Rights Watch
IDEA 
        Ruling: How It Adds Up
        
          A landmark Supreme Court decision declares 
          schools must cover one-on-one health care for disabled 
          students.
        Garret Frey was only four 
        years old when a motorcycle accident severed his spinal column.
        Now a high school sophomore in Cedar Rapids, Iowa, he motors around 
        his school in a specially equipped wheelchair that allows him to steer 
        by blowing into a straw.
        Because he is paralyzed from the neck down, Garret needs constant 
        one-on-one assistance to feed him, perform bladder catheterizations, 
        suction his tracheotomy tube, and monitor his ventilator.
        When he first went to school, Garret's 18-year-old aunt tended to his 
        health care needs. Later, his family used the proceeds from an insurance 
        settlement to hire a licensed practical nurse to care for him at 
        school.
        In 1993, his mother asked the Cedar Rapids Community school district 
        to foot the bill for Garret's school-related health care. When the 
        District refused, she sued.
        Frey argued that the district should pay for his nurse under the 
        Individuals with Disabilities Education Act (IDEA).
        In an important 7-2 ruling handed down in March, the U.S. Supreme 
        Court agreed.
        IDEA requires schools to provide disabled students with whatever 
        "health services" the student needs to attend school--except that 
        schools don't have to provide "medical services."
        In an opinion by Justice John Paul Stevens in Cedar Rapids 
        Community School District v. Garret F., the High Court said that a 
        "medical service" is a service that can be performed only by a licensed 
        physician. Since Garret's medical needs can be met by a nurse or trained 
        layperson, the Court reasoned, it is a "health service" for which the 
        school must pay.
        The Court rejected the school district's plea that hiring a full-time 
        nurse to care for Garret would be too costly.
        "The District cannot limit educational access simply by pointing to 
        the limitations of existing staff," the Court said, even if it means 
        that the school has "to hire specially trained personnel to meet 
        disabled student needs."
        Dissenting, Justice Clarence Thomas complained that the majority 
        "blindsides unwary States with fiscal obligations that they could not 
        have anticipated.
        "Congress enacted IDEA to increase the educational 
        opportunities available to disabled children, not to provide medical 
        care for them," he emphasized.
        It's too early to assess the impact of the Court's ruling, but 
        critics warn that it imposes yet another burden on schools, an unfunded 
        mandate that will drain resources from regular education programs.
        The Cedar Rapids school district claims it will cost $30,000 to 
        $40,000 a year to comply with the Court's order. "Who is going to 
        provide that money?" asked Sue Seitz, the school district's 
attorney.
        The National School Boards Association estimates that there are 
        17,000 "medically fragile" students who will need continuous assistance 
        from a nurse or aide--services with a total price tag of $500 million a 
        year. NSBA executive director Anne Bryant criticizes the Court's 
        decision, saying "it takes the focus of schools away from being 
        educators" and makes them "medical service providers."
        And in the end, a Los Angeles Times editorial cautioned, the 
        decision "may shortchange more students than it helps."
        Advocates for the disabled were pleased by the ruling and down-played 
        its potential impact on school coffers.
        Judith Heumann, assistant secretary for special education at the U.S. 
        Department of Education, said the decision "will help advance the 
        inclusion of disabled children into society. It says they have a right 
        to get an education in an inclusive setting."
        Mary Fitzsimmons, a Chicago-area mother of a disabled student, told 
        the Associated Press: "Every child should have the right to what they 
        need, and if that means spending a little more money so that the child 
        can have the same benefits that other children get, that should be 
        done."
        Other advocates argue that these costs can be borne by Medicaid in 
        many cases, and that teachers and aides can be trained to perform most 
        health care services.
        The problem is money, or rather the lack of it. The federal 
        government is not paying its fair share. When IDEA was first enacted, 
        Congress promised to fund 40 percent of the costs of educating students 
        with disabilities. But then Congress reneged.
        According to the U.S. Department of Education, the average excess 
        cost of educating a child with disabilities is $7,021. Yet the federal 
        government contributes only $702 for each disabled student. That's just 
        10 percent. It would take additional appropriations of $13.5 billion per 
        year to "fully" fund IDEA at the 40 percent level.
        People on both sides of the debate agree on at least one thing: 
        Home-bound students with chronic health problems that require constant 
        monitoring will now be able to attend school full-time.
        --Michael D. Simpson
NEA Office of General 
        Counsel