NEW UPDATED WEBSITE UNDER CONSTRUCTION, FALL 2017

 

MEANWHILE,

Here are links to the two Rumblestrip podcast interviews about:

1.  my mime and Parkinson’s projects, and

2. The play I am writing, called ACT 39.

A story about Mime and Parkinson’s Disease
RUMBLESTRIPVERMONT.COM

2. ACT 39, The Play. In December 2015 my best friend Bill asked me to help him die. He was suffering from a terminal illness and had less than 3 months to live, when his doctor informed us about the recent law passed by the Vermont legislature: Patient Choice at End of Life, known as Act 39. At that time Vermont was one of only 5 states to pass this version of a medical aid in dying law. I am writing a full evening play about the controversies around this issue, based on my experience as Bill’s proxy and how we implemented the protocols of Act 39, leading to his death. The background to the story can be heard on this Rumblestrip podcast when I was interviewed by Erica Heilman.

When Bill was diagnosed with terminal cancer, he asked his best friend to help him die. This is their story.
RUMBLESTRIPVERMONT.COM