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About
We are a small charity that supports families living with Smith-Magenis syndrome (SMS), a rare condition that occurs once in every 15-25,000 births. People with SMS have complex needs and behaviours, along with a learning disability. Our aim is to provide all caregivers and professionals with the knowledge and understanding to feel empowered and confident to support a person with SMS.
What they do
Who they help
How they help
Where they work
Finances
- £81,579
- Income
- £84,648
- Spending
- 10
- Trustees
Financial year ending 30 June 2024, from the Charity Commission register.