Myalgic Encephalomyelitis Support Services (M.E.S.S.)

M.E.S.S. is a volunteer organization dedicated to helping those who suffer from Myalgic Encephalomyelitis (ME), also known as Chronic Fatigue Syndrome (CFS). By keeping abreast of current medical research into ME/CFS, as well as the latest treatment strategies (both pharmaceutical and holistic), M.E.S.S. strives to foster understanding of this condition and the difficulties in living with it.

Based in Toronto, Ontario, Canada, M.E.S.S. currently has on file a substantial collection of formal research papers on ME/CFS, in addition to other reference sources. Ken Coleman, the Executive Director, also acts as liaison to support groups at the national level.

http://cfids-cab.org/mess/meamess.htm

The administrators of the ‘Living With ME’ website do not advocate the use of any particular type of medication, treatment or healthcare! YOU should ALWAYS seek advice from a DOCTOR / GP / CONSULTANT before undertaking or ceasing any treatment!

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