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The answer is: NO

Saturday, April 26th, 2008

I called the Pfizer help line this morning and spoke to the on-call weekend nurse. When Miles the nurse taught us how to do the injections he took us through from when you attach the meds cartridge to the Genotropin pen all the way through the injection. This made sense, since it was our first time, the cartridge was not attached, etc. 

After that, you’re on your own. You are left hanging about how to do the injections on a daily basis. Where do you pick up in the string of instructions? The DVD/website is not helpful on this, because it too begins when you attach the meds.Cut to the chase: I have been giving Natasha injections but no meds for the last two nights. The good news is that she is getting more used to the shots, and they hurt less without the meds, which could sting a bit (according to the on-call nurse), gradually reducing the fear factor. The bad news is, of course, three days of injections wasted. I definitely felt no need for a dress rehearsal of these. Oh well. At least I know now. And am prepared in case she feels the sting tonight. 

Am I doing this right?

Saturday, April 26th, 2008

Day 4 and all seems to be going well. Except I’m not sure I’m giving these shots correctly. Nurse Miles and the directions from the company instruct you from when you have to attach the meds cartridge all the way to giving the actual shot. 

Problem is, you only have to replace the meds cartridge every 12 days or so. It seems logical that in the interim I would proceed from the step following the cartridge attachment, which is what I have done for the past few days. I doubt myself, though. I am going to call my Prizer rep tomorrow and make sure I’m doing what I should be doing. I’d have to have given my kid “dummy” shots.On the positive side, today was really easy. Natasha let me give her the shot without the needle guard, which was much easier for me. She seemed pleasantly surprised with how painless it was. I hope I put the medication in her!And, she was starving at dinner time. Natasha is never starving. She’s hardly ever even hungry. Maybe that’s a good sign that this Genotropin is starting to work. Sending good thoughts into the universe…

New Blog in town

Friday, April 25th, 2008

Natasha started her own blog. Give her a day or two to get up and running and then check it out: Genogirl Grows On

Miles the nurse called…

Thursday, April 17th, 2008

…and although I was anxious for him to call yesterday, I hesitate to call him back. Setting up his visit will make this whole thing all too real.

My child on Genotropin

Friday, April 11th, 2008

Today my husband and I made the decision to begin our 10-year old daughter Natasha on Genotropin, a form of human growth hormone. If she reacts favorably, she will inject the drug daily for the remainder of her growth period. Given that her current bone age is roughly 7 1/2 years, this could be upwards of 5 years.

In my web-based information search I found no personal stories of anyone who has used this drug or given it to their child. Therefore, I decided to begin this blog. In it I will chronicle our experience, including the nurse home visit, which augurs the first injection, our experiences with the Pfizer Bridge program which makes the drug, effects, side effects, emotional effects– whatever comes up. I hope this will help others and possibly establish a forum for parents who make this scary decision.

Background:

A few years ago I noticed that my daughter was very, very small for her size. I am only 4′9″ and my husband is 5′8″, so we never expected her to be a giant. Nonetheless, she seemed excessively small compared to other children. Additional cause for concern was the fact that I am shorter than either of my parents, neither of whom is very tall, which indicates a possible hormone deficiency in my background. As puberty was not that far off, my gut told me we should check this out.

An endocrinologist from Denver Children’s Hospital began tracking Natasha’s growth. After a year and a half it emerged that her bone age is delayed by a few years (good), but that she is not growing at the pace of a normal child (bad). Thus, every time we visit the doctor her projected height–based on parental actual height– falls. Upon the doctor’s recommendation, we applied for insurance coverage.

 Last week I found out we were granted coverage. Today three months worth of the drug arrived, along with a tamper-safe needle disposal bin. On Tuesday we will get our “starter kit,” which among other things contains the injection device, designed to look like a pen. Somehow I don’t think too many kids are fooled by this. I will also be contacted by a nurse, who will come to our home and teach us how to inject our child.

I visited the Genotropin official site and cried through the video demonstration of a young girl preparing  the drug and injecting herself with the pen. She seems to think it’s no big deal but, then again, that’s her job.

To me right now this is a big deal. I go back and forth between being very calm and completely freaked out. My husband has been out of town all week and I am loathe to talk about this to her without him, so at this point all she knows is that we have been approved by insurance. So far she took it pretty well. I think is beginning to be conscious of how short she is and wants to grow. Over the weekend we will broach the topic in detail, talking about the nurse coming etc.

 If anyone has any experience or comments or knows of any other blogs about this, please share.