Establishment of Care: Klinefelter Syndrome Guide
Jack was the name we picked out for our son before we even knew he was a boy. There was no significance to [...]
Klinefelter Prenatal Testing Guide
“You tested positive for Klinefelter Syndrome, therefore you’re expecting a boy,” stated the genetic counselor, sitting across from me with a large binder [...]
Finding my “X”
My name is Gregory Duncan, I am 30 years old and I have Klinefelter syndrome and this is my story. It’s September of [...]
47 XXY Life WORTH Living
47 XXY Positivity Jack’s Story Our son, Jack Ryan, was born in June 2018—weighing in at 9 lbs, 2 ounces with a full head [...]
My son Joey is soon to be 28 years old, 14 years since he was diagnosed.
My son Joey is soon to be 28 years old. It’s been 14 years since he was diagnosed with Klinefelter syndrome. I was [...]
New Chromosome Clinic Offers Hope
Kids aren’t likely to bully Connor Blundin. At 16 years old, he’s well over 6 feet tall and built like a lumberjack. His [...]
Klinefelter Syndrome: Building A Community With Ryan Bregante.
Klinefelter Syndrome. When Ryan Bregante sees statistics estimating that 1 in 500 males has the extra X chromosome that causes Klinefelter syndrome. He [...]
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 participate in a study exploring [...]
Loving With XXY
Love is what keeps our community together, and one way we can show our dearest ones living with XXY, just how much we [...]
Giving Tuesday 2019
Our very first Giving Tuesday Today is #GivingTuesday and it is Living with XXY's first. We took on the challenge [...]