A blood test could have revealed the disorder far earlier The Washington Post, 24 Aug 2010 Years wreaking havoc on families who struggle to [...]

Original Article by LJWorld Julie and Brandon Urban only wish they had the cards sooner. Then they could have handed them to people [...]

The genetic condition is one of the most common in the UK and maybe a leading cause of infertility in men. Why does [...]

Families have a place to turn for help with sex chromosome disorders. Article By Pam Auchmutey Emory Health Digest Emma St. Germain [...]

Welcome Home! It’s hard to believe 2021 is soaring by so fast! We’ve been busy and we know you have too. That [...]

Dear Living With XXY Community, Let's go back to November 6th, 2019: Living with XXY was born, as an official nonprofit organization. We [...]

Hey Everyone! My name is Marci Tatham and I’m pleased to announce that I’ve officially joined the Living With XXY team as their newest [...]

Stanford BGAP Study Visit In late February, our team had the privilege of meeting the team at Stanford to get a [...]

Researchers at Stanford University are looking for boys ages 8-13 with confirmed non-mosaic Klinefelter syndrome (47, XXY) to participate in a study exploring [...]

Love is what keeps our community together, and one way we can show our dearest ones living with XXY, just how much we [...]