Description
The Williams Syndrome Foundation is the first point of contact for families whose child has been diagnosed with WS or individuals with the condition and for professionals involved with the care, education, and health of those with WS.
What they do:
- Support families with new diagnosis
- Operate UK wide regional network
- Hold social and information events
- Fund research into all aspects of WS
- Produce resources about WS and the management thereof
Location
- Address: Williams Syndrome Foundation, Box 103, Charter House, Lord Montgomery Way, Portsmouth, PO1 2SN
Who to contact
- Telephone: 0208 567 1374
- Email: enquiries@williams-syndrome.org.uk
- Website: