Tuesday, May 14, 2013

Dream D Device - The Life Long Test Strip


 
 
Today's suggested topic was to create a petition.  I've been reading through many blogs today and I really love all the petitions I've seen.  As it is, I would need to have a rubber stamp made to keep my hand from cramping from signing so many.  So I've decided to use a wildcard suggestion and tell you about my dream diabetes device.
 

My Dream Diabetes Device:  Permanent Test Strip
 
Think about it.  One test strip.. FOR LIFE!  No more random strips found literally everywhere.  no more money spent on an item smaller than my pen cap, but costs more than the entire pack of pens. 
 
I got to thinking about this at lunch.  About a month ago, a couple of us were chatting on Twitter about how many test strips we go through.  Jenny of Sugar Beat started collecting hers in a plastic container.  On April 14th I started collecting mine in my meter case. 
 
One Day

One Week


Almost One Month





I'm not sure I would want to see the size of the pile after six months, let alone a year.  What do you think?  Would you like a permanent test strip?


Monday, May 13, 2013

Hey Dr. Endo!

Often our health care team only sees us for about 15 minutes several times a year, and they might not have a sense of what our lives are really like. Today, let’s pretend our medical team is reading our blogs. What do you wish they could see about your and/or your loved one's daily life with diabetes? On the other hand, what do you hope they don't see? (Thanks to Melissa Lee of Sweetly Voiced for this topic suggestion.)

I love my doctors, especially my endo. Well, she not technically an endo, but she is who I see every three months for insulin adjustments, A1C tests, prescriptions, and life updates. I have mentioned in passing a little about my blog, ie: a post I had about a particular thing. I don't think she reads it. I could be wrong, I have been known to be wrong before, but I would be surprised. That being said, if she DOES read my blog, there are just a couple things I'd like her to know.

I may write about a lot of things, and not always my diabetes, but trust me.. it is ALWAYS first (or second) on my mind. I have a life outside of diabetes, and by golly that is what I find more interesting. My daughter is SUPER important to me and I try my darndest to not let diabetes interfere with me being with her and doing things for her. If that means I run higher for awhile because of the stress (Did you know that the HS senior year is a pain in the butt for the parents?! I sware it wasn't this way when I was a senior.. right?) it doesn't mean I'm not trying, it just means that diabetes is a pain in the butt and doesn't play well with others.

I am scared to make adjustments without your approval. I have done them, and I'm feeling more confident in doing them, but the kid in me still expects to be scolded for changing something without permission. I know ultimately I'm the one taking care of me, and I need to feel better about taking control of little things like that. I'm getting better, I really am, especially when the change I make actually works.

For the most part, things I don't want anyone to know I don't write about, so if she does read my blog, there is nothing there I want to hide. However, there are a few things I do (and I know others do as well) that aren't exactly best practice. I have changed my infusion set at 2am because my pump ran empty. I don't like wasting even 1 unit of insulin.. that stuff is expensive.. so I have had a snack before bed just to use the last little bit of insulin in my pump so I can replace the cartridge before going to bed so I don't have to get up at 2am. Yes.. this usually makes me run high all night, and I have a hard time getting it back down even after breakfast. Ok.. ok.. this is something I may need to reconsider. Is 1 or 2 units worth it? Hmm... let me consult my checkbook.