I, like millions of others, live with ME/CFS (Myalgic Encephalomyelitis/Chronic Fatigue Syndrome), a disease that drastically limits daily life and has no known cure or approved treatment. Despite its profound impact, especially in the wake of Covid-19, ME/CFS remains one of the most underfunded illnesses relative to its disease burden, and research funding is now being cut even further. That’s why I’m raising money to support critical scientific research. The majority of donations go directly to funding studies that bring us closer to understanding, treating, and hopefully curing this devastating condition. Your support could help change lives, mine included.

Your donations will go directly to the Open Medicine Foundation