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Williams Syndrome Foundation
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20 Convention
0:26
7.11.23 is a once-in-a-century date. Today we celebrate & raise awareness of Williams Syndrome. It corresponds to the area of deletion on the #7 chromosome, 7q11.23, that signifies Williams Syndrome. Later today, we're bringing you the story of Paul Glover and his daughters, who have Williams Syndrome and volunteer for The Foundation.💙 West Bromwich Albion | Williams Syndrome Foundation UK | The Albion Foundation
1.7K views
Nov 7, 2023
Facebook
The Albion Foundation
0:18
Williams Syndrome Association on Reels
5K views
Jul 13, 2022
Facebook
Williams Syndrome Association
0:31
Williams Syndrome Association on Reels
1.9K views
Feb 28, 2023
Facebook
Williams Syndrome Association
0:22
Williams Syndrome Association on Reels
2.2K views
Aug 5, 2020
Facebook
Williams Syndrome Association
8:58
Callie Truelove is diagnosed with Williams syndrome, a rare genetic condition known to cause a joyful demanor. She loves everybody and even sees hearts in common objects all around her. Callie's parents consider her positivity a blessing, but also try to teach her not everbody can be trusted. | Special Books by Special Kids
1.1M views
Jan 28, 2021
Facebook
Special Books by Special Kids
Home - Williams Syndrome Foundation
11 months ago
williams-syndrome.org.uk
1:15
NEW! UCL Maths Intervention Project – For Children with Williams Syndrome aged 5-11. 👩⚕️ This study will examine the effectiveness of two maths intervention programmes, in improving maths skills in those with WS. Watch this short video of PhD student Arcelia, explaining in more detail about what will be involved in this study. If you have any questions or would like more information, please email: nga.cheung.23@ucl.ac.uk | Williams Syndrome Foundation UK
118 views
5 months ago
Facebook
Williams Syndrome Foundation UK
Williams syndrome: Video, Causes, & Meaning | Osmosis
6.7K views
Oct 16, 2018
osmosis.org
1:52
Let’s be honest-fundraising can feel akward! The planning the posting the asking-it’s a lot. But here’s the truth: you don’t have to have experience or raise thousands. You just have to want to make a difference. ❤️ When you speak up for Williams syndrome awareness, you’re offering people a chance to make a difference. This is your sign to start. Your way, your voice, your impact. Let’s do this together! Click the link in our bio for more info on walks or how to set one up in your community! 🫶�
1.2K views
11 months ago
Facebook
Williams Syndrome Association
3:41
As we continue to celebrate 30 years of the ASF check out Dr. Charles Williams talking on the “Big Moments” of AS Research. | Angelman Syndrome Foundation
857 views
Jun 29, 2022
Facebook
Angelman Syndrome Foundation
0:28
💙 Psst! #weekendforwilliams is tomorrow!! We’re calling on everyone to come together & support Williams Syndrome! There are ✌🏼ways to give (you can start now!): text WEEKEND to 71777 or visit weekendforwilliams.org where you can also get more info on where your support goes! 🎥: Special thank you to our Adventure Seekers! #weekendforwilliams #makemaymatter #giveback #williamssyndromeawareness | Williams Syndrome Association
2.8K views
11 months ago
Facebook
Williams Syndrome Association
0:06
For kids with Williams syndrome ages 0-5, the early years are crucial for intervention and support. At the WSA, we’re here to help families every step of the way: 🧸 Providing information on early intervention programs that use play to address developmental delays through physical, occupational, speech and music therapy. 📋 Guiding families through the process of creating an Individualized Education Program (IEP) - the roadmap for your child’s public education. 👩🏫 Sharing strategies that work
4.1K views
May 6, 2024
Facebook
Williams Syndrome Association
0:42
The power of community! Individuals with Williams syndrome understand that community is family and that with family comes strength, resilience, and the power of love. The Williams Syndrome Association understands that too. We work to bring families together, to celebrate the joys of everyone’s accomplishments, and work together to overcome the challenges that Williams syndrome puts in their path. To help keep our WSA family strong despite the challenges of COVID-19, go to wsawareness.org to crea
1.9K views
Jun 25, 2020
Facebook
Williams Syndrome Association
0:53
Director of Family Support, Joel Liestman with a quick message for our WS families!Everything in one place so you can find what you need! ❤️🌟. 🔸For Family support groups & links: https://www.williams-syndrome.org/programs/supportgroups 🔸For Adventure Seekers: https://www.williams-syndrome.org/adventureseekers | Williams Syndrome Association
774 views
Sep 9, 2024
Facebook
Williams Syndrome Association
0:30
Kids with William syndrome often gravitate toward rhythm and music. Baby Declan is a future drummer and he's off to a good start! This sweet video was captured in his dad's studio. ♥️🥁. Happy Friday! Thanks for making us smile, Declan. 😍 #williamssyndrome | Williams Syndrome Association
3.1K views
Jul 16, 2021
Facebook
Williams Syndrome Association
6:11
While many of us may not have heard of Williams Syndrome, the parents of kids diagnosed with it are rewarded with a life of joy with children who want to make the most of it. However,it can be tinged with the knowledge that the worst could happen at any time. | The Project
1.2M views
Sep 6, 2023
Facebook
The Project
4:31
🌟 BIG ANNOUNCEMENT! 🌟 We’re thrilled to share that the 2028 WSA National Convention will be hosted in the Twin Cities, Minnesota, July 11–15, 2028! 🎉 The exciting news was announced at the Twin Cities Walk for Williams today by Minnesota Secretary of State Steve Simon and long-time WSA advocate Megan McNeil. Minnesota is ready to welcome our Williams syndrome community from across the country for connection, learning, and celebration. 💙❤️💚 BUT FIRST—get ready to join us next year in Buffalo
3.6K views
7 months ago
Facebook
Williams Syndrome Association
About Fragile X Syndrome | Fragile X Society | UK
Sep 9, 2016
fragilex.org.uk
0:12
Our camps provide many therapeutic activities and experiences for those with William syndrome. But the dancing? It is always a highlight when people with Williams syndrome of all ages get together! 💃🕺😍#williamssyndrome | Williams Syndrome Association
2.5K views
Aug 1, 2021
Facebook
Williams Syndrome Association
0:44
A number of celebrities have supported the WSA this year, including actor James Wolk, who appeared recently in the Watchmen series on HBO. He talks about the Williams Syndrome Association, which he knows through his friend Josh L. Join James and our supporters now and on #GivingTuesday December 1 so we can continue to be the go-to resource for families and individuals in 2021. Thank you! givewsa.org #givingtuesday #williamssyndrome #wsawareness #thanksgiving2020 #wsathankyouthursday | Williams S
7.3K views
Nov 19, 2020
Facebook
Williams Syndrome Association
0:36
Every year, many families in the U.S. begin the journey, and face the need for answers and support that a diagnosis of Williams syndrome sets in motion. For 40 years, the WSA has been here to help. We provide a wealth of knowledge from both experts who have studied or worked with children and adults medically or educationally, as well as from the networking of our members who have the past personal experiences to connect and share. Today, we need your help. We want to positively impact the life
1.2K views
Dec 12, 2022
Facebook
Williams Syndrome Association
1:17
𝐈𝐧𝐭𝐫𝐨𝐝𝐮𝐜𝐢𝐧𝐠 𝐭𝐡𝐞 𝐖𝐒𝐀 𝐒𝐨𝐜𝐢𝐚𝐥 𝐂𝐥𝐮𝐛! The WSA Social Club is your go-to hub for all virtual social and wellbeing programs for individuals with Williams syndrome—parents, caregivers, and siblings are always welcome too! All activities happen virtually on Zoom, from social hangouts to groups like Mindfulness Mondays and Wellness Wednesdays. View upcoming events and join anytime on the Social Club page at www.williams-syndrome.org/programs/wsasocialclub 📣 Big update: The Adve
2.5K views
4 months ago
Facebook
Williams Syndrome Association
25:50
Sofia is diagnosed with Williams syndrome, anxiety, and OCD. She has struggled throughout her life to create relationships with people her own age. The thing that Sofia wants most in the world is a true friendship. | Special Books by Special Kids
644.3K views
Apr 4, 2022
Facebook
Special Books by Special Kids
45:44
Steph is back!! She makes a brief appearance to give an update on her health and what's going on in her life! Then Jen and Producer Joel talk with WSA Educational Consultant Robin Pegg about the work she's doing to change how we think about education and our young people with Williams syndrome. Then they talk to Amy Nussbaum, mother of 4 (including Libi, who's 5 and has Williams syndrome), advocate, and member of the WSA Board of Trustees, about spreading awareness of WS in the month of May and
276 views
May 7, 2023
Facebook
Williams Syndrome Association
Genetic Therapy for Prader-Willi Syndrome
Oct 20, 2020
fpwr.org
21:09
Bess is diagnosed with Williams syndrome, a genetic condition that is known for causing a friendly and happy personality. Her favorite thing to do is play “Dinosaurs” with her younger brother as the two stomp and roar together. Bess hopes that everybody in the world is happy and wants others to know if you feel sad you just have to dance to feel happy again. | Special Books by Special Kids
2M views
May 16, 2023
Facebook
Special Books by Special Kids
1:03
📅 On Saturday May 20th 1pm - 5pm we are holding a family fun day Portway Lifestyle Centre to raise awareness for Williams Syndrome Association. From football and cricket to dance parties and bouncy castles there will be fun for everyone! #WBA | The Albion Foundation
2.7K views
Apr 25, 2017
Facebook
The Albion Foundation
0:15
Celebrating My Birthday with Williams Syndrome Foundation
5.6K views
4 months ago
TikTok
kaydijenae
5:01
Williams Syndrome
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Feb 23, 2021
YouTube
PATH CT
10:00
Williams Syndrome 1
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Oct 19, 2009
YouTube
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