FIBROMYALGIA SOCIETY OF ONTARIO INC

Association for ME/FM (CFS) Members
RR # 1, Site 15, Box 10, Mindemoya ON P0P 1S0


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WHO WE ARE & WHAT WE DO


FSO is a non-profit association of volunteers who were brought together in June of 1992 by a common interest in living better despite the chronic pain and fatigue of the Fibromyalgia and Chronic Fatigue Syndrome (FMS/CFS).

OUR MISSION:
To improve the quality of life as those directly affected by FMS/CFS

OUR OBJECTIVE:
To educate in order to encourage and facilitate:

*  Self-help for those whose lives are affected by FMS/CFS
*  State-of-the-art knowledge about FMS/CFS throughout the province of Ontario health care community
*  Research into FMS/CFS cause and treatment
*  Public and private sectors understanding and support for FMS/CFS - appropriate policies and actions
*  Advocate on behalf of FMS/CFS individuals having trouble with benefits
*  Sytemic advocacy with all levels of government, WCB, insurance companies, etc



OUR ACTIVITIES:
include:

*  Tracking and reporting on-going and planned FMS/CFS research
*  Issuing and distributing a quarterly newsletter and information materials
*  Special-issue meetings and seminars
*  Help in establishing small, local FMS/CFS self-help groups
*  Building an FMS/CFS lending and resource library of useful documents, books and audio/visual tapes to    share with self-help groups

*  Monitoring and reporting legislative progress relative to FMS/CFS
*  Exchanging information with other FMS/CFS groups across the country and internationally
*  To devise, implement and promote an education awareness campaign throughout Ontario about *  FMS/CFS, especially aimed at health care providers
*  To train representatives throughout the province in advocacy and self-help techniques
*  To solicit funds to promote the objective of the FSO and research on FMS/CFS


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