davidaugust, to me
@davidaugust@mastodon.online avatar
_elena, to me
@_elena@mastodon.social avatar

Belle-Île, France (2016)

(Funny that this pic was taken with a Canon 70D, which is now my daughter's camera)

DZGrizzle, to me
@DZGrizzle@mastodon.social avatar

My favorite tree. On the trail last Sunday at Sosebee Cove in the North Georgia Mountains. The hiking stick was handmade by my late father.

stefano, to photography
@stefano@bsd.cafe avatar

Me and my first phone Over 40 years ago.

This photo has been on my grandma's living room cabinet for as long as I can remember. She passed away a couple of years ago, and to keep her memory alive, my wife suggested we keep it in our living room.

A blast from the past looking towards the future.

No, the phone doesn't run Android or iOS 😆

#Photography #Photo #Me #JustMe #ThrowbackThursday #BackInTime

Journal article: Why the Psychosomatic View on Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Is Inconsistent with Current Evidence and Harmful to Patients (www.mdpi.com)

Abstract: Since 1969, Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) has been classified as a neurological disease in the International Classification of Diseases by the World Health Organization. Although numerous studies over time have uncovered organic abnormalities in patients with ME/CFS, and the majority of...

tomkindlon, to mecfs
@tomkindlon@disabled.social avatar

“In England, Conflicts Between Families and Hospitals Threaten the Lives of Young Women with ME” by David Tuller DrPH

https://t.ly/77JIT

About the desperate situation of patients not getting help from hospitals with necessary feeding tube fitting.

@mecfs

1/

NEWS: Chairman Bernie Sanders Releases Long COVID Moonshot Legislative Proposal | The U.S. Senate Committee on Health, Education, Labor & Pensions (www.help.senate.gov)

WASHINGTON, April 9 – Sen. Bernie Sanders (I-Vt.), Chair of the Senate Health, Education, Labor, and Pensions (HELP) Committee, today released a draft legislative proposal to address the Long COVID crisis that is negatively impacting the health of some 22 million Americans....

davidaugust, to Woman
@davidaugust@mastodon.online avatar
zhkbluerose, to photography
jo, to VintageOSes
@jo@wetdry.world avatar
tomkindlon, to mecfs
@tomkindlon@disabled.social avatar

Remembering ME activist (& my friend) Robert "Bob" Courtney, who passed away on March 7, 2018

This is from the @MEAssociation magazine

One can read about some of the specifics of Bob's work here: http://me-pedia.org/wiki/Robert_Courtney

@mecfs

andrewwet, to me

Haciendo el mono.


andrewwet, to me

El y
The and
Si soy ⚜️

AndrewGiffordphotography, to me
@AndrewGiffordphotography@mastodon.social avatar

Bit my lip three meals in a row - from my photo project about ME/CFS

https://glass.photo/andrewgifford/7Ox9KRuBCWodPgmzwzFdDH

ALT: colour photograph of male holding lip open to show mouth ulcer

I'm not sure why, but I'm more prone to biting my lip when crashed. It swells. I bite it again. Mouth ulcers soon join the party. Antiseptic mouth wash helps, but no doubt I'll bite again before gets chance to heal.

/CFS

bananabob, to me
@bananabob@mastodon.nz avatar
dmcahill, to me
@dmcahill@aus.social avatar

“Scientists have uncovered compelling evidence for abnormalities in the brain and immune systems of patients with chronic fatigue syndrome (CFS), also known as ().” via @hannahdev https://www.theguardian.com/society/2024/feb/21/scientists-find-link-between-brain-imbalance-and-chronic-fatigue-syndrome

mitexleo, to fediverse

You're amazing 👏 💖

CFS: number of patients is expected to double due to long-term effects of the COVID-19 pandemic: Scientists at MedUni Vienna have now identified possible biomarkers that could improve the diagnosis and treatment (www.meduniwien.ac.at)

The study by Eva Untersmayr-Elsenhuber and her team from MedUni Vienna's Center for Pathophysiology, Infectiology and Immunology builds on earlier research on immune disorders and the intestinal barrier function in patients with ME/CFS. It is well known that ME/CFS patients often differ greatly in the clinical manifestations of...

eladnarra, to cfs
@eladnarra@disabled.social avatar

Day 1 of my 2-day CPET done! Feeling pretty exhausted; hopefully that means all the numbers when I do it again tomorrow will show post exertional malaise (PEM).

/CFS

ME Research UK and the ME Association announce funding for a study that aims to create a diagnostic test for ME/CFS (www.meresearch.org.uk)

In 2019, Professor Ron Davis from America reported that researchers had developed a nanoelectronics test that could detect an impedance in white blood cells taken from people with ME/CFS1....

April 3-4 The 1st International Conference on Clinical and Scientific Advances in ME/CFS and Long COVID (free virtual registration) (conferencia-emsfc-pos-covid.pt)

The 1st International Conference on Clinical and Scientific Advances in ME/CFS and Long COVID aims to raise awareness, clarify misconceptions, promote understanding, and stimulate discussion among healthcare professionals, investigators, policymakers, patients, and community representatives on the clinical manifestations,...

A break in mitochondrial endosymbiosis as a basis for inflammatory diseases (Abstract) (pubmed.ncbi.nlm.nih.gov)

Mitochondria retain bacterial traits due to their endosymbiotic origin, but host cells do not recognize them as foreign because the organelles are sequestered. However, the regulated release of mitochondrial factors into the cytosol can trigger cell death, innate immunity and inflammation. This selective breakdown in the...

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