Livingwithxxy

Evan Flores was born and raised in NYC his entire life. He never left and met his amazing wife Sabrina on August 19th, 2010 After 3 to 4 years of trying to have a family, Evan and Sabrina decided to go in for testing to see why nothing was working. After testing, Evan was diagnosed with Klinefelter syndrome and was in utter shock. “How is it even possible for someone to have an extra chromosome,”...

Geoff Kruck 42 years old, lives just north of Melbourne, Australia. Geoff found out the hard way he had Klinefelter syndrome. When he got married to his wife, he didn’t have an overbearing desire to have children.  Geoff was just thrilled he was marrying his best friend.  He thought starting a family would come naturally down the road.  Geoff says "you just assume it’s going to happ...

Richard and Rosalie Bregante share information on what it was like to raise their son, who was born in 1985 when information for Klinefelter syndrome was very limited.   https://livingwithxxy.org/

Andrew was diagnosed with Klinefelter syndrome at the age of 16 after waking up one morning saying his testicles were hurting. A trip to the urologist and several doctor visits later he found out why.  He talks about what it was like to be diagnosed, being developmentally behind his peers, and how he caught up with life at 22.  He is actively involved with raising awareness online and ge...

Ryan Bregante shares what it was like growing up and going through grade school and middle school.   From bulling to believing in himself and self-advocating.  He also talks about how he got started raising awareness for Klinefelter syndrome and forming a non-profit organization to better help this amazing community come together to break down stigmas created by out of date informat...

Taking you all back to freshman year of high school as if it was yesterday.  Some key talking points are about being in an English class with 4 Japanese students, myself, and a teacher.  Also how I coped with bullying due to being a slow reader.  Playing sports freshman year and attending homecoming.  I hope you are able to learn more about my story and journey with Klinefelter...

What it was like for Kelsey to be diagnosed with Klinefelter syndrome at 27 years old while trying to build a family. Kelsey talks about when doctors told him he would not be able to have kids, that he wasn't going to let that stop him.  Even with the unknowns, emotions and anxiety Kelsey overcame the challenges of infertility using donor sperm with his wife.  Today they have two amazing...

We welcome you to join and subscribe to our brand new podcast series for Klinefelter syndrome awareness.  This is our introduction to what the podcast will be all about and how we will grow over time.  This podcast gives the voices of our community a chance to share the spotlight.  We look forward to having you.   Www.livingwithxxy.org