potency as a vaccine,” professor of biopharmaceutics Daan J.A. Crommelin and colleagues wrote in a review article in The Journal of Pharmaceutical Sciences late last year.”
  4. The BMJ asked Pfizer, Moderna, and CureVac, as well as several regulators, what percentage mRNA integrity they consider acceptable for vaccines against covid-19. None offered any specifics. [“Wow, that’s really comforting. <sarcasm off>”]
  5. The EMA told The BMJ that the levels of truncated mRNA “and the amounts of a potential protein produced by the truncated mRNA would be too low to constitute a safety risk.” [uh… how does the EMA know that exactly?]
  6. Health Canada told The BMJ that Pfizer had conducted investigations into the root cause of reduced integrity in the commercial vaccine batches, and “changes were made in their processes to ensure that the integrity was improved and brought in line with what was seen for clinical trial batches.” Health Canada said the three agencies subsequently determined that “there was no concern with the RNA integrity or any other product specifications.” [Whew! Now I’m relieved! No data on the new levels produced. If you can’t trust Pfizer, who can you trust?]

In general, the BMJ wasn’t happy about anything they heard from the regulators. They were basically stonewalled in their requests.

The fact that it’s illegal for anyone to analyze the vials (they are government property) doesn’t help inspire confidence at all.

Even if you are getting 100% intact mRNA which would be really rare, you’re still not getting anything that resembles the virus. So the efficacy as far as PROTECTING you will be next to nothing. However, what it will do very effectively, if you got reasonably intact mRNA, is to cause you significant harm. You are playing a game of chance with your immune system and what is in the bottle.

The video highlights some of the things we learned from the EMA data breach:

  1. The EMA claims the documents were manipulated to make them look bad, but won’t say how they were manipulated. I’m not buying the EMA story at all.
  2. The Members of the European Parliament (MEP) weren’t allowed to read the contracts with the vaccine makers (only heavily redacted versions). Again, if you can’t trust Pfizer and the EMA, who can you trust?
  3. The mRNA is unstable, even at the required temperatures because light, movement (like shipping it to a destination), and any temperature variation disrupts it.
  4. Unstable mRNA means the spike protein (which was artificially propped up) could collapse making the whole process useless to support immunity, but still dangerous in terms of damage to cells. So you get all the risk and no benefit.
  5. The mRNA integrity was better in the clinical trial than commercial batches. But don’t assume that the vaccine worked in the trials since the trials were heavily gamed to produce favorable outcomes, mostly by excluding people with weak immune systems from the vaccine group (this is why there were 5X the number of exclusions in the vax group). So you’re looking at a vaccine which likely does absolutely nothing except make people believe they are protected. This mind control works quite well. People bought the story for over a year before they realized they were getting infected at the same rate as people who didn’t get the vaccine.
  6. The mRNA integrity varied between countries.
  7. Pfizer never told anyone that the commercial vaccines had lower mRNA integrity than the vaccines used in the trials. This is unethical, bordering on fraud.
  8. The EMA tried to cover it up. Instead of protecting the public and making Pfizer look bad, the EMA basically covered up the problem.
  9. Pfizer never told the public or governments about the risks associated with mRNA integrity. If it wasn’t for the leak, we’d never have known. But it’s all OK because the drug companies are exempt from any liability. The patient takes all the risk here, not the drug companies.
  10. EMA was concerned about visible particles in the vials. The BMJ never investigated that. Is it still a problem? I don’t think anyone cares to know the answer to that.
  11. The deaths in the trials are all dismissed as “unrelated to the vaccine” without doing the proper analysis.
  12. There should be an investigation into these issues, but the governments are not going to expose their own fraud since it would be too embarrassing so nothing will happen.

Summary

  • This video summarizing the leaked EMA documents constitutes yet more evidence that the vaccines confer no benefits, only risk.
  • However, like everything else, it will be ignored by the authorities.
  • However, this is important information for the public to know about how they are being manipulated into taking a useless vaccine.
  • NOBODY is calling for any quality control here.
  • Have you ever seen a study where the authors collect vials randomly and sequence them? It’s not going to happen. Not in my lifetime.

____________________

**Comment**

Researchers HAVE studied the ingredients within the vials as well as the blood of the “vaxxed” and have found frightening things:

Category:

Activism, research, vaccines, Viruses

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Moderna Sues Pfizer, BioNTech Over COVID “Vaccines”

https://www.zerohedge.com/covid-19/moderna-sues-pfizer-biontech-over-covid-19-vaccines

Moderna Sues Pfizer, BioNTech Over COVID Vaccines

by Tyler Durden
Friday, Aug 26, 2022
Moderna announced on Friday that it’s suing rivals Pfizer and BioNTech SE, claiming that the mRNA technology in their Covid-19 jab infringes on its patents.

The lawsuit, filed in the US District Court in Massachusetts as well as in Germany, seeks unspecified monetary damages for patent infringement, and sets the stage for a massive legal battle between the three vaccine makers.

In a Friday statement, the Cambridge, Massachusetts-based Moderna accused partners Pfizer and BioNTech of violating key mRNA patents in the development of the Comirnaty vaccine. The company says it had patents from 2010 to 2016 on mRNA technology which made its Spikevax jab possible, which the other two companies copied without permission.  (See link for article)

________________

**Comment**

Evil always eats its own eventually.

The COVID debacle is and always has been about money and power.  It’s never been about health.  The lies and tales were spun from the very beginning, have continued to spin, and are now spinning out of control. 

Category:

Activism, vaccines, Viruses

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Tickease Founder On Dangers of Ticks, What We Need to Know About Prevention

https://www.wideopenspaces.com/tickease-founder-on-ticks/

TickEase Founder Dan Wolff on Dangers of Ticks, What We Need to Know About Prevention

By |
 

Dan Wolff, aka: “Tick Man Dan,” wore a tie emblazoned with images of ticks to his wedding. He regularly wears shirts and even a wristwatch with pictures of the arachnids on them. He has two tattoos of the creepy, blood-sucking pests permanently inked onto his left leg. He even goes on tick hunting expeditions, and he keeps jars of them around his home. This may strike some people as weird, but for Wolff, they’re conversation starters on a subject he’s passionate about. Plus, it’s part of how he makes his living. Tick Man Dan’s mission is simple: to educate the public on the dangers posed from the diseases and parasites carried by ticks, and to promote his brand, TickEase. The company makes a set of specialty tweezers designed by Wolff himself that are meant specifically for the removal of ticks and their nymphs once embedded in a person.

When I spoke to Wolff via Zoom from his home in Massachusetts, I learned more about ticks in one 40-minute sitting than I had learned my whole life. We spoke about TickEase and their Tick-Kits, proactively preventing issues, and his general enthusiasm for these tiny creatures that are capable of causing such big problems.  (See link for article)

___________________

SUMMARY:

  • Out of necessity, Wolff created Tickease when he couldn’t find a good tick removal device – particularly for an embedded nymph (which is as small as a poppy seed).
  • Unfortunately Wolff regurgitates the “warmer weather gets more ticks” mantra – essentially propelling the ‘climate change’ myth regarding tick and disease proliferation. 
    • Ticks are marvelously ecoadaptive and can survive virtually all weather by burrowing under leaf litter and snow – and anything else they can find. 
    • The repeated mantra of “climate change”, wildlife proliferation, and surburban sprawl ignores the very real spreading of ticks by our own government who has experimented on ticks for decades.
    • Willy Burgdorfer, the “discoverer” of Lyme disease was a researcher at the Rocky Mountain laboratory where he weaponized ticks by force-feeding them numerous pathogens.
  • Ticks can be active year-round – proving their ecoadaptability.  They can go into a dormant state called diapause due to a anti-freeze-like substance in their bodies which actually feeds the Lyme bacteria.
  • Wolff found ticks can wake up fast with a feeding frenzy if there are periods of cold interrupted by a sudden increase in temps. Please watch this short video demonstrating how quickly this can happen.
  • Wolff dispels the myth that it takes 36 hours for ticks to transmit Lyme.  (It can happen in a few of mere hours)
  • He also points out that viruses can be transmitted in minutes and that ticks carry far more than just Lyme.
  • When removing a tick, do not agitate it or get the contents of the abdomen on you.

For more:

 

Category:

Activism, Lyme, Prevention, Ticks, Transmission

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