From Seriously Sensitive to Pollution: For More Info, Go Here…
Guest post from Mordecai Cohen Ettinger,
The Health Justice Commons
I’ve had MCS for nearly 20 years. I’m a survivor of of the Three Mile Island partial nuclear meltdown, excessive x-ray radiation from medical treatment as a child from a teaching hospital that has since been ongoingly investigated for bioethics violations, and successive exposures to lead and mold from reckless landlords.
I’ve been a community activist for many years, along with a scholar and teacher of Critical Science, Technology and Medicine Studies.
In late 2016, I founded the Health Justice Commons, a non-profit. Our mission is to re-imagine and remake healthcare for our times.
To support efforts for MCS Awareness Month, we want to address the gap of basic research of our experiences.
Myself and my group, The Health Justice Commons, believe that because MCS is so discounted there is little documentation of our experiences & we want our experiences to count.
This is a survey for people who self-identify as having MCS and/or EII. There are limited studies that document the causes and impacts of these illnesses.
