Excellent!Again movement in this thread, I recognize that I am the first to find time to participate, my little son always has to sleep in his arms, so I take advantage of reads.
I want to encourage you to the "new" and the not so new, van, Antonio, Mcanrio, I always say it, this is the only club where we do not rejoice in having new members, but we will help you in what you need.
I am glad that you have decided that the bomb is the best treatment for your children, because it is, also in such little children, unthinkable to go with feathers.The feeling that you have had Antonio I have had many times, for me the bomb was a wonder and the meter continuously the sky.When I explained the "technological wonder" I found comments with those who have made you, at first I was very offended, it was something like "Oh! What has told me about our bomb of our meter, my Tesoooro! Little less what notMy mother hahaha!All those parents who explain how bad they are having with their children will try your solution.expectations or the idea that the pump is the perfect solution that will make your child no longer diabetic and unfortunately it is not so.
Van there is a post that began Velia, "problems with the continuous meter", where I think you can find a lot of information about the meter, if you have any questions, my son takes it since I was four years and we are delighted.
The degree of disability (it is not called disability) for children with diabetes, it is also a mystery to me, my son was also granted a 38% disability but not dependence, it is that! I also stay dead.Clarify that diabetes disability is temporary, I think they give it to you for a couple of years, then you have to go review it.
Well, let's see if I catch up, and I can follow this thread of parents regularly.