Williams Syndrome Info & Facts

10/13/2026

09/19/2026

09/16/2026

Unfortunately, my daughter, Kristina Juliano is sick & won’t be able to attend the Walk for Williams Syndrome fundraiser this Saturday but we are trying to raise our fundraising impact. Please consider a donation. The Williams Syndrome Association is the key to supporting our individuals with Ws in providing educational, social & research opportunities. Special camps & events. Individuals with Ws are living happier healthier lives. Support groups are provided for caretakers, parents, grandparents & siblings. Teachers can access educational resources, educational profile & strategies right on the website. Biannual conferences are held & this year a combined conference with the Canadian counterpart CAWS was held at Niagara Falls. The WSA is managed predominantly by parents & families of individuals with Ws. Key doctors & providers combine with the WSA to advance research & share new findings with families.

Check out all that is provided on their website: https://www.williams-syndrome.org

Our fundraising page:

https://fundraise.givesmart.com/vf/WSABOSTON/JudithMarino

THANK YOU IN ADVANCE FOR ALL YOUR SUPPORT. Judy L. Larsen Marino

Awareness is always in season at the 2026 WSA Fundraising Walk for Williams. I am actively fundraising for this meaningful event and invite friends like you to stand alongside me in supporting the Williams syndrome community. Lace up your walking shoes, join our campaign, and help us fund vital prog...

01/28/2026

Good morning. I am looking for a new P*P for my daughter. She is a 40 yo individual with Ws living in New Britain, CT. Anything in the Hartford area would be good. Please let me know if you have any recommendations. I appreciate it.