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Our work to improve the lives of people with F.M.S. includes:

  • producing a range of publications, e-newsletters and a membership magazine to help people understand the illness and take control of their lives
  • providing support services (support by telephone and email and a welfare rights helpline) to offer understanding, acceptance and information to cope with the practical and emotional difficulties of F.M.S.
  • campaigning to influence national policy and improve standards in healthcare, education, employment, welfare and social care
  • lobbying, networking and, where possible, strategically funding pilot projects to increase research into F.M.S.
  • working with professionals to achieve improvements
  • supporting people who want to help fundraise for F.M.S.
  • making our message heard through the media to increase understanding of F.M.S. and challenge misconceptions.