CALLING ALL U.S. CFS GROUPS!

If you are a US-based CFS organization please send your name and
contact information to me at pandorarebecca@aol.com  by October 3,
2008.  I need your organizations name, the president of the
organizations name, email and postal contact info and your website address.

I am collecting the information at the request of the Department of
Health and Human Services.  This will be used to disseminate
information about meetings and as a  tool for inviting patients to
participate in Chronic Fatigue Syndrome Advisory Committee Meetings.

Thanks,

Rebecca Artman