My Nonprofit Reviews

My family first found this organization 25 years ago when we needed information for our family member who was diagnosed with ME/CFS. We were greatly encouraged by the organization's 2008 decision to focus on funding cutting-edge research to be able to diagnose, treat and cure this illness. We believe that the organization's funding of the best scientists, along with creating infrastructure like their biobank which makes it possible for more researchers to study ME/CFS, offers the very best hope for patients and their families. Since 2010 I have served on the Board of Directors and have continued to be impressed by the board's and staff's dedication to the mission of solving this terrible illness. This is an effective, well-run organization that deserves support.