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Showing posts with label #kidney/pancreastransplant. Show all posts
Showing posts with label #kidney/pancreastransplant. Show all posts

Sunday, May 5, 2013

My Unusual Cinco De Mayo In 1998



 When I had the kidney/pancreas transplant, the kidney was slow to start working so I had to have hemodialysis treatments at the hospital until it started working on its own.  Fir this, a port was attached to the blood vessels in my neck.  There was a serious complication with the first one, which was done on Good Friday and led to a terrifying incident I write about earlier in the book.  It had to be removed and the second port was placed there later that evening.


For three weeks it clung to my neck.  The lines of the dialysis machines were fastened to it at each treatment and I couldn’t move my neck or head.  It was like having an octopus grab me by the throat.  Whiskers grew around it where it was too close for me shave.  The port had a few dangling parts where the lines attached to it and where nurses injected medications.  When I was able to start wearing my own clothes instead of a hospital gown, I had be extra careful putting on or taking off a shirt or else it would snag them.




It was still on my neck when I was released from the hospital because the kidney still wasn’t up to speed and I might need more dialysis treatments.  Fortunately, the kidney started working soon after that and no additional treatments were needed.
 
Here’s the excerpt from What Didn’t Kill Me Made Me Stronger.

At one appointment at Dr. Henry’s office, Judy, his nurse, removed the port from my neck.  On one hand, I was eager to have the thing off me.  On the other hand, I was still very nervous about letting anyone touch my neck.  The trauma of Good Friday was still fresh in my memory.  She gently cut the sutures holding it in place while I sat as still as I could, wincing now and then from the slightest tug and gritting my teeth.       
Is this what it’s like to get rid of a leech?  Am I going to end up with a scar on my neck? 
When I got back to my parents’ house, I finally got to take my shower.  It was May 5th – exactly one month since my last shower.  It made me a little nervous standing in the wet bathtub on my wobbly left leg, water cascading over the long surgical scar, which was still covered by a row of butterfly bandages.  But for the first time in thirty days of doing the best I could with a wet washcloth, I really felt clean.  After very carefully stepping over the edge of the tub, gently patting my tender torso dry, and getting dressed, I felt a hundred times better.      
    



Read more excerpts from Jim's book What Didn't Kill Me Made Me Stronger: How I Found Hope While Surviving Diabetes, Vision Loss, and Organ Transplant, published in April, 2013.

Tuesday, October 23, 2012

My Adventures In Health Insurance

I’m uniquely qualified to talk about healthcare.  In the past 25 years I’ve been disabled and non-disabled, diabetic and ex-diabetic, insured through employers, Medicare, and no one.  In the past couple of years the subject of socialized healthcare has been a divisive issue here in the U.S.  Aside from brief discussions with a few people I’ve kept quiet.
But the time has come for me to jump into the fray.  Lucky for me, I’ve got insurance if the fray hurts me.
My Type 1 Diabetes was a pre-existing condition (from age 12) which meant my employers’ insurance chose to ignore that area of my health needs.  I paid for the testing supplies, disposable syringes, alcohol swabs, and two kinds of insulin myself—when I could.  There were a few times when I had to use the syringes twice, risking infection.
And that was when I had insurance.  There were times when I had to cough up (pun intended) the cash to pay for every doctor’s appointment.
When I was 27, the diabetic complications started.  My vision and my kidneys started failing.  I had no problem proving I was in bad enough shape to get Social Security Disability.  Not long after that, Medicare became my only health insurance.
This is the part most lifelong healthy people miss.  If someone with a chronic health condition can’t get the help they need to take care of it, they can become disabled.  I went from paying into the system to being a consumer.  Maybe it was inevitable, but it could have happened later and I could have paid more to Social Security before needing it.
To keep from losing SSDI and the Medicare that comes with it, I worked part-time at a number jobs for which was severely overqualified and under challenged.  A diabetic with failing kidneys can’t expect a private insurer to go near them.  A VOUCHER WOULD NOT HAVE MADE ANY DIFFERENCE.  A voucher does no good if no one will take it.
Medicare paid for the kidney/pancreas transplant.  I was lucky enough to have people willing to help raise the money for the unpaid part of the surgery.  Not everyone is so fortunate.  I don’t even want to think about how a private insurer might have tried to dodge the whole issue.
Medicare also paid for a second transplant, four major eye surgeries, laser treatments, dialysis, and a host of other less serious procedures.
In 2004 I landed a state job and employee health insurance started paying for the deductibles and copayments.  Now that I’m a retired state employee, I’m covered by Medicare and private insurance.  I’m one of the tiny percentage of disabled people fully covered by insurance.
I can remember when my situation wasn’t so comfortable, which is why I don’t have that “I’ve got mine, Jack” attitude I hear too often from the chronically healthy.
Even if you don’t have a chronic health condition, an accident or sudden illness could make it impossible for you to work.  Then where would you be?  You’d end up with socialized healthcare.  You would be persona non grata to the private insurers.
You say you’re really careful?  You eat right and exercise?  Great, but your luck could run out.  Yes, luck is a factor, too.  A drunk or distracted driver could crash right into you.  Don’t let luck make you smug.
There’s an old saying, apparently forgotten my many: An ounce of prevention is worth a pound of cure.  Keeping people healthy is so much cheaper than playing catch-up later.
Not only do most healthy people work, they further their education, volunteer, and some even start businesses.
I’ve heard people say, “We can’t afford to cover everyone in this economy.”  With two-thirds of us overweight, we can’t afford not to.  Here is the Land of the Free it’s “eat now, pay later.” 
Well, I’ve seen the bill myself.  Millions of us won’t be able to stiff the restaurant and do a Dine-N-Dash this time.

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