I just read an article about type 3c diabetes on Diabetes Daily which was used with permission, as it was originally published by Beyond Type 1.
The article was very interesting but left me wondering.
I’ve heard type 3 used a few times before, 1) referring to those who are the caregivers for another with diabetes and 2) for those who have Alzheimer’s disease. I’m learning now there is another type 3, 3) referring to those who no longer have a pancreas. This type for the pancreas does have an addition of the “c” after the “3”, much like there is type 1a and type 1b.
How and when will healthcare get a handle on all of the various types of diabetes. The article I just mentioned addresses the fact that type 3 is not a recognized diagnosis, so for insurance purposes, they have a type 1 diagnosis.
As a community, I would like to see us better define type 3, so each group can seek and attain the assistance they need, without the confusion of three totally different types (caregivers, Alzheimer’s, no pancreas) all referred to as one entity, type 3.
Could it be that type 3a is for caregivers and 3b is for Alzheimer’s and now type 3c is for no pancreas?
Is there something we can and should do?