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Carer centres and services Smith-Magenis Syndrome (SMS) Foundation UK

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Our Vision is that every person with Smith-Magenis Syndrome shall have a fulfilling life within a supportive and understanding community.

The Smith-Magenis Syndrome (SMS) Foundation UK shall be at the heart of our community of individuals, families, carers and professionals living and working with Smith-Magenis Syndrome and 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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This information was supplied by Serco Global Services on 14 March 2024.