NIPT XXY Result

I just got the call from my geneticist today and he said they found that my future boy has a 50/50 chance at being diagnosed with Klinefelter. I think I am still in a bit of shock but also just relieved that nothing more serious was wrong so far. We can’t confirm until December, but I just wanted to reach out for support/resources/advice. Thank you ❤️

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I was told my boy could have it as well, he was born in April but we haven't done our follow up testing yet so we don't know if he has it or not yet

Thank you for sharing, Elli ❤️

If he does have it when we do the testing I'll come back to this group and let y'all know what I find out

Curious about this! I got the same result from my NIPT and am doing utero testing in 2 weeks to be certain. I know it’s nothing toooo serious but I can’t say I’m not terrified about it. This is my first and probably only baby and I’m just, scared

We got the diagnosis 10 weeks in utero. We had his cord retested at birth. I’ve followed Living XXY facebook and YouTube and have had lots of support through that community. They’ve even begun meetups within your state. Our toddler now has 2 KS friends who we meet with every month for playdates. Our guy is in speech and physical therapy. We also did early testosterone shots for him to meet milestones within his first year

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