Memo Opposing NY Bills A. 10059 and S. 7579

https://choiceisanillusion.files.wordpress.com/2016/06/ny-memo-05-31-16_001.pdf  

By Margaret Dore, Esq., MBA

I. INTRODUCTION  

I am a lawyer in Washington State where physician-assisted suicide and euthanasia are legal.[1] Our law is based on a similar law in Oregon.  Both laws are similar to the proposed bills, A. 10059 and S. 7579.[2]

The bills are titled “Medical Aid in Dying.”  There is, however, no requirement that patients be dying. “Eligible” patients may have years, even decades, to live. The bills are also sold as a promotion of patient choice and control. The bills are instead stacked against the patient and a recipe for elder abuse. Finally, the bills are deceptively written; they are not what they appear to be. I urge you to vote “No.”

John Norton: A Cautionary Tale

By Margaret Dore

In March 2012, I watched John Norton testify before the Joint Judiciary Committee of the Massachusetts Legislature.  A person with ALS, he had been told at age 18 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
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.

4. Six years after my initial diagnosis, the disease progression stopped. Today, my condition is about the same. I still can’t grip with my hands. Sometimes I need special help. But, I have a wonderful life. I am married to Susan. We have three children and one grandchild. I have a degree in Psychology and one year of graduate school. I am a retired bus driver (no gripping required). Prior to driving bus, I worked as a parole and probation officer. When I was much younger, I drove a school bus. We have wonderful friends. I enjoy singing tenor in amateur choruses. I help other people by working as a volunteer driver.

5. I will be 75 years old this coming September. If assisted suicide or euthanasia had been available to me in the 1950's, I would have missed the bulk of my life and my life yet to come. I hope that Canada does not legalize these practices.

Not Everyone Will Have the Support I Had

Dear Editor:
      

Terrie Lincoln

I am a 32 year old quadriplegic who works as a “Systems Advocate” in Rochester, New York. I am a college graduate and currently working on my Masters’ degree. I was disturbed to see Joel Marks’ forum piece, advocating for legalized assisted suicide.  (“Extending life no favor for some”).
        
When I was 19 years old, I was in an automobile accident, which led to my becoming disabled. I subsequently found myself in two different hospitals, where two different sets of doctors repeatedly and sometimes daily pressured my parents and later me directly, to agree to ending my life.  Fortunately, my mother was a strong advocate and refused to listen. Once I was better and recuperated, I was also a strong advocate for myself which helped me to advocate for others. Had we faltered, I would have missed out on some of the best years of my life.
        
Legalizing assisted suicide will expand the ability of doctors to legally kill their patients and/or pressure patients to kill themselves. With the “option” of assisted suicide, family members and others who might benefit from a death will be similarly empowered. Not everyone will have the support that I had. Our most vulnerable citizens will be at risk.

Terrie Lincoln