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Morton J. Kent Habilitation <strong>Center</strong> still a leader after 15 years<br />

In the early 1990’s, the Board of Directors at <strong>Orange</strong> <strong>Grove</strong> <strong>Center</strong> had<br />

an “awakening.”<br />

While the center was amassing a fi fty-year history of creating respected<br />

programs for individuals with intellectual and developmental disabilities,<br />

they realized that the increasing degree of complex disabilities demanded<br />

a new avenue of innovation. Thus, the idea for a dedicated center with the<br />

responsibility for identifying emerging and evolving challenges that<br />

would impact on clients with special needs began to catch both the<br />

collective imagination and zeal of the board. The Habilitation <strong>Center</strong><br />

would serve as the seat of innovation that would address the needs of an<br />

aging and increasingly fragile and vulnerable population.<br />

Several factors contributed to the Board’s vision. They saw the level of<br />

disabling conditions increasing. Technological advances in neonatal<br />

intensive care saw the survival of high-risk newborns that would have<br />

never lived even ten years before. These survivors had multiple and<br />

combined challenges in cognition, behavior, learning, sensory, motor,<br />

and medical areas. In addition, they foresaw the increasing longevity of<br />

Page4<br />

Dr. Rick Rader, Director of the Morton J. Kent Habilitation <strong>Center</strong>,<br />

and Ruth Toon, Director of Residential Habilitation, will be<br />

featured in an upcoming documentary called, “Living with Autism.”<br />

The video is produced by MassMutual to compliment the<br />

national survey conducted by Easter Seals.<br />

individuals who were previously considered “lucky” to live into their twenties and thirties. These challenges required a new breed of<br />

direct support professionals; highly trained and motivated with goals far beyond the traditional exhibition of “compassionate care.”<br />

Finally, the board echoed the growing societal movement to increase the level of “expectations” of what individuals with developmental<br />

disabilities could and needed to achieve. <strong>Orange</strong> <strong>Grove</strong> was given the “green light” to move forward with plans to establish a center that<br />

would refl ect the dictates of Lawrence Miller, “The achievement of excellence can only occur if the organization promotes a culture of<br />

creative dissatisfaction.”<br />

Thus, what was to become the Morton J. Kent Habilitation <strong>Center</strong> began to break ground in 1993. Mr. Kent, a veteran board member, had<br />

been given the reins to spearhead the creation of the center, outline its mission and formulate the benchmarks of its success.<br />

A national search for the <strong>Center</strong>’s fi rst director had some challenges of its own. For one thing, there wasn’t a “pool” of professionals<br />

who were currently engaged in “developmental disabilities medical futurism,” the term that was coined to identify and funnel potential<br />

candidates that might be able to “pull this off.” While there were certainly pockets of researchers involved in developmental disabilities,<br />

there was no existing similar setting that could describe what was envisioned at <strong>Orange</strong> <strong>Grove</strong>. Most of the research activities involved<br />

single agendas related to cause, prevention, special education, bio and adaptive engineering, employment, habitation, healthcare, and<br />

technology assistance. There was no single position that supported a researcher without borders, boundaries or beliefs.<br />

Thus the fi rst innovation didn’t come “out” of the Habilitation <strong>Center</strong>; it went “into” it. The idea and notion that a center could maintain<br />

multiple inter-connected research portfolios was an innovation itself. Before someone was even given the keys to the front door, the<br />

center had a radical platform; that their coordinated efforts could drive and deliver programs in areas that were seemingly unrelated to<br />

mainstream disability research.<br />

The selection of Dr. Rick Rader as the <strong>Center</strong>’s fi rst Director evoked the belief that the most successful people are those who are good<br />

at Plan B. This best described Dr. Rader who never even had a Plan A. Like most physicians, he had no formal training, experience or<br />

expertise in the fi eld of intellectual and developmental disabilities. What he did have was cross-training in both medicine and medical<br />

anthropology, and a key appreciation for the biocultural determinants of health and disease. Relying mostly on his training in anthropology,<br />

he approached the opportunity with a cultural model. People with intellectual disabilities were a culture unto themselves; albeit part<br />

of a greater cultural body. They and the community that supports them have their own beliefs, mythology, values, tools, language, social<br />

structure, and history. His belief that you needed to understand, incorporate and employ these components laid the foundation for his appointment<br />

as the Director of the Morton J. Kent Habilitation <strong>Center</strong> in 1994. It was at best a mutual leap of faith for the two unknowns;<br />

a neophyte in the fi eld coupled with an idea without precedence and devoid of a clear blueprint. While far more developed than a sketch<br />

on the back of a napkin, the Morton J. Kent Habilitation <strong>Center</strong> had no track record, no modes and no examples.<br />

In the ensuing fi fteen years, the Habilitation <strong>Center</strong> has had its footprint in virtually every aspect of the fi eld of intellectual and developmental<br />

disabilities. Signifi cant contributions have been made via the expansion of universal newborn screening, positioning OGC as the<br />

fi rst agency in the U. S. to adopt a code of ethics, medical school curriculum development, adoption of using parents in medical education,<br />

solid university teaching and research affi liations, invitations to participate in top level national disability task forces, including the<br />

President’s Committee for People with Intellectual Disabilities, the Dept. of Defense and the Surgeon General’s offi ce, as faculty in the<br />

fi rst national interactive webinars in developmental disabilities, in creation of the fi rst research organization in the fi eld of sensory processing,<br />

creation of comprehensive end of life programs, affi liation with Exceptional Parent Magazine, the professionalization of direct

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