Why would anyone subject their children to an experimental drug that has no long term studies on side effects. I'm so sorry about her child. The FDA , CDC, NIH, President Biden and anybody demanding mandates are in my opinion attempted murders and in 15,000 reported cases, are infact murdered. My option, my opinion and my right to refuse.
The rules of the trial were that all recipients experiencing side effects were to have them addressed by a study doctor. Seeking medical care outside of the study automatically results in the subjects removal from the study. Since severe side effects are likely to result in an emergency room visit at the local hospital, this ensures the majority of serious side effects will be pared from the study data.
Your letter is amazing. The phone call with the Pfizer trial principal investigator is disturbing. I can't imagine what this family has been through. How the FDA could approve this mRNA product for 12-15 year olds is beyond me.
I maintain that no clinical trials for any C19 "vaccine" should have been conducted because children have an extremely low risk from this virus. In light of this child's devastating injury, there can be no justification to risk grave injury (or worse) to another healthy child in an expanded trial. None.
Aaron Siri IMO has excellent judgement when it comes to the veracity of witnesses. I would think that because it fits exactly with mine. I watched an interview on Bitchute with Stephanie and she comes across as direct and truthful, a nice family who have a social conscience (which is why Maddie wanted to participate.)
Stephanie stated publicly that there was blood in the urine and that Maddie's fingers were white and cold to the touch. That speaks to endothelial dysfunction, the root cause of autoimmune illnesses and are objective symptoms that would have been documented during her frequent hospitalisations. I recall an opinion piece in the Lancet that was critical of pfizer for not even considering the potential of their drug to cause autoimmune conditions.
If you're young, you probably don't know how many times the government has poisoned Americans "for the greater good." And said it's all in their heads. They've been poisoning people at least since WWII using radiation and other poisons on purpose.
Until a politician's child is harmed or dies from a vaccine, we won't see these ill conceived liability indemnification laws change. The silver lining in these tragedies is that people are waking up to the big pharma mafia who put profits over people's lives. Their products rarely promote health. On the contrary, they create the diseases that they profess to cure. Until we change the liability laws, they will continue to act with impunity. Thanks again Aaron for giving victims a much needed voice and to wake up the populace that these vaccines were never about saving lives. It's all part of the New World Order agenda.
Pfizer should never have been permitted to skip a full set of animal trials. What we've learned from the Japanese release of information on Pfizer's inadequate preliminary animal trial is troubling. to say the least.
There are two CBER/FDA lists of possible serious adverse event outcomes known to be associated with these Covid-19 "vaccines" at least two months prior to the December, 2020, Covid-19 vaccine roll-outs; and, since then, the FDA has not been forthcoming with this information.
The FDA's withholding of this information from potential Covid-19 vaccine recipients is a violation of the FDA's disclosure requirement for EUA vaccines. All vaccines currently being administered within the U.S. are only EUA. The Pfizer Comirnaty vaccine, which has received full FDA approval, but is reportedly not chemically or structurally different from the EUA version, is not yet available within the U.S.. Apparently, Pfizer first wants to get rid of its current EUA packaged product.
There are two such serious adverse event outcome lists, which were included in separate October 22, 2020, CBER slide presentations to FDA heads:
1) Available at https://www.fda.gov/media/143530/download is the presentation by Tom Shimabukuro, MD, MPH, MBA, MBA of the CDC COVID-19 Vaccine Task Force, Vaccine Safety Team. Page/Slide 31 is titled, "Preliminary list of VAERS AEs of special interest". AE signifies "Adverse Event".
2) Available at https://www.fda.gov/media/143557/download is the presentation by Steve Andersen, PhD, MPP, who is the Director, Office of Biostatistics & Epidemiology, CBER. Page 17, known as "slide 16", is the "FDA Safety Surveillance of COVID-19 Vaccines : DRAFT Working list of possible adverse event outcomes"
Please note the differences between these two lists: The Shimabukuro slide additionally contains Multiple sclerosis (MS), Optic neuritis (ON), Chronic inflammatory demyelinating polyneuropathy (CIDP), and Ataxia; but, is missing Vaccine enhanced disease which is also known as Antibody Dependent Enhancement (ADE).
The fact there are eighty (80) Autoimmune diseases brings the total number of possible serious Adverse Event outcomes to approximately one hundred and ten (110).
If these CBER/FDA lists had been disclosed to Maddie and her parents, would they still have decided to enroll her in the trial?
If the medical community and the general public were to be made fully aware of these FDA lists of possible serious adverse event outcomes, the public narrative would be vastly different than it is at the moment, as the alleged Covid-19 "vaccines" would begin to lose all legitimacy,
In my opinion, by some means, we need to get these CBER/FDA lists into the hands of every physician and allied healthcare worker. Only then, will the physician and allied healthcare worker "vaccine-injury" doubters begin to realize that the diseases they are witnessing in their vaccinated patients are the vaccine-associated diseases in these FDA lists.
Thank you for your thoughtful response and comments. I do appreciate all you have said, and I agree with all you have said, including the statement about skipping animal trials. My comment was not intended to oppose, but rather to add a thought. It really gets very philosophical quickly as soon as ethics in research is touched upon. As I read all these comments, I appreciate the opportunity to be among all of you.
Consider: ozone therapy IV (for cellular healing), ivermectin, Colchine, plavix. Consider researching on your own and being your own advocate- get onto LinkedIn with Covid doctors throughout world. So sorry this has happened to you. Would be nice if this was in the news
As for the comments on this site slamming the de Garays for subjecting their children to an experimental drug, I'd like to point out that all over the world parents are subjecting their children to an experimental drug. They're guilty of nothing more than having misplaced trust in authority.
At least 3 children have died and 120 been hospitalised from Pfizer in Vietnam:
Maddie's parents are putting up with vilification because they are speaking out. They are trying to PREVENT what happened to their daughter happening to other people's children.
I listened very carefully to the interview with Stephanie below. There were other parents whose children were enrolled in the trial. How many of them are keeping quiet about a severe adverse reaction because they don't want people "wondering" why they enrolled their child in such a clinical trial?
Why would anyone subject their children to an experimental drug that has no long term studies on side effects. I'm so sorry about her child. The FDA , CDC, NIH, President Biden and anybody demanding mandates are in my opinion attempted murders and in 15,000 reported cases, are infact murdered. My option, my opinion and my right to refuse.
The rules of the trial were that all recipients experiencing side effects were to have them addressed by a study doctor. Seeking medical care outside of the study automatically results in the subjects removal from the study. Since severe side effects are likely to result in an emergency room visit at the local hospital, this ensures the majority of serious side effects will be pared from the study data.
Your letter is amazing. The phone call with the Pfizer trial principal investigator is disturbing. I can't imagine what this family has been through. How the FDA could approve this mRNA product for 12-15 year olds is beyond me.
I maintain that no clinical trials for any C19 "vaccine" should have been conducted because children have an extremely low risk from this virus. In light of this child's devastating injury, there can be no justification to risk grave injury (or worse) to another healthy child in an expanded trial. None.
This poor child and family. Now they are looking for approval in 5-11?!?! Criminals!
Aaron Siri IMO has excellent judgement when it comes to the veracity of witnesses. I would think that because it fits exactly with mine. I watched an interview on Bitchute with Stephanie and she comes across as direct and truthful, a nice family who have a social conscience (which is why Maddie wanted to participate.)
Stephanie stated publicly that there was blood in the urine and that Maddie's fingers were white and cold to the touch. That speaks to endothelial dysfunction, the root cause of autoimmune illnesses and are objective symptoms that would have been documented during her frequent hospitalisations. I recall an opinion piece in the Lancet that was critical of pfizer for not even considering the potential of their drug to cause autoimmune conditions.
It's all over for pfizer.
If you're young, you probably don't know how many times the government has poisoned Americans "for the greater good." And said it's all in their heads. They've been poisoning people at least since WWII using radiation and other poisons on purpose.
Until a politician's child is harmed or dies from a vaccine, we won't see these ill conceived liability indemnification laws change. The silver lining in these tragedies is that people are waking up to the big pharma mafia who put profits over people's lives. Their products rarely promote health. On the contrary, they create the diseases that they profess to cure. Until we change the liability laws, they will continue to act with impunity. Thanks again Aaron for giving victims a much needed voice and to wake up the populace that these vaccines were never about saving lives. It's all part of the New World Order agenda.
Pfizer should never have been permitted to skip a full set of animal trials. What we've learned from the Japanese release of information on Pfizer's inadequate preliminary animal trial is troubling. to say the least.
There are two CBER/FDA lists of possible serious adverse event outcomes known to be associated with these Covid-19 "vaccines" at least two months prior to the December, 2020, Covid-19 vaccine roll-outs; and, since then, the FDA has not been forthcoming with this information.
The FDA's withholding of this information from potential Covid-19 vaccine recipients is a violation of the FDA's disclosure requirement for EUA vaccines. All vaccines currently being administered within the U.S. are only EUA. The Pfizer Comirnaty vaccine, which has received full FDA approval, but is reportedly not chemically or structurally different from the EUA version, is not yet available within the U.S.. Apparently, Pfizer first wants to get rid of its current EUA packaged product.
There are two such serious adverse event outcome lists, which were included in separate October 22, 2020, CBER slide presentations to FDA heads:
1) Available at https://www.fda.gov/media/143530/download is the presentation by Tom Shimabukuro, MD, MPH, MBA, MBA of the CDC COVID-19 Vaccine Task Force, Vaccine Safety Team. Page/Slide 31 is titled, "Preliminary list of VAERS AEs of special interest". AE signifies "Adverse Event".
2) Available at https://www.fda.gov/media/143557/download is the presentation by Steve Andersen, PhD, MPP, who is the Director, Office of Biostatistics & Epidemiology, CBER. Page 17, known as "slide 16", is the "FDA Safety Surveillance of COVID-19 Vaccines : DRAFT Working list of possible adverse event outcomes"
Please note the differences between these two lists: The Shimabukuro slide additionally contains Multiple sclerosis (MS), Optic neuritis (ON), Chronic inflammatory demyelinating polyneuropathy (CIDP), and Ataxia; but, is missing Vaccine enhanced disease which is also known as Antibody Dependent Enhancement (ADE).
The fact there are eighty (80) Autoimmune diseases brings the total number of possible serious Adverse Event outcomes to approximately one hundred and ten (110).
If these CBER/FDA lists had been disclosed to Maddie and her parents, would they still have decided to enroll her in the trial?
If the medical community and the general public were to be made fully aware of these FDA lists of possible serious adverse event outcomes, the public narrative would be vastly different than it is at the moment, as the alleged Covid-19 "vaccines" would begin to lose all legitimacy,
In my opinion, by some means, we need to get these CBER/FDA lists into the hands of every physician and allied healthcare worker. Only then, will the physician and allied healthcare worker "vaccine-injury" doubters begin to realize that the diseases they are witnessing in their vaccinated patients are the vaccine-associated diseases in these FDA lists.
This reminds me of the documentary “Vaxxed. So much about dangers of MMR vax was wilfully covered up. Now this one, too. It’s infuriating.
That poor girl. I can’t imagine the guilt the parents must be feeling
Thank you for your thoughtful response and comments. I do appreciate all you have said, and I agree with all you have said, including the statement about skipping animal trials. My comment was not intended to oppose, but rather to add a thought. It really gets very philosophical quickly as soon as ethics in research is touched upon. As I read all these comments, I appreciate the opportunity to be among all of you.
Consider: ozone therapy IV (for cellular healing), ivermectin, Colchine, plavix. Consider researching on your own and being your own advocate- get onto LinkedIn with Covid doctors throughout world. So sorry this has happened to you. Would be nice if this was in the news
FDA, CDC ....Fauchi are liars !!!
They have falsified death counts since day one !!!!! There test is useless and they continue to lie and mislead the people every day ????
Dr. Nath's comment is very telling.
As for the comments on this site slamming the de Garays for subjecting their children to an experimental drug, I'd like to point out that all over the world parents are subjecting their children to an experimental drug. They're guilty of nothing more than having misplaced trust in authority.
At least 3 children have died and 120 been hospitalised from Pfizer in Vietnam:
https://trialsitenews.com/at-least-three-children-die-120-hospitalized-by-pfizer-biontech-vaccine-in-vietnam/
Maddie's parents are putting up with vilification because they are speaking out. They are trying to PREVENT what happened to their daughter happening to other people's children.
I listened very carefully to the interview with Stephanie below. There were other parents whose children were enrolled in the trial. How many of them are keeping quiet about a severe adverse reaction because they don't want people "wondering" why they enrolled their child in such a clinical trial?
https://trialsitenews.com/at-least-three-children-die-120-hospitalized-by-pfizer-biontech-vaccine-in-vietnam/
The blame should be ENTIRELY on Pfizer, the NIH and the FDA and NOT the de Garays.