The CFIDS Association of America has been at the leading edge of ME/CFS research, policy and education for more than 25 years. The Association responsibly represents the needs of ME/CFS patients and their loved ones, working to make ME/CFS widely understood, diagnosable and treatable. Inspired by the courage and passion of volunteers and fueled by gifts small and large from supporters committed to a vision of a world without ME/CFS, the CFIDS Association leads with purpose, collaboration, respect, integrity and innovation.
We strive for a world free of ME/CFS.
We will make ME/CFS understood, diagnosable and treatable.
- Identify safe and effective treatments for ME/CFS
- Strengthen the ME/CFS community by empowering patients and engaging greater numbers in our cause
- Aggressively expand funding for research that
will lead to approved treatments and cures for ME/CFS
Our Core Values:
FAQs about the Association