LIVING WITH XXY ARCHIVE
Welcome to our Non-Profit’s Klinefelter syndrome blog series. We are dedicated to giving people all over the world a safe space to share their stories. Living With XXY is changing the way the world views Klinefelter syndrome (47 XXY). Our community is growing fast as people focus on spreading awareness and learn to focus on the positive traits. Our Klinefelter syndrome blog series offers a wide rage of stories and information. Every week we launch a new story from families experiencing prenatal diagnosis, to parents finding out during the adolescences years, to men finding out after 18 years of age. Please celebrate these incredible stories with us and we hope you will one day feel empowered to share your own.
Finding Resources For Klinefelter’s In Rural Areas
Finding Resources For Klinefelter's In Rural Areas By Chelsea Castonguay When our son was born, my husband and [...]
Learning About Our Son’s XXY Diagnosis
Learning about N By Chelsea Castonguay When I got pregnant, my husband and I debated about finding out [...]
Putting one foot in front of the other – Living with Klinefelter syndrome.
Forty one-year-old Chef Geoff Kruck was diagnosed with Klinefelter syndrome (KS) in 2012. KS is a genetic condition [...]
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 [...]
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 [...]
Klinefelter Syndrome 47 XXY And Beyond: Nicholas Griwicki
In early January of 1994, we were planning for our first baby and we were so very excited. [...]
XXY Teenager: 15 Year Old Sean And His Story
A story about 15-year-old XXY teenager Sean written by his mother Kristin. On July 29, 2002, I gave [...]
XXY Syndrome Diagnosis Guide
Our Vision Our capacity to love has expanded because of our son, Jack. Our vision with this [...]
High school with XXY
How did I manage to get through High School with XXY? This is a small account of Ryan [...]
Living With XXY Newsletter: April 2020
Stanford BGAP Study Visit In late February, our team had the privilege of meeting the team [...]
Establishment of Care: Klinefelter Syndrome Guide
Jack was the name we picked out for our son before we even knew he was a boy. [...]
Klinefelter Prenatal Testing Guide
“You tested positive for Klinefelter Syndrome, therefore you’re expecting a boy,” stated the genetic counselor, sitting across from [...]
Finding my “X”
My name is Gregory Duncan, I am 30 years old and I have Klinefelter syndrome and this is [...]
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 [...]
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 [...]
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 [...]
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 [...]
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 [...]
Giving Tuesday 2019
Our very first Giving Tuesday Today is #GivingTuesday and it is Living with XXY's first. [...]
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