Pennsylvanians Urged to Protect Themselves Against Rising Tick-borne Diseases
http:// Approx. 8 Min
Pennsylvanians Urged to Protect Themselves Against Rising Tick-Borne Diseases
WGAL
March 16, 2022
http:// Approx. 8 Min
WGAL
March 16, 2022

On Tuesday, the FDA authorized Americans who are 50 years of age and older to receive a second booster of the Covid shot from either Pfizer-BioNTech or Moderna. The move comes after the Biden administration, disregarding the most basic “scientific” decorum and procedures, was reported to offer older Americans a fourth dose of the Covid vaccine. By fall, younger Americans will likely be able to get their second booster, too.
The news of the administration’s planning to make yet another dose available to the public was first reported by The New York Times over the weekend. (See link for article)
Important excerpt:
There’s a troubling caveat in that decision: it seems to have been made by the administration without discussion with the U.S. Food and Drug Administration’s (FDA) and the U.S. Centers for Disease Control and Prevention (CDC) “independent” panels. Meaning, the Biden administration is releasing the fourth vaccine booster without any public deliberation on the matter.
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SUMMARY:
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by Brian Shilhavy
Editor, Health Impact News
March 29, 2022
by Brian Shilhavy
Editor, Health Impact News
The FDA announced today that it has issued another emergency use authorization (EUA) for a second COVID booster vaccine for adults over the age of 50, and as young as 12 years old if they are “immune compromised.”
Pfizer had made the request for a second booster shot two weeks ago, but their request was for adults over the age of 65. The FDA, however, lowered that to age 50, and issued the EUA for both the Pfizer and Moderna COVID-19 vaccines.
Amid the ongoing debate over the need for another round of COVID-19 boosters, the FDA has acted quickly on the matter.
Only two weeks after Pfizer and its partner BioNTech asked the agency for an emergency use authorization (EUA) for a second round of COVID-19 boosters in people 65 and older, the FDA has granted the nod. The new FDA authorization covers those who have already been boosted with any COVID vaccine and are either 50 and older or 12 and older if they are immunocompromised.
At around the same time on Tuesday morning, Moderna said the FDA had granted its application for a second booster. The Moderna nod covers adults over 50 who have been boosted once, plus immunocompromised adults over 18. Moderna applied for a second booster on March 17. (Full article.)
Not likely.
As we have previously reported, the FDA does no safety oversight on these vaccines, but simply takes the drug manufacturers’ word for it, allowing them to police themselves. See:
So we will review the data on this age group in VAERS as a service to the public.
Here is what VAERS is reporting for people over the age of 50 following COVID-19 vaccines. (Source
There are currently 14,752 deaths recorded in VAERS for people over the age of 50 following a COVID-19 vaccine, covering a period of 15 months. That’s an average of 983 deaths a month for this age group.
Here are the results for this age group for the previous 30 years following ALL vaccines in VAERS. (Source.)
There were 1,590 deaths recorded following ALL vaccines for the previous 30 years for people older than 50. So if we divide that number by 360 months we get a monthly average of 4.4 deaths.
So we have seen a 22,000% increase in deaths for people over the age of 50 following COVID-19 vaccines, and the FDA just authorized another booster for those who are left in this age group.
But who cares? The corporate media owned by Big Pharma wants everyone to worry about Russia instead right now, while the FDA’s crimes go unpunished and they continue to produce and distribute more deadly shots.
Here is a video I put together last September when the FDA approved the first booster for seniors, which includes whistleblower testimonies from those who saw people die after taking the COVID-19 vaccines. This is on our Bitchute Channel. (Approx. 20 Min)
Media outlets mass-produce propaganda to control society, silencing those who dare to disrupt their narratives. Award winning journalist and ex-CBS Detroit employee, April Moss joined the Stew Peters Show Monday to expose Big Tech and Big Pharma’s collusion to kill the unvaccinated, the compliance of the media, nurses, doctors, and more.
Moss’s upcoming documentary, ‘Bad Medicine’ exposes how the media is killing thousands with the help Big Pharma, and the damage done so far. Visit FreedomMed.org to find clinics and doctors near you that prescribe ivermectin and effective treatments against the plandemic.
For appropriate COVID treatment:
For more:
The CARES Act provides incentives for hospitals to use treatments dictated solely by the federal government under the auspices of the NIH. These “bounties” must paid back if not “earned” by making the COVID-19 diagnosis and following the COVID-19 protocol. Government employees making the rules happen to have patents on nearly every aspect of COVID including the FDA approved treatments.
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https://thehighwire.com/videos/tv-exec-reveals-shocking-censorship-of-media/ Video Here (Approx. 17 Min)
Former British broadcasting executive, Mark Sharman, recently spoke out about the incredible failures of the media during Covid. Journalists were warned not to question the official government line in their reporting.

During the beginning stages of the Covid-19 pandemic, the British government threatened the media with penalties for reporting anything other than the official line, turning journalists into “cheerleaders for the government,” a former U.K. news executive said last week.
Mark Sharman, a former executive at ITV News and Sky News, told GB News that the U.K.’s Office of Communications (Ofcom) issued a bulletin to broadcasters in early 2020.
“It was a warning to basically say, ‘Do not question the official government line [on Covid-19],’” he said.
“Now, to be fair to them,” he continued, “they said, ‘You can have opposition voices on, but presenters must intervene if there’s any danger of harmful misinformation.’”
Ofcom meant what it said. The agency is empowered to impose a variety of sanctions on broadcasters that violate its dictates, up to and including revoking a broadcaster’s license, and it has done so repeatedly over the last two years. However, as Sharman pointed out, most of the penalties were meted out to smaller outlets that couldn’t fight back. (See link for article)
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Please go here to learn of how our government pays the media directly, puts “informants” in the national media and other institutions, uses reporters for information, and plants news stories.
SUMMARY:
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https://thenewamerican.com/lawsuit-biden-admin-pressuring-big-tech-to-censor-users/

The U.S. Surgeon General and the Department of Health and Human Services (HHS) of the Biden administration have directed social-media platforms, including Twitter, to suppress alleged “misinformation” about Covid, alleges a federal lawsuit filed on March 24.
The New Civil Liberties Alliance (NCLA), a conservative civil-rights group, filed the lawsuit in an Ohio federal court on behalf of social-media users Mark Changizi, Daniel Kotzin, and Michael Senger.
According to the lawsuit, all three garnered “tens of thousands of followers” on Twitter and other social-media platforms by actively criticizing restrictions imposed by governments and public-health authorities in response to Covid. As a result, the three have been unlawfully censored. (See link for article)
SUMMARY:
https://www.lymedisease.org/auto-antibody-lyme-test-tufts/
March 23, 2022

By Julie Rafferty, Tufts University
For scientists and clinicians alike, one of the holy grails for successfully treating and curing Lyme disease is developing tests that identify the disease sooner, show when people are cured of infection, and can diagnose reinfection.
Now, researchers at Tufts University School of Medicine say they have identified just such a testing mechanism. It detects a type of antibody that infected individuals produce against a substance the Lyme bacteria acquires from the host in order to grow.
The researchers believe tests to detect these autoantibodies – antibodies that mistakenly target and react with a person’s own tissues or organs – could provide clinicians with a way to diagnose the disease sooner, know whether treatment with antibiotics is working, and identify patients who have been reinfected.
Authors of the study, published today by the Journal of Clinical Investigation, are Peter Gwynne, Luke Clendenen, and Linden Hu of the school’s Department of Molecular Biology and Microbiology, and colleagues at the National Institute of Allergy and Infectious Diseases at the National Institutes of Health (NIH).
Lyme disease, which was identified five decades ago along the Connecticut coast and spread across New England and the mid-Atlantic region, affects almost 500,000 people in the U.S. every year. Caused by a bite from an infected tick, it frequently goes undetected unless a person notices the telltale rash that forms around the bite.
Lyme disease can lead to debilitating long-term complications including arthritis, fatigue, mental impairment, and in the most severe cases, attacks on the heart and brain tissue.
Caused by the bacterium Borrelia burgdorferi, Lyme disease can often be treated with antibiotics. But in 10 to 20 percent of cases, the disease’s effects can persist.
Testing to detect Lyme disease exists, but it has limitations, says Gwynne, the lead author of the study and research scientist at Tufts School of Medicine who received a Tufts Launchpad Accelerator award for his work on Lyme disease.
“Traditional Lyme tests can stay positive for prolonged periods of time after treatment – years or even a lifetime,” he says.
“As a result, for some individuals suffering from symptoms that resemble long-term Lyme disease infection, clinicians are never sure whether the patient has persistent Lyme disease, was cured and then reinfected, or was cured and is suffering from something else.”
“We started this current work to learn how Borrelia burgdorferi acquires key nutrients, like fats, for growth,” says Gwynne. “The Lyme bacteria, despite being a very successful pathogen, is much more dependent than other bacteria on acquiring nutrients from its environment.”
“In the process of our research, we found that the organism takes fats called phospholipids directly from its surroundings in the host, and puts them on its surface,” says Hu, the Vice Dean of Research at the school and Paul and Elaine Chervinsky Professor of Immunology.
“That finding led us to look to see if the direct use of a host fat by the bacteria might lead the immune system to recognize it as a foreign substance and create antibodies to it.”
What the scientists discovered is that both animals and patients infected with the Lyme bacterium developed autoantibodies to multiple phospholipids. Because autoantibodies can be damaging to the host, these autoantibodies are tightly regulated and tend to disappear quickly once the stimulating factor is removed.
“The antibodies also seem to develop much more quickly than traditional antibodies to the Lyme bacteria—likely because your body has previously created these autoantibodies and downregulated them,” says Hu.
While current testing makes it difficult to diagnose reinfection or successful treatment, “the anti-phospholipid autoantibodies—because of their quick increase and quick resolution with treatment—can fill these gaps as a novel additional test,” Gwynne says. “They may make it possible to tell whether treatment has eradicated the Lyme disease bacteria. And they therefore also make it possible to tell if a patient with a prior infection now has a new infection.”
Gwynne and Hu have a provisional patent pending describing the use of antiphospholipid antibodies in the diagnosis of Lyme disease. Their hope is that if their discovery is borne out by further research, a diagnostic company could begin development of a commercially available version of their test within a couple of years.
A bigger question, which was not examined in the current paper, is whether these autoantibodies may identify a subset of patients who will develop persistent symptoms of Lyme disease after treatment.
Up to 20 percent of patients can develop persistent symptoms after Lyme disease. Diagnosis of these patients is currently only by clinical symptoms, making it likely that patients with different causes of their symptoms are grouped together. And treatment trials in patients with persistent Lyme disease are unlikely to show benefit if that occurs.
“Anti-phospholipid antibodies are commonly seen in autoimmune diseases like lupus, and are associated with blood clots and persistent inflammation that causes other disease conditions,” says Hu. “Many of the persistent symptoms in patients who continue to have symptoms after being diagnosed with Lyme disease are similar to those autoimmune diseases.”
“If there ends up being a link between having persistent Lyme symptoms and these autoantibodies, this would be the first test that could be used to distinguish a group of patients who have persistent Lyme disease,” he says. “It would allow us to test specific new therapies targeted to a defined mechanism.”
SOURCE OF PRESS RELEASE: Tufts University
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**Comment**
A few points:
It’s imperative to understand this important backstory to understand where this current study is headed and the inherent bias. They are careful to bait patients into thinking this research is beneficial by mentioning things like “chronic infection”, the importance of early diagnosis, and identifying reinfection, but never ONCE do they admit the possibility of chronic, persistent, infection.
This, right here, is why Lyme/MSIDS has remained and continues to remain in a quagmire. Until this issue is dealt with utilizing unbiased studies, most probably from independent researchers without patents and ties to the government, we will never move forward with proper scientific information. It will all continue to be based upon a faulty paradigm which hasn’t shifted in over 40 years.
http://uknow.uky.edu/research/uk-study-explore-why-lyme-disease-symptoms-persist-some
LEXINGTON, Ky. (March 4, 2022) — Although most cases of Lyme disease can be cured with a two-to-four-week course of antibiotics, some patients still experience lingering, debilitating effects of the disease months after they finish treatment.
Researchers in the University of Kentucky’s College of Medicine are seeking to understand if the antibiotic regimen used to treat Lyme disease could also be contributing to Post-Treatment Lyme Disease Syndrome (PTLDS), which includes ongoing symptoms of pain, fatigue or difficulty thinking.
Antibiotics can cause imbalances to the gut microbiome, the trillions of microbes essential to health and immune system function. Known as dysbiosis, these disruptions are linked to various autoimmune and inflammatory diseases, as well as cardiovascular disease and depression.
The study, supported by the Global Lyme Alliance and co-led by Ilhem Messaoudi, Ph.D., and Brian Stevenson, Ph.D., in the Department of Microbiology, Immunology and Molecular Genetics, will be the first to assess the role of dysbiosis in the development of PTLDS.
Lyme disease is a tick-borne illness caused by the bacteria Borrelia burgdorferi. The Centers for Disease Control and Prevention estimates that 476,000 Americans are diagnosed with Lyme disease each year.
The research will provide new insights into the interaction between B. burgdorferi infection, antibiotics, and the gut microbiome that may lead to more effective ways to treat Lyme disease, says Messaoudi.
“Lyme disease can be just an acute episode, but for some people, it becomes a prolonged disease with a lot of complications and scientists don’t fully understand where these complications come from,” Messaoudi said. “This study may provide targets that could lead to the development of new antibiotic treatment plans that address the microbiome as well as the immune system.”
Messaoudi and Stevenson will be collaborating with researchers at the Oregon National Primate Research Center to carry out an in-depth analysis of host responses. The research will also establish an ideal animal model for future studies on the cognitive and physical effects of PTLDS.
The University of Kentucky is increasingly the first choice for students, faculty and staff to pursue their passions and their professional goals. In the last two years, Forbes has named UK among the best employers for diversity, and INSIGHT into Diversity recognized us as a Diversity Champion four years running. UK is ranked among the top 30 campuses in the nation for LGBTQ* inclusion and safety. UK has been judged a “Great College to Work for” three years in a row, and UK is among only 22 universities in the country on Forbes’ list of “America’s Best Employers.” We are ranked among the top 10 percent of public institutions for research expenditures — a tangible symbol of our breadth and depth as a university focused on discovery that changes lives and communities. And our patients know and appreciate the fact that UK HealthCare has been named the state’s top hospital for five straight years. Accolades and honors are great. But they are more important for what they represent: the idea that creating a community of belonging and commitment to excellence is how we honor our mission to be not simply the University of Kentucky, but the University for Kentucky.