Tag Archives: diabetes

It’s a busy month.

It is indeed a busy week inside of a busy month. So here’s a quick primer on some upcoming events:

– The American Diabetes Association is still collecting photos for their A Day in the Life of Diabetes project. They’re asking for people to take photos of their life with diabetes and upload them to the ADA Facebook page. CVS Pharmacy will donate $1 for every photo uploaded, up to $25,000 dollars. In addition to that, the Association is going to take some of the photos and project them onto the walls of Washington D.C’s iconic Union Station this Tuesday and Wednesday, which is World Diabetes Day. I’ve got Wednesday off of work… maybe I can get down there to get a look in person.

– Speaking of money for worthy causes, Diabetes Hands Foundation reminds you that you’ve still got a couple of days to participate in the Big Blue Test. Five dollars for every test logged will be contributed by Roche Diabetes Care to organizations that provide life-saving supplies and services to PWDs in need. If 20,000 take the test before World Diabetes Day, $100,000 life-saving dollars will be donated. As I publish this post, over 15,000 have participated. Only 5,000 more Big Blue Tests need to be logged before Wednesday! So get out there and work it out people! For more info, and to log your test, go to bigbluetest.org

– Locally, the Maryland JDRF chapter is hosting their Night of Hope Gala Saturday night in downtown Baltimore. They’re hoping you can attend. But if not, they’re also looking for volunteers to help with everything from checking coats to busing tables. For more information on the gala, go to jdrfmd.org/

– Finally… of course, there are many things happening this Wednesday on World Diabetes Day. All over the world, people will be dressed in blue and forming human Blue Circles and lighting monuments in blue. Many other happenings will be happening, and to find out more about all of it, go to http://www.idf.org/worlddiabetesday

Have a super (busy) week!
 
 
 

D-Blog Day. An open letter to the media.

It’s November 9th, and that means it’s D-Blog day. Today, the entire Diabetes Online Community is encouraged to write a post of similar topic on their personal blogs. And today, we’re encouraged to share them with media outlets far and wide. Want to include yours? Write your post and link it here: http://diabetestalkfest.com/blog/?p=507

Our topic today:

Choose a form of Media Outlet to write an open letter to, such as NY Times, CNN, Local/National Newspapers, TV and why it is so important for them to let the world know that diabetes is more than just being overweight and having too much sugar. It is about reporting stories about Type 1 and Type 2 diabetes. Let them know what kind of things you would like them to write about. If there are specific articles or reports they got wrong, let them know about it! Let’s get it right!

My letter is going to all of the local TV stations here in my city, and it goes like this:

Dear News Director,

We’re in the middle of a very important month for me, and others like me. November is Diabetes Awareness Month. Next Wednesday, November 14 is World Diabetes Day.

I’ve been living with Type 1 diabetes for nearly 22 years, from the time I was 28 years old. I’d like to take the opportunity during this important month to talk about how your organization covers diabetes over the course of the entire year. Over the years, I’ve seen stories about diabetes reported many times, and some of those times, I’ve become concerned about how diabetes is covered, or how issues related to diabetes are covered. I’m very concerned about how this affects the way people with and without diabetes view each other. So if I may, let me dispel a few diabetes myths.

Diabetes is all the same. Actually, there are many types of diabetes. The most common is Type 2, where the body has trouble using the insulin it produces. About 90% of new diagnoses are Type 2. There’s Type 1, which is an autoimmune disease characterized by the destruction of insulin-producing cells in the pancreas. But there’s also Type 1.5, or Latent Autoimmune Diabetes in Adults (or LADA), which researchers are still discovering more about, and Gestational Diabetes, where women have high blood glucose levels only during their pregnancy. It’s discovered in about 4 percent of all pregnant women.

It’s important to note the differences in diabetes, because while we all have the same serious, chronic condition, the way we approach and treat the different forms of diabetes can vary widely.

Diabetes is preventable. Let me say it clearly: People don’t get diabetes from too much sugar, or by being overweight. I developed Type 1 diabetes because my body’s immune system attacked my pancreas and killed the insulin-producing cells there. I was in great shape, at an optimal weight, active all the time, and otherwise, very healthy. In addition, many Type 2s are diagnosed without being overweight and while maintaining healthy diets.

Diabetes can be cured. Actually, it can’t. We can help mitigate the effects of diabetes through diet, exercise, and overall blood glucose management, but we can’t cure diabetes through drugs, or meditation, or blueberry yogurt, or anything. Anyone who says different is woefully under-informed.

People with diabetes cannot eat sugar. In fact, we can eat sugar. We just have to have the appropriate amount of insulin to account for it (your body already does this all by itself). We can also hold down a job, compete in athletics, bear and raise children, and do all of the other things that non-diabetics can do.

Those are just a few misconceptions I’m hoping you can help put to rest.

So, how can you help? What can you do to report on diabetes in an accurate, compassionate way? I would invite you to add media@diabetesadvocates.org to your e-mail contact list. Diabetes Advocates is a non-profit group of knowledgeable patients dedicated to advocating for, among other things, accuracy in reporting on diabetes. By using the e-mail address above, reporters can fact-check and get questions answered by people… actual patients… in the know. In case you’re wondering, I have no affiliation with this group. But I believe in what they do.

Through your efforts, your organization can help communicate a true, accurate portrayal of diabetes and People With Diabetes, and our many unique qualities. You can help dispel myths for those not living with this disease; reduce fear among those newly diagnosed or those at risk of developing this disease; and promote a positive message for everyone affected by diabetes. And that’s everyone.
 
 
 

Your Diagnosis.

Before today’s post, I want to let you know that I’ll be listening in on a health activist roundtable presented by WEGO Health on Friday, November 9th at Noon EST. I don’t know who will be on the panel, but I’m guessing there will be at least a couple of your favorite rock-star bloggers. Look for tweets by @WEGOHealth. You can follow along with the discussion on Twitter by going to http://tweetchat.com/room/hachat

Now on to the show!

In the past week or so, I’ve been reading a lot (at least to me it seems like a lot) of posts from PWDs telling their stories about being diagnosed. I must confess: I can’t stop reading them.

Like the proverbial race fan who only goes to the track to see the cars crash, I have to read them all. I’m hanging on every word, and I can’t turn away until I’ve read every last detail about someone’s bad experience with a doctor, or someone’s parents dealing with the diagnosis of their child.

Why? Why am I so intrigued by one of the saddest days in someone life?

I think (read: I hope) some of it has to do with the two things that People With Diabetes are blessed with: empathy and resilience. Let’s look at them one at a time:

Empathy. Once you’ve been cursed by the big D, you never look at another’s struggles the same way. Simply put, we don’t want another man, woman, or child to go through what we’ve gone through. And when we do see another diagnosis, we feel the same sadness, the same anger all over again. We want to do something about it. Every day I’m amazed at how much is being done to raise money, increase awareness, and provide grass roots support for all of us.

Resilience. When you consider where a lot of these stories begin, it’s uplifting to see how far all of us have come. Diabetes is difficult, it’s frustrating, it’s a full-time-never-ending-no-good-backstabbing-kick-you-when-you’re-down thing that never lets up. Yet we live real lives, with plenty of successes to go with the failure of our pancreases. Every day, PWDs are proving that we can do everything anyone else can do except produce insulin. Yeah… that is uplifting.

So if I take a particular interest in your diagnosis story, please don’t think I’m wacky. I want to support you. I want to be enlightened. I want to be uplifted and empowered.

Thank you for telling your story.
 
 
 

Wordless Wednesday. One week until World Diabetes Day.

I don’t do a lot of Wordless Wednesday posts, but I thought this might be nice since World Diabetes Day is one week from today.

I went to YouTube and entered Blue Circle into the search box. I found this video from about three years ago. It’s uplifting, but it also makes me a bit sad, since there are still so many who do not know about the blue circle. Take a look:

Enjoy your Wednesday!
 
 
 

Election Day. Your voice matters!

Happy Election Day in the USA. Today, America votes for a President, the entire House of Representatives, and one third of the Senate. In all 50 states, there are additional ballot initiatives on everything from gambling to schools to same-sex marriage to taxes.

If you haven’t informed yourself about the choices in your voting booth today, I hope you’ll do so. Then, if you’re of legal age and registered, go and vote!

I don’t usually make a big deal out of this kind of thing, but I will just this once. Listen… men and women have died to provide us with and protect our ability as a nation to determine our own destiny. Around the world, people still sacrifice their lives fighting for the same right we’ve had for over 200 years (though for women, it’s only been 92 years, I think).

We may not always like the outcomes on Election Day. But at least we get the opportunity to make our own choices. And the opportunity to make more choices in the future. Our right to vote is a precious commodity. Please don’t squander it by staying home.

I’m Stephen, and I’m proud to approve this message.