The point of this blog...my kid, of course.

Chamberlyn's T1 Diabetes D-Day (Diagnosis Day) was October 19, 2010. I decided to start writing her story almost nine months later because managing her diabetes is what our family does best. We have our "highs" and "lows" when dealing with this confounding autoimmune disease, and I hope our posts can provide some insight on the daily life of a person with T1 diabetes.

Friday, August 12, 2011

Fingers, toes, and syringes crossed!

It's official, we love the demo OmniPod and it doesn't even deliver her insulin yet.

Reasons why we love it:
1 - The mere idea that we won't be sticking her 3 times a day with an insulin filled syringe if we are approved to start using it.
2 - It withstood every test we could think of - showers, swimming, dancing, sleeping, doodling on it, and other daily abuses. The tape peeled up slightly around the edges, but it never was yanked off when she would rip her clothes off without caution.
3 - Finally, and most importantly, she would forget that she had it on. This was a big one for me because if she complained even once about "feeling it," or it "bothering her," I was going to throw in the towel and not think about a pump again. She would hit it on the wall, roll on it, catch her clothes on it, and say, "Oh yeah, I keep forgetting about the pod!"

She went through several nicknames, but the one we doodled on it in the picture below is her official name for it: "iPanc." We are keeping "fingers crossed" that our endo approves of us trying it out and taking the pump courses that the hospital requires before beginning pump therapy. I'll keep you posted!

No comments:

Post a Comment