Dating a girl with turner syndrome consolidating graduate plus loans
I was ordered to cease all growth hormone injections immediately as doctors believed a link existed between the two. If a TS girl is fortunate enough to receive an early diagnosis, like me, growth hormone injections would ordinarily be continued until twelve or 13 years of age.
By ceasing all treatment at just ten, I was missing out on a valuable three years of injections which would have serious implications for my final adult height.
I was so weak and fragile, just a hospital cold would have had devastating repercussions.
It took me a solid 12 months to make a complete recovery.
Over the next two years, life reverted to normal with the exception of some developmental delays such as speech and taking my first steps.
At the time of my diagnosis in 1986, information was sparse.
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Thus, this article is borne out of a need to educate the public and raise awareness of the everyday intricacies of living with TS.
The following article charts not only my personal medical complications but also the psychosocial difficulties experienced as an adult living with TS.
Constant hospital appointments gave me regular happy days away from school and usually a lollipop followed a visit to the doctor which always went down a treat (now I know where I developed my sweet tooth).