FAC is a community-based, voluntary organization founded by people with fibromyalgia, for people with fibromyalgia, their caregivers, and families.  FAC was federally incorporated as a not-for-profit organization on June 15, 2021.  FAC became a registered charity on  June 20, 2025.

As a national association, it is fundamental that FAC’s leadership represents the diversity, geography and marginalized communities in Canada.  FAC is committed to being a national association for all Canadians, regardless of where they live, accessibility needs, and whether they speak English or French.  With the help of volunteer translators, FAC is able to provide a bilingual website.

The Board of Directors endeavours to have representation from all Canada’s provinces and territories.  Only persons with fibromyalgia are eligible to serve on the Board of Directors.

The Board of Directors has identified four key areas of focus:

1. Awareness
2. Research
3. Education
4. Advocacy

Each of these core areas is managed by a committee which is responsible for identifying, considering, and recommending actions and project initiatives, subject to final approval by the Board of Directors. The Committee Co-Chairs are appointed by the Board of Directors, two for each Committee.

FAC will be compassionate, transparent, ethical, and respectful of all diversities. FAC will develop collaborations and share our learned knowledge. Together FAC will be resilient and not give up.