I had to make a less compelling but similar choice several years ago, when one of my cousins, who also had PKD, asked us all to get tested for possi
October 5, 2009


I had to make a less compelling but similar choice several years ago, when one of my cousins, who also had PKD, asked us all to get tested for possible transplant donation. I was out of work and uninsured, and I knew if I had any complications, I couldn't afford treatment. Even though I felt really bad about it, I didn't get tested.

Isn't it horrible that we're making moral decisions on such immoral grounds? The more I see of the disgusting horse-trading going on over the public option, the more convinced I become that a national (and probably single-payer) health care system is our only sane option.

Nick Kristof:

So what would you do if your mom or dad, or perhaps your sister or brother, needed a kidney donation and you were the one best positioned to donate?

Most of us would worry a little and then step forward. But not so fast. Because of our dysfunctional health insurance system, a disgrace that nearly half of all members of Congress seem determined to cling to, stepping up to save a loved one can ruin your own chance of ever getting health insurance.

That wrenching trade-off is another reminder of the moral bankruptcy of our existing insurance system. It’s one more reason to pass robust reform this year.

Over the last week I’ve been speaking to David Waddington, a 58-year-old wine retailer in Dallas, along with his wife and two sons. I’d love to know what the opponents of health reform think families like this should do.

Mr. Waddington has polycystic kidney disease, or PKD, a genetic disorder that leads to kidney failure. First he lost one kidney, and then the other. A year ago, he was on dialysis and desperately needed a new kidney. Doctors explained that the best match — the one least likely to be rejected — would perhaps come from Travis or Michael, his two sons, then ages 29 and 27.

Travis and Michael each had a 50 percent chance of inheriting PKD. And if pre-donation testing revealed that one of them had the disorder, that brother might never be able to get health insurance. As a result, their doctors had advised not getting tested. After all, new research suggests that lack of insurance increases a working-age person’s risk of dying in any given year by 40 percent.

“At the time David needed a transplant, the people closest to him couldn’t even offer a lifesaving donation — for insurance reasons,” said Mr. Waddington’s wife, Susan.

Travis, who is living in New York and working toward a math doctorate, is anguished at having to weigh insurance obstacles against the chance to save his dad.

“Can you put a price on your father’s life?” he asked. “My brother and I talked it over privately, and agreed that we should both go ahead and get tested anyway. It seemed like the only course of action. We presented our plan to our parents, and of course Mom immediately shot it down, with Dad firmly behind her.

“We had to respect their right to want to protect us. But it was enraging to be in that situation, and to be completely impotent to do anything to help. I told myself a number of times that we would reconsider the issue of testing if Dad’s dialysis stopped working before he got a transplant.”

David Waddington finally got that transplant when a kidney from a deceased donor became available. But our insurance system has had other excruciating consequences for the Waddingtons. Though PKD has no cure as such, there are experimental medications that may delay kidney problems. To get access to the medications, a patient must be tested — and since Travis and Michael Waddington don’t dare get tested, they don’t have access to these medications.

“The only way to do it is to lie about your name during testing, to use a fictitious name,” Susan Waddington said. “That was the advice we got from a major person in the field. We didn’t do that.”

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