It's no secret that, at least in the past, I have been very open about my diabetes and the treatments I'm on. I have injected openly in front of co-workers, family and friends; proudly displayed my insulin pump; and told almost anyone who will listen that I have diabetes.
However, I'm starting to put the wraps on that. I'm not ashamed of anything, I'm actually pretty tired of misinformed people and of trying to explain the difference between type 1 and type 2. I do enjoy setting people right (just ask The Mr.!), but I don't want diabetes to be any more of a focus than it already is.
I may be naive, but I believe that my friends, family and co-workers who knew me before diabetes don't see me any differently. I don't believe they take pity on me, I believe they see the same strengths in me--and hopefully more--that they saw before I outted myself to them.
But new people, people who only know the Michelle with diabetes, may not have that same non-judgmental view. These are the people I've decided to hide from. OK, not hide in the traditional sense, but hide in the sense that diabetes will not be revealed as haphazardly as it has been in the past.
This morning, one of my Diabetic Mommy sisters reminded us that people with diabetes are not covered under the Americans With Disabilities Act, which means we are not protected against job discrimination. A bill to close that loophole was being voted on today.
I'm not really sure why this message hit me the way it did today, but this non-protectionist state that we're lingering in right now is actually pretty scary.


Diabetic Recipes









Hmm... according to the American Diabetes Association Complete Guide to Diabetes, Second Edition (copyright 1999), which my health insurance company sent me upon diagnosis in 2002, the ADA *does* cover diabetes... but employers may still have discriminatory policies due to lack of education...
Color me "confused".
I, too, believe diabetics are covered by the Americans with Disabilities Act. I, however, don't see myself (type 2 for a year and a half now) as disabled.
I, too, had an issue with my comfort level about testing and injecting in front of people, but it lessened over time. It's just something I do, and I don't make a big deal or an issue about it. If people ask questions about diabetes, I'll answer them, but otherwise it's a non-issue. I manage testing and injections without anyone having to accomodate me. My boss knows, in case I'm in need of assistance, but otherwise it's work as usual.
So just go on with your job and your life, and don't worry about whether you might or might not be covered for something that hasn't even happened yet.