One in 18,000 people in the UK have Williams Syndrome.
Williams Syndrome is a micro-deletion of genetic material from a specific region of chromosome 7.
Only one in 30 GPs will ever see a patient with Williams Syndrome.
How we can help
The WSF is on hand to offer help and support to families, carers and people with WS.
The Foundation arranges and subsidises group respite breaks for WS adults and families.
However you choose to fundraise, we are here to help and support you every step of the way.
Watch nowMathew Baynton sets out to raise awareness of Williams Syndrome.
Our 2026 range of Christmas cards are available to buy now through our online shop.
Christmas cards are great way of raising awareness of WS and the WSF and ALL the profit raised goes directly to the WSF.
A hard copy of the brochure is available here or email us at enquiries@williams-syndrome.org.uk
The Autumn/Winter issue of the WSF’s member magazine ‘Talk to Me’ is out now! Full of fundraising stories, amazing achievements, Calvert Trust holidays, news, events, personal experience stories, research and more.
If you have any feedback or if there is anything you would like to see featured in our next issue, please email: mag@williams-syndrome.org.uk
If you haven’t yet received yours either by post or email, contact us at: enquiries@williams-syndrome.org.uk
We’re delighted to have partnered with Run for Charity to bring you access to an incredible range of sponsored events, giving you the opportunity to challenge yourself, have fun, and raise vital funds for the WSF at the same time!
Sign up online and get in touch – we would love you to share your journey from fundraising to the finish line, supporting you in any way we can!