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
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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
Williams Syndrome Association. Williams Syndrome Association · Original audio. 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 ...
1.2K viewsDec 12, 2022
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
FacebookSpecial Books by Special Kid
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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
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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
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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
FacebookWilliams Syndrome
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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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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
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