We support people affected by SMS to have a positive future
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Help us to ensure every person with Smith-Magenis Syndrome shall have a fulfilling life within a supportive and understanding community.
The Smith-Magenis Syndrome (SMS) Foundation UK is at the heart of our community. We will be the first point of contact for those seeking information and support. Nobody should ever feel isolated or alone. We value every person affected by this genetic disorder and shall empower them to reach their full potential as respected members of society.
Connecting Families – Raising Awareness – Building Futures
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We are the SMS Foundation UK, a small charity that supports families living with SMS in the UK.
As well as helping families that live with the syndrome we also work with and support a variety of professionals who treat, educate, and care for people with SMS.