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SMS Foundation UK

Supporting SMS families for a positive future

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?

Screenshot 2021-08-18 at 20.57.19

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Woman showing cataracts in her eyes on the left visible by the clouded appearance, and without cataracts on the right.

Woman showing cataracts in her eyes on the left visible by the clouded appearance, and without cataracts on the right

About Leeann Stevenson

For the past eight years, Leeann has been at the heart of our communications, information and branding as a Trustee of the charity. The transformation of the charity in this time has been exceptional. Leeann’s dedication has resulted in the Foundation becoming the go-to organisation for information on Smith-Magenis syndrome not only for the United Kingdom but across the world.

Leeann is the mother to three children, Lily who is 14 (SMS), William who is 10, and Teddy who is seven. Leeann is a director of a small Web Design agency in Marlborough, Wiltshire that specialises in charity websites and marketing.