The CFS/FM Center for Hope

To educate, advocate, inform, support, and provide self-help resources for either those who have Fibromyalgia &/or CFS/ME, their family, friends and associates or just the casual web traveler.

This Fibromyalgia and Chronic Fatigue Syndrome/ Myalgic Encephalomyelitis (CFS/ME) non-profit organization exists to educate, advocate, provide information, support, and self-help resources—including a user forum—for either those who have these illnesses, their family, friends and associates or just the casual web traveler.

You don't need to have CFS/ME or FM to join our group. You can join us in a simple show of support!

So please, join us today and make a difference in someone's life by showing that you DO care.

Gentle hugs!

Lori

1. We advocate for improved recognition, research, healthcare, and benefits for those with Fibromyalgia and CFS/ME.

2. We educate and increase awareness of Fibromyalgia and ME/CFS within all levels of government, media, healthcare organizations and the general public.

3. We provide self-help and support resources related to CFS/ME, FM and the related illnesses.

4. We attempt to provide the most accurate information whenever possible.

5. We comply with the HONcode standard for trustworthy health information.