Right now she's been pretty emotional with how other kids at school can eat and snack on food all they want. They don't have to count carbs, or have their food weighed and measured out. They don't have to go to the nurses room each day to get tested and bolused for their food. They don't have to deal with low and high blood sugars and the symptoms that come with it. She just wants to be like all the other kids and not have to worry about all these things.
She did get a pump last summer, what a blessing that has been. No more shots! She just has to change her site every 3 days, and that's almost painless.
Lately she has also felt very alone with having diabetes, she's the only kid in her school with it. She's not alone any more with Blake just getting diagnosed. As much as I wish Blake didn't have to have struggle with this, it will be really nice for them to have this in common so they don't feel alone in this.
I often think about how grateful I am for insulin, and that it's available to me. Without it, Brooklyn and Blake would not be alive. One day there will be a cure for diabetes and I'm confident that Brooklyn and Blake will be able to be here to be apart of it. What a happy day that will be for our family and for everyone who has this auto-immune disease. Until then, we will keep doing what were doing. We are all happy and healthy, we have good days and bad and those bad days make us stronger I'm sure of it.
March 7th, 2011 in the E.R. I remember we were in the E.R all night waiting for a room to become available. |
3 comments:
your kids are so brave and tough
Teri! What a trooper you and your kids are! YOU are such an example to them of how to handle something hard. You sound like you are doing everything right-- counting your blessings while still validating real feelings. Such a hard thing to have to deal with this disease! I have a few little cousins that have type 1 as well, and it is not fun. I pray for a cure someday, too.
Terri, thanks for this post-I needed it today. Gage has been struggling with his being different lately. sometimes he's good and sometimes he fights doing his bathroom routine every three hours. He's the only one with spina bifida in our school and that's hard, but you helped me recognize he's not the only one that has to go by the clock to help his body work right.
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