Prader-Willi Syndrome Association | USA
What’s YOUR story? Tweet us and tell us what it’s like #GrowingUpRare We hope you will suggest the PWSA | USA facebook page to your friends! Website: www.pwsausa.org PWSA (USA) is an organization of families and professionals working together to promote and fund research, provide education, and offer support to enhance the quality of life of those affected by Prader-Willi syndrome.
Founded
1977
15000
X (Twitter)
1178
Traffic
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Prader-Willi Syndrome Association USA - Supporting Families PraderWilli Syndrome Association USA Empowering Individuals Supporting Families PWS Advocacy Awareness PWS Family Support PWSA USA Family Support team provides individuals diagnosed with PraderWilli syndrome their families and care providers with critical information and resources on PWS. PWS Research PWSA USA seeks to support research projects with the potential for immediate and high impact for the PraderWilli Syndrome community. Registration is now OPEN for the 2025 International PWS Conference. Join PWSA USA IPWSO and FPWR June 2428 2025 in Phoenix Arizona.
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Prader-Willi Syndrome Association | USA
Our United We Brunch fundraisers are well underway. United We Brunch is all about raising awareness, fostering hope, and gathering resources-- one brunch, one state, and one family at a time—uniting communities and creating a ripple effect across the U. S.
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Legal name of organization: Prader-Willi Syndrome Association | USA
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