Mark is beloved by millions of kids, which makes it particularly great that he’s teaching them how to inform their parents that Tesla is a danger to children. This is another one of those “we don’t need a ‘Rogan of the left’, we need normal men” examples.
16.03.2025 17:06 — 👍 5814 🔁 1076 💬 87 📌 34
Mundus sine Caesaribus
14.03.2025 04:58 — 👍 2 🔁 0 💬 1 📌 0
Abstract
Myalgic encephalomyelitis (ME/CFS) a chronic, disabling illness with no established etiopathology. It has been indicated in some population-based studies that Black and ethnic minority populations are underdiagnosed with ME/CFS. The aims of the present study were to (1) identify the agreement between receiving an ME/CFS diagnosis and meeting diagnostic criteria, (2) identify the demographic characteristics associated with receiving a diagnosis, and (3) explore patient satisfaction with healthcare. Self-reported medical history and symptoms were collected via online survey from respondents with and without fatigue. The agreement between self-reporting an ME/CFS diagnosis and meeting the Center for Disease Control’s (CDC) ME/CFS criteria or Institute of Medicine (IOM) criteria was assessed with Cohen’s kappa. Patient characteristics predicting a physician diagnosis were analyzed with logistic regression. Associations between diagnosis, demographics, and healthcare satisfaction were assessed with chi-square tests of independence. There were 1110 responses. The agreement between meeting ME/CFS criteria and reporting an ME/CFS diagnosis was fair (CDC: κ = 0.29; SE = 0.02; IOM: κ = 0.28, SE = 0.03). White respondents had 2.94 greater odds of being diagnosed with ME/CFS than non-White respondents. Having an ME/CFS diagnosis was associated with dissatisfaction with healthcare (χ2 (3, N = 1063) = 14.17, p = 0.003). The findings suggest racial disparities in the diagnostic processes for ME/CFS.
Keywords: bias; social determinants of health; minority; long COVID; inequality
Possible Racial Disparities in the Diagnosis of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS)
www.mdpi.com/1660-4601/22...
"White respondents had 2.94 greater odds of being diagnosed with ME/CFS than non-White respondents"
#MEcfs #CFS
16.02.2025 13:58 — 👍 33 🔁 9 💬 1 📌 1
Area chart showing ME funding (£6m) vs. MS, IBD and Parkinson's by the UK Government, 2015-20
A comparison of UK Government research funding for ME/CFS compared to other diseases like MS, IBD and Parkinson's 🧐
@nihr.bsky.social and @ukri.org we need ring-fenced funding for ME as part of the Delivery Plan
Thank you to @mediumwhite.bsky.social & co. for analysis
#MECFS #NHS
16.02.2025 19:37 — 👍 37 🔁 25 💬 7 📌 0
Galician Medical Journal
ifnmujournal.com/gmj/article/... adolescent #t1dm clinic study - 25/70 pts (36%) positive bedside test for #POTS- HbA1c in that group high- 10.4%
16.02.2025 04:43 — 👍 6 🔁 1 💬 0 📌 0
This is a good and bad paper at the same time - if you compare #MECFS to #LongCovid in any scientific context, you must compare LC+PEM (i.e., ME from Covid) to #MECFS. Otherwise, you get the average of symptoms from any post-Covid condition.
15.02.2025 08:36 — 👍 13 🔁 4 💬 1 📌 0
With so much attention on NIH lately, can’t help but bring up lack of research focus of #myalgicencephalomyelitis #MECFS by NIH over the years. It’s so low make you wonder if intentional content.iospress.com/articles/wor...
15.02.2025 05:27 — 👍 2 🔁 0 💬 0 📌 0
I think it’s quite clear to outsiders- 🇺🇸 land of the bigsoda, bigsugar, bigfastfood, also the land of the biotech, pharma. Can’t make 🇺🇸 healthy without addressing the former
15.02.2025 03:51 — 👍 2 🔁 0 💬 1 📌 0
COVID-related conditions should be integrated into medical education rather than being left to so-called ‘Long COVID clinics.’ When those in charge lack a real understanding of the condition, these clinics end up becoming gaslighting centers. Physician education must come first.
12.02.2025 19:38 — 👍 13 🔁 2 💬 1 📌 1
Figure 3. Quercetin’s Enhancement of Macroautophagy for Cellular Regulation. The quercetin’s dynamic role in bolstering macroautophagy is a critical cellular process for maintaining homeostasis through the degradation and recycling of proteins and organelles. Quercetin modulates the mechanistic target of rapamycin (mTOR) pathway and activates AMP-activated protein kinase (AMPK), leading to decreased mTOR activity and the initiation of autophagy.
www.frontiersin.org/journals/pha... #Quercetin Enhancement of Macroautophagy for Cellular Regulation. Its dynamic role in bolstering macroautophagy is a critical cellular process for maintaining homeostasis
14.02.2025 23:21 — 👍 3 🔁 1 💬 0 📌 0
Just reflecting on the realisation that my medical education taught me much more about Munchausen’s, which I have rarely if ever seen, than ME/CFS, which I now see near daily.
12.02.2025 12:49 — 👍 7 🔁 3 💬 0 📌 0
It’s 2025, there really is no excuse to get blank looks from HCPs in Australia when #MyalgicEncephalomyelitis #MECFS is mentioned, policy makers should do more to ensure such given the health equity and access that pwME pwLC deserve
11.02.2025 23:23 — 👍 12 🔁 3 💬 0 📌 0
A small study but #mecfs pts with or without “psychogenic pseudosyncope “ diagnosis, greater orthostatic 🧠 blood flow drop pmc.ncbi.nlm.nih.gov/articles/PMC...
11.02.2025 05:52 — 👍 3 🔁 1 💬 0 📌 0
Logos for the British Psychological Society, Action for ME & ME Association
Good Practice Guidelines for Psychologists Working with People with ME/CFS
November 2024 Update
Screenshot of 1st 2 paragraphs
🧵
Good Practice Guidelines for Psychologists Working with People with ME/CFS November 2024 Update
meassociation.org.uk/wp-content/u...
Although this isn't brand new, I found it interesting so I'm going to post some extracts to this thread.
#MEcfs #CFS #PwME
1/
10.02.2025 21:16 — 👍 43 🔁 11 💬 4 📌 0
Humankind prior to 8 ka consisted of fewer than 50 million people, many of whom were migratory. Modern
human civilization in the 21st century is projected to near 10 billion people, hundreds of millions of whom live in permanent coastal communities that cannot be relocated inland.
30.12.2024 17:00 — 👍 13 🔁 5 💬 2 📌 0
GP Educational Webinar
on PVFS and ME/CFS
Dr Ros Vallings, a New Zealand GP who is an expert
on myalgic encephalomyelitis/chronic fatigue
syndrome (ME/CFS), will present a free talk entitled
'Key Messages for Primary Care on the Diagnosis
and Management of Post Viral Fatigue Syndrome
and ME/Chronic Fatigue Syndrome', followed by
a Q&A session on Tuesday, April 8 at 7:30pm.
Accreditation applied for from the Irish College of GPs
For more information, contact CPD@irishmecfs.org
38 FORUM January/February 2025
An ad we & the Irish ME Trust are running in this month's Forum magazine for Irish GPs in advance of our free webinar in April
#MyalgicEncephalomyelitis #ChronicFatigueSyndrome
06.02.2025 13:31 — 👍 10 🔁 5 💬 1 📌 2
Does COVID increase the risk of Alzheimer’s disease?
COVID-19, even in mild cases, is linked to changes in Alzheimer’s disease-related brain biomarkers comparable to four years of aging. This study raises concerns about long-term neurological risks and ...
“Overall, the study provided new evidence that COVID-19 may accelerate Alzheimer’s disease-related brain changes, even in individuals with mild infections. The observed alterations in plasma biomarkers suggested a potential long-term impact on brain health.”
www.news-medical.net/news/2025020...
03.02.2025 16:27 — 👍 64 🔁 33 💬 5 📌 1
1 in 22 COVID survivors develop debilitating chronic syndrome
A study suggests that catching COVID-19 significantly raises the risk of developing ME/CFS (formerly called "chronic fatigue syndrome"), a typically lifelong condition that can be debilitating.
When I trained in medicine I was told that Chronic Fatigue Syndrome (CFS/ME) was rare. I expected to see a handful of cases in my whole career.
Now I have Long Covid related CFS myself, I know of many affected colleagues, & saddest of all, 3 of my kids’ friends.
www.livescience.com/health/coron...
31.01.2025 09:34 — 👍 254 🔁 71 💬 12 📌 5
Important work from Australian group. It’s interesting that rather than novel, probably just forgotten by clinicians. Brain perfusion SPECT been used in #MECFS for years, it’s part of the diagnostic primer for medical practitioners from 2012 www.investinme.org/Documents/Gu...
30.01.2025 03:04 — 👍 17 🔁 4 💬 0 📌 0
Cochrane Review is...
29.01.2025 12:53 — 👍 4 🔁 1 💬 0 📌 0
Schematic representation of different signaling pathways and targets by quercetin as a potential therapeutic strategy in autoimmune diseases.
MMI vs autoimmune induced hypothyroidism, then potentially even more compelling mechanisms of quercetin - pmc.ncbi.nlm.nih.gov/articles/PMC...
Any human study on significant impact on thyroid function? Papers on in vitro studies, or in vivo rodent studies, tend to be quite speculative
29.01.2025 12:46 — 👍 1 🔁 0 💬 1 📌 0
Your leading source of international, cutting-edge research, review, and opinion in clinical #diabetes and #endocrinology. IF=41·8.
🌐 thelancet.com/journals/landia/home
Nutrition & Metabolism scientist. KevinHallPhd.com
Innovators in physiology research instruments. Family-owned, small business. Connecting great engineering to great science, enabling the next generation of researchers today!
www.technavance.com
There are #MillionsMissing from their lives due to ME (Myalgic Encephalomyelitis or #MECFS). We're fighting to make their voices heard. Sadly, many ppl with #LongCovid meet #ME diagnostic criteria - adding many more to the ME ranks.
Psychiatry, Public Health, People Power, Politics, Poetry | NSW Chair @RANZCP | Co-founder @seriphclinics | Research Fellow @UNSW | MD BMed BA MMed MSc FRANZCP GAICD
Not-for-Profit Organisation supporting Australians living with ME/CFS (mylagic encephalomyelitis / chronic fatigue syndrome) and long COVID.
Education | Research | Advocacy | Support Services
Website: www.emerge.org.au
Donate: www.emerge.org.au/donate/
Progressive bitch 💙 surviving stochastic terrorism. Used to work in science, healthcare, gov and higher ed before the dumbfucks took over. Watching #homeworthy just to talk shit about bitches with better #antiques than me. No DMs. Happily married. #resist
America’s Finest News Source. A @globaltetrahedron.bsky.social subsidiary.
Get the paper delivered to your door: membership.theonion.com
Radiologist. Interested in neuroimaging, molecular imaging and therapies, particularly theranostics.
Utrecht, NL
Physician (IM, EM, Pulm), Scientist. Dancer, Seamstress, Apprentice Balcony Gardener, Booklover, Foodie (more eating than cooking), Painter (badly), Traveller, Gamer. Living with Crohn's Disease.
Swiss (but not a fan of chocolate).
Columnist for The Saturday Paper, 7AM Podcast contributor, ABC Nightlife commentator, veteran political journalist. His views contestable but his own.
Independent Member for Kooyong. Authorised by M. Ryan 145 Camberwell Rd, Hawthorn East, 3123 #Mon4Kooyong
https://linktr.ee/moniqueryan
Fan of microglia, macrophages, glial-neuronal and brain-immune interactions (both innate & adaptive); flirted with oligodendrocytes, astrocytes and occasionally even neurons.
EIC Journal of Neuroinflammation
Sci-Fi and SDCC (Comicon)
opinions are my own
Neuropharmacology Lab at a major R1 in the south. We study mechanisms of and drug discovery for alcohol-induced neurodegeneration.
neural stem cells | adult neurogenesis | microglia | adolescent development | aging
Posts are our opinion.
Professor, Dept Path at the University of California Irvine. Focused on Aging and Alzheimer disease in people with Down syndrome, 🇨🇦, http://sites.mind.uci.edu/headlab/ and https://www.nia.nih.gov/research/abc-ds
Neuro postdoc at UCC 🇮🇪 PhD at MPI-NAT, 🇩🇪 | Alzheimer's x glia x sex differences x gut microbiome 🔬🧠 | (he/they) 🏳️🌈
Lab studying molecular evolution of proteins and viruses. Affiliated with Fred Hutch & HHMI.
https://jbloomlab.org/
PhD brain and genomic scientist. Ocean junkie. Computer wrangler. Open data believer. Geek. Punk. Not that kind of doctor. Views only my own. She/her
Neuroscientist and glial aficionado at NYU Grossman School of Medicine/NYU Langone Health in NYC. Posts in my individual/personal capacity.
My lab is full of awesome people doing amazing stuff - check them out: www.liddelowlab.com
he/him
My team and I study why pain can become chronic. We like the peripheral nervous system, neuroimmunology, stromal cells and sequencing. If you have similar interests - please say hi!