Shropshire ME Group

From MEpedia, a crowd-sourced encyclopedia of ME and CFS science and history
Revision as of 00:35, November 7, 2016 by Samsara (talk | contribs) (→‎Aims: expanded)

Shropshire ME Group (SMEG) is a patient charity that helps patients with ME/CFS/PVFS in and around Shropshire in the UK.

Aims[edit | edit source]

The Shropshire ME Group is a self-help support group which intends to provide advocacy, advice, and information for people in and around Shropshire suffering from ME/CFS/PVFS and their carers,[1] in particular by the provision of a network of contacts for such persons in order to provide mutual support and information exchange.[2]

Services[edit | edit source]

History[edit | edit source]

Shropshire ME Group was founded in 1987[3] by local couple Reg and Josephine Watson, and became a registered charity in 1999.[4] It currently has over 150 members.[5]

Notable people[edit | edit source]

British author Katie Flynn and Conservative MP Philip Dunne are patrons of the Shropshire ME Group.

Funding[edit | edit source]

Shropshire ME Group has been a registered charity since 1999.[4] Its charity number is 1072171.[1] The charity is self-funding and relies on individual donations to raise funds,[6] as well as occasional fund-raising events held by volunteers to support SMEG and M.E. research.[3] They charge an annual membership fee of £5.[7]

Online presence[edit | edit source]

See also[edit | edit source]

References[edit | edit source]