Thank you. I really appreciate all your comments and I read most of them. I feel badly that I was so matter of fact last time. If I agree, I don't say anything. So that must be the first time I disagreed on a strategic opinion kind of thing. Opinions are fair game to banter and critique. Facts are not. I just read my comment again and I know that I can sound harsh sometimes when I'm just laying out a case and going fast through stuff. Sorry about that.
No worries, John, and actually, your comment did not seem harsh to me, simply straight forward. (What is always challenging is to communicate by way of typing into these itsy bitsy text boxes.)
There, among many other interesting he has to say, Rees posts a link to the package insert for the gene therapy, and he notes:
***QUOTE***
CAR T Therapies get FDA Black Box Warning
FDA issues new boxed warning for CAR T-cell therapies, By Sabina Ray, Jan 30, 2024
Extract below:
Initially, the benefits of CAR T-cell therapy in lymphoma, leukemia, and multiple myeloma were thought to outweigh the risk of T-cell malignancy. However, in November 2023 the FDA emphasized a need to monitor CAR T-cell therapy clinical trials and post-marketing adverse event reporting throughout patients’ entire lives, enabling the identification of new malignancies and testing for the CAR gene when they occur.
Currently, six CAR T-cell therapies have been approved in the US:
tisagenlecleucel
brexucabtagene autoleucel
ciltacabtagene autoleucel
lisocabtagene maraleucel
idecabtagene vicleucel
axicabtagene ciloleucel
US FDA was quick to react, with
2024 Safety and Availability Communications
This is listed in November 27, 2024:
FDA Investigating Serious Risk of Hematologic Malignancy Following Skysona (elivaldogene autotemcel)
In layperson terms, it means there was evidence that CAR T therapies could cause secondary cancers.
This is the first CAR T therapy to be approved by FDA, in August 2017:
Kymriah (tisagenlecleucel) and the package insert.
John, If you or anyone happening to be reading this comment haven't seen Hedley Rees' work I can highly recommend it. I might also suggest, as a good general introduction to what Rees does, and what he's observed, watching the in-depth interview by UK Column's Debi Evans. For those who don't do video, I made a transcript of 6 excerpts:
Yes as do I. I wish someone could use the data. My father was killed by Remdesivir in 2021. I just met a woman who lost her 47YO husband to Remdesivir in the same year.
One puzzle here is that acute kidney injury deaths will occur almost exclusively in the intensive care unit, and death will occur while under clinical care, ie these deaths will be found on death reports, and not via autopsy of out-of-hospital sudden death.
It is hard to die of renal failure in the era of dialysis or continuous renal therapy (the temporary ICU version of dialysis).
This makes me wonder if some throttling of dialysis occurred from 2021 onward, such that cases of death attributed to kidney failure rose.
Have you touched base with nephrologists or intensivists regarding your findings?
The latter in particular should be aware of a surge in mortality.
Agreed on most. The thing I often say about AKI N17 is that if it's on a death record, then it happened. Unless they're sent home to die in a few days or hospice, they usually die in-hospital. And they usually have detailed medical charts like creatinine levels and protein levels. They have urine and blood tests every day. So the data is really good in the death records. Compared to cardiac arrhythmia or cardiac arrest, AKI is a specific and credible code that actually represents something traceable. The two cardiac ones are so abstract that they mean next to nothing except a change in data occurred. So N17 is a very good dataset. The dialysis issue is important. The market actually dropped when so many died from "covid" in 2020. But in a very short time, the dialysis market picked back up when they started vaccinating. The way to determine that is to do a study of "new" patients. Looking at patients for dialysis may not show any increase because of all the ones that were killed. But new patients to dialysis will show the truth
My then 21 y.o. daughter died on this day in 2007 of what had been diagnosed as a 'very rare' autoimmune disease called 'Goodpasteurs Syndrome' which has since been renamed.
Her problems started with sudden kidney failure in 2006.
She was the healthiest of my three children suffering few of the childhood illnesses that I had.
I now believe that any random collection of symptoms labelled a 'syndrome' is harmaceutical code for vaccine poisoning and that Frances was probably a victim of an NHS vaccine program.
"Medical science has made such tremendous progress that there is hardly a healthy human left." ~ Aldous Huxley, he died on the same day as JFK in 1963, how correct he was!
Well obviously we know Remdesivir causes kidney failure. And hospitals were/are financially incentivized to use Remdesivir on the unvaccinated. The 'Children's Health Defence' have had so many anecdotal stories from the bereaved relatives of it's victims and even some survivors of the Remdesivir protocol, though sadly not as many of the latter.
The Remdesivir administered was/is documented in the patients records.
Fauci's creation of the virus in Wuhan with US taxpayer money, and then the mandates to inject very dangerous and worse-than-ineffective experimental mRNA were the worst crimes against humanity ever.
Shortly after we relocated cross-country to Connecticut for a job, My husband had kidney cancer (stage 3B) in May 2020 and lost one of his kidneys. Connecticut (where we lived) and New York (Where he worked) were two of the biggest offenders with vax mandates, and vaccine passports to keep your job and ability to perform daily activities of life like grocery shopping. We paid a heavy financial, professional and personal cost but refused to jeopardize his one and only kidney. We had to sell our dream home, pick up and move to a place we never intended to live and start over again. However, we will never regret the decision to refuse the shot for our family. Reading articles such as this confirm for us that we made the correct decision, and our gut instinct and critical thinking were dead on.
I have a sister-in-law she’s in her 50’s. Perfectly healthy,thin and active. Suddenly hospitalized with end stage renal failure. Took them a couple of weeks to get her stable. We can’t get very detailed information about what is happening. Husband said they called it an amyloidosis protein that destroyed her kidneys and damaged her heart. She’s on dialysis 3 days a week and starts chemo today….We know that she got the initial 2 vaccines. As far as boosters go-don’t know…
Excellent and important. Thank you.
Thank you. I really appreciate all your comments and I read most of them. I feel badly that I was so matter of fact last time. If I agree, I don't say anything. So that must be the first time I disagreed on a strategic opinion kind of thing. Opinions are fair game to banter and critique. Facts are not. I just read my comment again and I know that I can sound harsh sometimes when I'm just laying out a case and going fast through stuff. Sorry about that.
No worries, John, and actually, your comment did not seem harsh to me, simply straight forward. (What is always challenging is to communicate by way of typing into these itsy bitsy text boxes.)
LOL. You missed the joke. That’s a parody list. There is nothing “cute” about kidney injury.
It’s increasingly obvious that Covid was created for the vax, not the other way ‘round.
Covid was created for a deep state coup d'état.
The vax was created for cover.
xfer of power
xfer of property/wealth
subjugation of the middle class
Hi John Beaudoin, I immediately thought your this post of yours when I saw pharma logistics expert Hedeley Rees's latest post:
https://hedleyrees.substack.com/p/big-pharma-companies-were-going-broke/comments
There, among many other interesting he has to say, Rees posts a link to the package insert for the gene therapy, and he notes:
***QUOTE***
CAR T Therapies get FDA Black Box Warning
FDA issues new boxed warning for CAR T-cell therapies, By Sabina Ray, Jan 30, 2024
Extract below:
Initially, the benefits of CAR T-cell therapy in lymphoma, leukemia, and multiple myeloma were thought to outweigh the risk of T-cell malignancy. However, in November 2023 the FDA emphasized a need to monitor CAR T-cell therapy clinical trials and post-marketing adverse event reporting throughout patients’ entire lives, enabling the identification of new malignancies and testing for the CAR gene when they occur.
Currently, six CAR T-cell therapies have been approved in the US:
tisagenlecleucel
brexucabtagene autoleucel
ciltacabtagene autoleucel
lisocabtagene maraleucel
idecabtagene vicleucel
axicabtagene ciloleucel
US FDA was quick to react, with
2024 Safety and Availability Communications
This is listed in November 27, 2024:
FDA Investigating Serious Risk of Hematologic Malignancy Following Skysona (elivaldogene autotemcel)
In layperson terms, it means there was evidence that CAR T therapies could cause secondary cancers.
This is the first CAR T therapy to be approved by FDA, in August 2017:
Kymriah (tisagenlecleucel) and the package insert.
https://www.fda.gov/media/107296/download
***END OF QUOTE***
From the PDF of that package insert
https://www.fda.gov/media/107296/download
***QUOTE***
------------------------------ADVERSE REACTIONS------------------------------
Pediatric and Young Adult B-cell ALL (up to 25 years of age): The most
common adverse reactions (incidence greater than 20%) are CRS, infections-
pathogen unspecified, hypogammaglobulinemia, fever, decreased appetite,
viral infectious disorders, headache, febrile neutropenia, hemorrhage,
musculoskeletal pain, vomiting, encephalopathy, diarrhea, hypotension,
cough, nausea, bacterial infectious disorders, pain, hypoxia, tachycardia,
edema, fatigue, and acute kidney injury. (6.1)
Adult Relapsed or Refractory Diffuse Large B-cell Lymphoma: The most
common adverse reactions (incidence greater than 20%) are CRS, infections-
pathogen unspecified, fever, diarrhea, nausea, fatigue, hypotension, edema,
hemorrhage, dyspnea, and headache. (6.1)
Adult Relapsed or Refractory Follicular Lymphoma: The most common
adverse reactions (incidence greater than 20%) are CRS, infections-pathogens
unspecified, fatigue, musculoskeletal pain, headache, and diarrhea. (6.1)
***END OF QUOTE***
Looks like a list of excess deaths I found 2.5 years ago. Amazingly similar list.
John, If you or anyone happening to be reading this comment haven't seen Hedley Rees' work I can highly recommend it. I might also suggest, as a good general introduction to what Rees does, and what he's observed, watching the in-depth interview by UK Column's Debi Evans. For those who don't do video, I made a transcript of 6 excerpts:
Transcript: https://transcriberb.dreamwidth.org/150689.html
Source video:
From Molecule to Man: The Lifecycle of an MHRA Medicine
UK Column News, Debi Evans, October 31, 2022
https://rumble.com/v1qsasc-from-molecule-to-man-the-lifecycle-of-an-mhra-medicine-that-will-fail.-uk-c.html
I don't know who might find it useful but I have a full set of medical records for analysis on a hospital death.
Make sure you tell the facts and story at CHBMP.org
Their database of murders by protocol will be used in court cases in the future.
Yes as do I. I wish someone could use the data. My father was killed by Remdesivir in 2021. I just met a woman who lost her 47YO husband to Remdesivir in the same year.
Make sure you tell the facts and story at CHBMP.org
Their database of murders by protocol will be used in court cases in the future.
Weep. I mean..its so sad. So sorry for you all
Excellent reporting, John.
One puzzle here is that acute kidney injury deaths will occur almost exclusively in the intensive care unit, and death will occur while under clinical care, ie these deaths will be found on death reports, and not via autopsy of out-of-hospital sudden death.
It is hard to die of renal failure in the era of dialysis or continuous renal therapy (the temporary ICU version of dialysis).
This makes me wonder if some throttling of dialysis occurred from 2021 onward, such that cases of death attributed to kidney failure rose.
Have you touched base with nephrologists or intensivists regarding your findings?
The latter in particular should be aware of a surge in mortality.
Agreed on most. The thing I often say about AKI N17 is that if it's on a death record, then it happened. Unless they're sent home to die in a few days or hospice, they usually die in-hospital. And they usually have detailed medical charts like creatinine levels and protein levels. They have urine and blood tests every day. So the data is really good in the death records. Compared to cardiac arrhythmia or cardiac arrest, AKI is a specific and credible code that actually represents something traceable. The two cardiac ones are so abstract that they mean next to nothing except a change in data occurred. So N17 is a very good dataset. The dialysis issue is important. The market actually dropped when so many died from "covid" in 2020. But in a very short time, the dialysis market picked back up when they started vaccinating. The way to determine that is to do a study of "new" patients. Looking at patients for dialysis may not show any increase because of all the ones that were killed. But new patients to dialysis will show the truth
My brother in law had the jab and a booster and all the sudden had the death of his left kidney with zero previous issues or health problems
That was an impressive piece. Fantastic writing. Lots of hard work goes into our education. Thank you.
My then 21 y.o. daughter died on this day in 2007 of what had been diagnosed as a 'very rare' autoimmune disease called 'Goodpasteurs Syndrome' which has since been renamed.
Her problems started with sudden kidney failure in 2006.
She was the healthiest of my three children suffering few of the childhood illnesses that I had.
I now believe that any random collection of symptoms labelled a 'syndrome' is harmaceutical code for vaccine poisoning and that Frances was probably a victim of an NHS vaccine program.
"Medical science has made such tremendous progress that there is hardly a healthy human left." ~ Aldous Huxley, he died on the same day as JFK in 1963, how correct he was!
So sorry.!!
Well obviously we know Remdesivir causes kidney failure. And hospitals were/are financially incentivized to use Remdesivir on the unvaccinated. The 'Children's Health Defence' have had so many anecdotal stories from the bereaved relatives of it's victims and even some survivors of the Remdesivir protocol, though sadly not as many of the latter.
The Remdesivir administered was/is documented in the patients records.
Written proof of this Democide.
More about Remdesivir Disaster
https://geoffpain.substack.com/p/remdesivir-deaths-was-endotoxin-a
Fauci's creation of the virus in Wuhan with US taxpayer money, and then the mandates to inject very dangerous and worse-than-ineffective experimental mRNA were the worst crimes against humanity ever.
https://patrick.net/post/1377537/2022-11-03-everyone-who-imposed-toxxine-mandates
Shortly after we relocated cross-country to Connecticut for a job, My husband had kidney cancer (stage 3B) in May 2020 and lost one of his kidneys. Connecticut (where we lived) and New York (Where he worked) were two of the biggest offenders with vax mandates, and vaccine passports to keep your job and ability to perform daily activities of life like grocery shopping. We paid a heavy financial, professional and personal cost but refused to jeopardize his one and only kidney. We had to sell our dream home, pick up and move to a place we never intended to live and start over again. However, we will never regret the decision to refuse the shot for our family. Reading articles such as this confirm for us that we made the correct decision, and our gut instinct and critical thinking were dead on.
I have a sister-in-law she’s in her 50’s. Perfectly healthy,thin and active. Suddenly hospitalized with end stage renal failure. Took them a couple of weeks to get her stable. We can’t get very detailed information about what is happening. Husband said they called it an amyloidosis protein that destroyed her kidneys and damaged her heart. She’s on dialysis 3 days a week and starts chemo today….We know that she got the initial 2 vaccines. As far as boosters go-don’t know…
No proofs will be sufficient for those who will not look, or search with G**gol.
What about what to.take.to remove.the damage and.poison?? Nattokinase?.ivermecrin? Fenben? Apple.Pectin? Vit C?
Also what about ongoing bladder infections? .when never before? Any body else have this?