The Plain Dealer and cleveland.com explore the U.S. model of Medical Aid in Dying (MAID) throughout 2026 in its End of Life Ohio Series. Read the articles below.

If you would like to share your experiences and thoughts, please email Mary Frances McGowan at mmcgowan@cleveland.com.

‘It just got too complicated’: Ohioans face steep barriers seeking medical aid in dying out of state

March 22, 2026

By Mary Frances McGowan

CLEVELAND, Ohio — Terminally ill Ohioans who want to decide when life should end have few options, with just two states on opposite coasts offering a legal path for nonresidents to access medical aid in dying: Oregon and Vermont.

On paper, the opportunity for patients and caregivers to avoid prolonged suffering by taking a trip out of state seems straightforward. But Ohioans who have taken on the challenge often find that the actual process is filled with financial and logistical obstacles that can end in frustration.
 
That was Liz Madigan’s experience. She helped her terminally ill sister, Pat Knippen, research traveling to Oregon — but Pat died before they could make the trip.
 

“She wanted the choice,” Madigan, a former hospice nurse from Concord, said. “And you know, the fact that we had to think about taking her either to one coast or the other to have that option … it just hurt.”

Dana Hollister of Chagrin Falls expressed similar frustration. She and her husband, David, investigated traveling to Vermont after he was diagnosed with ALS. Ultimately, they were forced to give up as David’s health began to decline.

“It just got too complicated,” Hollister said.

Ohio doesn’t allow medical aid in dying — a process to allow a terminally ill, mentally competent adult to hasten their death by taking a lethal dose of medication prescribed by a physician.
 
Advocates say it is a process that allows terminally ill patients to die with dignity on their own terms. Twelve states and the District of Columbia have enacted laws allowing it. In Montana, medical aid in dying is permitted through a court ruling.
 
Opponents fear that despite safeguards, the process clashes with the medical principle of “do no harm.” Some argue against the idea based on religious convictions.

But even in states where it is available for nonresidents, navigating complex medical logistics in a new place and doing that before the body becomes too weak is often too big of a burden.

Universal guardrails

In every jurisdiction where medical aid in dying is legal, patients must meet the same basic eligibility standards. They must be adults with a terminal illness and a prognosis of six months or less to live, mentally capable of making their own medical decisions and physically able to self-administer the medication.
 
State laws also include safeguards designed to prevent abuse or coercion. Only the patient may request the medication, and eligibility must be confirmed by both the patient’s attending physician and a second independent clinician. Both Oregon and Vermont require both medical professionals to be licensed physicians.
 
Patients are required to make multiple oral requests to their physician, separated by mandatory waiting periods that vary by state, as well as a formal written request that must be witnessed to ensure the decision is voluntary. In most states, patients must also be residents, a requirement Oregon and Vermont eliminated in 2023.
 
Out-of-state challenges
 
For Ohioans seeking medical aid in dying in Oregon or Vermont, the first, and most difficult task is often finding physicians willing to work with an out‑of‑state patient.
 
Neither state provides lists of participating providers, leaving patients and caregivers to navigate what one advocate described as a medical “black box.” While nonprofit organizations can offer guidance, securing even an initial appointment can take months.
 
“Physicians are happy, we know, just anecdotally, to support their own patients. But when it comes to supporting people that they’re meeting for the first time for a medical aid in dying request, there are far fewer that feel that they have the capacity in their practice to take that on,” said Amy Bruce, executive director of Patient Choices Vermont,
 
This is especially true in Vermont, which has fewer than 650,000 residents and a shortage of physicians. Nurse practitioners help fill in the gaps for local healthcare, especially in more rural parts of the state. But they are not allowed to prescribe medical aid in dying medications in Vermont or serve as the consulting physician.

“Getting that connection to find a physician to talk to you — that’s the biggest stumbling block,” Bruce said.

After physicians are identified, patients must complete all required evaluations while physically present in the destination state. Medical records must be transferred from Ohio, and appointments often need to be
 
Patients must make two oral requests to a prescribing physician, generally at least 15 days apart, and complete a separate evaluation with an independent consulting physician. A witnessed written request for medication by two individuals is also required.
 
The process, which could take weeks and even months, means patients
and families face either repeated long-distance trips or extended stays as they remain in Oregon or Vermont.
 
Once a prescription is filled, patients must take the life-ending medication while still in that state. That requires finding accommodations where people are aware of the situation and will allow an individual to die on premises.
 
Patients who die out of state must also make advanced arrangements for what happens with their remains and any final arrangements or services.
 
Timing is everything
 
Those realities can thwart patients, and their families, from attempting to venture to a state where they can die on their own terms.
 
In 2022, Pat Knippen — a Wapakoneta native, mother of triplets and lifelong public servant who dedicated her career to vulnerable children and families – noticed that her legs were shaking. Her primary care doctor referred her to a neurologist that kicked off a long and difficult road to be diagnosed with Multiple System Atrophy, a rare and progressive neurodegenerative disease with no treatment.
 
Eighteen months before Pat died, Madigan, her sister, raised the possibility of traveling for medical aid in dying. Pat said she was interested and the family began doing research. They decided that Oregon would be the best fit for them.
 
While she knew that it would be a significant undertaking, Madigan said she was surprised by some of the practical challenges – including finding accommodations in Oregon that would be willing to have a patient die on premises.
 
In the midst of planning, Pat’s health began to seriously decline – so much so that Madigan feared that she would no longer be eligible for medical aid in dying, as patients must be able to self-administer the medication.

Ultimately, Pat was placed in hospice care in Ohio before she and her family could make the trip to Oregon. She died two days later, in March 2025.

Even though they had months of planning, Madigan said she realized later that it is important to start the process early.
 
“It made me realize that you can’t wait on this,” Madigan said.
 
Dana Hollister watched similar events unfold at the end of her husband David’s life.
 
When David, a commercial real estate broker from Chagrin Falls, was diagnosed with ALS, he made it clear immediately that he did not intend to die from the fatal neurodegenerative disease, Hollister said.
 
“I knew what he meant,” Hollister said. “He wanted to end his life before that disease got him.”
 
David began researching medical aid in dying and became a passionate advocate for it — even penning
 
David eventually settled on Vermont – he talked to experts there, found places that he was interested in staying at, and understood what the process required.
 
Questions arose, though, as the pair pondered the logistics of not only traveling to Vermont, but whether to stay there or return to Ohio during the waiting periods as David’s health would continue to decline.
 
David was able to get in and out of his wheelchair and bed when they began their research. But as time progressed, he was unable to do either without the help of equipment. Transporting those supplies to Vermont became another complicating factor.
 
David was also in so much pain that he couldn’t tolerate even a short ride in a car, let alone more than 500 miles to Vermont.
Eventually, it became clear that the trip would be too difficult for David.
 
“When we realized we can’t do Vermont … he gave up,” Hollister said. “He just, everything just turned.”
David became depressed. About a month later, he stopped eating, and “willed himself to give up,” she said. He died in September.
“I don’t know if he had the option to do it in Ohio, if he would have lived longer,” Hollister said. “I’m not 100% sure, but I know he wanted out so badly. He wanted out.”
 
No option in Ohio
 

Legislation to allow medical aid in dying was introduced in 2018 in Ohio, but it went nowhere. There are no current proposals pending in the General Assembly.

Opponents often cite religious objections or fears that these laws are a “slippery slope,” that could be further expanded.

For those who have watched their loved ones suffer, allowing medical aid in dying is all about finding autonomy and comfort in a terminally ill patient’s final moments.
 
David urged lawmakers in Columbus to pass a law in Ohio in his opinion piece, which was published just one day before he died. In it he talked about dying on his terms.

March 1, 2026

 

With more than a dozen states having such laws, The Plain Dealer/cleveland.com is seeking to broaden understanding and gauge public views of what such a law might mean if adopted in Ohio.

With more than a dozen states having such laws, The Plain Dealer/cleveland.com is seeking to broaden understanding and gauge public views of what such a law might mean if adopted in Ohio.

As reporter Mary Frances McGowan noted in a recent story, “The question is one of the most personal in modern health policy: Should a mentally competent, terminally ill person be allowed — with state approval and medical oversight — to choose the timing of their death?”

But as McGowan also reported, opposition to the idea is fervent, with opponents calling it “physician-assisted suicide,” and many religious leaders strongly opposed to what amounts to an individual deciding to take their own life with the help of pills provided by a doctor.

A 2018 attempt in Ohio to legalize such a decision by a mentally competent, terminally ill patient never made it out of committee.

So how do members of our Editorial Board Roundtable view this possibility now?

Thomas Suddes, editorial writer:

No — absolutely not. True, the plan would require conscious, articulate consent by a dying person, and oversight by a physician, but the dangers of even implicit coercion by potential survivors could still factor into a patient’s decisions. And ascertaining a dying patient’s state of mind — as to intentions — may be nearly impossible. What Ohio must instead do is offer all Ohioans top-line end-of-life care, and full availability of palliative drugs.

[Ohio End of Life Options response on Facebook:

Believe it or not, we welcome this comment. Why? Because there are so many learning opportunities.

  1. We 100% agree that there should be full and robust funding for high-quality hospice and palliative care. Aid in Dying is a compatible end-of-life option.
  2. Over 80% of people who use the U.S. Model of MAID are enrolled in hospice at the time. Patients want the best quality of life for as long as possible (hospice/palliative care) AND the option of a peaceful, planned death (MAID).
  3. Only the patient may request medication, AND they must be able to self-ingest.
  4. Two different physicians would determine healthcare decision-making capacity of the requesting patient. This is something that is done everyday in America.]

 

Ted Diadiun, columnist:

My religious, spiritual and personal beliefs all scream against this, and I cannot imagine ever taking part on any level. But I have trouble arguing that it should be illegal for a person who draws different conclusions to make a different decision. This is a situation where “my body, my choice” applies. It’s different from abortion: The life you end is your own only. It should be up to you.

[Ohio End of Life Options response on Facebook:

Ohio End of Life Options respects the faith traditions of every citizen. The U.S. Model of Aid in Dying is 100% voluntary and patient-directed.

Each eligible patient deserves the freedom to make the decision that best aligns with their personal values and beliefs. Thank you, Mr. Diadiun, for being true to yourself and realizing that others hold different beliefs.]

 

Eric Foster, columnist:

No one questions the availability of health care directives, documents in which people can choose to decline medical treatment that could keep them alive. I don’t see a law allowing someone to choose medical treatment that would end his or her life as an entirely different thing. People should have that choice. Frankly, I don’t see it as my business to deny them that. Live and let live. Or die.

Lisa Garvin, editorial board member:

Extending the life of terminally ill patients wreaks an enormous emotional and financial toll. Why wouldn’t people want to spare their loved ones that burden and pass with dignity on their own terms? And why do some doctors insist on continued treatment of terminal patients, knowing that it’s futile? Medical aid in dying is a compassionate extension of the do-not-resuscitate order that allows us to refuse life-saving treatment.

Victor Ruiz, editorial board member:

Some people feel the need to control every part of human life, from forcing births, to policing how people live, to insisting that a terminally ill person must suffer through their final days. To me, that is cruel. If someone is competent, they should be able to choose dignity over pain. We should be fighting for quality of life for everyone, including health care that supports a good life and a good end.

Mary Cay Doherty, editorial board member:

The American Medical Association rightly opposes physician-assisted suicide and refuses to use the misleading “medical aid in dying” euphemism. While these laws purport to compassionately hasten death and preserve dignity for the terminally ill, they undermine and imperil the right to life for everyone. It’s a slippery slope from terminally ill patients “choosing” death to a culture of death where the right to life hinges on age, ability, and health.

[Ohio End of Life Options response on Facebook:

There is a lot to unpack here. Please be respectful to Ms. Doherty in the comment section. Everyone is entitled to their own opinion.
 
Our goal is to educate. Here is some information to help you respond when discussing Aid in Dying in the community.
 
Let’s start with the AMA. It is sometimes viewed as paternalistic in its thinking related to the patient-physician relationship. Many younger physicians have worked to try to encourage the AMA to adopt an “engaged neutral” stance and to use language that is used in all U.S. state laws and healthcare and public policy – Medical Aid in Dying. We encourage the AMA will adopt an “engaged neutral” stance at its next national meeting.
 
Some would argue that MAID is a “euphemism,” but language in healthcare evolves. We would counter that “physician-assisted suicide” inadvertently serves to stigmatize and shame terminally ill people and equate suicide with MAID, which is inaccurate and does not benefit genuine suicide prevention efforts or compassionately support terminally ill patients and their families.
 
Patients who consider MAID want to live, but they have a disease that will end their life.
 
As to the “slippery slope.” The term “slippery slope” is commonly used in pop culture, but it is a fallacy as it relies on fearmongering and exaggerated consequences. Medical advances such as anaesthesia during childbirth were once seen as “unchristian” as it removed the pain of labor, which would then lead to moral decay. Blood transfusions were also vilified as unnatural, with fears that transferring blood between people would mix souls, temperaments, or lead to risky, “unholy” practices.” (MDLinx). U.S. Aid in Dying laws are the strictest in the world and include robust safeguards for patients and providers.
 
Lastly, Ms. Doherty expresses concerns that “choosing” death will lead to a “culture of death” where vulnerable populations will be forced to die. The U.S. data and personal stories prove otherwise. The U.S. Model is available only to terminally ill adults with decision-making capacity. All U.S. state laws include a multi-step eligibility process and allow opt-outs for healthcare providers and systems.
 
All terminally ill people are asking is that they not be forced to suffer against their wishes. We do a disservice to those dying in America when we don’t allow or encourage people to talk about their end-of-life wishes.]

February 22, 2026

by Mary Frances McGowan, mmcgowan@cleveland.com

In a growing number of states, terminally ill patients now have a legal option that would have been unthinkable to many Americans a generation ago: a doctor’s prescription that allows them to end their own life.

The question is one of the most personal in modern health policy: Should a mentally competent, terminally ill person be allowed — with state approval and medical oversight — to choose the timing of their death?

Supporters call it “medical aid in dying,” a last-resort option for those facing unbearable suffering. Opponents call it physician-assisted suicide and warn it could put vulnerable people at risk.

The debate is accelerating — and it’s reaching closer to Ohio.

Cleveland.com and The Plain Dealer will publish a continuing series involving the multitude of issues involving end-of-life decisions, including hospice care, the costs of care for the terminally ill, ethics, legal issues and more.

If you’ve experienced these issues in your family and are willing to discuss your experiences and thoughts, please email Mary Frances McGowan at mmcgowan@cleveland.com.

More than a dozen states have adopted “death with dignity” laws, all with strict regulations. Last year, Illinois became the first Midwestern state to legalize the practice. Most recently was New York, where a law was signed this month.

The laws are an effort toward allowing a patient to choose when they die instead of prolonging a time of anguish and agony for themselves and their families.

A leading advocate in Ohio says she hears that story every day.

“You hear the same thing over and over. ‘I just wanted them not to suffer, and I wanted them to feel like they had a sense of control if that’s what they wanted,’” said Lisa Vigil Schattinger, the founder of Ohio End of Life Options.

When some Ohio lawmakers proposed legislation in 2018, a Public Policy Polling survey found 87% of Ohio voters either strongly support (71%) or somewhat support (16%) giving terminally ill patients the right to control the end of their lives and should be allowed to die in as humane and dignified a manner as they see fit. This was true across political party lines.

But opponents fear that despite safeguards, the process clashes with the medical principle of “do no harm” and that vulnerable people could still slip through the cracks.

“The guardrails (for medical aid in dying) are absolutely well intentioned. … But I just think there are so many vulnerabilities,” says Dr. Jason Kolb, an assistant professor of clinical emergency medicine at Northeast Ohio Medical University and member of the organization No Suicide Ohio.

“The guardrails are absolutely well intentioned. … But I just think there are so many vulnerabilities,” said Dr. Jason Kolb, an assistant professor of clinical emergency medicine at Northeast Ohio Medical University, and member of the organization No Suicide Ohio.

ORIGINS AND PARTICIPANTS

Medical aid in dying is the legal pathway to allow a terminally ill, mentally competent adult to hasten their death by taking a lethal dose of medication prescribed by a physician.

Medical aid in dying is often confused with euthanasia, but the two are fundamentally different. Active euthanasia is illegal in all 50 states and involves a physician taking a direct role in ending a patient’s life through lethal injection. Medical aid in dying, by contrast, is a patient-led process in which an individual must ingest the medication themselves.

“Physician assisted suicide,” is the preferred terminology of the American Medical Association, which has long opposed the practice. However, jurisdictions where the option exists do not legally consider it suicide.

Oregon became the first state to offer medical aid in dying nearly three decades ago with its Death with Dignity Act in 1997. Now there are similar laws in 13 states and the District of Columbia.

Legislation is also pending in several other states. But Ohio doesn’t have a similar law, and there is no legislation pending in the General Assembly.

In states where the option is available, individuals who use medical aid in dying skew older. A 2022 Rutgers University study found that of 5,329 patients from across the country who died with the help of medical aid, 60% were ages 65 to 84. Another 16% were older than 85. Just 8% were 54 years old or younger.

Men outnumbered women 53% to 47%. More than 72% of the patients had at least some college education. More than 95% were non-Hispanic whites, and nearly 75% had cancer.

“I definitely see it expanding, and I would love to see Ohio push back in a really productive, healthy way to say, end of life suffering is a real problem. Physician assisted suicide is the wrong solution.”

Dr. Jason Kolb, who became paralyzed from the waist down in a skiing accident years ago

STATE RULES AND LIMITATIONS

State laws have some variations — including differing waiting periods and residency requirements —the parameters that qualify patients for medical aid in dying are consistent. Patients must be adults who are terminally ill with a prognosis of six months or less to live. Those conditions mirror those needed to qualify for hospice care. In fact, a large majority of patients who use medical aid in dying are simultaneously enrolled in hospice care.

Patients must be deemed mentally capable of making their own health care decisions. They must be capable of taking the medication, usually pills, themselves. In most jurisdictions, except for Oregon and Vermont, patients also must be state residents.

State laws also include additional safeguards to prevent abuse and coercion.

Only the patient can request the medication and only after consulting multiple licensed healthcare providers to determine their eligibility, including the attending physician primarily responsible for the patient’s health care.

A second independent review of the patient’s medical records by another provider is required to confirm the patient’s terminal diagnosis, prognosis, and mental capacity. A mental health evaluation may also be required.

The process requires patients to make formal written and multiple oral requests with their physicians, separated by varying waiting periods. Witness signatures are needed on written requests to ensure no coercion. At least one witness must have no relationship with the patient and cannot benefit from their estate.

Patients can change their minds, too. They can decide to rescind their request for medical aid in dying or simply opt to never take the medication. About two-thirds of people with prescriptions ingest the medication and die, according to a report.

OPPONENTS FEAR A ‘SLIPPERY SLOPE’

There have not been any substantiated cases of abuse or coercion since the implementation of Oregon’s law in 1997, but opponents fear these laws are a “slippery slope,” that could be further expanded.

Some make religious arguments against the practice. Others fear laws in the United States could eventually be more expansive and less restrictive, as is the case in some other countries like neighboring Canada.

The American Medical Association acknowledges that physicians overall hold diverse opinions, and said in 2019 physicians could provide medical aid in dying “according to the dictates of their conscience without violating their professional obligations.” But it did not endorse the practice.

Since 1998, Oregon’s Death with Dignity Act has allowed Oregonians who meet certain conditions to receive prescription medications to help them end their life.

Kolb, the member of No Suicide Ohio, argues that determining that a patient’s prognosis is terminal can be imprecise, and that individuals who experience more subtle expressions of mental illnesses like depression or early cognitive impairment symptoms could slip through the cracks.

Kolb, who became paralyzed from the waist down after a skiing accident years ago, says his experience makes him personally understand acute suffering. However, he believes assisted death is the wrong solution to very real problems.

His hope is that Ohio becomes a leader in opposing medical-aid-in-dying laws.

“(Nationally) I definitely see it expanding, and I would love to see Ohio push back in a really productive, healthy way to say, end of life suffering is a real problem. Physician assisted suicide is the wrong solution,” he said.

ADVOCATES SEEK A SENSE OF CONTROL

Vigil Schattinger, the founder of Ohio End of Life Options, says she hears from families every day who wanted their loved ones with terminal illnesses to suffer less and find comfort in their final days.

Advocates say that’s the point. Giving patients the autonomy to make their own decisions about their lives, including how it ends, is at the center of what drives them.

New York Gov. Kathy Hochul focused on that point when she signed her state’s law this month. Hochul said she grappled with competing influences — her Catholic faith, which opposes these laws, and her belief that government should protect individual rights. She found clarity at a funeral where the priest discussed death as being called home to eternal life.

“I think that as people understand how these laws work effectively in other states, that they will just continue to ask for this option, as they are in Ohio.” Vigil Schattinger, who watched her father-in-law die after using Oregon’s law in 2014

“I realized we’re not talking about ending life early, we’re talking about dying early. So that people can transition surrounded by family, loved ones, not in a hospital bed with strangers … after grueling pain, sometimes just unbearable for loved ones to witness,” Hochul said.

That was Vigil Schattinger’s experience, and the beginning of her advocacy. She watched her stepfather, Dr. Jack Rowe, die after using Oregon’s Death with Dignity Act in 2014.

“Now there’s 14 jurisdictions that allow this. At the time that Jack died, there were three,” Schattinger said. “I think that as people understand how these laws work effectively in other states, that they will just continue to ask for this option, as they are in Ohio.”

Retired Assistant U.S. Attorney Ann Rowland, who leads Ohio End of Life Options’ policy advisory group, experienced caring for her brother-in-law at the end of his life after he was diagnosed with glioblastoma multiforme, a form of brain cancer.

“The hospice team was outstanding, but they could do nothing about many of the predictable indignities John suffered at the end of his life,” Rowland wrote in an opinion piece for cleveland.com/The Plain Dealer in 2019. “I don’t know if he would have chosen medical aid in dying if it had been available to him, but I know I would if I were suffering the way he did.”

Rowland said her eventual hope for Ohioans is that they have all the end-of-life options possible available to them.

“We want, for Ohioans, the ability to choose from a whole array of options as they’re facing their terminal illnesses, whether it be palliative care, hospice care, medical aid in dying or at various times, all three,” Rowland said. “This is not an either-or situation.”