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Birth Pains of Inclusion

by Nicolai Ordahl

The house I grew up in stands five blocks from a notorious state institution in Cambridge, Minnesota. Riding my Huffy through that place was like entering a strange cartoon land—grand buildings forming rows into the distance, rolling expanses of green grass, a curious stillness in the air. Occasionally, I would see someone walking around, looking lost. I always wondered what went on inside those buildings. Thankfully, I didn’t hear the story until years later.

One day a man came out of nowhere as I rode through. “Hey!” He said. “Hey, I’m looking for a friend!” I didn’t know what to think—words like “retarded” and “dangerous” had been put into my mind by the well-meaning townsfolk. So when this man yelled at me, I turned up the heat and left a streak of fire in my wake. I felt sad looking back, watching him give up and turn away. I realized that he wasn’t looking for a particular friend. The guy was looking for anybody.

Serendipity brought me to Life Pages, a community inclusion project funded by Administration on Developmental Disabilities (ADD) fifteen years later. The point of my position at Life Pages, was to facilitate a greater diversity of life experiences for people with disabilities. As the Life Pages’ Web site matured into a megalith of accessible community happenings, I ventured out into the Twin Cities to promote the work: standing at exhibits, presenting at conferences, and meeting the people for whom I had been toiling. It became clear to me that to some, I was the rookie reporter whistling through an office full of disenchanted veterans—they were dying to see me trip.

Forging ahead, we developed interactive Web site features that addressed vulnerability concerns, while creating personal connections between users. But it became clear that in the real world, improving community inclusion was no cakewalk. Many bright-eyed exchanges of business cards resulted in silence, unreturned messages, even dropped telephones and mysterious disconnections. I could have sworn a man from Houston, panicked by the prospect of being solicited by a community inclusion project, used his voice to imitate a dial tone. Other talks with disability professionals yielded clearer results; the phrase “no way in hell” was indeed spoken.

Of course it was a good idea! A network of localized, yet connected Web sites where people could march under the banner of community inclusion while finding local information and connecting with each other—clearly a progressive way to approach the problem. People with disabilities needed more diversity in their leisure experiences, more self-direction, more opportunities to connect with each other and the community—everybody was high five-ing over that one. But did I, a starry-eyed tenderfoot with a college education burning a hole in my pocket, have any idea of the kinds of things these professionals were up against? There was red tape. There were incidents. There were dismal finance meetings in which heads sunk into hands, burned coffee was glumly sipped, and the mere mention of investing real money in a community inclusion network was met with a prompt discussion of American Idol.

Hope dwindled. The data seemed to indicate that while institutions were out, self-direction had not exactly seized the tiller. The federal government thought Life Pages was a solid concept, but everyone has their own impression of Uncle Sam’s slugging percentage. We did enjoy brief courtships with a handful of organizations, but in the end we were always disapproved of by the parents—the people in charge of the money, or vice versa. Disability advocates from New York to California sang the praises of this original idea, but nobody was willing to ante up. This isn’t anybody’s fault —it takes a lot of faith and momentum to put resources into an instrument of systems change. Everybody knows that the disability world is not characterized by people lighting cigars with hundred dollar bills. In the meantime, the project marches on and waits, much like those individuals with few connections to the community around them.

Drawing the curtains on the state institution in Cambridge was a laudable step for the State of Minnesota. The next step, not only for Minnesota but for the country, is drawing the curtains on monotony, one individual at a time. Using fast, user-friendly technology to explore the community, facilitate friendships, and nurture the interests of individuals is a reasonable place to start.

Partners in Community Supports (PICS) was founded by some of Minnesota’s most respected non-profits to promote inter-agency cooperation, improve legislation, develop best practices and change the system to put people first. Our Partner Agencies:

Life Pages - www.LifePages.org This site was developed to help you find information about recreation and leisure activities, services, advocacy, and other useful things about life in Minnesota. Life Pages offers information for Minnesotans of all ages and abilities who want to enrich their leisure lifestyle as well as their connections to the greater community.

The Administration on Developmental Disabilities (ADD) is the U.S. Government organization responsible for implementation of the Developmental Disabilities Assistance and Bill of Rights Act of 2000, known as the DD Act.

 


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