After Sierra Westley Wilson became pregnant at 27, she wanted to know the gender of their baby, so they did NIPT, and they were told they had a 36% chance of their baby having Klinefelter syndrome.  Once her son was born, they did a routine blood draw, and two weeks later, they learned their son had 48, XXXY. 

In 2021, the day after Christmas, Elliott was hanging out with his niece and nephew, who were 8 and 12. The kids were telling him that he was a fantastic uncle. Suddenly his niece told him he couldn't have kids and that he could adopt if he wanted to. He felt they knew something he didn't know. Elliott Day, from Scotland, in his late 30s, looked into getting his medical records from the NHS. He was diagnosed very young, but no one bothered to tell him.

At 41 years old, Ryan Brown opens up to spread more awareness about his life with Klinefelter syndrome.  When he had been trying to have kids with his ex-wife for over a year, the doctors recommended they both do fertility testing. After a sperm sample and a series of other tests, Ryan discovered he had XXY.  Ryan is now on track to compete in bodybuilding and is a head chef at a group home. 

Jennifer Fritz Voige spent eight agonizing years trying to find her son's Klinefelter syndrome diagnosis.  At the age of 5, Toby started to show challenges after they took away his nap.  In kindergarten, his teachers noticed some blank stares and let Jennifer know something might be happening. This was the start of their long journey.  Toby, now at 14 after his diagnosis in December of 2021, is thriving and started on TRT,  making huge strides toward success.

Gareth Landy was the first person on our podcast from Ireland. He was diagnosed with Klinefelter syndrome while trying to start a family.  Gareth did his first podcast in March of 2021. Since March, he has been on a mission to raise awareness about male infertility. Gareth talks about his experience and becomes an advocate for other men across western Europe and his fight to normalize life with XXY.

Jose Ferreira was diagnosed with Klinefelter syndrome while trying to have kids with his wife. A doctor gave them a blood test, and Jose had no idea what XXY was. After learning he was infertile, he experienced mixed emotions and finally realized there was some answer to knowing why he was different. He never thought it was related to his diagnosis. After his diagnosis, he was in denial for years, pushed away support, and tried to live everyday life.  Now Jose has come to a level of acceptance to share his extraordinary story to help others.  Jose gives excellent insight into his thoughts and has built confidence in himself.  He has his dream job and loves learning more about himself. 

Whitney Lance received a prenatal diagnosis of Klinefelter syndrome via email from the hospital after a NIPT. In big red letters, it read XXY. Her doctor urged her to see a geneticist, and Whitney panicked and went to google. The geneticist printed information directly from google and didn't have much more information to share. 

Bradford Stucki was diagnosed with Klinefelter syndrome/47 XXY while trying to create a family with his wife.  After his diagnosis, their quest to create a family turned to adoption. Despite his diagnosis, Bradford went on to earn his Ph.D. in Human Development and Family Science. 

Bradford is a Licensed Marriage and family therapist with 7+ years of experience working with individuals, couples, parents, children (ages 5-12), and families with many relationships and mental health challenges. https://www.bridgehopefamilytherapy.com/

A very special daughter from donor sperm shares her unique story.  She learned about her father having XXY 30 years after she was born from DNA testing. Make sure you grab your tissues for her captivating story.  By far one of the most extraordinary stories in the entire podcasting community.  

Matthew Keller is a 21-year-old man born and raised in Texas. Matthew was diagnosed with Klinefelter syndrome in high school at 17 years old. After diagnosis, he became angry and didn't want to understand his diagnosis. Learning he was infertile, his family offered to try Micro-TESE (a procedure that takes sperm directly from the testicular tissue of a man's reproductive system). Now that Matthew fully accepts his diagnosis, he wants to help other men and boys with XXY to accept themselves and share their own stories to help others! https://livingwithxxy.org/