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jen brea

Thread
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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Jen Brea to step down as Executive Director of MEAction to focus on health

https://www.meaction.net/2020/11/12/important-news-from-jennifer-brea/?fbclid=IwAR3_GgqUDp3qe3woHXjeH04-n_sdapO-xKepc1EvJ4Gz0TTvCLXmo12st0U...

Thread by: InitialConditions, Nov 12, 2020, 5 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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Jen Brea: My ME is in remission

This is a hard post to write because there are no words that can do this justice. I can hardly believe it myself. My ME is in remission. For the...

Thread by: Dr Carrot, May 20, 2019, 305 replies, in forum: General ME/CFS News
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Do you have ICC-ME and other FAQs - Jen Brea

I just wanted to respond to a few comments and questions raised in response to recent posts in this series. If you aren’t a part of the ME...

Thread by: Sly Saint, Apr 1, 2019, 1 replies, in forum: General ME/CFS News
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Canada: 19th Annual Illuminations Jan 2019 - guest speaker Jen Brea

"Date January 24, 2019 Time 11:30am - 2:00pm Location Fairmont Waterfront, 900 Canada Pl, Vancouver BC Illuminations is our much-anticipated...

Thread by: Sly Saint, Nov 9, 2018, 0 replies, in forum: General ME/CFS News
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Epidemiology of ME and CFS

In conjunction with the master list of facts @JaimeS is discussing in this thread...

Thread by: JenB, Aug 10, 2018, 11 replies, in forum: MEpedia
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Treatment of ME patients in ERs and Hospitals

Hi all! I'm working to improve the quality of information for patients with ME, fibro, EDS, POTS, mast cell activation disorder having surgery as...

Thread by: JenB, Jul 27, 2018, 34 replies, in forum: General Advocacy Discussions
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#MEAction: Next steps: a letter to our community [from Jen Brea]

Hi everyone, I just wanted to take a moment to comment on some of the confusion and concern of these last few weeks and offer some steps forward...

Thread by: Andy, Jun 28, 2018, 3 replies, in forum: General ME/CFS News
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USA: JAX ME/CFS Center and Derya Unutmaz news

Derya Unatmaz of Jackson Laboratories explains the partnership between Bateman Horne Center, Jackson Laboratory, and many other collaborators as...

Thread by: Andy, Nov 15, 2017, 48 replies, in forum: News from Organisations
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Jen Brea $100,000 crowdfund for 2018 #MEAction activities

You'll need to unmute the audio: [MEDIA] Donation page here: [MEDIA] Please retweet: [MEDIA] And share on FB - except I can't seem to...

Thread by: Sasha, Apr 26, 2018, 53 replies, in forum: Fundraising
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CBT- Jen Brea Twitter

From twitter [MEDIA] Hit link.to see thread

Thread by: Amw66, Mar 16, 2018, 121 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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Jen Brea - Lavin agency speaker

" THE LAVIN AGENCY is the world’s largest intellectual talent agency, representing leading thinkers for speaking engagements, personal...

Thread by: Sly Saint, Mar 8, 2018, 3 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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Jen Brea comments on Esther Crawley's behaviour

I've made a practice of not publicly calling out Esther Crawley in part because the issues we face are so much bigger than any one researcher. 26...

Thread by: Alvin, Dec 31, 2017, 47 replies, in forum: General ME/CFS News
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Unrest - Screenings 2018

Galway Premiere of the award winning medical documentary film 'Unrest' (97 mins) about Myalgic Encephalomyelitis (M.E). " The screening of...

Thread by: Sly Saint, Nov 23, 2017, 19 replies, in forum: General ME/CFS News
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Unrest - reviews and general articles

When Fatigue Disables - Newcastle Herald Australia Chronic fatigue syndrome documentary UNREST to screen in Newcastle 10 Nov...

Thread by: Sly Saint, Nov 12, 2017, 157 replies, in forum: General ME/CFS News
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ME - The Movie. Ouch Disability Podcast BBCRadio

An interview with Jen Brea on the Ouch Disability Podcast On BBC iPlayer Radio http://www.bbc.co.uk/programmes/p05mgjjz 19 minutes long eta -...

Thread by: Skycloud, Nov 9, 2017, 7 replies, in forum: General ME/CFS News
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Jen Brea talks to Dr Phil Hammond about Unrest: BBC Radio Bristol

Haven't listened yet but should be interesting: http://www.bbc.co.uk/programmes/p05j3qr6#play Edit: Jen's bit starts around 2:20.

Thread by: Sasha, Oct 21, 2017, 2 replies, in forum: General ME/CFS News

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