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
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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
Special Books by Special Kids. . 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.
1.1M viewsJan 28, 2021
Williams Syndrome Explained
About Fragile X Syndrome | Fragile X Society | UK
About Fragile X Syndrome | Fragile X Society | UK
fragilex.org.uk
Sep 9, 2016
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
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
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2M viewsMay 16, 2023
Williams-Beuren Syndrome Explained Causes, Symptoms and Treatment, All Insights
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Williams-Beuren Syndrome Explained Causes, Symptoms and Treatment, All Insights
YouTubeDisease Decoder
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Williams Syndrome Association on Reels
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Williams Syndrome Association on Reels
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Actress, singer, and author Kristen Bell went to the same Michigan elementary school as one of our adult friends with Williams syndrome and she lends her voice to many good causes. Thanks for kicking off our walk week in style, Kristen! We really appreciate it and we know many in our community can be counted as fans! Show your support this week, and join us for our opening ceremony at 11:30 a.m. EST August 1st! Our campaign: wsawareness.org (or via the post). Thank you! #Walk4Williams #Everywher
0:19
Actress, singer, and author Kristen Bell went to the same Michigan elementary school as one of our adult friends with Williams syndrome and she lends her voice to many good causes. Thanks for kicking off our walk week in style, Kristen! We really appreciate it and we know many in our community can be counted as fans! Show your support this week, and join us for our opening ceremony at 11:30 a.m. EST August 1st! Our campaign: wsawareness.org (or via the post). Thank you! #Walk4Williams #Everywher
FacebookWilliams Syndrome
27.9K viewsJul 26, 2020
Williams Syndrome Walk to Support Local Student
Williams Syndrome Walk to Support Local Student
patch.com
May 4, 2011
Williams Syndrome Stories
No one size fits all when it comes to Williams Syndrome! Autumn and her dad, WSA Board President, William Palmer share their Sunday with us! Every person with Williams Syndrome brings their own stories, strengths, and individuality. ❤️ #williamssyndrome #williamssyndromeawareness #dualdiagnosis | Williams Syndrome Association
2:06
No one size fits all when it comes to Williams Syndrome! Autumn and her dad, WSA Board President, William Palmer share their Sunday with us! Every person with Williams Syndrome brings their own stories, strengths, and individuality. ❤️ #williamssyndrome #williamssyndromeawareness #dualdiagnosis | Williams Syndrome Association
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7.1K views11 months ago
As we say goodbye to 2023, we can't help but be excited for 2024: Convention, Camp, and Events all over the country will see so many of us get together to share our stories, strategies, and successes! Happy New Year from all of us to all of you! 🎉🎉🎉 #williamssyndrome #williamssyndromeawareness #wsa | Williams Syndrome Association
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As we say goodbye to 2023, we can't help but be excited for 2024: Convention, Camp, and Events all over the country will see so many of us get together to share our stories, strategies, and successes! Happy New Year from all of us to all of you! 🎉🎉🎉 #williamssyndrome #williamssyndromeawareness #wsa | Williams Syndrome Association
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948 viewsDec 31, 2023
This week our blog was about the effects of convention, and we're continuing the thread (see link for blog in comments). Mom Jennifer Ryan sent her stories/observations--feel free to share yours if you were at #SetSail2018! And enjoy a few more pictures! 1. "We take turns with childcare during the convention. While Granny (Cathy Minnella) was at a session, I took Elise (8, and dually diagnosed with Williams syndrome) to the Hard Rock Café. The adults arrived (The Dream Team--ages 38+). My daught
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This week our blog was about the effects of convention, and we're continuing the thread (see link for blog in comments). Mom Jennifer Ryan sent her stories/observations--feel free to share yours if you were at #SetSail2018! And enjoy a few more pictures! 1. "We take turns with childcare during the convention. While Granny (Cathy Minnella) was at a session, I took Elise (8, and dually diagnosed with Williams syndrome) to the Hard Rock Café. The adults arrived (The Dream Team--ages 38+). My daught
FacebookWilliams Syndrome
1.8K viewsAug 2, 2018
Williams Syndrome Association on Reels
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Williams Syndrome Association on Reels
5K viewsJul 13, 2022
FacebookWilliams Syndrome Association
Actress, singer, and author Kristen Bell went to the same Michigan elementary school as one of our adult friends with Williams syndrome and she lends her voice to many good causes. Thanks for kicking off our walk week in style, Kristen! We really appreciate it and we know many in our community can be counted as fans! Show your support this week, and join us for our opening ceremony at 11:30 a.m. EST August 1st! Our campaign: wsawareness.org (or via the post). Thank you! #Walk4Williams #Everywher
0:19
Actress, singer, and author Kristen Bell went to the same Michigan elementary school as one of our adult friends with Williams syndrome and she lends her voice to many good causes. Thanks for kicking off our walk week in style, Kristen! We really appreciate it and we know many in our community can be counted as fans! Show your support this week, and join us for our opening ceremony at 11:30 a.m. EST August 1st! Our campaign: wsawareness.org (or via the post). Thank you! #Walk4Williams #Everywher
27.9K viewsJul 26, 2020
FacebookWilliams Syndrome Association
Williams Syndrome Walk to Support Local Student
Williams Syndrome Walk to Support Local Student
May 4, 2011
patch.com
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! 🫶�
1:52
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 views10 months ago
FacebookWilliams Syndrome Association
What a perfect weekend to #walkforwilliams! 💚Congratulations to Twin Cities for crushing their original goal of raising $5000 and topping that with a total number of $14,728 raised!!!!!🎉 Way to go Minnesota! 👏🏼 Did you walk with Twin Cities this weekend? 🎥 credit: Joel Liestman #williamssyndrome #twincities #walkforacause | Williams Syndrome Association
2:56
What a perfect weekend to #walkforwilliams! 💚Congratulations to Twin Cities for crushing their original goal of raising $5000 and topping that with a total number of $14,728 raised!!!!!🎉 Way to go Minnesota! 👏🏼 Did you walk with Twin Cities this weekend? 🎥 credit: Joel Liestman #williamssyndrome #twincities #walkforacause | Williams Syndrome Association
973 viewsSep 16, 2024
FacebookWilliams Syndrome Association
💙 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
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💙 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 views11 months ago
FacebookWilliams Syndrome Association
💙 Every Step Matters ❤️ Awareness is always in season,It blooms in hearts for every reason.Through every moment, every year,The need for love and hope is clear. A walk is more than just a stride,It is stories shared, it is hands held wide.It is the ones who walk with joy and grace,And those who find a brighter place. When we gather for Williams, side by side,We honor those we love with every stride. We raise our voices, loud and strong, Because in this fight, we all belong. It’s not about the m
2:02
💙 Every Step Matters ❤️ Awareness is always in season,It blooms in hearts for every reason.Through every moment, every year,The need for love and hope is clear. A walk is more than just a stride,It is stories shared, it is hands held wide.It is the ones who walk with joy and grace,And those who find a brighter place. When we gather for Williams, side by side,We honor those we love with every stride. We raise our voices, loud and strong, Because in this fight, we all belong. It’s not about the m
3.4K views11 months ago
FacebookWilliams Syndrome Association
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Walk for #williamssyndrome today!! We’re headed to #mississippi first ever #walkforwilliams ❤️💚💙 #teamreagan on the road!!! Come with us today and experience Reagan’s first Williams syndrome activity!!! #senior2026🎓❤️ #williamssyndromeawareness #senioryearloading #reagansworld #inclusionmatters #ilovesomeonewithwilliamssyndrome #morethanasyndrome | Jen Pulliam
8.9K views11 months ago
FacebookJen Pulliam
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No one size fits all when it comes to Williams Syndrome! Autumn and her dad, WSA Board President, William Palmer share their Sunday with us! Every person with Williams Syndrome brings their own stories, strengths, and individuality. ❤️ #williamssyndrome #williamssyndromeawareness #dualdiagnosis | Williams Syndrome Association
7.1K views11 months ago
FacebookWilliams Syndrome Association
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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 viewsJun 25, 2020
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Where are we going in 2026?!📣 The Williams Syndrome Association (WSA) & the Canadian Association for Williams Syndrome (CAWS) are thrilled to announce the first-ever international biennial convention & awareness walk! Join us in Niagara Falls/Buffalo from July 7-11, 2026, for five days of education, support, & community building. Event Details: Convention Dates: July 7-11, 2026 Location: Niagara Falls/Buffalo Awareness Walk: Niagara Falls State Park - at the American & Canadian border This land
6K viewsJul 10, 2024
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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 viewsJul 16, 2021
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🌟 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 views7 months ago
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Families and volunteers from around the country have been planning and attending great fall events this year with more to come! From picnics to zoo and adventure days at nature centers, gathering with WS families is always a great time. Want to plan an event in your region? We can help with that: https://williams-syndrome.org/volunteer/resources_events | Williams Syndrome Association
454 viewsOct 3, 2017
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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
2.4K viewsAug 1, 2021
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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
7.2K viewsNov 19, 2020
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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 viewsDec 12, 2022
FacebookWilliams Syndrome Association
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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
2.4K views4 months ago
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'Walk for Williams' aims to raise awareness on rare disorder
May 9, 2022
wkow.com
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
644.2K viewsApr 4, 2022
FacebookSpecial Books by Special Kids
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This Saturday join us for a special Walk for Williams Syndrome with Daren #ProgressiveMedicalCenter
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