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We found 10 result(s) that match your search "letter writing":

It's that time of year again...fundraising! So I've written my letter. And here it is, for the world to see!

Dear______,

 

 On March 3rd, 1993, I was diagnosed with type 1 diabetes. I was 4 years old. It’s been over sixteen years since that day. I’ve struggled, grown, and I’ve gained and lost precious moments from this disease.

 

 In October of 2007, my dad was diagnosed with type 1 diabetes as well. To this day, hearing that he had this dreadful disease like me has been one of the worst days of my life. Now, it isn’t just about my own diabetes, my risk of complications, or my lows and highs with this disease. It’s about my dad’s A1c, the genetic risks of diabetes, and the worry that comes with having a diabetic loved one.

 

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What do you say to the person/people you haven't spoken to in four years? It wasn't a break up, it was just...  distance and history.

 

You all know that I can talk/write up a storm. Especially about my life. But there's this letter I need to write that I can't figure out how to start. And I'm sure I've told you before that I'm the kind of writer who likes to start from the beginning. I've never been able to write the middle of a story first; I have to get the first paragraph down before anything else will fit.

 

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In my last post, I mentioned that I would be wearing some Continuous Glucose Monitoring Systems (CGMS) and deciding if any were right for me. 

 

I tried both the DexCom and the Navigator.  My decision was this: there is simply no way a separate device is going to work for me.  This was proven by the HOURS worth of dead zones - where I'd accidentally left the device behind.  Further evidence, the fact that I regularly leave my cellphone behind when I leave my house in the morning - and that since childhood I've been known as someone who "would lose their head if it weren't tied on."  Really, I think I'd lose my pump if that weren't tied on!  

 

So, I am starting the process of trying to get a Minimed Real-Time System.  I've got new insurance with my new job- so the pump part shouldn't be too great a struggle.  But the CGM to go along with it is a different story. 

 

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I usually have my JDRF Walk to Cure Diabetes fundraising letter done and distributed by mid-July. This year has been different. I've been in a fundraising funk. I'm just tired of writing the same statistics year after year. The lower life expectancy; the long-term complications; adding up the number of finger pricks since November of 2003. I finally did sit down and write our letter - deciding to simply write what I was feeling at that moment.

 

Dear Friends and Family,

 

"A cure for diabetes is just around the corner."

 

"Scientists are closer than ever to finding a cure."

 

"A cure for diabetes is now within reach."

 

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Today, I'll write about freedom. The letter f.
I really don't feel like writing about diabetes today. I don't feel like thinking about it. I don't feel like testing or bolusing. I will, of course, test and bolus, because as much as I'd like a break, I value my health and the feeling of well-being and well, being alive that infused insulin brings me...
But today, I'm going to share another piece of writing. To remind myself that it isn't all about diabetes. My life, that is. My existence. My writing. None of these things are all about diabetes. And I hope that by sharing something else here, someone else will realize the same. That your life is not all about diabetes, despite the fact that it seems to take up so much room. (READ MORE)

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Driving over the highway on a route I usually don't take I was thinking about the letter I had just drafted to the bank that holds our mortgage in Missouri. I was pleading with the bank president because we see no hope for selling that house and even if we do we won't recoup the money we've put into it in the last 15 months.

 

I had butterflies. I felt strange. I felt light and heavy. It was a weird feeling considering how confident I felt as I was writing the letter. That's when it dawned on me that I actually felt low. It wasn't about the letter after all.

 

I try not to test while I'm driving -- especially on the highway -- but as soon as I realized what was happening I knew I needed to test right that second.

 

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In April 2008, I went to my urgent care doctor for several reasons. The first was a strange side pain that I'd been having for two days. The second was that my blood sugars were just not budging from the 200s and 300s. Then there was an intense shoulder pain.

 

The side pain started out tolerable on my lower right side. It was just a burning twinge that I noticed throughout my day. It got a little worse and the blood sugars seemed to follow over the next day. By the morning of my doctor's visit, I was wanting to curl in pain and forget the world.

 

It turned out that I had a ruptured ovarian cyst. It was bleeding into my ovary which was causing the intense pain. It was most likely brought on by an aggressive workout that I did a few days prior (the rupturing, not the cyst). It eventually helped me obtain my diagnosis with PCOS (that and the acne, irregular periods, hair growth, hair loss, and other lovely symptoms).

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When you see the check-mark-y swoosh, you think Nike, right? An apple gets you the computer company, golden arches make you think of cheesburgers, a peacock will have you thinking Must See TV, a red cross... you get the picture.

 

And when it comes to health there are several very recognizable symbols of support, perhaps the most popular is the pink ribbon for breast cancer. I was doing some research today on breast cancer and realized that the pink ribbon is quite possibly the only symbol synonymous with only one health condition. Even the red ribbon went from AIDS to a host of other causes.

 

You see a pink ribbon you instantly think breast cancer; you see a red, green or yellow ribbon and you have to do some thinking or asking. While many diabetes organizations and associations have their own symbols, there is not one that is universal for diabetes.

 

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I debated where to wear Toohey today: in my pocket (out of sight) or on my belt as I always do. Prior to this morning, I had been to my new office three times: twice for interviews and once to sign my offer letter.* All three times Toohey was tucked neatly in my pocket, no tubing was visible, I was a normal-looking person.

 

So I debated for several days and ultimately decided not to hide, to wear Toohey on my belt as always, to be myself. I decided though to not come out and say "Hey, I have diabetes" on my first day. I just wanted it to flow, to just happen naturally. I really thought I would have had some questions since Toohey was so visible.

 

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Both of my doctors, my endocrinologist and the doctor in charge of my bio-identical treatment, have sent disability status letters for me. It actually took very little effort, despite the initial feedback from the nurses in the beginning. I'm happy to get these out of the way and go forward with the process. I'll also be writing my own letter to support my case with a personal note.

 

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