Fight Diabetes, Not Each Other

The one thing that I have always appreciated about the DOC as a whole is the diverse assembly of types, individuals, blogs, communities, etc… that exist within it.

People need to see all aspects of life with this disease.  Some people prefer to focus on the positives.  Others focus on the negatives.  And others fall in between.  Personally, as a blogger, I write about the good and the bad, because life with this disease is a mixed bag.

Whether you prefer to keep it real or you prefer to ride a unicorn and toss glitter everywhere, there is a place for you in the DOC.

When you’re blogging, advocating, etc… just be yourself and do so from the heart.  Remember why you started doing so in the first place.  Remember that your experience with diabetes will be different than someone else.

But most importantly, remember this:  Diabetes is the enemy; not your fellow DOC members!

Posted in Diabetes, Lessons Learned, Rants | 9 Comments

30 Things About My Invisible Illnesses

This past week has been Invisible Illness Week.  As someone who has been living with Type 2 Diabetes and Congestive Heart Failure for nearly 3 years, I’d say I know a thing or two about living with such illnesses.  And since stealing ideas from Kerri seems to be the trendy thing to do these days, I’ve decided to take a shot at the 30 Things About My Invisible Illness Meme.  Since I live with two invisible illnesses, though, I’ll be making slight tweaks to accommodate them.  So, go grab a diet coke, sit back, and enjoy.

1. The illnesses I live with are:  Type 2 Diabetes & Congestive Heart Failure

2. I was diagnosed with them in the year:   2008

3. But I had symptoms since:   Longer than I really care to admit.  Looking back, I probably had the symptoms of type 2 diabetes for at least a few years before I developed the yeast infection that led me to the doctor.  I’d been experiencing some chest pain, shortness of breath, fatigue, etc… related to the congestive heart failure for a while too.  As with so many people, I didn’t have insurance and couldn’t afford a doctor visit.

4. The biggest adjustment I’ve had to make is: Has been in my attitude and outlook on life.  And I’m thankful that it has changed for the better.

5. Most people assume: That because I’m a big guy I must have given myself Type 2 Diabetes and Congestive Heart Failure.  And you know the saying about the word “assume”.

6. The hardest part about mornings are:  Is that my mornings are really afternoons.  I work nights. And working nights with diabetes and congestive heart failure is a bitch.  You might even say it’s not for the faint of heart. (Pun) haha.

7. My favorite medical TV show is: I don’t really have one.

8. A gadget I couldn’t live without is: My meter.  My cell phone is a close second. I use it to keep track of all of my doctor appointments, med refills, etc…

9. The hardest part about nights are: Well, I work nights as a professional code monkey for a newspaper. So, I’ve got thoughts about diabetes, heart failure, etc… racing around while I’m working through complex algorithms needed to make things work properly and what I end up with is a clusterf **k topped off with a migraine headache.   By the way, chronic migraines is another invisible illness I deal with.

10. Every day I take 10 different oral medications, some multiple times a day, take two injections of Byetta, use an asthma inhaler, and a nasal spray. And this is my blog, and I’ll comment if  want to. 😛

11. Regarding alternative treatments I:  If by alternative treatments you mean cinnamon, miracle diets, and snake oils, I’m not a subscriber to the philosophy.

12. If I had to choose between an invisible illness or visible I would choose: I’ll stick with my invisible illnesses.  They are easier to conceal on days when I really don’t feel like talking about them.

13. Regarding working and career:  Honestly, I work for the insurance, and for the money to pay the co-pays forced on me by the insurance company.  And I’ve been doing this work thing in the same place for 5 years now. I guess you can call that a start to a career.

14. People would be surprised to know:  That prior to my diagnoses, I really didn’t give a shit about Twitter. Had no use for it, and thought it was just another trendy thing that would fizzle.

15. The hardest thing to accept about my new reality has been:  The overwhelming financial burden that has come with it.

16. Something I never thought I could do with my illness that I did was:  when I was diagnosed with Congestive Heart Failure, I gave up all hope of ever being able to fly on an airplane.  Everything I read and heard indicated that I shouldn’t it.  I’m so thankful that I’ve had that opportunity, and that my first flights were taken to meet my DOC friends.

17. The commercials about my illness: Annoy the hell out of me.

18. Something I really miss doing since I was diagnosed is:  If anything, I miss not constantly thinking about my health.  It gets old.

19. It was really hard to have to give up:  You know, I don’t believe that I’ve given up much at all.  Unless you count giving up my sanity, and I didn’t have much of that to lose to begin with.

20. A new hobby I have taken up since my diagnosis is:  Traveling to meet strangers I meet on the internet.

21. If I could have one day of feeling normal again I would:  Normal scares me.  Besides, I can’t change what’s happened in the past. I can only make the best of the days I have yet to live.

22. My illness has taught me:  That it is OK to stop and think about what is best for ME.  And that life is precious.

23. Want to know a secret? One thing people say that gets under my skin is:  “You don’t look sick.”

24. But I love it when people: Actually take an interest in how I’m doing, and show that they genuinely care.

25. My favorite motto, scripture, quote that gets me through tough times is: “Stick to the fight when you’re hardest hit.  It’s when things seem worst that you must not quit!”

26. When someone is diagnosed I’d like to tell them:  That there is great life after diagnosis.

27. Something that has surprised me about living with an illness is: that so many good things have come to my life because of something bad.

28. The nicest thing someone did for me when I wasn’t feeling well was: Give me a hug and tell me that she loves me. 🙂

29. I’m involved with Invisible Illness Week because: People need to know that we are living with these Invisible Illnesses.  Because we need to raise awareness. And if it’s going to be, then it’s up to me!

30. The fact that you read this list makes me feel:  That you care.  Thank YOU!

Posted in Diabetes, Heart, Inspiration, Invisible Illness Week, Shout outs | 2 Comments

Photos: Annual visit to the Zoo.

April and I made our annual visit to the Fort Wayne Children’s Zoo yesterday afternoon and, naturally, I shot a boatload of pictures.  So, I went through them, edited the ones I liked, and threw them together in a set on flickr to share with my readers.  Enjoy!

http://www.flickr.com/apps/slideshow/show.swf?v=107931

If you like the photos, let me know.  Feedback is always appreciated.

Posted in Life, Photos | 1 Comment

Help me reach my Step Out goal

Help us Stop Diabetes!

On October 2, I will be taking part in the American Diabetes Association’s Step Out: Walk to Stop Diabetes event in Indianapolis.  This will be the very first time I’ve been able to participate in a diabetes walk since being diagnosed with Type 2 diabetes and Congestive Heart failure in late December 2008. I am extremely excited and proud to be doing so.

I’m hoping to meet and exceed the $100 fund raising goal that I’ve set and that’s where you come in.

By making a donation on my behalf, you will be helping the ADA provide community-based education programs, protect the rights of people with diabetes and fund critical research for a cure.

No matter how small or large, your generous donation will help us Stop Diabetes.

Thank you so much for your consideration.  Together, we can make a difference!

All the best!

Mike Durbin, PWD Type 2

Posted in Announcements, Diabetes, Diabetes Walks | Leave a comment

Ten Years Later – I Remember

Today marks the 10th anniversary of the terrorist attacks that rocked our nation on September 11, 2001.  More than 3,000 people died on that morning in the wake of two air craft crashing into the twin towers of the World Trade Center in New York, another into the Pentagon in Washington D.C., and in the crashing of Flight 93 in Pennsylvania.  And like so many, I remember exactly where I was and what I was doing when I heard the news.

I was sitting in my senior English class that Tuesday morning, when someone entered the room and announced that a plane had crashed into one of the towers of the World Trade Center.  I remember the teacher turning on the television and everyone watching in horror as the second plane hitting the other tower.  I remember lots of crying, screaming, and not being able to think about anything more than the events unfolding.  I personally didn’t lose anyone to those horrific events, but many of my friends at school did. I remember trying to offer what comfort and support I could to them.

I remember feeling the same anger, sadness, helplessness, and disbelief that so many others around felt then and still feel today.

I remember sitting in the living room at my grandmother’s house that evening with the rest of my family.  All of our eyes glued to the television news as the events of the morning  played over and over.  As more and more details were made available.  The images. My God the images were horrific.  I remember everyone, my uncle especially, making comments that war was at hand.

I remember it all as if it were yesterday.  But it wasn’t.  It was 10 years ago.  But the painful memory is ever present.

Today, on this 10th anniversary of the attacks of September 11th, I mourn for those who lost their lives on that tragic morning.  I mourn for the families of those who died.  I mourn for the thousands of additional lives that have been lost the ten years since, as we sought to bring justice to those responsible for the attacks.

I mourn for those whose birthdays, anniversaries, and other special events which too fell on September 11th, have been forever tarnished by the events of that morning.

April’s parents were married on 9/11, about 30 years ago.  And given her mother’s battle with cancer, today I have mourned for them. Because this 9/11 may very well be the last that they have.  On this day when we should be celebrating them, we are mourning. Yet another link to a tragic day, which we will never forget.

Today, I mourn.  I pray for peace and comfort to all who lost someone dear on that day.  I pray we never forget.

Ten years later, I remember!

Posted in Lessons Learned, Life | 3 Comments

If I Can Help Somebody

“If I can help somebody, as I pass along, If I can cheer somebody, with a word or song … Then my living shall not be in vain.”

Those simple words of that great old song have weighed heavily on my mind over the last week, as I’ve read the comments of so many trying to thank me and commend me for my efforts to help Dustin and his family after their devastating loss.

Dustin has said “I can’t thank you enough for all of this. I don’t have the words to describe how great all of you are.”

“Thank you doesn’t seem like enough for all you’ve done to support my guy and his family, but it’s all I can say. Thank you for being the best adopted brother a girl could ask for.” says Ashley.

And I’ve heard things like “you’re my hero” and “you’re such an amazing part of the DOC” and ‘you have a heart of gold”.

While I so appreciate the sentiment behind all of those kind words, and they’ve brought tears to my eyes, they really aren’t necessary.  I don’t do the things I do for praise, fame or fortune.  My reward comes from knowing that I’ve made the effort to help someone else. From knowing that I’ve paid forward the second chance at life with which I’ve been blessed. From knowing that I haven’t wasted it by only thinking about myself.

If you wish to thank me, simply pay it forward. Then neither of our lives will have been in vain.

 

Posted in Inspiration, Lessons Learned, Life | Leave a comment

A DOC Logo – Diabetes Art Day

So today is the second annual Diabetes Art Day, and I’m so excited to be contributing again this year.  I decided to stick with the community theme that I started with the last year’s Diabetes Family Tree, and having been inspired by a question during DSMA last night, I present you with what I believe a Diabetes Online Community Logo should look like.

In addition to this being my submission for Diabetes Art Day, I have set up a section on my CafePress shop with merchandise bearing the logo.  And all of the proceeds from selling the merchandise will be donated to help Dustin Iris and his family.  So, not only will you be able to wear your DOC pride on your sleeve, you’ll be helping a community member in need.

Feel free to leave some comment love and tell me what you think of the logo.

Happy Diabetes Art Day!

Posted in Announcements, Diabetes Art, Shout outs | 9 Comments

Help The Iris Family

Dustin's street under several feet of flood water. His home was rendered uninhabitable, and has been condemned as a result.

As you might have heard, our friend Dustin Iris (@deejaybetes) and his parents have lost their home as a result of Hurricane Irene.  And they need our help!

Dustin’s friend has started the effort to help them by setting up the “Help The Iris Family” relief fund.  If you are in any position to help Dustin and his family, please consider doing so.

Pulling together to help friends in need is a hallmark of the Diabetes Online Community, and I sincerely hope that we can all work together to provide Dustin & his family with the love and support that is needed to get through this very difficult time.

Help The Iris Family

Thank You!

Posted in Announcements, Shout outs | 3 Comments

Stepping Out to Walk to Cure Diabetes

Over the last couple of years, I’ve given considerable thought to participating in the various diabetes walks hosted by the American Diabetes Association and the JDRF, but because of the weakened state of my heart,  I just didn’t have strength or energy to do so.   Wanting to be involved in some way, though, I decided that if I couldn’t walk myself, I could at least make contributions to the fund raising efforts of fellow Diabetes Online Community members.  And I’ve done so proudly.

While I’ve found great reward in being able to support everyone else, though, it just isn’t the same as participating in the walk and fund raising efforts myself.  And that’s what I’ve really wanted. To be out there among my fellow PWD’s walking to support the cause.  And now, I’m at a stage in my journey where I feel that I’m able to do that.  And with that in mind…

I have registered to participate in not one, but two, diabetes walks during the month of October.  I will be traveling to Indianapolis on October 2nd to join my friend Cherise and her Team DSMA in participating in a Step Out walk  hosted by the ADA.  And I’ll follow that up by traveling to Louisville, KY on to join my friend Meredith and her team in participating in the Walk to Cure Diabetes hosted by the JDRF.  Now, who says I don’t support all PWDs. 🙂

I am super excited about participating in these walks, not only because I’ll be supporting a cause near to my heart along with my friends, but also because of what that participation symbolizes for me personally.  It’s a big indication of just how far I’ve progressed since my diagnosis.  It’s an amazing feeling.

I’ll be posting more about preparations for each of those walks, as well as information about how you can get involved, in the coming days.  Until then…

Keep Living!

Posted in D-Meetups, Diabetes, Diabetes Walks, Inspiration, Life, Shout outs | 2 Comments

September 1st is Diabetes Art Day

The 2nd annual Diabetes Art Day will take place just over a week from now on Thursday, September 1, 2011.

For those who don’t know, Diabetes Art Day was created last year by my friend, fellow DOC member and art therapist, Lee Ann Thill. She blogs over at The Butter Compartment.
The inaugural Diabetes Art Day was an unqualified success, and I’m proud to say that I’ll be participating again this year. And I hope that the rest of the Diabetes Online Community will join the fun again as well.

And that’s what Diabetes Art Day is all about; having fun with our DOC family and friends while offering a glimpse into life with Diabetes by way of artistic expression.

It doesn’t matter whether you’re an experienced artist or a beginner, everyone is welcome to participate in Diabetes Art Day.

To find out more about Diabetes Art Day and how to participate, visit the official event website at www.diabetesartday.com.

I can’t wait to see what everyone comes up with this year. So go grab some art supplies, and get crafty!

20110824-041902.jpg
This collage is made up of images of works from last year’s event.

Posted in Announcements, Diabetes Art, Diabetes Art Day, Shout outs | 2 Comments