Archive for the ‘Activism’ Category

Emergency Petitions to Halt Numerous Clinical Trials of COVID-19 Vaccine Unless ALL Adverse Reactions Are Tracked
The NIH and Moderna have rigged the clinical trial of their COVID-19 vaccine, mRNA-1273, to avoid capturing adverse reactions that occur more than 28 days after injecting this experimental vaccine. ICAN’s legal team has filed an emergency petition to stop this unethical conduct.
ICAN previously filed a petition to the FDA demanding that this clinical trial include a placebo. The clinical trial for this vaccine was then delayed and when its design was finally issued, it included a placebo. But it appears that NIH and Moderna have decided to play a different game to avoid capturing safety issues that could prevent licensure of their mRNA-1273 vaccine. 
Their trick is to only capture adverse reactions that occur more than 28 days after injection if the participant withdraws from the clinical trial. This is nonsensical, since there is little for a participant to withdraw from after getting two doses during the first 28 days of the clinical trial. Once a participant has received both doses, if anything, a participant would have an incentive to remain part of the follow-up check-ups to address any adverse effects.
There could be many autoimmune, neurological and chronic health disorders which have a major impact on the quality of life that this experimental vaccine could cause. All of which may only arise more than 28 days after the injection. But yet, as long as the participant does not withdraw from the clinical trial, these will nonsensically be ignored as if they did not occur. This is unethical and renders vacuous any claim of safety for this product based on this trial.
Given that efficiency in this trial will be tracked for two years, the only reason to not track safety for this same duration is to avoid detecting safety issues that would prevent licensure.
ICAN’s legal team, headed by Aaron Siri, has therefore filed a citizen petition and an emergency stay petition demanding that the clinical trial design for this vaccine be updated to require that all adverse reactions for the entire period of the clinical trial be tracked. These petitions also demand that the number of participants in this trial be increased and that they be tested before and after injection for any T-cells to SARS-CoV-2. ICAN intends to take further legal action if its rational and sensible requests are not met.
Pfizer and BioNTech have also rigged the clinical trial of their COVID-19 vaccine, BNT162b, to avoid capturing many potential life-altering adverse reactions that may occur from this experimental vaccine. ICAN’s legal team again filed an emergency petition to stop this unethical conduct.
While Pfizer and BioNTech have now included a placebo control group in their clinical trial, these companies have decided to play a different game to avoid capturing safety issues that could prevent licensure of their COVID-19 vaccine, BNT162b.
The study design for the clinical trial for BNT162b provides that — despite reviewing efficacy for at least 2 years — it will only capture “adverse events” for 1 month and “serious adverse events” for only 6 months after each dose.
The adverse events captured beyond a month after injection should not be limited to “serious adverse events,” since there are many autoimmune, neurological, and chronic health disorders which have a major impact on the quality of life, yet are categorized by the FDA as “adverse reactions” and not categorized as “serious adverse reactions.” To wit, there are a myriad of post-licensure adverse reactions reported by consumers and physicians and are also listed in the package inserts for one or more vaccines that any individual living with would categorize as “serious”; yet the FDA, under its current guidelines, may not. These include, but are not limited to: alopecia, autoimmune disease, lupus erythematosus, vasculitis, Bell’s Palsy, hypotonia, migraine, myelitis, neuropathy, seizures, mental disorders, rhinitis, and vertigo. 
The study design for BNT162b nonetheless provides that these adverse events should be captured for only 1 month after vaccination while “serious adverse events” are captured for 6 months. These artificial limitations are unethical and make any claim of safety for this product based on this trial specious at best.
Incredibly, the efficiency of Pfizer and BioNTech’s vaccine in this trial will be tracked for two years. As such, the only reason to not track safety for this same duration is to avoid detecting any safety issues that would prevent licensure. If BNT162b causes a systemic autoimmune issue to arise two months after vaccination, it would be irresponsible and unethical not to capture that reaction just because an autoimmune issue falls into the artificially defined zone of being an “adverse event” or “non-serious adverse event,” rather than what the FDA has decided to label a “serious adverse event.”
ICAN’s legal team filed a citizen petition and an emergency stay petition demanding that the clinical trial design for this vaccine be updated to require that all adverse reactions for the entire period of the clinical trial be tracked. These petitions also demand that the number of participants in this trial be increased and that they be tested before and after injection for any T-cells to SARS-CoV-2. ICAN intends to take further legal action if its rational and sensible requests are not met.
AstraZeneca and the University of Oxford have also rigged the clinical trial of their COVID-19 vaccine, ChAdox1 nCoV-19, to avoid capturing many potential life-altering adverse reactions that may occur from this experimental vaccine. ICAN’s legal team once again filed an emergency petition to stop this unethical conduct.
Unlike the clinical trials for Moderna and Pfizer’s vaccines for COVID-19, which are occurring in the United States, the current clinical trial for AstraZeneca’s COVID-19 vaccine is not under the direct authority of the FDA, since this clinical trial is not occurring in the United States.  
News reports have indicated that AstraZeneca will be starting a new clinical trial in the United States for its COVID-19 vaccine that presumably will include a placebo control group. In the meantime, its current clinical trial occurring outside the United States persists in using a MenACWY vaccine as a control. As if that were not enough to rig this trial’s safety results, the study design for their vaccine, ChAdox1 nCoV-19, like the design of Pfizer’s vaccine, provides that, despite reviewing efficacy for at least 2 years, it will only capture “adverse events” for 1 month and “serious adverse events” for only 6 months after each dose. 
Therefore, ICAN’s legal team has also filed a citizen petition and an emergency stay petition demanding that the clinical trial design for this vaccine be updated to require that all adverse reactions for the entire period of the clinical trial be tracked against a placebo control group. These petitions also demand that the number of participants in this trial be increased and that they be tested before and after injection for any T-cells to SARS-CoV-2. ICAN intends to take further legal action if its rational and sensible requests are not met.
Just as the pharmaceutical companies will never rest when it comes to promoting and selling their vaccine products, we will never rest in exposing the truth regarding these products.  
Stand for vaccine truth and help us keep winning! Help us start 2020 strong. Donate $50, $100, $500, or $1000 today!

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**Comment**

Ponder this:

All of a sudden, after decades of over the counter use in travelers, being on the WHO’s List of Essential Medicines (the safest and most effective drugs needed in a health system), and being used by billions of people for autoimmune issues like Lupus, HCQ is supposedly dangerous. Yet, an experimental – never used before COVID-19 vaccine that’s bypassing the normal 5-19 year observation period, that manufacturers insist upon and have been granted indemnification by public officials, doesn’t use a true placebo and will only track adverse reactions that occur more than 28 days after injection if the participant withdraws from the clinical trial, is acceptable.

Anyone else see a problem here?

This is scientific hypocrisy at work reminiscent of the Lyme debacle:  https://madisonarealymesupportgroup.com/2020/04/26/cdc-playbook-learning-from-lyme/

 

 

 

 

Category:

Activism, vaccines

Litigating for the Truth

https://childrenshealthdefense.org/advocacy-center/litigating-for-the-truth/

AUGUST 20, 2020

Litigating for the Truth

Print

One of our allies has filed many Freedom of Information (FOIA) requests to uncover what is known about the origins of the COVID-19 pandemic and the coronavirus SARS-CoV-2, and whether it emerged from a laboratory in Wuhan. They are also investigating the dangers of gain-of-function experiments, which aim to increase the transmissibility or deadliness of potential pandemic pathogens, and the use of our tax dollars to finance this potentially dangerous work.

Their investigation is crucial, but they are being stonewalled by some federal agencies and state universities.

Are you a lawyer? You can help.

They are seeking lawyers who can litigate Freedom of Information cases pro bono against these federal agencies and state universities. Are you interested? If so, please do fill out this form:  (Go to link)

Sign up for free news and updates from Robert F. Kennedy, Jr. and the Children’s Health Defense. CHD is implementing many strategies, including legal, in an effort to defend the health of our children and obtain justice for those already injured. Your support is essential to CHD’s successful mission.

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**Comment**

This work is crucial and relates to Lyme/MSIDS as well. We can not allow these issues to be hidden and denied.  Currently, we are still waiting on an investigation regarding ticks, our government, and bioweaponization:  https://madisonarealymesupportgroup.com/2020/07/22/house-passes-chris-smith-measure-to-probe-if-government-turned-ticks-into-bioweapons/

For more:  https://madisonarealymesupportgroup.com/2019/07/19/biological-warfare-experiment-on-american-citizens-results-in-spreading-pandemic/

 

 

 

 

Category:

Activism

Questions for Dr. Fauci

https://spectator.org/questions-for-dr-fauci/

Questions for Dr. Fauci

By George Parry

Aug. 17, 2020

As you may be aware, health-care providers across the country and around the world have reported great success in using Hydroxychloroquine + Zinc + Azithromycin (the “HCQ cocktail”) to treat COVID-19. According to these physicians and researchers, the key to success is to use the HCQ cocktail within the first seven days after onset of COVID-19 symptoms.

Nevertheless, ever since President Trump endorsed Hydroxychloroquine (HCQ), its use has become a highly politicized and controversial matter. The opposition to HCQ started with Dr. Anthony Fauci…

Three practicing physicians have published the following “Open letter to Dr. Anthony Fauci regarding the use of Hydroxychloroquine for treating COVID-19.” It is a devastating written cross-examination of Dr. Fauci that contains much valuable life-saving information and squarely addresses the needless deaths that have occurred due to the opposition to the HCQ cocktail.  (See link for article & letter)
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**Comment**
Seems many people have questions for mafia-overlord, Dr. Fauci:
Also, I found this short video enlightening.
“9 Minutes Explaining the Connections between Gates, Fauci, Google, and Epstein:

http://

June 23, 2020

Patrick Howley exposes how COVID-19 is being used to exert control over American citizens.

Politics aside, just listen to the facts and “follow the money.”

Category:

Activism, Treatment, Viruses

The Lyme Voices You Didn’t Hear at TBDWG Meeting

https://globallymealliance.org/the-lyme-voices-you-didnt-hear-at-tbdwg-meeting/

The Tick-borne Disease Working Group (TBDWG) issued a public request to hear from patients willing to share their stories for its July 8, 2020 meeting. It’s an important part of these meetings, where the public and the TBDWG members can hear directly from patients, to better understand the dire need for answers and results.

Four of Global Lyme Alliance’s Educational Ambassadors submitted their public comments for this meeting. We’d like to highlight their stories and share them with you now. Below are the unedited submissions from Lyme patients Fawna Bough, Rhonda Howdyshell, Jen Kenley, and Robin Reich.

FAWNA BOUGH

My name is Fawna Bough and I have struggled with tickborne diseases (Lyme, Babesia, Bartonella, Ehrlichiosis) for at least 14 years. I struggled for years to get a diagnosis which finally came in 2015. Since then I have been battling these tickborne diseases–most of which the costs have been solely my burden to bear as my insurance refuses to pay for most of the treatments, and my doctor appointments, related to my illness.  I have spent 10s of 1000s of dollars fighting this disease. The financial burden has changed most every plan I had for my life and retirement. I had to retire early from a job that I loved, realized that most of my family and friends thought I was a hypochondriac as I watched them distance themselves from me, and I continue to fight these diseases on a daily basis.

This disease brought me to my knees and almost took my life. I have heart and neurological involvement, have been bedridden, have permanent muscle damage, the list goes on and on… and I still struggle with mobility from time to time. These diseases have disrupted my immune system so much that I have now progressed into other issues i.e. POTS, Reynauds, etc. I will also share that these diseases have sadly changed me from the inside out. My personality morphed into a person that I literally did not recognize and I’m still trying to get myself back.  The neurological suffering of patients like myself is simply indescribable.

I am grateful that the Tick-Borne Disease Working Group is allowing TBD victims to voice their comments as this disease changes the trajectory of your life in every way possible. The barriers that are currently in place that discard us as patients need to be removed quickly and permanently.  There have been a variety of treatments that have been prescribed to me to help me heal; however, because of my diagnosis of TBD, my insurance will not approve those treatments due to their claim that chronic TBD does not exist and/or because the treatments that I prefer lean more toward holistic healing vs. traditional Western medicine. The treatment decisions for any disease should fall solely on the patient. There should be equality toward coverage of both holistic and traditional medicine.

I have suffered long enough, as has my fellow Lyme Warriors.  There are thousands of children that are getting TBD and not being diagnosed and these kids are being set up for a lifetime of suffering.  We have NO RELIABLE TESTING.  We have NO CURE.  Please help us gain equality in treatments.  Please help us.

Thank you for your time and consideration.

Fawna Bough
GLA Education Ambassador, Illinois

RHONDA HOWDYSHELL

Just last week another doctor shared with me that it wasn’t possible to have advanced or undiagnosed Lyme Disease. Find that contrary to my own experience. I was only 8 years old growing up in Northern Virginia when my family thought sending me to camp in the Shenandoah Valley for 6 weeks would be a wonderful adventure! It was horseback riding, pond swimming, hiking, and outdoor showers and privies were all part of my summer adventure! Then one day a counselor was helping to brush and braid my hair when they found an engorged and embedded tick in my hair. It was a big deal and the nurse had to remove it, using a match to burn and make it come off. When I came down with a disseminated rash a while later—they quarantined me with measles. It was determined later it wasn’t measles. My later childhood was marked by allergy issues that had me on antibiotics often. Later I developed a strange blood disorder where I would bruise and bleed upon the slightest bump.

I moved to the Shenandoah Valley in 1979. Ticks were commonplace. Most symptoms Drs and I wrote off to getting older. including thyroid disorder, skin mottling, confirmed arthritis (suspected RA) in my hands and feet, and joint deterioration in my hip that required a replacement to walk.

I retired at 62 early, as the cumulative deterioration was making work very difficult. The next spring I found a tick attached to my chest. I had no bulls-eye, it was only on 8-10 hours. The subsequent flu, neck pain, and facial paralysis didn’t give me a clue. but a migrans rash that appeared on my calf sent me to the doctor and they diagnosed Lyme based on symptoms (note no blood test was administered! Which means the health dept/CDC didn’t have to count the case as confirmed Lyme). The speaking difficulty (not being able to remember words) and cognitive disfunction got more severe. (Like writing this account would have been impossible.). They gave me 14 days of doxycycline. Cured… NO, so I tried to accept my new normal of no energy, cognitive lapses, and arthritis throughout my body as my lot in life.

Then a friend suggested an LLMD doctor and I went to one near me. The blood tests were done and I tested “wildly positive” for Lyme. Treatment of 28 days of Doxy began and I felt some better. Then a course of two antibiotics followed. The treatment was harsh and I was sick (Herxing) daily on it. But still, I felt 60% better and I was grateful. Then I showed the LLMD the massive bruises on my legs and arms (had this since childhood) and a sore that wasn’t healing. Diagnosis? Secondary Lyme infection .. and this time the doctor tried a new trial – the WEIGMAN protocol. I remember it was just before Christmas and I decided to wait until after the holiday and I was tired of being sick every day from the meds. The protocol was cheap and effective, It gave me back my life.! It was a pulsed Mindi / Tindi antibiotic that has proven studies that show a complete kill of spirochetes over others that foster the formation of round cysts. (you know the ones that hatch out after the antibiotic cure and then multiply so you stay sick). It included boosting the immune system before starting it, to allow your body to fight along with the meds.

So my advice is:

  1. Change the CDC recommended 14-28 day doxycycline treatment to Weigman Protocol.
  2. Recognize that Lyme disease not addressed or under-treated will resurface when your body allows the remaining spirochetes to multiply.
  3. Encourage doctors to think “advanced” Lyme disease when seeing a patient with disseminated migrans rash, joint pain, thyroid disorders, MS, Parkinson like symptoms, and temperature of 97.
  4. Order health departments to count all cases of diagnosed Lyme even without a blood test (you see the test is so unreliable docs aren’t bothering to do it) – so we have no idea the number of cases. Keep in mind over a million dogs are diagnosed every year in the US.

Rhonda Howdyshell
GLA Education Ambassador, Virginia

JEN KENLEY

As a patient with Lyme disease, and an Ambassador for the Global Lyme Alliance, it is difficult to put into tangible words what I want to convey to your team. The Lyme community just lost one of our greatest advocates this past week (as of June 24th), Dr. Neil Spector. Following your last meeting, I know that I speak for many Lyme patients when I say that we are deflated, crushed, and incensed by things that were said.  Most pointedly at the disregard for two million lives (“Post Treatment Lyme Disease” patients) in refusing to update the CDC’s treatment guidelines. The CDC’s guidelines have and continue to fail the Lyme community shamefully.  I know this personally, I have done the CDC’s advises Doxycycline regimen and am left with almost no immune system (after years of “PTLD”), terrible arthritis, ongoing night sweats, heart abnormalities and debilitating brain fog and loss of memory.  I am 33 years old, crying over my 5-year-old son at night because there is nothing else that can be done for me because of the “guidelines” in place. In September we had to sell our house to pay medical debts, because again, thanks to the CDC’s guidelines my continued treatment is not covered by insurance.  There have been NUMEROUS studies indicating that Lyme disease can hide in the joints and that people are affected for years despite these Doxycycline doses (Please see Tulane and John Hopkins studies). Many suggest a three-antibiotic cocktail and others, like Dr. Sapi (New Haven) propose enzymes and drugs to break down biofilms in remaining bacteria to enhance antibiotics.  To be completely candid, myself and a lot of others in the Tick / Vector-Borne Disease community have lost faith in the ability of this group to make empathetic, fact-based decisions following this past meeting. With Lyme now in all 50 states and enough PTLD patients to fill the city of Chicago, we can no longer be ignored.  We are pleading with every one of you to revisit and amend the CDC guidelines. For those unwilling to bend, please put aside your conflicts of interest and stand on the side of history that fights for humanity.

My life (and my 5 year old’s) is (are) in your hands.

Jen Kenley
GLA Education Ambassador, Tennessee

ROBIN REICH

I need HELP in the Orlando Florida area… Will a doctor please message me if willing and able to assist me with this Babesia created with Lyme Disease. I have had it too long now…..and I am frightened. I want to live a wholesome life as best I can and I can not find a doctor who is legally able to treat me past the 21 days IV antibiotic treatment. Unless I PAY CASH. Also, is an Infectious Disease doctor LEGALLY ABLE to take care of patients for this (Babesia/Lyme) yet past the 21 day IV antibiotics? If so, who? I am having a very difficult time trying to find a doctor who will treat me past 21-day treatment and is able to use my health insurance coverage of any kind. I am going on 5 years with the exact symptoms of Babesia after having been treated for Lyme Disease with an integrative and natural medicine doctor who was guided by Dr. Richard Horotwiz’s books out of NY. The book entails details and treatments of my disease(s) to the T. I have gone to ANOTHER 2 local infectious doctors here in Orlando, Florida who say they DO NOT treat Lyme Disease. This is SURREAL at this day and age … I don’t have $$$ thousands of dollars to treat myself at [redacted] doctors … Sadly, I can buy a gun but I can not use my $384.00 a month Health Insurance to treat my disease when there ARE treatment options available out there, but only for cash … or am I severely missing something here?

Also, I’m on the backstretch of this thing or things/diseases Lyme or and Babesia…And I am already in debt from treating basic Lyme … 2 years unable to work (I only made six figures). And yes I have the credit cards I am paying off for that paid for treatment and or living without being able to work … I am a strong person and I insist on working again … I am working … willing to work … never took charity … have health insurance and yet … there ARE solutions out there … documented … but I need large amounts of cash to use them.

Maybe I will try this angle … Who has about $5,000 to $20,000 to give me to travel and treat my disease because of the Health MR. OZ’s of our world do not believe Insurance should pay for treatments found for my illness???? Please message me … I will keep all receipts to assure you that that is where the money will go … And I am an organ donor so science can study this mess … But … GOD BLESS AMERICA there are options out there but I have to be wealthy in order to use them!!

I am going on 10 years since my positive Western Blot diagnosis of Lyme Disease… and I do realize Babesia is a co-infection… However, I am currently treating myself -no doctor supervision. Because I choose to pay my mortgage … and possibly die in my own house without legal professional treatment versus moving into a tent because I had to pay CASH for the treatment … I am not sure if the “Samsara Herbs TICK Immune Support” will treat Babesia or only Lyme Disease … I started to lightly herx after 2 days so it’s doing something. Herx symptoms include morning headaches, eye inflammation/blurry, sweating, anxiety, neuropathy on the entire left side and is now agitated with tingling hot/cold increases. Or…. are these Herbs bringing the Lyme symptoms back that went into hiding versus KILLING these miniature beasts??

Who or where do I go for help? My mind has become boggled or continues to stay fogged with all the internet info and NO SOLID covered health insurance doctors who can legally treat me.

Robin Reich
GLA Education Ambassador, Florida

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**Comment**

I share our story here, which serves as a perfect example of how two infected people achieved their health back with extended, varied, and many antimicrobials.

But patient experience, doctor experience and worldwide, Peer-Reviewed Evidence of Persistence of Lyme:MSIDS copy just doesn’t matter to The Cabal, just as the truth about COVID and mounting reports on the experimental, fast-tracked, dangerous COVID injections causing serious harm and death doesn’t matter to them.

These ‘authorities’ are riddled with conflicts of interest and should not direct public health.

 

Category:

Activism, Lyme

On the Couch With Dr. Kuna: Lyme Disease With Guest Colleen Schake

https://soundcloud.com/user-499704216/on-the-couch-with-dr-kuna-guest-colleen-schake-on-lyme-disease  Program here  (Approx. 30 Min)

On this episode of “One the Couch,” Dr. Kuna (Psychology Associates) welcomes guest Colleen Schake who discusses Lyme disease.

Check out “On the Couch” each Saturday at 12:30pm on terrestrial radio 94.3 FM in the Scranton/Wilkes-Barre Pennsylvania region, or for more information please visit: drjohngkuna.com.

 

 

 

Category:

Activism, Lyme