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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)

WSF National Convention 2013

Have you booked your place yet to attend our 1st National Convention for many years on 12/13 October 2013.  Spaces are going fast, so don't miss out. Click here for more information

Williams Syndrome Study - Volunteers Wanted   

Research Psychologists at the Centre for Brain and Cognitive Development are looking for families who have a child with Williams Syndrome between 8 and 36 months of age to take part in a study on perception and attention click here...

Regents Park Picnic 2013

See the news and events page for full details of this year's WSF picnic.  We hope to see another great turnout.

Midlands Area Summer Event 2013

The next meeting for your group is coming up soon, so check out the full details here as Gareth and Liz would love to see some new families joining them.