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Allen's avatar

Excellent post.

I would suggest this story might be much bigger than an adverse, albeit massive, reaction to a series of vaccines. Full disclosure- I'm in opposition to all vaccines as they are all toxic and should never be injected or swallowed into any biological system.

That said, let's look at the drug treatment in question- that drug is Novartis' FABHALTA® (iptacopan) which received FDA fast track approval on August 8, 2024. It is advised as the "first oral monotherapy for adults with PNH." The risk profile for this drug is not good and they require vaccination with it.

Lexi’s sister stated that a nurse mentioned giving her a different medication outside of the vaccine vials and it was also mentioned in the interview w/Polly at CHD that some doctors laughed and were saying she was a "scientific experiment."

Analysts at Jefferies predicted that Fabhalta could hit $3.6 billion in peak annual sales IF it gets approved for all its target indications, which along with PNH and IgAN include atypical haemolytic uraemic syndrome (aHUS), C3 glomerulopathy (C3G), and idiopathic membranous nephropathy (IMN).

It still has a long way to go to reach that objective. In the second quarter, sales from PNH were $22 million, with Novartis pointing to "encouraging early launch indicators" with the rollout.

Over a two-year span, Pakbaz’s clinic, which served solely benign hematology patients, registered a significant demand that crossed various zip codes and cities. Huh? How did this happen? What was the process?

Were Pakbaz and associates fishing for subjects and shaping diagnoses to fit the objectives of the drug trials? Was Alexis caught up in this "sweep?" Are certain hospitals/clinics programming EPIC software to create this diagnosis to prime the pump for an accompanying financial windfall?

Pakbaz highlighted the logistical challenges in implementing this therapy, particularly its prohibitive cost, ($550,000 a pop- that's not a typo) and drew attention to the ongoing negotiations with insurance companies to ensure patient access to these innovative treatments and stressed the invaluable role of Non-Malignant Hematology Clinics in enhancing patient outcomes and the "remarkable potential" of gene therapies to heal diseases that were once deemed incurable.

Gene editing therapy, CRISPR, etc. are all the rage in the medical industry and with their financial backers- the BioPharma frontier. The investors and the Pharma cartel only wait so long before they need to see a return on their investments.

This "new era of therapeutic options", as the investors and Pharma PR flacks call it, lies on the horizon for individuals with non-cancer blood disorders. More of these people must be located (invented) for this noble cause.

HOW was Alexis diagnosed with Paroxysmal Nocturnal Hemoglobinuria (PNH), in January 2024?

WHO did the diagnosis and WHERE was it done? WHAT were the mechanisms and processes that were employed for this diagnosis?

BTW In July 2020, Novartis agreed to pay $678 million to settle allegations that the company violated the False Claims Act and Anti-Kickback Statute by paying physicians to induce them to prescribe certain of the company's drugs. Novartis allegedly spent hundreds of millions of dollars on fraudulent speaker programs that served as a means to bribe doctors with cash payments and other extravagant rewards.

"FABHALTA is only available through a program called the FABHALTA Risk Evaluation and Mitigation Strategy (REMS). Before you can take FABHALTA, your health care provider must: Enroll in the FABHALTA REMS program. Counsel you about the risk of serious infections caused by certain bacteria. Give you information about the symptoms of serious infections. Make sure that you are vaccinated against serious infections caused by encapsulated bacteria and that you receive antibiotics if you need to start FABHALTA right away and you are not up to date on your vaccinations."

California Girl's avatar

"The massive amounts of EMF’s she is being subjected to from hospital equipment."

Two days ago I was released from the local hospital after 3 days of their trying to "lower the numbers" that supposedly reflect my heart condition. I have contended for years that my AFIB was caused by EMF (smart meters), and been largely tolerated for such foolishness. And now you claim that the hospital equipment itself emits EMFs. I certainly suspected that was how the readings from heart monitors attached to my body were displayed on terminals in the nurse's station. I was radiated for their convenience. The hospital relied on drugs to "lower the numbers". I conclude tentatively that I was given more drugs to compensate for the hospital's technology.

Maybe I will have to carry an EMF meter into the hospital when next I am there.

Thanks for an informative article!

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