Showing posts with label Diane Coleman. Show all posts
Showing posts with label Diane Coleman. Show all posts

Tuesday, November 18, 2025

We mourn the death of the great John Kelly

Alex Schadenberg
Executive Director, Euthanasia Prevention Coalition

I am shocked and saddened by the loss of John Kelly, the leader of the disability rights group, Second Thoughts an activist with Not Dead Yet and a leader of Progressives Against Medical Assisted Suicide.

John was an amazing disability rights activist leader and tireless in his opposition to medical assisted suicide. John was an amazing leader, advocate, speaker, a warrior for truth.

John was a gifted orator and incredibly funny and witty.

He was a great collaborator, life few others. He worked with everyone.

I remember John coming to Toronto to speak at our Euthanasia Prevention Coalition conference. He was profound, excellent and funny. 

But life with a disability was always present. The next morning he thanked one of the doctors who was attending the conference for saving his life. I can't remember exactly what happened, but in the night he had a medical emergency.

Similar to Diane Coleman, the founder of Not Dead Yet who died last November and Stephen Mendelsohn who died in June, John's death is an incredible loss.

Here are some articles by or about John Kelly.

Tuesday, December 17, 2024

Putting Suicide Prevention Stickers Over the Dignity in Dying Ads.

Meghan Schrader
By Meghan Schrader

Meghan is an autistic person who is an instructor at E4 - University of Texas (Austin) and an EPC-USA board member.


Before getting to the main topic of this post I want to acknowledge the recent passing of Not Dead Yet director Diane Coleman. I never had the pleasure of meeting Diane in person, but I was honored to have NDY post some of my articles on its social media accounts and republish one of my EPC blog posts on its blog. I am deeply grateful for Diane’s decades of disability justice work and my condolences go out to her family and friends.

The rest of this post will address the use of suicide prevention resources to defy the right to die movement’s ideology. Despite the fact that the UK’s subway system usually forbids advertisements for controversial social policies and the fact that suicidal people are known to take their own lives in subway tunnels, Dignity in Dying UK posted glossy, expensive assisted suicide advertisements on the walls of London England’s subway system, such as one that fit into the assisted suicide movement’s pattern of foregrounding the assisted suicide advocacy of upper middle class white women by featuring a young, attractive white woman jumping for joy over the prospect of being able to die by physician assisted suicide. In response, assisted suicide opponents covered the advertisements with posters with the contact information for the UK’s largest suicide prevention organization, the Samaritans.

In my opinion, the act of putting suicide prevention posters over Dignity in Dying’s posh advertisements is the kind of nonviolent cvil disobedience we need more of. It was a powerful statement that the death with dignity movement does not own the cultural lexicon; that not everyone is willing to buy into the death with dignity movement’s rebranding of assisted suicide as “aid in dying.” It was an example of regular people ignoring the desires of the elite; it was a case of someone putting the interests of marginalized, struggling individuals ahead of young, privileged white women leaping in exultation at the prospect of getting to die with champagne in their hands. I think it was the kind of action that Diane Coleman would have been proud to imitate.

In a culture where the assisted suicide movement enjoys a great amount of power and prestige, assisted suicide opponents need to find creative ways of resisting its influence. Covering Dying with Dignity’s advertisements with suicide prevention posters did just that.

Friday, November 22, 2024

Honoring Diane Coleman. Founder of Not Dead Yet.

Alex Schadenberg
Executive Director, Euthanasia Prevention Coalition

Diane Coleman
I have written and published previous articles honoring Diane Coleman, the founder of Not Dead Yet. The most recent article was written by Clay Risen and published in the New York Times on November 20, 2024. 

Risen begins:

Diane Coleman, a fierce advocate for disability rights who took on Dr. Jack Kevorkian, the right-to-die movement and the U.S. health care system, which she charged was responsible for devaluing the lives of Americans like her with physical and mental impairments, died on Nov. 1 at her home in Rochester, N.Y. She was 71.

Her sister Catherine Morrison said the cause was sepsis.

Risen explains what Diane did before founding Not Dead Yet:

Ms. Coleman was born with muscular spinal atrophy, a disorder that affected her motor neurons. She was using a wheelchair by 11, and doctors expected her to die before adulthood.

Instead, she blossomed, graduating as valedictorian from her high school and receiving a joint J.D.-M.B.A. from the University of California, Los Angeles, in 1981.

It was only after several years of working as a consumer protection lawyer that she shifted her energies to disability rights, joining a flourishing movement that was pushing for anti-discrimination laws at every level of government, including improvements on transit and in buildings.

Ms. Coleman was a member of Adapt, considered one of the most militant disability rights groups.  She participated in scores of protests, blocking the entrances to buildings where conferences were held or government offices were housed.  She was arrested more than 25 times.

Risen explains why Diane focused on preventing assisted suicide:

In the 1990s, she shifted her attention yet again, to assisted suicide and the right-to-die movement. Though the movement was aimed at people with terminal illnesses, legislation in many states expanded to include people with significant disabilities.

Gifted with a dark sense of humor, in 1996 she founded a group called Not Dead Yet, a reference to a memorable scene in the movie “Monty Python and the Holy Grail” in which a man tries to pass off an infirm — but very much alive — relative to a man collecting dead bodies.

“To put it bluntly, she was blunt,” Jim Weisman, a disability rights lawyer, said in an interview.

Working on a shoestring budget, Ms. Coleman organized protests against right-to-die legislation, became a regular guest on television news programs and testified four times before Congress.

Diane explained why assisted suicide threatened people with disabilities:

At the core of her critique was the argument that the idea of a “right to die” was evidence of how little society valued people like her and a warning that the health care system was broken.

“It is already possible in some states for impoverished disabled, elderly and chronically ill people to get assistance to die,” she told the House Judiciary Committee in 1996, “but impossible for them to get shoes, eyeglasses and tooth repair.”

Diane challenged Peter Singer and Jack Kevorkian. Risen writes:

Not Dead Yet showed up at Princeton University in 1999 after the university announced the hiring of Peter Singer, an Australian philosopher who had argued for voluntary euthanasia for people with disabilities.

Never shy with a quote, Ms. Coleman told the British newspaper The Independent that Mr. Singer was “a public advocate of genocide, and the most dangerous man on earth.”

Her biggest target was Dr. Kevorkian, who became a household name in the 1990s and early 2000s for assisting patients in ending their lives. She sent protesters to his house outside Detroit, and she reveled in his 1999 conviction for second-degree murder after he helped a man with amyotrophic lateral sclerosis end his life.

“It’s the ultimate form of discrimination to offer people with disabilities help to die,” she told The New York Times in 2011, “without having offered real options to live.”

Risen finishes the article by recounting some of Diane's many accomplishments:

When she was 6, Diane was diagnosed with muscular dystrophy, which doctors later said was actually muscular spinal atrophy and would require surgery. The adoption agency told the Colemans that they could send her back. They declined.

Instead, they encouraged her to work hard in school and to attend college, at a time when many people with disabilities did not. She graduated with a degree in psychology from the University of Illinois in 1976, and she received law and business degrees from U.C.L.A. five years later.

She spent eight years working for the California Department of Corporations, where she focused on consumer fraud. She attended her first protest in 1985, against the lack of wheelchair lifts on Los Angeles buses, and she joined Adapt a year later.

In 1989, she moved to Nashville, where she developed plans for an independent living facility for people with disabilities. She continued that work after moving to Chicago in 1996, the same year she founded Not Dead Yet.

Ms. Coleman’s first marriage, to Michael Yester, ended in divorce. She later married Stephen Drake. Along with her sister Catherine, he survives her, as does another sister, Denise Coleman.

Ms. Coleman and Mr. Drake moved to Rochester in 2008, to be close to his family. By then the muscles controlling her breathing had begun to weaken, and she was using a ventilator. 

Still, she remained the chief executive of Not Dead Yet until her death, insisting that her fight was not just for people with disabilities but for everyone.

The disability community is the canary in the coal mine,” she told The Village Voice in 1996. “This assisted suicide-euthanasia issue is a test for our nation. If we as disabled, chronically ill or terminally ill people are declared better off dead, who will be next?”

More articles honoring Diane Coleman:

  • The Great Diane Coleman has died. She has left an amazing legacy (Link)
  •  Not Dead Yet comments on the passing of Diane Coleman (Link)

Wednesday, November 6, 2024

Not Dead Yet comments on the passing of Diane Coleman.

Dear Not Dead Yet Family, Allies, and Supporters,

Diane Coleman
It is with heavy hearts and deep sorrow that we announce the passing of our beloved founder and leader, Diane Coleman. Diane’s legacy as a tireless advocate for the rights of people with disabilities, and as a fierce and unyielding voice against assisted suicide and euthanasia, will forever shape our movement and the world we strive to change.

Diane founded Not Dead Yet in 1996, establishing a national disability rights organization committed to fighting for the inherent dignity of every person with a disability. Through her vision and leadership, Not Dead Yet grew into a powerful force for justice, protecting our right to live and ensuring that disabled lives are valued, respected, and protected from discriminatory medical practices, including the non provision and forced removal of life sustaining care, QALYs, and most of all, the inherently discriminatory public policy of assisted suicide and euthanasia law. Her work was visible not only in the courts, boardrooms and legislatures the halls of legislative chambers but also on the streets, where she led protests, organized, and mobilized countless other disabled people people with disabilities from across the globe to fight for their rights.

Diane was an intellectual powerhouse, a strategist, a passionate advocate, and a mentor to so many of us. Her understanding of policy, her commitment to the principles of the social and disability justice models of disability, and her ability to cut through the ableist rhetoric surrounding assisted suicide and euthanasia were unparalleled. She spoke with clarity and conviction, both in the media and in legislative hearings, where she presented testimony before Congress, co-authored amicus briefs in state, federal and Supreme Court cases for the U.S. Supreme Court, and tirelessly worked to ensure that the voices of disabled people were heard and respected in the development and implementation of public policy.

As many of you have shared, Diane's impact on individuals—colleagues, activists, students, and friends—was profound. She shaped the lives of so many, whether through direct mentorship or through the sheer force of her example. Diane was a leader who never wavered in her commitment to the movement. Her strength was, in many ways, a beacon for all of us who continue the fight for freedom, dignity, equality and inclusion of people with all kinds of disabilities, as well as women, elders, LGBTQ+, BIPoC and other marginalized populations.

Diane’s legacy will endure through all the work that continues in her name—through the Not Dead Yet community and through the work of every person whose life she touched. She built a movement that will not stop fighting, and she taught us to mourn for the dead and fight like hell for the living.

While we grieve her loss, we also celebrate her extraordinary life and the powerful mark she left on the world. Diane was a friend, a teacher, and a champion of justice. Her spirit, her intellect, and her fierce commitment to disability rights will live on in each of us who continue the work she began.

Our deepest condolences go out to Diane's family, her colleagues, and to all who loved her. We stand united in our grief, but also in our commitment to carry on Diane’s work. Rest in power, Diane. Your legacy is eternal, and the fight for the rights of disabled people will continue in your name.

With Love and Solidarity,

The Board of Not Dead Yet

Emily Wolinsky, Chair
Samantha Crane, Treasurer
Lydia Nunez Landry, Secretary
Horacio Esparza
Amy E. Hasbrouck
Germaine Martin
Michael Volkman