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720 results for “criquaer”
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“Krimi um das #ChronischeFatigueSyndrom
#Hörbilder
#PostCovid ist ein Rätsel. Dabei ist das Syndrom gar nicht so neu. Schon 1955 wurde eine ähnliche Krankheit beschrieben, die nach viralen Infekten auftritt: das Chronische Fatigue-Syndrom, #MECFS. Warum gibt es bis heute keine Therapien?” -
#Dylexia can be rather irksome; sometimes frustrating.
“Colin, why don’t we get greedy for the next lesson.”
I read that sentence several times. I knew it was meaningless. After remaining puzzled for what seemed ages, I worked out that the word greedy was ‘ready’. Even then, it still looked like greedy.
Ay!
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@thegrumpyenby For any new query I have on something #MyalgicEncephalomyeltis related, I generally have a quick loon at me-pedia.org. There is a page item on #shingles - http://me-pedia.org/wiki/Varicella_zoster_virus References appear at bottom of page. Additionally I put shingles into the search-box and links to other pages do appear.
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@tomkindlon I disagree with pts. 2 & 5. Having #SevereME I do very much #suffer with/from #MyalgicEncephalomyeltis. #NICE use the term ‘mild’ however infuriating - using different terminology is not necessarily helpful. In this case ref. to #NG206 / #NICE classification &/or the caveat re 50% loss of function ought to be included in articles.
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#GoodFriday dinner: baked, fresh salmon; boiled, new potatoes; steamed asparagus; boiled petits pois; steamed, purple-sprouting broccoli; lemon; tartare-sauce. Delish! The chilled #GrünerVeltliner 🇦🇹 was a refreshing accompaniment.
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Per #ONS:
“An estimated 1.9 million people living in private households in the UK (2.9% of the population) were experiencing self-reported #LongCovid (symptoms continuing for more than four weeks after the first confirmed or suspected #coronavirus (#COVID19) infection … as of 5 March 2023”
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@naga @tomkindlon I think I read in the past few weeks that due to the heterogeneity of #MyalgicEncephalomyelitis, that to have any really useful data research needs to have c.1500 contributors. I think the article was on phenotypes or something similar - or I could be merging what I have read! #Dyscognition #BrainFog
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@Judyintheskynet Ich wünsch’ allen Österreicher*innen mit #MyalgischeEnzephalomyelitis, „Alles Gute!“
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@Judyintheskynet Ich wünsch’ allen Österreicher*innen mit #MyalgischeEnzephalomyelitis, „Alles Gute!“
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@Judyintheskynet Ich wünsch’ allen Österreicher*innen mit #MyalgischeEnzephalomyelitis, „Alles Gute!“
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#BhupreshPristy (following earlier comments I previously tooted here) tweeted on 30.03.23:
“#MECFS #LongCovid You don’t have to wait long. We will present our work in Berlin & Hinxton meeting. As always, we believe in functional & meaningful, data driven biomedical research that can make sense for understanding complex molecular processes. Let’s dive deeper this time.”
#pwME #MyalgicEncephalomyelitis #ChronicFatigueSyndrome #PostViralDisorder
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For German-speakers, yesterday evening #ORF (the #Austrian equivalent to the #BBC) in their news-programme #ZeitimBild, broadcast an item on #MyalgischeEnzephalomyelitis.
I have to say I cried a few tears. I cannot imagine the BBC’s main news even making such an item.
#pwME #MyalgicEncephalomyelitis #ChronicFatigueSyndrome #MECFS #LongCovid #PostViralDisorder
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“Pandemic or no, [#Cochrane are] hoping no one is looking too closely at their promise.
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There IS an answer out there. It WILL be found. I’m an optimist.”
Alicia Butcher Ehrhardt, #pwME, author
#MyalgicEncephalomyelitis #ChronicFatigueSyndrome #MECFS #LongCovid #PostViralDisorder
This in response to David Tuller’s blog of 21st March:
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@evel If you did, you would have to keep the blind down &/or curtains drawn to to protect against #photophobia. 😞
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CW: Bit of a ramble, bonus points for MECFS and fibro chat.
@Splodgenoodles I also am officially diagnosed as a #pwME, a #pwFM & a #pwOA inter alia other maladies. I both hear & feel you. {{{gentle}}}
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CW: Bit of a ramble, bonus points for MECFS and fibro chat.
@Splodgenoodles I also am officially diagnosed as a #pwME, a #pwFM & a #pwOA inter alia other maladies. I both hear & feel you. {{{gentle}}}
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CW: Bit of a ramble, bonus points for MECFS and fibro chat.
@Splodgenoodles I also am officially diagnosed as a #pwME, a #pwFM & a #pwOA inter alia other maladies. I both hear & feel you. {{{gentle}}}
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CW: Bit of a ramble, bonus points for MECFS and fibro chat.
@Splodgenoodles I also am officially diagnosed as a #pwME, a #pwFM & a #pwOA inter alia other maladies. I both hear & feel you. {{{gentle}}}
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CW: Bit of a ramble, bonus points for MECFS and fibro chat.
@Splodgenoodles I also am officially diagnosed as a #pwME, a #pwFM & a #pwOA inter alia other maladies. I both hear & feel you. {{{gentle}}}
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A painter who cannot paint is tasked with creäting the World’s flowers via his paintings - the result is a sense of failure and deep loneliness. But the Fates have other plans… This is a moving & beautiful #webcomic.
Check out #Incarnation on #Tapas. Link: https://tapas.io/series/Incarnation
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Lack of services provided by #NHS for #pwFM i.e. #Fibromyalgia (another of my conditions). I can honestly say that other than an ill-fitting (thus useless and so did not help!) neck-brace, I have received no specific treatment or medication for my illness from primary- or secondary-care.
Link to UK’s #NHE website:
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Lack of services provided by #NHS for #pwFM i.e. #Fibromyalgia (another of my conditions). I can honestly say that other than an ill-fitting (thus useless and so did not help!) neck-brace, I have received no specific treatment or medication for my illness from primary- or secondary-care.
Link to UK’s #NHE website:
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Lack of services provided by #NHS for #pwFM i.e. #Fibromyalgia (another of my conditions). I can honestly say that other than an ill-fitting (thus useless and so did not help!) neck-brace, I have received no specific treatment or medication for my illness from primary- or secondary-care.
Link to UK’s #NHE website:
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Lack of services provided by #NHS for #pwFM i.e. #Fibromyalgia (another of my conditions). I can honestly say that other than an ill-fitting (thus useless and so did not help!) neck-brace, I have received no specific treatment or medication for my illness from primary- or secondary-care.
Link to UK’s #NHE website:
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Lack of services provided by #NHS for #pwFM i.e. #Fibromyalgia (another of my conditions). I can honestly say that other than an ill-fitting (thus useless and so did not help!) neck-brace, I have received no specific treatment or medication for my illness from primary- or secondary-care.
Link to UK’s #NHE website:
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I just tweeted - the orgs are not on Mastodon as far as I know:
“Housemate made a rare visit home during the working-day, so I got a snack - a buttered hot-cross bun with an espresso. 😊
#SocialCareCrisis #Bedridden #SevereME
Only average 1 meal/day usually.
@CareQualityComm @TraffordCouncil @gmpolice “
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Over the past few days I went 26 hours without a meal, at which point ex-boyf stepped in, came over and cooked some pasta. Then another 49 hours without a meal. In the past 13 weeks I have averaged exactly one day/week with no food. I ate 1 meal per day on average. #SocialCareCrisis #pwME #bedridden #SevereME #Malnutrition #BloodSugar #Dehydration
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@jlthoughts I am inter alia a #pwME #SevereME & #pwFM and I have a blog. I try to publish several blog-posts each year as energy & cognition permit. Please share the link to your blog - once published - as I am happy to share. 🙏🏻🌈💕🤓💙
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@jlthoughts I am inter alia a #pwME #SevereME & #pwFM and I have a blog. I try to publish several blog-posts each year as energy & cognition permit. Please share the link to your blog - once published - as I am happy to share. 🙏🏻🌈💕🤓💙