🌟 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
🌟 BIG ANNOUNCEMENT! 🌟 We’re thrilled to share that the 2028 WS…
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You know the song that you hear at the beginning of every episode? Our first guests, Mariella Elm and Tommy Barbarella, wrote that song. Mariella is 17 and has Williams syndrome, and her dad has been a professional musician for years, playing with such artists as the Jonas Brothers and Prince! They join us to discuss their musical, "The Girl Who Cried Different." Next, Kristen Van Handel talks to us about working for make-up giants Sephora and knowing that beauty can come in all kinds of package
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Boots and cats and boots and cats…🎤 Our Teen group crushing it today! It’s been a fantastic week! #wsaphx2024 #beatbox #williamssyndrome | Williams Syndrome Association
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When Debbie's daughter Laura was 8-years-old (now 44), she "finally" heard of the WSA, which led to years of active involvement and convention attendance that continues today. Back then, the internet was not available to spread information like it is today, so these connections looked a bit different when the WSA was officially incorporated 40 years ago. Her convention attendences provided information and opportunties for Laura that she never would have known about otherwise, and she was graciou
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