A letter to the Federal Minister for Health and Aging Mr. Greg Hunt


The Honorable Greg Hunt MP
Federal Minister for Health and Aging
PO Box 647
Somerville, Vic 3912

Dear Mr. Hunt,

On behalf of the tens of thousands of members and supporters of The Australian Vaccination-Risk Network (AVN), we write to you with numerous concerns about the COVID-19 vaccination cycle. We demand, in accordance with the precautionary principle, that current mRNA and viral vector vaccination experiments be immediately discontinued until independent safety science and efficacy tests can be made available. We are aware that Queensland, from 21st May 2021, has abandoned the AstraZeneca viral vector vaccination program due to injuries and deaths after vaccination.

We are very concerned that COVID-19 vaccines are only given temporary TGA approval under the State of Emergency declaration and that the decision to vaccinate the Australian public is made on the basis of short-term effectiveness and safety. in the data. It is provided by TGA and AHPRA with no longitudinal scientific data related to the risk / benefit profile. Why is our government forcing Australians to have experimental indices made, sold and distributed less than a year ago when previous vaccine development took between 10-15 years?

In a conversation with Contents you stated:

“The world is doing the most clinical trials, the most vaccination trials in the world, and we have a lot of data.”

As you have publicly acknowledged, these injections have even gone through clinical trials, and anyone who can shoot is already part of an experiment.

Why don’t you instruct health professionals to let every person who receives the shot know that they are participating in an experiment? Informed consent is essential for any medical procedure such as the Australian Vaccination Handbook and the Nuremberg Code.

These Covid vaccines are not necessary. Consistent with the CDC’s best estimate today, the “infection death rate” (IFR) for Covid-19 is less than 1 percent for people age 69 and older. Vaccine makers say COVID-19 vaccines are 95 percent “effective,” but the FDA allows companies to describe effectiveness as “avoiding mild symptoms.” Studies were not designed to determine the reduction in outcomes such as severe illness, hospitalization or death. For individuals who have developed severe symptoms, the vaccine is not the solution. However, nutritional and oxidative support can help prevent the disease from going into “overdrive.” Peter Doshi from the British Medical Journal is concerned that current trials are not designed to show whether injections can save any lives. In fact, reports from the start of the launch in countries around the world indicate that vaccines cause death and injury.

Participants in each COVID-19 vaccine trial reported adverse reactions including high fever, chills, muscle aches and headache. Some even report severe reactions requiring hospitalization and invasive treatment. According to the FDA, potential long-term effects may include Guillain-Barré syndrome, brain inflammation, muscle weakness and paralysis, nausea and vomiting, stroke, narcolepsy, thrombosis with thrombocytopenia syndrome (TTS), shock. , heart attack, autoimmune disease, arthritis and joint disease, multisystem inflammatory syndrome in children, and death.

Some health workers in the UK have experienced anaphylactic shock after receiving a dose of the approved vaccine and the UK government has warned those with severe allergies to avoid Pfizer injection. Providers are given full compensation, freedom from liability even if all previous attempts to create coronavirus vaccines have caused harm and
never advanced in regulatory approval.

Sadly, we have seen dire consequences of government-supported and unnecessary, untested experimental injections in people around the world. As of May 14, 2021, the number of reported deaths in the U.S. following COVID-19 vaccines was 4,201 according to data released today by the Centers for Disease Control and Prevention (CDC). Data comes directly from reports submitted to the Vaccine Adverse Event Reporting System (VAERS). A U.S. Harvard Study concluded that “fewer than 1% of injuries were reported” in the database. Each week, VAERS notifies all reports of vaccine damage received as of a specified date, usually about a week before the release date.

Between December 14, 2020 and May 14, 2021 there were a total of 227,805 adverse events, including 4,201 deaths. This is alarming but not surprising because there is no data suggesting safety for the following groups of people: Anyone younger than age 18 or older than age 55, pregnant or breastfeeding mothers , those with autoimmune conditions and immunocompromised individuals. Safety for other age groups is not as convincing as the clinical trial for Pfizer, and AstraZeneca will not end in 2023.

In Australia, more than 19,598 adverse events were reported on May 20, 2021 according to a report on the TGA website. We have also heard that thousands of women around the world report that the menstrual cycle is disrupted after receiving COVID-19 vaccines. The UK government’s vaccine malpractice reporting system has collected more than 2,200 times of reproductive diseases after coronavirus injections, including excessive or no menstrual bleeding, delayed menstruation, menstrual cramps. vaginal, annihilation, and stillbirth.
Two prominent doctors, including the ex-head of respiratory research Pfizer, warn that Covid-19 vaccines contain a protein called syncytin-1, essential for placental formation. If the vaccine triggers the immune response to this protein, it can result in female infertility, miscarriage or childbirth.

On Monday 22 February 2021, COVID-19 vaccination began in Australia. As of May 12, TGA had received 6 reports of Guillain-Barre Syndrome (GBS) after injection of the AstraZeneca COVID-19 vaccine. There have also been TGA reports of 18 cases of Thrombosis with thrombocytopenia syndrome (TTS), a debilitating condition that leaves the patient with low platelet levels and a tendency to bleed at the same time, and with fat fat rate of 25%. Reports on May 2 showed that there were approximately 20 cases of anaphylaxis reported in Australia per million doses of Comirnaty vaccine. How many vaccination reactions are actually reported in the TGA database as adverse reactions? Do frontline medical staff know they can and should report a suspected adverse event following vaccination? We know that according to a study done by Harvard less than 1% of all adverse reactions are submitted to VAERS, so we can only assume (because there is no study done by the government in Australia) whose percentage is the same as in Australia.

Known consent was omitted. According to the Australian Immunization Handbook on the TGA website, informed consent is essential. It says:

Valid consent is the voluntary agreement by an individual on a proposed procedure, provided after sufficient, appropriate and reliable information about the procedure, including potential risks and benefits, is communicated to the individual and must be provided voluntarily. without. by undue coercion, coercion or manipulation.

Approved by the Royal Australian College of General Practitioners:

Informed consent is the process by which a patient makes a voluntary decision about their medical care with knowledge and understanding of the benefits and potential risks involved. A patient should only agree to the proposed treatment if he or she has been provided with sufficient information including benefits, associated risks and management options, so that they can make an appropriate decision about their own care. health.

Obviously, we cannot make an informed choice unless we have the full information to do so. This clinical trial we participated in did not meet the full disclosure requirements and therefore this vaccination program had to be stopped immediately. Many Australians have been pressured and pressured to take the vaccine against their will due to the ongoing Australian government discussion about restrictions imposed on those who do not agree with the Covid-19 vaccine. This is against Australia’s values ​​as an independent country where citizens have the right to make their own informed medical judgments.

We look forward to receiving a written response to our concerns and we call for urgent action in response to the information above, ensuring a halt to the launch of COVID-19 vaccines for the safety of all Australians.

Sincerely,
Ms. Meryl Dorey
President, Australia Network (AVN) Risk
On behalf of AVN Members and our supporters
Cc: / The Hon Mark Butler MP, Shadow Minister for Health and Aging

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