The Smith-Magenis Syndrome (SMS) Foundation UKSupport us
The SMS Foundation is the leading support charity in the UK for children and adults living with Smith-Magenis Syndrome (SMS), a rare genetic disability due to a microdeletion or abnormality of chromosome 17. The Foundation is the authoritative voice for this condition and provides support for families and professionals living and working with SMS across the UK.
The Foundation was created by families, for families, and is fuelled by a heart-felt passion to ensure children, adults and their loved ones with SMS have the information and support they need to live life to the full.
Registered Charity 1186647.