View of the U.S. Capitol in Washington on April 22. (Bonnie Jo Mount/The Washington Post)
Reporter

In January 2017, Betsy DeVos, who was soon to become President Trump’s education secretary, appeared before Congress at her confirmation hearing and displayed ignorance about a key federal law aimed at protecting students with disabilities.

The law is the Individuals With Disabilities Act, known as IDEA, and DeVos appeared not to realize it is a federal law that all states must follow.

During conversations about it, first with Sen. Tim Kaine (D-Va.) and later with Sen. Maggie Hassan (D-N.H.), DeVos repeatedly said it was up to the states to decide whether to follow the law. Hassan at one point told her that IDEA is a federal civil rights law and asked DeVos: “So were you unaware when I just asked you about the IDEA that it was a federal law?”

DeVos responded, “I may have confused it.”

DeVos did, in fact, confuse it, but it is also true that Congress hasn’t lived up to its promises about IDEA — and that failure has harmed many students with disabilities. This post explains the broken promises and the consequences.

It was written by Meghan Schrader, who has a master’s degree in musicology and has served as an affiliate faculty member in disability studies. Her experience growing up with a learning disorder also inspired her to serve on the governing board of Boston ASAN (Autistic Self Advocacy Network) in 2015 and to volunteer as an education advocate for disabled students in foster care.

Her research exploring bioethics issues in respect to musical representations of disability in 1950s America was published by Oxford University Press in 2014. She maintains a personal blog called Diary of a Learning-Disabled Academic, through which she expresses her perspective on disability-rights issues. She is the recipient of the 2018-2019 Quell Foundation Fighter scholarship. You can find more of her writing on her blog.

This was first published on the website of Rooted in Rights, which posts stories to challenge stigma and redefine narratives around disability, mental health and chronic illness. I was given permission to republish it.

By Meghan Schrader

In the U.S. Supreme Court’s historic 1954 Brown vs. the Board of Education case, the justices stated:

Today, education is perhaps the most important function of state and local governments…. It is the very foundation of good citizenship. Today, it is a principal instrument in awakening the child to cultural values, in preparing him for later professional training, and in helping him to adjust normally to his environment. In these days, it is doubtful that any child may reasonably be expected to succeed in life if he is denied the opportunity of an education.”

Although disability-based discrimination and race-based discrimination are separate, specific experiences, I quote this case because advocates for people with disabilities used the premise of equal educational opportunity to advocate for the inclusion of disabled children in their neighborhood schools.

Moreover, the statement perfectly describes the connection between education and social justice: education helps determine the degree to which people can participate in and influence society.

Advocacy for the extension of such opportunities to people with disabilities led to the passage of the Education for all Handicapped Children Act (EAHCA) in 1977. Today, the EAHCA is known as the Individuals with Disabilities Education Act (IDEA). As a learning-disabled woman who grew up receiving special education services, I couldn’t be more passionate about IDEA. It opened a critical door to disability justice.

However, IDEA was so unpopular when it was passed that President Gerald Ford signed it in secret rather than in the Rose Garden where most major legislation was signed. There were two reasons for the legislation’s lack of popularity: it promised to end the segregation of disabled students from non-disabled students and it was expensive.

The bill contained a promise that the federal government would fund 40 percent of the costs of implementing IDEA. Today, the government funds just 14.7 percent.

Noting this discrepancy, legislators have filed the IDEA Full Funding Act to fully fund IDEA by 2023. I’m glad that this bill has been filed, but what I don’t understand is why IDEA wasn’t fully funded 44 years ago.

I also don’t understand why legislators didn’t take up this cause as a bipartisan issue in the ‘80s, ‘90s or ’00s when I was going to school. There really is no excuse for that lapse.

In Massachusetts where I grew up, people discussed civil rights and social justice, but they didn’t apply those insights to people with disabilities. I don’t feel comfortable chalking this failure up to simple ignorance.

The disability rights movement has been going strong since the 1970s, so the bipartisan legislators who voted to lower special education standards in Massachusetts from Maximum Feasible Development to Free and Appropriate Public Education (FAPE) in 2000 to save money had already had ample time to learn about it. Special education students just weren’t on their list of priorities.

That decision was part of a pattern both in and out of the classroom. For instance, in high school, I constantly overheard teachers complaining about the presence of special education students.

I was fortunate enough to take mostly advanced college preparatory courses, and sometimes the teachers would tell us things like, “We can’t go into the computer lab because the special kids are in there,” or, “I used to work with retards — oh, I’m sorry we can’t say that anymore, emotionally disturbed. Well, all I did was rip people apart to keep people from killing each other.”

During that same year, the school yanked accommodations in some of the college prep courses that I was taking. When I complained, I was repeatedly reminded that kids in special education “didn’t usually go to college.”

It was over that summer that the Massachusetts legislature lowered the standard of progress for special education students from Maximum Feasible Development — the de minimis standard of progress required by FAPE. My school decreed that students needed to be failing before they received special education services.

As a result, students like me who were succeeding in their academics became allegedly ineligible for special education services. Some of my services were cut, which made accessing the curriculum even harder than it already was. I think that was the point. The message from the state legislature and my school was clear: You are here to take the opportunities other people choose to give you. Be grateful and stay in your place.

Attitudes like that are a shame. Fully funding IDEA would help break down this kind of systemic ableism in a big way. For instance, full funding for special education would help pay for the services that high-schoolers with disabilities need to succeed academically and attain a four-year degree. With college and graduate degrees, such students will be more likely to avoid poverty, access job opportunities and be allies to one another in situations where ableism rears its head.

Yet, despite knowing the statistics about education’s connection to enfranchisement, Congress has broken its promise to fund IDEA for the last 44 years. This is largely due to the fact that too many people in the United States think that special education is a waste of money. For instance, Ford’s statement about the original EAHCA read in part:

Unfortunately, this bill promises more than the Federal Government can deliver, and its good intentions could be thwarted by the many unwise provisions it contains. Everyone can agree with the objective stated in the title of this bill — educating all handicapped children in our Nation The key question is whether the bill will really accomplish that objective. Even the strongest supporters of this measure know as well as I that they are falsely raising the expectations of the groups affected by claiming authorization levels which are excessive and unrealistic.

Despite my strong support for full educational opportunities for our handicapped children, the funding levels proposed in this bill will simply not be possible if Federal expenditures are to be brought under control and a balanced budget achieved over the next few years.

Ford’s statement was built on a faulty premise. He asserted that the government didn’t have the money to fund special education, which really isn’t true: the government pours billions of dollars into its pet projects every year and it always has. Hence, Ford’s statement wasn’t a response to true fiscal constraints, but a value judgment about the social benefit of educating people with disabilities.

Today, utilitarian objections to the cost of educating kids in special education continue to abound, and they have a connection to even darker arguments about resource allocation, such as those in favor of eugenics, euthanasia and organ transplant discrimination. Essentially, disabled people are viewed as resource-suckers.

Ultimately, not funding special education represents the influence of that perspective on the field of education. The denial of educational opportunities can be understood as the nonlethal counterpart of asking disabled people to give up their lives

Hence, the lack of full funding for IDEA is rooted in the same phenomenon that drives every other mechanism of disability oppression: social hatred of people with disabilities for being burdensome and expensive.

Underfunding IDEA has helped put disabled people in a terrible Catch-22: the powers that be express resentment toward disabled people for needing public assistance but perpetuate a special education system that leads to increased dependency in adulthood.

Given that there is no way for people with disabilities to “win” in this system, underfunding IDEA is one of the ways in which society expresses its wish for disabled people to disappear.

If Congress finally funds IDEA in 2023, its members shouldn’t pat themselves on the back for promoting justice for kids with disabilities: They should apologize to all of the people whose education has been stymied for almost 50 years.