Insulin pumps are crazy expensive. Even when I looked at refurbished ones, the cheapest still came to over $900. Maybe, if we aren't in dire straights again when the next PFD comes around, I could get one. But then, I always find that the kids need something, or bills need to be paid. I wish medical care wasn't so expensive. I wish insurance companies were more affordable and didn't shut out those of us with pre-existing conditions.
So, later today, my son will hopefully start a new chapter, that will give him near perfect control that will add years to his life and prevent any complications. My hope for him, is that his life will draw a little closer to normal and he won't feel so left out when there are special foods during celebrations, or have to compromise and decide whether or not a treat is worth getting a shot. I hope even more, that we will be able to prevent the low blood sugars that robbed me of much of my sight. This is huge and I wish everyone with type I diabetes, all kids and mothers who have this unfair disease could have a pump. It should be standard after proving ability to properly utilize it.
So, wish us luck. This is a huge step. I am a little scared, but so much more excited... and envious. Maybe someday, a pump of my own will be within my grasp.
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