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SMS Foundation UK

Supporting SMS families for a positive future

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We are a small charity that supports families living with Smith-Magenis syndrome (SMS)

Never feel isolated or alone. Call our helpline and leave a message: 0300 101 0034 (we aim to respond to messages within 48 hours).

Newly Diagnosed?

SMS Springboard Project & Community Survey Update

April 16, 2026

WEBINAR
Date: 14th May 2026

Time: 19:00 (GMT)
Register for this event

Please join us for a webinar providing an update on the SMS Springboard Project, together with early findings from the 2026 SMS Community Survey. Using routinely collected healthcare data, the Springboard Project is exploring key questions about health and wellbeing in Smith-Magenis syndrome, including how health changes as people get older and why outcomes may vary between individuals. Early insights will also be shared from the 2026 SMS Community Survey, which captures real experiences of living with Smith-Magenis syndrome across areas such as education, health, mental health, daily living,  employment, and support services. The session will focus on sharing progress to date and highlighting what we are learning at this early stage.

The webinar will be co-presented by Dr Kate Baker and Dr Millie Wagstaff from the Department of Genetics at the University of Cambridge, and Leeann Stevenson, Executive Director of the SMS Foundation UK.

The webinar will be recorded automatically, and all registered attendees will receive a link to the recording once it has been published.

Register for this event

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Never feel isolated or alone. Call our helpline: 0300 101 0034

Please note: This is an answer phone service that will alert us as soon as a message is left. A member of the team will call you back as soon as possible – we aim to respond to messages within 48 hours.

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