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Anne Stitch it to Brexit #FBPE 2h
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Jack Croxall 27 Oct 17
Last night I saw + Q&A with . Wonderful, heart-wrenching film. My thoughts here:
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Will T.N Allen ∞ Jan 13
. That was a great film. Especially since it's up in the air that I might have M.E myself. I just wasn't sure if anyone even considered it a real illness. So I was accepting it was maybe depression, yet so many other people have been fighting people calling (1/3)
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Dragonflies & Dreams May 7
is a severe, debilitating chronic neuro-immune disease with more than 60 symptoms that worsen after even minimal physical, emotional or mental activity, but do not improve with rest. ME is NOT just "feeling tired".
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Eleanor Dryden 22 Oct 17
Incredible film making, and a necessary film
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Mo Schoenfeld 4 Dec 17
Just saw the Sundance award-winning film which focuses on the millions suffering w/ . Very moving, informative, often shocking & it opened my eyes wide to this debilitating condition
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Simone Jan 24
A cousin messaged me tonight to say that she watched on Netflix. She said she was sad to see what I'm going through. She said that I'm not forgotten, that she sees me, that I am not invisible. I cried.
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Ilona Dougherty 15 Jan 18
Finally had a chance to watch . Beautiful, moving, important. Take the time to watch it.
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Steve Topple Aug 22
CALLING ALL THE : "The UK’s General Medical Council just threw 250,000 disabled people under a bus" The have snubbed hundreds of complaints about . So here's my response. WARNING: not for the faint-hearted
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Dragonflies & Dreams May 6
I am one of the . Millions with (ME) are missing from our careers, social lives, families and hobbies. We miss having a life. Please support the OMF ().
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hank sturgis 10 Jan 18
There’s a very active reddit discussion going on right now on r/documertaries, which has more than 12.7 million subscribers. Good time to drive traffic there to upvote and comment.
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Peter Tatchell Apr 7
Patients with ME are demanding justice. There are political, social & medical issues surrounding the trial. READ:
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Chris Evans MP 24 Oct 17
Attended today's viewing of the film Unrest - a must watch. The condition ME urgently needs more research funding
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Uncle B Jan 23
I post often about because my wife has dealt with it for yrs. Few know how life-altering it can be. If anything, pls help those afflicted via this petition that demands fund ME research fairly & equally. And say DONE! TY
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🌹 Witch, Hunting 💀 15 Jan 18
Whether or not you think you know anything about Chronic Fatigue Syndrome, I urge you to watch on Netflix. It's beautifully made and incredibly eye-opening. CFS is not what I thought it was.
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Nevra Elis A. Jul 5
Wow, after our meeting changed their website already! At least M.E & post extertional malaise are mentioned. This is an accomplishment! It's far from perfect but we'll continue to work together to spread awareness!
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Hannah🐝 Jan 17
Unrest, a New Documentary Now on Netflix, Unpacks What Chronic Disease Means for Us All - Vogue
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Raeka Aiyar 16 Jan 18
Hosted an house party to show friends how devastating is & how urgent the research is. Sign the petition to demand fair funding for this disease:
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Gregor McAbery Jan 30
Tonight we are at the Scottish Parliament for an event linked to the new ME film Unrest Here is the linked P&J story
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Anton Mayer 31 Oct 17
Replying to @MECFSNews
From my angle, it looks like a lot like millions of patients were denied medical care & advances of 30 years of research.
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