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When I tell my "real-life" friends stories about my friends from the Diabetes Online Community (DOC), I'm often told that my stories make these people sound real.
"Well," I say, "They are real. In many ways more real than some people I've met face to face."
I usually get the look then. The one that says: Nicole has been spending too much time online. Nicole's friends all live in the box.
That's the furthest thing from the truth. I mean - really - who can spend too much time online? And my friends don't live in the box, they just talk to me through it. Right?
I'm getting to the point. Patience. (READ MORE)

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This morning, I went for a second opinion on my current reproductive status. Back in late August, my Well Woman Exam turned into a possible endometriosis diagnosis. So I decided to go for another opinion before pursuing further treatment options.

 

And I have to say that I was pleasantly surprised by the doctor. New doctors are always interesting, especially those related to gynecology. But this doctor reinforced the idea that doctors can actually be helpful, understanding, and interested in what you actually feel or need.

 

So his opinion was that endometriosis is the likely choice as to the causes of some of my reproductive issues. Since I've tried most of the obvious treatment choices (NSAIDs, birth control pills, and pain management), the next step for a woman my age is surgery.

 

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Do you ever have that "D'oh! Why did I make such a big deal out of that" feeling/moment/day? That's kind of what I've been going through lately.

 

I feel really terrible saying this, but I think I'm doing OK without Dex. Which is kind of weird to me considering the amount of energy I put into getting my insurance company to approve the sensors.

 

I think one reason I fought so hard to get the sensors is because I had just started exercising again and I was (still am!) terrified of going low while walking. In the last twoish months since I started walking I haven't had any blood-sugar-related issues.

 

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Patti LaBelle is on the TV singing about how a certain glucose monitor changed everything. "Back then, food was the enemy," she says. My mind flashes to a host of studies I've come across recently touting different foods as the "cure." I can't help but see the humor in it.
We all know diabetes and food are so closely linked that often it's hard to deal with daily diabetic life without feeling like you have a major eating disorder. And while these new studies shouldn't give anyone a license to eat with abandon, it's nice to see research money being spent investigating food and nutrition, instead of new drugs.
Here's a look at some of my favorite new finds: (READ MORE)

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See that cat, he's jumping for joy - in spite of early-morning stressors...
I thought for sure I was going to be late.
I got in my car at 7:20 - I'd have enough time to make it into Providence for my 8:00 appointment with the doc - with time to spare. But there was traffic. A lot of it.
I was fairly certain my blood pressure would be through the roof when I finally arrived at the doctor's office 5 minutes late. (READ MORE)

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There was the researching, and the chats with the doc,. There was the mental tug-o-war between my daily injection comfort zone and my need for more flexibility, and now, like the quickness of a self-inserting cannula, I am pumping insulin by way of the OmniPod. (READ MORE)

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I was diagnosed with type 1 diabetes twenty-five years ago. Twenty-five years is a long time to live with something. It is an especially long time to live with something that requires tight control. Twenty-five years is enough time to have seen lots of bad days, lots of good days, and lots and lots of in betweens. And it is enough time for me to have had the good fortune of seeing vast improvements in access to information and treatment, developments and improvements in technology and even some improvements in (GASP!) what health insurers are willing to cover. (READ MORE)

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I want to think a fellow blogger, Carey Potash, for the idea behind this blog. It was him that I got the motivation to write this entry. Thanks man. You're a great father and you do an amazing job with your child with diabetes.
I hate going to my Endocronologist. I can't stand the overcrowdedness, the parking, some of the staff (you know who you are), the blood work (see my post entitled, "Disappointing Endo Visit"), The rookie University medical students, and the list goes on forever. (READ MORE)

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When I wrapped my last entry, I had just received my diagnosis of type 2 diabetes, in a non-standard manner.
In hindsight, I'm sure she was just trying to scare me straight. Maybe I'm not really a type 2, but that's what the paperwork says and as you'll see; if it's not 1000% correct today, chances are very high that it will be within the next 10 years.
Gosh, definitely don't tell my insurance company, or I'll be scrounging for strips like my friend Julia. (READ MORE)

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After a month of contemplation, phone calls, and hassle, I've finally made an appointment with a new doctor. If you haven't followed along, my old endo wasn't being as cooperative or helpful as I wanted him to be. So I decided to pursue a new endo that might walk me through the next few years of my life as I prepare for the "real world," babies, and possibly even marriage. I called several doctors recommended by my pediatric endo, only to find out that my insurance either will not let me see them or I'd have to go about a massive ordeal just to get an appointment.

 

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