Long Covid Advocacy 💙(@LongCovidAdvoc) 's Twitter Profileg
Long Covid Advocacy 💙

@LongCovidAdvoc

📘Legislate
⚕️Investigate
🌬️Ventilate
👥Educate
Advocacy4 #LongCovid #MECFS #COVIDisAirborne

ID:1416846409865867267

linkhttps://linktr.ee/longcovidadvocacy calendar_today18-07-2021 19:45:00

19,1K Tweets

13,9K Followers

13,4K Following

davidtuller(@davidtuller1) 's Twitter Profile Photo

I am touched that Berkeley's May crowdfunder for Trial By Error has reached 150 donations and almost 30 percent of the goal. Thanks to all past, current and future donors! crowdfund.berkeley.edu/project/42302

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davidtuller(@davidtuller1) 's Twitter Profile Photo

Wow, now almost 26K views! That's a lot of people watching Peter Judodihardjo deconstruct the PACE trial and explain why it's so awful. This video was based on my Trial By Error investigation. If you'd like to donate to this month's crowdfunding effort, here's how: crowdfund.berkeley.edu/project/42302

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A 😎 Long Covid + MECFS Billboards(@AaronCa11) 's Twitter Profile Photo

iTunes 59p

Or stream for free on Spotify, Apple or YouTube and leave it on repeat with volume low (not muted, won’t count to charts)

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betsy ladyzhets 📊(@betsyladyzhets) 's Twitter Profile Photo

Excited to announce we are now open for pitches at The Sick Times, and also hiring for two part-time roles, an engagement editor and podcast producer! More info here: thesicktimes.org/write-for-us-p…

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CoRE Mount Sinai(@CoRESinai) 's Twitter Profile Photo

Understanding the potential roots and drivers of chronic illnesses plays an important role in advancing our treatment and knowledge of post-acute infection syndromes. Join us on 5/21 for a live virtual education session about persistent pathogens. Links to tune in, in the thread.

Understanding the potential roots and drivers of chronic illnesses plays an important role in advancing our treatment and knowledge of post-acute infection syndromes. Join us on 5/21 for a live virtual education session about persistent pathogens. Links to tune in, in the thread.
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Putrino Lab(@PutrinoLab) 's Twitter Profile Photo

Calling all folks who have, care about or treat , and chronic and other PAIS: we are planning out a new live education initiative but first we need folks to subscribe to our YouTube channel. We need 100 subscribers to be able to broadcast. Please help!

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Cambridge ME group(@CBMEgroup) 's Twitter Profile Photo

Worth reading on legal funding routes for class action cases similar to post office scandal etc. May be relevant to and people if we ever get act together and take a civil case for negligence, etc.

theguardian.com/uk-news/articl…

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Long Covid Advocacy 💙(@LongCovidAdvoc) 's Twitter Profile Photo

The free speech union was founded by Toby Young and Paul Garner is happy to platform his views here.
Showing how desperate he is for attention as pushes into extreme culture war territory.

The free speech union was founded by Toby Young and Paul Garner is happy to platform his views here. Showing how desperate he is for attention as pushes into extreme culture war territory.
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UniteToFight2024(@U2Fight_World) 's Twitter Profile Photo

Finally, we made it into the German news!

Here is a short article about in Handelsblatt, a major news outlet in Germany

Please share it in your network !

German: handelsblatt.com/dpa/gesundheit…

English: www-handelsblatt-com.translate.goog/dpa/gesundheit…

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MortenGroupOxford(@OxMEDiscovery) 's Twitter Profile Photo

Funding delay with our Chronic Lyme, ME/CFS PhD project. Issues with Oxford mean that our funding will be delayed for 12 months. We need to find £70K to cover the 1st year costs to start on time. Can anyone help? . Ideally we need a large donor.

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Kimberly Prather, Ph.D.(@kprather88) 's Twitter Profile Photo

Now that the world realizes many respiratory viruses are airborne and can be inhaled...what next? My view is the biggest quick impact is to ramp up filtration in all schools (including pre-school) and measure the massive impact it has on reducing the spread of disease. Why not?

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Dianna Cowern(@thephysicsgirl) 's Twitter Profile Photo

is unimaginably isolating, especially for severe patients like Dianna. The disease just doesn't make sense; even for me, it's taken a year of caring for her every day to start to understand.

To get a sense, Dianna has spent the last year and a half in her room, unable to

#MECFS is unimaginably isolating, especially for severe patients like Dianna. The disease just doesn't make sense; even for me, it's taken a year of caring for her every day to start to understand. To get a sense, Dianna has spent the last year and a half in her room, unable to
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