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The Turner Syndrome Foundation, based in Hazlet, NJ, is a non-profit organization dedicated to supporting and advocating for individuals with Turner Syndrome, a genetic condition that affects 1 in 2,000 females. They provide specialized care and resources for women and babies diagnosed with Turner Syndrome, including a patient handbook and support for families and healthcare providers. Through fundraising and awareness initiatives, the foundation aims to improve the lives of girls and women with Turner Syndrome and their families. The foundation also focuses on education and research, offering resources for healthcare professionals and promoting healthcare equity for women with Turner Syndrome. They organize events such as walks, runs, and fundraisers to raise awareness and funds for their mission. With a commitment to communication and collaboration, the Turner Syndrome Foundation strives to make a difference in the lives of those affected by Turner Syndrome.Generated from the website

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