The Witch Hunt continues
Another Questioning Voice is removed from the Medical Register
Health Advisory & Recovery Team | September 13, 2024
A chill wind passed through the dissident medical profession this week when Dr Sam White was permanently erased from the medical register. But it will not cause us to stop speaking truth to power or more importantly being open and honest with our patients about the potential harms of mRNA vaccines.
For those who don’t know of Dr White, he was an experienced General Practitioner who, like many others, found himself conflicted between his NHS practice expecting him to promote Covid-19 vaccines to his patients, while in his clinical practice seeing increasing numbers of people with vaccine injuries. After much soul-searching he resigned from his post in February 2021. A few months later, in June 2021, he recorded a short face to camera video explaining why he had decided to quit, which he then posted on a social media site. Perhaps to his surprise, it was viewed by millions and within a few days had come to the attention of his employer, namely NHS England, who blocked him from any NHS work, which he legally challenged. A GMC investigation then followed and his NHS suspension was reversed, but an Interim Orders Tribunal put conditions on his registration, namely that he must not use social media to express any medical opinion about the pandemic. Dr White challenged this in the High Court on the grounds that it breached his right to freedom of speech. The court upheld his challenge, as described in the BMJ here, though oddly enough the link to the actual judgement is no longer available, except via Wayback machine. Mr Justice Dove ruled that there had been “an error of law and a clear misdirection in the interim orders tribunal’s decision making process.” Its decision was “clearly wrong and cannot stand,” he added. He stressed that he was expressing no views on the merits of Dr White’s claims on social media. But he said the tribunal had failed to consider a provision in the Human Rights Act 1998. This states that a court or tribunal should not restrain somebody’s freedom of expression before a full hearing unless it was satisfied that after a full hearing the application to restrict publication was more likely than not to succeed.
At the time, the GMC clearly didn’t think that Dr White was a danger to his patients (there had been no clinical complaints against him) nor even sufficient danger to public health for them to suspend him and for the next 3 years he was entitled to work and to speak freely, and many of his supporters had thought this was the end of it. But the wheels of ‘justice’ (ironically in this case more like the wheels of ‘injustice’) grind slowly and in August 2024, the GMC set up a full hearing by the Medical Practitioners Tribunal Service (MPTS). By this stage, Dr White had moved entirely to a practice of naturopathic medicine and decided that he would not engage with the process – he neither attended nor was he legally represented. No-one who has experienced a GMC investigation will blame him at all for this decision – it is time-consuming, emotionally draining and very costly. But his absence may have enabled a serious miscarriage of justice.
The charge against Dr White concerned 5 video interviews about the pandemic which he had recorded between June 2021 and July 2022, and the hearing hinged around details of the Human Rights Act 1998.
Article 10, paragraph 1 states:
“Everyone has the right to freedom of expression. This right shall include freedom to hold opinions and to receive and impart information and ideas without interference by public authority and regardless of frontiers. This Article shall not prevent States from requiring the licensing of broadcasting, television or cinema enterprises.”
However in certain circumstances, the law allows for these rights to be restricted, as in Article 10, paragraph 2:
“The exercise of these freedoms, since it carries with it duties and responsibilities, may be subject to such formalities, conditions, restrictions or penalties as are prescribed by law and are necessary in a democratic society, in the interests of national security, territorial integrity or public safety, for the prevention of disorder or crime, for the protection of health or morals, for the protection of the reputation or rights of others, for preventing the disclosure of information received in confidence, or for maintaining the authority and impartiality of the judiciary.”
The Tribunal chairman quoted from the case of Adil v GMC [2023] EWCA Civ 126. Mohammad Adil is a surgeon who was suspended by the GMC in 2020, again for a face to camera video which went viral. He also took the GMC to court but in his case he lost. In that case, “the Court held that the fact that a doctor expresses a minority view, even a view shared by a small minority is not sufficient of itself to render his conduct improper. Medical progress depends upon such debate and is littered with examples of what were thought to be heretical views becoming accepted wisdom, and vice-versa. Article 10 and the common law protect the right to express views with which most people disagree. Views contrary to widely accepted medical opinion are not sufficient to establish misconduct.” However, the judgement went on to say that this does not apply to views so far removed from any concept of legitimate medical debate and must be considered on the facts of each individual case. “There is an important qualitative difference between a doctor’s views which have some supporting scientific basis, even if not widely accepted, and views whose validity or accuracy is unconnected to any supporting evidential basis, in other words baseless.”
With Dr White absent from the proceedings, the Tribunal seem to have assumed that his views on the safety of the Covid-19 mRNA vaccines were ‘baseless’, whereas of course they are shared by a significant minority of doctors who have assembled a huge amount of scientific literature on vaccine harms. However, the judgement in quoting from his interviews has barely mentioned Dr White’s criticisms of the vaccine, for all of which he had provided many references to the GMC in 2021. It has instead focussed almost entirely on discussions about the ‘why’ of the vaccine rollout and the censorship, quoting Dr White speaking of: ‘evil’, ‘planned’, ‘globalists’, ‘tyranny’, ‘totalitarianism’, et cetera. These, of course, are all issues which are widely discussed but are not subject to testing and writing up in peer-reviewed journals. They are a matter of opinion. The question of whether Dr White’s opinions in any way harmed public health has not been demonstrated by the GMC, yet the Tribunal “determined that, it was more likely than not, such comments undermined public confidence in the medical profession.”
Another aspect of Dr White’s absence was that, whereas the GMC were actually asking for a suspension rather than for his name to be permanently erased from the register, the Tribunal interpreted his absence as showing a lack of insight into the seriousness of his actions and a lack of any effort at mitigation or remediation. For a surgeon who has cut off the wrong limb or a physician who has missed a potentially treatable fatal condition, remorse and a desperate wish to ensure you never make the same mistake again, would be the universal reaction, even without censure from the GMC. But for a doctor who is in effect a whistleblower, it is hard to show remorse, whilst still hoping that your actions have indeed saved lives.
The irony is that if the GMC really believed that Dr White was a danger to public health, they would have suspended him in 2021, at a time when the vaccine rollout was in full swing and we were heading towards a second winter of masks and lockdowns. Yet they appear to have made no effort to bring forward a full hearing, and have instead waited a full 3 years after his initial video before bringing this case. The rules for deciding on a penalty are that the Tribunal must consider whether the doctor poses a risk to future patients rather than only past. Given the government messaging with which Dr White disagreed all came to an end during 2022, it is hard to see what harm he is thought to be causing in 2024.
It was, however, made very clear that the penalty was not only intended for Dr White but also to send a clear message to other doctors considering speaking out. “Sanctioning doctors for comments likely to undermine public health and confidence in the medical profession so as to deter such behaviour engages the aim of the protection of public health and safety.” Indeed, coming close in the heels of Dr White, is a consultant psychiatrist, Dr Daniel Armstrong, also facing the possibility of being struck off for a single online video, “Navigating the Truth-deception duality”. And there are others with hearings in the near future. This is not about clinical complaints of patient safety. This is about doctors questioning the government about the management of the pandemic, especially the poor safety record of the vaccines.
In May of this year, Professor Dame Carrie McEwen, chair of the GMC, published a statement in response to the contaminated blood scandal. She commented robustly on the importance of protecting whistleblowers. “There is extensive commentary within the report about the importance of speaking up about both mistakes and near misses and a cautionary note about the need to protect those who do so from detriment to their career.” She said, “We are of course aware that referrals to us are sometimes used to intimidate. This is completely unacceptable, has significant consequences for doctors’ wellbeing and puts the safety of patients at risk….We’ve put a number of safeguards in place” and she committed to assessing “whether further interventions are needed to prevent retaliatory or weaponised referrals.” “also seen investigative media reports alleging that a number of NHS managers have taken actions to silence whistleblowers, including threatening referral to the GMC.” The Telegraph (15th May 2024), published one such report under the title “The four-step ‘playbook’ the NHS uses to break whistleblowers”.
A large group of doctors and other health professionals wrote to the GMC in June, highlighting their concerns over what appeared to be a witch hunt of doctors speaking out about covid-vaccine harms. The ongoing correspondence is published here. Several of the signatories to that letter had previously signed a fully referenced scientific letter to the Chief Medical Officer in June 2021 calling on him not to recommend covid vaccines for children, and found themselves referred by the DoHSC to the Counter Disinformation Unit.
A recent BMA survey showed that the proportion of doctors being discouraged from or even afraid of speaking out has risen significantly between 2018 and 2024, to the point where 61% of those polled in 2024 said they may not raise concerns because they were “afraid” they or colleagues could be “unfairly blamed or suffer adverse consequences”.
The UK is not alone in its efforts to stifle free speech with eminent doctors being similarly sanctioned in Canada, Australia, and most recently the USA. Whistleblowing in academia is no easier.
If public confidence in the medical profession has fallen, rather than blaming dissenters for speaking out against the prevailing message, perhaps doctors need to take a hard look at their unquestioning acceptance of the ‘Safe and Effective’ message and ask themselves why is covid continuing, why are their vulnerable patients being recommended for another booster every 6 months, and yet why are they apparently busier than ever?
Many of the doctors currently being hounded for speaking out on social media, are the same doctors who are repeatedly thanked by members of the public for their honesty and integrity and especially for their efforts to support the vaccine injured, often ignored and disbelieved by others. Comments beneath an article in the Mail about Dr White’s erasure, suggest that many members of the public have rather more faith in Dr White than they have in the GMC.
The current situation of self-censorship amongst doctors combined with GMC overreach, risks serious ongoing harms to patients and must not continue.
The Truth: About COVID-19 Shots
Millions were exposed without informed consent — this fight is for accountability & justice
Gaz’s – A Defender’s Voice – September 7, 2024
This video delves into the alleged concealment of critical information regarding the safety and efficacy of COVID-19 mRNA injections, focusing on how regulatory bodies and authorities misled the Australian public. It claims that significant contamination of genetic material was found in Pfizer and Moderna vaccines, far exceeding safety thresholds, with potential links to severe health risks like cancer and autoimmune diseases. Despite independent verification from multiple labs, global regulators, including Australia’s Therapeutic Goods Administration (TGA), dismissed concerns, claiming there was no safety risk without conducting proper tests.
The video argues that the mRNA injections are in fact gene therapies rather than traditional vaccines, citing how these injections modify genetic material within cells to stimulate an immune response. It criticizes the lack of rigorous testing on the long-term effects of this genetic modification, accusing manufacturers and health authorities of withholding important information about the risks, such as the bio-distribution of modified RNA throughout the body and its potential to disrupt cellular functions.
Legal challenges against Pfizer and Moderna are outlined, notably the case of Dr. Julian Fidge, who accused the companies of bypassing Australia’s regulatory requirements for gene therapies. The lawsuit was dismissed due to a lack of legal standing, but the video highlights potential conflicts of interest, including Judge Helen Rofe’s undisclosed connections to Pfizer. This raises questions about the integrity of the judicial process, especially regarding the dismissal of critical evidence related to genetic contamination.
The video also condemns the narrative pushed by health authorities that the vaccines were “safe and effective,” arguing that data showed minimal absolute risk reduction and high infection rates among vaccinated individuals. It accuses authorities of fearmongering, particularly regarding children, and asserts that pregnant and breastfeeding women were given false assurances about the safety of the vaccines, despite being excluded from clinical trials.
Ultimately, the video calls for accountability and justice, emphasizing that millions of Australians were subjected to experimental gene-based treatments without adequate informed consent. It demands transparency, thorough investigations into regulatory failures, and reparations for those harmed. The script ends with a strong appeal to hold responsible parties accountable and to ensure that such breaches of public trust are never repeated.
Their vaccine injury reports disappeared from VAERS — So they developed a tool for anyone to track their own reports
By Brenda Baletti, Ph.D. | The Defender | September 11, 2024
A team of researchers is developing a tool to track reports in the Vaccine Adverse Event Reporting System (VAERS), so vaccine-injured people can follow what happens to the reports they submit.
As part of a broader effort to hold public health agencies accountable, the tool will also make it possible to audit the VAERS system by identifying what types of reports are deleted, insufficiently updated or contain errors.
The Centers for Disease Control and Prevention (CDC) and the U.S. Food and Drug Administration (FDA), which jointly oversee VAERS, have refused to do this work despite multiple appeals by advocates for the vaccine-injured, according to React19, the group leading the initiative.
React19, founded by a small group of medical professionals injured by COVID-19 vaccines, works with institutions and providers to increase understanding and awareness of patients experiencing lasting effects following COVID-19 and/or COVID-19 vaccines.
The group is teaming up with computer programmer Liz Wilner, founder of OpenVAERS — a website that provides tools for more easily accessing and searching VAERS data — and Children’s Health Defense (CHD) to develop the tool.
The idea for developing the automatic VAERS report tracking tool came out of a VAERS audit the group conducted in 2022 to assess how the FDA and CDC were following up on COVID-19 vaccine injury reports.
React19 worked with outside experts to review a sample of 126 VAERS reports filed by some of its members who wanted to know what happened to their reports.
After tracking down each person’s reports and following them through the VAERS system, they “were kind of shocked at how bad it is,” members of React19 told The Defender.
They found that only 61% of the reports filed were correctly logged and published in VAERS. Twenty-two percent of the reports were never issued a permanent ID and are therefore not publicly visible, 12% were deleted and in 5% of the cases, a report couldn’t be filed or their report number remains unknown due to system errors.
That means more than 1 in 3 reports searched couldn’t be found in a database that is meant to be publicly accessible and transparent. It also suggests that problems of “omission of data and underreporting may be even greater than estimated,” according to the audit report.
The group also found that the medical status of the deleted reports, “by and large, had a worse outcome than the ones that were still in the system,” they said. For example, they said, in the public-facing VAERS system, 23% of reports were for permanent disabilities — but in the deleted reports, 53% were for permanent disability.
“One of the more alarming things we found out was that not all death reports are investigated,” Brianne Dressen, React19 founder, told The Defender.
The group brought this to the attention of public health officials in their meetings, sharing examples of reports that had been updated by people’s families when they died, but didn’t show up on the public system.
They also found that many follow-up reports containing updates on worsening symptoms were gone from the system.
At the time, the group was meeting regularly with top officials, including Peter Marks, M.D., Ph.D., director of the FDA’s Center for Biologics Evaluation and Research, to discuss vaccine injuries and why the agencies were doing nothing to address them.
In those meetings, according to Dressen and React19 member Dr. Joel Wallskog, when they raised the issue that the agencies weren’t following up on VAERS reports, the FDA told them VAERS wasn’t a reliable indicator for vaccine injuries, because anyone could file an injury complaint, including “Mickey Mouse or Michael Jackson.”
“We told them we know thousands of people that have not had any follow-up on their VAERS reports that are not Mickey Mouse, and they’re suffering it every single day waiting for you guys to get back to them to investigate what happened to them,” Dressen said.
“And of course then they never did anything. So we were like, OK, fine. If they’re not going to generate the evidence, then we will ourselves.”
The group submitted their findings to Marks during a meeting with him and his team. Based on their findings they also requested an external audit of the entire VAERS system and posed a series of questions listed on their audit report webpage.
They never heard from the agencies again.
“We were like, really?” Dressen said. “We were having these regular meetings with them every one month or every two months, and then after that, they wouldn’t meet with us anymore.”
Dressen, who was injured in the AstraZeneca clinical trials and whose diagnosis of post-vaccine neuropathy and other vaccine-related disorders was confirmed by the National Institutes of Health, said her own VAERS report is not visible to the public. The agencies haven’t told her why.
More recently, still hoping for accountability from the public health agencies, React19 submitted its audit and complaint to the Office of Inspector General at the U.S. Department of Health and Human Services.
The only response they received was an autoresponse confirming receipt of the complaint.
Attempt to ‘bring power back to the people’
In its small pilot audit, React19 found the VAERS system is “obviously broken from top to bottom.” According to Dressen, “One thing we can easily conclude is that the FDA and CDC have no interest in addressing these issues.”
Now, the group is scaling up the project to do a larger audit with more data.
With help from OpenVAERS and CHD, the team built a backend, automated administrative tracking system that eliminates the need to manually search for each report and its journey through VAERS — something the analysts had to do for the first iteration of their audit.
Participants will register on the React19 website and will be invited — if they are interested — to share their stories as part of the organization’s project to collect and publish vaccine injury testimonials.
Users can share any information they have about their VAERS report — their ID number if they have one, or if not, details about their case. Then they will receive a monthly email with the status of their report.
For example, someone who has a user ID and a public-facing report will be informed if their report disappears. In the case of those people who filed a VAERS complaint but never got an ID number, the system will search each month for the record and try to find the ID.
“We’ll be able to track these reports through the system and figure out what happens to them,” Wilner said. “Do they disappear? Do they appear and the person doesn’t get notified? Do they appear incorrectly?”
“So people will be able to track their own reports with less effort and React19 will be able to audit a much larger user base than they initially did.”
Wilner said auditing VAERS in this way also reveals details about how the agencies are “either lying or deliberately obfuscating the process.” In the first audit, it was clear there was no systematic or automated way that, for example, reports were deleted.
The tracker and the audit will provide valuable data that no one else has. Rather than having only the stories, Wilner said, they will have the data backing up those stories. “Now we have a group of injured people that are all talking with one voice.”
“Without more pressure and more discovery,” Wallskog said, “I don’t think we’re ever going to get the truth out. Ultimately, we want to get this information to the masses of people that just don’t know what’s happening, particularly with this data, and that we’ve all been duped.”
Dressen said the project is an attempt to “bring the power back to the people.”
The COVID-19 vaccine produced a large swath of vaccine injuries all at the same time, she said. Auditing the COVID-19 entries in VAERS will provide an opportunity “to show through massive numbers where those problems are, not just with the systems that are supposed to be monitoring vaccine safety, but also the actual harms themselves and what those are, but the government’s not doing their job on that.”
The two faces of VAERS and the problem of accountability
Wilner said Dressen’s injury report, sitting in VAERS limbo, spoke to one of the major issues around claims of transparency in the database — that there are two versions of VAERS, a public-facing database and a private one.
The BMJ reported last year that it investigated the VAERS database and found that the public facing database contains only initial reports. And “a private, back end system containing all updates and corrections — such as a formal diagnosis, recovery, or death.”
The CDC told The BMJ that this was part of patient confidentiality, but the publication found that in the FDA’s Adverse Event Reporting System, they do update the database — “raising the question of why VAERS can’t do the same.”
And during the React19 audit, the group found that VAERS was sometimes deleting people’s legitimate reports or the more detailed updated reports that some people were submitting.
Another problem, Wilner noted, is that a lot of key information — such as race, pregnancy and report provider — is unnecessarily withheld from public VAERS reports. She also said the agencies sometimes leave reports on there that are clearly false or jokes, which then discredits the database in the public’s eyes.
On the CDC website, Wilner said, “you’re basically looking at a doctored set of books.”
Wallskog said the agencies “try to live on both sides of the fence” with VAERS, presenting it as a key tool for monitoring vaccine injuries. But when it shows a safety signal or an issue with vaccines, they discredit it as a problematic surveillance system with a lot of limitations that can’t be trusted.
“It’s incredibly frustrating for injured people,” he said.
The team working on the new VAERS tracking system and audit said they hope it will raise public awareness and force the public health agencies to take responsibility for the vaccine injuries.
“Rochelle Walensky said the CDC is charged with finding legitimate vaccine injuries and reporting them,” Wilner said. She added:
“If that’s the case, where is that? We don’t have access to the actual database to figure it out so we want to know where is the report from the CDC on the people that were actually injured by the COVID vaccine that the government accepts were legitimately injured? That report doesn’t exist.”
This article was originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.
Demand for Justice: World Council for Health urges the immediate release of Dr. Reiner Füellmich
World Council for Health | September 10, 2024
The international human rights community is rallying to demand the immediate release of Dr. Reiner Füellmich, a lawyer from Germany who has been in pre-trial detention for over 10 months. Arrested under dubious circumstances at Frankfurt Airport on October 13, 2023, Dr. Füellmich’s case has raised serious concerns regarding the legality of his detention and the integrity of the judicial process. Of the initial 18 charges made against Füellmich, only one remains regarding personal loans.
According to German law, the maximum duration of pre-trial detention is six months, as outlined in 121 para. 1 of the German Code of Criminal Procedure (StPO). “Special or important reasons for an extension of pre-trial detention beyond the 6 months are not apparent.” This assertion highlights the urgent need for a re-evaluation of Dr. Füellmich’s ongoing detention.
In a significant development, it has come to light that Dr. Christof Miseré, one of the defense attorneys representing Füellmich, obtained a dossier from the German secret services. This document explicitly outlines a directive to halt Füellmich by any means necessary. Alarmingly, it details a strategy to infiltrate individuals within his inner circle of collaborators. Furthermore, the dossier reveals a clear objective: to convict Fuellmich, thereby obstructing any future aspirations he may have for public or political office. This information raises serious questions about the lengths to which authorities may go to silence dissenting voices. This dossier, given to Miseré by a whistleblower, demonstrates that Reiner Füellmich was already under special surveillance as far back as 2021.
Adding to the controversy is the manner of Dr. Füellmich’s arrest. He was reportedly “kidnapped” from Mexico, where he had been residing legally. A German and a European arrest warrant were issued against him, ostensibly to circumvent lengthy international extradition procedures. The Göttingen public prosecutor’s office collaborated closely with officers from Interpol and the Federal Criminal Police, orchestrating a deceptive plan to lure Dr. Füellmich to the Mexican consulate under false pretenses, an act that raises significant legal and ethical questions about the conduct of authorities involved.
Despite multiple assertions from both his defense and Dr. Füellmich himself regarding the illegality of his deportation, these concerns have been largely dismissed in court. Lawyers argue that the circumstances surrounding his abduction and subsequent detention underscore critical national and international legal issues that must be addressed.
Currently held in Rosdorf Prison near Göttingen, Dr. Füellmich faces harsh and isolating conditions. He is segregated from other inmates, permitted only solitary yard time, and restricted in his communication with the outside world, limited to a mere three hours of private visits per month. This punitive environment raises further questions about the treatment of individuals in pre-trial detention, particularly when contrasted with the lack of substantial evidence to justify such measures. On June 11, Reiner Füellmich was once again placed in solitary confinement, a status he continues to endure. This isolation means he is prohibited from any interaction with other inmates. The authorities justified this extreme measure by alleging that Füellmich had been providing legal advice to his fellow prisoners, a situation deemed unacceptable by those overseeing his incarceration. Füellmich is required to eat in isolation and is granted just one hour each day for outdoor activity, which is also spent in complete solitude. He is not allowed access to the gymnasium and can only use the telephone after other inmates have returned to their cells. This strict regimen underscores the severity of his confinement and the restrictions imposed upon him.
The charges against Dr. Füellmich include embezzlement, yet many observers, including his defense, contend that this trial has transcended ordinary judicial proceedings and has become a politically motivated effort to silence a prominent critic of COVID-19 measures. The trial has seen troubling shifts in legal parameters, further complicating the case and undermining the principles of justice.
In light of these serious allegations and the apparent disregard for due process, World Council for Health is calling for the immediate release of Dr. Reiner Füellmich. This situation not only affects one individual but also serves as a stark reminder of the potential for political influence to infiltrate the judiciary, compromising the very foundations of justice and fairness.
As the international freedom movement watches closely, it is imperative that justice prevails and that Dr. Füellmich is granted the freedom he deserves, freedom that is essential not only for him but for the integrity of the legal system itself.
Take action now – Sign the petition calling for the release of Reiner Füellmich
Episode 388: SIRI TESTIFIES: NEW HAMPSHIRE “POST-LICENSURE SAFETY”
The HighWire with Del Bigtree | September 5, 2024
The next installment of attorney Aaron Siri’s expert testimony before the New Hampshire House Committee on COVID Response Efficacy. In this episode, ICAN’s lead attorney exposes the shortcomings of post-licensure safety, and shatters the claim that the connection between vaccines and autism has been ‘thoroughly studied.’
Guest: Aaron Siri, Esq.
My Biggest Battle – The Movie
August 21, 2024
Narrator: John Bowe
HART:
A new documentary titled “My Biggest Battle” explores the life-altering journey of renowned
extreme triathlete Heiko Sepp after receiving a COVID-19 vaccination. The 35-minute film
highlights Heiko’s incredible athletic accomplishments, the onset of debilitating health
complications, and his relentless search for answers while suffering from post-vaccination
injuries.
“My Biggest Battle” is more than just a documentary—it’s a conversation starter. Our hope is
that Heiko’s battle encourages the public to share this powerful film to raise awareness about
the challenges faced by individuals like Heiko. By sharing his story, you contribute to an
important dialogue supporting those impacted by vaccine-related events.
The documentary paints a vivid picture of Heiko’s life in Norway, where he lives with his wife
and their two young sons. Known for his remarkable achievements in extreme triathlons,
including podium placements in grueling races like the Norseman, Heiko’s passion for the sport
is central to his identity. However, everything changed in September 2021 when Heiko received
his second COVID-19 vaccination. What began as chest pain rapidly escalated into a series of
debilitating symptoms, including heart inflammation, joint pain, and muscle spasms, leaving
Heiko’s once vibrant life shrouded in pain and uncertainty.
The film follows Heiko’s challenging journey through countless hospital visits, medical tests, and
consultations with healthcare professionals. Despite his lifelong peak health and athletic
prowess, Heiko faces a healthcare system that offers few answers and little relief. As Heiko’s
search for a diagnosis leads him to an esteemed immunologist, the documentary delves into the
emerging understanding of vaccine-induced autoimmunity and its implications for people like
Heiko. The film concludes with a message of hope and resilience, raising critical questions
about vaccine safety and healthcare accessibility.
FUNDRAISER FOR HEIKO’S FAMILY:
Due to Heiko’s illness, he has been unable to maintain stable employment, depleting his
savings on costly private treatments. Facing the brink of bankruptcy, Heiko has launched a
personal fundraiser to alleviate the financial strain and continue his necessary treatments.
Despite the risks, Heiko’s decision to share his story is vital, bringing attention to post
vaccination injuries—a topic few are willing to address.
We urge the media and public to support Heiko’s fundraiser and spread the word about his
story.
Support Heiko’s Fundraiser: GoFundMe
CONTACT INFORMATION:
heikoseppfilm@gmail.com
http://www.heikosepp.com
Heiko’s story of injury after the first dose and yet still being advised to take a second shot with devastating consequences, is unfortunately a common occurrence. Any doctor will tell you that if you have penicillin allergy you must never receive it again, and yet the medical profession seemed happy to follow this quite extraordinary advice re covid vaccines, as if they couldn’t get the mantra ‘Safe & Effective’ out of their minds. His story of the failures of the medical profession in Norway to diagnose and treat him, is also mirrored across the world.
Most Variation in All-Cause Mortality Explained by Mass COVID-19 Vaccination
Australian Ecological Analysis Points to Vaccine Campaign Causing Rising Death Counts
By Peter A. McCullough, MD, MPH | Courageous Discourse | September 1, 2024
After a pandemic, all cause mortality should go down due to a culling effect of the frail and vulnerable. We saw acute COVID-19 become the proximate cause of death in many seniors who were in the final year of natural life.
Now an analysis from Allen indicates that all-cause mortality is up in heavily vaccinated Australia and that at least two thirds in the variation per region is explained by mass COVID-19 vaccination. There are numerous well-documented fatal vaccine serious adverse events which are piling up months and years after the shots. Cumulative toxicity is another factor as a single person is not vaccinated just with the primary series (first two injections), but continued dosing every six months.

Allen, DE. 2024. The correlation between Australian Excess Deaths by State and Booster Vaccinations. Medical Research Archives, [online] 12(7).https://doi.org/10.18103/mra.v1 2i7.5485
These data call for a direct data merge of the vaccine administration and death data in Australia to explore these very uncomfortable relationships. Because the Australian government pushed the vaccines so hard, officials have been stonewalling the public on this important next analysis.
Japan’s Largest MSM Broadcaster, NHK, Releases Groundbreaking Feature on mRNA Vaccine Harms
PharmaFiles by Aussie17 | August 30, 2024
Japanese citizens were shocked on the morning of August 28 as their largest national broadcaster, NHK, decided to air a special feature on the COVID-19 vaccine relief system. This program highlighted real-life experiences of individuals who have suffered severe side effects, prompting an overwhelming public response with over 2000 messages received.
In a surprising turn of events, NHK’s popular Morning Show, Asaichi, has taken a bold step. Once dismissive of doubts about vaccine safety, the show recently focused on the challenges and realities faced by those affected by mRNA experimental vaccine side effects. This change in stance marks a pivotal U-Turn in the ongoing national conversation about the experimental mRNA’s safety and transparency.
The program’s new focus was echoed in the unexpected surge of viewer engagement. “We have received more than 2000 messages from viewers today. Thank you very much,” the host announced, signaling widespread public interest and concern.
One chilling account came from a viewer who detailed their struggle after the third vaccine dose: “My headaches became severe. Although they have lessened since the beginning, the symptoms have persisted for more than two years. It has been two and a half years of vaccine aftereffects.” Frustration with the bureaucratic hurdles in seeking relief was evident: “It’s difficult to go collect documents because of my leg pain, so I urgently wish the process to be simplified as soon as possible.”
Another viewer recounted a deeply personal tragedy: “Right after vaccination, my mother developed a serious illness and passed away.” Their story was not just about personal loss, but also about the social repercussions of questioning vaccine side effects. “During the period when I was collecting application documents after my mother’s illness and passing, I’ve been met repeatedly with heartless comments just for questioning the connection with the vaccine.”
The show also featured Misu from Ibaraki Prefecture, a former healthcare worker in her 40s, who shared her ongoing battle. Since receiving her third dose, she has struggled with “pain and numbness in the vaccinated arm, fatigue, and other symptoms.” Misu’s plea was simple yet profound: “I hope the government and media report this properly. Voices are being raised to spread awareness about the suffering caused by side effects.”
This feature on NHK’s Asaichi has not only brought attention to individual struggles but has also highlighted a broader societal issue: the difficulty in openly discussing vaccine side effects without backlash. It presents a call to action for society to foster an environment where sharing such experiences does not invite judgment but rather understanding and empathy.
Two days following the national broadcast, Japan’s Health Minister, Keizō Takemi, made an unexpected statement: “Regarding whether health damage from the COVID-19 vaccine constitutes drug-induced injury, our response at this point is that we would like to refrain from commenting.”
It looks like they are no longer saying that it is 100% safe and effective!
$3,000 and a Toy: Novavax Dangles Incentives to Fill Clinical Trials on COVID Shots for Babies, Kids
By Brenda Baletti, Ph.D. | The Defender | August 29, 2024
Novavax is offering parents up to $3,000 to enroll their children in the vaccine maker’s Phase 2/3 COVID-19 vaccine trial for infants and children ages 6 months to 11 years. The offer also includes a stuffed animal for each child.
The “Hummingbird” trial is testing two primary shots and a booster shot of Novavax’s adjuvanted recombinant spike protein nanoparticle vaccine in children. The study, which began in 2022, is enrolling 3,600 children.
The study, which began in the U.S., is expected to run through 2025 and will be conducted in the U.S. and other countries.
The children will receive three injections and visit the clinic eight times. Parents will participate in three phone calls and keep an e-diary of the vaccine’s effects on their child. Some children will receive two additional injections, for a total of five shots.
The study website promises, “You will be compensated for your time and travel regardless of your immigration status. Transportation to the study site may also be provided, as available. No health insurance is required to participate.”
Recruitment materials from Be Well Clinical Studies, which is running one of the U.S. trials, state that compensation can be more than $3,000 over two years.
A 2023 video explaining the study also promises incentives for the children, including “a Covid stuffed animal.”
In the video, a pastor from Louisiana who has four children enrolled in the study said incentives like the stuffed animal made the kids even “more excited than the parents” to participate.
The video features Dr. Jibran Atwi who is running a Hummingbird trial in Lafayette, Louisiana. He encouraged people to participate in the study, because COVID-19 severely affected kids, particularly through lockdowns and lost schooling.
Atwi also said that COVID-19 can be “very disruptive” because if a child has to stay home from school, parents may not be able to go work and the child may have to be isolated from their grandparents.
“Prevention,” he said, “is the best medicine.” He added that there had been an “impressive response” from parents who wanted to participate.
Research shows that young children rarely get sick from COVID-19 and that the illness is typically mild in older kids.
Atwi received over $2 million in research funding in 2023 from Big Pharma, according to the Open Payments website.
Most of that funding came from Genzyme — a Sanofi subsidiary — and from Sanofi, which shares the co-exclusive licensing agreement with Novavax to commercialize its COVID-19 vaccine.
In 2022, Atwi received over $1 million, largely from AstraZeneca and Genzyme.
Last week, the U.S. Food and Drug Administration (FDA) granted emergency use authorization to Pfizer and Moderna’s 2024-2025 mRNA COVID-19 shots, but Novavax’s 2024-2025 formula has not yet been authorized.
The FDA has authorized previous versions of the Novavax vaccine, but only for children ages 12 and up.
High payments place children ‘at risk of coercion’
Other pharmaceutical companies that have paid research subjects large sums of money have come under scrutiny. In the United Kingdom (U.K.), Moderna was criticized for initially offering children’s families 1,505 pounds ($1,984 dollars) to participate in its NextCOVE clinical trial, which is testing Moderna’s mRNA vaccine in children ages 12 and up.
The Children’s Covid Vaccine Advisory Council submitted a complaint to the U.K.’s Prescription Medicines Code of Practice Authority (PMCPA) — an industry trade group that regulates ethical practices — raising concerns about “inappropriate financial inducement” offered to children and their parents to participate in the trial.
The council cited concerns raised by the research ethics committee (REC) that approved the clinical study. Regarding the 1,500-pound payment they wrote:
“This amount seems much higher than what would be considered a reasonable reimbursement and therefore would contravene clinical trial regulations. The Medicines for Human Use (Clinical Trials) Regulations (2004) explicitly prohibit the giving of incentives or financial inducements to children… or their parents.”
The REC said the amount, “placed the children at risk of coercion,” and the organization required that Moderna reduce the offer before recruitment could begin. Moderna reduced the amount to 185 pounds ($244 dollars).
Yet, according to the complaint, at least one pediatrician continued to offer the high enrollment compensation.
The PMCPA sanctioned Moderna, and the case report on the issue is currently pending.
If the PMCPA determines a pharmaceutical company has breached the industry code, it can require the company to pay administrative charges or issue a corrective statement. Or, it may request a compulsory audit of the company.
In the U.S., Be Well is also advertising that it will pay parents $2,400 for enrolling their infants and toddlers, ages 5-23 months, in Moderna’s Rhyme Trial for an mRNA RSV and a human metapneumovirus (hMPV) vaccine.
According to the clinicaltrials.gov website, Be Well withdrew from the Moderna RSV study, but the website is still advertising to recruit participants.
Be Well is run by founder and director Dr. Mark Carlson, a geriatrician, who has taken nearly $3 million in research funding from Big Pharma, mostly from Moderna, since 2021.
Moderna did not respond to The Defender’s inquiry about compensation offered to children’s families to participate in these studies.
This article was originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.
Biden-Harris Administration Defends Big Tech Censorship Pressure Following Zuckerberg’s Admission

By Didi Rankovic | Reclaim The Net | August 28, 2024
The Biden-Harris White House looks determined to justify and normalize the practice of the government colluding with private companies, in this instance Big Tech, to censor speech.
After Meta CEO Mark Zuckerberg on Monday sent a letter to the House Judiciary Committee, admitting that his company came under pressure from the current administration to conduct censorship and that he “believes” that was wrong – the White House doubled down on the controversial, and quite possibly, unconstitutional, policy.
In his letter, Zuckerberg chose to focus on Meta censoring content related to COVID-19, and in response, a White House spokesman revealed the government does not share Zuckerberg’s stance that the policy of pressure was wrong.
“Encouragement” is how that’s phrased. “When confronted with a deadly pandemic, this administration encouraged responsible actions to protect public health and safety,” stated the White House spokesman to media requests.
He further justified the actions described by Zuckerberg as needed because the White House believes private companies, including those from the tech industry, “should take into account the effects their actions have on the American people.”
And with the stage set in this way – the spokesman concluded that these companies are then free to make “independent choices about the information they present.”
But Zuckerberg’s letter to the Judiciary Committee Chairman Jim Jordan does a pretty good job of explaining how these “independent choices” get made. Senior figures from the Biden administration, Zuckerberg stated, in 2021 “repeatedly pressured our (Facebook, Instagram) teams for months to censor certain COVID-19 content, including humor and satire.”
The decision on content removal, and introduction of new rules into platform policies to facilitate censorship, Zuckerberg concedes, was “ultimately ours” – but made under pressure.
If Meta tried to defy these “suggestions” – the administration showed “a lot of frustration.”
“I believe the government pressure was wrong, and I regret that we were not more outspoken about it,” the letter, sent in response to the Committee’s subpoena first issued in early 2023, reads.
The Committee has been investigating how the government may have colluded with private companies to suppress speech it disapproves of, and whether those actions constitute First Amendment violations.
Even before the current Biden-Harris administration came to power, Facebook was being steered in a desired direction, one example being the notorious case of the censorship of the Hunter Biden laptop news story, the Zuckerberg letter reveals.
The FBI contacted the social media giant with a “warning” that there could be an anti-Biden family “Russian disinformation” campaign – and Facebook heeded it by “fact-checking and temporarily demoting (links to the article).”
