161 High Street
Tel: 01732 365152
The Foundation finds many ways to help Williams' syndrome children and their families. There are regional contacts around the country - all parents of a Williams' syndrome child - who keep in touch with local families, visit new contacts, arrange meetings, and organise fund-raising events. The Foundation organises national meetings, as well as local gatherings for families.
The Foundation acts as an information and advisory service and keeps parents in touch, with half yearly newsletters and magazine. It also keeps a register of all known Williams' syndrome cases and provides access for professionals to assist research.
Last updated on 25/09/2013
Disclaimer: This article is for information only and should not be used for the diagnosis or treatment of medical conditions. Patient Platform Limited has used all reasonable care in compiling the information but make no warranty as to its accuracy. Consult a doctor or other health care professional for diagnosis and treatment of medical conditions. For details see our conditions.