My daughter was diagnosed with mosaic TS in February 2012 aged 16 and a half. Best of luck to you and your daughter also. I am sure she will still be a wonderful mother someday through other options. My daughter is still young so it doesn't bother her yet. What mom doesn't dream of her daughter having her own baby. The thing I struggle with is the infertility. She has always been little (never even been on the growth chart which I am sure is the case for a lot of the girls) and she has never started puberty so it's only good and exciting news that she will get a little taller and eventually start having girly feelings. It is all bit overwhelming in some ways but in others it's not. Depending on how her growth goes, I think we are going to start estrogen next summer. Her bone age test came back of that for a 12 year old which is great because now we have time for her to be on just the hormone before we introduce the estrogen. Fortunately we didn't have any insurance problems so we were able to get them going right away. Yes, my daughter has been on growth hormones for about a month now. She always felt guilty! Don't feel guilty, your daughter can have an amazing life, I have! This is a great tool to connect with others and gain knowledge to help your daughter. I am also happily married to a wonderful man that helps me navigate my medical challenges. There is so much research out there now.there was one paragraph when I was diagnosed. I will have that done ASAP since my research says they should be removed. I probably should have had my ovaries removed a long time ago, but I didn't know. My arm span is 3 inches longer than my height. I was very short, under 5 feet tall, until I turned 16 1/2. As I was 19 when diagnosed, I didn't receive any HRT until that time. I found out recently that my 2nd chromosome in the 23rd set probably has a mutated y or 'some y material'. Is the doctor calling it Turners? I am 65 and was diagnosed Turners just before my 19th birthday.

Mosaic turner syndrome