Stanford Medical Students Watch Unrest

Many thanks to folks at Stanford University for screening Unrest with #MEAction twice this month to educate health care professionals and medical students.

Medicine & the Muse sponsored the first screening on October 15th with many medical students in attendance asking thought-provoking questions about ME/CFS. Read this great article in Stanford Daily

The Medicine & the Muse Program is the home for the arts and humanities at the medical school, with programs that support diversity and integrate the arts and humanities into medical education, scholarly endeavors, and the practice of medicine.

The facilitator, Dr. Jonathan Berek, thanked Jennifer Brea and Laurie Jones for coming to discuss the film. He added,” Very informative and I must say that I admire you very much for your work and your courage, as I said, it also kind of reminds me of how important it is for all of us in medicine to listen to our patient advocates and to include our patient advocates in all of our activities, when we’re teaching when we’re developing educational programs and outreach programs in my area of oncology, that’s, that’s, I think, essential to hear from our from our patients.”

Jonathan Berek reflected #MEAction’s values right there. We fight so hard for patient advocates to be at the table and hearing those words brought music to our ears, and we want to share it widely.

The Stanford Medicine Abilities Coalition screened the film again on the 31st with a robust panel discussion!

The discussion was moderated by Terri L. Wilder, MSW. Panelists included the filmmaker, Jennifer Brea; Dr. Ron Davis; Dr. Jennifer Curtin; and former nurse and pwME, Ashanti Daniel.

The Stanford Medicine Abilities Coalition (SMAC) is composed of people who have disabilities and their allies. Membership is open to everyone at Stanford Medicine, including Stanford School of Medicine, Stanford Health Care, University HealthCare Alliance (UHA), Lucile Packard Children’s Hospital Stanford, Packard Children’s Health Alliance (PCHA), and Stanford Children’s Health.

Dr. Peter Poullos and the Stanford Medicine Abilities Coalition advocates for greater inclusion for people with disabilities at Stanford and are recruiting more medical practitioners with disabilities as well. The discussion prompted lots of questions about research, practice, long COVID, and personal experience.

#MEAction is so grateful for these two screenings and for Stanford University and all of the organizers (including Terri, Kristian, Daniel, Christy and many others) for bringing the topic of ME/CFS to such a prestigious university. 

 

To share Unrest with your clinician, you can have them take the CME opportunity here

To host a screening of Unrest through #MEAction, learn more here:

Facebook
Twitter
WhatsApp
Email

Latest News

black square image with two white lines at the top and bottom of the image. Then another two white lines come out from the sides to the middle over the #MEAction logo and the words, #NotJustFatigue Video Series Elizabeth Ansell Interview.

#NotJustFatigue Video Series: Interview with Creator Elizabeth Ansell

Over the past year, the #NotJustFatigue website, created by Elizabeth Ansell, releases a 10-part, documentary style, short form video series on different aspects involved in living with ME. Titles of the videos include topics such as: You Have No Idea How Serious This Is, Nobody Believes ME, and It’s Not Hysteria: It’s Sexism. In these

Read More »
navy blue square. there are two white lines at the top and bottom of the square. The #MEAction logo in at the top of the image. The words #MEAction Georgia Voice of the Patient in coordination with the Center for Disease Control and Prevention & Emory School of Nursing.

#MEAction Georgia: Voice of the Patient in Coordination with CDC & Emory School on Nursing

Back in September, #MEAction Georgia State Chapter partnered with the Centers for Disease Control and Prevention (CDC) and Emory School of Nursing to host, Voice of the Patient: A Panel Discussion with #MEAction Georgia. This event was a continuation of #MEAction Georgia’s #MillionsMissing 2024: #TeachMETreatME programming. Erin Lee and Liz Burlingame of the #MEAction Georgia

Read More »
a light blue square image with medical instruments/tools as a border (pill bottles, scales, needles, covid protein spike, etc). At the top of the image is the Home Test to Treat Program logo, in blue font: Findings Summary. Below that the #MEAction logo and Body Politic Logo.

Home Test To Treat – Findings Summary

#MEAction and Body Politic collaborated last spring, with a new national telehealth program, Home Test to Treat. We are now able to share initial findings from the program! Here are some highlights: 80K + enrolled in the program across the country! 40K + test distributed 6K + individuals treated for COVID-19 or flu 5.6K+ organizations

Read More »
Scroll to Top