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The mission of the Fibromyalgia Care Society of America (FCSA) is to provide education, care and supportive services to individuals living with fibromyalgia, their families and the community at large. FCSA will also work to educate medical providers on the appropriate diagnostic, care and treatment of those living with this condition.
Founded in 2015, the Fibromyalgia Care Society of America (FCSA) is devoted to revolutionizing how fibromyalgia is cared for in this country by introducing a comprehensive holistic approach to care, family supports and support groups. The organization was founded by Mildred Velez, who has been living with fibromyalgia since 2007, in response to the lack of direct services for those living with fibromyalgia and to the dearth of dedicated medical care and support. Mildred, along with a dedicated board of trustees, has developed a concise and direct approach to helping those living with fibromyalgia and their families.
The FCSA is committed to the highest standard of care and services that also promotes equality in care so that everyone living with fibromyalgia is able to take advantage of care regardless of their socioeconomic status and geographical location. The FCSA is committed to a holistic and cutting-edge approach to services, which will be offered through three key areas: Centers of Excellence, FibroCares and Empowerment Groups.