Giving Tuesday 2019
Our very first Giving Tuesday Today is #GivingTuesday and it is Living with XXY’s first. We took on the challenge of becoming a NonProfit 501(c)(3) charitable organization to bring our community more support,
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 care for them. Sure, flowers and chocolates
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 how puberty affects the brain and behavioral
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 is acutely aware of his minority status
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 size is the result of being born
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 a young mom so I never had
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 of luscious hair, piercing blue eyes, and
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 2017, my wife and I are celebrating
