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Jennifer Brea🦒 Profile
Jennifer Brea🦒

@jenbrea

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Filmmaker @4mmfilm @unrestfilm @longroadhomedoc. @MEActNet co-founder. Dropped out Harvard Poli Sci/Stats Ph.D after virus. #MECFS, #longCOVID

Los Angeles, CA
Joined July 2008
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@jenbrea
Jennifer Brea🦒
2 years
Working on a film about neurosurgical diagnoses and related comorbids (#MECFS, #longCOVID, #EDS, #POTS, #MCAS, #fibro). What would you like to see in such a film?
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@jenbrea
Jennifer Brea🦒
8 months
RT @pfatech: This makes me cry each time I watch it. And I'm curious how long it took @jenbrea to recover from having done this in-person s…
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@jenbrea
Jennifer Brea🦒
9 months
RT @IrishMECFSAssoc: 🧵 May is Myalgic Encephalomyelitis (ME) Awareness Month. You can help by liking and/or sharing this video. This 2017…
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@jenbrea
Jennifer Brea🦒
9 months
RT @missmunchkinz: May is Myalgic Encephalomyelitis (ME) Awareness Month! You can help by liking and/or sharing this video. This 2017 TED…
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@jenbrea
Jennifer Brea🦒
9 months
RT @Really_Richelle: The first time I saw someone else experience what I did was when I watched Unrest by @jenbrea , during the parade scen…
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@jenbrea
Jennifer Brea🦒
9 months
RT @loscharlos: 2. Watch the incredible @netflix documentary about #MECFS by @jenbrea — @unrestfilm — it’s now free on YouTube. This is a…
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@jenbrea
Jennifer Brea🦒
9 months
RT @loscharlos: “[#LongCovid] is a full NIH activity.. We must find better ways to.. restore the lives of these people” “We are not where…
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@jenbrea
Jennifer Brea🦒
9 months
RT @BPaulShelton: I've been putting off watching this since I first heard about it a couple years ago, but I ended that procrastination ton…
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@jenbrea
Jennifer Brea🦒
9 months
RT @loscharlos: This is a big deal — the absolute best bet for more #LongCovid research funding in next year is through the appropriation p…
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@jenbrea
Jennifer Brea🦒
10 months
@RoxiiLee_ I've recovered completely from ME and POTS
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@jenbrea
Jennifer Brea🦒
10 months
@RealLucyLawless Really appreciate your panel at Sundance. Love Never Look Away. Congrats!
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@jenbrea
Jennifer Brea🦒
10 months
RT @ar_pnw: More and more #longcovid patients, like #mecfs patients, are learning they have a connective tissue / structural problem that i…
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@jenbrea
Jennifer Brea🦒
10 months
RT @ahandvanish: To those who tried Truvada, how long until the side effects went away? It’s been 2 weeks - the nausea has decreased a lot…
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@jenbrea
Jennifer Brea🦒
10 months
RT @jayletay: Today we need to stand (or sit or lay down in my case) in solidarity with Millie, who is in hospital with very severe M.E.. S…
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@jenbrea
Jennifer Brea🦒
10 months
RT @ahandvanish: Bernie Sanders (@SenSanders) has released a #LongCovid Moonshot Legislative Proposal calling for $10b in research funding!…
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@jenbrea
Jennifer Brea🦒
10 months
@kirstler31 Yes, I know several who have but primarily via surgeries for neurological pathologies/compression syndromes.
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@jenbrea
Jennifer Brea🦒
10 months
RT @ar_pnw: Starting to see a pattern in patients who undergo jugular decompressions and their #POTS symptoms are greatly reduced or go awa…
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@jenbrea
Jennifer Brea🦒
10 months
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@jenbrea
Jennifer Brea🦒
10 months
@joleen_frick @jason_isaia But there are many syndromes that can cause dysautonomia, e.g., compression syndromes, spinal pathologies.
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