Fraoch (Heather) 🏞️🌌🌅

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Fraoch (Heather) 🏞️🌌🌅

Fraoch (Heather) 🏞️🌌🌅

@FraochL

Mainly thoughts on: politics, place & design ; respecting nature & people ; living with IBCancer & #MyalgicE. Once fae Edinburgh, now in Argyll🏴󠁧󠁢󠁳󠁣󠁴󠁿

Argyll, Scotland Katılım Şubat 2020
329 Takip Edilen193 Takipçiler
Fraoch (Heather) 🏞️🌌🌅
@DecodeMEstudy Recent immunology research (summarised👇) which looks to align with your findings may be be getting sidelined for publication due to the location of the researcher. Might any of the Decode team act as a reviewer or somehow help this inform others work? x.com/JackHadfield14…
Jack | amatica health@JackHadfield14

🔬New @BhupeshPrusty paper breakdown - very cool paper: The study finds that people with ME/CFS & Long COVID have antibodies in their blood that may directly interfere with mitochondria (how human cells create energy and regulate inflammation) In simple language all findings 🧵

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DecodeME the ME/CFS Study
DecodeME the ME/CFS Study@DecodeMEstudy·
"DecodeME is now calling on researchers worldwide to join us in accelerating ME/CFS research.” - Prof Chris Ponting (DecodeME Investigator). We encourage researchers to explore and build on our findings. Apply for access to our rich dataset now shorturl.at/F8aOM
DecodeME the ME/CFS Study tweet media
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Bhupesh K Prusty
Bhupesh K Prusty@BhupeshPrusty·
Publishing a paper on ME/CFS and long COVID in a descent journal without an elite stamp is a nightmare.
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Cinnamon rolling along
Cinnamon rolling along@LongCovidFight·
@KSchnickelfritz @useless_priest I think so too, that stress isn’t the disease or underlying cause. Where there’s room for CBT it leaves the door open for exercise. Faulty illness beliefs, nervous system stuck in fight or flight, thinking your way better. Exercise is part of the next step, ignoring symptoms.
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Brian Fog
Brian Fog@useless_priest·
@KSchnickelfritz I'm sure I'm reading too much into it but is there an FND vibe permeating that somehow? Also no mention of severe. But we'll take the apology.
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KimH
KimH@KH118118·
@FraochL @SMC_London What has that got to do with FND? He also confirms in that same thread he doesn’t do ME research. I would like to see the supporting evidence of your claim if possible please.
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KimH
KimH@KH118118·
@FraochL @SMC_London “Prof Carson advocates that ME is a Functional Neurological Disorder.” Can you share your sources please?
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Fraoch (Heather) 🏞️🌌🌅
@WoollerEmma @DecodeMEstudy Definitely doesn't - he wrote NHSScotland’s good practice guide for ME based on the BSP model (that guide’s only just been thrown out😤) and just last week was posting comment that ME is a functional neurological disorder (a problem in how the brain and body communicates).
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Fraoch (Heather) 🏞️🌌🌅 retweetledi
DecodeME the ME/CFS Study
DecodeME the ME/CFS Study@DecodeMEstudy·
Our initial DNA results! DecodeME have discovered that people with an ME/CFS diagnosis have significant genetic differences compared to the general population. Summary of our results: shorturl.at/pgsjk Check out our full preprint paper: shorturl.at/VwN3s
DecodeME the ME/CFS Study tweet media
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Carole Bruce
Carole Bruce@CaroleBruce17·
@FraochL @DecodeMEstudy Thank you for finding this. A C really reaching for his negative bias. It wasn’t all questionaire we spat, we all spat!!
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Fraoch (Heather) 🏞️🌌🌅 retweetledi
Channel 4 News
Channel 4 News@Channel4News·
ME, or Myalgic encephalomyelitis, is linked to your genetics, an early study by Decode ME has suggested. They’ve found eight areas of genetic code in people with ME are ‘significantly different’ to the DNA of people without the disease. The results still need to be reviewed, but the University of Edinburgh research team hope these results will pave the way for future research and the development of drugs.
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Fraoch (Heather) 🏞️🌌🌅
@DecodeMEstudy Can someone please find and gag Prof. Alan Carson so the news articles on Thursday arnt full of him casting shadows over the findings because they arnt based on his pet hypothesis 🙏
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DecodeME the ME/CFS Study
DecodeME the ME/CFS Study@DecodeMEstudy·
The initial DNA results from DecodeME are coming this week! We will release them on our website on Wednesday 6th August at 7pm (approx). We're letting you know the timing in advance so you can pace beforehand. Thank you to our participants & supporters.
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Anna Wood
Anna Wood@Annakwood·
Thanks so much lovely people. I did it! Came back at lunch and had a sleep then went to a couple more talks online. Really nice to see people who I normally see online, in person And no, I didn't take the scooter, but it worked out ok
Anna Wood@Annakwood

Big day today - I'm off to give my first ever keynote speech! I've even put makeup on! Luckily just a mile or so down the road,and I'm getting a lift. Still dithering about whether I need the scooter (more for a guaranteed seat than the distance)

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Nick Ray
Nick Ray@LifeAfloat·
03.30. I’m excited to reach the western point of my adventure today. I’m cocooned in my wee tent against the rain. I’ve a warm glow of a job pretty well done & there’s more to come. This undertaking is more significant than my others. At the age of 61, I’ve rediscovered joy.
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Anna Wood
Anna Wood@Annakwood·
The common spotted orchids in our front lawn are going from strength to strength - currently there are 30! A photo didn't do it justice so here's a video
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Fraoch (Heather) 🏞️🌌🌅
@BylinesScotland The ones which grind my gears are those who think Access Rights extend to vehicles so off-road their campervan or 4x4&rooftop over other’s land to ‘wild camp’. These vehicles are sold with the promise of freedom but they need to obey the same road/land laws as any other motor.
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