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May 23rd, 2012
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I think he's just about had enough.

 

If I went through what he goes through, I suppose I would too.

 

Two days of low ketones that wouldn't go away no matter how hard we prayed for mercy. Waiting for the other shoe to drop. Two days home from school. Maybe a third tomorrow. High blood sugars and ketones that proved to be an omen for one hell of a nasty cold.

 

He's had enough of the long, sharp needles in his ass and the tiny sharp needles in his fingers. Our constant handling of his pump like he's some sort of appliance. Out of defiance yesterday, he wouldn't let me near his pump because he couldn't eat what he wanted to eat. He took a stand against the injustice.

 

He's had enough of the food requests that get rejected; the waiting like a dog while we count and weigh his food; the grabbing of his fingers in the middle of the night; the brightness of the lamp at 2 am. He's had enough of my ill-timed silliness. My dopey sensor inquiries - "Hey Charlie, what does Pumpy Pumpington say?" A sigh. A roll of the eyes when we ask him to test himself before a snack. It's all wearing on him. He's had enough.

 

You can see it in his eyes at times. He's fed up with how this disease is affecting his life as a 9 year old. He's pissed off and beginning to lash out. There's a new anger; moodiness; a definite dark side that has taken over. 

 

During site changes and sensor insertions, he screams louder than he ever has before, in a pitch that will seemingly break the windows.  It makes the moment more difficult - more stressful for me and Susanne. I think Charlie knows that. It's our punishment for being his torturers. He is vengeful and it's hard to blame him for that due to the very unpleasant circumstance we find ourselves in.  Like an abused puppy, he pulls away and retreats when we try to console him.

 

When the moment passes, he comes back to us - burying his head into our bellies.

 

Until the dark side comes calling again.

 

I think we've all had enough.




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Carey,
This post hit home, and I know exactly how difficult it is to be the parent! There is no way to explain to your child that you are trying to help, when all they feel is pain, sickness and anger! I wish I could say that I don't know about the anger and hurt looks, but I do. We went to a counselor and it really helped. I was skeptical at first, but figured that it could not hurt, and it was a good decision. Now at 19 she understands when I bug her about testing and other diabetes "stuff", I just say it's part of my job as her mom.

Good luck!


Sounds to me like he's growing up. He wants more independence, but the diabetes (and the way parents need to worry more about their d-kids than their non-d kids) keeps you on your toes (and eating anti-stress pills instead of food), and him more tightly tethered than the average 9-year-old. I suspect you went through (and continue to go through) the same sort of thing with Maeve, it just wasn't complicated by diabetes. (Just wait until she starts dating...)


Carey, this post hit home. My 11yo did the same thing with his site change last night. Absolutely refused to have one more needle of any kind poking him. I'm thinking it's an age vs. diabetes thing; we haven't hit the 2 year diaversary yet. It's heartbreaking and I'm tired of it too.


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Kerri Sparling
Kerri SparlingKerri Sparling, diagnosed with type 1 diabetes when she was six years old, doesn't let diabetes define her. It just helps explain some things.
Creator of the diabetes blog Six Until Me and an editor for dLife, Kerri is an awareness advocate and an active member of the diabetes community. She'd also like a kitten.
(Read More)
Lindsey Guerin
Lindsey GuerinLindsey is a typical, yet unique, Texas girl who loves shopping, movies and reading. She loves to travel and take risks. She dreams of diabetes cures, never-ending cheesecake and her own airplane. The rest you can discover in her blog! (Read More)
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