heyy My name is Leanne and i also have TS i was Diagnosed when i was 10. im 13 now! i still strugel with it so if anybody could give me any advice..that would be great :)
Yeah i think we probably have spoken lol and i can be ocassionally at conferences depends where they are don't have time or ways of getting to some of them x
i was born with TS and am now 14 and my height is 4'9...im not going to grow more than another inch. you videos are awesome and you should conyinue doing them( :
I was also born with TOTAL TS (I have only 1 X chromosome), and now, I'm 16, and my height is about 4' 8''. I'm glad to learn about someone who's also going through it. I'm now in estrogen and progesterone replacement therapy, because they switched me out of the growth hormone about 2 years ago.
I didn't have as many ear infections, but I do have a tri-valve defect in my heart and the horse shoe-shaped kidneys. And clothes ARE hard to buy! Thanks for making this video, I really appreciate it!
I have TS and am only 4ft 9inches tall unfortionatly I didn't recieve any treatments as a child and understand about it being hard to find cloths I also have hearing loss due to ear infections as a child so i know what you have gone through love your videos think they are great thank you for putting them up here
Hi My daughter is almost 12yr old, she was DX at birth with classic TS.Started GH aged 4yrs. And Estrogen 7 months ago. She too has puffy feet so shoes can be a problem.Last checkup she grew 2" in 6 months(so is 4ft 3") and for the 1st time since she was 6 weeks old was on the very bottom line on a regular growth chart for height. She's in mainstream school and doing well. great vid BTW xx
Hi EMZ! Good video! Keep em coming. My daughter Tess was born with Turners. We diagnosed her very early, 18 months and started her on GH. She is now 2.5 yrs and in the 25th % on the growth charts! She too is mosaic and "normal" in every other way. I'll check out your website later. Thanks for sharing! -Tessie's Dad
Hi thanks so much for getting in touch really good to hear from people watching the videos. Wow she sounds like she is doing well which is good and its lucky that it was early diagnosed like mine so that she can get all support and things that some girls havent had not being diagnosed. Anyway just wanted to reply quickly to your comment. Emma
thanks for all the comments sorry i havent got back to everyone havent really been on this much but glad to see theres been interest in the videos =]
Emz1402 1 year ago
heyy My name is Leanne and i also have TS i was Diagnosed when i was 10. im 13 now! i still strugel with it so if anybody could give me any advice..that would be great :)
LeanneRR14 1 year ago
@LeanneRR14 its tough but just gotta find your own way of dealing with it but talk to people around you if you need to =]
Emz1402 1 year ago
Thank you so much for posting this. I have ts myself and am 4ft 8. Apart from short stature it really hasn't affected my life at all. Thanks again xx
barbie0919 2 years ago
Diagnosed with mosaic TS yesterday.
I'm 27, 5ft7.
So I am shocked.
I'm also getting a lot of conflicting info.
I found out because after 2 miscarriages I got pushy and had some tests done, karyotyping was one.
I'm now under the impression that I can and will pass this on to my children, which is why they died before they were born.
I sunno it's a huge thing to learn at the age of 27 ..
..all I am thinking about is if I'll ever have a baby.
Or if I'm going to hit menopause soon.
beraucracy 2 years ago
I Lost my baby at 17 weeks Gestation.....
She had Turners Syndrome
6pimpette9 2 years ago
@6pimpette9 really sorry to hear that
Emz1402 1 year ago
FAB video. I got TS, was diagnosed at 10. Think i might have spoke to you on MSN, lol. Keep up the good work!
Ella x
PS. Do you ever go to the Conf. in October??
elrhia 3 years ago
Yeah i think we probably have spoken lol and i can be ocassionally at conferences depends where they are don't have time or ways of getting to some of them x
Emz1402 2 years ago
i was born with TS and am now 14 and my height is 4'9...im not going to grow more than another inch. you videos are awesome and you should conyinue doing them( :
ltgbear1995 3 years ago
I was also born with TOTAL TS (I have only 1 X chromosome), and now, I'm 16, and my height is about 4' 8''. I'm glad to learn about someone who's also going through it. I'm now in estrogen and progesterone replacement therapy, because they switched me out of the growth hormone about 2 years ago.
I didn't have as many ear infections, but I do have a tri-valve defect in my heart and the horse shoe-shaped kidneys. And clothes ARE hard to buy! Thanks for making this video, I really appreciate it!
giligara30492 3 years ago
I have TS and am only 4ft 9inches tall unfortionatly I didn't recieve any treatments as a child and understand about it being hard to find cloths I also have hearing loss due to ear infections as a child so i know what you have gone through love your videos think they are great thank you for putting them up here
elrond98031 3 years ago
Thanks for getting in touch appreciate hearing form everyone
Emz1402 3 years ago
Hi My daughter is almost 12yr old, she was DX at birth with classic TS.Started GH aged 4yrs. And Estrogen 7 months ago. She too has puffy feet so shoes can be a problem.Last checkup she grew 2" in 6 months(so is 4ft 3") and for the 1st time since she was 6 weeks old was on the very bottom line on a regular growth chart for height. She's in mainstream school and doing well. great vid BTW xx
fluffyfairy321 3 years ago
Hi thanks for getting in touch glad to hear your daughter is doing well x
Emz1402 3 years ago
great vid! keep up the good work!
lbpmchoir 3 years ago
Hi EMZ! Good video! Keep em coming. My daughter Tess was born with Turners. We diagnosed her very early, 18 months and started her on GH. She is now 2.5 yrs and in the 25th % on the growth charts! She too is mosaic and "normal" in every other way. I'll check out your website later. Thanks for sharing! -Tessie's Dad
finley1970 3 years ago
Hi thanks so much for getting in touch really good to hear from people watching the videos. Wow she sounds like she is doing well which is good and its lucky that it was early diagnosed like mine so that she can get all support and things that some girls havent had not being diagnosed. Anyway just wanted to reply quickly to your comment. Emma
Emz1402 3 years ago