Chossidmom's Spam Thread of Covid Vaccine Info - welcome

amother

↑ Gladiolus ↓

Tue, Jul 19 2022, 2:19 pm

Thinking about it all day…
CM you are right
People who fell into the lie are not heard enough saying “I made a mistake. Now more information has been revealed. I am sorry.” All the more so people to whom we may have looked up to and followed. A great person can be humble b’ezras Hashem.

amother

↑ Gladiolus ↓

Tue, Jul 19 2022, 2:31 pm

Heard rabbi Abraham sutton discussing this at length and don’t want to misrepresent his words about how there is an opportunity in this darkness. A great opportunity.

↑ ChossidMom ↓

Tue, Jul 19 2022, 2:40 pm

Who is Rabbi Sutton?

And notice that not only are people not saying "whoops", many people on this site are attacking me for posting this info. I was called a "shill" and people here suspect I have ulterior motives. Well guess what? My ulterior motive is to save lives. I am certainly not too popular for what I am doing. People do not want to be faced with the sheer evil and ugliness of what is happening.

amother

↑ Gladiolus ↓

Tue, Jul 19 2022, 2:53 pm

True
It can be overwhelming for some who can get defensive/aggressive R”L
Not an excuse
We are living through challenging times
May we be blessed to have this pressure bring out the best in us our higher and highest levels of our neshoma and our mission here now.
I really appreciate the information you are bringing and your really genuine kavana.
Rabbi Sutton is an amazing person he and his family Iive in E”Y worth looking him up his books videos shiurim. He is a living treasure. Very kind humble and makes himself accessible.
Much of what I have heard him say seems to me to be aligned with what you have posted.
He is empowering and inspiring and grasps the big picture. Insightful and illuminating.
A transformer of klipah

amother

↑ Pear ↓

Tue, Jul 19 2022, 2:58 pm

amother [ Gladiolus ] wrote:

Yes at least we can admit and apologize for any mistakes we have made while acting under misinformation or lack of updated and accurate info .

Who apologized?

amother

↑ Apple

Tue, Jul 19 2022, 2:59 pm

Thank you for posting all this info.

amother

↑ Gladiolus ↓

Tue, Jul 19 2022, 3:00 pm

I really feel for you CM. I know friends who left
E”Y for a time who felt the pressure was so intense and unrelenting.
And others who stayed and were more able to just do their own thing.

↑ ChossidMom ↓

Tue, Jul 19 2022, 3:17 pm

amother [ Gladiolus ] wrote:

I really feel for you CM. I know friends who left
E”Y for a time who felt the pressure was so intense and unrelenting.
And others who stayed and were more able to just do their own thing.

h

Nah. I am strong and I B"H have a lot of strong backbone in the form of my husband. We are the kind of people about whom they say במקום שאין איש תהיה איש or something like that. I know that I have a mission in this world. It may change from time to time but I know clearly, that right now it is very important to use whatever tools and forums I have to publicize the Emes. So, maybe I lose friends over this but if this is what is going to make me lose friends - they couldn't have been real friends to begin with. I never attack anyone personally and try to keep all my discussions respectful.

At the beginning of this plandemic, my siblings were pressuring me horribly about taking it. I was being accused of being the cause of all the ECMO machines being taken up by the "unvaccinated" and I was told that people like me were causing the health system to collapse. Really. But, since I am only interested in Shalom Bayis with my family and real friends, I just stopped reacting to their messages and kept up positive communications with them. B"H today, they are all triple (and maybe more) jabbed and I am not. They all had Covid and even gave it to me recently. But we have Shalom because that is the most important value. I do not inundate them with all the info that I put here. This is a topic we do not discuss. Because I value Shalom over doing the same thing to them that they did to me last year. I don't lord it over them either, that most of the people in the hospitals and most of the severe cases are jabbed. No point in that. For that I come here and post. Whoever has an open mind is welcome to read my posts. Whoever doesn't want to can just skip them. This way I know that I have done MY hishtadlus.

amother

↑ Gladiolus ↓

Tue, Jul 19 2022, 3:21 pm

I hear you.
Much continued hatzlocha in health and happiness.

tryinghard ↓

Tue, Jul 19 2022, 4:08 pm

ChossidMom, do you have any information about J&J? Everything I’ve been able to find about AEs and studies has been Pfizer with occasional Moderna.

amother

↑ Pear ↓

Tue, Jul 19 2022, 4:12 pm

tryinghard wrote:

ChossidMom, do you have any information about J&J? Everything I’ve been able to find about AEs and studies has been Pfizer with occasional Moderna.

Wondering the same. I'm hoping jj wasn't as dangerous because it doesn't have mrna.

mommyof5

Tue, Jul 19 2022, 6:13 pm

The Novavax Covid vaccine was approved by the FDA last week and approved by the CDC today. It is more of a traditional vaccine - similar to the shingles vaccines. So - it is not giving MRNA instructions to make spike protein (like Pfizer and Moderna) and not giving instructions via an adenovirus (like th J&J). I’m both It actually delivers the spike protein with an adjuvant (bark of a tree) to boost the reaction. Like all viruses - there are side effects but nothing major. This is already available in Canada, the UK and other countries. This should be available in the US in next week/month. If I had to take any I would take this one.
There were very few cases of myocarditis and pericarditis seen - but these are also seen in rare cases after Covid. IY”H this will be available soon.
Much less side effects than the other Covid vaccines and no deaths so far -that I have heard of.
It will only be available to people above 18.

amother

↑ Gladiolus ↓

Tue, Jul 19 2022, 6:14 pm

But what is the point of taking it now?
And is it even geared to the current strains of mutation of covid?

↑ ChossidMom ↓

Tue, Jul 19 2022, 6:23 pm

amother [ Gladiolus ] wrote:

But what is the point of taking it now?
And is it geared to the current strains of mutation of covid?

Have a look at this very short clip regarding Novovax. Dr. Cole explains how it works.

https://rumble.com/v17wpbt-doe......html

amother

Tulip

Tue, Jul 19 2022, 6:35 pm

amother [ Gladiolus ] wrote:

But what is the point of taking it now?
And is it geared to the current strains of mutation of covid?

There are still those that are being required to take it at this date - any person starting medical or nursing school for example.
Most medical or nursing schools will NOT give any exemptions to the vaccine - so even if you managed to avoid it until now - if you want to go school -you need to take it.

amother

↑ Gladiolus ↓

Tue, Jul 19 2022, 6:47 pm

I see. Thanks for the update. Not taking anything and have that choice B”H

↑ #BestBubby ↓

Tue, Jul 19 2022, 6:56 pm

Delete

Last edited by #BestBubby on Wed, Jul 20 2022, 10:28 am; edited 1 time in total

amother

Crocus

Tue, Jul 19 2022, 10:37 pm

#BestBubby wrote:

There are some doctors who will write they vaxxed you....

But only if you are their patient and they know you a long time and trust you.

Why would you trust a doctor like this? If he'll lie for you, why wouldn't he lie TO you?

↑ ChossidMom ↓

Tue, Jul 19 2022, 11:49 pm

05/06/22

COVID › NEWS

FDA Limits Use of J&J Vaccine Over Blood Clotting Disorder, But Experts Say Pfizer, Moderna Shots Pose Similar Risk

The U.S. Food and Drug Administration on Thursday put strict limits on the use of Johnson & Johnson’s COVID-19 vaccine, citing the risk of a blood clotting condition, but experts say that Pfizer and Moderna pose similar risks.

By

Julie Comber, Ph.D.

28

The U.S. Food and Drug Administration (FDA) on Thursday put strict limits on the use of the Johnson & Johnson (J&J) COVID-19 vaccine, citing the risk of a blood-clotting condition the agency described as “rare and potentially life-threatening.”

In a statement Thursday, the FDA said the risk of vaccine recipients developing thrombosis with thrombocytopenia syndrome (TTS) after receiving the vaccine “warrants limiting the authorized use of the vaccine.”

The FDA said it has identified 60 cases of vaccine-induced thrombosis with thrombocytopenia syndrome, including nine deaths, out of about 18 million doses administered — although the condition is likely underreported.

Women 30 to 49 years old are at the highest risk of TTS from the J&J vaccine, with about eight cases per 1 million doses of vaccine administered, according to the FDA.

According to the latest data from the Vaccine Adverse Event Reporting System (VAERS), between Dec. 14, 2020, and April 29, 2022, there were 13,873 reports of blood-clotting disorders following COVID-19 vaccines in the U.S.

Of those, 6,227 reports were attributed to Pfizer, 4,943 reports to Moderna and 2,662 reports to J&J.

In the U.S., 575 million COVID-19 vaccine doses had been administered as of April 29, including 339 million doses of Pfizer, 217 million doses of Moderna and 19 million doses of J&J.

The agency said the “known and potential benefits” of the J&J vaccine for preventing COVID-19 outweigh the known and potential risks for individuals 18 and older “for whom other authorized or approved COVID-19 vaccines are not accessible or clinically appropriate,” or “who elect to receive the Janssen COVID-19 vaccine because they would otherwise not receive a COVID-19 vaccine.”

The agency described TTS as “a syndrome of rare and potentially life-threatening blood clots in combination with low levels of blood platelets with onset of symptoms approximately one to two weeks following administration of the Janssen [J&J] COVID-19 vaccine.”

The updated restrictions to the Emergency Use Authorization (EUA) of the vaccine, marketed under the Janssen brand, also apply to booster doses, CNN reported.

People who can still get the Janssen vaccine include:

Those who had a severe allergic reaction to the Pfizer/BioNTech or Moderna mRNA vaccine.Those with personal concerns about the mRNA vaccines who would remain unvaccinated unless they can choose the Janssen vaccine.Those with limited access to mRNA COVID-19 vaccines.

Symptoms of TTS include shortness of breath, chest pain, leg swelling, persistent abdominal pain, neurological symptoms (like headaches or blurred vision) or red spots just under the skin called “petechiae” found beyond the site of injection.

Experts question timing, and why just J&J?

Peter Marks, M.D., Ph.D., director of the FDA’s Center for Biologics Evaluation and Research, said limiting the authorized use of the Janssen vaccine “demonstrates the robustness of our safety surveillance systems and our commitment to ensuring that science and data guide our decisions.”

Marks said:

“We’ve been closely monitoring the Janssen COVID-19 Vaccine and occurrence of TTS following its administration and have used updated information from our safety surveillance systems to revise the EUA.

“The agency will continue to monitor the safety of the Janssen COVID-19 Vaccine and all other vaccines, and as has been the case throughout the pandemic, will thoroughly evaluate new safety information.”

However, Brian Hooker, Ph.D., P.E., Children’s Health Defense chief scientific officer and professor of biology at Simpson University, had a different take on the news.

“It seems like the FDA pays lip service to the fact that the spike protein can cause clotting, and to the widespread reports of clotting, by punishing Janssen, who has become the ‘whipping boy’ of the COVID-19 vaccine manufacturers through the pandemic,” Hooker said.

“I believe this is partially because of the limited use of the Janssen vaccine in the U.S. as compared to Pfizer and Moderna,” he added.

Hooker said the FDA can limit the use of the J&J vaccine without significantly impacting vaccine distribution overall, “while having the appearance of addressing the myriad vaccine adverse events caused by all the types of COVID-19 vaccines.”

As of Thursday, CNN reported only 7.7% of those considered fully vaccinated received the J&J vaccine.

Dr. Pierre Kory, founder and president of Front Line COVID-19 Critical Care Alliance, told The Defender:

“My only hypothesis is this action is some attempt for the FDA to be able to claim that they took at least some action to protect the safety of the public, akin to ‘virtue signaling.’

“Having been a keen observer of their actions throughout the pandemic, I find this action to be completely insufficient and demonstrates a calculated attempt to ensure vaccinations with similarly dangerous vaccines continue.”

Dr. Meryl Nass questioned the timing of the FDA’s restriction of the EUA.

“Why did the FDA just throw the kill switch on the Janssen vaccine, when it knew of the thrombosis problems since the rollout?” Nass asked.

Nass told The Defender the FDA may have known about the thrombosis problem even before the Janssen vaccine rollout, “since the adenovirus vector platform is known to be associated with thrombosis” for “more than 15 years.”

Kory, who noted that all COVID-19 vaccines have had a high rate of adverse events, also questioned the timing of the new restrictions.

It's Time to Follow the Science. Join our Campaign!

“I find the timing of this action to be both irrational and alarming given there is extensive data from around the world, much of it being censored from media and medical journals, that all the COVID-19 vaccines, not just Janssen, have long had unacceptable and diverse toxicity signals — beyond just clotting disorders from numerous pharmacovigilance databases and epidemiological and public health data reports,” Kory said.

As far back as April 2021, U.S. and European health officials were investigating whether the J&J COVID-19 vaccines were causing blood clots.

However, there was already mounting evidence the Pfizer and Moderna vaccines could cause similar adverse reactions. U.S. regulatory officials were alerted to this risk as far back as December 2020.

The Centers for Disease Control and Prevention (CDC) in December 2021 recommended the Pfizer and Moderna mRNA COVID vaccines over the J&J vaccine due to the risk of blood clots, despite data showing the Pfizer and Moderna shots also cause blood-clotting disorders.

In January 2021, shortly after the rollout of Pfizer’s vaccine in the U.S., The Defender reported on the death of a 56-year-old Florida doctor who developed a blood-clotting disorder after the Pfizer vaccine and died 12 days later.

The Defender also reported on numerous other deaths related to blood-clotting disorders that developed after the Moderna and J&J vaccines.

The J&J vaccine received EUA on Feb. 27, 2021.

On April 13, 2021, the FDA and CDC paused use of the vaccine to investigate six reported cases of TTS.

The agencies lifted the pause only 10 days later, after confirming a total of 15 cases of TTS had been reported to VAERS, including the original six reported cases, out of approximately 8 million doses administered.

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Julie Comber is a freelance science reporter for The Defender.

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↑ ChossidMom ↓

Wed, Jul 20 2022, 12:03 am

04/27/22

COVID NEWS WATCH

Guillain-Barré Rates Unusually High After J&J Vaccine + More

The Defender’s COVID NewsWatch provides a roundup of the latest headlines related to the SARS CoV-2 virus, including its origins and COVID vaccines.

By

The Defender Staff

Guillain-Barré Risk After COVID Vaccines Low, Surveillance Data Show — but Rates Continue to Be Unusually High After Johnson & Johnson Shot

MedPage Today reported:

Risk of Guillain-Barré syndrome after COVID-19 vaccines was low overall, but unusually high after the Johnson & Johnson shot, surveillance data showed.

Among 15.1 million doses of COVID-19 vaccines included in the Vaccine Safety Datalink, the unadjusted incidence rate of confirmed Guillain-Barré syndrome 1 to 21 days after receiving the Johnson & Johnson vaccine was 32.4 per 100,000 person-years, significantly higher than the background rate, reported Nicola Klein, MD, PhD, of Kaiser Permanente Northern California in Oakland, and colleagues.

The findings confirm data seen in the Vaccine Adverse Event Reporting System (VAERS) that led to the FDA warning about the Johnson & Johnson vaccine in July 2021.