Archive for the ‘Activism’ Category

Worth Repeating: COVID Shot Alters DNA & May Pass Genetic Code From Parent to Child. CHD Sues FDA

The following information isn’t new.  Dr. McCullough continues to remind the public that studies showing the COVID shots alter DNA and may pass the genetic code to fetuses have gone unchallenged.  Similarly to Dr. John Campbell’s appraisal, we hear nothing from corrupt public health ‘authorities,’ other than silence.  Now, the FDA wants people to be “vaccinated” yearly with a clot shot is linked with more reports of adverse reactions and death than any other vaccine in the history of VAERS, which only has a 1% capture rate.

https://www.newstarget.com/2023-01-25-mrna-vaccine-experiment-does-alter-human-dna.html

The mRNA “vaccine” experiment does alter human DNA and may pass genetic code from parent to child, warns Dr. McCullough

01/25/2023 / By Lance D Johnson
The mRNA “vaccine” experiment does alter human DNA and may pass genetic code from parent to child, warns Dr. McCullough

Dr. Peter McCullough, the leading cardiologist fighting for the health of the next generation, gave a grave warning about the long-term effects of the mRNA “vaccine” experiment.

“Once people take these vaccines, it’s long lasting, it may get into the nucleus, change the human genome, and pass down to daughter cells… which means that this could actually be passed down to the progeny of vaccinated young parents,” he said. “There couldn’t be worse news right now. We were hoping this vaccine would be in and out of the body. It looks like it’s long lasting, causing a tremendous amount of damage.”

Vaccine spike protein doesn’t degrade, persists in lymph nodes, causes immune imprinting

Dr. McCullough mentioned two important studies that have gone unchallenged. In a study at Stanford, the Pfizer spike protein mRNA actually persists in the lymph nodes for several months, instead of degrading in the deltoid muscle, as was initially promised by the vaccine manufacturers. The scientists found that this predisposes the vaccinated individual to some degree of immune imprinting. In other words, the person’s immune system is being engineered to have preferential responses to the viral variants it initially encountered, negatively affecting the development of antibodies against new viral variants that will continue to challenge the immune system.

Basically, the mRNA vaccines are programming human immune systems for failure, making it harder for immune cells to respond to the ever-changing mutations that are taking place in coronaviruses. Because the spike proteins from the mRNA persist in the body for weeks (and months in some cases), vaccinated individuals are not having robust immune responses; instead, they are being burdened by long term cardio-toxins. The vaccine’s lipid nano-particle delivery system is so stealth, it is able to deliver the mRNA instructions to several organs such as liver, spleen, heart, kidney, lung, and brain.

The Pfizer mRNA vaccine is reverse transcribed in human liver cell lines

Pfizer’s bio-distribution study showed that the spike proteins target the liver, causing enlarged liver, vacuolation, increased gamma glutamyl transferase levels, and increased levels of aspartate transaminase and alkaline phosphatase.

In the other study that Dr. McCullough referenced, scientists found that the entire genetic code from Pfizer’s vaccine gets installed into human liver cell lines.   (See link for article)

________________

https://childrenshealthdefense.org/defender/chd-lawsuit-fda-vaers-covid-vaccine-injuries-deaths/

CHD Sues FDA to Obtain Documents Related to VAERS Reports on COVID Vaccine Injuries, Deaths

Children’s Health Defense today filed a federal lawsuit against the U.S. Food and Drug Administration to obtain documents related to the agency’s safety monitoring of COVID-19 vaccines through the Vaccine Adverse Events Reporting System database.

Children’s Health Defense (CHD) today filed a lawsuit in D.C. Federal Court against the U.S. Food and Drug Administration (FDA) to obtain documents related to the agency’s safety monitoring of the COVID-19 vaccines through the Vaccine Adverse Events Reporting System (VAERS) database.

The lawsuit alleges the FDA violated provisions of the Freedom of Information Act (FOIA) by refusing to provide key analysis of reports in the vaccine safety database.

CHD submitted the FOIA request in July 2022.

The FDA claimed the records sought are fully exempt from disclosure under FOIA because they are part of internal and intra-agency memoranda that include opinions and discussions protected by law, and because the records include discussions of legal and policy matters protected by attorney-client privilege.

Mary Holland, CHD president and general counsel, took issue with the FDA’s position.

“The public must have truthful, complete information about the risks and benefits of these drugs, and others,” Holland told The Defender.

FDA analyzes VAERS data but doesn’t make its results public

(See link for article)

________________

**Comment**

We pay for this agency yet we don’t get to see what we pay for.

Withholding, hiding, deleting, manipulating, botching, falsifying, and twisting data is what these corrupt public health agencies do best.

And in case you are wondering what waived good”vaccine” manufacturing practices as well as liability and informed consent, look no further than laws that were changed under Obama in 2016:  https://frankspeech.com/video/obama-changed-laws-2016-waved-good-manufacturing-practices-informed-consent-and-liability

Obama and 114 Congress change of informed consent

According to these documents, as long as medical professionals are following the government, they are not liable – even if you die.

This is called “medical kidnapping.”
If you go to a hospital today, you do not have any rights and will be subjected to whatever whims the staff are following that are coming down from the government.

For more:

46% Increase Risk in All-Cause Death in “Vaccinated” vs Placebo, Excess Deaths in 30 Countries & UK Ends COVID Boosters For Healthy People

https://popularrationalism.substack.com/p/acceptable-adverse-event-profile?

“Acceptable Adverse Event Profile?” At Six Months Follow-Up, the Pfizer-Vaccinated Had a 46% Increase in Mortality Compared to the Placebo Group

Of course they then vaccinated the placebo group.

The patients in the BNT162b2 (Pfizer) vaccine trial (Funded by BioNTech and Pfizer; ClinicalTrials.gov number, NCT04368728) were followed up to assess health outcomes.

From their data, 20 of 20,334 (98 per 100K) who received both doses of their experimental mRNA jab died.

In the placebo group, 14 out of 20794 (67 per 100K) had died.

The ratio 98/67 = 146; thus, 46% increase risk of all-cause death in the vaccinated compared to placebo.

The authors nevertheless concluded:

“Through 6 months of follow-up and despite a gradual decline in vaccine efficacy, BNT162b2 had a favorable safety profile”.

and then

“BNT162b2 continued to be safe and have an acceptable adverse-event profile.”

This is on you, #NEJM. And on you, Pfizer. And on you, FDA.

And on you, the authors of the study.

Also from the study, in case any Attorneys General read #PopularRationalism:

“The authors’ full names, academic degrees, and affiliations are listed in the Appendix. Dr. Dormitzer can be contacted at philip.dormitzer@pfizer.com or at Pfizer, 401 N. Middletown Rd., Pearl River, NY 10965.”

http://  Approx. 16 Min

Excess Deaths in 30 Countries

Dr. John Campbell

Jan. 26, 2023

“We can say definitively that for pretty well seven months now in the UK, excess deaths have been increasing….This demands an explanation.  And we are not getting one.  We hear nothing from the Chief Medical officer.  We hear nothing from the Chief Scientific Officer, we hear nothing from Prime Minister, and we hear essentially nothing from national media, it’s left to eccentrics in their back room to try and publicize the fact that thousands of people extra are dying every week in my country and probably in your country as well. ~ Dr. John Campbell

UK Prevalence

  • 2.61% in England (1 in 40 people)
  • 3.94% in Wales (1 in 25 people)
  • 4.22% in Northern Ireland (1 in 25 people)
  • 3.26% in Scotland (1 in 30 people)

Deaths and excess deaths (W/E week 13th January 2023) A total of 19,916 deaths were registered in the UK 20.4% above the five-year average. 

https://childrenshealthdefense.org/defender/uk-covid-vaccine-booster-post-pandemic

UK to End COVID Booster Program for Healthy People Under 50 in Shift to ‘Post-Pandemic Life’

The U.K. said Wednesday it will no longer recommend COVID-19 boosters for healthy people under age 50 and will discontinue free distribution of the primary two-shot series.

The U.K. will no longer recommend COVID-19 boosters for healthy people under age 50, and will discontinue free distribution of the primary two-shot series, the UK Health Security Agency (UKHSA) announced Wednesday.

The policy change comes as the U.K. government shifts away from its “pandemic emergency response,” The Telegraph reported. The Daily Mail characterized the changes as a sign the country is “settl[ing] into post-pandemic life.”

The U.K.’s autumn COVID-19 booster drive for those over 50 will end Feb. 12, according to the UKHSA, along with its booster offer for 16- to 49-year-olds who are not in a clinical risk group.

The agency cited “dwindling uptake” of the primary series and booster, which up until now were available to healthy people ages 16 to 49, in its decision to end “its evergreen offer,” according to The Telegraph.

This announcement came one day after Esther McVey, a member of the UK Parliament with the Conservative Party, called for an urgent and thorough investigation into excess deaths while speaking in parliament.

British cardiologist Dr. Aseem Malhotra, who recently “truthbombed” the BBC during a live appearance telling viewers the mRNA COVID-19 vaccines pose a cardiovascular risk, welcomed the changes. He tweeted:

Some other European countries, including Denmark, already ended their universal COVID-19 vaccination campaigns for healthy individuals.

The U.S. Food and Drug Administration (FDA) today is meeting to discuss a new vaccination schedule wherein adults would be vaccinated once a year to “stay protected” against COVID-19.

(See link for article)

____________________

**Comment**

Please remember that the CDC recommended the bivalent boosters without any clinical trial data.

When people finally discover that Western Media is owned by three global news agencies that are heavily used by intelligence agencies and defense ministries that have more than 27,000 PR specialists with an annual propaganda budget of nearly $5 BILLION, all spouting the accepted narrative, and actually refuse the spin about the COVID gene therapy injections, ‘the powers that be’ will make moves similar to the one being made in the UK: simply stop recommending the shot due to “dwindling uptake,” exactly like when they pulled Lymerix, the vaccine for Lyme disease that maimed a bunch of people, but cited “lack of demand,” as the reason.

It’s ingenious PR.

If our corrupt public health ‘authorities’ were only half as good with science as they are with public relations and propaganda – they’d actually be respectable.

Pfizer Exposed Exploring “Mutating” COVID For ‘Vaccines” Via ‘Directed Evolution’ in Living Monkeys

**UPDATE**

Intelligence Analyst Brian O’Shea recently did this article on Jordon Rishton Walker, the “doctor” in the Verita’s video: https://brianoshea.substack.com/p/who-is-jordon-trishton-walker?  O’Shea admitted that finding anything out about him was tough.  In the comment section, a writer for Brownstone (Debbie Lerman) states that there are inconsistencies and a strangeness about the information, including that it all might very well be fake.  

https://rumble.com/v274lsi-pfizer-exposed-for-exploring-mutating-covid-19-virus-for-new-vaccines-via-d.html  Video Here (Approx. 10 Min)

Project Veritas released a new video today exposing a Pfizer executive, Jordon Trishton Walker, who claims that Pfizer is exploring a way to “mutate” COVID via “Directed Evolution” to preempt the development of future vaccines.

Walker says that Directed Evolution is different than Gain-of-Function, which is defined as “a mutation that confers new or enhanced activity on a protein.” In other words, it means that a virus such as COVID can become more potent depending on the mutation / scientific experiment performed on it.

The Pfizer executive told a Veritas journalist about his company’s plan for COVID vaccines, while acknowledging that people would not like this information if it went public.

“One of the things we [Pfizer] are exploring is like, why don’t we just mutate it [COVID] ourselves so we could create — preemptively develop new vaccines, right? So, we have to do that. If we’re gonna do that though, there’s a risk of like, as you could imagine — no one wants to be having a pharma company mutating f**king viruses,” Walker said.

“From what I’ve heard is they [Pfizer scientists] are optimizing it [COVID mutation process], but they’re going slow because everyone is very cautious — obviously they don’t want to accelerate it too much. I think they are also just trying to do it as an exploratory thing because you obviously don’t want to advertise that you are figuring out future mutations,” he said.

“Don’t tell anyone. Promise you won’t tell anyone. The way it [the experiment] would work is that we put the virus in monkeys, and we successively cause them to keep infecting each other, and we collect serial samples from them.”

Walker drew parallels between this current Pfizer project and what may have happened at the Wuhan Institute of Virology in China.

“You have to be very controlled to make sure that this virus [COVID] that you mutate doesn’t create something that just goes everywhere. Which, I suspect, is the way that the virus started in Wuhan, to be honest. It makes no sense that this virus popped out of nowhere. It’s bullsh*t,” he said.

“You’re not supposed to do Gain-of-Function research with viruses. Regularly not. We can do these selected structure mutations to make them more potent. There is research ongoing about that. I don’t know how that is going to work. There better not be any more outbreaks because Jesus Christ,” he said.

Walker also told the Veritas journalist that COVID has been instrumental for Pfizer’s recent business success:

Walker: Part of what they [Pfizer scientists] want to do is, to some extent, to try to figure out, you know, how there are all these new strains and variants that just pop up. So, it’s like trying to catch them before they pop up and we can develop a vaccine prophylactically, like, for new variants. So, that’s why they like, do it controlled in a lab, where they say this is a new epitope, and so if it comes out later on in the public, we already have a vaccine working.

Veritas Journalist: Oh my God. That’s perfect. Isn’t that the best business model though? Just control nature before nature even happens itself? Right?

Walker: Yeah. If it works.

Veritas Journalist: What do you mean if it works?

Walker: Because some of the times there are mutations that pop up that we are not prepared for. Like with Delta and Omicron. And things like that. Who knows? Either way, it’s going to be a cash cow. COVID is going to be a cash cow for us for a while going forward. Like obviously.

Veritas Journalist: Well, I think the whole research of the viruses and mutating it, like, would be the ultimate cash cow.

Walker: Yeah, it’d be perfect.

Walker went on to explain how Big Pharma and government officials, such as at the Food & Drug Administration [FDA], have mutual interests, and how that is not in the best interest of the American people:

Walker: [Big Pharma] is a revolving door for all government officials.

Veritas Journalist: Wow.

Walker: In any industry though. So, in the pharma industry, all the people who review our drugs — eventually most of them will come work for pharma companies. And in the military, defense government officials eventually work for defense companies afterwards.

Veritas Journalist: How do you feel about that revolving door?

Walker: It’s pretty good for the industry to be honest. It’s bad for everybody else in America.

Veritas Journalist: Why is it bad for everybody else?

Walker: Because when the regulators reviewing our drugs know that once they stop regulating, they are going to work for the company, they are not going to be as hard towards the company that’s going to give them a job.

_________________

**Comment**

Dr Robert Malone says this is ‘gain of function.’  No question. Ongoing serial passage leading to a little “directed evolution” is ‘gain of function.’

“Pfizer has completed regulatory capture.  Is quite proud of it.” ~ Dr. Robert Malone

The corruption is prolific and seemingly everywhere.

Bring back the moratorium on gain of function research (serial passage, directed evolution, or any other made up euphemism).

Meanwhile in Boston, researchers have created a new version of the virus, combining the spike protein that studs the surface of omicron with the backbone of the ancestral strain yielding a “chimeric” virus only a little less deadly than the Wuhan strain, which killed 80% of the lab mice rather than 100%, but it’s still deadlier in the mice than omicron.

Mother Nature “is not being coy with us. She’s telling us exactly what she’s going to do. She says, ‘I’m hurling another coronavirus epidemic at you every 7 to 10 years. Mother Nature is the most advanced, sophisticated weaponeer ever invented.’”  ~ Peter Hotez, vaccinologist at Baylor College of Medicine

I, for one, would rather take my chance with Mother Nature.

For more:

Lyme Disease Misinformation Has Physicians Searching For Guidance Part 3

https://www.change.org/p/the-us-senate-calling-for-a-congressional-investigation-of-the-cdc-idsa-and-aldf/u/31256356

Lyme disease misinformation has physicians searching for guidance (Part 3)

Carl Tuttle

Hudson, NH, United States

JAN 25, 2023 — 

This petition update is a continuation of the attempts to alert Dr. Arnold Chen, Senior Researcher at Mathematica that the CDC (Grace Marx, MD, MPH) is deliberately misrepresenting Lyme disease which will lead to inappropriate guidance for the medical community.

———- Original Message ———-
From: CARL TUTTLE <runagain@comcast.net>
To: “achen@mathematica-mpr.com” <achen@mathematica-mpr.com>, “info@mathematica-mpr.com” <info@mathematica-mpr.com>, “pdecker@mathematica-mpr.com” <pdecker@mathematica-mpr.com>
Cc: “lwx1@cdc.gov” <lwx1@cdc.gov>, “frederick.chen@ama-assn.org” <frederick.chen@ama-assn.org>, “gmarx@cdc.gov” <gmarx@cdc.gov>, “acoyne@mathematica-mpr.com” <acoyne@mathematica-mpr.com>, “jconstantine@mathematica-mpr.com” <jconstantine@mathematica-mpr.com>, “ctrenholm@mathematica-mpr.com” <ctrenholm@mathematica-mpr.com>, “tbarnes@mathematica-mpr.com” <tbarnes@mathematica-mpr.com>, “sboudreau@mathematica-mpr.com” <sboudreau@mathematica-mpr.com>, “jdevallance@mathematica-mpr.com” <jdevallance@mathematica-mpr.com>, “sara.berg@ama-assn.org” <sara.berg@ama-assn.org>
Date: 01/24/2023 8:29 AM
Subject: Fwd: Lyme Disease Updates and New Educational Tools for Clinicians -Grace Marx, MD, MPH

Mathematica
Princeton, NJ
Attn: Arnold Chen, Senior Researcher
Dear Dr. Chen,

Please see the email below dated one day before Dr. Marx presented her Clinician Outreach and Communication Activity (COCA) Webinar on May 20, 2021.

There are 9 important facts about Lyme disease missing from Dr. Marx’s presentation and I assume these facts will also be missing from the upcoming guidance created by Mathematica
Carl Tuttle
Hudson, NH

Email to Grace Marx, MD, MPH:

———- Original Message ———-
From: CARL TUTTLE <runagain@comcast.net>
To: “lwx1@cdc.gov” <lwx1@cdc.gov>, “coca@cdc.gov” <coca@cdc.gov>
Cc: Lynn Durand <ldurand@crhc.org>, Tricia Aiston <tricia@aiston.net>, “Dr. Frank Hubbell” <bearhubbell@aol.com>, Mary Mayville <mj4ok@aol.com>, “Dr. Rex Carr” <rcarrmd@comcast.net>, “benjamin.chan@dhhs.nh.gov” <benjamin.chan@dhhs.nh.gov>, “apara.dave@nhms.org Apara” <ApDave@ehr.org>, Charles McMahon <cmcmahon55@gmail.com>, William Marsh <wmarshmd@gmail.com>, Kathie Fife <kathie@kathiefife.com>, Christina Dyer <Christina.Dyer@leg.state.nh.us>, Jeb Bradley <Jeb.Bradley@leg.state.nh.us>, Mary Freitas <Mary.Freitas@leg.state.nh.us>, Tom Sherman <Tom.Sherman@leg.state.nh.us>, Jeb Bradley <jebebrad@metrocast.net>, Michelle Wagner <mwagner@naminh.org>, “yzhang@jhsph.edu” <yzhang@jhsph.edu>, “jc.salloway@unh.edu” <jc.salloway@unh.edu>, “barbarabuchman@ilads.org” <barbarabuchman@ilads.org>, “dandmhamp38@gmail.com” <dandmhamp38@gmail.com>, “killinger888@comcast.net” <killinger888@comcast.net>, “drhegnauer@h2health.org” <drhegnauer@h2health.org>, “Gary.Woods@leg.state.nh.us” <Gary.Woods@leg.state.nh.us>, “chris.smith@mail.house.gov” <chris.smith@mail.house.gov>, “Sununu.Press@nh.gov” <Sununu.Press@nh.gov>, “alexa011@mc.duke.edu” <alexa011@mc.duke.edu>, “governorsununu@nh.gov” <governorsununu@nh.gov>
Date: 05/19/2021 1:20 PM
Subject: Lyme Disease Updates and New Educational Tools for Clinicians

Lyme Disease Updates and New Educational Tools for Clinicians
https://emergency.cdc.gov/coca/calls/2021/callinfo_052021.asp

During this COCA Call, presenters will review updates in Lyme disease epidemiology, diagnosis, treatment, and prevention and share new educational tools for both healthcare providers and their patients.

“Planners have reviewed content to ensure there is no bias.”

May 19, 2021

Grace Marx, MD, MPH
LCDR, U.S. Public Health Service
Medical Epidemiologist, Bacterial Diseases Branch
Division of Vector-Borne Diseases
Centers for Disease Control and Prevention

Dear Dr. Marx,

As a member of the New Hampshire Lyme Disease Study Commission appointed by Governor Chris Sununu, I have some concerns/questions regarding your upcoming presentation.

If there is to be no “bias” in your presentation does that mean that the CDC will finally recognize persistent infection after extensive antibiotic treatment? Please take a moment to read my letter to the editor published in the BMJ as I have identified seven documented cases of treatment failure; there are actually hundreds.

Letter to the editor of the BMJ

Lyme borreliosis: diagnosis and management
https://www.bmj.com/content/369/bmj.m1041/rr-1

Dr. Marx… will you be sharing the following facts/references with the intended audience?

  1. It takes 4-6 weeks for humans to fully develop both IgM and IgG antibodies to Lyme disease in order to produce a positive Western blot test result. [1]
  2. Treatment delay of over thirty days often leads to Chronic Lyme Disease. [2]
  3. Bulls-eye rash has been recorded in less than 50% as reported by the State of Maine Department of Health. [3]
  4. Seronegative disease has been identified [4] (no antibody production to infection producing a false negative lab result)
  5. You can become horribly disabled or die [5] from Lyme disease and routinely denied Social Security Disability Compensation.
  6. 35% of acute Lyme disease patients (21out of 63) who were treated with the IDSA’s short course of antibiotics were found to meet the case definition of “Post Lyme Disease Syndrome” at six months. (Johns Hopkins) [6]
  7. Single dose Doxycycline after tick bite as prophylaxis against Lyme disease failed 80% of the time in the mouse model so why would this be recommended in humans? [7]
  8. There are hundreds of references to failed treatment of the one-size-fits-all IDSA Lyme treatment guideline. [8]
  9. Congenital transmission of Lyme disease has been identified dating back to 1985 [9]

I want to make this perfectly clear Dr. Marx; The current dogma propagated for the last thirty years has misguided an entire medical community and misclassified Lyme as a simple nuisance disease; “hard to catch and easily treated.” [10] Take a moment and read the public comments from the Tick-Borne Disease Working Group website and you’ll see that we have a public health crisis on our hands with hundreds of thousands (if not millions worldwide) left in a debilitated state. The deliberate bias against persistent infection after extensive antibiotic treatment is 100% responsible for this unimaginable pain and suffering.

Will your presentation continue on this path of deception and omit the facts/references I have provided?
A response to this inquiry is requested. Please hit reply-all.

Respectfully Submitted,

Carl Tuttle
Hudson, NH

Cc: All members of the NH Lyme Study Commission
Governor Chris Sununu

When “evidence-based medicine” has been spun to fit bias agendas and the patient voice has been intentionally ignored who investigates the dishonest science? -Carl Tuttle

References: Please read them!

1. Notice to Readers Recommendations for Test Performance and Interpretation from the Second National Conference on Serologic Diagnosis of Lyme Disease https://www.cdc.gov/mmwr/preview/mmwrhtml/00038469.htm

2. Treatment Delays Increase Risk of Persistent Illness in Lyme Disease
https://www.hopkinslyme.org/news/treatment-delays-increase-risk-of-persistent-illness-in-lyme-disease/

3. State of Maine Department of Health has been tracking incidence of rash and found an average of under 50% for the four years listed below:

2011 42%
http://www.maine.gov/dhhs/mecdc/infectious-disease/epi/vector-borne/lyme/documents/2011-lyme-legislature.pdf

2012 49%
http://www.maine.gov/dhhs/mecdc/infectious-disease/epi/vector-borne/lyme/documents/2012-lyme-legislature.pdf

2013 51%
http://www.maine.gov/dhhs/mecdc/infectious-disease/epi/vector-borne/lyme/documents/2013-lyme-legislature.pdf

2014 57%
http://www.maine.gov/dhhs/mecdc/infectious-disease/epi/vector-borne/lyme/documents/2014-lyme-legislature.pdf

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

5. Deaths From Lyme Disease Compiled by: John D. Scott, Research Scientist 17 April 2018
https://www.dropbox.com/s/eo794dx7zspc1ln/Ld%20deaths.doc?dl=0

6. Post-treatment Lyme disease syndrome symptomatology and the impact on life functioning: is there something here?http://www.lymemd.org/pdf/aucott_et_al_qol_research.pdf

7. A sustained-release formulation of doxycycline hyclate (Atridox) prevents simultaneous infection of Anaplasma phagocytophilum and Borrelia burgdorferi transmitted by tick bite
https://www.dropbox.com/s/jc0h9g9arjhc8l1/Zeidner%202008.pdf?dl=0

8. 700 articles LYME Evidence of Persistence-V2
https://www.dropbox.com/s/n09sk90eo6xz7ua/700%20articles%20LYME%20EvidenceofPersistence-V2.pdf?dl=0

9. Congenital Transmission of Lyme
https://www.dropbox.com/s/xlju8w25phkypy0/Congenital%20Transmission%20of%20Lyme.pdf?dl=0

10. Lyme Disease Is Hard to Catch And Easy to Halt, Study Finds

New York Times By GINA KOLATA Published: June 13, 2001
http://www.nytimes.com/2001/06/13/us/lyme-disease-is-hard-to-catch-and-easy-to-halt-study-finds.html

___________________________________________________________________________

Announcement of Dr. Marx’s Presentation:

                Notice from the CDC

Lyme Disease Updates and New Educational Tools for Clinicians
Date: Thursday, May 20, 2021

Time: 2:00 pm – 3:00 pm (ET)

From: Centers for Disease Control and Prevention < no-reply@emailupdates.cdc.gov>
Sent: Monday, May 17, 2021 11:15 AM
Subject: Reminder: CDC COCA Call—Thursday, May 20: Lyme Disease Updates and New Educational Tools for Clinicians

Go here for Part 1

Go here for Part 2

German Health Minister Warns of Incurable Immune Deficiency From COVID But Ignores Elephant in the Room: COVID Injections

https://philipmcmillan.substack.com/p/warning-from-german-health-minister

Warning from German Health Minister!! – Immunodeficiency after COVID infection

Or more appropriately, after injection?
Approx. 11 Min
 “It’s sad that at this stage we still have to be speaking in code.  But we do.  And it’s important for people to read between the lines and recognize that at the end of the day science is what we have to follow. We have to become determined that no matter what we are looking at, we mustn’t be afraid to face it. That seems to be the challenge that we have today.”
“Sadly at the moment, it seems that politics and finance seems to be leading most of the charge.  ~Dr. Philip McMillan

Headline NTV/Politics – 21st January 2023:

Read full article here (Translate German to English) >

It is important to note that the unmentioned elephant in the room is covid “vaccines.”

The mechanism of immunodeficiency through vaccination is four fold:

  • SARS-COV2 infection causes transient T and B cell immune depletion. That is a normal part of the immune changes. However, natural immunity prevents recurrent infection.
  • Covid “vaccines” impact on the immune response to cause a mainly spike furin epitope antibody response which is not effective against Omicron.
  • Recurrent Omicron infection leads to interferon suppression and immune dysregulation in those that are vulnerable (vaccinated and interferon autoantibodies)
  • Covid “vaccines” also increase the risk for interferon autoantibodies which exacerbates the risk of recurrent infection.

For more: