Josh Crane, reporter and producer for Brave Little State with Vermont Public says, "If you’re like me, you may not have realized Vermont is one of just 10 states with a Medical- Aid-in-Dying (MAiD) law on the books. Act 39, as it’s known here, passed in 2013. And there’s a bunch of criteria you must meet in order to use it, like being a Vermont resident over the age of 18 with a terminal illness." ​

In some of her final words before using medical aid in dying, Karen Oelschlaeger made a powerful statement advocating for improvements to Vermont’s Act 39. Vermont Public Radio (VPR) reporter Howard Weiss-Tisman interviewed her about a week before she died. VPR's report, published on April 20, includes statements from PCV Board Member, Dr. Diana Barnard and PCV President, Betsy Walkerman.

Among the changes proposed in Senate Bill 74 is an adjustment to the patient’s timeline so that dying people won’t have to wait an extra 48 hours before receiving their medication after already spending weeks at appointments, filing a written request, and obtaining confirmation by two doctors.

In the words of Duncan Allen-Burns (son of Dee Allen whose video is featured on PCV’s website)... “Those 48 hours were a nightmare. Just the sheer emotional toll it took on her [his mother] was so painful to watch... I couldn’t be more appreciative of Act 39 and the work that you are doing. My mom was passionate about it.”

This spring, PCV is sponsoring several educational events for hospice personnel. A few weeks ago, PCV Board Member Dr. Jaina Clough hosted more than 50 UVM Hospice volunteers on zoom. Participants discussed the special role of hospice workers in providing neutral, trusted support, both in the qualification process under Act 39 and in connection with medical aspects of the process.

Two more sessions will be hosted by PCV Board Chair, Toni Kaeding, MS RN, in April and May for hospice organizations in Rutland and Brattleboro.

Act 39 patients consistently tell us how much they value the comfort their hospice workers provide. Thank you to all the people and organizations that make that work possible.

Vermonters reflect on five-year anniversary of the state's Medical Aid in Dying law.

Tom Ozahowski, is shown walking on a wooded trail near his Thetford home. He made his career at Dartmouth-Hitchcock Medical Center in Lebanon, New Hampshire where he worked with patients who often stared death in the face.

"People have cardiac arrests and have near death experiences that, it's not everybody, but some of them have had profound situations that have helped me," he said those situations have helped him find peace with his fate. 
"I was diagnosed in 2008," Ozahowski said regarding his prostate cancer, which has spread to his bones. "I have no idea exactly whats in store."h

The one thing he does know is how he plans on dying.
"My sons are totally in agreement that I can use Medical Aid in Dying and get a prescription to be self-administered," he said.

Dr. Diana Barnard, with the University of Vermont Medical Center, would like to see more Dartmouth-Hitchcock doctors on board.
The palliative care specialist said most of her patients worry about losing their sense of control, something many wish to gain using Act 39.
"Most people that I talk to don't want to die. They want to live, but they are dying from their underlying illness and we cant stop that," Board Member Dr. Diana Barnard said.

In the past five years, the state's Department of Health said 52 people have qualified to utilize the law, but only 29 people have chosen to end their lives.

"The law itself was really carefully crafted and is working very well," said PCV President Betsy Walkerman, also featured in the story.

​​Click to Watch the Story...

Dr. Diana Barnard appearing before the New York State Legislature's hearings on medical aid in dying.