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Thank you for visiting the Williams Syndrome Foundation website.

We aim to be the first point of contact for individuals with Williams Syndrome, their families and professionals needing support and information regarding the Syndrome. We actively support research into the educational, behavioural, social, scientific and medical aspects of the Syndrome. We will seek to organise our financial and personnel resources so as to achieve our mission on a sustainable basis.

I am a Parent/Carer

My son Ethan was diagnosed with Williams Syndrome when he was 13 weeks old and the support and information that the WSF have provided since then has been invaluable. read more

I am a Professional

I first became involved with the Williams Foundation as a paediatric registrar in London. Over the subsequent 35 years I have met, talked to and enjoyed the company of many hundreds of children and adults with Williams Syndrome ... read more

I am a WS Person

Hi my name is Katy, I am 25 and have Williams Syndrome. read more

News & Events (read all news)

Chester Zoo Trip, Sunday, 28 September 2014 

Fancy an outing to Chester Zoo with other Williams Syndrome families then see the "News and Events" page for more details.

Wild Warrior, 21 September 2014

Fancy a challenge and want to raise some money for Williams Syndrome, then why not join Gareth Martin and "Team Williams" at the Wild Warrior Event in Derbyshire.  For more details click here.

Marwell Zoo, 27 September 2014

If you would like to join Jane Nash at this event please let her know ASAP.  See "News and Events" page for full details.

WSF 2014 Christmas Card Brochure

Help support Williams Syndrome Foundation by buying our charity Christmas cards.  Click here to look at the brochure in full.