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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)

Kent Family Fun Day, 31 August

We would like to welcome Danielle and Jon Thwaites as new Regional Contacts for Kent and invite you to their Family Fun Charity Day on 31 August.  For full details go to the "News and Events" page. 

Alton Fun Day, 31 August 2014

Go to the "News and Events" page for full details of this fundraising and awareness event for Williams Syndrome Foundation.
 

Northern & Yorks Meeting 31 August

Don't forget the Northern & Yorks group will be meeting on 31 August.  For full details go to the "News and Events" page.

Short Survey Re Genetic Disorders

We have been advised of a survey being carried out by Genetic Disorders UK and they are asking for the participation of WS families.  If you have a few minutes and would like to know more click here.