Business Description Prader‐Willi Syndrome Association | USA was established in 1975 to unite parents, professionals, and other interested citizens to enhance the quality of life for those affected by Prader‐Willi syndrome (PWS). The organization plays a crucial role in the PWS community by providing a platform for shared experiences, advancing research, promoting education, advocating for patient rights, and offering comprehensive support to individuals with the syndrome and their families. With chapters across most states, PWSA | USA stands as the only national PWS supporith Prader-Willi syndrome t organization dedicated exclusively to assisting individuals w and their families at every stage of their journey.
Mission and Vision Mission: To empower the Prader-Willi syndrome community through shared experiences, research, education, advocacy, and support. Vision: To enhance the quality of life of those affected by Prader-Willi syndrome and ensure they receive the necessary support and resources. Services and Programs Support Services: Emotional and informational support for families and individuals. Assistance with accessing healthcare and educational resources. Crisis intervention and management. Education and Awareness: Educational resources for families, professionals, and the general public. Workshops, webinars, and conferences on PWS. Advocacy: Advocacy for policies and legislation that benefit individuals with PWS. Collaboration with other organizations and stakeholders to promote awareness and research funding. Research: Funding and supporting research initiatives aimed at understanding PWS. Promoting and disseminating research findings to the community. Community Building: Facilitating connections among families, caregivers, and individuals with PWS. Organizing community events and support groups.
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