World Diabetes Day-WDD

Today is my 100th blog post. Considering the number 100 is lauded as one of the most prized numbers in the diabetes community (think winning the diabetes jackpot, when that one-zero-zero pops up on your glucose meter), I find it ironic that this 100th post ended up being on, World Diabetes Day.

In support of this day, and in celebration of my 100th post, Seth and I both are wearing the official World Diabetes Day color, blue:

Dinner with Ryan Reed

Several weeks ago, Seth and I were fortunate enough to have dinner with up-and-coming Nascar driver Ryan Reed and his family while they were in San Diego for an event. We met them at Roy’s on the Bay Downtown, and ended up having a wonderful evening filled with fabulous conversation. It was like we’d known their family forever. Truly down to earth people, on an important mission.

Seth, Myself and Ryan

Savanna (Girlfriend), Myself, Ryan, Jodi (Manager), Karla (Mom) and Mark (Dad)

Ryan, 19, was diagnosed with type 1 diabetes when he was 17 years old and thought his racing career had ended until he met Dr. Anne Peters. He quickly learned when armed with proper healthcare, education, and technological tools, his dream of racing could become a reality.

In addition to founding his own organization Ryan’s Mission, http://ryanreedracing.com/mission/ he is involved in the diabetes community in varying ways, building relationships and collaborating to improve the lives of those living with diabetes and raise awareness:

  • JDRF, Celebrity Advocate (if you’ve seen him race, JDRF is all over his car!)
  • ADA
  • The Iaccoca Foundation (involved with researcher Denise Faustman)
  • University of FL Diabetes Center of Excellence
  • Diabetes Hands Foundation
  • TuDiabetes
  • TalkType1
  • Athletes with Betes
  • IDF
  • Marjorie’s Fund
  • No More DIabetes Foundation
  • Type 1 Rider (Tony Cervati)

You can find Ryan on Twitter @driverryanreed and on Facebook: https://www.facebook.com/home.php?ref=tn_tnmn#!/driverRyanReed

Working at Dexcom, and experiencing firsthand how the device has changed my life with diabetes, it was inspiring to meet Ryan and learn how his use of the Dexcom System has helped his career progress. Seth and I are anxiously waiting to hear what’s next for Ryan!

Myself and Ryan, Go Dexcom!

We can’t wait until they’re in town again 🙂

Diagnosis of Type 1 Diabetes

I’ve been cleaning and organizing recently, and I’ve come across all of my paperwork and lab work from when I was diagnosed with type 1 diabetes (it makes me laugh at how comical the healthcare was, although at the time, I did not think it was funny). I’ve also been reflecting back on what I went through at that time, and how I got to where I am today. Some have read this, but for those that have not, here is my story.

December 23, 2006

After moving to Puerto Rico with the Navy in September 2006, December came, and it was time for my favorite yearly doctor appointment (joy). The gynecologist insisted that I have complete blood work just to make sure everything was okay (how did he know?). I went to Clinica Las Americas Guaynabo for my appointment. One week later I received a phone call from the lab that my results came back abnormal and I should try to get to my PCM as soon as possible. They refused to send the results to my doctor (down the hall); I had to physically pick them up and hand deliver them to her, when I could get in.

I went the same day to pick up my results, and sat in the car looking at them. Right away, I noticed the low and high markers that were out of clinical range. The glucose was 399, with a clinical range of 70-110, and the glucose in my urine registered 4+. I went home, called my best friend Michelle, a nurse, and told her. She hesitated and said “Linds, you need to go to the doctor right away, that’s really high, and might mean that you have diabetes.” I was able to get an appointment on December 22nd to see my PCM, who said “you might have type 1 diabetes, I’m going to send you over to the lab to redo the blood work and we’ll see what it says,” she put a rush on it. The result was 256, not quite 399 (go pancreas go!), but still too high, so she said, “you have to go to the hospital and get insulin, we can’t help you here,” I thought, “insulin? Puerto Rican hospital?” Uh oh.

I was referred to AshfordPresbyterianCommunityHospital in San Juan. I went home from the clinic and called Seth, and said, “We’re supposed to go to the hospital, because the clinic can’t handle my case, and this is the only hospital that will accept our insurance.” At this point, the importance of this trip was greatly misunderstood, and Seth happened to be getting off work early that day so his command could have their holiday celebration. I decided to go with, have lunch, and then we were going to go to the hospital (which I laugh about now). After the celebration, we left for the hospital with printed directions in hand, and whoa, with traffic, it took us quite a while to get there. When I saw the hospital, and after we finally found parking in this cramped and congested touristy area, I grew uncomfortable. We went to the ER, filled out insurance paperwork, gave them my PCM referral, and they brought me right back. Upon initial check in, they tested my blood glucose and it was 389, he said, “we’re going to have to admit you, and get your blood glucose down into a safe range.”

There were no open beds in the ER, so they put me in the very back corner on a gurney, next to another patient’s day old food tray. It was dark and scary. I got up to go to the bathroom, and the bathroom floor was covered in urine, the soap dispenser was broken, there were no towels. I came out of the bathroom and there sat 10 or so staff members sitting at the desk with their feet up chatting.

I was immediately hooked up to saline, and they came to inject insulin into my arm…right into my muscle (no subcutaneous injections here!). Every hour they would come and draw blood from my bony small wrists (no IV, just repeated digging around in veins in my wrist), and check my blood sugar. It was starting to drop. Two technicians came by to perform an EKG to check my heart, but they couldn’t figure out how to work the machine. They kept laughing and saying “you have to be smarter than the EKG machine.” At one point, the ER doctor came by and I asked “do I have type 1 diabetes?” she nodded and said yes, and then walked away. At this point, neither Seth nor I really understood what was going on, nobody explained anything to us, and were both so overwhelmed that we sat and cried together. I told Seth I was scared, he told me that he would take care of me and protect me (which he has done 1,000,000%).

When my glucose was in a safer range, the doctor gave me a prescription for insulin, and referral to an internist whom I could call on Monday (this was Friday) and make an appointment with. I asked where the pharmacy was, she said the hospital pharmacy was closed but there was a Walgreen’s up the street. After eight hours in the ER, I signed the discharge papers, and off we went at 12:00 am.

Trying to find Walgreen’s in the middle of a very popular tourist area, on a Friday night was interesting and apparently this is peak time for filling prescriptions. It took a while, so we walked around, waited, and I called my mom to update her, and then they finally called our name. After that entire wait the pharmacist couldn’t get our insurance to go through, so the bill was a couple hundred dollars. Again, completely misunderstanding the severity of this situation, we said, forget it, we’ll go to our primary care clinic in the morning which has a pharmacy and get it there. We did purchase a glucose meter to test blood sugar (this was never explained to us), although neither of us knew what any of the numbers meant or when we should actually use it. On the way home from this overwhelming day, we got stuck in rush hour traffic at 1:00 am in the morning, which gave me a good opportunity to call my best friend Michelle again. I told her everything, and asked her “how do I give myself an injection?” She was totally flabbergasted that nobody took the time to show me how to give myself a subcutaneous injection. She was crying, telling me that she wished she was there with me, and to call anytime day or night.

Once we got home, we tried to decompress by playing with our new golden retriever puppy Lucy, who’d been alone that day, more than she’d ever been in her short life. The next morning, we woke bright and early and went to the primary care clinic with prescription in hand. The pharmacist filled the prescription, and we talked with her briefly about how we received no information or instruction on type 1 diabetes at the hospital, so she told us to hang on while she quickly ran next door to the clinic and got me in to see another PCM who could help me. Her name was Dr. Roselyn Martinez-Olivieri, and I will never forget her. She gave Seth and I the most important (you know, life saving) information, when to test blood sugar, how to inject insulin, and started me on an insulin regimen. This was December 23rd, and the clinic closed early that day, at 3:00 p.m. for the Christmas holiday, so she gave me her cell phone number (mind you it was a “moviestar” cell phone which rarely worked where she lived in the jungle in PR), and for the next three days, I called her regularly with updates, numbers, etc, and she told me how to proceed. Seth and I had finally received some decent information, and had, so we headed home, to try and enjoy our first Christmas in Puerto Rico, with a new disease (Merry effing Christmas!).

Several hours later, we went to get some insulin to inject (thanks to Seth for giving me my first injections, I couldn’t do it myself), and much to our surprise (although no surprise now), the pharmacist had given us insulin two years past the expiration date. Again, Seth and I set out to find some insulin for the third time, and eventually found an ER (the 3rd hospital we went to) doctor that wrote me a new script and we proceeded to the hospital pharmacy. They wouldn’t fill it because I’d already had one vial filled that same day (and so begins the insurance shenanigans that accompany T1D)…so we fought with insurance to explain the necessity, and it wasn’t our fault the second pharmacy gave me two year expired insulin and is closed for the holidays. Finally, insurance gave in and filled the prescription.

We headed home with fresh insulin to start our new life together. A life that in most ways, replaced the life I had been living for 25 years up until that point, and a life that Seth and I had been living together for four years. Looking back now, you could say that this really was the worst Pap smear ever; I went in for one test, and I came out with T1D!

Vaccinations…and Brittle Diabetes?

Seth and I are headed to Africa in December; last Friday I had my appointment at the travel clinic to go over our itinerary, get vaccinations, and medications.

Going through the questions with the nurse, went something like this:

Nurse: I see you’re taking insulin? Me: Yes. Nurse: Are you wearing a pump? Me: Yes. Nurse: How do you like it? Me: (what?) I like it, it provides a lot more freedom for me. Nurse: Yeah, that’s what my mom says, she really likes hers. Me: Oh, does your mom have type 1 diabetes? Nurse: No, she has type 2, but she’s insulin dependent, and (wait for it), really brittle. Me: Oh. Nurse: But the pump is really cool, it does everything for her. I’ve seen it when she tests her blood sugar, and it tells the pump everything to do, she doesn’t even have to do anything or look at it. Do you have that kind? Me: (does that exist?) No.

Everybody knows somebody with diabetes, but everybody’s diabetes is different. Mine, is not your mom’s. I can’t help but think, if I’d had another chronic condition, that the nurse would’ve been so open and inquisitive into my condition. If I were in remission from cancer, would he have asked me personal questions about my cancer, and tell me about his mom’s?

Probably not.

Why is diabetes different?

Diabetes Art Day 2012

Today, September 24, 2012 is Diabetes Art Day: http://www.diabetesartday.com/.

I absolutely love this idea, and this is my first time participating. I’m just getting into Diabetes Social Media, so it snuck up on me this year, therefore, I wasn’t feeling too inspirational on short notice. Then I woke up yesterday morning, and was greeted with a 445 on my blood glucose meter, and my first thought was the emotion that this invoked, which to me, can be a form of art, if for nobody else but myself.

So, in all its simplicity, here is my contribution this year. I’m looking forward to getting more involved next year!

 

Title: Speaking the Truth