We are very grateful to all the people who have responded to PCV’s spring fundraising letter with generous contributions. Our education programs and our work to improve Act 39 are possible only with your support. Thank you for making end-of-life choice a priority in your giving. 

In the past month, PCV board members have given five educational seminars for healthcare providers and community members around the state. We've been pleased to respond to numerous requests for our brochure, Vermonter's Guide to Medical Aid in Dying, coming from churches, community centers, and hospice organizations. 

Our Videos make up the most popular page on our website. 

As one donor recently wrote, “The video of a woman going through the actual process of using Act 39 gave me a lot of reassurance. Keep up the good work!” 

People have had a particularly powerful response to our video of Karen Oelschlaeger. Karen was extremely grateful for medical aid in dying and chose to be an advocate even in the last week of her life when she spoke to a reporter from VPR. The recent Vermont Public Radio story powerfully framed the struggle that certain parts of the Act 39 process have on people seeking aid in dying.

May 20th was the eight-year anniversary of Act 39. Let us know that you're celebrating by making a donation of $88, or $888, or perhaps a multiple of $8, such as $48, or $96…be creative!

Many thanks, and happy spring!
Betsy Walkerman, President

Patient Choices Vermont
email: info@patientchoices.org
phone: 802.448.0542

“Those 48 hours were a nightmare. Just the sheer emotional toll it took on my mother was so painful to watch.” - Duncan Allen-Burns, son of Dee Allen, who used aid in dying in Dec., 2020

When we heard Duncan’s words, we were more convinced than ever that we have to work hard for patient-focused improvements to Act 39.

Duncan was referring to the mandatory 48-hour delay that all patients must endure after all other parts of the rigorous Act 39 approval process have been completed. The Act 39 process also requires that two separate requests to use Act 39 be made at least 15 days apart — in the physical presence of the doctor.

“I could not wait to get through that timeline. Removal of that [in-person] requirement would be a huge relief.” - Karen Oelschlaeger

Karen was 37 years old and dying from stomach cancer. You can hear the pain and frustration in her voice on the PCV video as she describes the arduous process of traveling to required appointments.

At PCV’s urging, Senate Bill S.74 was introduced in February, 2021 to make three important improvements to the law:

— First S.74 would adjust the timeline to eliminate the final 48-hour delay. 

This change would be a huge relief for people like Dee Allen. Dee’s health was deteriorating so quickly from a devastating neurological disease that she feared she would lose the ability to self-administer the medication while waiting the last 48 hours before the prescription could be written. As she expressed in her video on PCV’s website, this period seemed to have no purpose and caused needless suffering. 

— Second, S.74 would enable people to make their Act 39 requests via telemedicine.  

This change would remove a tremendous burden for people like Karen, for whom an hour-long ride to an appointment was a nightmarish experience. 

—Third, S.74 would correct a technical deficiency in the immunity clause of Act 39.

Act 39 currently provides legal immunity only for doctors. Access to medical personnel and pharmacists would be more consistent and predictable if legal immunity were explicitly spelled out for everyone involved in the process. 

When Act 39 was created, legislators placed great weight on preventing improper use of the law. The current process includes five qualification requirements, an eight-step process including certification by two doctors, and full documentation. (PatientChoices.org/act-39-overview) Now, with eight years of experience and zero reports of abuse, it’s time to listen to the people who the law is intended to serve and make proper use of the law less onerous for dying people. The next year will be critical for our work on S.74.

Patient Choices Vermont is the only Vermont organization focused on the rights of people who want the option of medical aid in dying.  

• We provide the only aid-in-dying hotline to both doctors and patients in Vermont.
• The PCV website PatientChoices.org provides the most comprehensive set of resources on medical aid in dying in Vermont. 
• Our educational programs have trained hundreds of medical and hospice personnel and brought greater knowledge to community members across the state.
• Our materials explain a person’s options in plain English. We are pleased to enclose our new brochure. We hope you find it useful and will share it with a friend.

​We only fundraise twice a year. We count on you to determine how much end-of-life choice means to you.

Many thanks to all of you who have supported PCV’s work over the years. Thank you to those who give monthly, like a Netflix subscription. Thank you to our major donors who can afford and choose to give $1,000 or more to this important cause. Thank you to those who send notes of encouragement and share stories. Thank you to those who make gifts in honor of dear friends. All donations speak to the strength of our community and commitment to this basic civil right.

For me, the best part of this work is seeing the impact we have on such a meaningful time of life. From Dee Allen’s son, Duncan: “I couldn’t be more behind her decision, and that’s coming from a place of pure love. We really appreciate the work that you are doing. We’re very thankful our mom was in a state where she got to choose the way she went out.”

With appreciation,

​Betsy Walkerman, President

Patient Choices Vermont
email: info@patientchoices.org
phone: 802.448.0542