Throughout the country there are Regional Co-ordinators who are there to help any parents or carers with a child or adult who has Williams Syndrome. The details of the co-ordinator for your area can be found in the "Members Area".
Please contact your co-ordinator 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.
