Hi Everyone...
I was wondering if anyone has been on Genotropin or have children who are/were on it. My daughter, Kaitlyn, is 11 1/2, perfectly normal for weight (over 50% on charts) but her height is behind (5-10%). Our CF doctor sent her to an endocrinologist (he works with several CF patients). He did testing to determine if she is not making growth hormone. The end result is that one test showed normal and the other showed a defiency. He said most insurances require both tests to show a defiency before it is covered but he wanted to see if he can get her started on it. Well, our insurance agreed to cover it but now I am skeptical. If it typically requires two positive tests and she only has one, does she really need it? It means a shot every single day and then the risk of side effects. Also, I read on their website that it can cause death in people with respiratory problems (I take that lightly because I know all drugs run a risk but still, it scares me). I don't think she is all that small for her age. She is not tall, but really she isn't all that short compared to her friends...The dr said that she should be growing at a rate of 4 inches per year and she is only growing 2 so she won't reach her full potential without help.
Any advice? If anyone has dealt with this drug, what are the side effects you noticed? How do you determine if it's worth the risk. The idea of the shots freaks Kaitlyn out. I give her sister allergy shots at home and Kaitlyn won't even be in the room when I do it. I have called our CF doctor to ask her opinion but of course I haven't gotten a response (nothing unusual)...so I figured I'd ask you guys. You always respond faster than the clinic.
Thanks!
I was wondering if anyone has been on Genotropin or have children who are/were on it. My daughter, Kaitlyn, is 11 1/2, perfectly normal for weight (over 50% on charts) but her height is behind (5-10%). Our CF doctor sent her to an endocrinologist (he works with several CF patients). He did testing to determine if she is not making growth hormone. The end result is that one test showed normal and the other showed a defiency. He said most insurances require both tests to show a defiency before it is covered but he wanted to see if he can get her started on it. Well, our insurance agreed to cover it but now I am skeptical. If it typically requires two positive tests and she only has one, does she really need it? It means a shot every single day and then the risk of side effects. Also, I read on their website that it can cause death in people with respiratory problems (I take that lightly because I know all drugs run a risk but still, it scares me). I don't think she is all that small for her age. She is not tall, but really she isn't all that short compared to her friends...The dr said that she should be growing at a rate of 4 inches per year and she is only growing 2 so she won't reach her full potential without help.
Any advice? If anyone has dealt with this drug, what are the side effects you noticed? How do you determine if it's worth the risk. The idea of the shots freaks Kaitlyn out. I give her sister allergy shots at home and Kaitlyn won't even be in the room when I do it. I have called our CF doctor to ask her opinion but of course I haven't gotten a response (nothing unusual)...so I figured I'd ask you guys. You always respond faster than the clinic.
Thanks!