We aim to raise awareness of ME/CFS by informing and educating the public and medical practitioners about the illness and its devastating effects on patients and their loved ones.
The foundation sources experts on ME/CFS to contribute meaningfully to the education process, diagnose those affected, and provide some form of basic treatment.
We provide information on available resources when patients suspect they have ME/CFS.
We provide comprehensive support to those affected in South Africa.
The foundation aims to contribute to international research efforts to identify a cause and treatment for ME/CFS.
We aim to build on the work previously done by the ME Association of South Africa, led by the late Arlene Vermaak.