Rocky Mountain Way ~ Joe Walsh + BIO TERROR ALERT ‼️ LINKS

Highest Alert ‼️ Biological Threat To Carson Army Base and Cheyanne Space Force Base, Colorado.

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New Injections Of “ Live “ Ebola Vaccines being given to medical 🏥 staff at
Carson Army Base, Colorado in Cheyanne Mountain ⛰️
Fort Carson, the Mountain Post, is a proud Army post located southwest of Colorado Springs, Colorado, between Interstate 25 and Highway 115 in El Paso county.

https://twitter.com/RealAlexJones/status/1748474475304133038

Near : Cheyenne Mountain ⛰️ Space Force Base.
Near https://www.norad.mil/Newsroom/Fact-Sheets/Article-View/Article/578775/cheyenne-mountain-complex/

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Sheriff Prepares People Of Ohio About Coming Conflicts Inside America - https://gab.com/graymaze/posts/111906692541790082
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Autoimmune Technologies LLC, New Orleans
Gulf War Syndrome
ANTI-SQUALENE ANTIBODIES LINK 
GULF WAR SYNDROME TO ANTHRAX VACCINE
Data published in the February 2000 and August 2002 issues of Experimental and Molecular Pathology strongly suggests that Gulf War Syndrome is caused by a vaccine contaminated with squalene.

The August 2002 article is entitled "Antibodies to Squalene in Recipients of Anthrax Vaccine" (Exp. Mol. Pathol. 73,19-27 (2002)).

Gulf War Syndrome, or GWS, is the term which has been applied to the multi-symptom rheumatic disorder experienced by many veterans of the 1990-1991 Persian Gulf war. A similar disorder appeared in 1990-1991-era personnel who were never deployed to the Persian Gulf theater of operations and also in other military personnel, including participants in the Anthrax Vaccine Immunization Program, or AVIP, which was inaugurated in 1997. No data has ever suggested that the disorder experienced by the deployed 1990-1991 soldiers is different from the disorder experienced by the other groups of patients, but the other cases have not been considered to be cases of GWS.

Squalene was found by the U.S. Food and Drug Administration in five lots of the AVIP anthrax vaccine. The discovery of serum anti-squalene antibodies and the development of a test to detect these antibodies has made it possible to see that links appear to exist between the contaminated AVIP vaccine lots, the illness experienced by post-1997 vaccine recipients, the illness experienced by non-deployed 1990-1991-era patients, and the illness in deployed 1990-1991-era patients that has been referred to as GWS.

The data establishing these links is presented in the peer-reviewed February 2000 and August 2002 articles. The published findings (1) strongly suggest that the GWS-like illness being reported by all of the various patient groups is the same illness, (2) strongly suggest that the contaminated vaccine caused the illness in the AVIP group, and (3) further suggest that squalene contamination of one or more 1990-1991-era vaccines accounts for the GWS cases from that era.

Before the anti-squalene antibody test was developed, there was no specific laboratory test for GWS. Both articles suggest that the antibodies can serve as an excellent laboratory marker to help identify patients with GWS. Using the antibodies as a laboratory marker for GWS could be very useful in helping physicians diagnose the disorder and in differentiating it from other rheumatic illnesses.

Anti-squalene antibodies might also provide a key to more effectively treating GWS patients. The presence of the antibodies in GWS patients indicates that the immune system is involved in the development of GWS. Effective drugs which modulate the human immune system are already in wide use, but they have not been previously considered to be appropriate for GWS patients. The published data now suggests that the use of immune modulators in GWS patients should be studied.

A detailed discussion of the data in the February 2000 and August 2002 articles can be found in the Autoimmune Technologies news release dated July 15, 2002.

Further information about the discovery of squalene in the AVIP vaccine lots can be found in the statement made by former U.S. Congressman Jack Metcalf on September 27, 2000 to the House Subcommittee on National Security, Veterans Affairs, and International Relations.

In March 1999, the United States General Accounting Office (the GAO) encouraged the Department of Defense to investigate the discovery of anti-squalene antibodies. In GAO/NSIAD-99-5, "Gulf War Illnesses - Questions About the Presence of Squalene Antibodies in Veterans Can Be Resolved," the GAO urged the DoD to conduct its own research into anti-squalene antibodies with two objectives in mind: (1) to confirm the existence of the newly-discovered antibodies, and (2) to acquire patient data, explore the apparent link between the antibodies and the illness in GWS patients, and attempt to confirm or disprove the existence of such a link. Click on GAO/NSIAD-99-5 for a PDF version of this report. See Notes on PDF Files if you would like help with the PDF format.

To satisfy the first GAO objective, the Army researchers confirmed that anti-squalene antibodies do indeed exist and can reliably be detected. They published their findings in an article entitled "Induction and Detection of Antibodies to Squalene," which appeared in the November 2000 issue of the Journal of Immunological Methods (J Immunol Methods 2000 Nov 1;245(1-2):1-14). The Army researchers conducted their testing by applying squalene to the wells of ELISA plates. Dr. Robert F. Garry, the Tulane Medical School professor who discovered anti-squalene antibodies and developed the test for detecting them, and his colleagues conducted their testing for the February 2000 and August 2002 articles by applying squalene to nitrocellulose strips in a Western-blot-type assay. There is no material difference between the two test methods, and both are covered by the patent which subsequently issued to Tulane.

Although the Army researchers confirmed the validity of the test and thus added support to the February 2000 patient data, their November 2000 article included no patient data of its own and as a result did not specifically address the GAO's second objective. The Army researchers also failed to embrace the peer-reviewed February 2000 data itself, as is discussed in the statement submitted by Dr. Garry to the House Subcommittee on National Security, Veterans Affairs and International Relations for the record of its hearing into Gulf War illnesses on January 24, 2002. Dr. Garry's statement can be seen on the Subcommittee's Web site on the Autoimmune Technologies Web site at Garry 24 Jan 2002 House Subcommittee Statement.

Tulane has licensed the anti-squalene antibody technology to Autoimmune Technologies. U.S. Patent No. 6,214,566 covering the anti-squalene antibody test, which the Company calls the Anti-Squalene Antibody Assay or ASA Assay, was awarded to Tulane in April 2001. Because this patent covers the method which was used by the Army researchers to verify the existence of the antibodies, Autoimmune Technologies has offered the ASA Assay technology to the Department of Defense for use in conducting a large confirmatory study of the patient data in the February 2000 and August 2002 articles. The Company has urged the DoD to sponsor such a study.

For information about the patented Anti-Squalene Antibody Assay, go to the Gulf War Syndrome Laboratory Test Page.

See the Autoimmune Technologies GWS News Release dated July 15, 2002
See the Autoimmune Technologies GWS News Release dated January 31, 2000

Mudder Phucker 59
The Gulf War Illness Causing Vaccine 💉 Adjuvant / Additive Autoimmune Technologies LLC, New Orleans
https://www.autoimmune.com/SqualeneInVaccine.html
[ Place where Dr. Pamela Asa discovered Squalene Antibody in Sick Gulf War Veterans ] - She also created what is called the ASA ASSAY TEST that can check for this. This test MIGHT be able to be ordered in quantity from them in order to determine conclusively in court if someone has developed an antibody to this synthetic foreign substance.

Can anybody help subsidize this type of “Test Kit” rallying cry?

It is my sincere hope that you will consider not only punitive, antitrust actions against those responsible for so much death, pain, and anguish, but to please consider a class action lawsuit on a massive scale for citizens and soldiers alike.

I am also asking for this type of landmark case to become an automatic assumed criteria within the VA to trigger granting of long overdue service connected disability for all affected veterans.

Guess What !!! THEY NEVER TOOK IT OUT !!!!!!!!!!!!!

They jack us up on Synthetic Squalene which is a precursor to cholesterol and STEROIDS !!!!

Is that what they mean by a Super Soldier Program?

Breaking News 📰
Attention All Veterans - Legendary Grassroots Veterans Activist - Highly Decorated USMC Purple Heart 💜 Vietnam Veterans Latest Conference Call ☎️- working on a Veterans Gathering in Eagle 🦅 Pass Texas in Support of Border Defense Forces. - https://www.freeconferencecall.com/wall/recorded_audio?audioRecordingUrl=https%3A%2F%2Frs0000.freeconferencecall.com%2Fstorage%2FsgetFCC2%2FaG1s5%2FboZWY

Declaration Of Military Accountability Sign Up Form
- Read the Declaration.pdf | DocDroid

https://bardsnation.docdroid.com/58x0KsV/read-the-declaration-pdf

Patent # For Morgellons Disease US6245531B1 - Polynucleotide encoding insect ecdysone receptor - Google Patents

New Vaccine 💉 Hazard ☣️ Summaries.
The Vaccine 💉 Safety and Hazard ☣️ awareness level is about as realistic as 1940’s cigarette safety.

Anything - absolutely anything that can end up in a vial will circumvent the immune system. And does.

Hard to sum up.

Mold can be present. Inject mold straight into the body and watch the fun begin.

Synthetic SQUALENE ( MF59 ) is a big industry secret because without Adjuvants / Additives , Vaccines 💉 Simply Don’t Work.
It’s as if the other 95% of each vaccines are snake 🐍 oil toxins . - which they are. They are completely trying to harm us, although maybe 🤔 75 % of them are flunkies and genuinely believe in the compartmentalized information they are exposed to.

MF-59 is patented which by definition means that is a synthetic SQUALENE oil & water mixture and our bodies hate synthetic substances just like breast implants and artificial knee joints, etc.

The other red flag 🚩 on this is that it goes by over 100 different designations / aliases.

The synthetic SQUALENE triggers the body to permanently hyper activate the immune system as well as attack ALL natural SQUALENE in the body. Which is especially concentrated in the brain, 🧠 spine, spinal cord, nervous system and Mylan Sheath that protects the spine.

The results are surprisingly like Fibromyalgia , Chronic Fatigue, Mental Health Problems, and mind bending chronic pain. I have them all. I got the milky white liquid ( I watched ) at RAF Lakenheath in 1990.

Best book 📖 to read on this topic is Vaccine 💉 A by Gary Matsumoto.

https://www.basicbooks.com/titles/gary-matsumoto/vaccine-a/9780786728060/

Gary’s book was based on the research of Tulane University Scientists 👩‍🔬 Dr. Pamela Asa ons Dr. Robert F. Garry.

Imagine me finding this out in 2002 and trying to engage with ANYONE about it up right now.

Why? Because it could have been discontinued at any time. It started in the Anthrax Vaccine 💉 and then went worldwide. It has NEVER 👎 BEEN TAKEN OUT !!! 

This weighs heavily on my heart and mind.

New Topic : 
Micoplasmas , particularly Weaponized, like Micoplasma Fermentans are basically a Crime Against Humanity ( along with MF-59 ) invented by Dr. Carl Alving who was an Army Scientist at Ft. Dietrich - our base for Chemical and Biological Weapons.

I think that less than 1000 people know the full story or have a good overview on this topic.

The main guy on this topic is Dr. Garth Nicolson.

Dr. Garth Nicolson

1.) Weaponized ( and patented ) Micoplasmas https://youtu.be/9ZN-kXZMzqU?si=CMj-iu4WwER1JxA8

2.) Days. Garth Nicolson https://youtu.be/9ZN-kXZMzqU?si=CMj-iu4WwER1JxA8

3.) Wiki https://en.wikipedia.org/wiki/Garth_L._Nicolson

4.) Gulf War Syndrome https://en.m.wikipedia.org/wiki/Gulf_War_syndrome

5.) Peter Kawaja & Captain Joyce Riley https://youtu.be/gzxnfZ2Hm90?si=0iqkxvyGAohh1dXu

Peter Kawaja https://www.linkedin.com/in/peter-kawaja-b8588610b

Dead Men Tell No Tails - http://pages.suddenlink.net/anomalousimages/images/text/kawa2.html

Peter demanding answers about the PATENTED GERM 🦠 WARFARE AGENT Micoplasma Fermentans https://groups.google.com/g/misc.activism.militia/c/3rL3itgMxxA

Government Created Diseases https://www.nairaland.com/1847086/government-created-diseases-joyce-riley

Gulf War Illness Links https://gulflink.health.mil/vet_help/med_research/epidemiology/med_research_epidemiologyjsp.shtml

Dr. Garth Nicolson - Institute For Molecular Medicine https://www.immed.org/

Dr. 👨‍⚕️ Garth Nicolson ~ Research 🔬 Gate - https://www.researchgate.net/profile/Garth-Nicolson

Micoplasmas - https://youtu.be/67-bQLS4ZI4?si=Fpr8SUR0569LzFeP

Tom Trefts Note 🗒️- Extremely Interesting 🤨 MICOPLASMAS ROLE IN AUTISM - https://youtu.be/cdk6cZtLXyY?si=eRKqxYgEKhHaPuXW

Needle 💉 And The Damage Done ✅
AMG NEWS 📰 @amgnews | Linktree

The Poisonous ☠️ Anthrax Vaccine

THE NEEDLE AND THE DAMAGE DONE ( PT. 1. )

As a Gulf War Veteran and Veteran Activist I have been carrying the burden of knowledge of the purposeful poisoning of the world's vaccine supply through the use if an extremely inexpensive and far too powerful additive known as Squalene Oil. It is also known by over 110 different names.

Why is that you may ask?

It's licensed in Europe isn't it?

Well yes. We know that.

It's licensed in the USA right?

Yes. But for one thing only, the military Anthrax Vaccine.

Isn't that the one that both killed and got a vast number of servicemen sick during the Gulf War?

Yes.

But it's no longer in the DOD Anthrax Vaccine is it not?

No, those **** left it in.

It's as simple as that.

Not only that, but they have hundreds of vaccines and vaccine adjuvants already patented and sitting on shelves just waiting to go for just the precise time in history when they won't really be needed.

That's right. It's simple logic. It causes dozens of illnesses that share something special in common. They all cause chronic pain!

Chronic Pain? I live in constant agonizing chronic pain. I use it to hyper focus on research on any topic I choose. Anything to divert my attention from pain.

So,who could that benefit from all of this pain and misery? Obviously the Opiate Industry, that's who.

A time honored way to harvest vast sums of money. The Opium Trail.

Today, I will not be content to try to prove that various vaccine ingredients produce horrific death and damage across the globe. To me and many others, that point has long since been proven.

Instead, I will give you a guided tour of this Hell on Earth that has been intentionally woven into the World Health Care Community.

It's so insidious that it drives vaccine advocates to relentlessly take to the battlefield of public opinion through the internet and in any public capacity available. Just like any other Satanic Manifestation here on Earth, once you see this Evil Abomination, it is impossible to forget.

Doctor's, as we are told, pledge themselves to the Hippocratic Oath. Scientists, on the other hand have no obligation to do so. They take their allegiance elsewhere.

So then, let's take a field trip to the Battlefield of Lies in the “Occult” realm of “Blood Related” studies.

 It should be known by all that the Vaccination Industry is exactly that. It’s a business, TYPICALLY RUN WILLFUL AND PERSISTENT FOREIGNERS.

Its mechanization's are finely tuned towards mass production and massively corrupt and unconscionable methods.

Let me introduce an analogy for the entire BUSINESS MODEL that appears to be at work here.

Let's take the classic image of a heavy stone being thrown into a flat pond. [ Those who oppose us make the stones. ] They also make medicine, the also make poison, and they all get fabulously wealthy by Poisoning the so called Cure. They are fully aware of what they are doing and they've been doing it for decades. They even are quite good at inserting self-protective narratives into everything they do. Like any other criminal enterprises, they all plant seeds of plausible deniability at every opportunity.

So, if you would now imagine a huge heavy stone throwing machine adjacent to a massive pond of fiat currency and Pure Gold. It takes a while to load, but seems to launch every Fall like clockwork. They like to feign ignorance by touting the party line that they just can't figure out what strain of FLU they are putting out each year.

How cute.
Why spoil the surprise?

The financial concept here is that as the water moves outwardly from the center of the splash in the pond it makes rings upon rings of gainful opportunities from its epicenter.

The pond and therefore our lives are turned upside down by the rock thrown into the pond.

They like to do this.

If they make a good batch they win massive governmental contracts. If they make a bad batch they win even more lucrative grants and contracts.

How can this be?
That's easy. These sick puppies are very clever. So now imagine a multilayered plot that  produces tremendous windfall profits, just sitting there for the taking.

I see these rings in the water as obvious movements of money. Now imagine that at multiple points, on multiple rings there are businesses, investments and funds that profit enormously whenever a flow of money passes through their hands.

From a Business Model standpoint my head swims when I glimpse the Economic Dynamics at work here. Wave upon wave, industry by industry, executive by executive, investor by investor, and finally onto the Stock Market and beyond.

Each supporting financial entity or holding simply has to wait to sell the Ventilators, The Masks, The Medicines, The Hospital Equipment, The Scientific Equipment, and even the Communications equipment.

In Economics, there is a concept of the flow of money, that if cycled repeatedly in certain ways the production of windfalls is virtually guaranteed. What I mean by this, imagine owning the stone, the launch system, the industries that would profit the most,the transportation of the product, etc. 

Now imagine a group of people with seemingly unlimited wealth and unlimited power. They are professionals. They have private armies, weapons caches, and hired thugs and assassins in their arsenal.

These sick bastards have absolutely no concern for their fellow man. If anything, these people regard the World's Entire Population as a looming threat to their comfort, power, and greed. Anything in the way of Agenda 21 is an obstacle. They've done the math. They know that the maintenance of the world's population is unsustainable. That's just a fact.

So like drowning men and women, they drag us down, they stand on our shoulders, they do anything to survive. All for the sake of their families and constipated ideologies.

All of this has been taking place, all of the Wars started by the Rothschild's and Bilderberger’s. All of it geared towards population control [ Eugenics ]. Less of us means more for them. Less of us who have are now almost fully awake. Make way, for we are coming to track them down.

 Many of them have even had extensive training at The Bohemian Grove School of Impropriety. Once they get their “End of Cares” summer camp badges there is no looking back. None at all.
 
But as much as they wish it wouldn't, life goes on for those of us with hearty genetic dispositions.

Now they have new and improved brainwashing techniques and all of the Mainstream Media in their hands. Thanks to the CIA and Project Mockingbird.

But their days are numbered, their time has come. They will be vanquished. They will be no more.

Autoimmune Technologies LLC, New Orleans
https://www.autoimmune.com/SqualeneInVaccine.html
[ Place where Dr. Pamela Asa discovered Squalene Antibody in Sick Gulf War Veterans ] - She also created what is called the ASA ASSAY TEST that can check for this. This test MIGHT be able to be ordered in quantity from them in order to determine conclusively in court if someone has developed an antibody to this synthetic foreign substance.

Can anybody help subsidize this type of “Test Kit” rallying cry?

It is my sincere hope that you will consider not only punitive, antitrust actions against those responsible for so much death, pain, and anguish, but to please consider a class action lawsuit on a massive scale for citizens and soldiers alike.

I am also asking for this type of landmark case to become an automatic assumed criteria within the VA to trigger granting of long overdue service connected disability for all affected veterans.

Guess What !!! THEY NEVER TOOK IT OUT !!!!!!!!!!!!!

They jack us up on Synthetic Squalene which is a precursor to cholesterol and STEROIDS !!!!

Is that what they mean by a Super Soldier Program?

That is what's been making me so nuts all these years!!!

Then seeing it cross over into influenza vaccines after getting licensed in Europe!!!

Now researching with you and CHD and finding it ALREADY IN USE IN THE USA under secretive aliases has made me so possessed by my quest.

I am not just dedicated. I am permanently pissed off. This will not stand. This will not go on unchallenged. 

AddaVax | MF-59 like Squalene Adjuvant for Vaccine Research
https://www.invivogen.com/addavax

'Direct Order'- Full Documentary | Soldiers Ordered To Take Anthrax Vaccine resulting in Brain Damage
https://oye.news/documentaries/direct-order-full-documentary-anthrax/

Direct Order: The Military Anthrax Vaccine Experiment
http://www.omsj.org/corruption/anthrax4nov

FDA Tests Find Squalene in Anthrax Vaccine
https://www.dynamicchiropractic.com/mpacms/dc/article.php?id=31995

Squalene MF59 Adjuvant - Our Imaginal Cell (Creative Life) Options
 https://ourimaginalcells.info/squalene-mf59-adjuvant.html

PRIME Pub Med | AF03, an alternative Squalene emulsion-based vaccine adjuvant prepared by a phase inversion temperature method
https://www.unboundmedicine.com/medline/citation/22941944/AF03_an_alternative_squalene_emulsion_based_vaccine_adjuvant_prepared_by_a_phase_inversion_temperature_method_

Antibodies to Squalene in Recipients of Anthrax Vaccine - Pub Med https://pubmed.ncbi.nlm.nih.gov/12127050/

Squalene (oil-in-water nano emulsion, Vaccine adjuvant) - Creative Diagnostics
https://www.creative-diagnostics.com/squalene-oil-in-water-nano-emulsion-vaccine-adjuvant.htm

H. Dept. 106-556 - THE DEPARTMENT OF DEFENSE ANTHRAX VACCINE IMMUNIZATION PROGRAM: UNPROVEN FORCE PROTECTION | Congress.gov | Library of Congress https://www.congress.gov/congressional-report/106th-congress/house-report/556/1

Antioxidative Protection of Squalene Adjuvant and Rabies Vaccine with Adjuvant https://www.jstage.jst.go.jp/article/bpb/40/7/40_b17-00026/_html/-char/en

WHO | Squalene-based adjuvants in vaccines
https://www.who.int/vaccine_safety/committee/topics/adjuvants/squalene/questions_and_answers/en/

WHO | Safety of Squalene
https://www.who.int/vaccine_safety/committee/topics/adjuvants/squalene/Jun_2006/en/

Vaccine Injury in the Military - Vaccine Choice Prayer Community
https://www.vaccinechoiceprayercommunity.org/blog/vaccine-injury-in-the-military

Recent research on Gulf War illness and other health problems in veterans of the 1991 Gulf War: Effects of toxicant exposures during deployment - Science Direct
 https://www.sciencedirect.com/science/article/pii/S0010945215003329?via%3Dihub

Gulf War Syndrome: A Review of Current Knowledge and Understanding - Pub Med https://pubmed.ncbi.nlm.nih.gov/25895403/

Manufacture of Oil-in-Water Emulsion Adjuvants | Springer Nature Experiments
 https://experiments.springernature.com/articles/10.1007/978-1-4939-6445-1_12

In adjuvant-induced arthritis the disease-triggering adjuvant Squalene accumulates in draining lymph nodes but not affected joints | Arthritis Research & Therapy
https://arthritis-research.biomedcentral.com/articles/10.1186/ar220

Gulf War Illness and the Health of Gulf War Veterans: Scientific Findings ... - United States. Department of Veterans Affairs. Research Advisory Committee on Gulf War Veterans' Illnesses
https://books.google.com/books?id=IJ_CrkE1jdgC&pg=PA119&lpg=PA119&dq=squalene+adjuvants&source=bl&ots=fH0db2nWyp&sig=ACfU3U00xbvWBBPTPSE7HiDnQbk2TQGt9Q&hl=en&sa=X&ved=2ahUKEwja9tXf35_qAhUxJzQIHdjvA-44MhDoATAFegQIBRAB#v=onepage&q=squalene%20adjuvants&f=false

Vaccination, Squalene and Anti-Squalene Antibodies: Facts or Fiction? - Pub Med https://pubmed.ncbi.nlm.nih.gov/20206873/

Anthrax Vaccine Efficacy - The Anthrax Vaccine - NCBI Bookshelf
https://www.ncbi.nlm.nih.gov/books/NBK220536/

FDA Tests Find Squalene in Anthrax Vaccine
https://www.dynamicchiropractic.com/mpacms/dc/article.php?id=31995

Development of a novel oil-in-water emulsion and evaluation of its potential adjuvant function in a swine influenza vaccine in mice
https://link.springer.com/article/10.1186/s12917-018-1719-2

SAILORS INJECTED WITH OUTDATED ANTHRAX VACCINE - Daily Press
https://www.dailypress.com/news/dp-xpm-19980528-1998-05-28-9805280077-story.Hamburger

Our Next Evolution Thru Love ❤️

https://rumble.com/v1jp6aj--we-are-from-the-future-next-stage-is-the-revolution-of-love.html

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( Keep ) Vaccine 💉 Notes - Lowered Resistance after repeated Flu Vaccinations 💉.

Would it surprise you to learn there is ‘new’ information questioning the so-called benefits of annual flu vaccines? Not me.
 
 
 
As covered in an AFLDS Daily Dose episode this week, a recent study co-authored by the CDC U.S. Flu Vaccine Effectiveness Network Investigators found that repeat annual flu vaccines are associated with an INCREASED risk of getting the flu.
 
 
 
This is alarming news for anyone who has been repeatedly told by Big Pharma and their cronies that flu vaccines are safe and effective.
 
 
 
But the truth is, this information isn’t new. As far back as the 1970s, studies have shown that repeat flu vaccination was linked to reduced vaccine protection. The more a person is vaccinated against a particular strain of the flu virus, the less effective the vaccine becomes.
 
 
 
This means that the flu shots you receive every year are actually making you more susceptible to getting the flu.
 

My firsthand experience with this issue likely contributed to my advocacy over Covid. As a board-certified emergency physician, I have taken care of hundreds of influenza patients. After just a few years, I noticed that every person I admitted into the hospital with influenza had taken the annual influenza shot. I myself took the flu shot because it was a job requirement, but I always knew it was foolish.
 
 
 
It is well known in the medical community that natural immunity obtained by contracting an infection is more effective than the short-term immunity gained from flu vaccines.
 
 
So, why the push each year for the vaccine? You guessed it: money.
 
The financial interests of Big Pharma drive the annual flu vaccine campaigns, prioritizing profit over public health. As we’ve consistently cautioned, do NOT trust Big Pharma over your own natural immunity.
 
 
 
We are dedicated to exposing the profit-driven agendas of Big Pharma and their involvement in the Medical Industrial Complex, which prioritizes financial gain and power above all else. Through our unwavering commitment to truth and independent research, we will persistently expose the hidden lies behind the manipulation and corruption.
 
 
Your help is crucial in this fight. Stand with America's Frontline Doctors today and together, let's create a healthier, more informed America.<http://alerts.aflds.org/rd/9z4zfg7u3uild22fupjuek545lp30gforair6ou5an8_rp22sh2s8h66ob1cdi6cob24no>
 
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For Liberty!
 
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The Problems Associated With Ebola Vaccine by Professional Vaccine Hazard Researcher Thomas W. Trefts
Founder of Veterans Against Treason

Veterans Health Chairman of The National Vietnam And Gulf War Veterans Coalition

Paid Researcher ( one month , part time ) for Robert F. Kennedy’s Children’s Health Defense

Long Time Activist Against Allen Experimental Vaccines 💉Given Without Informed Consent.

Note 📝 : Vaccines 💉 Given Without Informed Consent are by their very nature defined as a War Crime Offense.

From September 15, 2023

Ebola Vaccine: Information about ERVEBO®

On This Page
• Why an Ebola Vaccine is Important
• The Ebola Virus Vaccine
• Ebola Vaccine Eligibility
• Booster Dose Eligibility

Why an Ebola Vaccine is Important
A safe and effective vaccine is an important tool to protect frontline workers and prevent the introduction and spread of Ebola disease in the United States.

Ebolaviruses are zoonotic pathogens that cause severe hemorrhagic fever in humans, known as Ebola disease. There are four species of Ebolaviruses that are known to cause disease in humans.

Of these, Ebola virus (EBOV; species Zaire ebolavirus), the cause of Ebola virus disease (EVD), is the most lethal, with case fatality rates of 70–90% if left untreated. EBOV is responsible for the majority of recorded Ebola disease outbreaks. This includes the two largest Ebola disease outbreaks in history, the 2014–2016 West Africa outbreak and the 2018 outbreak in eastern Democratic Republic of the Congo, where over 32,000 people were infected, and more than 13,600 deaths were reported.
Importation of Ebola disease to the United States by an infected traveler from an outbreak area is a recognized risk with the potential for spread to other people. During the 2014–2016 Ebola disease outbreak in West Africa, 11 people were treated for EVD in the U.S., and two of them died. Nine of these cases were imported into the U.S. Two were domestic healthcare workers who were infected while caring for the first travel-associated Ebola disease case diagnosed in the U.S. Both healthcare workers recovered.

The Ebola Virus Vaccine
ERVEBO® (Ebola Zaire Vaccine, Live also known as V920, rVSVΔG-ZEBOV-GP or rVSV-ZEBOV) is approved by the U.S. Food and Drug Administration (FDA) for the prevention of disease caused by Ebola virus (EBOV; species Zaire ebolavirus) in individuals 12 months of age and older as a single dose administration. ERVEBO is a replication-competent, live, attenuated recombinant vesicular stomatitis virus (rVSV) vaccine manufactured by Merck. It is not possible to become infected with EBOV from the vaccine because the vaccine only contains a gene from the Ebola virus, not the whole virus.

Specifically, it contains a gene for the EBOV glycoprotein that replaces the gene for the native VSV glycoprotein. ERVEBO does not provide protection against other species of Ebolavirus or Marburgvirus.
Antibody measurements are often used as a surrogate test to predict when protection by a vaccine can be expected. Clinical trials have shown that the vaccine elicits rapid antibody response in 14 days after a single dose. Clinical efficacy of the vaccine was supported by a randomized cluster (ring) vaccination study during the 2014–2016 outbreak in Guinea. In this study, 3,775 people in close contact with diagnosed EVD cases (contacts) and their close contacts (contacts of contacts) received immediate vaccination.

No one who was vaccinated immediately developed EVD 10 or more days after vaccination.
The correlate of protection, or the specific immune response to the ERVEBO vaccine that closely relates to protection against infection with EBOV, is unknown and still being studied. It is also not known whether it is effective when administered concurrently with antiviral medication, immune globulin, and/or blood or plasma transfusion. The duration of protection conferred by an initial dose of ERVEBO is also unknown. A booster dose for people who have been previously vaccinated may extend the duration of protection for ERVEBO. Scientists continue to monitor people who have received the vaccine to learn more.

Ebola Vaccine Eligibility
ERVEBO is not currently commercially marketed in the U.S. but is currently stockpiled in the Strategic National Stockpile and is made available through CDC for pre-exposure vaccination of individuals who fall into one of the three occupational categories:
1. Ebola virus disease (EVD) responders to an Ebola virus (EBOV; species Zaire ebolavirus) outbreak.
2. Laboratorians and support staff working at biosafety level 4 (BSL-4) or Laboratory Response Network facilities in the United States that handle specimens that contain or might contain replication-competent EBOV.
3. Healthcare personnel (HCP)* at federally designated Ebola Treatment Centers or state-designated Special Pathogens Treatment Centers** involved in the care and transport of patients infected or suspected to be infected with EBOV.
Disclaimer: The mention of any product names or non-United States Government entities on CDC Ebola websites is not meant to serve as an official endorsement of any such product or entity by the CDC, the Department of Health and Human Service, or the United States Government.

Booster Dose Eligibility
Given booster dose vaccination is not covered under ERVEBO’s FDA-approved indication, the Centers for Disease Control and Prevention (CDC) is sponsoring an expanded access Investigational New Drug (IND) program

[PDF – 600 KB] to allow booster dose administration for pre-exposure prophylaxis in adults (≥ 18 years of age) who were previously vaccinated (e.g., ≥ 6 months since prior vaccination) and who have potential risk of occupational exposure to EBOV. Final eligibility decisions of booster doses will be assessed on an individual basis.

Resources
• ERVEBO® package insert
• ERVEBO® patient information 
[PDF – 58 KB]
• Choi MJ, Cossaboom CM, Whitesell AN, et al. Use of Ebola Vaccine: Recommendations of the Advisory Committee on Immunization Practices, United States, 2020. MMWR Recomm Rep 2021;70(No. RR-1):1–12. DOI: http://dx.doi.org/10.15585/mmwr.rr7001a1external icon
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• Malenfant JH, Joyce A, Choi MJ, et al. Use of Ebola Vaccine: Expansion of Recommendations of the Advisory Committee on Immunization Practices to Include Two Additional Populations—United States, 2021. MMWR Morb Mortal Wkly Rep 2022;71:290–292. DOI: http://dx.doi.org/10.15585/mmwr.mm7108a2

Footnotes
*Healthcare personnel (HCP) refers to all paid and unpaid persons serving in healthcare settings who have the potential for direct or indirect exposure to EVD patients or infectious materials, including body substances (e.g., blood, tissue, and specific body fluids); contaminated medical supplies, devices, and equipment; contaminated environmental surfaces; or contaminated air. These healthcare personnel include, but are not limited to, emergency medical service personnel, nurses, nursing assistants, physicians, physician assistants, technicians, clinical laboratory personnel, autopsy personnel, therapists, phlebotomists, pharmacists, students and trainees, contractual staff not employed by the healthcare facility, and persons not directly involved in patient care, but who could be exposed to infectious agents that can be transmitted in the healthcare setting (e.g., clerical, dietary, environmental services, laundry, security, engineering and facilities management, administrative, billing, and volunteer personnel).
Adapted from https://www.cdc.gov/infectioncontrol/guidelines/healthcare-personnel/index.html
**

Healthcare facilities that intend to receive and are able to provide care for a suspected or confirmed patient with Ebola disease for the duration of their illness, as assessed by their state health department. In addition to Ebola disease, these facilities may also be designated by the states to treat other high consequence pathogens.

Last Reviewed: September 15, 2023

EBOLA 🦠 DISEASE 🦠 TRANSMISSION
https://www.cdc.gov/vhf/ebola/transmission/index.html

Let’s go over this one more time :

Tested for ten days in New Guinea ( pigs ? ) New 🆕 Guinea 🇬🇳 Pigs 🐷?
Dark Humor ?

What are the exact names of the participants. How long did they live after the 10 day mark ?

Random Ring ? Are you shitting me ? Where are the statistics ? Who was ruled in / who was ruled out ?

**** See Below ****

Why an Ebola Vaccine is Important
A safe and effective vaccine is an important tool to protect frontline workers and prevent the introduction and spread of Ebola disease in the United States.
Ebolaviruses are zoonotic pathogens that cause severe hemorrhagic fever in humans, known as Ebola disease. There are four species of Ebolaviruses that are known to cause disease in humans. Of these, Ebola virus (EBOV; species Zaire ebolavirus), the cause of Ebola virus disease (EVD), is the most lethal, with case fatality rates of 70–90% if left untreated. EBOV is responsible for the majority of recorded Ebola disease outbreaks. This includes the two largest Ebola disease outbreaks in history, the 2014–2016 West Africa outbreak and the 2018 outbreak in eastern Democratic Republic of the Congo, where over 32,000 people were infected, and more than 13,600 deaths were reported.
Importation of Ebola disease to the United States by an infected traveler from an outbreak area is a recognized risk with the potential for spread to other people. During the 2014–2016 Ebola disease outbreak in West Africa, 11 people were treated for EVD in the U.S., and two of them died. Nine of these cases were imported into the U.S. Two were domestic healthcare workers who were infected while caring for the first travel-associated Ebola disease case diagnosed in the U.S. Both healthcare workers recovered.
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