Throughout the country there are Regional Contacts who are there to help any parents or carers with a child or adult who has Williams Syndrome.  The details of the Contact for your area can be found in the "Members Area".

Please get in touch with your Contact if you feel you would like to speak to another family who has experience of Williams Syndrome.  If they are unable to assist you personally they will be able to put you in touch with other parents or professionals who may be able to help you.

We are a small Foundation run by parents for parents, families, professionals, etc.  Please do not hesitate to draw on the wealth of experience within our organisation.  We also need help with funding our ambitious medical research projects and family support programme, so if you feel able to assist us in any way, please contact us.

For more information, please contact the Head office.












Disclaimer: The information provided on this website is intended to give general information about Williams Syndrome. The information is not intended to be relied upon or to be a substitute for medical or legal advice. Accordingly, we do not accept any liability for any damages or loss which may arise from reliance upon this information.