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unrest

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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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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: 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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Scotland: Email and/or call your SMP today, asking them to attend the Unrest screening and conversation about ME, Tuesday 30th January

From their Facebook post [MEDIA]

Thread by: Andy, Jan 27, 2018, 2 replies, in forum: Advocacy Action Alerts
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Ask Francis Collins to watch UNREST and screen film at the NIH

The Unrest film team sent out a rather long email today. At the bottom of the mail there are links to three actions to take. I thought the action...

Thread by: ahimsa, Jan 25, 2018, 0 replies, in forum: Advocacy Action Alerts
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Academy Award Nomination Announcements; January 23, 2018

Will Unrest survive the cut, from 15 to 5, and acquire the sought after Academy Award Nomination for “Best Documentary Feature”? Find out on...

Thread by: MErmaid, Jan 20, 2018, 30 replies, in forum: Advocacy Action Alerts
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PacificStandard: How Disabled People Care for Each Other When Doctors Can't

[Note to moderators: I think this belongs in general news - please move if this is the wrong forum] New article by David M. Perry (twitter handle...

Thread by: ahimsa, Jan 16, 2018, 1 replies, in forum: General ME/CFS News
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Unrest now on Netflix

Unrest is in Netflix from today! https://www.netflix.com/title/80168300 I don't know in which countries apart from the US. The Unrest team said in...

Thread by: Joh, Jan 15, 2018, 53 replies, in forum: General ME/CFS News
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Leave a Comment about 'Unrest' on Independent Lens Site

You can leave a comment about 'Unrest' on the Independent Lens site. If you have FB, Twitter or Google you can link it to Disqus (which can be a...

Thread by: Melanie, Jan 10, 2018, 1 replies, in forum: Advocacy Action Alerts

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