My Nonprofit Reviews

ME/CFS has robbed me of the last thirteen years of my life. When I was first diagnosed, there was hardly a whisper about this horrible illness, let alone any kind of real research or possible treatments/cure. When OMF was established, I had no idea that they would not only help finance some of the worlds most prominent researchers and their projects, they would also help change the way researchers around the globe communicate and collaborate. Since it’s inception Open Medicine Foundation has worked continuously to bring awareness of ME/CFS, encouraged teaching institutions to add ME/CFS to their curriculum and have brought hope to millions of patients worldwide.