Vermont Becomes the 3rd State with A Death with Dignity Law
On May 20, 2013 Vermont made history by becoming the first state to pass a Death with Dignity law by legislation. Governor Shumlin, Senator Ayer, and other dedicated supporters packed the Statehouse room for the bill's signing into law.
Vermonters reflect on five-year anniversary of the state's Medical Aid in Dying law
Liz Strzepa reporting for Vermont's NBC 5
May 16, 2018
May 16, 2018
PCV Board Member Dr. Diana Barnard Testifies in New York
Living While Leaving
Patient Choices Vermont is pleased to launch the Living While Leaving video series to share the heart-felt and compassionate stories of Vermonters who have used medical aid in dying.
The two films (below) are the second in our series... They feature a dialogue with wife and mother Peggy Stevens and daughter Samantha Stevens regarding Eric Stevens, husband and father. The interview is conducted by Betsy Walkerman, PCV President. These films were created by Stephen Kastner at DesignWise Studios, videographer and editor with music by Eric Stevens (and his band in Part 2).
Part 1
Part 2
The first video in the series (below), is an interview that spans three generations: with wife and mother, Ginny Walters, co-founder of PCV; her daughter Betsy Walkerman, President of PCV and daughter/granddaughter Karen Walkerman. It is the story of Dick Walters, also co-founder of PCV, his relentless advocacy and his journey at the end of his life using medical aid in dying.
Please, contact us if you would like to share your story.
Are you an individual near the end of life, or a caregiver? Were you close to someone who used or considered using Act 39? Others may benefit from your experience and insights. (Please recognize that not all stories will be suitable for posting.)
Maggie Lake - Putney, Vermont
Barb Bardin - Burlington, Vermont
Burlington, Vermont, July 27, 2015 - Burlington, VT resident Barb Bardin wanted to share her story in the hope that it would help others. WCAX Story. Please note that some of the details of Act 39 are incorrect (no one has to swallow 100 pills). However, the story is still meaningful.
Kimiko Yumoto - South Burlington, Vermont
Terri Hallenbeck | Seven Days | June 4, 2015
Read in full at Seven Days
[…] After initially being diagnosed with Parkinson’s disease in 2007, Yumoto learned in 2011 that she had multiple system atrophy, her obituary says. That is a degenerative condition that diminishes the body’s involuntary functions, including heart rate and digestion.
“Kimiko chose to end her life through physician-assisted suicide under Vermont’s Patient Choice and Control at End of Life Act (Act 39),” the obituary says. “Kimiko left us on the day and in the manner of her choosing, but long before her time.” […]
Read in full at Seven Days
[…] After initially being diagnosed with Parkinson’s disease in 2007, Yumoto learned in 2011 that she had multiple system atrophy, her obituary says. That is a degenerative condition that diminishes the body’s involuntary functions, including heart rate and digestion.
“Kimiko chose to end her life through physician-assisted suicide under Vermont’s Patient Choice and Control at End of Life Act (Act 39),” the obituary says. “Kimiko left us on the day and in the manner of her choosing, but long before her time.” […]