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January 8th, 2009
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I have spent nearly 72 hours trying to figure out how to describe my appointment at the Mayo Clinic on Thursday. I just can't decide what to tell you first.

 

Although I arrived much earlier than I had been told to (it's hard to judge traffic patterns at off hours) and was getting ancy when numerous people were called back before I was, I was quite pleased when the nurse called me at 8:04 a.m.

 

No nurse came in to take my temp or blood pressure or ask me why I was there. I barely had time to observe my surroundings -- an actual desk with a computer, phone and other medical necessities including an ergonomic chair; a couch!; and other non-medical-feeling necessities -- before Dr. A came in. He shook my hand and we got down to business.

 

We talked like people, not like a doctor to an idiot patient. He treated me like I understood my body and my condition. Before I even had the chance to launch into my here's-who-I-am-and-you're-gonna-listen-to-me-damnit speach, Dr. A understood the value of getting my input.

 

He went through all of my notes on the patient medical history form in a pretty detailed fashion: who in your family had cancer? is there a history of diabetes in your family? how did you get all those blood clots? He didn't just glance over the form, he went through it one "yes" at a time. And he took notes and took time to discuss my conditions with me.

 

"So what can we do for you," he asked in a wonderful Hispanic accent.

 

"I want to be able to communicate with someone on a weekly or bi-weekly basis so that my basals and bolus ratios can be examined...," I said.

 

"We have the people for you," he assured me.

 

Dr. A spent an hour with me. He never left the room. He connected with me the way Dr. C did -- like a person, not a patient. I go back in a week to talk with the pump educator and a nurse practioner, who Dr. A says are better at working with patients on the day-to-day issues of diabetes. And I'm totally fine with that.

 

This doesn't begin to adequately describe my appointment with Dr. A. I left there feeling empowered, not left behind. I left feeling like this doctor cared about me and understood me.

 

This, my friends, is a feeling we should all seek from our medical team. And if I hadn't found it here, believe me I would have kept searching, kept fighting for the care I know I deserve.



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Yahoo!


Inspirational! And good news - all d-people deserve that treatment!!!


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Michelle Kowalski
Michelle Kowalski, a writer, editor and photography hobbiest living in Phoenix, was diagnosed with Type 2 diabetes in February 2005. In January 2008, as part of her quest to start on an insulin pump, Michelle learned that she actually has type 1 diabetes. (Read More)

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Kim Doty
Kim is a computer systems administrator for a major food manufacturer and lives in Colorado with her husband, Steve, and their children. She currently battles the bulge and tries to develop an exercise habit to better manage her blood sugars. (Read More)

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