Archive for the ‘Testing’ Category

Oct. 31 Webinar: A Rash of Tickborne Illnesses: Current Challenges With Diagnostic Testing

Upcoming Webinar: A Rash of Tickborne Illnesses: Current Challenges With Diagnostic Testing

Date: Oct 31, 2023 9 a.m. PDT/12 p.m. EST

Please join us for an upcoming webinar, “A Rash of Tickborne Illnesses: Current Challenges with Diagnostic Testing,” an hour-long webinar featuring Elitza S. Theel, Ph.D., D(ABMM) and Elizabeth Lee-Lewandrowski, Ph.D.

  • Understand the incidence and prevalence of tickborne illness
  • Review the current testing methodologies available for Lyme disease
  • Explore current diagnosis guidelines for Lyme disease
  • Discuss the advantages of Point-of-Care diagnostics for Lyme disease

Go here to register:  https://gateway.on24.com/wcc/eh/3300431/lp/4379756/a-rash-of-tickborne-illnesses-current-challenges-with-diagnostic-testing

“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?

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)

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**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.

Lyme & Coinfection Update: Dr. Armin Schwarzbach

http://

An Update for Lyme & Co-infections

Dr. Armin Schwarzbach/Nordic Laboratories & dnalife

Oct. 9, 2023

Within the field of infections, new research is in constant development. During his discussion, Dr. Schwarzbach will cover both what tests he offers through Nordic and dnalife, looking at what could potentially be a great alternative to what the national health service may have to offer. He will also be informing us about new and ongoing testing and considerations, while also touching on the topic of co-infections as an additional concern for patients.

If you go to the Youtube link, you can also view the transcript.

Yet Another “Unique” EM Rash

https://danielcameronmd.com/unique-presentation-em-rash/

A UNIQUE PRESENTATION OF AN EM RASH

unique-EM-rash

The rash, indicative of Lyme disease, does not always present as a classic “bull’s-eye rash,” as this case report demonstrates. A broad spectrum of lesions has been reported in patients with Lyme disease (LD). In fact, one study found only 6% of the lesions in LD patients had the “classic bull’s-eye or ring-within-a-ring pattern.” [1]

In the case report, “A Non-Classical Presentation of Erythema Migrans in a 51-Year-Old Woman With Early Manifestation of Lyme Neuroborreliosis (Bannwarth Syndrome),” Lorquet et al. describe a 51-year-old female who presented with general malaise, headache, neck stiffness, and an expanding rash consistent with Lyme neuroborreliosis.2

The woman reported having a worsening of her symptoms over a 4-day period and a rash which expanded on her upper back but she did not recall any tick bites.

“She stated that [the rash] started as a small area of redness, spreading rapidly,” the authors wrote.

Clinicians suspected she might have cellulitis and prescribed cephalexin and valacyclovir. But her symptoms did not improve.

“The “bull’s-eye” appearance of erythema migrans is not the only cutaneous manifestation of the acute stage of Lyme disease. There can be multiple variations of the rash, as demonstrated in the patient.”

According to the patient, “the rash had gotten larger and more pruritic [itchy] and that her headache had become more severe, also causing severe pain that radiated to the right side of her neck,” the authors wrote.

The erythema migrans (EM) rash covered two-thirds of her back and had a 5 cm crusted plaque in the center. There was a second circular rash that appeared, as well, behind the woman’s right ear.

READ: The many presentations of the Lyme disease rash

Clinicians treated her symptoms with intravenous ondansetron, ketorolac, pantoprazole, and saline. But also empirically treated for Lyme disease with doxycycline.

After Lyme disease testing was positive, the woman was diagnosed with Lyme Neuroborreliosis, also known as Bannwarth syndrome in Europe.

Bannwarth syndrome (BS) is a typical manifestation of early Lyme neuroborreliosis (LNB) in Europe. It is characterized by painful radiculopathy, neuropathy, varying degrees of motor weakness and facial nerve palsy, and cerebrospinal fluid (CSF) lymphocytic pleocytosis.3

“Several weeks later, the patient had made a full recovery and was back to her baseline level of functioning,” the authors wrote.

They point out, “The “bull’s-eye” appearance of erythema migrans is not the only cutaneous manifestation of the acute stage of Lyme disease. There can be multiple variations of the rash, as demonstrated in the patient.”

References:
  1. Schotthoefer A M, Green C B, Dempsey G, et al. (October 25, 2022) The Spectrum of Erythema Migrans in Early Lyme Disease: Can We Improve Its Recognition? Cureus 14(10): e30673. doi:10.7759/cureus.30673
  2. Lorquet JR, Pell R, Adams J, Tak M, Ganti L. A Non-Classical Presentation of Erythema Migrans in a 51-Year-Old Woman With Early Manifestation of Lyme Neuroborreliosis (Bannwarth Syndrome). Cureus. 2023 Jun 4;15(6):e39931. doi: 10.7759/cureus.39931. PMID: 37416051; PMCID: PMC10319937.
  3. Shah A, O’Horo JC, Wilson JW, Granger D, Theel ES. An Unusual Cluster of Neuroinvasive Lyme Disease Cases Presenting With Bannwarth Syndrome in the Midwest United States. Open Forum Infect Dis. 2017 Dec 23;5(1):ofx276. doi: 10.1093/ofid/ofx276. PMID: 29383323; PMCID: PMC5777478.

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**Comment**

So many thoughts here.

  • The rash issue has caused frequent, unnecessary delays in diagnosis and treatment as doctors are not properly educated on actual science, but have been fed a CDC-narrative.  Most doctors are unaware that this rash is diagnostic for Lyme disease, and that misdiagnosis can have fatal consequences.
  • Aucott reports that 54% of Lyme disease patients who present without a rash are misdiagnosed.
  • The designation of Bannwarth Syndrome is also confusing and has caused massive misdirection.  The symptoms are nearly synonymous with most cases of Lyme & can cause severe burning, stabbing, biting, or tearing pain & responds poorly to analgesics:
    • radicular pain (100%)
    • sleep disturbances (75.3%)
    • headache (46.8%)
    • fatigue (44.2%)
    • malaise (39%)
    • paresthesia (32.5%)
    • peripheral nerve palsy (36.4%)
    • meningeal signs (19.5%)
    • paresis (7.8%)
  • This case study shows many of the problems that continue on unabated in Lymeland.

Review: Borrelia Miyamotoi

https://danielcameronmd.com/review-borrelia-miyamotoi/

REVIEW: BORRELIA MIYAMOTOI

borrelia-miyamotoi

Borrelia miyamotoi is an emerging tick-borne illness that is transmitted by the deer tick. The most common symptoms of a B. miyamotoi infection include fever, fatigue, headache, chills, myalgia, arthralgia, and nausea.

In their article, “Human Borrelia miyamotoi Infection in North America,” Burde and colleagues discuss the frequency and location of infection in ticks and people, clinical presentation and complications, diagnosis, treatment, and prevention.

Prevalence of B. miyamotoi

B. miyamotoi-infected ticks have been reported throughout the northeastern, northern Midwestern, and western United States. They’ve also been detected in all Canadian provinces except Newfoundland and Labrador.

The prevalence of Borrelia miyamotoi infections is difficult to determine, since the illness is not nationally reportable in the U.S. but reportable in only a few states including Connecticut, Maine, Massachusetts, Minnesota, New Jersey, Vermont, and Wisconsin. And, confirmation of the diagnosis depends upon laboratory testing, which is not always available.

Furthermore, diagnosis can be challenging. “The discrepancy between diagnosed and undiagnosed infection is probably even greater for B. miyamotoi, a tick-borne disease that lacks an easily identifiable clinical marker, such as the erythema migrans rash, and is less well known by health care workers and the general public,” the authors write.

Transmission

B. miyamotoi can be transmitted to humans through the bite of an infected black-legged (deer) tick. Several studies have found that it may be transmitted through blood transfusions, as well.

The B. miyamotoi pathogen can be transmitted from an infected female tick to her eggs, which may result in some larval ticks harboring the infection and transmitting it to a host. “Other larvae become infected after taking a blood meal on an infected mouse reservoir host, molt to the nymphal stage, and then transmit infection to another mouse or human,” they write.

Symptoms & Treatment

B. miyamotoi symptoms can be non-specific and an individual may appear to have a viral-like illness with fever, chills, headache, myalgia, fatigue, arthralgia, and gastrointestinal complaints, according to the authors.

“The most striking clinical feature of B. miyamotoi is relapsing fever with an initial febrile episode followed by a period of wellness and then one or more additional febrile episodes,” the authors write.

Some studies have found that the “average time between relapses was 9 days with a range of 2 days to 2 weeks.”

However, not all individuals develop relapsing fever. “In the largest case series of B. miyamotoi cases in the US, only 2 of 51 cases (4%) developed relapsing fever.”

READ: Don’t Rely on Relapsing Fever to Diagnose B. miyamotoi 

Treatment of B. miyamotoi disease typically involves using the same antibiotics to treat Lyme disease: doxycycline, tetracycline, erythromycin, penicillin, and ceftriaxone. However, there have been no trials to evaluate the effectiveness of these treatments.

Co-infections worsen disease

Co-infections can worsen the illness. There have been reported cases of B. miyamotoi co-infection with B. burgdorferi and/or Babesia microti.

“Previous studies have found that coinfection of B. burgdorferi with either Babesia microti or with Anaplasma phagocytophilum are often associated with more severe disease compared with that caused by B. burgdorferi infection alone,” the authors write.

Testing for the infection can include blood smear, polymerase chain reaction (PCR), and/or antibody detection.

Authors’ Conclude:

“The possibility of B. miyamotoi infection should be considered in any patient with a febrile illness who resides in or has recently traveled to a region where Lyme disease is endemic, especially during the late spring, summer, or early fall.”

References:
  1. Burde J, Bloch EM, Kelly JR, Krause PJ. Human Borrelia miyamotoi Infection in North America. Pathogens. 2023 Apr 3;12(4):553. doi: 10.3390/pathogens12040553. PMID: 37111439; PMCID: PMC10145171.

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For more:

Since Borrelia miyamotoi is not a reportable illness to the CDC, no one has any clue about prevalence but reports are coming in continually that it’s highly likely to be a much bigger problem than ‘authorities’ believe.
It was recently discovered that:

Also, Borrelia miyamotoi has been in California ticks for a long time:

https://madisonarealymesupportgroup.com/2018/02/15/b-miyamotoi-in-ca-ticks-for-a-long-time/

The following case shows how you can become infected while traveling:  https://madisonarealymesupportgroup.com/2020/10/24/a-case-of-borrelia-miyamotoi/