Our Community
Inspirational stories from people all over the world who have been affected by Klinefelter syndrome 47 XXY. These are the voices of our community and their experiences are helping to make a bigger difference. Many of these posts have been published in magazines and newspapers.
Marathon Baby by Cedars-Sinai Magazine
Marathon Baby Feb 26, 2020 Amy Paturel, Photos by Ted Catanzaro Original Article - Here Fueled by the power [...]
The hope of fathering children snatched away at 20.
Original Article by Bourn Hall Fertility Clinic When Fraser was diagnosed with Klinefelter Syndrome, it was possible he [...]
The Diagnosis of an Extra X Chromosome Helped Mathew Find Himself
This article was written by Children’s Hospital Colorado In a tunnel beneath Willow Park Drive in Parker, Colorado, along [...]
A New Zealand mother and her XXY Kid
I am writing this from a mother's perspective, my son Noah is aged 5 and is an XXY [...]
Jack’s Mom
This blog is created for families or expectant parents of sons living with Klinefelter Syndrome 47 XXY. By sharing our journey and experiences, we hope the content provides clarity, inspires hope, and brings a smile to many faces. We aren’t experts—we are parents just like you, figuring this out day-by-day, yet determined to give Jack the best launch to an amazing life ahead of him. We are excited to link arms with you, building this community together while providing a brighter future for our sons.
Try Try Try
“TRY, TRY, TRY!” were the words that came out of Jack’s mouth as he attempted to run up [...]
Klinefelter Syndrome Speech Therapy Tips
“But your son doesn’t sound like he needs speech therapy.” or “But he’s only 10 months old. What [...]
XXY Syndrome Diagnosis Guide
Our Vision Our capacity to love has expanded because of our son, Jack. Our vision with this [...]
Establishment of Care: Klinefelter Syndrome Guide
Jack was the name we picked out for our son before we even knew he was a boy. [...]
News & Updates
Marci Tatham “Jack’s Mom” Joins Living With XXY
Hey Everyone! My name is Marci Tatham and I’m pleased to announce that I’ve officially joined the Living With [...]
Living With XXY Newsletter: April 2020
Stanford BGAP Study Visit In late February, our team had the privilege of meeting the team [...]
Stanford’s Brain, Genes, and Puberty (BGAP) Study!
Researchers at Stanford University are looking for boys ages 8-13 with confirmed non-mosaic Klinefelter syndrome (47, XXY) to [...]
Loving With XXY
Love is what keeps our community together, and one way we can show our dearest ones living with [...]