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ME/CFS Worldwide Patient Alliance Has Its Own Website and Forum!

  [ 10 votes ]   [ Discuss This Article ] • October 6, 2010

The ME/CFS Worldwide Patient Alliance is a newly formed grassroots advocacy community, and as of October 5, now has a lovely home at

People around the world (1,300 so far) are joining hands to create positive ads & other publicity, events, fundraising campaigns, and more to project a positive image of ME/CFS patients and raise awareness of patients’ needs. Joining is a snap, and it's free.

Go to to learn, chat, network, and share ideas that will add to worldwide patient power and “win the public’s heart." 

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