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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)

New Trustees

We would like to welcome Liz Martin and Tim Cooper as new Trustees of the Foundation following our Trustees Meeting yesterday. 

Northumbria Meeting

Go to the "News and Events' page for full details of the next meeting in this area.
 

Merseyside Meeting 27 July

Don't forget the Merseyside group will be meeting on 27 July with a special Teddy Bear picnic.  Put it in your diary

New Regional Contacts

We would like to welcome our new Regional Contacts in Herts/Beds, Kent and Surrey and West London.  Go to the "Regional Contact" page for her details.