Where fibromyalgia knowledge meets community.
The Fibromyalgia Association is a national nonprofit connecting people living with fibromyalgia with trusted information, practical education, community support, and advocacy—while working with healthcare professionals and researchers to move fibromyalgia understanding and care forward.
Find Your Path
Whether you're living with fibromyalgia, caring for patients, or looking to support our mission, we're here to help you find what you need.
Support
Connection
Education
Community
Advocacy
SUPPORT, EDUCATION & COMMUNITY
Support & Education Group
Join our regular virtual Support & Education Group, led by our founder, who has lived with fibromyalgia for 30+ years and is a board-certified health and wellness coach. It’s a safe, welcoming space to learn from experts, share real-life experiences, connect with others who understand, and know you are not alone.
ANNUAL CONFERENCE
Fibromyalgia Awareness Day
Each year, Fibromyalgia Awareness Day brings our community together to raise awareness, share trusted information, and amplify the voices of people living with fibromyalgia. Through education, expert speakers, and community connection, we shine a light on fibromyalgia and help move understanding forward.
POLICY & RESEARCH
Making Patient Voices Heard
We believe healthcare policy, research, and treatment decisions should be shaped with the voices of people living with fibromyalgia. We bring the lived experience of our community to the table—working alongside researchers, healthcare professionals, policymakers, and other advocates to help create meaningful change.