Archive for the ‘research’ Category

Novel Therapy Destroys Lyme in Lab

https://projectlyme.org/novel-therapy-destroys-lyme-in-lab/

Novel Therapy Destroys Lyme In Lab

Research Identifies New Investigational Therapy Regimen Capable of Irreversibly Damaging Lyme Bacteria in Laboratory Tests

Inspired by research that targets cancer tumors, these new findings in Lyme could also lead to novel R&D strategies for other diseases. This project was partially funded by Project Lyme, in partnership with the Bay Area Lyme Foundation. Learn more about our funded research here.

http://

Dr. Neil Spector Research Project

Nov. 1, 2023

PORTOLA VALLEY, Calif. November 1, 2023 – Bay Area Lyme Foundation, a leading sponsor of Lyme disease research in the US, today announced the development of a potential new drug, HS-291, that targets and destroys Borrelia burgdorferi, the bacterium that causes Lyme disease. Published in the peer-reviewed journal Cell Chemical Biology, this laboratory study represents a novel paradigm shift for anti-microbial treatment research as it is the first to target and inhibit Borrelia burgdorferi HtpG (high-temperature protein G), a specific type of enzyme within the bacteria that causes Lyme disease— a condition affecting nearly 500,000 new patients annually. The research was conducted at Duke University School of Medicine, with collaboration from the University of North Carolina, Tulane University, and Stanford University, and HS-291 is currently in preclinical stage testing at UC Davis.

“As Lyme disease is currently treated with broad-spectrum antibiotics and there are no targeted treatments, we are particularly excited about this discovery, and hopeful that our novel Lyme disease therapeutic HS-291 will specifically destroy the Lyme bacterium without off-target effects or antibiotic resistance,” said Timothy Haystead, PhD, professor of Pharmacology and Cancer Biology, Duke University School of Medicine, Bay Area Lyme Foundation grantee, and co-lead author. “This research has been an incredible opportunity to leverage knowledge from oncology to Lyme disease to design an investigational therapeutic that could one day benefit hundreds of thousands of patients with Lyme.”

This discovery has implications beyond Lyme disease as it demonstrates that using the drug HS-291 to deliver cellular toxins to HtpG, a type of non-essential enzyme that assists the folding or unfolding of large and complex proteins, greatly expands what can be considered druggable within any pathogen and opens a whole new area of infectious disease research.

When activated, HS-291, an inhibitor of HtpG tethered to the photoactive cellular toxin verteporfin, causes discrete protein modifications, which wreaks havoc on the Lyme disease bacterium’s DNA. This impacts multiple processes including nucleoid collapse and cell wall disruptions. A single dose of HS-291, when activated by light, irreversibly damages Borrelia proteins in close proximity of Bb HtpG in vitro.

“Antibiotics used to treat Lyme disease do not always work for all patients, which causes many to suffer for years with extreme symptoms including neurocognitive issues, disabling fatigue and sleep disruption,” said Linda Giampa, executive director of the Bay Area Lyme Foundation. “Bay Area Lyme concentrates on funding innovative research, including projects where knowledge can be deployed from other areas of medicine. We hope that this discovery will inspire others to join us in investing in impactful, translational research to bring relief to patients.”

This research was made possible by a 2020 Bay Area Lyme Foundation grant of more than $2 million to Duke University School of Medicine in honor of Neil Spector, MD, a renowned oncologist who passed away from complications of Lyme disease that had been misdiagnosed for years. He encouraged scientists to take cancer staging techniques and immunotherapy learnings from oncology and apply them to Lyme research. Dr. Spector was the Sandra Coates associate professor in the Duke University Department of Medicine and also served on Bay Area Lyme Foundation’s Scientific Advisory Board.

Haystead and Spector joined forces as Spector sought to leverage his knowledge of oncology to help better understand Lyme disease, and Haystead’s research is focused on the use of chemical biology approaches to define novel drug targets focused on the treatment of hypertension, obesity, cancer, inflammatory and infectious disease.

Bay Area Lyme Foundation also funded University of North Carolina collaborator, Matt Redinbo, PhD’s research on HS-291; his lab’s crystallography work was instrumental in the discovery process.

Bay Area Lyme Foundation’s research grant program was made possible by the support from the Fairbairn Family, the Younger Family Fund, and Project Lyme.

For more:

Category:

Lyme, research, Treatment

Not Good: Medscape – New Federal Oversight of Lab Developed Tests

The following information about “FDA approved” tests is a perfect example of corrupt government agencies doing what they do best: monopolize and control disease for their own purposes – usually financial.

They have restricted doctor and patient choice, care, and access in a number of ways, but one way they cling to like a survivor on a raft is testing. Lyme testing has been fraudulent from the get-go and their suppression of other tests is something that should be made into a movie.  In so many ways the CDC and FDA are maniacal evil twins – both doing all within their power to monopolize medicine.

Dr. Sin Hang Lee has sued the CDC for suppressing direct detection tests for Lyme disease, and promoting their own newly patented, unproven metabolomics technology for diagnosis of LD. Current and former CDC representatives receive royalties as a result of working on the approval and promotion/CDC endorsement of a Lyme disease serology test.

Lee has been fighting back with equal tenacity and performed independent research on faulty COVID testing which showed COVID cases will be overstated by a factor of 72%!

Instead of fixing the obvious errors (no positive control sample, no data on false positives, faulty cycle thresholds, and refusal to publish Ct values due to it being “proprietary”,) HHS, FDA, and CDC opted for arbitrary and perpetual diagnosis of COVID.

It’s important the CDC and FDA control testing because then they can completely steer the narrative about any disease – even if the numbers are all based on faulty testing.  They’ve been doing this in Lymeland for over 40 years by

“setting arbitrary level of antibodies to diagnose a disease that has not been amenable to Koch’s postulates seems open to question.  By the same token, ignoring antibody results unless they meet arbitrary levels seems suspect.  The vast majority of patients in this series showed some WB antibody exposure, but many did not meet the arbitrary limits set….in our present state of knowledge, the diagnosis of chronic Lyme disease is a clinical one.  Many of the patients in this series have suffered serious ‘hurts’ when they have been told that they could not have LD because their WB did not meet arbitrary limits.”  ~ Dr. Burton Waisbren  IDSA founder who disagreed with his colleagues.  RIP

https://www.change.org/p/the-us-senate-calling-for-a-congressional-investigation-of-the-cdc-idsa-and-aldf/  Video within link (Approx. 10 Min)

Medscape: New Federal Oversight of Lab Developed Tests

Carl Tuttle

Hudson, NH, United States

NOV 1, 2023 — 

Please see the following inquiry sent to Dr. Paul Auwaerter regarding his commentary (verbal diarrhea) published on Medscape.  He has yet to respond to my serious question. Why not email Dr. Auwaerter and demand a response?

Auwaerter’s image was found on his Hopkins profile page:
https://www.hopkinsmedicine.org/profiles/details/paul-auwaerter

———- Original Message ———-
From: CARL TUTTLE <runagain@comcast.net>
To: “pauwaert@jhmi.edu” <pauwaert@jhmi.edu>, “pgauwaerter@gmail.com” <pgauwaerter@gmail.com>
Cc: “aaguilar@webmd.net” <aaguilar@webmd.net>, “DFlapan@Medscape.net” <DFlapan@Medscape.net>, “lkane@medscape.net” <lkane@medscape.net>, “gamiller@medscape.net” <gamiller@medscape.net>, “dolmos@webmd.net” <dolmos@webmd.net>, “sarah.wright@webmd.net” <sarah.wright@webmd.net>, “editor2@webmd.net” <editor2@webmd.net>
Date: 10/25/2023 9:51 AM EDT
Subject: Medscape: New Federal Oversight of Lab Developed Tests

Medscape COMMENTARY
 
New Federal Oversight of Lab Developed Tests
https://www.medscape.com/viewarticle/997365

Paul G. Auwaerter, MD

Excerpt:

“I often see patients who are concerned they might have Lyme disease, or they’ve been told by other physicians that they have a tickborne or multiple infections. I’ve had patients who claim to have five or six infections: Lyme disease, Babesia, Bartonella, Mycoplasma, or Epstein-Barr virus. They bring LDT results from outside laboratories, which often have a proviso that these tests are only for research or educational purposes. Yet, they purport finding analytes (antibodies or proteins) that suggest the patient has an active infection. These patients may have been treated but are not improving, so they are referred to me.”

Oct 25, 2023

The IDSA Foundation
1300 Wilson Boulevard Suite 300
Arlington, VA 22209
Attn:  Paul Auwaerter, vice chair of the IDSA Foundation

Dear Dr. Auwaerter,

As a member of New Hampshire Governor Chris Sununu’s 2020-2021 commission to study diagnostic testing for Lyme disease, I read your commentary with great interest. After a full year of deliberation, study results concluded that the FDA approved two-tier serologic immunoassay for Lyme was not reliable in all stages of disease. (No better than a coin toss)

COMMISSION TO STUDY TESTING FOR LYME AND OTHER TICK-BORNE DISEASES
https://www.gencourt.state.nh.us/statstudcomm/committees/default.aspx?id=1515

“A commission to study the role of clinical diagnosis and the limitations of serological diagnostic tests in determining the presence or absence of Lyme and other tick-borne diseases”
 
With that conclusion, serology cannot be used to determine who has or does not have Lyme disease.

“FDA approval” (Federal Oversight) has failed miserably in this example.

The CDC has warned the medical community that “surveillance case definitions” (which include the IgM and IgG Western blot serologic bands) are not to be used for making a clinical diagnosis:

From the CDC website:

Lyme Disease (Borrelia burgdorferi)
2022 Case Definition
https://ndc.services.cdc.gov/case-definitions/lyme-disease-2022/

NOTE: A surveillance case definition is a set of uniform criteria used to define a disease for public health surveillance. Surveillance case definitions enable public health officials to classify and count cases consistently across reporting jurisdictions. Surveillance case definitions are not intended to be used by healthcare providers for making a clinical diagnosis or determining how to meet an individual patient’s health needs.
________________________

Recent announcements:

1. “Standard” Lyme testing once again proves fatal
https://www.lymedisease.org/lyme-testing-proves-fatal/

“Lyme disease helped kill our son. A better test might have saved him.”

2. Sensitivity of Two-Tiered Lyme Disease Serology in Children with an Erythema Migrans Lesion 
https://doi.org/10.1093/jpids/piad073

Abstract

In our prospective cohort of 192 children with a physician-diagnosed erythema migrans (EM) lesion, two-tier Lyme disease serology had higher sensitivity in children with multiple EM lesions (76.8% multiple lesions vs. 38.1% single EM; difference 38.7%, 95% CI 24.8 to 50.4%). The diagnosis of cutaneous Lyme disease should be based on careful physical examination rather than laboratory testing.

3. Jury awards $6.5M to Maine family for wrongful death, negligent misdiagnosis
https://fox23maine.com/news/local/jury-awards-65m-to-maine-family-for-wrongful-death-negligent-misdiagnosis-mercy-hospital-dr-john-henson-peter-smith-lyme-disease-lyme-carditis-physicians

Court records show Dr. Henson diagnosed smith with a skin disorder and a virus, writing “no sign of Lyme Disease.” Smith died of Lyme carditis.

(I understand that serology was NEGATIVE in this case)

Question:

Dr. Auwaerter…  I would like to call attention to the following 2009 tick study conducted here in New Hampshire:

Correlation between Tick Density and Pathogen Endemicity, New Hampshire
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2671416/

The study found deer ticks were carrying multiple pathogens (co-infections) that could be transmitted in a single bite.

What FDA approved Tick-Borne Disease Panel are you recommending so as not to miss any of these infections?

A response to this inquiry is requested
Carl Tuttle
Hudson, NH

Cc: MEDSCAPE EDITORIAL STAFF

Additional reference:

“Seronegativity in Lyme borreliosis and Other Spirochetal Infections” 16 September 2003
https://www.dropbox.com/s/3d6m45jzlhhwalu/Seronegativity.pdf?dl=0

“If false results are to be feared, it is the false negative result which holds the greatest peril for the patient.”

Category:

Activism, Lyme, research, Testing

Spike Protein in Heart Cells Within 48 Hours of Injection

https://www.theepochtimes.com/health/mrna-covid-vaccines-form-spike-protein-in-heart-cells-but-cause-different-anomalies-research-article

mRNA COVID Vaccines Form Spike Protein in Heart Cells, but Cause Different Anomalies: Research Article

New research observing rat and human heart cells shows that within 48 hours of vaccination, the COVID-19 mRNA vaccines form spike proteins.
10/22/2023

New research out of Germany observing rat and human heart cells shows that within 48 hours of vaccination, the COVID-19 mRNA vaccines form spike proteins.

Spike proteins, made from the mRNA instructions inside the vaccines, were detected in the heart cells. While both Pfizer and Moderna vaccines caused cell abnormalities, the two induced different anomalies.

The different responses the cells had to the two mRNA vaccines suggest an mRNA toxicity reaction in these cells, according to Dr. Peter McCullough, a leading internist, cardiologist, and epidemiologist who has published over 1,000 research reports and is the lead author of one of the first widely utilized treatment regimens for SARS-CoV-2 patients. He added that 48 hours was a short amount of time to observe this.

“The findings support both the diagnosis and treatment of cardiac events following mRNA-based COVID vaccination,” the authors wrote, adding that the findings may explain persistent cardiac symptoms among long-COVID patients.(See link for article)

_____________

**Comment**

The article has now been updated and includes a video comparing unvaxxed rat heart cells vs vaxxed.  They found:

  • Pfizer-“vaxxed” cells displayed stronger, sustained contractions (1B) due to increased protein kinase A (PKA) activity. PKA levels are linked to heart performance; the higher the PKA level, the stronger the heart contractions.
  • Moderna-“vaxxed” cells developed irregular heart contractions and disrupted calcium regulation. The authors attributed the change in cell activity to disturbances in RyR2 receptors. These receptors play a key role in coordinating heart contractions using calcium. Some of the heart muscles administered Moderna vaccines developed irregular and peristaltic contractions (1C and 1D), whereas others had irregular and arrhythmic contractions (1E and 1F).

The authors also found damage is closer to cardiomyopathy by toxic stress (heart muscles are structurally and functionally abnormal in the absence of other heart diseases) than myocarditis & pericarditis (heart muscles are inflamed and damaged.)

Also, the varying responses indicate the cardiac abnormalities may suggest toxicity in the mRNA itself rather than the spike protein which both injections have.

For more:

How ‘the powers that be’ are covering up the injection damage:

How the injections are causing heart damage:

Category:

Heart Issues, research, vaccines, Viruses

The Link Between Nightshades, Chronic Pain and Inflammation

https://greenmedinfo.com/blog/link-between-nightshades-chronic-pain-and-inflammation

The Link Between Nightshades, Chronic Pain and Inflammation

March 8th 2023
Written By: Elisha McFarland
“© [Article Date] GreenMedInfo LLC. This work is reproduced and distributed with the permission of GreenMedInfo LLC. Want to learn more from GreenMedInfo? Sign up for the newsletter here //www.greenmedinfo.com/greenmed/newsletter.”

Few people are familiar with the term nightshades, and many will be surprised to learn that consuming foods from this plant group may be contributing to their pain and inflammation

Nightshades belong to the Solanaceae family which includes over 2,000 species. They also include some of the most popular foods consumed today; such as tomatoes, potatoes, all types of peppers, and eggplant. Although not truly nightshades, blueberries, huckleberries, goji berries and ashwaganda all share the same alkaloids which may have inflammation-inducing properties.

The Solanaceae family contains cholinesterase inhibiting glycoalkaloids and steroid alkaloids including, among others, solanine in potato and eggplant, tomatine in tomato, nicotine in tobacco, and capsaicin in garden peppers. The glycoalkaloids in potatoes are known to contribute to Irritable Bowel Syndrome (IBS) and negatively affect intestinal permeability. (1,2) According to Dr. Marvin Childers, “When these inhibitors accumulate in the body, alone or with other cholinesterase inhibitors such as caffeine or food impurities containing systemic cholinesterase inhibiting pesticides, the result may be a paralytic-like muscle spasm, aches, pains, tenderness, inflammation, and stiff body movements.” (3) These symptoms may dissipate in a few hours or days if ingestion is stopped, based on the sensitivity of the individual, the amount of nightshades consumed on a regular basis and their level of inflammation. However for some heavy consumers of nightshades the process of inflammation and pain reduction can take up to 3 months.

After reading the symptoms associated with nightshade consumption, it is easy to understand why one of the major problems attributed to nightshade is arthritis. Arthritis is also the most common disability in the U.S. (4,5) Statistics from a 2007-2009 study show that doctor diagnosed arthritis affects 49.9 million people in the United States alone (6). Osteoarthritis is the most common form of arthritis affecting more than 20 million people. More than 2 million people are affected by rheumatoid arthritis, the most disabling and painful form of arthritis. Arthritis has no boundaries to gender, race or age, it affects young and old alike. (5, 7) In fact it may be surprising to some that an estimated 294,000 children (age 18 and under), have some form of arthritis. (7) In 2003 the medical cost of arthritis alone was approximately 128 billion annually. (4) Since 1994, disability-related costs for medical care and lost productivity have exceeded an estimated $300 billion annually in the United States, this includes arthritis and other rheumatoid related illness (8) Add to these numbers the report released in 2011 by the Institute of Medicine of the National Academies, where an estimated 116 million adults live with chronic pain, which costs the United States $635 billion annually in health care and lost productivity. (9) So the question is how much of these problems are nightshade related? That is the question some researchers are asking, as they believe that arthritis is often misdiagnosed in people who may in fact be experiencing severe side effects of nightshade consumption.

Many who suffer with arthritis or an arthritis related disease such as lupus, rheumatism, and other musculoskeletal pain disorders, have found that consuming foods from the nightshade family is in fact adversely affecting their health. Norman F. Childers, PhD, founder of the Arthritis Nightshades Research Foundation stated: “Diet appears to be a factor in the etiology of arthritis based on surveys of over 1400 volunteers during a 20-year period. Plants in the drug family, Solanaceae (nightshades) are an important causative factor in arthritis in sensitive people.” (3)

Three month challenge

If you want to know if nightshades negatively affect you, take the three month challenge. Avoid all nightshades for three months. (It’s called a challenge for a reason).Be careful to note the nightshade list, and become a label reader as some homeopathics, prescriptions, over the counter medications as well as numerous processed foods contain nightshades. Prescriptions and over the counter medicines may require a discussion with your pharmacist or a phone call to the manufacturer of your over the counter medicines to determine ingredients.

After three months, begin to reintroduce one nightshade at a time. Take note of any aches, pains, stiffness, and loss of energy, headaches, respiratory problems or any other symptoms. You may find as many others have, that the quality of your daily health will dramatically improve after eliminating nightshades from your diet.

The nightshade list

  • ­ tomatoes (all varieties, including tomatillos)
  • ­ potatoes (all varieties, NOT sweet potatoes or yams)
  • ­ eggplant (aubergine)
  • ­ okra
  • ­ peppers (all varieties such as bell pepper, wax pepper, green & red peppers, chili peppers, cayenne, paprika, etc.)
  • ­ goji berries
  • ­ tomarillos (a plum-like fruit from Peru)
  • ­ sorrel
  • ­ garden huckleberry & blueberries (contain the alkaloids that induce inflammation)
  • ­ gooseberries
  • ­ ground cherries
  • ­ pepino Melon
  • ­ the homeopathic “Belladonna” [note: this is highly precautionary as homeopathics contain virtually no measurable “active” chemical]
  • ­ tobacco
  • ­ paprika
  • ­ cayenne pepper

Soy sauce made in the U.S. is generally made with genetically modified (GMO) soy beans, which are cut with the nightshade plant Petunia.

The condiments black/white pepper and pepper corns are not nightshades

Other ingredients and products to avoid

  • ­Homeopathic remedies containing Belladonna [note: this is highly precautionary as homeopathics contain virtually no measurable “active” chemical]
  • ­Prescription and over-the-counter medications containing potato starch as a filler (especially prevalent in sleeping and muscle relaxing medications)
  • ­Edible flowers: petunia, chalice vine, day jasmine, angel and devil’s trumpets
  • ­Atropine and Scopolamine, used in sleeping pills
  • ­Topical medications for pain and inflammation containing capsicum (in cayenne pepper).
  • ­Many baking powders contain potato starch
  • ­Don’t lick envelopes, many adhesives contain potato starch
  • ­Vodka (potatoes used in production)

Read labels carefully because you could be doing everything else right, and still be sabotaged by one small amount of an ingredient.

Never buy a food has that uses the generic term of seasoning or spices…. nightshades may be included in the ingredients.

Learn more about the similarity of tomato lectin with wheat germ lectin (WGA), as well as lectins found in rice and barley:

Rice, Potato, and Tomato May Be As Inflammatory As Wheat

References

1. Potato glycoalkaloids adversely affect intestinal permeability and aggravate inflammatory bowel disease. www.greenmedinfo.com/article/potato-glycoalkaloids-adversely-affect-intestinal-permeability-and-aggravate

2. Naturally occurring glycoalkaloids in potatoes aggravate intestinal inflammation in two mouse models of inflammatory bowel disease. www.greenmedinfo.com/article/naturally-occurring-glycoalkaloids-potatoes-aggravate-intestinal-inflammation-two-mouse

3. Journal of Neurological and Orthopedic Medical Surgery (1993) 12:227-231.An Apparent Relation of Nightshades (Solanaceae) to Arthritis https://www.noarthritis.com/research.htm

4. National and State Medical Expenditures and Lost Earnings Attributable to Arthritis and Other Rheumatic Conditions — United States, 2003 https://www.cdc.gov/mmwr/preview/mmwrhtml/mm5601a2.htm?s_cid=mm5601a2_e

5. Differences in the Prevalence and Impact of Arthritis Among Racial/Ethnic Groups in the United States, National Health Interview Survey, 2002, 2003, and 2006 https://www.cdc.gov/pcd/issues/2010/may/10_0035.htm

6. Prevalence of Doctor-Diagnosed Arthritis and Arthritis-Attributable Activity Limitation – United States, 2007-2009 https://www.cdc.gov/mmwr/preview/mmwrhtml/mm5939a1.htm?s_cid=mm5939a1_w

7. Prevalence of and annual ambulatory health care visits for pediatric arthritis and other rheumatologic conditions in the United States in 2001-2004. Sacks JJ, Helmick CG, Luo YH, Ilowite NT, Bowyer S. https://www.ncbi.nlm.nih.gov/pubmed?Db=pubmed&Cmd=ShowDetailView&TermToSearch=18050185&ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum

8. Prevalence and Most Common Causes of Disability Among Adults — United States, 2005 https://www.cdc.gov/mmwr/preview/mmwrhtml/mm5816a2.htm

9. Relieving Pain in America: A Blueprint for Transforming Prevention, Care, Education, and Research https://www.iom.edu/Reports/2011/Relieving-Pain-in-America-A-Blueprint-for-Transforming-Prevention-Care-Education-Research.aspx

After sixteen years of struggling with MCS, Elisha McFarland recovered her health through alternative and natural healing methods. It was this experience that encouraged her to pursue an education in natural health.  She has the following designations:  Doctor of Naturopathy, Master Herbalist, D.A. Hom., B.S. in Holistic Nutrition, Certified Wholistic Rejuvenist and EFT-ADV. You can visit her website at:  https://www.myhealthmaven.com or follow her on Facebook  at  https://www.facebook.com/myhealthmaven

Disclaimer: This article is not intended to provide medical advice, diagnosis or treatment. Views expressed here do not necessarily reflect those of GreenMedInfo or its staff.

Category:

diet and nutrition, Inflammation, Pain Management, research, Supplements

“We Admit The Shot Has SV40, But We Found Some ‘Experts’ Who Don’t Think It’s a Problem”

If you are new to SV40, read this, and watch this.

https://kirschsubstack.com/p/ok-you-were-right-we-admit-vaccine

“OK, you were right. We admit the vaccine is contaminated with SV40, but we found some experts who think it’s not a problem.”

How is it that Kevin McKernan, and not any world health authority, found the contamination in April 2023? And why are the FDA, CDC, and the mainstream media still silent about this?

 
STEVE KIRSCH
OCT 19, 2023

Executive summary

Kevin McKernan is a friend of mine and his work is unimpeachable. His results have been replicated by others all over the world. He found that the COVID vaccines contain therapeutic levels of plasmid DNA. DNA lasts forever, and if it integrates into your genome, you will produce its product forever

The main takeaways are:

  1. The mRNA vaccines are contaminated with SV40 and who knows what else. This should never have been allowed.

  2. The vials exceeded the guidelines by “orders of magnitude.”

  3. The discovery was confirmed by Health Canada.

  4. The FDA and CDC are remaining silent. As far as anyone knows, they are no doing anything to assess the implications of the finding. I presume that they must believe that by not knowing the implications, they won’t have to disclose them so they are better protecting themselves against the public who might be very upset to learn they were guinea pigs. But that’s just an educated guess.

  5. We don’t know what the implications are. Experts disagree. Some claim the contamination is meaningless. Others say it could be very serious.

  6. The experts who claim there is no risk of harm have NO EVIDENCE to back up their claims. So that’s really comforting, isn’t it? Trust the experts :). Don’t worry.

  7. The politicians seem happy to let YOU take the risk. And they aren’t giving you any informed consent about this issue. Nobody seems to be requesting the CDC warn anyone of the potential risk. Wouldn’t want to scare anyone, would we?

  8. It was not the government regulators who first discovered the contamination. It was my friend Kevin McKernan. This should never have happened. The government should have discovered this at the very outset, 3 years ago.

  9. It would have been discovered sooner by independent researchers, but people were threatened with arrest if they supplied vials for analysis. I know this first hand because I was warned I would be arrested and criminally charged if I participated in trying to analyze the vials.

  10. We don’t fully know the ramifications of the contamination, but they probably aren’t good, and they could be devastating and irreversible. We don’t know yet because nobody has done the necessary studies.

  11. The experts I consulted thought that it was likely to be very serious. But they couldn’t quantify “likely” but said only that it was “more likely than not.”

  12. I volunteered for a full gene sequencing study, but they said they’d have to cut off my deltoid muscle, so I changed my mind.

  13. The regulators apparently never QAed any of the vials. If they did, they would have found contaminations such as this before it was ever injected into a single human being. Or they did and simply chose to remain silent and look the other way. Health Canada said the sequence was disclosed to them, but that the drug company never pointed out that the SV40 promoter sequence was specifically identified in the gene sequence provided.

  14. The SV40 promoter contamination has been known since April 9, 2023 when McKernan published a paper on it. But the CDC and FDA have remained silent on this issue. That’s comforting, isn’t it? <sarcasm off>

  15. The mainstream media is silent as well.

  16. And the mainstream medical community is silent as well. After all, they recommended you injected the stuff so they are not going to admit they f _ _ _ _ d up, are they?

  17. There is absolutely no doubt this is happening, so the silence of the formerly “trusted” health authorities is telling.

  18. The longer they delay telling you they forgot to QA the vials, the bigger the hole they are going to dig for themselves.   (See link for article and resources)

_________________
**Comment**
 
Public Health, mainstream medicine and media have used the silent treatment in Lymeland for over 40 years so I don’t hold out much hope of transparency.  These people have far too much invested in their power structure for honesty at this point.  They’ve been finding “experts” to tell them what they want to hear for so long they wouldn’t know real science if it hit them in the face.
 
In the “For more Info” section of Kirsh’s paper is an important key:

In-depth explanation from WCH and 14 minute video of Kevin McKernan. There is also a 2 minute excerpt entitled “Bait & Switch” on the page. Read this article first. Key excerpts:

  1. “By using qPCR to detect DNA but fluorometry to measure RNA, manufacturers had managed to mislead the regulators regarding the presence of DNA in the vials!”

Regarding the presence of SV40:

An NIH researcher, Bernice Eddy, found that hamsters who were injected with the Salk polio vaccine developed cancerous tumors. She was instructed not to publish her research but she did it anyway. Her lab was taken from her and she was demoted and moved to another position. Soon after her findings were corroborated and the carcinogen identified in the virus was SV-40.  The fly in the ointment is that every scientist on planet earth witnessed the treatment of Eddy and nobody wants to determine what component of SV40 is carcinogenic (can you blame them?) – so we remain ignorant, and now ‘the powers that be’ have yet another loophole to make excuses with.  The same issue is alive and well in Lymeland which is why nothing happens.

Rigging testing has always been a foundational component in corrupt public health’s playbook.  If you control the testing you control virtually the entire narrative.  

Hirsch states he is “arranging funding for a researcher with the necessary samples and equipment to do the research. This is because protecting the public is the responsibility of the public, not the government.“

And this, my friends, is the only way Lymeland will ever move forward. We must do it ourselves.

Category:

Activism, research, Testing, vaccines, Viruses