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About
The charity provides local and national support, advice and information for people affected by myasthenic syndromes (Myasthenia Gravis; Ocular Myasthenia Gravis; Congenital Myasthenic Syndromes and Lambert Eaton Myasthenic Syndrome) and their families. It raises medical and public awareness of these conditions and funds research to reduce their impact and ultimately a find cure.
What they do
Who they help
How they help
Where they work
Finances
- £449,135
- Income
- £1,054,088
- Spending
- 9
- Trustees
Financial year ending 31 March 2025, from the Charity Commission register.