Original Article from Healthy Male My husband and I have been together since we were teens and we had our first son Ayden when I was 21, he’s now 17, followed by Jacob, 13 and Amelia [...]

Hello, I’m Brian. I’m 36 years old, and I have Klinefelter Syndrome. I’ve been following Living With XXY for about a year now. Since finding this organization, I’ve finally started to understand what Klinefelter Syndrome is [...]

Written by Sierra Westley Wilson I've hesitated to share this publicly for the past year because I didn't want our son to be looked at or treated differently, & I wanted him to be the one [...]

Hello, My name is Max, and this is my story.  You can find me here on Instagram. Two years ago today, I was diagnosed with Klinefelters Syndrome or XXY. Most of you probably have no idea [...]

This is my story. Written by: Cesar Cortes Something has been on my mind for quite some time, and I’m entirely comfortable sharing it with the world. I was born with a rare condition called [...]

Understanding Adoption Many men in our XXY community find out they are infertile when trying to have kids. Understanding adoption can be one of the many ways to build a family. We have built this [...]

Hi, everyone. I'm Dr. Shanlee Davis. I'm a pediatric endocrinologist that works at the Children's Hospital, Colorado, and the University of Colorado Anschutz Medical Campus. Here we have the Extraordinary Kids Clinic, a specialty clinic [...]

A Mom’s Tale of XXY:  We lived in blissful unawareness until our son was almost 20 in the fall of 2018 and the doctor told us Ethan may have Klinefelter syndrome.  We had absolutely no [...]

This Story was written by a Mum that lives in Germany who has a son with Klinefelter syndrome. Using translation software, we do our best to bring you their story. I am a Mum of [...]

Klinefelter educations are something people have never even talked about openly on the internet.  There are people all over the world who have Klinefelter syndrome, though no one until now has put together a list [...]

XYY A Missed Diagnosis When asked the question, “Tell us about your son’s journey to an XYY diagnosis,” it almost seems like too much to put into words. Too much time, too many doctors, too [...]

Created By EMILIA LOUISA PUCCI UX, INTERACTION & WEARABLE TECHNOLOGY DESIGN Original Content Creator LIVING WITH XXY A human-friendly logo for a Project on Klinefelter Syndrome Awareness GOAL For this project, I had [...]

English translation from Spanish I wanted to have an amniocentesis. Although you do it by detecting early any anomaly detectable by this method, you never expect that there will be. In fact, I was also [...]

By Chelsea Castonguay In my time working with Living With XXY, there’s been a change in our family. Before we met Ryan and joined the community, we were extremely private about our son Noah’s diagnosis [...]

To my surprise, I found out I was pregnant at 45. My husband & I already had 3 children. At the time, my youngest was our 13-year-old son, who does not have 47 XXY syndrome.  Because [...]

Written By Ryan Bregante To give some context to this blog post, the first part in quotes is from a conversation I was having with a mother of a son born with XXY.  She was [...]

What is Klinefelter's confidence, you might be asking yourself? Did you know that most men with Klinefelter syndrome fall under the lack of Klinefelter confidence and believing in themselves?   Some say we are genetically pre-disposed [...]

English translation from Spanish. On June 30, 2008, they called us on the phone to tell us that they already had the amniocentesis results. We started to suspect that something was wrong when the nurse [...]

Mom Vs. Teacher  A few details from a “Teacher that is a Mom”  regarding my son’s academics and how it relates to Klinefelter Syndrome Diagnosis by: GLSS  Note: I have written more about my Klinefelter Syndrome [...]

People often ask how I live with the mindset to be an optimistic XXY knowing that I have Klinefelter Syndrome and XXY. Many years passed where I looked at the negative before the positive, and [...]

English translation from Spanish. It has been many years since I wrote this message in a forum about Klinefelter Syndrome, and many of you will see yourself reflected in my words: “I’m 37 years old, [...]

Written By: An Australian Mother I had to arrange my 13 weeks scan privately and Sydney UltraSound for Women recommended the NIPT test. I willingly had this due to the greater accuracy for Downs Syndrome… [...]

A man who only discovered he had Klinefelter syndrome when he and his wife failed to conceive naturally. FRI, 09 OCT, 2020 - 7:46 Written by: Ailin Quinlan THROUGHOUT childhood and adolescence, Luke* was tall [...]

XXYKindaGuy: Klinefelter syndrome diagnosis a relief after childhood woes. February 16, 2018 The Courier News Letter Samuel Pierce knew something was amiss growing up. He lacked hair growth and muscle mass, experienced numerous learning difficulties [...]

Written by: A Mother in Australia Our journey began after 6 years of IVF. I had decided not to go one more round and my husband Pete decided we would (yay for Pete) we received [...]

Motherhood is Tough. It hasn’t been easy for me. The caring, nurturing, looking after has been a breeze, it was becoming a mother that was difficult. Having suffered from endometriosis, I knew that becoming pregnant [...]

Marathon Baby Feb 26, 2020 Amy Paturel, Photos by Ted Catanzaro Original Article - Here Fueled by the power of knowledge and unparalleled access to supportive resources, Matt and Marci Tatham take their young son’s genetic [...]

Original Article by Bourn Hall Fertility Clinic When Fraser was diagnosed with Klinefelter Syndrome, it was possible he would never become a dad. Thanks to sperm donation, he is now a father to three boys. [...]

This article was written by Children’s Hospital Colorado In a tunnel beneath Willow Park Drive in Parker, Colorado, along the Sulphur Gulch Trail, a series of five-foot tall painted hands spells out “L-O-V-E O-T-H-E-R-S” in American [...]

I am writing this from a mother's perspective, my son Noah is aged 5 and is an XXY kid. When Noah was 2 weeks old we nearly lost him. His tiny wee body was starting [...]

There is perhaps no more remarkable moment in our lives than -if we are lucky enough- the experience of welcoming a child into the world. For the Hutchinson family, the birth of their son Colton [...]

Another amazing story about a baby with Klinefelter syndrome here This is my 6-week-old son. He is a very happy and healthy baby that breastfeeds well, has great muscle tone and is extremely alert and [...]

My name is Stefan Schwarz. I have Klinefelter Syndrome, XY/XXY mosaic, and found out in February 1996 at the age of 25. Throughout my life before my Klinefelter diagnosis, my parents took me to many medical [...]

How did we miss this? One family looks back at the “soft signs” of XXY that were overlooked in early childhood. This article was written by a Mother for Living with XXY. These are her words. [...]

Sam Carson "As people know my Thomas has been born with a syndrome. The syndrome Thomas has is Klinefelters. His syndrome is also called XXY. Meaning my boy has an extra X chromosome. The X chromosome [...]

The following is a bit of my story… "We all have a story to tell, and a perspective from which our experiences determine who we are". Kelsey Maffei Starting from my childhood, I attended a [...]

My husband and I got married a few years ago. I was 34 and he was 44. We dated for 4 years and I was super keen on trying for a baby by then as [...]

Free Forest School: The benefits of Free Play in Nature Written by Kat Pacheco.  Please also take the time to listen to our podcast series.  XXY Mom Squad with Kat Pacheco is available here. Today [...]

After being married in 2015, life was amazing.  My wife and I had really dug in our careers, myself as a police officer and her as a correctional officer. Our biggest worry was where to [...]

Finding Resources For Klinefelter's In Rural Areas By Chelsea Castonguay When our son was born, my husband and I considered moving to a more urban area for the sake of gaining access to more resources. [...]

Learning about N By Chelsea Castonguay When I got pregnant, my husband and I debated about finding out the sex of our baby. We decided to skip genetic testing, and wait to be surprised when [...]

Forty one-year-old Chef Geoff Kruck was diagnosed with Klinefelter syndrome (KS) in 2012. KS is a genetic condition that affects fertility, energy levels and bone and muscle strength. One in 550 boys and men have [...]

A story about 15-year-old XXY teenager Sean written by his mother Kristin. On July 29, 2002, I gave birth to my second child, a baby boy. He was identical in weight and length to my [...]

How did I manage to get through High School with XXY? This is a small account of Ryan Bregante's high school years, we will dive into more details on our Living With XXY Podcast Series. [...]

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 an amniocentesis during my pregnancy. [...]

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 with an extra X chromosome. [...]