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 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 viewsJan 28, 2021
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Williams Syndrome Association on Reels
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Williams Syndrome Association on Reels
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Williams Syndrome Association on Reels
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Williams Syndrome Association on Reels
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Williams syndrome: Video, Causes, & Meaning | Osmosis
Williams syndrome: Video, Causes, & Meaning | Osmosis
6.7K viewsOct 16, 2018
osmosis.org
💙 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 views10 months ago
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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
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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
4K viewsMay 6, 2024
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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
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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
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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 viewsSep 6, 2023
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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 views6 months ago
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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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True Love: The Film is now streaming! This award-winning film gives viewers a glimpse of what it’s like to experience life through the eyes of Callie Truelove, a teenage girl with Williams syndrome who has blessed her with the superpower of LOVE! Learn more about the film: https://pulse.ly/c8yi4i6yqs | Williams Syndrome Association
7.4K viewsSep 14, 2023
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Williams syndrome is caused by a tiny but powerful deletion of genes on chromosome 7 — This genetic change affects about 1 in 10,000 people and leads to unique strengths and challenges. 💙 May is Williams Syndrome Awareness Month — let’s celebrate the vibrant, kind, and musical individuals who light up our world with their extraordinary spirit. #WilliamsSyndrome #WSAwarenessMonth #Chromosome7 #GeneticAwareness | The Birch Family
25.7K views11 months ago
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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
7K viewsNov 19, 2020
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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
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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
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What is Williams Syndrome? The rare condition that makes people unusually friendly
11 months ago
MSNTOI Lifestyle Desk
What is Prader-Willi Syndrome
Feb 4, 2022
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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
644.1K viewsApr 4, 2022
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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 viewsMay 16, 2023
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HER FIRST CONCERT EVER! 🎸 Emotional Journey Reaction in Memphis! ✨
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