“I do not like the late resurrection of the Jesuits. … the Jesuits in the U.S. are more numerous than everybody knows. Shall we not have swarms of them here, in as many shapes and disguises as ever a King of the Gypsies, Bamfied More Carew himself, assumed? In the shape of printers, editors, writers, school masters etc?… If ever any congregation of men could merit eternal perdition on earth and in hell… it is this company of Loyola [founder of the Jesuits].”
Letter From 2nd U.S. President John Adams to Thomas Jefferson, 6 May 1816 (see here)
“The Jesuits are the deadly enemies of civil and religious liberty.”
This is a continuation of this post reporting on the comments of medical staff on the Medscape forum.
I have a patient who developed cranial nerve 3 palsy 4 days after the 2nd dose of Pfizer. The following week she cannot open her left eye. I referred her to a neurologist. MRI did not show stroke or aneurysm.
2 other patients with stable stage 1 cancer, developed progression of their disease after the second dose of the vaccines within days.. COINCIDENCE? I don’t think so. We need to look closer into this. We just can’t ignore the side effects. “FIRST DO NO HARM”. I have 100% success with either HCQ or Ivermectin. Treat early!!!
Dr. Erich Glenn Acebedo
I am a Master’s prepared Registered Nurse with 41 years experience, and the elected coroner for my county. Since Covid vaccinations began this year, I have seen 16 post Covid vaccine deaths, some immediate, and 2 complete cardiovascular collapse after the second injection (Moderna). They had immediate third spacing, became cyanotic, and it was impossible to obtain post-mortem blood samples due to highly clotted blood, even pericardial. One patient who received her first injection of Moderna in the pharmacy had an immediate allergic reaction, followed by a myocardial infarction that week. A stent was placed, and clotted off 2 days after discharge while she was on her way home. I have diligently reported all to the FDA, and pray that these vaccines do NOT get approved.
Marie Lasater
Is anyone hearing of stories of blood clots months after getting Pfizer covid shot?…I’m a pharmacist
The website Medscape put up a forum in February of this year for medical professionals to discuss their expectations and concerns about the new COVID-19 injections.
I spent over an hour today reading through all these comments.
There are both positive comments towards the shots and negative comments. This is the kind of dialog that should have been happening in a public forum on a much larger scale from the beginning, but of course that was never the plan, to monitor the execution of the emergency use authorization of these shots to determine if they were safe.
This is more than 3 hours long; about the last 1 1/2 hours is Dr Mike Yeadon explaining all the deliberate lies of most of our governments and their medical agencies. He explains that only logical conclusion one can draw is that it has all been about getting the world to sign up for a digital identity and thus totalitarian control.
The SARS-CoV-2 virus is a little worse than a bad flu and is nothing to be worried about. But the same cannot be said of the experimental injections, especially the gene modifying mRNA vaccines. All COVID vaccines are dangerous and with unknown long term safety issues. There is evidence now that suggests they do interfere with pregnancy causing abortions. But the real danger is if we give into this totalitarian control over our lives we will never get our freedoms back. It is pure evil what the deep state cabal have planned.
I implore you to watch this video. And please share it with your friends and family. I believe we are on the cusp of total mass extermination. The so-called booster shots for the so-called COVID variants may be the real programmed death shots. He says if the vaccines work your immune system can easily handle any variants. That is basic immunology. So why are the manufacturers preparing billions of booster shots. They are the extermination shots the sheeple will line up to get.
Stew Peters interviews Brittany Galvin who after her second Moderna shot has develop the very serious Guillain-Barre Syndrome. She is the same 35 year old mother who showed how keys and other magnetic objects would stick to her body after the experimental injections.
All the vaccines (flu, polio, MMR, etc) are contaminated with many different animal viruses which cause all the diseases people have been experiencing for many decades now. This includes coronaviruses in the experimental COVID injections. This means the current COVID injections spread the disease. But we also know the so-called vaccines are the real bio-weapons.
But Dr Judy Mikovits real message is that the medical industrial complex, which is driven by profits and power, is corrupt to the core. It is a plague of corruption more than plague of disease. The blood supply has been contaminated by the vaccines which have been contaminated by animal viruses for many many decades.
Our world, once thriving with energy and life, has now become a dystopian landscape of barren streets and masked people with a look of foreboding in their eyes.
Governments around the world have enforced unprecedented restrictions on people’s lives, imposing lockdowns that closed down most of society for months at a time. Stopping people from visiting their family, isolating the elderly in care homes and destroying millions of people’s livelihoods.
By Gavin Phillips
These draconian laws were brought in to control an alleged pandemic created by a new virus called SARS-CoV-2 that creates the respiratory illness of Covid 19. The numbers of so called ‘cases’ and deaths ‘attributed to Covid’ are churned out daily by the media fanning the fear. The hurricane force driving this pandemic is the reverse transcription polymerase chain reaction test (RT-PCR). So, it’s vitally important that we understand exactly how the RT-PCR test works and its limitations.
The PCR test was invented by the late American Kary Mullis in the mid 1980’s for which he received the Nobel Prize in 1993 in Chemistry. Mullis died in August 2019.
The European Medicines Agency is misleading citizens into medical experimentation, experts warn. Doctors and scientists from 25 countries have today issued a rebuttal letter to the European Medicines Agency (EMA), following the regulator’s dismissal of their earlier warnings regarding COVID-19 vaccine dangers from clotting and bleeding.
Within days of the EMA receiving the group’s original letter on March 1st, outlining risks of blood disorders from COVID-19 vaccines, over a dozen countries suspended the AstraZeneca vaccine following deaths from clotting and bleeding, as the doctors had warned.
On March 23rd, however, the EMA dismissed the group’s concerns as relating to “minor” and “rare” events, concluding that “a positive benefit-risk balance has been established.”
The doctors and scientists have today hit back, accusing the EMA of misleading the public on the vaccines’ true risk-benefit profile. “Your reply of March 23 is unconvincing and unacceptable,” they wrote, noting that recorded cases of life-threatening cerebral venous thrombosis (CSVT) post-vaccination likely “represent just the tip of a huge iceberg”. Common reactions to vaccination, including headache, nausea, blurred vision and vomiting, they state, are symptoms of CSVT, and should be assessed as such, immediately.
Clotting and bleeding after vaccination can also “be expected to increase with each re-vaccination, and each intervening coronavirus exposure” the group warned. Over time “this renders both repeated vaccination and common coronaviruses dangerous to young and healthy age groups, for whom — in the absence of ‘vaccination’ — COVID-19 poses no substantive risk.
The European database of suspected drug reaction reports is EudraVigilance, which also tracks reports of injuries and deaths following the experimental COVID-19 “vaccines.”
Here is what EudraVigilance states about their database:
This website was launched by the European Medicines Agency in 2012 to provide public access to reports of suspected side effects (also known as suspected adverse drug reactions). These reports are submitted electronically to EudraVigilance by national medicines regulatory authorities and by pharmaceutical companies that hold marketing authorisations (licences) for the medicines.
EudraVigilance is a system designed for collecting reports of suspected side effects. These reports are used for evaluating the benefits and risks of medicines during their development and monitoring their safety following their authorisation in the European Economic Area (EEA). EudraVigilance has been in use since December 2001.
This website was launched to comply with the EudraVigilance Access Policy, which was developed to improve public health by supporting the monitoring of the safety of medicines and to increase transparency for stakeholders, including the general public.
The Management Board of the European Medicines Agency first approved the EudraVigilance Access Policy in December 2010. A revision was adopted by the Board in December 2015 based on the 2010 pharmacovigilance legislation. The policy aims to provide stakeholders such as national medicines regulatory authorities in the EEA, the European Commission, healthcare professionals, patients and consumers, as well as the pharmaceutical industry and research organisations, with access to reports on suspected side effects.
Transparency is a key guiding principle of the Agency, and is pivotal to building trust and confidence in the regulatory process. By increasing transparency, the Agency is better able to address the growing need among stakeholders, including the general public, for access to information. (Source.)
