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November 21st, 2008
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It took us just short of a year, but we finally discovered the right time of day to change Charlie's infusion set.

From the start of our pump training, we were instructed to change his site in the mornings. Before bed was not recommended for fear of low blood sugars.

So, we did as told.

And for months, Charlie's blood sugars were extremely high for a good part of the morning and into the early afternoon on site change days.

Our doctors weren't sure what to make of it. We all theorized that it was the stress of the site change sending him out of the stratosphere. Seemed to be a good enough explanation. He did absolutely flip out with site changes. The hope was that he would eventually not stress so much with the site changes and the blood sugar levels would fall into place.

Never happened and never happened.

At this point we were doing the change after breakfast. We started to wonder if it really was the stress that was bringing him up. Could it be absorption? A combination of stress and absorption?

Still months later, we revisited the site change day dilemma with Gary Scheiner, author of Think Like a Pancreas. Gary, who didn't look anything like a pancreas despite his ability to think like one, seemed to have the answer we've been so desperately looking for.

Timing and absorption. Of course! How could we have been so blind. It made perfect sense. Change the site before breakfast rather than after. Gary illustrated on a piece of paper how the post breakfast insulin from the new site would take a long time to make it through Charlie's subcutaneous tissue. This, of course, resulted in high blood sugars. A site change timed just prior to a large meal bolus would surely get that stream of insulin flowing.

Or not.

We then spent the next few months setting a temporary basal increase for the mornings of site changes. This helped occasionally but it didn't feel like a solution. Our pump educator offered a suggestion in the way we primed the pump. Yet another theory that failed.

Just for the hell of it, we recently gave nighttime a try. Just before Charlie went to bed. Guess what? We don't have site change highs anymore. So odd this disease. A disease in which so often the parent of the patient or the patient himself finds the answer before the doctor does. Diabetes is very unique in that way.

So often a work in progress. So often trial and error. So often uncertainty.



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Email this Comments (4) :: Add a comment

I so glad you found something that works, knock wood. I think what I hate the most about diabetes is how individualized it is and what works for one person doesn't work for another. It really is so much of a guessing game most of the time. And even when you do have it all figured out, whammo, something changes. I really hope the night changes keep working for you!!!


We were also told not to change Brendon's site at night just in case the set wasn't inserted correctly and we wouldn't be awake to check him and correct the mistake.

But, we're rebels and decided to change it at night anyway because getting it done in the morning when everyone is trying to get out the door was too crazy.

His numbers have been fine overnight and in the morning. That is our preferred time to do it.


Congrats on finding a solution for those nasty morning highs. Hopefully the routine continues to bring good results and another diabetes wrench isn't thrown into the mix.


Is it possible to get your email address. I am a grandmother of a 8 yr old diabetic diagnosed in May 07'. We are having a terrible time regulating her #'s, she was 350 at snack time this morning. Her endo quit (Kaiser) 2 mths ago, and now all we have is a diabetic nurse. The endo said to give her more insulin inbetween if she was high. The nurse says no, so now we are really confused. She refuses to put her on the pump (think it's Kaiser refusing to pay for it myself). We are seriously thinking of putting her on medi-cal so she can go to Childrens.
This constant highs and lows is making my daughter a basketcase. Kaiser offers no classes for her or her daughter. She is low income (can't work much when you have to run to school to do shots etc...) so she will qualify. And, hopefully get some help with her med. supplies. We are at a quandry on what to do.
Judy
fastax@aol.com


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Carey Potash
Carey is a full-time hater of diabetes. The benefits stink. His 6-year-old son, Charlie, was diagnosed with type 1 diabetes when he was 22 months old. Carey's parenting humor has appeared in various websites and print magazines. He resides in the suburbs of Philadelphia with his wife and three children. (Read More)

Latest Posts: The Adventures of Gleevec and Sutent | Permanent Remission? | It Was a Blizzard (5 Years Ago)

Michelle Kowalski
Michelle Kowalski, a writer, editor and photography hobbiest living in Phoenix, was diagnosed with Type 2 diabetes in February 2005. In January 2008, as part of her quest to start on an insulin pump, Michelle learned that she actually has type 1 diabetes. (Read More)

Latest Posts: Waiting Impatiently for CGMS OK | Back to the Find-A-Doctor Drawing Board | A Day in My Life

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