Emmi Skyten
emmiskyten.bsky.social
Emmi Skyten
@emmiskyten.bsky.social
1.4K followers 230 following 56 posts
Sustainability science studies on hold because of POTS + Long covid / suspected ME. Previously interesting, now mostly into resting. Here to connect with other sick people and for science stuff.
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Reposted by Emmi Skyten
Love Ed’s work! A gap I see in covid coverage is a need to hear from the organizers responding to the crisis. There are mask blocs, people organizing for funding & legislation like Long Covid Justice Network. People’s
cDC. Berlin Buyers Club. The public needs to hear how they can fight covid.
There are a lot of people, even among experts, in our country who believe long covid and ME are functional disorders. This makes life very hard for us patients. And so little accurate reporting unfortunately.
Hi @edyong209.bsky.social I just shared your opinion piece on Twitter quoting the poem you also quoted. A fellow patient from Finland asked me to pass on her thanks because she is not on Bluesky. I think she felt seen.
Reposted by Emmi Skyten
I love the idea that maybe sleep is the purpose of your life and being awake is the inconvenient but necessary disturbance.
Reposted by Emmi Skyten
Alarming thread/convo.

A high-profile paper on #LongCovid contains a mystery section apparently written by AI that perpetuates unfounded ablist stereotypes, presumably skewed by LLM verbiage.

One of the authors is even listed as affiliated to an "AI lab"!

Great sleuthing by @lucibee.bsky.social
There's something bothering me about this review.
Something about it is very odd.
🤔
A new, very good review on Long Covid
www.nature.com/articles/s41...
Reposted by Emmi Skyten
'The long COVID figure for those at the lowest income levels was a staggering 50%, versus a 29% average for all adults and 22% for those at the highest income levels.'

Class had tremendous influence on who got COVID in the first place, and now it's long-term outcomes. Best health care in the world!
Poverty and Long COVID Go Together
The lowest income Californians are more likely to have lingering symptoms, and more likely to lose jobs.
capitalandmain.com
Reposted by Emmi Skyten
🔬Wondering how OMF selects treatments used for clinical trials? Let us illuminate our process for you. Learn more 👉 www.omf.ngo/treatment-trials.

Join us on this complex journey towards understanding the intricacies of ME/CFS. 🌟
Reposted by Emmi Skyten
The UK's Covid inquiry has heard that a major imperfection of standard issue PPE was that, although marketed as 'gender neutral', it was designed for male bodies.

This included masks, which even now fail to take account of female-male differences in facial dimensions

#Covid #MedicalSexism
Another truth from the Covid inquiry: women were being ignored over ill-fitting PPE long before the ...
NHS England denied there was a problem with unisex equipment. But it was well known that most neither fits nor protects female healthcare workers, says feminist campaigner Caroline Criado Perez
www.theguardian.com
Reposted by Emmi Skyten
Unfortunately, the authors' conclusion of "some evidence" is contradicted by their conclusion that *all* studies had "unclear or high" risk of bias.

There was "no" evidence here, not "some".

This is the same as for CBT/GET in #MECFS treatment: lots of studies; all bad; ergo, no evidence.

#pwME
Is there a role for traditional & complementary medicines in managing chronic fatigue [#CFS]? a systematic review of RCTs

Full text now available here:
www.frontiersin.org/articles/10....

"future studies should employ more objective diagnosis standards and outcome measurements ..."

#MEcfs #PwME
Tldr: onko bluesky miljardöörinkestävä?
Reposted by Emmi Skyten
With several recent advances and funding, Covid nasal vaccines now have momentum. Really needed and exciting to see!
erictopol.substack.com/p/covid-nasa...
Reposted by Emmi Skyten
The latest weekly Science for ME news in brief is online with items on ME/CFS and Long Covid research, advocacy and coming events.

You don't need to be a forum member to read the news. To suggest an item for future bulletins, join the forum and start a discussion.
www.s4me.info/threads/news...
News in Brief - October 2023
This thread has a Science for ME 'News in Brief' post for each week in October 2023 by a team including @Trish, @Kalliope and @ahimsa. Scroll down to...
www.s4me.info
Reposted by Emmi Skyten
Today the PolyBio research foundation will host a webinar on infection-associated chronic diseases. ME/CFS and Long Covid will be discussed.

It's open to the public. Join here polybio.org/polybio-fall...
I can't believe someone actually wrote this in their name. Discusting.
Reposted by Emmi Skyten
Amalia Fleming was an amazing person but her cat was clearly not impressed. 1971. press-ert-gr.translate.goog/grafeio-typo...
Haetaanko yleensä ensin paikka vai ensin rahoitus? Voiko yliopistolle sanoa, että aloitan vasta sitten, kun saan rahoituksen? Tämä välimaasto on jäänyt minulle epäselväksi.
Reposted by Emmi Skyten
It's that time of year again! Today I look at the history of so-called "Medically Unexplained Symptoms" with my students (part of our #pseudoscience class).

Migraines? Rooted in "perfectionism"
Ulcers? "stress"
AIDS? "shame/guilt"
MS? "childhood trauma"

Tropes now recycled for #MECFS & #LongCovid
Ohh I'd love to attend!
I'm gathering evidence for a complaint and this might work for that 🤞
Thank you! I had been searching for this info 🙏