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Illness (In)action: CFS and #TimeForUnrest, 2021, Diedrich

Illness (In)action: CFS and #TimeForUnrest Lisa Diedrich Literature and Medicine Johns Hopkins University Press Volume 39, Number 1, Spring 2021...

Thread by: Dolphin, Jun 30, 2021, 0 replies, in forum: General ME/CFS news
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Article: When the Chronically Ill Go into Remission: Filmmaker Jennifer Brea’s Life After “Unrest”

Excellent article in the Los Angeles Review of Books about the trauma of illness and the double edge of remission. Written by Megan Moodie, who...

Thread by: kikala, Jul 18, 2020, 2 replies, in forum: General ME/CFS news
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Media Impact Award 2019 Invisible Disabilities Association goes to Jen Brea

[MEDIA] "Jennifer Brea is impacting the world for people living with the invisible disability, M.E. with her award winning film, "Unrest!"...

Thread by: Sly Saint, Jan 18, 2020, 2 replies, in forum: General ME/CFS news
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Postcards to Doctors - new project from ME Action

A new project from ME Action: #MEAction is excited to announce the launch of our Postcards to Doctors medical education campaign. Send...

Thread by: ahimsa, Aug 1, 2019, 15 replies, in forum: Advocacy Projects and Campaigns
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Unrest Continuing Medical Education Program (CME/CE)

#MEAction has teamed up with the Time for Unrest Campaign to make using Unrest as a tool for medical education easier than ever. US healthcare...

Thread by: Andy, Feb 11, 2019, 4 replies, in forum: General ME/CFS news
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2019 Ann W. Caldwell Lecture on ME at MGH Institute of Health Professions

Learn About the Millions Missing from ME/CFS – Sundance Award-Winning Film Screening and Panel Discussion January 15, 2019 5:30 PM - 7:00 PM...

Thread by: Sly Saint, Dec 31, 2018, 18 replies, in forum: Advocacy Projects and Campaigns
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US action: Ask your health care professional (doctor, nurse, therapist, etc) to watch Unrest online for credit

Here's a relatively easy advocacy action for patients in the USA: Ask your health care professional to watch Unrest online and get continuing...

Thread by: ahimsa, Nov 1, 2018, 8 replies, in forum: Advocacy Projects and Campaigns
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Film Gives Voice to Chronic Fatigue Patients Seeking Understanding, Treatment

Shame about the title. "Last year, the National Institutes of Health awarded grants totaling more than $7 million to develop a coordinated...

Thread by: Sly Saint, Oct 14, 2018, 2 replies, in forum: General ME/CFS news
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US healthcare providers receive CME credit for watching Unrest and new diagnosis and management video

From the Unrest website: Watch Unrest and receive CME credit US healthcare providers can now watch Unrest and receive continuing education...

Thread by: Joh, Sep 24, 2018, 15 replies, in forum: General ME/CFS news
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Best news article that gives background info on Unrest, Brea, #MEAction and MillionsMissing?

I would be very grateful for suggestions for the most useful articles from big international newspapers (or similar sources) in giving background...

Thread by: Kalliope, Sep 21, 2018, 3 replies, in forum: General Advocacy Discussions
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Accessible Film Festival presents VR experiences of disabled individuals - Unrest VR features

DAILY SABAH ISTANBUL "The festival's virtual reality program has three projects this year: Unrest VR, created by Jennifer Brea and Amaury La...

Thread by: Sly Saint, Sep 10, 2018, 1 replies, in forum: General ME/CFS news
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Unrest on YouTube

The link to a copy of Unrest has been deleted from this post as @JenB has confirmed that is was a pirated copy and asked that we don't share the link.

Thread by: MeSci, Aug 6, 2018, 10 replies, in forum: General ME/CFS news
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Vote for Unrest as your favorite 2017-18 Independent Lens film

It’s that time of the year again: Now that Independent Lens has concluded another season, we need you to vote for the recipient of this year’s...

Thread by: Andy, Jun 18, 2018, 16 replies, in forum: Advocacy Action Alerts
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MP Nicky Morgan to raise awareness of ME illness

" LOUGHBOROUGH MP Nicky Morgan has said she will work in Parliament to raise awareness of the devastating illness, ME. She spoke after joining...

Thread by: Sly Saint, May 10, 2018, 12 replies, in forum: General ME/CFS news
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Video: "After Unrest"

This was retweeted by @JenB, [MEDIA]

Thread by: Indigophoton, Apr 23, 2018, 6 replies, in forum: General ME/CFS news
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Jen Brea tweets about U.K. Unrest campaign

[MEDIA]

Thread by: NelliePledge, Mar 27, 2018, 97 replies, in forum: Advocacy Projects and Campaigns
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Video: Unrest panel discussion in Melb, Sun Mar 18

Here is the video of the Q&A which followed the screening of Unrest in Melbourne on Sunday March 18. The panel members were: Patient advocate:...

Thread by: Simone, Mar 20, 2018, 4 replies, in forum: General ME/CFS news
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Australian radio program: Jen Brea & Panel Discussion

Uncommon Sense with Amy Mullins "Tuesday 13th March: US film director Jennifer Brea will talk to Amy about her Oscar-shortlisted documentary...

Thread by: Sly Saint, Mar 10, 2018, 18 replies, in forum: General ME/CFS news
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ProHealth is Proud to Announce its 2017 ME/CFS Patient Advocate of the Year: Jennifer Brea

" In 2017, Jen Brea did the impossible. She catapulted ME/CFS onto the public stage, and into the international spotlight, all in one fell swoop...

Thread by: Sly Saint, Mar 8, 2018, 9 replies, in forum: General ME/CFS news
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Tues 20 Feb: Livestream of post-Unrest panel discussion, incl. Ron Davis, Lily Chu, Montoya, Tuller

[MEDIA] 3am on Wednesday UK time, apparently - what's that, 7pm on Tuesday Pacific Time or something?

Thread by: Sasha, Feb 17, 2018, 33 replies, in forum: General ME/CFS news

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