Cancer v. the Constitution

I don’t get into political debates here much since I want this to be a happy place. But I can’t help it with this one. As I was saying to a co-worker the other day, if anyone is against the Affordable Care Act, I believe they are too rich to worry about things like medical insurance or the ability to pay for a catastrophic illness, or they just do not understand what it’s all about. Or, more likely, they simply are against it because it wasn’t an idea that came from the right (even though Obamacare is a close brother to Romneycare in Massachusetts)

For those who argue they don’t want the government to come between them and their doctor: well, if you don’t think insurance companies are doing that now then you, or no one you know, have ever had a complicated illness and had the experience of an insurance company telling you that the treatment you are receiving, or that your doctor is recommending, is medically unnecessary or “experimental” and therefore denied. Maybe it’s just me, but I would much rather have the government making those calls than an insurance company that financially benefits each and every time they deny a claim.

And what about Medicare? Are all of those screaming about “socialized medicine” going to turn down (federally-funded) Medicare coverage when they are eligible for it? I don’t think so.

This excellent blog post from Dr. Jen Gunter (which I copied in its entirety) gives a real-world example of why this matters and why it will be a damn shame if the Supreme Court overturns this.

The patient in the emergency department smelled of advanced cancer. It is the smell of rotting flesh, but even more pungent. You only ever have to smell it once.
She had been bleeding irregularly, but chalked it up to “the change.” Peri-menopausal hormonal mayhem is the most common cause of irregular vaginal bleeding, but unfortunately not the only cause.
She hadn’t gone to the doctor because she had no health insurance. The only kind of work she could get in a struggling rural community was without benefits. Her coat and shoes beside the gurney were worn and her purse from another decade. She could never afford to buy it on her own. She didn’t qualify for Medicaid, the local doctor only took insurance, and there was no Planned Parenthood or County Clinic nearby.
So nothing was done about the bleeding until she passed out at work and someone called an ambulance. She required a couple of units of blood at the local hospital before they sent her by ambulance to our emergency department.
I looked at the fungating mass on her cervix. Later the Intern wondered why she hadn’t picked up on the smell. Probably a combination of it being so gradual and denial. It’s amazing what people learn to tolerate when their options are limited.“I’m very sorry to tell you this looks like a cancer of the cervix,” I said.
She looked surprised. “Oh.”
She paused in silence as she adjusted to the news. And then quietly she added, “But the doctor back home said you could fix me up. He said you can offer free care because you have the university.”
But we didn’t have free care at the university hospital. While resident salaries come from Medicare dollars, there is very little, if any, money from the State for the medically indigent. We were in the same situation as her local OB/GYN. The cost of caring for those without insurance was born by the profits from those with insurance. But medical care was becoming more expensive and what insurance companies were willing to reimburse was decreasing. In addition, with more unemployment there were fewer insured patients and more uninsured. Not a sustainable model.
She needed a biopsy to confirm the type of cancer and a CT scan to see if the tumor had spread beyond the cervix. If she were lucky, she would have a some combination of a hysterectomy, chemotherapy, and radiation with a 50-65% chance of survival. If the cancer had spread, she would have radiation and chemotherapy with about a 25% chance of surviving.
But the cancer surgeons were not allowed to offer an uninsured woman a hysterectomy. Every now and then they snuck someone in, claiming to the administrators that the patient was more emergent than they really were. But one surgery doesn’t cure stage 2 or 3 cervical cancer, or even stave it off for long. It takes multiple admissions and week after week of expensive chemotherapy and/or radiation.The radiation doctors were also not allowed to see uninsured patients. They could not even give a dying women a few weeks of radiation to ease her tumor’s stench while it caused her to bleed to death or killed her another way. They could give her one dose today. A very temporary measure for the bleeding, but only if her blood count was low enough. It wasn’t because she’s had the blood transfusion to get her here.
There was a charity program that paid providers and hospitals pennies on the dollar for cancer care. One hospital had signed up, resigned to the fact that they were seeing those patients anyway so better to get something for the cost of the care than nothing. Our hospital administrators had declined to participate. Better to get no money and keep seeing these uninsured patients over and over in the emergency room, each time providing the same stop-gap care that has no hope of cure or even palliation like a purgatory version of Groundhog Day, than to be inadequately reimbursed for the right care.
I had never encountered this clinical scenario during my training in Canada. I had never seen a woman suffer because she couldn’t afford something as simple as a Pap smear, never mind deal with the indignities of shopping around her sorrow and hard luck to try to patch together what would inevitably be inadequate medical therapy. It is this reality of medical care in America for which I was wholly unprepared. Many times I found the residents comforting me.
I gathered my thoughts before explaining the situation. To get her care through the charity program there was a catch. A set of hoops to jump through and we could jeopardize her eligibility with specific tests. I explained the ins and outs of accessing care through the program, where she needed to go, and what specifically she must say. The Intern printed out the sheet of community resources and advocacy groups that might also be able to help her patch together some kind of treatment.
It’s not health care, not by any stretch. But as long as the Supreme Court finds it constitutional I guess they’ll sleep better than I do.

via Cancer v. the Constitution.

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About travelerontherun

I am a chronic adventurer who loves to see and experience new places. What I really love most is experiencing those places after parking my RV and lacing up my running shoes.
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2 Responses to Cancer v. the Constitution

  1. Great Post, even though I do not agree. I love your thoughts and I love your friendship so I will not go into my reasons because let’s face it, you will never come to my side and I will never come to yours. But I do appreciate you sharing!

    • I don’t mind at all hearing other opinions, so don’t feel like you have to edit yourself 🙂 But, you are right, you likely won’t change my mind. I think our opinions are rooted in personal experiences and knowledge and I am all too familiar with injustices handed down by insurance companies and a broken health care system. But I’m sure as many examples of injustice I have, there are an equal number of stories people have about injustices handed down by the government. Again — personal experiences and knowledge guiding our opinions. But I’ll never tell someone I don’t want to hear their opinion because it differs from mine.

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