What Happened to Physics Girl? How Long COVID Has Changed Her Life
Dianna Cowern, widely known as Physics Girl, has made significant contributions to science communication through her engaging and educational content. Her sudden absence from
In mid-2020, Open Medicine Foundation (OMF) launched a three-year study to find answers. We’re leading a large-scale international study following the potential conversion of Long Covid to Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (ME / CFS), a chronic, life-altering disease. This study is an unprecedented opportunity to find ME/CFS drug treatments and prevention strategies at an accelerated pace.
As leaders of the largest worldwide nonprofit effort to diagnose, treat, and prevent ME / CFS and related complex diseases, such as Post Treatment Lyme Disease Syndrome and Fibromyalgia, we know one thing to be true: If we don’t do the research now, millions will be left behind. Join us in our mission to find the answers.
“We do know for absolutely certain that there is a Long Covid …Anywhere from 25% to 35%—or more—have lingering symptoms well beyond what you would expect from any post-viral syndrome like influenza and others. It’s fatigue, shortness of breath, muscle aches, dysautonomia, sleep disturbances, and what people refer to as brain fog.”
Anthony S. Fauci, MD.
Because many people develop ME/CFS after a viral infection, researchers question whether some viruses might trigger the disorder.
Source:Mayo Clinic
In one study, 27% of hospitalized SARS patients met the CDC’s criteria for ME/CFS one year after recovery from SARS itself.
Source:Lam et al. (2009)
About 1 in 10 infected with Epstein-Barr virus, Ross River virus, or Coxiella burnetti develop symptoms that meet the criteria for ME/CFS.
Source: CDC (2018)
History shows us that a documented percentage of those who were sick with a post-viral syndrome will end up developing symptoms of ME/CFS.
have ME/CFS worldwide
are affected in the USA alone
25% are homebound
No FDA approved treatment
No cure
$17 to 24 billion in USA
men, women and children.
Anyone. Any time.
ME/CFS is a debilitating illness that has upended too many people’s lives. With no FDA-approved treatments or cure, millions have been left behind, forced to put their lives on hold as they wait for answers. In the aftermath of COVID-19, millions more are now at risk of developing the disease.
OMF secured a $1 million grant to launch the first year of our three-year international study. It already being conducted across the globe at the OMF funded Collaborative Research Centers spearheaded by some of the world’s top researchers and ME/CFS experts.
We are actively working to raise an additional $2 million to fund the next two years of the study. We all need this research now. We need your help today, so millions can return to health tomorrow.
Too many people already suffer from this debilitating disease, and now millions more are at risk.
Dianna Cowern, widely known as Physics Girl, has made significant contributions to science communication through her engaging and educational content. Her sudden absence from
Post-exertional malaise (PEM) is a defining symptom of myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS), marked by a significant worsening of symptoms or the development of flu-like
In 2020, OMF secured a $1 million grant to launch the first year of an international, multi-year study across the five OMF funded Collaborative Research Centers (CRC). The aim of this study is to examine Post-COVID Syndrome transitioning to ME/CFS. We are actively working to raise an additional $2 million for years two and three of the study. I am pleased to share with you an update on the first phase of this groundbreaking — and urgently needed — research project.
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