How you can Help?

The SDS/MSA Support Group needs your help to increase the public awareness of SDS/MSA. Some of the ways this can be accomplished are:

    1. Encourage Physicians to learn as much as possible about the diagnosis and treatment of SDS/MSA.
    2. Encourage donations!  The SDS/MSA relies entirely on donations to provide it services.  Finding corporate sponsors and individual donors is not only important to the growth of the Group, its longevity may depend on it.
    3. Write or call your U.S. Representatives and Senators, encouraging them to allocate more funding for Autonomic Research.
    1. Volunteer your time! The SDS/MSA Support Group needs volunteers as Local Area Support Leaders, recruiting membership and chapters; fund raising; and information gathering for newsletter and website distribution.

We also need financial help to keep the support group going.  If you are able to contribute financially, contact the group president, Don Summers.

You all have a part!   Remember our Mission:

"To Educate and Support"

We see the process as a circle with information and support constantly making the rounds from patient, to caregiver, to family member, to physician.

Please join us in our efforts to educate and support one another!