Assisted Suicide and Euthanasia Will Be Practiced Through the Prism of Social Inequality and Bias

  

By Kathryn Lopez

When Gov. Andrew Cuomo’s father, Mario, was governor, the New York State Task Force on Life & the Law released a report in 1994 unanimously rejecting assisted suicide, and cautioned: “No matter how carefully any guidelines are framed, assisted suicide and euthanasia will be practiced through the prism of social inequality and bias that characterizes the delivery of services in all segments of society, including health care. The practices will pose the greatest risks to those who are poor, elderly..." 

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Bevelyn Beatty in NYC: "Take Your Country Back"

Watch video here

Slow Euthanasia: No One to Blame for Andrew Cuomo Putting 6,000+ Coronavirus Patients in Nursing Homes

https://www.frontpagemag.com/point/2020/07/cuomo-no-one-blame-me-putting-6000-coronavirus-daniel-greenfield/

by Daniel Greenfield

"Hi Bob, got a question for you."

"Yes, Andy."

"How many thousands of nursing home patients can you kill before it impedes your presidential chances?"

Dore Bio

Margaret Dore is a fourth generation lawyer in Washington State USA. Her father was a lawyer and a Democratic politician who ultimately served as Chief Justice of the Washington State Supreme Court. Her mother was a politician’s wife and a political activist in her own right, best known for her work to raise awareness about Sudden Infant Death Syndrome (SIDS), and also to help affected families and to promote medical research. Growing up, other families went camping. Dore’s family went campaigning.

Press Release Opposing New York Act

To view as sent, click here.

Attorney Margaret Dore, president of Choice is an Illusion, a nonprofit corporation opposed to assisted suicide and euthanasia, made the following statement in connection with the Medical Aid in Dying Act, now pending before the New York State Legislature. (Bills A 2694 and S 3947).

“The Medical Aid in Dying Act is a recipe for elder abuse, financial exploitation and legal murder," said Dore. "Older people with money, meaning the middle class and above, will be especially at risk to their heirs and other financial predators." Dore added, "The poor will also be at risk, but for a different reason.”

Reject Medical Aid in Dying Act (Assisted Suicide and Euthanasia)

By Margaret Dore, Esq., MBA

Click the links to view a pdf version of this document, consisting of a memorandum and appendix.

I. INTRODUCTION 

The proposed bills amend New York’s public health law by  adding a new article (28F), the Medical Aid in Dying Act.[1] The Act is based on similar laws in Oregon and Washington State.[2]

“Aid in Dying” is a euphemism for euthanasia.[3] The Act, however, purports to prohibit euthanasia. On close examination, this prohibition will be unenforceable.

If enacted, the Act will apply to people with years or decades to live. It will also facilitate financial exploitation, especially in the inheritance context. Don’t render yourself or someone you care about a sitting duck to heirs and other predators. I urge you to reject the proposed Act.

Join Us in Albany on January 14th

Event to be live streamed
To link, click here.

     

John Norton: A Cautionary Tale

Hearing Room

By Margaret Dore, Esq., MBA

In March 2012, I watched Massachusetts resident, John Norton, testify before the Joint Judiciary Committee of the Massachusetts Legislature. A person with ALS, he had been told at age 18 or 19 that he would die in three to five years from paralysis. Below find his story, at age 74, as submitted to a Canadian court via this affidavit: 

AFFIDAVIT OF JOHN NORTON IN OPPOSITION TO

ASSISTED SUICIDE AND EUTHANASIA

THE UNDERSIGNED, being first duly sworn on oath, STATES:

1. I live in Florence Massachusetts USA. When I was eighteen years old and in my first year of college, I was diagnosed with Amyotrophic Lateral Sclerosis (ALS) by the University of Iowa Medical School. ALS is commonly referred to as Lou Gehrig’s disease. I was told that I would get progressively worse (be paralyzed) and die in three to five years.

2. I was a very physical person. The diagnosis was devastating to me. I had played football in high school and was extremely active riding bicycles. I also performed heavy labor including road construction and farm work. I prided myself for my physical strength, especially in my hands.

3. The ALS diagnosis was confirmed by the Mayo Clinic in Rochester Minnesota. I was eighteen or nineteen years old at the time. By then, I had twitching in both hands, which were also getting weaker. At some point, I lost the ability to grip in my hands. I became depressed and was treated for my depression. If instead, I had been told that my depression was rational and that I should take an easy way out with a doctor’s prescription and support, I would have taken that opportunity.