I had three broken bones before I got out of high school;  and I think I recall being told that TS girls were a little more predisposed to brittle bones.    I know I even had a bone age study done at one point.

Can anyone confirm or deny this, or point me to some information?

Hi, ladies. If any of you are out there, I came across this very informative article. I found the parts on the thyroid and the liver noteworthy because I have hypothyroidism now and a recent blood test showed one of my liver enzymes elevated. I copied and pasted it as best I could.

( Turner's Syndrome in Adulthood )

Hi there ( Read more... )

Do any of you (all 14 members...) have Lymphangioma/Cystic Hygroma? The research says that it is common when you have Turner's. I've just never met anyone like me who had it. They say 1 out of 4000 are born with it. That's 4000 in general population, not 1 out of 4000 turnergirls.

  Hello everyone! My name is Kai and I am an English grad student at San Jose State, and I am really happy to have found this community! I was diagnosed at about 9 mos. old and I am really looking forward to hearing everyone's stories.

Hello everyone ( Read more... )

...just in case anyone read or heard about a certain article in the Times recently and was worried at all.

( Taken from the TSSS UK Website (www.tss.org.uk) )

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Okay, I really hate to do this; I know that this is (literally) a sensative issue for a lot of girls with TS; so if this question hurts anyone, I apologize in advance and will understand if it is deleted ( Read more... )

Well, first of all, I want to thank you all for joining ( Read more... )