Jini Fairley developed retinitis pigmentosa (rp) as an adult. As her vision progressively diminished, she made changes to her life as needed, always remaining fiercely independent. As Director of Services at MWCIL for x years, Jini mentored IL Coordinators and helped many, many consumers achieve new levels of independence. Today she is the staff person …
Don’t Let the Pity Party Last Too Long – Jini Fairley Read More »
Growing up pre-ADA, both Joe and Linda’s parents had high expectations that each would be independent. Joe contracted polio at 8 months. He went to “special school” until 4th grade, and then switched to public schools. He went on to college, and got his first job in billing at the Center for Living and Working …
There Was Never Any Doubt – Joe Bellil and Linda Long-Bellil Read More »
Karen Schneiderman describes her growth as she learned about the wide range of disabilities, the commonalities of wanting to stay independent, and her activism. She was not allowed to attend public schools, so attended a special school. After getting degrees at Boston University and Northeastern College as well as a doctorate at another school, she …
Michael speaks about his journey since his injury in 1976. He has been a key member of the Boston Center for Independent Living since 1981. He describes his appreciation of the Independent Living and Disability Rights movements. His advocacy contributes to improved access to transportation, housing, jobs and services.
