Battling the Complications: An Interview with Diabetes Patient Michael Burke (Part II)

Posted November 9th, 2011 by

Last week, in Part I of this interview, PatientsLikeMe member and blogger Michael Burke shared his sister Linda’s struggle with type 1 diabetes.  Today, we learn about his own type 1 diabetes journey, including his June 2011 kidney transplant as a result of diabetes-induced kidney failure.

1.  What diabetes complications have you faced?

PatientsLikeMe Member and Diabetes Blogger Michael Burke

Diabetes is a disease that appears to be misunderstood by most people, in that the consequences of the disease can lead to many different complications.  As I mentioned earlier, both Linda and I suffered from diabetic retinopathy…essentially, you can go blind from diabetes.  Another complication is nephropathy, or kidney disease.  For me, this led to kidney failure and the eventual need for a kidney transplant this past June.

Heart disease is another major complication.  Personally, I never knew that I had any heart disease until one day my primary care physician sent me for a routine stress test.  During the stress test, the cardiologist felt it necessary to immediately admit me to the hospital and do a cardiac catheterization the next morning.  When he did, he found two blockages in my right coronary artery – one was a 90% blockage and the other was an 85% blockage.  I then had several stents placed.  After two years, those stents were becoming ineffective, and I required heart bypass surgery.  Lucky for me, there was a heart surgeon in Boston who was doing bypass surgery robotically.  What this meant for me was a much smaller incision (about an inch and a half compared to the whole chest being opened up), and being a diabetic, less risk of infection and a shorter recovery time.

Another complication is [diabetic] neuropathy, or nerve damage.  Typically, this usually affects the feet, but other parts of the body can be affected as well.  As for Linda and I, the neuropathy is/was primarily in our feet.  For Linda, it was extremely painful, with the feeling that you are constantly being poked in your feet with something very sharp.  For me, the feeling has been quite different, in that there is no feeling, at least around my big toes, which in turn has caused some balance issues for me.  Neuropathy is serious, it’s not just that it is painful for some and a loss of feeling for others.  It can also lead to amputation of your toes, your foot, or in drastic circumstances, part of or all of your leg.

2.  What was your kidney transplant experience like, and how are you doing now?

I went through a whole lot of emotions over the course of getting this new lease on life.  Although I had been prepared by my kidney doctor over the last several years that I was most likely going to need a kidney transplant, the day I sat with the transplant team for the first time was absolutely frightening and surreal at the same time.  It’s hard to explain.

I just remember sitting with the transplant team and when the transplant doctor said, “Ok, we will put you on the transplant list within the next few days, and we will move forward,” my heart was pounding so hard I thought it was going pop out of my chest.  There is also a lot of anxiety that goes along with the whole transplant process.  At first, I didn’t know where the kidney would come from.  I knew there were family members who said that they wanted to be tested and now I was also on the national transplant list.

Michael Burke's Brother and Kidney Donor Tommy

When my brother Tommy was starting the testing process, I kept going back and forth in my head.  It would be great to have someone close to me donate, but then there was the guilt.  If I ever rejected their kidney now they are left with just one.  As it turned out, Tommy was a 5 out of 6 antigen match, and he donated his kidney to me in June.

I had often heard before the transplant that you won’t understand how badly you felt or how sick you were before the surgery until after the surgery.  That could not be a truer statement.  I never really felt sick before, and I have been told that is because kidney disease can be very slow and progressive.  However, looking back today, I can honestly say that there has been a 180 degree turnaround.  I have much more energy and I just generally feel well – it has been a huge difference, and I have Tommy to thank for that.

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Are you a diabetes patient as well?  In honor of American Diabetes Month, share your thoughts and stories at CallingAllTypes.com.


8 Comments

  1. Way to go. This so parallels my older sister, and I’s experience. She had to deal with multiple amputations, years of dialysis, and bad nerve damage as well as sight loss. She was not compliant with her diabetes while I was more careful. She was not eligible for transplant due to her non-compliance with diabetic treatments. I was fortunate to get a close match, but it was from a diseased donor of only 18 years of age. It’s been 2 1/2 years this month, and I am doing great! Hang in there Burke, it all gets better and better!

  2. HELLO!, I’M NOT A DIABETES PATIENT OR SUFFERER! I CAN RELATE TO FATIGUE AND WITH MIGRAINES AND SEIZURES THAT LEAVE ME DRAINED OF ENERGY! I FIND IT DIFFICULT, COPING, ON A DAILY BASIS! I MAY HAVE SEVERAL MIGRAINE HEADACHES A WEEK!, ESPECIALLY WHEN I’M DUE FOR MY SEIZURE!
    SO!, YES, YOU MAY HAVE MORE COMPLICATIONS WITH YOUR ILLNESS, THAN MINE!, BUT WE ALL HAVE OUR BURDENS TO BARE!
    I WELCOME!, ANY FELLOW SUFFERERS, NO MATTER, WHAT YOUR CONDITION! KEEP UP THE GOOD FIGHT!

    BARRY

  3. Very interesting story about your sister, especially because my name is also Linda, I was diagnosed in 1970 at age 5, which I believe puts me at approximately the same age as your sister. I, too, always wanted to be a nurse although I never followed through on that. I lost the vision in one eye due to diabetic retinopathy, and have had laser treatment and cataract surgery on the other. More recently, I was diagnosed with MS. One thing I do not have much to the amazement of several doctors is neuropathy. Thanks so much for sharing!

  4. Wow Micheal, reading your story was inspiring. I couldn’t help and think of the dear friends I have w/ diabetes. They keep telling that they are falling repeatedly, and about the eyes. The idea of losing your sight becuase of the disease is frightening. I am glad new kidney has given you another chance for a more quality life.

    Q: has the esperience changed the way you eat and care for your life?

  5. Michael,
    How well I can relate to your story. I was diagnosed with Type I Diabetes at age 5 and have overcome many of the complications associated with it. I have retinopathy, with left me blind in one eye after a retinal detachment in 1992. I have had 2 kidney and 2 pancreas transplants and are currently awaiting my third kidney transplant. This past March, I underwent open heart surgery for a mitral valve replacement and bypass. This surgery has taken the longest to recover from, but I am doing well. Like you, I have had all my surgeries done in Boston,MA. Have you considered having a pancreas transplant? It will prolong the life of your new kidney. You are very lucky to have received the gift from your brother. Best of luck to you.

  6. i have recently bout a report called diabetes uncut which has lots of great info on how to prevent complications.
    a must read if your worried about complications

  7. interesting story

  8. Nice post.

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