From Our FounderWelcome Back to the Living with XXY Newsletter! We look forward to producing our newsletter more frequently [...]

THE ORIGINAL ARTICLE CAN BE FOUND HERE BIOTECHNOLOGYWhat to expect when you’re expecting an extra X or Y [...]

Original article from SDvoyager found Here Today we’d like to introduce you to Ryan Bregante.  Hi Ryan, thanks for [...]

Apr 13, 2021, 4:25 PM Original Article HERE Hi there, I’m Sam. I’m 27 and I got diagnosed [...]

Dear Community, This year was the first year building an annual report; it was extremely challenging and frustrating. [...]

XXY Males – Klinefelter syndrome HEALTH TOPIC BY GLENDA FAUNTLEROY DEC 2012 Although considered the most common chromosomal [...]

At age 21, Graham loves to spend time on his favorite pastime of writing mysteries and screen plays. [...]

By JANE E. BRODY AUG. 31, 2004 The New York Times 2004 Sam’s parents began to suspect something was not [...]

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

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

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

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

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

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

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

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

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

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