TONIGHT! Don't miss our webinar with WSF trustee, Jon Stevens, who will be offering information and advice on Financial Planning for those with Williams Syndrome. Tuesday 6th May @ 7.30pm. Email: [email protected] to join us. . #williamssyndrome #webinar #WSF

Life with Williams Syndrome is more than you can imagine... By Liz Martin – Williams Syndrome Genetic Alliance UK

Hello and welcome to the Williams Syndrome Foundation #TuesdayTakover! We are grateful to be given this opportunity to tell you all about Williams Syndrome, especially during Williams Syndrome Awareness Month! Williams Syndrome UK #WilliamsSyndrome #Charity #Genetics #Rare

Williams Syndrome is a rare genetic condition affecting around 1/18,000 people in the UK. It’s caused by a deletion on chromosome 7. It causes cardiac, physical and mental health problems as well as learning disabilities. williams-syndrome.org.uk #WilliamsSyndrome Williams Syndrome UK

The Williams Syndrome UK is a small UK charity, providing help and support for individuals with Williams Syndrome. We fund research, create resources and organise regional events to keep families connected. williams-syndrome.org.uk #WilliamsSyndrome #Charity #Rare #Support

Williams Syndrome UK supports individuals with WS and their families through research, resources, and events. Learn more: williams-syndrome.org.uk #RareDisease #WilliamsSyndrome #Charity #Genetics #Chromosome #Rare #Healthcare #NHS

We are fortunate to have a fantastic Professional Advisory Panel (PAP) - a panel of professionals who have expertise in WS and/or a special interest in voluntarily supporting families with WS. #WilliamsSyndrome #WilliamsSyndromeSupport Williams Syndrome UK

We celebrate #WilliamsSyndrome Awareness Month in May. By raising awareness, we can improve early diagnosis and intervention, promote research as well as reduce feelings of isolation and discrimination. Join us and help spread the Williams Syndrome word in May! Williams Syndrome UK

The Williams Syndrome UK Family Convention provides excellent opportunities for everyone to make friends and share support. There are presentations and workshops hosted by professionals and experts in WS. Find out more about our conventions by watching this video: williams-syndrome.org.uk/wsf-family-con…

Thank you for following our #TuesdayTakeover! If you would like to find out more about #WilliamsSyndrome or the Williams Syndrome UK, please contact us at [email protected] or visit williams-syndrome.org.uk 0208 5671374 #Charity #Genetics #Rare #Awareness

Thank you to our wonderful WSF Patrons Elizabeth and Peter for helping to spread awareness of #WilliamsSyndrome for their niece Molly!❤️ Find out more about Williams Syndrome at williams-syndrome.org.uk . #williamssyndromeawarenessmonth #williamssyndrome #shareyourheart #DrWho

See the plain English england.nhs.uk/long-read/heal… and easy read england.nhs.uk/wp-content/upl… guidance on how to the complete the health and care passport template which is for people with a learning disability, autistic people, their families/carers.

Please watch this wonderful video starring Ashlee and Isabel - two inspirational ladies with #WilliamsSyndrome and ambassadors for the WSF ❤️

Participants needed for research study! Durham University require young people with Williams Syndrome aged 12 - 25 and their parents, to take part in a study on the social world of people with WS. Please scan the QR codes or email: [email protected]. youtube.com/watch?v=WL-Y4M…

This week is Carers Week. Thank you to all of the carers in the U.K. and all over the world. #CarersWeek #CarersWeek2025 #Carers

Proud to have contributed to Jamie Oliver’s Dyslexia Revolution documentary on Channel 4 with The Jamie Oliver Group, which shines a spotlight on what needs to change in our education system for children with SEND (📚💡 #SEND #EducationReform #Dyslexia #JamieOliver #ComeOnBridget

It's learning disability week. This year's theme is about being seen, heard and being valued. People over 14 with a learning disability should have a health check every year. youtu.be/ocU8XhD1kh8 Make sure you ask your GP for your health check youtu.be/TBZpaJbeg2g

NEW WEBINAR!⭐️ Wednesday 25th July - Upholding the legal rights of people with WS with Eliza Sharron and Imogen Jolley. Our webinars are designed to support parents and carers of children and adults with WS. Email: [email protected]

Participants needed! @durhamuniversity require people with Williams Syndrome aged 12 - 25 and their parents, to take part in a study looking at the social world of people with WS. Watch the short video to find out more. youtube.com/watch?v=WL-Y4M… email: [email protected]

On Wednesday 25th July, Williams Syndrome UK are holding a webinar on 'Upholding the legal rights of people with William Syndrome (and similar conditions)' - designed to support parents and carers of children and adults with Williams Syndrome. Book your pace now: forms.office.com/pages/response…