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SMS Foundation UK

Supporting SMS families for a positive future

  • What is SMS?
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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?

Living with SMS

Personal stories from individuals sharing their experiences of life with Smith-Magenis syndrome.

A Guide to SMS Booklet

Ellen Wotherspoon and her remarkable sporting journey

At the SMS Foundation UK, we take immense pride in celebrating individuals who are dedicated to pursuing their aspirations. Ellen Wotherspoon, a 28-year-old from Scotland, has become a shining example …

Louie Martland: Thriving in the World of Hospitality

Meet Louie Martland, a remarkable 17-year-old from Wigan, Greater Manchester, who has shown incredible determination and resilience in pursuing his passion for customer service and hospitality. Louie, …

Elizabeth proudly wears her cadet uniform ready for Armed Forces Day

Elizabeth’s Inspiring Journey: Marching with Confidence on Armed Forces Day

At just 16 years old, Elizabeth Dudley from Belton in South Yorkshire has proven that determination and an inclusive environment can turn aspirations into reality. This year, she had the opportunity …

Lily on her work experience rolling up the hair of a mannequin

Lily’s Dream Comes True: A Remarkable Work Experience Journey

At the age of 16, Lily Stevenson has recently completed her school work experience placement at Bliss Hairdressers in Devizes, Wiltshire. This opportunity not only allowed Lily to explore her passion …

Facts about SMS

A series of factual videos from parents, carers, and professionals who live and work with people that have Smith-Magenis syndrome. When was Smith-Magenis syndrome discovered, and who first described …

Videos About SMS

Sharing My Syndrome ‘Sharing My Syndrome’ is a video filmed during our 2017 SMS conference. That Defining Moment Broadly focusing on the diagnosis and early planning aspects of Smith-Magenis syndrome, …

Young SMS man with wood working

Everyday care and living with SMS

Living with SMS, finding support and building futures.

Frequently asked questions

If we have one child with SMS, will our other children also have SMS? Smith-Magenis syndrome is typically not inherited. It usually results from a genetic change that occurs during the formation of …

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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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Become a Member of The SMS Foundation UK

Connect with SMS families in your region and be the first to receive updates on any social meetings, conferences, and fundraising events going on!

Family & Carer Membership
Professional Membership

Registered UK Charity (CIO) 1186647

Scottish Charity (SCIO) SC050921

Registered with the Fundraising Regulator

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