By Diane Coleman
On February 8, the Maryland Senate's Judicial Proceedings Committee held a public hearing on a proposed assisted suicide bill (SB0443). That morning prior to the hearing, the Patients Rights Action Fund organized a press conference of opponents. Anita Cameron represented Not Dead Yet and made the following compelling arguments against the bill:
I'm Anita Cameron, Director of Minority Outreach for Not Dead Yet, a national disability organization opposed to medical discrimination, healthcare rationing, euthanasia and assisted suicide.
SB 0443 will put sick people, seniors and disabled people, especially, at risk due to the view of doctors that disabled people have a lower quality of life, therefore leading them to devalue our lives.
The problem for us disabled people is that we are already treated badly in the medical system. As medicine has focused increasingly on patient “quality-of-life” as a barometer of life-worthiness, death has been re-characterized as a benefit to an ill or disabled individual. Most physicians (82%, a 2020 Harvard study found) view our “quality-of-life” as worse than non-disabled people.
In an effort to provide information and resources about Alzheimer’s disease, the Alzheimer’s Association entered into an agreement to provide education and awareness information to Compassion & Choices, but failed to do appropriate due diligence. Their values are inconsistent with those of the Association. We deeply regret our mistake, have begun the termination of the relationship, and apologize to all of the families we support who were hurt or disappointed. Additionally, we are reviewing our process for all agreements including those that are focused on the sharing of educational information.
By Alex Schadenberg*
Spiked published an in-depth article by Lauren Smith on January 15, 2024 titled: "Canada has revealed the horror of assisted dying." Smith tells the stories of the many people who have felt forced into considering death by euthanasia.
Smith sets the stage for her article by calling Canada's euthanasia law a gruesome, state-sanctioned industry. Smith states:
There is nothing remotely civilized about Canada’s medical assistance in dying (MAID) programme. Assisted dying in Canada was initially considered a last resort for terminally ill patients suffering from incurable pain. But in the space of just a few years, euthanasia has been made available to pretty much anyone who is struggling with an illness or a disability. Even Canadians facing homelessness and poverty are feeling compelled to end their lives, rather than ‘burden’ the authorities.
Tallahassee, Fla. — On December 6, 2023, Surgeon General Dr. Joseph A. Ladapo sent a letter to the United States Food and Drug Administration (FDA) Commissioner Dr. Robert M. Califf and Center for Disease Control and Prevention (CDC) Director Dr. Mandy Cohen.
Ladapo outlined concerns regarding contaminants in the approved Pfizer and Moderna COVID-19 mRNA vaccines ... Ladapo also stated: "Providers concerned about patient health risks associated with COVID-19 should prioritize patient access to non-mRNA COVID-19 vaccines and treatment. It is my hope that, in regard to COVID-19, the FDA will one day seriously consider its regulatory responsibility to protect human health, including the integrity of the human genome."
For more information about the Florida Department of Health, visit www.FloridaHealth.gov.
Assisted suicide laws are dangerous because though these laws are supposed to be for people with six months or less to live, doctors are often wrong about a terminal diagnosis. In 2009, while living in Washington state, my mother was determined to be at the end stage of chronic obstructive pulmonary disease. I was told her death was imminent, that if I wanted to see her alive, I should get there in two days. She rallied, but was still quite ill, so she was placed in hospice. Her doctor said that her body had begun the process of dying.
Though she survived 6 months of hospice, her doctor convinced her that her body was still in the process of dying, and she moved home to Colorado to die.
My mum didn’t die. In fact, six weeks after returning to Colorado, she and I were arrested together in Washington, DC, fighting for disability justice. She became active in her community and lived almost 12 years!
By Margaret Dore, Esq.
In 2010, Kathryn Tucker, Director of Legal Affairs for Compassion & Choices, published an article in the Idaho Bar Association magazine, The Advocate. The article referred to assisted suicide and euthanasia as “aid in dying,” which Tucker claimed was legal in Idaho.
The reaction to Tucker's claim was swift and brutal. In the next issue of The Advocate, there were nine letters against her. The writers included a former Chief Justice of the Idaho Supreme Court, Robert E. Bakes, who characterized her article as a “gross misunderstanding of Idaho law.” Another writer termed the article "malarkey."
Delaware’s assisted suicide bill is based on legislation in Oregon, where assisted suicide was first legalized. Data from Oregon provides insight into the top reasons that patients ask for assisted suicide. The top five reasons that people gave were the loss of autonomy, being unable to participate in activities that make life enjoyable, loss of dignity, loss of bodily functions and becoming a burden on family, friends and caregivers. These reasons are all disability-related. Contrary to popular belief, pain does not even make it into the top reasons people give to justify their application for assisted suicide.
An increase in deaths among younger people last year was attributable in part to deaths under investigation by a coroner or medical examiner, which typically include suicides, homicides and drug toxicity deaths.Further to that, the Canadian Press reported:
New Brunswick saw the biggest decline in life expectancy among provinces, dropping more than a year to 79.8 years from 80.9 in 2021, the report said. Saskatchewan's life expectancy has fallen the most over the past three years combined, dropping a full two years to 78.5 in 2022 from 80.5 in 2019. Prince Edward Island was not included in the yearly data breakdowns by province.Health Columnist Andre Picard was published by the Globe and Mail on December 5 as stating:
A one-year loss in life expectancy may not seem like a big deal, but it is. It’s only the second time this sharp a drop has happened in Canada in the past century. In fact, life expectancy has been climbing steadily for decades: 71 in 1960, 75 in 1980, 79 in 2000, and 82.3 in 2019. Life expectancy is an oft-misunderstood measure. It’s not so much a prediction of how long an individual can expect to live, but rather a crude measure of a country’s health, the only real measure of overall population health we have.To read Schadenberg's article as originally published, please click here: https://alexschadenberg.blogspot.com/2023/12/canadians-life-expectancy-drops-three.html
By Margaret K. Dore, Esq.
Here, the proposed Act’s title is: “The Ron Silverio/Heather Block End of Life Options Law." The title thereby implies that the Act is "optional," meaning "left to one's choice."
On close examination, however, the Act has no enforcement mechanism to ensure that the Act is voluntary. Involuntary and non-voluntary death are allowed via the Act.
The Act, as proposed, is therefore unconstitutional. The Act cannot be legally enacted via its present title.
On June 6, 2023, attorney Margaret Dore filed an amicus brief in the Supreme Court of New Jersey, seeking to overturn Petro v Platkin, 472 N.J. Super. 536, 277 A.3d 480 (2022). Dore's brief also supports the petitioners, including Dr. Joseph Glassman, MD, pictured here.
Dore and the petitioners seek to overturn New Jersey's Medical Aid in Dying for the Terminally Ill Act, as unconstitutional. The Act legalized aid in dying, previously known as assisted suicide, physician-assisted suicide and euthanasia.
The Act allows these practices on both a voluntary and involuntary basis. The Supreme Court has not ruled as to whether it will take the case. The case was previously titled Glassman v. Grewal and also Petro v Grewal.
https://www.thegatewaypundit.c
Amicus Curiae Margaret Dore, who argued the cause below in Petro v. Platkin, 472 N.J. Super. 536, 277 A.3d 480 (2022), seeks to overturn the Medical Aid in Dying for the Terminally Ill Act as unconstitutional.
The case was initially filed as Glassman v. Grewel, then renamed Petro v. Grewel, and then renamed Petro v. Platkin. This brief is submitted in support of the petitioners: Dr. Joseph Glassman, MD; Manish Pujara, a licensed pharmacist; and Anthony Petro, a patient.
The Act’s findings describe the Act as “entirely voluntary.” There is, however, no enforcement mechanism to make this so. Deaths per the Act are allowed to occur in private, without a witness or even a doctor present....
Although we recognize the paramount importance and profound significance of all end-of-life decisions, after careful consideration, we conclude that the Massachusetts Declaration of Rights does not reach so far as to protect physician-assisted suicide.3 We conclude as well that the law of manslaughter may prohibit physician-assisted suicide, and does so, without offending constitutional protections.
By Margaret Dore, Esq.
This document is a shorter and more formal version of my presentation at the Caring About Everyone Conference in Hartford Connecticut, on October 15, 2022. The conference was generously sponsored by the Euthanasia Prevention Coalition and the Family Institute of Connecticut.I am an attorney licensed to practice law in Washington State. I have been working against assisted suicide and euthanasia since 2008. I am also president of Choice is an Illusion and the Foundation for Choice is an Illusion.
.jpg)
By Margaret Dore
Zena loved to make friends with the people who came to Annie’s office. Sometimes they brought her treats. She made friends [with me] at the local Starbucks, meaning more treats. She reached out to a lonely woman at the bank, making the woman’s day.
Yesterday, I submitted a formal legal analysis detailing problems with the proposed Act, that it is not what it's sold to be.
I also encourage you to look at my website, which has an online version of my analysis, which can be viewed here.
In 2011, I met a beautiful blonde woman at a Euthanasia Prevention Coalition Conference in Vancouver BC Canada. To me, she looked like a movie star. She was in fact a jazz singer and also a teacher.
We talked and she explained that her mother had been starved and dehydrated to death in a Canadian long-term care home. She also told me that she had published an article about her experience and agreed to let me republish the article on the Choice in an Illusion website.[1] We also became friends.
In April 2013, Alex Schadenberg, head of the Euthanasia Prevention Coalition, wrote Kate regarding the impact of her republished article:
I want you to know that I had a meeting with a head nurse at a local nursing home today who was converted by your article about your mom's death.
She cried and cried . . . she is trying to change her nursing home.
To read a pdf version, click here.
I. INTRODUCTION
The proposed Connecticut Act, Raised Bill No. 88, seeks to legalize physician-assisted suicide and euthanasia as those terms are traditionally defined.[2] This will be on both a voluntary and involuntary basis.
The Act is based on similar acts in Oregon and Washington State. I urge you to protect yourselves and the people you care about. Vote “No” to reject Raised Bill No. 88.