Declaration of Jeanette Hall 23 Years After She Was Talked Out of Assisted Suicide in Oregon

Jeanette with her son Scott, shortly
after she changed her mind

I, JEANETTE HALL, declare as follows:

1.  I live in Oregon where assisted suicide is legal. Our law was enacted in 1997 via a ballot measure that I voted for.

2.  In 2000, I was diagnosed with cancer and told that I had 6 months to a year to live. I knew that our law had passed, but I didn’t know exactly how to go about doing it. I tried to ask my doctor, Kenneth Stevens MD, but he didn’t really answer me. In hindsight, he was stalling me.

3.  I did not want to suffer. I wanted to do our law and I wanted Dr. Stevens to help me. Instead, he encouraged me to not give up and ultimately I decided to fight the cancer. I had both chemotherapy and radiation. I am happy to be alive!

Proposed Bill Renders Delaware Residents Sitting Ducks to Their Heirs and Other Predators

Attorney Margaret Dore, President of Choice is an Illusion, which has fought against assisted suicide and euthanasia legalization throughout the United States, and internationally, has issued the following statement regarding House Bill 140, still pending in the Delaware General Assembly. The proposed bill seeks to legalize assisted suicide, physician-assisted suicide and euthanasia, on both a voluntary and involuntary basis. The Act, deceptively titled End of Life Options, refers to these practices as medical aid in dying.

“Aid in Dying has been a euphemism for physician-assisted suicide and euthanasia since at least 1992," said Dore. “Per the American Medical Association, ‘physician-assisted suicide’ occurs when a doctor facilitates a patient’s death by providing the means or information to enable a patient to perform the life-ending act. ‘Euthanasia’ is the administration of a lethal agent by another person.”

Anita Cameron’s Powerful Statement At Maryland Press Conference

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.

John Kelly's Testimony Opposing Assisted Suicide in Minnesota

There is no way to contain eligibility to a narrow set of people. Especially when thousands of disabled Americans now live with conditions that in some states are seen as “worse than death.” Anorexia nervosa and diabetes can now qualify as terminal conditions. Once death is accepted as a positive outcome of medical care, it inevitably gets offered to more and more people.

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.

Alzheimer's Association Terminates Relationship with Compassion & Choices, fna the Hemlock Society

Interesting news from last year.

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.

This Is Where the Right to Die Leads Us

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.

Australia: Legalising Assisted Dying Has Led to More Suicide

The Anscombe Bioethics Centre Press Release, 9 January 2024

New research published in the Journal of Ethics in Mental Health has found that the introduction of Voluntary Assisted Dying (VAD) has failed to reduce the rate of unassisted suicide in the State of Victoria. 

In fact, since the law came into force, suicide among older people in Victoria has increased by more than 50%.

Florida Surgeon General Calls for Halt in Use of COVID mRNA Vaccines

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.

Anita Cameron: "My Mum Didn't Die"*

Good morning. I’m Anita Cameron, Director of Minority Outreach for Not Dead Yet, a national, grassroots disability organization opposed to medical discrimination, healthcare rationing, euthanasia and assisted suicide.

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!

Good News Worth Remembering

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."