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Families across country feel Latimer ruling better protects life of people with disabilities

(15 February 1999) — In an action the Saskatchewan Association for Community Living (SACL), calls appropriate, the Saskatchewan Court of Appeal recently overturned a lower court's unprecedented two year sentence given to Robert Latimer for killing his daughter, Tracy, who had cerebral palsy. Latimer had been convicted of second-degree murder, but the judge created an exemption to the mandatory 10-year sentence and gave Latimer only two — only one of which to be served in prison.

Hugh Scher Swears Affidavit in Genereux Case

(8 January 1999) — CCD is seeking to intervene in the Genereux case. In its affidavit, CCD outlined its general position on the Genereux case to the court. CCD's position is summarized below:

People with disabilities are frequently victimized by prejudicial, paternalistic and stereotypical ideas about the quality of our existence. This is true for people who are HIV positive and/or are living with AIDS and for people who depend on doctors and care givers for survival and nurturing.

The Latimer Case: The Reflections of People with Disabilities - Biography of Tracy Latimer, 1980-1993

A Life Cut Short

by Elizabeth Semkiw

Tracy Latimer was born on 23 November 1980. She had Cerebral Palsy and was the eldest of four children. Tracy lived on a farm with her family near Wilkie, Saskatchewan.

The Latimer Case: The Reflections of People with Disabilities - Introduction

by Hugh R. Scher, Chairperson, CCD Human Rights Committee

Annual Report: 1998-1999

Making Change Work for Us

Submitted by Eric Norman

The Latimer Case: The Reflections of People with Disabilities - Media

Latimer Wins Case in Media

by Prof. Dick Sobsey, University of Alberta Abuse and Disability Project

The Latimer Case: The Reflections of People with Disabilities - A Parental Perspective

A Father's Concerns

by Brian Stewart

Forty plus years ago my parents were told not to take me home. Those concerned for my parents' well being, the medical profession, could not see my life as being worth living. Born with Cerebral Palsy, their vision was that I would not have a future and they did not, would not, or could not, see a place in the community for me.

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