The Evans Foundation for Molecular Medicine, established in 2006, promotes research into Multiple Systems Atrophy and seeks to make information on the disease, research progress, and patient care available to people living with MSA and their caregivers.

Our activities include:

  • A support group for MSA and PSA patients and their caregivers in the San Diego area.
  • Research funding and support for projects involving MSA.
  • Summarizing and reporting on current MSA research for patients, caregivers, and the public.