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In 1989, a small group of people with
fibromyalgia, who had been meeting on a regular basis, formally organized and created the
Fibromyalgia Association of British Columbia. Since that time, we have grown and expanded
and currently have a membership of over 800 people throughout the world. In 1995 we
achieved non-profit status and became known as the British Columbia Fibromyalgia Society.
In 1996, we also became a registered non-profit charitable organization, allowing us to
issue tax receipts for charitable donations. The key concept
by which the Society defines itself is empowerment, the belief that members must have the
information resources necessary to maintain and/or regain control of their lives. The
commitment to this principle has shaped the Society's priorities, defined its purposes and
provided the impetus for its growth. Since its creation in 1991, the Society has earned
respect at local, national and international levels for its information, education and
self help services, encouragement of self help coping strategies and for its knowledge and
experience on issues relevant to fibromyalgia.
Information provided on this site is for
education purposes only. Please consult your physician or allied health professional for
treatment. This site is free for personal use only. For further information contact |
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