Our Blog

Insights from the XXY Community Blog

  • Voices Of Adults With XXY
    May 4, 2025

    I Felt Like Something Was Missing.

    At 21, Cesar’s Air Force dreams uncovered a surprise diagnosis: Klinefelter Syndrome. He turned adversity into confidence being XXY.

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  • Voices Of Adults With XXY
    Apr 25, 2025

    Tyler Indermill - I have forty-seven chromosomes! - Living with XXY Non-Profit

    When Tyler Indermill was diagnosed with Klinefelter syndrome (XXY) at age 33, it changed his life—but not in the way he expected.

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  • Community
    Apr 12, 2025

    Finding Your XXY Parenting Community

    With time I’ve developed a community of Klinefelter syndrome moms. There’s such importance in finding your XXY parenting community.

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  • Voices Of Adults With XXY
    Apr 12, 2025

    Ben Redefining His Life At 28

    Discover Ben’s inspiring journey living with Klinefelter Syndrome (XXY)—from childhood hearing loss and a surprise diagnosis to finding love, purpose, and a life filled with gratitude and adventure.

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  • Prenatal Diagnosis
    Apr 10, 2025

    My Pregnancy With A Klinefelter Syndrome Boy

    Google can be a scary place for new parents after doing prenatal testing (NIPT) and receiving A Klinefelter syndrome boy diagnosis.

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  • Community
    Apr 9, 2025

    Living With Klinefelter syndrome, I didn’t look like I had a disability

    Discover Pete Cowley's inspiring journey of Living with Klinefelter syndrome. Pete shares his story of resilience and hope

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  • Prenatal Diagnosis
    Apr 6, 2025

    What if my NIPT is Positive

    You receive a “Screen Positive” test result from your NIPT. This test result doesn’t necessarily mean that your baby has genetic condition.

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  • Community
    Mar 26, 2025

    Born With 48, XXYY

    At 11 weeks pregnant my doctor asked if I wanted NIPT, our doctor told us that it was all suggestive that our son would be born with XXYY.

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  • Post
    Mar 10, 2025

    Types of Testosterone

    Types of Testosterone from a guy who has been using TRT for more than 24 years. Check out our YouTube Channel Living With XXY.

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  • Do It Yourself Therapy Guides
    Dec 27, 2024

    XXY Syndrome Diagnosis Guide

    Our vision with this guide is to provide hope & encouragement to parents or expectant parents to boys just like Jack who are born with xxy syndrome.

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  • Early Childhood Diagnosis
    Dec 1, 2024

    Discovering Diagnosis Klinefelter Outline

    Discovering Diagnosis Klinefelter Outline. I am a mom of a 17-year-old son with XXY. Since then, we’ve seen a lot of specialists

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  • Doctors Information
    Nov 28, 2024

    Common Questions About XXY

    What are the most Common Questions asked About XXY? Here is an extensive list from the top doctors in the community.

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  • Community
    Nov 26, 2024

    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 with an extra X chromosome.

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  • Community
    Nov 26, 2024

    Kelsey Maffei: We all have a story to tell

    Kelsey Maffei says by sharing his story about Klinefelter syndrome he can shape people's perceptions before they build conclusions from online infromation.

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  • Community
    Feb 6, 2024

    Raising a son with Klinefelter syndrome

    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 10.

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  • Voices Of Adults With XXY
    Feb 1, 2024

    Josh Lutz’s Klinefelter Syndrome Diagnosis

    Josh received his diagnosis of XXY when trying to become a father. Initially, while it was a shock, Josh worked to be his best self.

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  • Community
    Dec 27, 2023

    XXY Teenager - 15 Year Old Sean And His Story

    When xxy teenager finally got his diagnosis, the neurologist was only able to tell him he would have severe learning disabled and unable to have children.

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  • Voices Of Adults With XXY
    Dec 27, 2023

    XXY Male - Born Different by James Nimmo

    The most important thing that I hope would be taken away from reading my story as an XXY male is to never give up, whatever the struggle is. You are brave.

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  • Community
    Dec 27, 2023

    XXY Early Diagnosis Signs

    One family looks back at the “soft signs” of XXY that were overlooked in early childhood. We found out about my son’s Klinefelter’s diagnosis when he was 9.

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  • Do It Yourself Therapy Guides
    Dec 27, 2023

    Try Try Try

    “TRY, TRY, TRY!” were the words that came out of Jack’s mouth as he attempted to run up a steep grass hill around 18 months of age.

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  • Voices Of Adults With XXY
    Dec 27, 2023

    "This Might Be Me"

    JT received his diagnosis of Klinefelter Syndrome in May of 2015, at age 28. JT “blanked” after the urologist delivered the news.

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  • Voices Of Adults With XXY
    Dec 27, 2023

    The Voice of Jordan Truax

    Jordan is a 29-year-old man who is very open about his diagnosis, and ready to share about his life with Klinefelter Syndrome.

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  • Voices Of Adults With XXY
    Dec 27, 2023

    The Voice of J

    J is a man in his late seventies who resides in the UK. As an older gentleman with Klinefelter Syndrome he is helping increase awareness.

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  • Voices Of Adults With XXY
    Dec 27, 2023

    The Voice of Drew Gagnon

    When he was a young boy, Drew knew what he wanted to do with his life.

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  • Voices Of Adults With XXY
    Dec 27, 2023

    The Voice of Armin: Every diagnosis is different

    Armin is a 29-year-old man with Klinefelter Syndrome living in New Zealand. Armin learned of his diagnosis as a young teenager.

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  • Community
    Dec 27, 2023

    The hope of fathering children snatched away at 20

    When Fraser was diagnosed with Klinefelter Syndrome, it was possible he would never become a dad. Thanks to sperm donation, now a father to three boys.

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  • Community
    Dec 27, 2023

    The Diagnosis of an Extra X Chromosome Helped Mathew Find Himself

    Mathew’s pediatrician began to suspect Klinefelter when Mathew was 15. Since he was very young, Mathew has struggled with speech and auditory processing.

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  • News And Updates
    Dec 27, 2023

    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 development in adolescent boys.

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  • Community
    Dec 27, 2023

    Putting one foot in front of the other - Living with Klinefelter syndrome

    I found out the hard way I had Klinefelter syndrome. I married my wife and we started trying for a child. We tried for nineteen months with no success.

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  • Community
    Dec 27, 2023

    Puberty Hormones In Klinefelter Syndrome

    Here we have the Extraordinary Kids Clinic, a specialty clinic for children with XXY and other X and Y variations. I will review some of the most common questions.

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  • Community
    Dec 27, 2023

    My son Joey is soon to be 28 years old, 14 years since he was diagnosed.

    I am very proud of my son. He is kind, considerate and forever loyal to family and friends. He manages to always be positive and help others before himself.

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  • Community
    Dec 27, 2023

    My first time telling people my son has XXY

    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.

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  • News And Updates
    Dec 27, 2023

    Many men have an extra X chromosome - but are rarely diagnosed.

    “Most men are only diagnosed when they struggle to conceive,” Yap says. “This will be when they are in their 30s or older.

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  • News And Updates
    Dec 27, 2023

    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.

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  • Community
    Dec 27, 2023

    Learning About Our Son's XXY Diagnosis

    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 the baby was born. However,

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  • Do It Yourself Therapy Guides
    Dec 27, 2023

    Klinefelter Syndrome Speech Therapy Tips

    This journey isn’t always easy and certainly doesn’t come with a step-by-step manual. Our guide is designed to help with Klinefelter syndrome speech therapy

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  • Community
    Dec 27, 2023

    Klinefelter Syndrome Genotype

    We became aware of the possibility that our son had Klinefelter syndrome genotype through a NIPT test (non-invasive prenatal test) I had done at 8 weeks.

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  • Voices Of Adults With XXY
    Dec 27, 2023

    Klinefelter Syndrome: Building A Community With Ryan Bregante.

    An article about Founder and President of Living With XXY, Ryan Bregante. This article is about Ryan's vision for the future of XXY.

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  • Do It Yourself Therapy Guides
    Dec 27, 2023

    Klinefelter Prenatal Testing Guide

    The Klinefelter prenatal testing guide for expectant mothers to help you in next steps after undergoing genetic testing in the first trimester of pregnancy.

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  • Termination To Life Stories
    Dec 27, 2023

    Klinefelter Pregnancy Termination Story

    Devra shared her story of learning about Declan’s diagnosis of 47, XXY, and how they were offered Klinefelter pregnancy termination.

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  • Community
    Dec 27, 2023

    Klinefelter Diagnosis - Stefan Schwarz

    I had learning, social, anger, and behavioral issues. But they couldn’t put their finger on it until my XY/XXY Klinefelter diagnosis occurred.

    Read More
  • Early Childhood Diagnosis
    Dec 27, 2023

    I Feel Alone In The UK With My Son’s Diagnosis

    A year after their son's diagnosis, they traveled to Italy for a follow-up appointment since the UK did nothing to help with their young son.

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  • Community
    Dec 27, 2023

    High school with XXY

    How did I manage to get through High School with XXY? Sophomore year English was one of my hardest classes, I remember taking notes was extremely difficult.

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  • Community
    Dec 27, 2023

    Free Forest School - The benefits of free play in nature

    Free Forest School gives boys with Klinefelter syndrome free play in nature. It is not leisure time; it’s an essential investment in our children’s health.

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  • Community
    Dec 27, 2023

    Finding Resources For Klinefelter's In Rural Areas

    When our son was born, my husband and I considered moving to a more urban area for the sake of gaining access to more Klinefelter's resources.

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  • Voices Of Adults With XXY
    Dec 27, 2023

    Finding my "X"

    My name is Gregory Duncan, I am 30 years old. This is my story about being diagnosed with Klinefelter syndrome and finding my "X".

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  • Do It Yourself Therapy Guides
    Dec 27, 2023

    Fears Are Changing Into a Community of Hope

    Have you ever felt like no one truly understands what living with XXY means or feels like? Only view your son to what the internet suggests?

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  • Community
    Dec 27, 2023

    Father Learns of Son’s XXY

    Father Learns of Son’s XXY. Seeing the joy on my wife’s face was priceless. We were both established adults and were ready to handle this.

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  • Do It Yourself Therapy Guides
    Dec 27, 2023

    Establishment of Care - Klinefelter Syndrome Guide

    We hope this Establishment of Care: Klinefelter Syndrome Guide will encourage families to customize their own approach to establishing their son’s plan.

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  • Community
    Dec 27, 2023

    Colton’s XXXtraordinary Cause

    At nine months old, Colton was diagnosed with 48XXXY. Colton’s XXXtraordinary Cause is for every child that has been diagnosed with a rare syndrome.

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  • Community
    Dec 27, 2023

    Baby Boy Born With Klinefelter XXY

    Jaclyn Childers, A Pregnant mother story about NIPT testing and how they found out their son had Klinefelter XXY, syndrome.

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  • Voices Of Adults With XXY
    Dec 27, 2023

    An XXY Diagnosis - The Voice of Luke Breard

    This is the story of Luke's XXY diagnosis, and how he became an adoptive father to two boys, while living with XXY.

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  • Community
    Dec 27, 2023

    After 6 Years of IVF Our Journey Began

    In December we had a CVS test done as I was 43 and my obstetrician recommended it. Days passed and we were anxiously awaiting the results.

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  • Community
    Dec 27, 2023

    A New Zealand mother and her XXY Kid

    Are you mum?, Have just been told about your son being an XXY kid? I just want to show you that life isn’t bad after a Klinefelter syndrome diagnosis.

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  • Community
    Dec 27, 2023

    A few days later I canceled our XXY abortion

    Diagnosed with XXY and a doctor said “mental retardation, severe delays in development… but she could help me have and XXY abortion without any difficulty”.

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  • Community
    Dec 27, 2023

    47 XXY Life WORTH Living

    The genetic counselor cut straight to the chase and informed me that I tested positive for a chromosomal abnormality 47 XXY that was only present in males.

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  • News And Updates
    Dec 27, 2023

    Living With XXY September Newsletter

    Welcome to the Living with XXY Newsletter!

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  • News And Updates
    Dec 27, 2023

    Living With XXY October Newsletter

    It's better late than never, and our October newsletter is a special issue of all the fantastic things happening this month.

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  • News And Updates
    Dec 27, 2023

    Living With XXY December Newsletter

    Thank you all for your continued support as I take time to focus on self-care, during an especially busy time of year.

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  • Voices Of Adults With XXY
    Dec 24, 2023

    The Voice of Matthew Roseworne

    Matthew Roseworne is 39 years old and lives in Gulgong, New South Wales, Australia He shares about life with Klinefelter Syndrome is like.

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  • Community
    Oct 15, 2023

    Hello, I Am Brian Winters

    I’m Brian a 36 years old male born with Klinefelter Syndrome. I wasn't diagnosed till my adult years. Let’s talk about mental health.

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  • Prenatal Diagnosis
    Jun 8, 2023

    A Mother’s Journey - The Unknowns of XXY

    While pregnant with her first child, Nina learned that her son might have Klinefelter syndrome. She had never heard of it before.

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  • Prenatal Diagnosis
    Jun 5, 2023

    Perhaps The NIPT Was Wrong

    Haddie and her husband met with a maternal-fetal medicine specialist, but the appointment was jarring and disappointing. Their son has XXY.

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  • Community
    Jun 4, 2023

    Wyatt Will Move Mountains

    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 to decide if & when to share it.

    Read More
  • Prenatal Diagnosis
    May 31, 2023

    An Ill-Informed Provider

    Beth was told her son with XXY would be “mentally retarded” and to see a genetic counselor so they could discuss termination options.

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  • Early Childhood Diagnosis
    May 30, 2023

    Our Doctor Suggested Termination For XXY

    Meet the Jenkins-Nardelli family. Here is the story of their remarkable little XXY boy Preston, who will turn 5 in February!

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  • Prenatal Diagnosis
    May 26, 2023

    Our Beautiful Rainbow Baby

    Our rainbow baby's story with XXY. Our Genetic Counselor "I know you said let's not discuss abortion, but maybe you need to think about it."

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  • Community
    Apr 24, 2023

    Sharing My Diagnosis With The World

    Two years ago today, I was diagnosed with Klinefelters Syndrome or XXY. Most of you probably have no idea what this is.

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  • Infertility
    Feb 20, 2023

    Male Infertility & Pursuing Parenthood

    Jared Pike is helping raise awareness for Male Infertility & Pursuing Parenthood. Sharing his succesfull adoption story is essential.

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  • Infertility
    Feb 14, 2023

    The Journey To Baby Indermill

    After more than a year of trying to conceive, Tyler Indermill and his wife, Tasia, underwent testing. Tyler then learned he was infertile.

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  • Early Childhood Diagnosis
    Feb 7, 2023

    Unexpected Klinefelter Pregnancy Diagnosis

    Soon-to-be mother Femke Weidema had an unexpected Klinefelter pregnancy diagnosis with her son Ender when they met with her doctors.

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  • Community
    Jan 31, 2023

    Sharing My Klinefelter Diagnosis Worldwide

    When applying for the Air Force, the doctor noticed something odd during the medical/physical exam. I found out I had Klinefelter syndrome.

    Read More
  • Voices Of Adults With XXY
    Jan 24, 2023

    Michael Palumbo's Klinefelter Adult Diagnosis

    Michael Palumbo was born in Toronto, Canada. Now 35, Michael was 32 years old when he learned about his Klinefelter adult diagnosis.

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  • Termination To Life Stories
    Jan 17, 2023

    Lois Ivanoff's Klinefelter Mother Termination

    Lois' doctor suggested an amniocentesis to ensure everything was ok with the baby. She was offered a Klinefelter mother termination

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  • Community
    Jan 5, 2023

    Understanding Adoption For XXY Men

    Men with XXY find out they are infertile while trying to have kids. Understanding adoption i one of the many ways to build a family.

    Read More
  • Termination To Life Stories
    Jan 4, 2023

    Klinefelter Pregnancy Abortion

    Heather's son Tyler, was diagnosed with Klinefelter syndrome. She shared her story of being offered a Klinefelter pregnancy abortion.

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  • Prenatal Diagnosis
    Jan 3, 2023

    A Mother's XXY NIPT Diagnosis

    I wanted to write my story. My point of view of being a mom to a now toddler with Klinefelter Syndrome.

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  • Prenatal Diagnosis
    Jan 2, 2023

    United States Klinefelter Diagnosis

    united-states-klinefelter-diagnosis

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  • Prenatal Diagnosis
    Jan 1, 2023

    Amnio Klinefelter Diagnosis

    At 20 weeks, Beverly received an amniocentesis. They were surprised by the results of an amnio Klinefelter diagnosis.

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  • Prenatal Diagnosis
    Oct 16, 2022

    Klinefelter Diagnosis Stress

    Kasia's doctor required early prenatal testing. The results for Kasia and her husband resulted in Klinefelter diagnosis stress.

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  • News And Updates
    Sep 30, 2022

    What to expect when you’re expecting an extra X or Y chromosome

    What to expect when you’re expecting an extra X or Y chromosome.

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  • Voices Of Adults With XXY
    Sep 30, 2022

    48 XXXY - The Voice Of Aron Capon

    Aron is a 41-year-old man living with a variant of Klinefelter Syndrome 48 XXXY. Aron resides in Gabriola Island, BC with his wife Nikki.

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  • Prenatal Diagnosis
    Sep 29, 2022

    Klinefelter Syndrome And Autism

    Annette Flannery lives in Maryland with her husband and their son, Ronan. Ronan is a fantastic boy with Klinefelter syndrome and autism.

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  • Prenatal Diagnosis
    Sep 11, 2022

    Early Prenatal Klinefelter Diagnosis

    At the age of 35, Nina found out she was pregnant. Five days later, Nina’s phone rang . She received a prenatal Klinefelter diagnosis.

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  • Prenatal Diagnosis
    Sep 8, 2022

    Infant Klinefelter Diagnosis

    The pregnancy was a surprise. As Amy was 39, her doctor suggested a NIPT. The couple was surprised with an infant Klinefelter diagnosis.

    Read More
  • Voices Of Adults With XXY
    Aug 25, 2022

    Life with KS - The voice of Daniel Hellinger

    Daniel Hellinger is a 30-year-old man living with mosaic Klinefelter Syndrome/KS. He resides in Seattle, where he was also raised.

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  • Voices Of Adults With XXY
    Aug 20, 2022

    Klinefelter Man Diagnosis

    Dan shared his Klinefelter man diagnosis, as he received the news later in life. He lives with 47, XXY, or Klinefelter syndrome.

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  • News And Updates
    Aug 18, 2022

    Meet Ryan Bregante of Living With XXY

    In 1985, while my mother was pregnant with me, I was diagnosed with 47, XXY, or Klinefelter syndrome. When I was 9, I was told about XXY.

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  • Prenatal Diagnosis
    Aug 9, 2022

    A Surprise Klinefelter Pregnancy

    Anne and Mike weren't expecting a pregnancy after their daughter was born. They had a surprise Klinefelter pregnancy with their son Brent.

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  • Community
    Aug 5, 2022

    A Positive 48 XXXY NIPT

    When I was pregnant with Wyatt, I opted to do NIPT. When he was two weeks old, we were informed he had Klinefelter syndrome, 48 XXXY NIPT.

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  • Voices Of Adults With XXY
    Aug 4, 2022

    Young Adult Klinefelter Life Story

    Jason noticed unexpected body changes. Despite an active lifestyle he began developing breast tissue as young adult Klinefelter diagnosis.

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  • Early Childhood Diagnosis
    Jul 28, 2022

    An Unexpected Klinefelter Diagnosis

    When a nurse noticed something during a routine exam, Max's family was shocked by an unexpected Klinefelter diagnosis.

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  • Prenatal Diagnosis
    Jul 13, 2022

    A Klinefelter Abortion

    When Ashley found out she was pregnant, she couldn’t wait to learn more about her baby. Her doctor suggested a Klinefelter abortion.

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  • Community
    Jul 7, 2022

    Teenage Klinefelter diagnosis

    15-year-old Cassiel, who received a teenage Klinefelter diagnosis two years ago, and what it's like living with 47, XXY.

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  • Community
    Apr 21, 2022

    Living With Fear “And” XXY

    Tyler and his wife learn their unborn son has 47, XXY. Well, it was a BOY! And then the “but”… but he has Klinefelter syndrome.

    Read More
  • Prenatal Diagnosis
    Mar 16, 2022

    A doctor's son with Klinefelter syndrome

    A Doctor's son with Klinefelter syndrome. Emily who was 26 years old after experiencing a miscarriage learned her son may have 47 XXY.

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  • Infertility
    Mar 15, 2022

    47XXY Adoption Story: George Tomkin's

    In 2015, George was told he would be unable to have children. He never imagined his journey would include 47XXY adoption.

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  • Early Childhood Diagnosis
    Feb 8, 2022

    Klinefelter Teen Diagnosis

    The Keller family was surprised by a Klinefelter teen diagnosis when Matthew was diagnosed in Texas at age 17.

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  • Prenatal Diagnosis
    Jan 28, 2022

    Prenatal Diagnosis Klinefelter Baby

    Ali and her husband did not expect a prenatal diagnosis Klinefelter baby. This is their story of acceptance.

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  • News And Updates
    Dec 26, 2021

    Sam's story

    Hi there, I’m Sam. I’m 27 and I got diagnosed with Klinefelter Syndrome at age 23, but those 23 years of not knowing were somewhat uncomfortable.

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  • Voices Of Adults With XXY
    Dec 14, 2021

    Klinefelter Syndrome Male - Joey Schiffman

    Joey Schiffman is a 29-year-old man, working with the cars he dreamt of, while also living as a Klinefelter syndrome male

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  • News And Updates
    Dec 8, 2021

    Living With XXY 2021 Annual Report

    Dear Community, This year was the first year building an annual report; it was extremely challenging and frustrating.

    Read More
  • Voices Of Adults With XXY
    Dec 2, 2021

    The Voice of Richard Martinez

    Richard Martinez is living with Klinefelter syndrome. This is his story about what it was like to like to discover he had KS later in life.

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  • Voices Of Adults With XXY
    Nov 26, 2021

    The Voice of Ben Henrickson

    Ben Henrickson is 22 and resides in Chapel Hill, North Carolina. Ben was in fifth grade when he noticed signs of gynecomastia.

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  • Infertility
    Nov 22, 2021

    Using Donor Sperm - Greg and Katie Duncan

    Katie’s OB-GYN ordered a sperm test for Greg, and the results left the couple stunned. The first test showed Greg had zero viable sperm.

    Read More
  • Infertility
    Nov 22, 2021

    The Road To Adoption - Matt Troxler

    When Matt Troxler was in kindergarten, he received an unexpected diagnosis. His teacher noticed some symptoms, and encouraged his parents to get Matt tested.

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  • Voices Of Adults With XXY
    Nov 2, 2021

    Mosaic Klinefelter Syndrome: Stefan Schwarz

    An avid foodie with Mosaic Klinefelter syndrome, 51-year-old Stefan Schwarz is living a healthy, happy, full life.

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  • Termination To Life Stories
    Oct 30, 2021

    She hopes it doesn't happen to other mothers

    After her son's diagnosis of Klinefelter syndrome was delivered bluntly, Sophia hopes it doesn't happen to other mothers .

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  • Voices Of Adults With XXY
    Oct 27, 2021

    Navigating the World With Klinefelter Syndrome - The Voice of Andrew Curry

    Andrew Curry is an Eagle Scout. He’s an avid gamer and an excellent swimmer. Andrew is also navigating the world with Klinefelter syndrome.

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  • News And Updates
    Oct 25, 2021

    Finding community with Living with XXY

    In case we haven’t met yet, I’m Chelsea, the writing director for Living With XXY. Our son Noah lives with 47, XXY, or Klinefelter syndrome.

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  • Voices Of Adults With XXY
    Oct 21, 2021

    The Voice of Ken Widelski

    Ken Widelski believes setting goals and consistency is the key to success; when fitness training, and living with Klinefelter syndrome.

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  • Prenatal Diagnosis
    Oct 18, 2021

    A Surprise Diagnosis

    Jacqueline Lightcap is a mother raising a son with Klinefelter syndrome. This is her story of receiving an unexpected childhood diagnosis.

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  • Prenatal Diagnosis
    Oct 12, 2021

    Lacy and Dan's Prenatal Diagnosis Story

    Dan and Lacy are parents to a baby boy with Klinefelter syndrome. They agreed to NIPT testing to learn the sex of their baby.

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  • Voices Of Adults With XXY
    Oct 11, 2021

    The Voice of Nate Biklen

    Nate Biklen is a 41-year-old man living with Klinefelter syndrome. Nate enjoys a variety of hobbies, spending time withfamily and family.

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  • Voices Of Adults With XXY
    Oct 8, 2021

    The Voice of Geoff Kruck

    Geoff Kruck is 43 and living with Klinefelter syndrome. He shares his story about his wife Beth, their dog living near Melbourne, Australia.

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  • Voices Of Adults With XXY
    Oct 7, 2021

    The Voice of Dave Ruckle

    Dave Ruckle is a 48-year-old man living with Klinefelter syndrome.

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  • Voices Of Adults With XXY
    Oct 5, 2021

    The Voice of Porter Declan

    Porter Declan is a 29-year-old man living with Klinefelter Syndrome/47 XXY. Despite rough patches in his life he continues to drive forward.

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  • Community
    Oct 2, 2021

    Why Telling Your Story Matters

    He’s smart as a whip, photographic memory, and is ready to strike a pose for a photo. Noah also lives with 47, XXY, or Klinefelter syndrome.

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  • Prenatal Diagnosis
    Oct 1, 2021

    Everything is going to be fine - Leah's story

    Following her doctor’s recommendation, Leah participated in NIPT testing and learned her unborn son had Klinefelter syndrome, or 47, XXY.

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  • Termination To Life Stories
    Sep 30, 2021

    From Termination to Life - Jenn's story

    Stories of parents who were advised to terminate their prenatally diagnosed 47, XXY pregnancy and why they chose to go forward.

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  • Voices Of Adults With XXY
    Sep 28, 2021

    The Voice of Seamus Denison

    Seamus Denison shared his story of growing up in Australia without knowledge of his diagnosis and learning about XXY as an adult.

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  • Voices Of Adults With XXY
    Sep 7, 2021

    The Voice of Jake Gray

    Jake Gray has seen and done things at twenty-six that many of us could only dream of and he’s doing it while living with Klinefelter syndrome.

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  • Community
    Sep 4, 2021

    Klinefelter syndrome - You are worthy

    Having Klinefelter syndrome doesn't make you any less worthy. Like autism, Klinefelter syndrome is a spectrum disorder.

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  • Community
    Aug 12, 2021

    Living With XXY Response to 1,000-Year-Old Remains May Be Nonbinary

    Living With XXY NonProfit 501(c)(3) Charitable Organization response to recent news about 1000 year old remains.

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  • Community
    Jul 20, 2021

    “Your son has Klinefelter’s Syndrome.”

    We had absolutely no idea that our sons learning difficulties, his stature, and thin physique were indicative of having Klinefelter 47 XXY.

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  • Prenatal Diagnosis
    Jul 14, 2021

    They told their son "You’re an X-Man!"

    Noelle Davidson is the mother of a boy diagnosed in utero with Klinefelter Syndrome. Her pregnancy was considered geriatric.

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  • Prenatal Diagnosis
    Jul 9, 2021

    Blood work indicated “something was wrong"

    Andrea Holdren is the mother of 3-year-old Connor, who lives with Klinefelter Syndrome and Autism. Andrea shares her story to help others.

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  • Community
    Jul 6, 2021

    A German Klinefelter Story

    I am a Mum of a 24-year-old Klinefelter syndrome boy. He was diagnosed while I was pregnant. I was sent to an endocrinologist consultant.

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  • Community
    Jun 29, 2021

    The People Behind Colton’s XXXtraodinarY Cause

    Boys with 48 xxxy often face physical struggles due to low muscle tone, complications with language and speech, and developmental issues.

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  • Community
    Jun 23, 2021

    XYY A Missed Diagnosis

    I think it is a journey that many X Y variant moms could have been through, so I feel like I owe it to my son and other moms to write it.

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  • News And Updates
    Jun 19, 2021

    XXY Males – Klinefelter Syndrome

    Klinefelter affects only males. Instead of having the usual XY chromosome pattern of most males, boys are born with an extra X chromosome.

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  • News And Updates
    Jun 19, 2021

    The Havoc of an Undetected Extra Chromosome

    Sam’s parents began to suspect something was not quite right when at age 2, their son was not walking and he said nothing they understood.

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  • Early Childhood Diagnosis
    Jun 19, 2021

    Matthew was diagnosed with XXY at 14

    I credit Matthew's pediatrician who thought that his enlarged breast tissue was something more than just puberty.

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  • News And Updates
    Jun 19, 2021

    Graham's Klinefelter Syndrome Story

    As a young child he was involved in Early Intervention following his diagnosis at age 2 of Klinefelter’s (47XXY).

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  • Community
    Jun 19, 2021

    A human-friendly logo for Klinefelter Syndrome Awareness

    I had to create a logo for Living with XXY. Their mission is to spread positivity and awareness around Klinefelter Syndrome.

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  • Community
    Jun 18, 2021

    My Son’s Klinefelter Story (Spanish)

    When the gynecologist phoned me to give me the results, he told me the karyotype had left XXY, Klinfelter syndrome. I was frozen with worry.

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  • Prenatal Diagnosis
    Jun 18, 2021

    Klinefelter’s Syndrome Story

    She said: Your son has Klinefelter’s Syndrome. We had no idea whaT it meant or if our baby was going to be okay, I started shaking from fear.

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  • Community
    Jun 17, 2021

    What To Say When Someone Tells You About Their Son’s XXY Diagnosis

    What tell someone about their son’s Klinefelter Syndrome diagnosis can be challenging. Here are some tips to support loved ones .

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  • Voices Of Adults With XXY
    Jun 15, 2021

    The Voice Of Dylan Mathis

    Dylan Mathis is a man living with Klinefelter Syndrome, or 47,XXY. Dylan works as a residential service tech for Xfinity. Dylan has a fiance.

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  • News And Updates
    Jun 14, 2021

    XXY Syndrome Blood Test

    Two weeks later, the results came back from the lab. “You’re not going to believe this one,” she recalled Bean ‘A punch in the gut’.

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  • News And Updates
    Jun 12, 2021

    Years of misdiagnoses, Lawrence teen found to have little-known disorder.

    “My child has Klinefelter Syndrome, a genetic condition in which boys have an extra ‘X’ chromosome — 47, XXY,” the cards say.

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  • Community
    Jun 11, 2021

    47 XXY Syndrome Awareness

    Because of my age, I had to have an amniocentesis. The results included a thin, little book of information I never heard of 47 XXY syndrome.

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  • Community
    Jun 8, 2021

    Changing The Stigma - A New Perspective

    When surrounded by nothing but negativity and stigmas, how do you change that information? How do you bring hope to XXY famlies in your shoes?

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  • Prenatal Diagnosis
    Jun 7, 2021

    XXY Baby is Born

    This is to the mothers who are really struggling and not understanding what it means to have a baby with Klinefelter syndrome or XXY.

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  • Community
    Jun 5, 2021

    Klinefelter Educations

    There are people all over the world who have Klinefelter syndrome. Klinefelter Educations list helps people see what careers people have.

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  • Prenatal Diagnosis
    Jun 4, 2021

    OBGYN Diagnosed Mosaic 47 xxy

    I was excited to tell my husband he was going to be a dad then, my OBGYN said "don’t freak out, but the test shows that your baby has XXY."

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  • Prenatal Diagnosis
    Jun 2, 2021

    Our Genetics Counselor Said Most People Terminate Their XXY Pregnancy

    Karla is a mother of a man with Klinefelter Syndrome. She shared what it was like to have a prenatal diagnosis of 47 XXY.

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  • Community
    Jun 1, 2021

    Klinefelter Confidence

    Did you know that men with Klinefelter syndrome fall under the lack of Klinefelter confidence and believing in themselves?

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  • Voices Of Adults With XXY
    May 18, 2021

    The Voice Of Russell Martin

    Russell Martin lives with mosaic Klinefelter Syndrome. The diagnosis was missed when he was 13, and wasn’t confirmed until 30 years later.

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  • Community
    May 18, 2021

    Mexican Mother’s 47 XXY Story

    Our doctor called with results of the amniocentesis. The news was a shock, our son had XXY, the gynecologist did not know much about it.

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  • Voices Of Adults With XXY
    May 4, 2021

    The Voice of Gerald Mynard

    Gerald Mynaard, a social media developer and youth leader shares what his life with Klinefelter Syndrome is like living in St. George, Utah.

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  • Early Childhood Diagnosis
    May 3, 2021

    A Story about Kyle born with XXY

    With Kyle’s initial diagnosis I was extremely upset. It was a lot to take in and I had never heard of Klinefelter Syndrome before.

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  • News And Updates
    May 1, 2021

    Sex Chromosome Disorders

    “Emma loves school and her teachers,” says Tori St. Germain. “But she struggles with reading and math. Socialization is hard for her.

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  • Voices Of Adults With XXY
    Apr 28, 2021

    The Voice of Charles Plaisance

    Charles Plaisance is a man living with Klinefelter Syndrome in the Midwest. He’s married, and has three children of his own.

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  • Community
    Apr 21, 2021

    Optimistic XXY Mindset

    People often ask how I live with the mindset to be an optimistic XXY knowing that I have Klinefelter Syndrome and XXY.

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  • Prenatal Diagnosis
    Apr 20, 2021

    Melissa felt “pretty hysterical” when given the news

    Melissa, the mother of a toddler with Klinefelter Syndrome, shares what it’s like to raise a child with 47XXY in New York State.

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  • Community
    Apr 18, 2021

    Spanish Mother’s 47 XXY Story

    I’m 37 years old and I’m pregnant with twins. Last week I had the amniocentesis test, and we discovered that of the two babies being 47 XXY.

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  • Community
    Apr 3, 2021

    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

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  • News And Updates
    Apr 1, 2021

    Your Quarterly Newsletter: April 2021

    Welcome Home! It’s hard to believe 2021 is soaring by so fast! We’ve been busy and we know you have too. That is why we’re so glad you’ve subscribed to stay up to date with our current projects, accomplishments, meetups, and more.

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  • Prenatal Diagnosis
    Mar 30, 2021

    Julian is going to be the best baby!

    Sarah Winner is a mother whose son was diagnosed with Klinefelter Syndrome while she was pregnant. To help raise awareness this is her story.

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  • Early Childhood Diagnosis
    Mar 22, 2021

    A Mother's Intuition Led to Her Son's Diagnosis

    Luke continued to be extremely fatigued, lagged behind his peers both academically, and physically, the Greenes pushed for genetic testing.

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  • Voices Of Adults With XXY
    Feb 21, 2021

    The Voice of Alex H.

    Alex is a 34-year-old man with Klinefelter Syndrome. He’s a gregarious, self-described ginger, with a bright smile, and infectious laugh.

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  • Community
    Jan 13, 2021

    I was Googling every chance I got!

    XXY can’t be “cured”, but on the other hand, it isn’t something that needs to be managed every minute or even every day.

    Read More
  • News And Updates
    Dec 27, 2020

    Our Annual Letter for 2020

    In the midst of a global pandemic, our community came together in the toughest of times and offer support to one another all across the world

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  • Community
    Nov 18, 2020

    Facing Uncertainty

    Daniel’s speech was the first red flag, years later unable to talk Paul & I decided that we needed to see our paediatrician to find out why.

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  • Community
    Oct 9, 2020

    Struggle to be a father due to an extra X chromosome

    A man who only discovered he had Klinefelter syndrome when he and his wife failed to conceive naturally. Challenging times ahead.

    Read More
  • Community
    Sep 8, 2020

    Marathon Baby by Cedars-Sinai Magazine

    Fueled by the power of knowledge and unparalleled access to supportive resources, Matt and Marci Tatham take their young son’s genetic disorder in stride.

    Read More
  • Voices Of Adults With XXY
    Dec 27, 2019

    Giving Tuesday 2019

    Our very first Giving Tuesday Today is #GivingTuesday and it is Living with XXY's first.

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  • Community
    Feb 16, 2018

    XXYKindaGuy Sam Pierce

    Samuel lacked hair growth, muscle mass, had learning difficulties, and at the age of 23 his “sex drive decided to die”.

    Read More

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