triplekon

With the cancellation of Wednesday's ACIP meeting the horror and cruelty continues. "The suffering they have endured—and the cruelty many have faced from government health agencies, medical institutions, legislators, and even journalists—has been beyond anything I would have believed possible in modern America." Following is the public comment I submitted for the ACIP meeting that is no longer taking place: "For the past five years, through my work with @React19org - the largest organization in the United States advocating for individuals injured by the COVID-19 vaccines—I have been in continual contact with people across the country whose lives were devastated following COVID-19 vaccination. Adults and children alike are now facing life-long disabilities. Some individuals—including children—have died after taking the vaccine. Many others lost their health, their careers, and in some cases their ability to ever work again. Over these years, I have heard their stories and witnessed firsthand the systemic failures they encountered while seeking help. Families that were once stable and productive have been financially and physically destroyed. Some have lost their entire life savings searching for treatments that might restore even a fraction of their former health, while others have been forced to sell their homes simply to survive. The suffering they have endured—and the cruelty many have faced from government health agencies, medical institutions, legislators, and even journalists—has been beyond anything I would have believed possible in modern America. Some injured individuals have faced such profound despair—living in bodies that feel as though they are attacking themselves, with no clear path to treatment and being left completely abandoned and censored—that they have taken their own lives. The magnitude of this suffering must be acknowledged. Early in 2021, federal health agencies were aware that serious vaccine injuries were occurring. Some injured individuals were flown to the NIH in Bethesda to be studied, with the promise that their conditions would be investigated and that the public would be informed. Instead, the research was quietly abandoned and the injured were left without answers. That silence led to devastating consequences At the same time, widespread censorship took place across the country. Government officials worked with media platforms and technology companies to suppress discussion not only from the vaccine injured themselves, but also from physicians, scientists, and researchers raising legitimate concerns. This prevented the public from understanding what was happening in real time and discouraged many physicians from speaking openly. The chilling effect within the medical community was real. I personally know individuals in our area who experienced serious health problems following COVID vaccination, and I also know physicians who believe those injuries are vaccine-related. Yet many doctors have been reluctant to speak publicly because of the professional backlash faced by physicians who questioned vaccine policy or reported concerning observations. As a result, many injuries were never fully documented or investigated. Numerous patients report that their physicians did not file reports to the Vaccine Adverse Event Reporting System, and even when reports were filed, there was little to no follow-up. Those who sought help through the federal government’s Countermeasures Injury Compensation Program encountered overwhelming barriers. Approximately 97 percent of claims have been rejected, leaving the vast majority of injured individuals without compensation, medical support, or even acknowledgment of what happened to them. If restoring public trust is truly a goal, it cannot happen without openly acknowledging the injuries that have occurred and the institutional failures that followed. Trust cannot be rebuilt by ignoring the suffering of those who stepped forward in good faith. Immediate action is required. These injuries must be openly researched without delay. Physicians and scientists must be encouraged—not discouraged—to investigate possible treatments and therapies. Proper medical classification must also be established so these injuries can be accurately tracked. Appropriate ICD-10 diagnostic codes should be created so clinicians can document vaccine injuries consistently and researchers can properly study their prevalence and outcomes. The American people deserve honesty, and the injured deserve recognition, research, and care. Until the profound harm—and the horror—that many Americans have endured is openly acknowledged, trust will not be restored." The paintings below titled (Left) "Gaslighted" and (Right) "Silenced" by @melania_jayne reflect well the agony of the injured. Please keep fighting for them. @NIHDirector_Jay @DrJBhattacharya @SecKennedy @RetsefL @TracyBethHoeg @RWMaloneMD @DrMakaryFDA

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Vaccines save millions of lives. Unfortunately, a small fraction of people develop debilitating diseases after vaccination. Thank you @WSITYpod for having me on the show to discuss post-vaccination syndrome. Please listen and understand what the patients are going through and why many of them lost trust in the medical and scientific establishment. We must do better.

Let's look at how the FDA is treating $SRPT and $QURE differently. The FDA grants accelerated approval to Amondys and Vyondys to treat Duchenne muscular dystrophy. Sarepta conducts a post-marketing confirmatory study that fails to show a benefit for either drug. There is no evidence that patients are benefiting from either drug, based the outcome of a randomized, controlled study. Still, Sarepta pushes forward, seeking to convert accelerated approval to final approval. The FDA allows Sarepta to submit an application. "The adequacy of the data to support conversion to traditional approval will be a matter of review," the FDA concludes, according to Sarepta. Amondys and Vyondys should be withdrawn from the market. My opinion. I've said that repeatedly. There's a process, of course, so FDA should review the data. That's what regulators are supposed to do. And then, there's UniQure and AMT-130, its treatment for Huntington's disease.... The FDA won't even allow UniQure to submit an application for accelerated approval. Bar the door, the FDA says, not even a review. investorrelations.sarepta.com/news-releases/…