International Support Forums for 47XXY, including Klinefelter Syndrome & variants

Never replace the advice of a qualified medical professional with anything you read in our forums.
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"Harry Fitch Klinefelter was born March 20, 1912 (now deceased) and was the physician for which Klinefelter Syndrome was named. We at XXYTalk.com shall observe Klinefelter Syndrome Awareness Week each and every year starting in 2007 on March 18th. We encourage the world to join with us in helping to establish the week that includes March 20th as a week of awareness of Klinefelter Syndrome, XXY, and the Variants."
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Username Post: Welcome        (Topic#5346)
Loc: Lancashire, England
Reg: 03-26-06

07-01-09 04:54 AM - Post#55390    

Welcome to XXYTalk!

We are a family of the X: XXY persons, their partners, parents of XXYs and mothers-to-be. Guests who are curious about XXY are also welcome.

Please take a moment and fill out your profile (under My XXYTalk, upper left). If you have a confirmed XXY diagnosis note it in your bio. No matter what you write about yourself in the profile, you are as anonymous as you want to be. So don't be shy.

The board is divided into topical forums and there is an appropriate section for whatever your interest is.

People may read your profile but they may not write to you about it. Please use the Forums to engage people in conversation.

XXY persons with confirmed diagnosis: after you have filled out your profile, please take a moment to answer a survey titled "XXYs only - what do you do for a living?" - this is our XXY wall of pride and we would be pleased to have a contribution from every XXY person.

Mothers-to-be: if you are struggling with a decision whether to continue your pregnancy, please give us a chance to tell you what we know about XXY. Our information comes of research and first hand experience, and may be quite different from what a doctor or geneticist has told you.

If you are a person who suspects he is XXY but hasn't been to a doctor about it, post about yourself in the forum titled "Am I XXY?" Do note that we are not doctors, we cannot diagnose or give medical advice, please don't expect us to.

The only way to confirm if you have the condition is to get the genetic test done.

If you haven't used a bulletin board system before this will be a new experience. There are lots of tips and tricks under the "Information" forums. And don't hesitate to ask for help.

We curious to know how you found us. Could you send Paul a Private Topic message and let him know?

This site is an offshoot of a UK Charity which funds the web hosting etc. more details can be found at www.ksa-uk.net

Again, welcome to the board!

the moderators
XXYTALK joint-Admin

Klinefelter's Syndrome Association (UK) [Founded 1990].
KSA Website: www.ksa-uk.net
KSA UK Conference June 2015 @ Derby, England.

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