Klinefelter Syndrome Podcast: Connor age 17

Connor and his mother Kelly Stine share their experiences with understanding and learning about Klinefelter syndrome. Connor was diagnosed last year at 16 years old, during his junior year in high school.
Connor hopes that by sharing his story more of his peers will come forward to share theirs. He hopes this will help create a more positive and friendly XXY community for young men.

[@fernandamartinez3734]

I love the way his mum looks at him. so proud and so amazed by everything he says. so much love and positive energy for Connor. Thank you for helping other people with your story.

[@cooperwa]

Very interesting info from you all about fingerprints. I've been wondering most of my adult life why it's hard to lift fingerprints from me. Everytime I go to the sheriff's office to renew my firearm carry permit they can never get my prints electronically and they have to do it manually the old fashioned way with ink and pad. Now I know it's a fluke with XXY's.

[@SCCheaters]

16:20 broke me. Connor will be a fabulous father! and a great man!

[@cooperwa]

Best LWXXY podcast of all from my perspective -- goes to show that with proactive parents the XXY can overcome obstacles easier than those without. I think we XXY's do need a tutor and nothing better than a parent who is an educator. Looking forward to the interview with Kelly and another one just with Connor. Thanks for reminding me that Ryan doesn't enjoy compliments. 🙂 Yes to Control-F !!! But, there's also Control G (find next).

[@LivingwithXXY]

Thank you

[@natscat4752]

What a fantastic podcast. What an intelligent young man and fabulous Mom. Thanks all

[@LivingwithXXY]

Glad you enjoyed it!

[@jennifervoige6484]

Thank you Connor & Kelly for your honesty & openess in sharing your story - it really embodies throughout the hard work, perserverance & just love on both sides. Enjoyed your interactions so much and learn something new. Thank you, cause it really does help & make such a difference. Amazing job! So glad you are part of this community 🩵

[@LivingwithXXY]

Thank you so much!

[@princessdollyllama]

What about XY females. Not everyone with a y is male. (CAIS)

[@shannonefteland9539]

One son with KS and one with Down Syndrome, it has definite challenges but it has its gifts and joys just the same.😊

[@gaylecheung3087]

Great talk

[@shannonefteland9539]

Thank you for all of this. Dealing with this right now and you give me so much hope.

[@j.b.4340]

Great chat. I always learn new things. @11:46, that gets me. Many times, I’ll view an xxy/xyy, or related video, and they’ll mention some symptom, in Latin. Then I look it up, and it’s always a curse word moment, because I’ll have it. (Fifth finger clinodactyly was a recent one. I looked down at my hand, and cursed. I’m 6/10 with clinodactyly). To help me understand, I recorded a list of symptoms, with 27 items, and I checked off 17 boxes.

[@sherrisutton6809]

MicroTESE in Michigan is $20,000

[@neverstoplearning3451]

I am 18 years old and have no beard so can I start TRT or try to boost testosterone naturally. I was a topper in high school and get qualified for Jee Advanced exam which is one of the toughest exams in the world. But in Btech I can not do coding like others due to dyslexia. What can I do ?? Drop out and go for a hobby or do Btech and then go for a hobby ??

[@natscat4752]

Getting good advice from others is always a positive step. You don’t always have to take their advice. So seek knowledge from someone experienced in that area could be a good move.

[@neverstoplearning3451]

@@arturfil thank you so much sir . Sir do you use Instagram so that I can ask some questions ?

[@Sushilkumar92]

You can learn UI/UX design, as I assume you might have an creative brain. It pays equally well as a coder

[@ashishpkrl]

​@@Sushilkumar92It is very difficult to learn the coding part of those who are affected by KS people.

[@benjaminstewart4332]

Just had my semen analysis and my results came back and they said it will be next to impossible for me to impregnate my wife. Has anyone else been told this after there diagnosis of Klinefelter’s. Has anyone had any success

[@LivingwithXXY]

Check out our podcasts.

[@Jacob-wn4lp]

They have! There are still options available to you. On this channel they have a series of podcast that go over things like this

[@belmckee590]

If you have any live sperm, the doctors can get it and inseminate your wife. There has been success in the past. Australian 60 minutes did a story on xxy a fair while back but you might find it on you tube. Good luck. My son is xxy he has no chance at being a dad. 😢

[@hibache4532]

Thank you for sharing this.

[@LivingwithXXY]

My pleasure!