Researcher Disinterest Still Hampering ME/CFS Field Plus Avoiding Burnout, The “Real” NIH, Staying Homeless, Moving Forward
A Freedom of Information Act (FOIA) reveals that during the three grant review panels from July 2017 to April 2018, chronic fatigue syndrome (ME/CFS) researchers applied for a total of 12 grants. It was the lowest number of grant applications to the panel dating back...
The Autoimmune Virus? Groundbreaking EBV Finding Could Help Explain ME/CFS
It’s not every day that a noted researcher calls a study “the capstone” of his career or asserts that it’s more important than the rest of his 500 studies put together. That’s pretty amazing but the exciting part for those of us with...
POTS Rising! Research & Advocacy Producing Breakthroughs in Neglected Disease
If you think ME/CFS and FM are behind the eight ball at the NIH, then check out postural orthostatic tachycardia syndrome (POTS), a common comorbidity. The NIH doesn’t even measure POTS funding but then how could it? POTS doesn’t even have a designated...
Huge “All of Us” NIH Initiative Offers Possibilities for ME/CFS and Fibromyalgia
“It will be transformative.” Francis Collins Neither chronic fatigue syndrome (ME/CFS) or fibromyalgia (FM) exactly feel welcome at the NIH. Funding for both diseases is pitiful, but a program has just opened up which welcomes everyone’s participation. A top...
Pain, Genes, Drugs and You: How Your Genetic Makeup May Be Keeping You in Pain
From Dr. Trescott’s lecture given to the Physician Partners of America: “Your Genes, Your Pain Drugs and You Or “Why Every Pain Physician Should be Testing Your Genes” When the patient says, “This doesn’t work,” or, “I’ve been too sensitive,”...Lives Interrupted Latest Story
Megan
Randolph, United States
Former occupation: Day care worker
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