Retsef Levi

@RetsefL

Professor Retsef Levi, MIT Expert in Analytics, Risk Management, Health Systems, Food & Agriculture Systems, Manufacturing & Supply Chain Management

Cambridge, MA

Joined January 2023

Retsef Levi
@RetsefL
14h
A baby dying shortly after birth from ruptured spleen is ‘classified’ by some as unvaccinated measles death based on positive antibodies test! Be assured that if the baby would be vaccinated against measles 2 days before, they will argue the cause of death is the spleen! The
Retsef Levi
@RetsefL
Aug 27
The US allocated almost $2.5B to research and clinical trials addressing long-COVID patients who report on chronic symptoms, such as fatigue, brain fog, pain, neuropathy and dysautonomia 3 months or longer after COVID infection. The US allocated $0 to research and clinical
Retsef Levi
@RetsefL
Aug 26
Hope state health authorities and congress/senate will demand @CDCgov to follow up with the VSAFE enrollees! @RonJohnsonWI @SecKennedy @NIHDirector_Jay @FLSurgeonGen @la_surgeon
Maryanne Demasi, PhD
@MaryanneDemasi
Aug 26
Replying to @MaryanneDemasi
“This is not something one can ignore,” said @RetsefL. “The CDC had a plan to follow up with V-SAFE enrolees in real time. This plan, to say the least, was not executed,” he said.
Retsef Levi
@RetsefL
Aug 26
Breaking: @CDCgov planned to follow up with VSAFE enrollees reporting on injuries but didn’t! Our analysis of VSAFE data shows that 1.87% of ~10 million enrollees reported 3+ months post vaccination on prolonged health worsening self-attributed to the vaccine. ~50% of them or
Retsef Levi
@RetsefL
Aug 25
Adding to that: 1) In 4 trials the mRNA vaccine had more serious adverse events and the largest pivotal trial showed statistically significant additional 60 serious adverse events, or about 3 additional per 1000 vaccinees that will switch! 2) In all 4 trials there were more
Robert W Malone, MD
@RWMaloneMD
Aug 24
FDA REFUSED Moderna’s mRNA flu vaccine because the company hadn’t tested it against the vaccines seniors actually receive. Moderna called for White House intervention. Trump intervened. 14 days later, FDA reversed itself. The missing trial was never done. Instead, FDA approved