As the Globe’s Patricia Wen documented in a series in December, the $10 billion-a-year Supplemental Security Income program, which was originally meant for families of children with such disabilities as Down syndrome or cerebral palsy, has long since expanded to cover such mental conditions as attention-deficit disorder. In 1990, 8 percent of the poor children on SSI had qualified because of mental, learning, or behavioral disorders; in 2009, more than half did.
To some degree, the change reflects an acknowledgment that certain mental disabilities can strain a family just as physical ones do. But it also suggests that, in an era of stagnant wages and dead-end jobs, many poor families are looking to SSI less to defray expenses associated with a child’s disability than to help make ends meet more generally.
SSI has clearly given some hard-up parents a strong financial incentive to seek federal aid by having their children classified as disabled — and in some cases to get drugs prescribed. “To get the check,’’ one regretful mother told the Globe, “you’ve got the medicate the child.’’ The program has also made some ostensibly disabled teens reluctant to seek work for fear of jeopardizing their families’ benefits. “If I work and I get a certain amount,’’ one teen lamented, “then they’ll take money away from my mom.’’
But teens, including teens with diagnosed disabilities, learn useful skills from paying jobs. In this way and others, when SSI becomes a substitute for other benefits, it has deeply distorting effects on the families who receive it.
Some advocates for the poor defend the current system as a substitute for welfare, the only recourse for some needy families. But the damage done to children who are misclassified as mentally ill is incalculable: Some linger in special ed classes when they are capable of accelerated work; others come to believe themselves to be impaired when no such impairment exists.