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104 lines
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104 lines
6.6 KiB
Plaintext
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[From the Wall Street Journal]
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"A Mother Talks to Mrs. Clinton"
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by Marianne M. Jennings
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[The author is a professor of legal and ethical studies in the College of
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Business at Arizona State University and a columnist for the Arizona Republic,
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a newspaper.]
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My husband and I have the privilege of raising a child with severe mental
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and physical impairments. If you were to ask me the most difficult aspect of
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rearing this unique little girl, the answer would not be the countless
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hospitalizations, the equipment demands, the sleepless nights or the too-long
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stares when we're in public. It would be the government bureaucracies we face
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to provide for her, protect her, and help her tap her potential.
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As I listen to Hillary Rodham Clinton tout the wonders of a national
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health care plan, I want to say: "Come follow me, Mrs. Clinton. I can show
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you what government does to those it sets out to help."
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I would begin by introducing Mrs. Clinton to the five or so caseworkers
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assigned to our Claire. One is from Arizona's Department of Development
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Disability. Another is with Arizona Long Term Care. Another is with the
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Arizona Health Care Cost Containment System. Another is with APIPA, and I
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don't know what that stands for. I lost track of acronyms, agencies and
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caseworkers long ago.
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These caseworkers, assigned as advocates for my daughter's needs, come to
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our house, one by one, once each year to conduct two-hour interviews and verify
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in person that Claire, a child who is now six and has never spoken, has not
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been the recipient of a miracle cure.
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I don't know what caseworkers do beyond this interview, but two things
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have occurred to me. First, burglars could just arrive at our door with a lot
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of forms and an acronym and anyone in the household would let them in. Second,
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there must be yet another contrived constitutional privacy right or some
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insider trading rule that prohibits state and federal employees who work with
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the same family from using one file, comparing notes, sharing information or
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even carpooling for interviews. My favorite interview was last fall, when a
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caseworker was assigned to re-do hundreds of interviews as part of a new total
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quality management program. [That's "TQM", to those fortunate non-initiates --
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L.D.]
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If I could introduce Mrs. Clinton to our five caseworkers, I would ask her
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to pose a hypothetical question to them about Claire's coverage. Mrs. Clinton
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would get five to eight different answers. The eight is because some of the
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caseworkers who buy into the new TQM program would go beyond the call of duty
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and give us two to three wrong possibilities.
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I would then take Mrs. Clinton into the world of Title XIX, a federal
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benefits program administered by the state for children under 19 who have
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permanent disabilities. Theoretically, Title XIX means summer school, swimming
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programs, respite care, therapy and a host of services that make it sound like
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a luxury spa. Reality is quite another story.
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Title XIX qualifies children on the basis of need (ie., income) or degree
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of disability. Claire qualified on the basis of disability, but we are still
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required once each year to submit to an in-office interview (with yet another
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case worker) in which I must give copies of our car titles, house deed, bank
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account statements, W2s, and the like. A sample caseworker comment from one
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year's interview: "I see you have a new piano in your home. Claire doesn't
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play this, does she?" I had to wonder why someone looking at a child who can't
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sit, hold her head up or make any discernable voluntary movements felt
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compelled to ask such a question.
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One year we made the monumental mistake of adding Claire to our car title.
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Claire must be on the car title in Arizona for us to have a handicapped
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license plate. When we had only a moveable permit that was placed in the front
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window, people yelled at us in parking lots. With our official plates, we were
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saved from such grocery store skirmishes. But I had to face the glare of a
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Title XIXer who said, "Is Claire driving this car?" I was required to sign a
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witnessed statement that said our cortically blind kindergartner did not take
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the Chevrolet Suburban out for spins.
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During our income interview last year, a caseworker spotted our medical
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expenses. They are our biggest expense even with insurance, exceeding our
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house payments and food costs each month. The caseworker askes, "Why would you
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pay medical bills?" I never know about trick questions in bureaucratic
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territory, so I responded, "Because we owe them?"
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She then explained -- the first government employee in four years to spot
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the issue -- that Title XIX covered all of Claire's medical expenses not
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covered by insurance. I asked, "How come no one ever told me this?" To which
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she responded, "Because they didn't know?"
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Once you're in Title XIX, it is Disney's Space Mountain -- dark and
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twisted. In 1992 I began asking for summer school approval in April. I
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received approval on July 22 -- three days before summer school ended. Last
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year I began the summer school approval quest in February. I got it in April,
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but someone forgot to put Claire's name on the registration list. I found this
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out after a two-hour wait in the registration line. I paid for summer school
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myself and have since learned the term "refund" is not part of Title XIX.
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I began using our newly discovered Title XIX medical benefits in August,
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In just six weeks, I received authorization for a new wheelchair and a
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scoliosis jacket. In October I got a call from a caseworker who informed me
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that Claire's Title XIX benefits were being terminated as of that day. He had
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discovered on the forms that I fill out for the financial interview that a
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$1,600 bank account for Claire. It was a burial account within the $1,500
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limit allowed by statute, but it had earned interest. Claire had too much
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income. I offered to close the account. "Too late," he said. Then he added,
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"But you can always come down and reapply for Title XIX." It took me six
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months to get qualified the first time. I should have us reinstated just in
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time for summer school this year.
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I am a lawyer who teaches and writes about administrative process. Yet
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this system is beyond my expertise. How do parents with language barriers,
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little or no knowledge of due process and noncompulsive personalities cope?
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I can show Mrs. Clinton that programs like hers already exist. I can show
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her the paperwork, the idiosyncratic rules, the insensitivity, the ill-trained
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workers and a bureaucracy as deep as the Mississippi at St. Louis. I can show
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her a system, that, much like her proposal, was intended to help. The reality
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is that help rarely makes it to our Claire.
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[End]
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