Quick update re foundation: TEMPI foundation (tempi-stiftung.at) will establish a yearly grant worth 100k USD for #mecfs research. We plan to be open for applications by 2023. My family finances the budget for this specific grant for the next five years, guaranteed./1
Christoph Ströck
@cstroeckw
Board member |
Soon, people will look back in disbelief at what has happened to patients with #mecfs |
Vienna, AustriaJoined January 2016
Christoph Ströck’s Tweets
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Gene expression data in the Cornell Center’s latest preprint (tinyurl.com/4e7cdeum) suggests monocytes are receiving signals from tissue under assault—perhaps from infection or injury. More work to do—what are these signals and where are they coming from?
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Thank you very much for supporting us via the first-ever “Johadamis ME/CFS Research Grant.” 🙌 We are very excited to work with to identify signs of infection in #ME/CFS blood + cerebrospinal fluid, in concert with
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My special thank you to @cstroeckw who taught me so much about #MECFS and has been so generous with his effort to educate the public and promote research on this understudied disease

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So grateful to receive the 2022 Johadamis ME/CFS Research Grant! In collaboration with @polybioRF @BjornBragee we will test blood & CSF samples from #MECFS patients for immune phenotypes and antibodies to various pathogens. This will inform us about potential drivers of disease. twitter.com/tempi_stiftung…
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Thank you, to everyone involved.
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Covid infections disrupt the gut microbiome and increase vulnerability to secondary bloodstream infections
nature.com/articles/s4146
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Replying to @foundmyfitness
Great timing Rhonda!- I just posted this (my favorite topic, aging biology) pub’d last week.
Kynurenine Pathway Metabolites in the Blood and Cerebrospinal Fluid Are Associated with Human Aging
They ID’d age-related
of potentially neurotoxic QA in
.
hindawi.com/journals/omcl/
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Every mitochondria in a cell imaged over 10 min. Depth-coded LUT (8 μm range). The ability to rapidly image full cell volumes came from a SoRa tip he posted here. Movie uploaded using a trick. LUT from 's NeuroCyto Fiji plugin. See the pattern? 🙌
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Worsening POTS Is Associated With Increased Glucose-Dependent Insulinotropic Polypeptide Secretion
pubmed.ncbi.nlm.nih.gov/35232225/
The glucose-induced worsening orthostatic tachycardia in POTS occurred while GIP, a splanchnic vasodilator, was maximally elevated.
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If you want to understand how MDs treat #mecfs and #longcovid patients, please dive deeply into this subreddit. I will repeat it. MDs and academics knowing about the severity of these diseases and who stand by idly are part of the problem!
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Hey @economicsbrooke @CatiaNicodemo, have you seen r/medicine’s reaction to your study?
Looks like you hit a sensitive nerve — dead on
reddit.com/r/medicine/com
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Spermidine activates mitochondrial trifunctional protein and improves antitumor immunity in mice
New insight into the properties of SPD may facilitate the development of strategies to prevent and improve outcomes of age-related immune pathologies.
science.org/doi/abs/10.112 
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B cells from old mice induce the generation of inflammatory T cells through metabolic pathway
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"Given its central importance, it is logical that cells would modulate mitochondrial membrane potential in response to demand and environmental cues [...]". Membrane potential is a widely conserved biological integration site - cell membrane and likely mitochondrial membrane too.
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Congrats @Yeyunouyang for your pre-print from the @RutterLab coming out today!
Check out this fascinating body of work - learn about some fascinating ways mitochondria sense and respond to mitochondrial dysfunction.
biorxiv.org/content/10.110
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Vielen Dank für Ihre Hilfe/Unterstützung!
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Wichtige Folge-Empfehlung!
Die @Tempi_Stiftung, eine Initiative der Familie Ströck, unter anderem @cstroeckw, fördert Forschung zu #MECFS.
Neu mit einem jährlichen $100.000-Grant, zu dem Details in den nächsten Wochen bekannt gegeben werden!
tempi-stiftung.at
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"These six genes were further upregulated in the 22 bedridden participants who suffer not only from ME/CFS but also from other autoimmune diseases. These genes are involved in T cell, B cell and autoimmunity functions." ncbi.nlm.nih.gov/pmc/articles/P
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(Ugh, one paragraph got lost, but the point I am trying to make comes across nevertheless, I hope)
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is used in a quasi religious manner. It is "where" medicine puts many of the things we don't know or understand. In doing so upholding old dogma. This comes at a high cost for patients in many or most cases.
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is or can be psychosomatic, depending on an intuitive process of any given MD or certain specialties (i.e. psychiatrist). No questions asked. It is interesting to note that unfalsifiability is a "no go" in medicine unless it serves the idea of psychosomatism which
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The alternative (and unfortunately the status quo in medicine) is ludicrous. At its core, it says that every medical diagnoses must be falsifiable (i.e. biomarker) unless it is psychosomatic. Which means that every disease that can exist but is not understood
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Psychosomatic diagnoses shouldn't be existent as long as they are not falsifiable. Even if there were psychosomatic "appearances", and this whole conundrum was not mostly "magical thinking" MDs should be held accountable to (per default) err on the side of caution.
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"The results show physicians discuss ME/CFS, depression, and Lyme disease with more negative language [...]. The results for ME/CFS included over four times more negative words than the results for depression."
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Amazing.
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PS: The website and Twitter are at the very bottom of our priority list atm. Tempi is run entirely by very few volunteers; most of our time is used to find and advance good funding opportunities.
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Tempi-Foundation runs its own Twitter profile now. Please follow to stay up to date. 💙
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Hallo Herr ! Würden Sie uns helfen und untenstehenden Tweet teilen? Wären davon unabhängig für jeden Tipp dankbar! Vielen Dank! 💙
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Arzt/WissenschaftlerIn in Österreich die/der am Interplay von Stoffwechsel und Infektion im Zusammenhang #mecfs forschen möchte und/oder daran interessiert ist am Aufbau einer Forschungsplattform mitzuwirken?
Bitte teilen!
Bei Interesse:
christoph.stroeckcfs@gmail.com
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Arzt/WissenschaftlerIn in Österreich die/der am Interplay von Stoffwechsel und Infektion im Zusammenhang #mecfs forschen möchte und/oder daran interessiert ist am Aufbau einer Forschungsplattform mitzuwirken?
Bitte teilen!
Bei Interesse:
christoph.stroeckcfs@gmail.com
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Arzt/WissenschaftlerIn in Österreich die/der am Interplay von Stoffwechsel und Infektion im Zusammenhang #mecfs forschen möchte und/oder daran interessiert ist am Aufbau einer Forschungsplattform mitzuwirken?
Bitte teilen!
Bei Interesse:
christoph.stroeckcfs@gmail.com
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I am not a doctor, but if your gut- and blood-brain barriers are "leaky", you would not necessarily need abnormal standard blood testing to be in big trouble. There is no "normal amount of X" if it travels freely where it should not. #mecfs #longcovid
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The normal structure and permeability pathways of blood-brain barrier (BBB)
#cancer #oncology #neurology #braincancer #neurotwitter #MedEd #MedTwitter #SciComm #AcademicTwitter
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On the one hand, it makes sense not to "overrepresent" phenomena that appear "psychological"(they are not) if you want to establish a clear demarcation line between psychological disease and #mecfs. Still, on the other hand, you lose an opportunity to detect "early cases."
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What this points to in my opinion, is that severe cognitive symptoms are underreported in the literature of #mecfs. Available information I found to be a good description of what I experienced were always biased towards Alzheimer, PD, MS, Psychosis, all excluded by MDs.
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That is the good news; the bad news is brain fog remained and, in some facets, intensified over the years. It is likely tied to hypoperfusion, neuroinflammation, and the resulting metabolic reprogramming and maybe also some of what doctors would call "actual damage".
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Anyways, the depersonalization and derealization went away by themselves. These phenomena are likely to appear time-restricted in many or most patients. They seem to correlate with an early, more intense (neuro) inflammatory process that subsides to some degree.
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way of knowing this, and I followed my doctor's orders. I also know that if I had listened to what my body told me, despite what everyone else said, I would not have ended up with very severe #mecfs, though.
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I was in grave danger of making myself worse by keep pushing mentally as well as physically (I did 30 repetitions per set of pull-ups with mild mecfs) to regain what I understood to be my former health. To this day, I beat myself up about this. I know there was no
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While physical symptoms were already quite severe (POTS, PEM,..), they were in the background. When you can't remember your own birthday, your arm feels by all means like a foreign entity, and the whole world loses its "normalcy" it is not surprising I did not understand that
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