wigglethemouse

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wigglethemouse

wigglethemouse

@wigglethemouse

49ers and Swindon Town supporter. Engineer. #mecfs has got in the way of having a life

49ers Land Katılım Ocak 2009
140 Takip Edilen894 Takipçiler
wigglethemouse
wigglethemouse@wigglethemouse·
@JackHadfield14 Mast cells also have receptors that release Granzyme just like Killer T and NK cells. That kinda blew my mind.
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Jack | amatica health
Jack | amatica health@JackHadfield14·
Non exhaustive list of receptors on mast cells: ∙FcεRI (high-affinity IgE receptor) ∙FcγR (IgG receptors) ∙c-KIT (CD117) ∙MRGPRX2 ∙TLR1 ∙TLR2 ∙TLR3 ∙TLR4 ∙TLR5 ∙TLR6 ∙TLR7 ∙TLR8 ∙TLR9 ∙C3aR ∙C5aR ∙ST2 (IL-33 receptor) ∙IL-1R ∙NK1R (substance P receptor) ∙CRLR/RAMP1 (CGRP receptor) ∙PAR1 ∙PAR2 ∙PAR3 ∙PAR4 ∙S1PR1 ∙S1PR2 ∙CysLT1R ∙CysLT2R ∙H1R ∙H4R ∙A2A (adenosine receptor) ∙A2B (adenosine receptor) ∙A3 (adenosine receptor) ∙CB1 ∙CB2 ∙VPAC1 ∙VPAC2 ∙EP2 ∙EP3 ∙EP4 ∙DP1 ∙DP2 (CRTH2) ∙CCR1 ∙CCR3 ∙CCR5 ∙CXCR1 ∙CXCR2 ∙CXCR4 ∙LPA receptors ∙P2X7 ∙P2Y ∙TRPV1 ∙TRPV2 ∙TRPA1 ∙ERα (oestrogen receptor alpha)
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Jack | amatica health
Jack | amatica health@JackHadfield14·
Further to this, most low-level mast cell treatments are semi-useless in excluding mast cell involvement. Mast cells have numerous downstream mediators and upstream triggers Oversimplifying them to histamine and IgE is extremely narrow in scope and does not represent the reality
Jack | amatica health@JackHadfield14

Not reacting to food does not exclude mast cell involvement. Research shows mast cells may be implicated in Alzheimer’s, MS, migraines, neuropathy, ALS, pain, reflux, and blood pressure, despite these patients not reacting to food. Food hypersensitivity is just one presentation.

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wigglethemouse
wigglethemouse@wigglethemouse·
@violinvet @Naomi_D_Harvey Yep. We got sunblock curtains and I reacted to the smell of them 😂 Six months airing in the garage before we hung them up.
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Naomi Harvey “PhD Witch” #WearAMask
The sun ☀️ is finally in our garden in the mornings now so I’ve tried to sit in it for a bit to help my circadian rhythm etc. but it’s immediately causing the skin on my face to sting & feel like it’s burning. Other areas of my skin are fine though 🤷🏻‍♀️ it’s still sore hours later.
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wigglethemouse
wigglethemouse@wigglethemouse·
@violinvet @Naomi_D_Harvey Thanks for the feedback both of you. It was good to be reminded that repeated exposure can desensitize the skin somewhat sometimes. Sunblock clothes and good quality sensitive skin sunblock can help too. Unless you start reacting to the sunblock as well.
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Hannah
Hannah@violinvet·
@Naomi_D_Harvey @wigglethemouse For me, there was absolutely no change in anything that I could tell. It just happened, and went away the next year.
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wigglethemouse
wigglethemouse@wigglethemouse·
@JackHadfield14 Sorry if I missed it what is the outer green line? Is it 3 standard deviations above high normal or something like that?
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wigglethemouse
wigglethemouse@wigglethemouse·
@violinvet @Naomi_D_Harvey I'm allergic to the sun since 2000. Did you have any thoughts on what might have caused it and why it disappeared E.g. perhaps a medication making you sun sensitive?
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Hannah
Hannah@violinvet·
@Naomi_D_Harvey I got randomly allergic to the sun on my arms a couple of years ago for just one summer. It was random, and quite vexing. And I didn't want to be on an antihistamine every time I went outside so I just went around with a parasol like a Victorian lady.
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wigglethemouse
wigglethemouse@wigglethemouse·
@Z3R0Gravitas @Naomi_D_Harvey @clarejdaly I don't get much light all year round but I do get seasonal changes. Leaves appearing on trees and leaves disappearing from trees are two very stark downturns for me. Second week March, second week October. Mike Snyder had a very good seasonal study a few years ago.
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Richard Lewis
Richard Lewis@Z3R0Gravitas·
@Naomi_D_Harvey @clarejdaly I mean to say, are there many who feel *better* in summer but get no notable UVB exposure? Counter-evidence. Windows tend to block basically all UVB. Less so NIR. I'd look at if NIR lamps compliment UV exposure, too. I think it may prime the skin to protect against damage.
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wigglethemouse
wigglethemouse@wigglethemouse·
@Sally_writes ❤️❤️❤️. That marketing career is being put to good use. 😍
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wigglethemouse
wigglethemouse@wigglethemouse·
@nwagoner Fred said it wasn't up to him, it was a business decision. 49ers insure their top wages. Could he need to meet an insurance demand before returning? Reinjury could be a significant cost for the insurer. How do these policies work?
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Nick Wagoner
Nick Wagoner@nwagoner·
RE: Fred Warner and a potential return to #49ers. This Sunday would mark 21 days until the Super Bowl. Opening his practice window at any point from then would give maximum time possible to evaluate if he's ready to go with no real down side. (That's probably true now, too, given that it's close enough to the time left on the season as a whole running out relative to the window).
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wigglethemouse retweetledi
Maureen Hanson
Maureen Hanson@DrMaureenHanson·
In pre-2020 ME cases, analysis of over 7000 proteins demonstrates that exertion disrupts T and B cell signaling, IL-17 pathways, and mitochondrial metabolism in comparison to healthy sedentary controls. Protein signatures correlate with symptom severity.
Maureen Hanson tweet media
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wigglethemouse
wigglethemouse@wigglethemouse·
@mecfsskeptic I would say for neurological/peripheral nerve effects sjogrens is a close match.
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ME/CFS Science
ME/CFS Science@mecfsskeptic·
Question: of all medical conditions and diseases*, which one's presentation do you think is most similar to ME/CFS? * Excluding overlapping syndromes such as fibromyalgia, Long Covid, POTS, MCAS, hEDS, etc., which are equally poorly understood.
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wigglethemouse
wigglethemouse@wigglethemouse·
@lifeanalytics @OpenMedF I thought that summary was fascinating. You don't normally write 3 papers for null results. Fingers crossed. And this work has been progressing for quite a number of years. I'm looking forward to see how well the radioisotope labelling worked that was on previous web version.
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Michael R Scoma MD
Michael R Scoma MD@DrMichaelScoma·
Severe and very severe ME/CFS patients are the sickest patients I’ve ever seen - even compared to septic transplant or end-stage cancer patients. The unrelenting suffering and lack of research or definitive treatments puts severe ME/CFS on another level. Nothing compares...
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wigglethemouse
wigglethemouse@wigglethemouse·
@Z3R0Gravitas I've enjoyed seeing them and knowing that you were able to get out and about. And yes the hedges were fun!
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Richard Lewis
Richard Lewis@Z3R0Gravitas·
@wigglethemouse A Mr Man of taste I see; you like hedges too. 🙂 Yeah, I see 17 too, thanks. But low 100s view count on a double sunny flowers post is a sign it's time to wrap these posts up soon, I think. For various reasons.
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Richard Lewis
Richard Lewis@Z3R0Gravitas·
Is Thursday dead internet day? I thought this colourful post would do better? Zero likes in the other place too. I say something silly? The algo here is definitely decreasing my reach, tho. Showed this to no humans for first 15min, before tags. Then seemingly not to all those.😞
Richard Lewis tweet media
Richard Lewis@Z3R0Gravitas

1/2 #ThrowbackThursday, bonus pics from the corner house September shoot (linked below), for November cheer!: - Cyclamen (hederifolium Aiton), in the sun out front. - Different Dahlias, out back. - Nice colour but poor focus. #MEcfsEgress #BloomScrolling DailyNaturePics 204

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Stanford Medicine
Stanford Medicine@StanfordMed·
Twelve years ago, Stanford Medicine geneticist Ron Davis shifted his focus to study severe chronic fatigue syndrome — the disease that has profoundly affected his son. Today, each new discovery, big or small, gives him hope for a path forward. stan.md/4nqAOBu
Stanford Medicine tweet media
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wigglethemouse
wigglethemouse@wigglethemouse·
@RorPreston @wecrunchme @ThereForME_UK FYI - you are missing the most significant team in terms of funding and length of research. Dr Jackie Cliff at Brunel. Dr Cliff runs the lab for the UK Cure ME group. I think Dr Nacuul's role is minor now he is in Canada.
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Ror Preston
Ror Preston@RorPreston·
Earlier this year, @wecrunchme created a report on the UK ecosystem emerging around solving ME/CFS and long COVID, in collaboration with the wonderful @ThereForME_UK 🌱 The goal is to help sharpen our advocacy, and make it clear where support is needed & where gaps remain. V happy to bring to this to X in a more social-ready version - please share and tag MPs etc! 🤝 #MECFS #LongCovid 🧵
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wigglethemouse
wigglethemouse@wigglethemouse·
@mecfsskeptic Its worth remembering that this Stanford center has published recently on red blood cells deformability (with UC Davis), myelin basic protein breakdown, and a sizeable WGS study that concluded similar findings to DecodeME - before DecodeME.
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ME/CFS Science
ME/CFS Science@mecfsskeptic·
1) We watched the 2025 Stanford Symposium on ME/CFS and summarized many of the presentations. While it's great to see so many talented people focusing on ME/CFS, we also noted that a lot of research is focused on hypotheses that are not yet supported by strong evidence.
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MortenGroupOxford
MortenGroupOxford@OxMEDiscovery·
Annual Meeting with OMEGA, including an Oxford ME/CFS research update. November 13th, 17.15. Talks from Aleyna Lumsden, Beata Godlewska, Patrick Esser, Edie Guo & Inga Williams. Live streamed on TEAMS. eventbrite.co.uk/e/174811226383…. Full programme soon.
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wigglethemouse
wigglethemouse@wigglethemouse·
@OxMEDiscovery Thanks for making the start time more accessible this year for those of us with large timezones differences.
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