The High Cost of ObamaCare

This is the reason many people don’t like ObamaCare. It’s also part of why people wind up making fun of the president at state fairs. (On that, everyone should breathe deep and remember, as the noted political philosopher Orson Welles once put it: “It’s the business of the American people to take the mickey out of the president.” It’s not only what we do, it’s what we should do. Welles was speaking on a talk show; it was the 1970s; he was talking about people making fun of some Republican president, Nixon or Ford. So what? They can take it. And they’re not kings. Let me suggest a classy Obama move that might go over well. From his Vineyard vacation spot he should have the press office issue a release saying his reaction to finding out a rodeo clown was rudely spoofing him, was, “So what?” Say he loves free speech, including inevitably derision directed at him, and he does not wish for the Missouri state fair to fire the guy, and hopes those politicians (unctuously, excessively, embarrassingly) damning the clown and the crowd would pipe down and relax. This would be graceful and nice, wouldn’t it? He would never do it. He gives every sign of being a person who really believes he shouldn’t be made fun of, and if he is it’s probably racially toned, because why else would you make fun of him?

But back to health care. The piece I linked to, by Yuxing Zheng of the Oregonian, makes quick work of a complicated subject. A woman in Cornelius, Ore., takes care of her disabled 22-year-old daughter. The daughter has cerebral palsy, spina bifida and a condition called automonic dysreflexia. She requires 24-hour care. The mother provides it, receiving for this $1,400 a month. The mother fears—and is apparently right to fear—a provision of the Affordable Care Act that will, as Zheng reports, “largely prohibit guardians from serving as the paid caregiver of an adult child with developmental disabilities.” The mother is afraid this will mean foster care for her daughter, or a lengthy and costly process in which she herself will be forced to transfer legal guardianship to someone else. The provision, the paper says, will likely cause hardship for hundreds of Oregon families in which the guardian and the caregiver are the same person.

Oregon officials are asking the administration for an exemption to the provision.

Four points. First, no mother or child should be put in this position by a government ostensibly trying to improve their lives. Second, everyone in America knows health care is a complicated and complex subject, that a national bill will have 10 million moving parts, and that when a government far away—that would be Washington, D.C.—decides to take greater control of the nation’s health care it will likely get many, maybe a majority, of the moving parts wrong. A bill that is passed and is meant to do A will become Law U—a law of unforeseen, unplanned and unexpected consequences. And that’s giving Washington the benefit of the doubt, and assuming they really meant to honestly produce Law A. Third, because health-care legislation is so complex, it is almost impossible for people to understand it, to get their arms around what may be a given bill’s inadequacies and structural flaws. Stories of those inadequacies and flaws dribble out day by day, in stories like this one. They produce a large negative blur, and a feeling of public anxiety: What will we find out tomorrow? The administration reacts, as the president has, with protestations about how every large, life-enhancing bill has hitches and bumps along the way. But this thing looks now like one large hitch, one big and never ending bump. Fourth, when a thousand things have to be changed about a law to make it workable, some politician is going to stand up and say: “This was a noble effort in the right direction but let’s do the right thing and simplify everything, with a transparent and understandable plan: single payer.” Will that be Mrs. Clinton’s theme in 2016?