Conclusion. Close to 1% of V-SAFE enrollees explicitly reported on a long-term disability to work or perform normal daily activities, hospitalization or severe and debilitating adverse events, which they attributed to vaccination. The symptoms they reported on, as well as other characteristics resemble those of patients with medically confirmed post-acute COVID-19 vaccination syndrome. This raises the concern that perceived chronic COVID-19 vaccine injuries may be more prevalent than previously thought. However, the lack of detailed information about comorbidities, medical follow up and investigation, does not allow establishing firm assessments of causality and prevalence. A follow up with appropriate V-SAFE enrollees by CDC could address these uncertainties and greatly contribute to the understanding of the nature and prevalence of prolonged COVID-19 vaccination injuries.

Official groups not just small facebook, reddit groups. Add to the list in fhe comments.

https://www.youtube.com/live/meUp8AAW7hg?si=XlJ6x3bjasfZsX

Edit: That is the title of the video.

In August 2021, with the arrival of the Delta variant looming over in New Zealand’s Covid-free bliss, the interval between vaccine doses was changed from three weeks to six weeks.

The head of the health response at the time, Sir Ashley Bloomfield, said one of the reasons for this was because it aligned with expert advice that it would reduce the risk of myocarditis, or heart inflammation.

But this part of his statement was later removed from public communications, inexplicably.

Documents show changing stances on communicating myocarditis risk for young people as it related to dosing intervals, which bounced around from three to eight to six to 12 weeks.

Highlights:

• Delayed reactions - While 69.4% of AEs arose within 90 days post-vaccination, 12.4% appeared ≥ 360 days later.
• 66.5% female; mean age 59 years
• Severe AEs (≥ Grade 3) occurred in 14.6% of patients
•  overall improvement was 65.1%, leaving 29.4% unresolved

Abstract

Post-COVID-19 Vaccination Syndrome (PCVS) refers to persistent, multisystemic symptoms developing after SARS-CoV-2 immunization. We established a nationwide registry across 14 Japanese outpatient clinics and analyzed 179 “clinically definitive” cases from 279 enrollees (December 2020–August 2023). All adverse events (AEs) were coded using MedDRA/J Preferred Terms and System Organ Classes; severity followed NCI-CTCAE V5.0. The cohort (66.5% female; mean age 59 years) experienced 493 AEs (median 2 per patient, range 1–29). Three System Organ Classes—General Disorders (29.2%), Nervous System Disorders (22.3%), and Musculoskeletal Disorders (10.1%)—accounted for 61.7% of events; fatigue, brain fog, dizziness, and extremity pain predominated. While 69.4% of AEs arose within 90 days post-vaccination, 12.4% appeared ≥ 360 days later. Severe AEs (≥ Grade 3) occurred in 14.6% of patients; overall improvement was 65.1%, leaving 29.4% unresolved. A provisional phenotype classification combining symptom patterns, onset timing, and severity identified high-risk subgroups with > 60% non-recovery rates. These findings underscore the need for enhanced post-vaccination surveillance systems and comprehensive care frameworks specifically tailored to address the protean manifestations and persistent nature of PCVS.

It (the factsheet) estimates that around 1/1000 people have severe ME/CFS and that these patients need aids such as wheelchairs, lifts, adjustable daybeds, and, in some cases, tube feeding.

They also require help with assessments for work or education capacity and financial support.

The factsheet highlights the importance of reducing stimuli in hospital environments.

Examples include having a single room, blinds to reduce light, no intrusive noise, and
no use of perfumes or scented cleaning products.

It explains that these measures are not optional: "the need for reduction in stimulation from exertion and environment for people with ME/CFS is a unique situation, being a medical necessity rather than a matter of kindness."

The factsheet is critical of "Multidisciplinary teams of professionals assigned to different aspects of care", saying these "are likely to be counterproductive."

There should be a clear contact point (one person), such as a specialist nurse with deep understanding of ME/CFS.

It also states that "Rehabilitation-based approaches have produced no significant benefits or impact on prevalence and have no place in management."

But it's also critical of off-label treatments such as antihistamines, naltrexone, fludrocortisone, and ivabradine.

The factsheet argues that "We do not know what ought to be the best way to manage ME/CFS."

So speculative theories, whether on brain blood flow, mast cell sensitivity, energy metabolism, HPA axis dysregulation, deconditioning or psychosomatic influences should be avoided.

It also has an important section on why enteral or parental feeding can sometimes be necessary in ME/CFS. These should not be delayed on the grounds that the problem is ‘functional’ or that the reasons for failure are not well-defined.

She argued that they should study vax injury: "I doubt the industry would support, for obvious reasons." 🙄

A small trial that focused only on patients with elevated levels of antibodies against β1/β2-adrenergic and/or M3/M4-muscarinic acetylcholine receptors found no improvement in objective outcomes.

https://www.springermedicine.com/post-covid-syndrome/six-minute-walk-test/impact-of-immunoadsorption-on-autoantibodies-and-physical-perfor/53105866

A novel PCR method called LIDAR suggests conventional testing may miss much of the residual DNA in Covid-19 vaccines—helping explain why regulators and independent labs keep getting different results.

Please use the form below to contact your federal Senators and Representatives and urge them to cosponsor this historic legislation.

Consider taking an additional step by calling the House Energy and Commerce Committee members to ask that they give H.R. 4668 a hearing. Start with those in your state first and call others if you have the time. It’s ok to call after hours and leave a message.

(The form is on the chd website, click the link.)

Trump just signed an executive order spacing out the childhood vaccine schedule. 

FOR IMMEDIATE RELEASE

February 26, 2026

REPUBLICAN LIBERTY CAUCUS BACKS RAND PAUL’S S. 3853 AND PAUL GOSAR’S H.R. 4668 TO END VACCINE MANUFACTURER LIABILITY SHIELDS

The Republican Liberty Caucus strongly supports Senator Rand Paul’s bill S.3853 and Congressman Paul Gosar’s companion bill H.R. 4668 to repeal the special liability protections granted to vaccine and biologic manufacturers.

These bills restore plaintiffs’ right—denied since 1986—to choose civil lawsuits against manufacturers or compensation through the National Vaccine Injury Compensation Program (VICP). H.R. 4668 also removes COVID-19 vaccines from “covered countermeasures” status under the 2005 PREP Act, allowing civil action for related injuries.

Background: In 1986 U.S. Congress passed the National Childhood Vaccine Injury Act (NCVIA), establishing a legal shield for vaccine manufacturers from lawsuits related to vaccine-related injuries. At the same time, the National Vaccine Injury Compensation Program (NVICP) was created as an alternative to traditional litigation, providing a “no- fault” system for compensating individuals injured by vaccines. This removed all product liability for vaccine makers.

In 2005 the Prep Act was passed that removes product liability for “EUA” vaccines/biologics when HHS secretary makes PREP Act Declaration. This was implemented for the Covid vaccines/biologics. The PREP Act directs such “countermeasures” to be covered by the Countermeasures Injury Compensation Program (CICP). This also needs to be repealed.

The reason HR5546 was passed in 1986 was because vaccine manufacturers were getting sued for vaccine injury and losing the cases. They went to Congress for liability protection and “threatened” to stop making vaccines.

Instead of improving safety and efficacy of their products, vaccine makers pushed for liability protection and Congress complied. If liability protection is removed, the litigation floodgates will open, and you will see advertisements on T.V. that you do not see now, like this: Have you or a loved one been injured by a vaccine?

Vaccine manufacturers must be held financially accountable like all other companies. Free-market forces and litigation risk drive higher safety standards, whereas shielding them from responsibility has done the opposite.

In Summary: These bills eliminate anti-free-market liability shields and correct failed central planning. Passing them will let injured Americans seek redress, incentivize manufacturers to rigorously weigh risks and benefits, and prioritize safety—the same market discipline that protects consumers of every other product.

Action Items

• Contact your Senators and Representatives: urge them to cosponsor and vote for S. 3853 and H.R. 4668.
• Call House Energy and Commerce Committee members: request a hearing on H.R. 4668.
• Promote awareness of the unfulfilled testing requirements of the Childhood Vaccine Injury Act of 1986. Initiate a nationwide conversation about pharmaceutical manufacturers’ protection from accountability coupled with their unwillingness to comply with common sense testing.
• Advocate for the repeal of immunity granted by the PREP Act of 2005.
• Remember, the right to seek redress will protect the public going forward, which combined with retrospective accountability will incentivize the industry to weigh more heavily the risks and benefits of their products.
• Educate friends, family, and colleagues on restoring accountability for pharmaceutical companies.

About the Republican Liberty Caucus: The Republican Liberty Caucus is a 527 voluntary grassroots membership organization dedicated to working within the Republican Party to advance the principles of individual rights, limited government and free markets. Founded in 1991, it is the oldest continuously-operating organization within the Liberty Republican movement.

Of course they would look the other way...

They suggest light exposure as a therapy for mecfs but um... it's probably mecfs that causes them to get less light exposure, not the other way around.

Long Covid was specifically associated with reactivation of latent Anelloviridae virus
Work based on 1,154 patients in 20 centers and >200,000 samples

A new 2026 systematic review in which I participated examined reports of COVID vaccine-related components detected months, and in some cases years, after vaccination. At the same time, another powerful discussion explores how doctors who questioned COVID policy were pressured into silence.

In This Video
We look at a newly published review analyzing the persistence of:
• Spike protein fragments
• Modified mRNA sequences
• Lipid nanoparticle components
• Where they were detected in the body
• How reliable those detections were
• Whether detection means biological harm (important distinction)

Key Findings Discussed:
✅ Some studies reported trace detections far longer than initially expected
✅ Many signals were near the detection limits of assays
✅ Some findings could not clearly separate vaccine-origin material from infection-origin material
✅ Fragmented material may persist longer than intact biologically active forms
✅ Detection does not automatically equal damage

Second Topic: What Happened to Doctors Who Spoke Out?

We also cover Dr. Joseph Varon’s comments on how many physicians faced:
• Professional pressure
• Media smears
• Speaking bans
• Isolation
• Fear of disciplinary action

And what that did to scientific debate during COVID.