What About Providing Aid in Living?

Yesterday, the New York State Assembly voted to pass legislation (A136/S138), the Medical Aid in Dying Act, to legalize state-sanctioned suicide [and euthanasia] for those diagnosed with a terminal illness. We strongly urge the New York State Senate to reject this legislation and we urge you to contact your state senators and ask them to vote against this legislation. Click here to contact your state senator.  

Proceeding down this path would be both a moral and practical failure, violating the sanctity of life and leading to a further erosion in the health and well-being of society’s most vulnerable.

New York Talking Points, Including Commentary by Dawn Eskew & Margaret Dore

Dear Angela & Senator Palumbo, 

In attachments are the talking points I referred to you in our conversation this morning. I can not stress enough to urge everyone on our side to stay clear away from bringing up religion, moral theology, prolife, and things like that.

The problem is the proposed Bill is a Bad Policy Bill, and the reasons pointed out should be our mantra.

One can be for the concept, but not these bills. (2025 #A136 & #S138).

I will be dropping off to your office , as discussed, our brochure which contains all of the short bullet points.

Most Sincerely, 

Dawn C . Eskew1.631.487.7578

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My friend Margaret Dore [pictured above], who is copied here, provided me with four publications, which may be of help.  Please see below.

1)

Margaret Dore Featured by Hope Australia

Vote No! on S. 136: New York Should Not Be Considering Assisted Suicide When So Many People Struggle to Live.

By Lisa Blumberg (pictured right)  and Not Dead Yet.

It is disturbing that at a time when the healthcare system is so broken and so many people struggle to get the care and practical support, they need that New York would want to try repeatedly pass legislation which would legalize doctor assisted suicide. The state has shown good judgment in rejecting the idea before and should reject it now.

The pandemic has made evident the deadly health care disparities that people of color, older people and persons with disabilities have always been subjected to. Any law which enables doctors to write lethal prescriptions at the request of people deemed to have six months or less to live, as this bill would, increases risk for devalued patients.

Despite common misconceptions, uncontrollable pain is not a primary reason that people turn to assisted suicide. Data indicates that people often request lethal prescriptions due to perceived lessening of autonomy, or feelings of being burden. As Cliff Perez, a disability rights activist, states, “these reasons are… existential or disability related and ought to be addressed with quality, multidisciplinary care, not death.” It is not so much how individuals view living with limitations caused by illness or disability, but society’s stigma and failure to provide practical supports to address such limitations.

New York Times: Diane Coleman has Died

https://www.nytimes.com/2024/11/20/us/diane-coleman-dead.html?smid=url-share

By Clay Risen, published 11/20/2024, updated 11/22/24  

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. [Diane pictured right with sign stating "freedom rider"]

Her sister Catherine Morrison said the cause was sepsis.

Ms. Coleman was born with spinal muscular 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.

Judicial Watch Sues New York State for Records on Controversial Killing of ‘Peanut the Squirrel’ and ‘Fred the Raccoon’

(Washington, DC) – Judicial Watch announced today that it filed a Freedom of Information Law (FOIL) lawsuit against the New York State Department of Environmental Conservation for records about the seizure, testing and euthanizing of a squirrel named “Peanut” and a raccoon named “Fred” belonging to Pine City, New York, resident Mark Longo (Judicial Watch Inc. v Sean Mahar, Interim Commissioner, New York State Department of Environmental Conservation (No. 902596-25)). 

Judicial Watch filed suit in the Supreme Court of the State of New York, Albany County, after the Department of Environmental Conservation failed to comply with two FOIL requests for written and video records related to Peanut and Fred. The first, filed on November 6, 2024, seeks: