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        It has been 80 years since Harry Klinefelter discovered Klinefelter syndrome in 1942. Each generation of individuals diagnosed has faced its own set of challenges and difficulties. With hard work and determination, our community has come a long way. Transparency on where your donations go: Our writing team works on biographies and blog posts. Our website brings the latest information to people's fingertips. Building educational materials for parents, teens, and adults. Male Infertility resources, Managing our social media presence, producing podcasts, youtube videos, and documentary films. 

        We represent individuals, families, and friends from 40 different countries. "Hi, Ryan! My XXY boy was born a week and a half ago, and I just wanted to thank you for everything you're doing! We were being led to believe termination was our only option, and my husband and I found your Instagram. It has made accepting and advocating for our son so much easier, honestly changed our lives, and given us the tools to give our son the best possible life. THANK YOU" - Kori Fuchs 

        A clear and present vulnerability exists for Living With XXY: Each year, we face more babies wrongfully terminated, as NIPT (noninvasive prenatal testing) is becoming more readily available. Klinefelter syndrome is not a death sentence; we bring kindness, creativity, and empathy to a desperately needed world. 

        "The stigmas of the past will not take away the voices of the future." – Ryan Bregante.

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