Our mission: Living with XXY changes how the world views Klinefelter syndrome (47 XXY). Focusing on community, awareness, and positive traits.
"Hello Ryan, this is Anderson. He is two months old today and has Klinefelter syndrome/47 XXY. We love him to pieces!!! He sleeps through the night, rolling over, smiling at us, and babbling. We were apprehensive when the doctors told us our results from NIPT testing.
It wasn't enjoyable finding out my son had XXY. My doctor gave me the worst image of Klinefelter syndrome. Telling me, he would be a tall, overweight, very low-intelligence man-child who would never be able to have children. I asked about terminating if I chose that option, and he said he could give me referrals. I left in a daze and cried all the way home in the car, talking to my husband. I vented to my mom while I googled it and the cost of abortions.
Then I found your site and nonprofit and read the positive messages from people with XXY. I especially loved the page listing all of the positive characteristics. We knew our baby would be perfect with his extra X. You gave us hope to face the rest of my pregnancy with peace and excitement. Thank you for your incredible life-changing work." - Proud Mother.

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