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The note above is one that I dictated into my phone last year and then forgot about. Other than edits for punctuation this is how it came out that night lying in bed. Fortunately something this dramatic doesn't happen very often, but there are always going to be nights like this that make no sense. This is reality for people with Type 1.
The image below is my JDRF footprint through this evening. It's based on an average of 5 finger pricks a day - I'm typically close to double that. The injections are an average of 7 a day, which is probably a little low but not too far off. And the hours of sleep lost? I have no idea. They usually aren't quite as dramatic as the night above, but it's a good example. In comparison, I was up at 4 AM today doing an injection because I was higher than I like to be. It goes both ways. These numbers represent just 4.5 years. I never knew anything about this before I was diagnosed, but I'm going to keep telling my story and watching these numbers climb until somebody figures out a solution.
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