In January of 2018 I was invited to speak in front of the FDA in Washington D.C about Testosterone Replacement Therapy. This was regarding two pharmaceutical companies who are still trying to get a pill form of Testosterone passed. I find that this can be a benefit towards people born with Klinefelter syndrome that use …
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 of my age, I had to have an amniocentesis. I was elated when the results came back Down Syndrome …
Another wonderful story here. May 8th, 2017 is a day I will never forget. It was the due date of a baby we never got to meet, and the same day I found out I was pregnant with my son. I was excited to tell my husband he was going to be a dad, as …
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 to create a logo for Living with XXY, the life project of a dear friend, Ryan Bregante. His mission is to …
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. At 20 Fraser felt he and his partner Nina were still too young to consider starting a family, but then …
Original Article by LJWorld Julie and Brandon Urban only wish they had the cards sooner. Then they could have handed them to people who stared at them whenever their son had a tantrum in public. “My child has Klinefelter Syndrome, a genetic condition in which boys have an extra ‘X’ chromosome — 47,XXY,” the cards …
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 the most lovable lips. Immediately, he exhibited the sweetest demeanor. We were looking at perfection. Anyone who laid eyes on him couldn’t agree more. …
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 interactive. He is just like any other 6-week-old and he has Klinefelter syndrome genotype. We first became aware of the …
By JANE E. BRODY AUG. 31, 2004 The New York Times 2004 Sam’s parents began to suspect something was not quite right when at age 2, their son still was not walking and he said nothing that made any sense. Laboratory and neurological tests showed no abnormalities. But a genetic test revealed that Sam’s cells contained an …
XXY Males – Klinefelter syndrome HEALTH TOPIC BY GLENDA FAUNTLEROY DEC 2012 Although considered the most common chromosomal disorder in humans, the subtle symptoms of Klinefelter syndrome can result in a man living with the condition his entire life without ever being diagnosed. Klinefelter affects only males. Instead of having the usual XY chromosome …
XXY Adult Mathew My son Matthew is 26 years old and was diagnosed with Klinefelter syndrome when he was 14 years old. I credit his pediatrician who thought that his enlarged breast tissue was something more than just puberty. He sent us off to CHOP (Children’s Hospital of Philadelphia) where we received his diagnosis. At …
XYY A Missed Diagnosis When asked the question, “Tell us about your son’s journey to a XYY diagnosis,” it almost seems like too much to put into words. Too much time, too many doctors, too many tests, too many feelings of failure as a mom … just too much. However, I think it is a …
A Klinefelter Story from Germany 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 a 24 year old Klinefelter syndrome boy. He was diagnosed while I was pregnant. …
Klinefelter Educations 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 of these amazing individuals and their Klinefelter educations. With hard work we can do anything we put our …
Extraordinary Care Families have a place to turn for help with sex chromosome disorders. Article By Pam Auchmutey Emory Health Digest Emma St. Germain (above right) talks with pediatric nurse practitioner Sharron Close (middle) and PhD nursing student Amy Blumling (left). Photo by: Jack Kearse Emma St. Germain, a dark-eyed, dark-haired eight-year-old, loves playing with dolls …
