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.
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About Fragile X Syndrome | Fragile X Society | UK
About Fragile X Syndrome | Fragile X Society | UK
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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
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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💙 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
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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
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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/o | 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
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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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🌟 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
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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
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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
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