This article was published in the Valley Reporter on April 16, 2015.
By Meghan Schrader
I love Vermont. My family has owned a home here since the 1980s and I guess you could say that I've adopted the state as my own. I am also a disabled woman and much of my own identification with that community was forged here as I grew up role playing, painting and dreaming alongside the streams and rivers that run through the town of Waitsfield.
Being disabled has also made me very cognizant of the right-to-die movement. Since 2007, I have engaged in an extensive exploration of what disability studies scholar Rosemarie Garland Thompson refers to as the "cultural logic of euthanasia" which I incorporated into recently published research regarding the representation of disability and assisted suicide in film music. However, the issue of assisted death is personal for me, which is why I am dismayed that Act 39 was ever implemented in the first place.
For instance, in the course of doing research for my aforementioned book chapter, I had occasion to review the writings of many utilitarian bioethicists whose arguments concerning disability and death with dignity are framed in regard to familial burden, which tends to be situated as a legitimate reason for choosing or being obliged to die. Such statements are similar to hate speech I experienced growing up and I was shocked when I first saw it in bioethics literature.