Michael Stingl @neurostingl
Facharzt für Neurologie ME/CFS ▪ Long Covid ▪ Nervenultraschall ▪ ENG/EMG ▪ Hirngesundheit ▪ Telemedizin neurostingl.at Garnisongasse 7/13, 1090 Wien Joined May 2018-
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Wenn man über Post Exertional Malaise was lernen mag, sollte man @sunsopeningband zuhören.
Wenn man über Post Exertional Malaise was lernen mag, sollte man @sunsopeningband zuhören.
Vor kurzem gab es einen hochkarätig besetzten Workshop von @theNASEM zu Infekt-assoziierten Erkrankungen, zB ME/CFS. Die ausführliche Zusammenfassung kann hier nachgelesen werden. nap.nationalacademies.org/catalog/27462/…
In dem Moment, wo dieses Faktum zu Post Exertional Malaise der common ground der medizinischen Diskussion über ME/CFS ist, wird man über Nuancen auch wirklich diskutieren können.
In dem Moment, wo dieses Faktum zu Post Exertional Malaise der common ground der medizinischen Diskussion über ME/CFS ist, wird man über Nuancen auch wirklich diskutieren können.
Spannende Studie, mit Hinweisen auf Viruspersistenz und Veränderungen des Immunsystems bei Long Covid, ~24 Monate nach Infektion.
Spannende Studie, mit Hinweisen auf Viruspersistenz und Veränderungen des Immunsystems bei Long Covid, ~24 Monate nach Infektion.
Die Awareness-Kampagne von @weandmecfs zeigt die Drastik von ME/CFS sehr gut. Der Schwung, der gerade mit Referenzzentrum und gesteigerter Aufmerksamkeit für ME/CFS entsteht, muss endlich zu einer besseren Versorgung der Betroffenen führen.
Die Awareness-Kampagne von @weandmecfs zeigt die Drastik von ME/CFS sehr gut. Der Schwung, der gerade mit Referenzzentrum und gesteigerter Aufmerksamkeit für ME/CFS entsteht, muss endlich zu einer besseren Versorgung der Betroffenen führen.
Interessanter Artikel über eine neue Methode zur Diagnostik bei Liquor Leak. link.springer.com/article/10.100…
Bei aller Kritik an der Methodik, wenige Leute sind es halt auch nicht, die in England noch an Long Covid (unpräzise Definition) leiden.
Bei aller Kritik an der Methodik, wenige Leute sind es halt auch nicht, die in England noch an Long Covid (unpräzise Definition) leiden.
Ein nationaler Aktionsplan - der auch umgesetzt wird - ist dringend notwendig. ME/CFS ist nämlich weiterhin eine höchst relevante Erkrankung ohne Versorgungsstruktur. science.apa.at/power-search/1…
Dieser Thread mit den Antworten von @sunsopeningband zu PEM und 2-day CPET bei ME/CFS ist lehrreicher als jede Fortbildung.
Dieser Thread mit den Antworten von @sunsopeningband zu PEM und 2-day CPET bei ME/CFS ist lehrreicher als jede Fortbildung.
Studie, wo Nachweis von SC2-RNA in verschiedenen Geweben sehr deutlich mit Long Covid (unpräzise definiert) nach milder Infektion verbunden war. Insofern wieder ein Hinweis, dass Viruspersistenz bei einem Teil der Betroffenen eine Rolle spielen könnte. thelancet.com/journals/lanin…
Dr.C.Werner @DrCWerner
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3K Followers 121 Following 100% crowdfunded LC & ME/CFS conference project. community-driven. independent. global.Michael Mitterwallner @Mit48218Michael
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2K Followers 661 Following Writer. Troublemaker. Rhetoric Professor @UTAustin 🏳️⚧️🏳️🌈🥄#pwME Words in @HuffPost @TheHill @BostonGlobe Author of Constellating Home https://t.co/MRhE1rgTwMProf. Dr. Nils Kroemer // @cornu_copiae @UniklinikBonn @uktuebingen on “Targeting motivation with vagus nerve stimulation” scheduled lecture on Thursday, 29.08; 2 pm – 3 pm #CSSBP2024 @UniCologne @joseph_kambeitz
Thrilled to be part of the #CSSBP2024 summer school with a focus on focus on transitions & frontiers. Thank you for organizing this @koeniglab and @joseph_kambeitz
Prof. Dr. Nils Kroemer // @cornu_copiae @UniklinikBonn @uktuebingen on “Targeting motivation with vagus nerve stimulation” scheduled lecture on Thursday, 29.08; 2 pm – 3 pm #CSSBP2024 @UniCologne @joseph_kambeitz
Reminder: This Friday, 5/3 at 1:00pm ET - @RenegadeRes & @MEActNet bring you this Clinican's roundtable with @sunsopeningband - Clinican's can earn 1 CME credit. Register at: us06web.zoom.us/webinar/regist… #MedTwitter #MECFS #longcovid #IACI
Would you like to ask Prof. Akiko Iwasaki (@VirusesImmunity) a question? You can do so during her session at #UniteToFight2024 ! Register now for free or send the link to people who should attend
I'll also point out there's a lot of daylight between No PEM and Mild (50% impairment). This is a challenging population requiring special monitoring and education, because they feel lousy but are good enough at faking being well that we clinicians may assume there's no problem.
These guidelines are from the International Consensus Criteria for ME. 50% reduction in pre-illness activity levels is required for mild. Moderate is housebound. These levels don't belong together in patient stratification for clinical decision-making. ncbi.nlm.nih.gov/pmc/articles/P…
We have a few more speakers if you like ?! ☺️ Please welcome Megan Fitzgerald @TheMegascope from @patientled ! Megan will provide insights into the reinfection study. She will talk about the effect of reinfections on self-reported measures of post-exertional malaise (PEM) 👍…
This is important, common and underecognised by neurologists. It can take different forms including feeling ill, symptoms worsening without explanation, brain fog and even momentary unrousability when sitting
33 years after our 1st joint paper, my mentor & friend Gert van Dijk (now retired) and I published new article together. Highly relevant: hypotensive “twilight zone”, often missed in persons with #Parkinson. Timely recognition is important: it is debilitating & treatable.
@bmsgpk Unterstützt uns z.B. am 12. Mai und helft uns, den Anliegen von #MECFS-Betroffenen mehr Sichtbarkeit zu geben! 👉mecfs.at/politik/#petit… 👉mecfs.at/unversorgtseit… 8/8
@bmsgpk Erschwerend für unseren weiteren Einsatz ist, dass eine Entschließung sich immer nur auf die aktuelle Zusammensetzung des Nationalrats bezieht und daher nach der anstehenden Wahl nicht mehr als politische Willensbekundung gültig ist. Wir bleiben weiterhin dran! 7/8
Anerkennung, medizinische Versorgung & Absicherung von Betroffenen sowie Forschungsförderung”. Die Entschließung war das Ergebnis eines 1,5-jährigen Petitionsprozesses mit enormem Engagement und führte zu viel Hoffnung bei den Betroffenen. 2/8
📍1 Jahr ME/CFS-Entschließung im Nationalrat: Viel Hoffnung, keine Umsetzung für ME/CFS-Betroffene📍 Vor einem Jahr wurde im Nationalrat einstimmig beschlossen, die #MECFS Situation verbessern zu wollen: “Entschließung des Nationalrates vom 27. April 2023 betreffend ME/CFS: 1/8
@U2Fight_World Thank you #UniteToFight2024 for including me in your speaker list. I am hoping to show you how ME/CFS differs from long COVID and how we can predict the severity of long COVID very early. Hopefully it will help us in developing better treatment strategies.
Quick reminder 🗣️ You may saw @johanvawe tweet today! Johan is speaking at #UniteToFight2024 next month. You can watch his session live and free of charge 👍
if there is someone that still doesn’t believe Long Covid is a real biological condition, and similar ME/CFS, in 2024, I can only say 1- I am sorry 4you 2- you should seriously consider how you study new literature 3- you should also reconsider your role if you are a doctor
#LongCovid is complex to diagnose and treat, so we need #biomarkers! 1. to confirm viral persistence, and 2. to map the failing/overactive immune response. So we tried to hit two birds with one stone using digital transcriptomics 👇👇 (1/n) thelancet.com/journals/lanmi…
This is a real-world #LongCovid cohort, based on general practice of Marc @jamoulle who has become a beacon of hope for patients in Belgium & beyond. From his practice 48 patients and 12 controls were carefully matched for age, sex, time since COVID, vaccination and comorbidities
We believe clinically useful #biomarkers should be non-invasive: while it is interesting to know what happens with #SARSCoV2 in muscle or colon/gut, these biopsies are too painful and laborious to integrate in daily care for #LongCOVID patients. Hence a blood test!