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David Stanley Ford

Duncan transplant patient loses drug benefit
AFTER 3 YEARS, MEDICARE PROGRAM STOPS PAYING FOR ANTI-REJECTION MEDICATION

BY WENDY K. KLEINMAN    Comments Comment on this article4
Published: November 30, 2008

All a Duncan man knows about his organ donor is what they had in common: They were about the same age and were outdoorsmen. The Arizona man died following a motorcycle crash; his kidney and pancreas now belong to Mike Reddin.


Mike Reddin

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Transplant patient Mike Reddin

Nov 29Patient Mike Reddin talks about hardship of paying for medication...

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at a glance
BY THE NUMBERS

MEDICARE

Figures for Medicare’s private fee-for-service plans (as of July 1, 2007):


• 355,249: Number of chronic kidney failure enrollees


• $106,000: Cost of a kidney transplant


• $71,000: Per dialysis patient, including other health care needs


• $17,000: Per patient with a functioning transplant, for anti-rejection drugs and other health care needs

TRANSPLANTS

Oklahomans on the national transplant waiting list (as of Nov. 21)


• 436: Number waiting for a kidney


• 21: Number waiting for a kidney and pancreas

Sources: Centers for Medicare & Medicaid Services, National Kidney Foundation, Organ Procurement and Transplantation Network, Dr. Jose Elamm, End Stage Renal Disease Network 13


WHAT’S AHEAD
Help on the way?
Bills were introduced in the U.S. House and Senate this year that would have eliminated the three-year limit on anti-rejection drug coverage, but neither bill was heard, said Troy Zimmerman, vice president of government relations for the National Kidney Foundation. The bills would have extended coverage only for the drugs, not for other health costs. Zimmerman said the change would be good economically because the drugs are cheaper than dialysis. It also would allow more people to consider a transplant and improve their quality of life.

Zimmerman hopes legislation gets passed. "The fact that they (members of President-elect Barack Obama’s administration) are going to be looking at health care coverage in a broader sense, that helps our chances,” he said.

Medicare doesn’t have a position on the issue. "The limit on the anti-rejection drugs is statutory. Congress is the boss,” agency spokeswoman Ellen Griffith said.

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But in August, three years after his double-transplant, Reddin, 46, was dropped from a special Medicare program that covered the cost of his anti-rejection drugs. The Basco Leather Goods mechanic now can’t afford the drugs he needs to hold onto his health.

Wondering why
Medicare’s policy is to cover people with chronic kidney failure, regardless of age. It pays for dialysis, transplants and even some medical expenses that aren’t related to kidney problems.

Although End Stage Renal Disease Medicare will pay for dialysis indefinitely, the federal health insurance program stops paying for post-transplant drugs after three years.

Patients in most cases must take the drugs the rest of their lives to keep transplanted organs, which their bodies view as foreign objects.

Reddin knew his three-year mark was approaching, but didn’t realize just how much he would have to pay because he never saw a bill from the time he went on dialysis in 2003 until a few months ago.

"Six hundred dollars out of me and my wife’s paycheck, that’s a big chunk,” Reddin said.

The $600 is after his employer pays a portion and he uses manufacturer’s coupons.

There are no generics for the three Prograf and six Myforic pills he has to take every day.

Reddin relies on his parents to pay for the drugs.

"It’s embarrassing,” Reddin said. "And it makes you wonder why. I mean, I pay thousands of dollars worth of taxes out of my paycheck — and I know every American does — and it’s not just kidney people, it’s people with cancer, heart problems, diabetes — all this medicine is high.”

There are assistance programs available, but Reddin is not eligible for them because he works.

"It looks like if you’re working you get punished. ... I’m hoping somewhere out there’s assistance, but it’s not looking good,” he said.

"It’s been hard,” said his wife, Delisa.

"There’s things that we’re not able to do for our kids. ... We have one that’s trying to work hisself through college. ... We’d love to go send him to college but financially we’re not able to.”

Don’t plan ‘too far ahead’
There is a drop in survival for transplant patients after three years because some patients can’t afford the drugs, said Dr. Jose Elamm, a transplant nephrologist at Integris Baptist Hospital, where Reddin goes for checkups. Some patients ration their supply, he said.

That accounts, in part, for what Elamm said is a "significant number” of people on a waiting list for another transplant.

About 3,000 transplanted kidneys fail every year and an estimated 12 percent of those are due to noncompliance associated with drug costs, said Troy Zimmerman, a vice president with the National Kidney Foundation.

Reddin was diagnosed with diabetes at age 5.

He should live at least another decade if he continues taking the anti-rejection drugs.

The average life expectancy of a diabetic on dialysis is three years, Elamm said. But the average life of an organ from a living donor is 15 years, and the recipient can live longer back on dialysis.

The Arizona donor’s body was kept alive until the transplant.

"I take everything day-by-day now,” Reddin said. "You don’t want to plan too far ahead.”

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David Stanley Ford





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I do realize this article was in regards to Medicare however, I am from Illinois and Iowa and in thosed states this would not have happened as they have much better healthcare to residents of those states. At the very mimimum, Mr. Reddin would have qualified for a "Spenddown" type of Medicaid coverage that kicks in after any existing insurance he has, and after a certain amount has been amassed each month in medical expenses. I know this because that is what I had before moving here. Had I known Oklahoma cares so little for its residents, maybe we would have accepted a job in another state at the time that thinks a bit more kindly of those that live there. I think it is bad enough that the Federal programs are dropping people all the time let alone your own state ignoring your needs as well. I agree, it becomes a choice between living and being alive all to quickly for too many people. You either have to work and be denied access to healthcare or have no job, no money for housing, heat/electricity, or water and then receive access to healthcare. This is wrong on so many levels in my opinion, that is all I was trying to get across.
Paula, Oklahoma City - Dec 2, 2008 at 8:43 am
It's not about the "great state of Oklahoma" here, this is referring to the "Federally funded Medicare". I agree that states could and should do more to provide adequate healthcare for their citizens. The problem is with the pharmaceutical companies that control a big chunk of our entire healthcare system. They drive the prices up so high nobody can afford them and insurance companies won't cover them. Then give doctors kickbacks for prescribing their medications. You go into see a doctor for one thing and leave with 4 prescriptions... ever wonder why? Hospitals want to charge outrageous prices as well and forces the insurance companies to deny claims there as well. So with insurance companies that don't care, pharmaceutical companies that want to get as much money as they can and hospitals charging the highest rates possible... we get stuck with poor poor standards in heathcare. In the United States of America, people should not have to choose to live or die because they can't afford healthcare. If you want assistance your better off quiting your job and everything, instead of helping the working middle class, they want to help all the bums.
Jess, Warr Acres - Nov 30, 2008 at 10:42 pm
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I just have to say a few things here, to Mr. Reddin, hang in there somthing's gotta give sometime. My family and I moved to this "great state of Oklahoma" a year ago and I must say that until a month ago, we absolutely loved it here. Until I found out just how much this "Great state of Oklahoma" thinks of its inhabitants. Their lack of compassion to those in need of medical attention is absolutely disgusting and appalling, to say the least. I was told, point blank by several agencies, that my Cancer is of no concern since it is not Breast or Cervical Cancer. However, if it was one of those they would be more than happy to assist me any way they could and provide financial assistance via the Medicaid program. Other than that, I didn't even get a "Sorry for your pain and need. Wish we could help." , that is appalling to say the least. Cancer is Cancer and they ALL KILL!! But, Oklahoma doesn't care about that, they don't care about any of the people that live here either as a matter of fact. I do hope you can get some help somehow, I really feel for you and your family and I will keep you in my prayers. You should not have to choose between living and being alive, which is exactly what this oh-so "great state of Oklahoma" expects you to do.
PJ
Paula, Oklahoma City - Nov 30, 2008 at 7:29 pm
Mike Reddin, you are in my prayers. I once almost died from lack of sufficient healthcare. I pray God's blessings to you and your family.
Kathryn, Oklahoma City - Nov 30, 2008 at 5:01 pm

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