When things start moving, help shows up in the most unlikely places. Take a recent blog from a University of Michigan sports blogger – Ace. Ace has been sick since high school but only in the last couple of years has he been diagnosed as having chronic fatigue...
ME/CFS needs witnesses – people who can stand firm in the face of denial and rejection and tell their story to the world. Each time we responsibly speak the truth to the medical profession, or our families, or our friends, or the NIH or whomever we begin to move...
More Than Just a Film “riveting……equal parts medical mystery, science lesson, political advocacy primer and even a love story.” San Francisco Chronicle From the beginning Jen Brea’s vision has been a very large one of which Unrest was...
Welcome to Lives Interrupted – a project by Health Rising designed to make clear on a personal level, the economic and other costs of having diseases like chronic fatigue syndrome (ME/CFS), fibromyalgia, postural orthostatic tachycardia syndrome (POTS), and long...
Pike was in a bind. His severe ME/CFS meant that he needed financial help, but two trips by medical examiners produced such biased reports as to bring him to tears. He was so dismayed by the inaccurate reports that he regretted trying in the first place. A month...
The Jaspar’s and the Gilmete’s were like family, but it wasn’t Michael Jaspar and his wife saw “The Forgotten Plague” film about ME/CFS that he understood why their best friend Terri disappeared so much…Terri was sick – really...
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