People with diabetes know the score. We've all seen "revolutionary" drugs and treatments introduced with fanfare, and we know that that much of the time they're evolutionary at best. But something has changed in the world of diabetes care.
I've been type 1 diabetic for 15 years. It hasn't been easy and I'm still grasping to keep my feet on the ground medically. Every time I think I've got this disease figured out, something new gets thrown at me and I stumble over and over again. From insulin resistance to pump failures to carbohydrate/insulin sensitivity changes to exercise regimens to health insurance issues to medical bill payments to a seemingly innocent cut on the sole of my foot, etc., I'm getting worn out.
I spent a month in a major insulin pump center and saw several things. Many of the female patients seemed to have wings on their sides where the pump tubing was inserted and they got lipohypertrophy from localized injections, but that was the least of it. None of them actually had remotely normal blood sugars.
People today have an incredible array of methods for finding the latest news and information about diabetes: the Internet, social media, and print publications. But perhaps the most powerful is the strong relationships they develop within the tight-knit diabetes community.
I wanted to interview my husband about my diabetes. He played a huge part in helping me accept my type 1 diabetes and he has never made me feel inferior for having it. Rick and I just celebrated the 15th anniversary since our first date, and since I've only had diabetes for 18 years, he's been there for most of it. He was there during the times I was out of control and in denial, and he's been there while I work on treating myself right and trying to take good care of myself.
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