I too have joined the ranks. My dad discovered his Type 2 Diabetes at the same age in his life that I have. I'm mirroring his progress, though I don't know that I ever heard him say that he lost the feeling in his feet.
My story is one of denial and as a nurse makes me a little ashamed...but I am also human. I go to the beach every year and take my family...don't go on vacation without them, Ha. But you know how the surface around the pool makes you want to dance it's so hot? Well, from one year to the next, I lost the ability to feel the hot. Still didn't do anything. About 2 or 3 years before that, I noticed the Plastic Wrap feel to the bottoms of my feet as I would get up in the mornings. My fastings were not bad at this time and my Internal Medicine MD is excellent. She was keeping an eye on me. So all told, I've really been a diabetic for about 8 or 9 years, only 3 with treatment. I wonder if I will ever get some of this feeling back in my feet. I've done a little research online, but nothing speaks to that point...it's just that part of it really bothers me.
I'm currently taking oral diabetic agents including amaryl, glucophage, and just started Byetta a month ago. My A1C was 7.4 last month. I know it needs to come down lower, but that was not even trying to adjust my diet...not that I am a constant splurger, but I don't go by the strict "3 pieces of bread a day...etc" diet.
Bad nurse! Not taking care of herself. I need a spanking.
I really think it's already affected my autonomic nervous system because I have gastroparesis, and I sweat a lot. My B/P is mildly elevated and controlled by diovan, and I frequently feel the pulse elevating "on it's on".
Scary. It seems that even when you do it "right" with DM, you lose. It's such an insidious disease.
A bad example for my patients,
jen