"Long before I became a whistleblower, I’d been conditioned to keep secrets. As a child, I was sexually abused by my father during an era when no one spoke about such things."
Why did you omit this revelation and instead only mention that her father may have been schizophrenic?
Anyway... from this interview I discovered one very important nugget: You can investigate if your doctor is "on the take" or a doctor you've looked at, but are still not a patient of, is on the take.
Lastly: The drug that was being used "offlabel", in a dosage that was suboptimal according to package insert, is still being manufactured and prescribed in suboptimal doses, and currently costs not $28,000.00 per vial, as it did when the DoJ investigated, but $45,000.00 US per vial.
It still takes 5 doses for this drug to be of any substantial benefit to MS patients...
It is derived from the pituitary gland of slaughtered pigs so the cost to the drug manufacturer is NEGLIGIBLE.
I couldn't help notice that Lisa's son was "special needs". There is a high probability that those "special needs" developed as a result of childhood vaccine injury/injuries. So she gets a double whammy from Pharma: her son was injured by Pharma product(s) and her company turns out to be the worst kind of parasite, making billions off of people's suffering.
i wonder how many of these $28,000 "vials" a bonafide patient needed per year?
a couple i know in their 60s were both diagnosed with some unusual type of lung cancer within a year or two of the covid vax rollout (they totally believed the covid scam, got all the shots including boosters, and probably are still getting them). first the husband was diagnosed in mid 2021 and later the wife. they are now both taking some kind of unusual chemotherapy drug (gene therapy maybe) at $20,000 per month each!! naturally they are not paying this amount; most is covered by their insurance and/or medicare, which of course means we all are paying.
this is what the pharma industry is doing to our country, on an increasing basis, and with increasing prices. is there no government oversight? i guess not.
in this, she reveals that for an MS patient having an exacerbation of their disease, the appropriate dose (approved by the FDA) was 4 vials in a 20 day period (1 vial every 5 days) - but the company she worked for was pushing it to desperate MS patients as only one vial within 5 days, period, in order to get medicare, medicaid and other insurance approval "and i knew the patients were never gonna get better . . ." . so that 20 day treatment cost was $112,000 - for just one flare-up of MS.
and people around the world wonder why US so-called "healthcare" is the most expensive in the world.
Whistle-blower, Lisa Pratta:
"Long before I became a whistleblower, I’d been conditioned to keep secrets. As a child, I was sexually abused by my father during an era when no one spoke about such things."
Why did you omit this revelation and instead only mention that her father may have been schizophrenic?
Anyway... from this interview I discovered one very important nugget: You can investigate if your doctor is "on the take" or a doctor you've looked at, but are still not a patient of, is on the take.
https://youtu.be/6I6qj4dXbGI
https://openpaymentsdata.cms.gov/
Lastly: The drug that was being used "offlabel", in a dosage that was suboptimal according to package insert, is still being manufactured and prescribed in suboptimal doses, and currently costs not $28,000.00 per vial, as it did when the DoJ investigated, but $45,000.00 US per vial.
It still takes 5 doses for this drug to be of any substantial benefit to MS patients...
It is derived from the pituitary gland of slaughtered pigs so the cost to the drug manufacturer is NEGLIGIBLE.
YOU CANNOT HATE BIG PHARMA ENOUGH!!!
A very insightful comment!
Thanks Tony. Just doing my own follow up aka "due diligence". 😉
You should listen to Lisa Pratta's
"8 extra things" she didn't cover in the book.
She not only was employed by Big Pharma: she and her son both have been "victims" of the medical industry, regarding "drugs".
Having a hard time with this woman who's "on a book tour" and shopping it around for the best "film rights" deal.
I dunno. Just a vibe.
https://youtu.be/-1LUR0BaYp8
Perverting the use of a drug that works—a case study in the reality of evil.
Exactly right!
I couldn't help notice that Lisa's son was "special needs". There is a high probability that those "special needs" developed as a result of childhood vaccine injury/injuries. So she gets a double whammy from Pharma: her son was injured by Pharma product(s) and her company turns out to be the worst kind of parasite, making billions off of people's suffering.
i wonder how many of these $28,000 "vials" a bonafide patient needed per year?
a couple i know in their 60s were both diagnosed with some unusual type of lung cancer within a year or two of the covid vax rollout (they totally believed the covid scam, got all the shots including boosters, and probably are still getting them). first the husband was diagnosed in mid 2021 and later the wife. they are now both taking some kind of unusual chemotherapy drug (gene therapy maybe) at $20,000 per month each!! naturally they are not paying this amount; most is covered by their insurance and/or medicare, which of course means we all are paying.
this is what the pharma industry is doing to our country, on an increasing basis, and with increasing prices. is there no government oversight? i guess not.
Excellent work.
Weird piece of trivia but "Suits" (Netflix) had an episode that must have been based on this story. Hiding in plain sight again.
to answer my own Q, i just watched Lisa Pratt here:
https://www.youtube.com/watch?v=27qUyMuYZJw
in this, she reveals that for an MS patient having an exacerbation of their disease, the appropriate dose (approved by the FDA) was 4 vials in a 20 day period (1 vial every 5 days) - but the company she worked for was pushing it to desperate MS patients as only one vial within 5 days, period, in order to get medicare, medicaid and other insurance approval "and i knew the patients were never gonna get better . . ." . so that 20 day treatment cost was $112,000 - for just one flare-up of MS.
and people around the world wonder why US so-called "healthcare" is the most expensive in the world.
https://timothywiney.substack.com/p/titanic-courage-from-dr-redfield
I have a feeling a lot of MS as diagnosed might be better described as BS. Disclaimer: I have no medical qualifications whatsover:).
All of this is so familiar to me . Clearly common practice .