I🖤 @inadarkroom247
25, UK and Dying from covid induced severe ME. POTS + mild MCAS Joined April 2015-
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WESTMINSTER HALL DEBATE ON #MEcfs As promised please find below an open letter everyone can sign asking @sajidjavid to raise #BringMillieHome #SaveCarlasLife & more during 1 May's debate We will send it on 30 April. So get involved and get signing. LINK with a CW - suicide:…
#MEAwarenessHour I am bed-bound with severe ME. I am terrified of going into hospital & would refuse as I can’t even imagine how much worse I’d end up. This is the biggest medical scandal of the 21st century. Our cries are falling on deaf ears. #SaveCarlasLife #ExposeMENow
#MEAwarenessHour I am bed-bound with severe ME. I am terrified of going into hospital & would refuse as I can’t even imagine how much worse I’d end up. This is the biggest medical scandal of the 21st century. Our cries are falling on deaf ears. #SaveCarlasLife #ExposeMENow
NHS hospitals are extremely dangerous places for #SevereME patients. Carla, Millie and Karen are just the cases we know about, there could be so many more being abused without us ever knowing about it #MEAwarenessHour #SaveCarlasLife #BringMillieHome
The NHS are going to kill yet another severe ME patient #SaveCarlasLife
The NHS are going to kill yet another severe ME patient #SaveCarlasLife
To all pwME who menstruate: what are we doing about periods? Has stopping them lead to improvement? If so what are you taking? (Especially curious if you're severe)
This is horrific. Carla is having frequent seizures and yet the hospital STILL this her condition is psychosomatic! #SaveCarlasLife #Severe
This is horrific. Carla is having frequent seizures and yet the hospital STILL this her condition is psychosomatic! #SaveCarlasLife #Severe
Carla is having seizures and repeatedly losing consciousness while in hospital. She's lost the ability to speak and move yet still isn't being believed. Her case has been taken over by psychiatry and she's at risk of death. She has #SevereME #SaveCarlasLife #ExposeMENow
Yet another young woman with #SevereME is being harmed in an NHS hospital who refuse to follow NICE guidelines. The worst part is that @gmcuk let them get away with it every time #SaveCarlasLife #ExposeMENow #DontLetMEDie
What is the point of NICE guidelines if hospitals refuse to follow them for #MECFS ? Severe patients are at risk of dying in hospital because psychiatrists are taking over their care and ignoring advice from experts @rcpsych @RCPhysicians @gmcuk #SaveCarlasLife #ExposeMENow
thecanary.co/uk/analysis/20… #SaveCarlasLife #ExposeMENow #MECFS The abuse of severe ME patients in NHS hospitals has to stop!
Imagine being so ill it’s agony to eat, going into hospital for help, instead doctors cancel all your referrals, ignore experts & NICE guidelines leaving you having seizures & losing consciousness because they think #MECFS is psychological #SaveCarlasLife #ExposeMENow
UPDATE on #SaveCarlasLife #ExposeMENow - we've been involved with the family for a week, now - and she has been deteriorating since then. The video we put out earlier showed she could still partially speak. This has now stopped.
This is so so cruel. The NHS tortures #SevereME patients. WHERE IS THE NEWS COVERAGE??! #SaveCarlasLife #ExposeMENow
This is so so cruel. The NHS tortures #SevereME patients. WHERE IS THE NEWS COVERAGE??! #SaveCarlasLife #ExposeMENow
Toolkit for Carla’s Twitter storm on Thursday! Huge thanks to @fionarh289 for putting this together using the one I made for Millie, I’m severe & pretty burnt out but the community comes together! Pls suggest edits in the comments 👇 #SaveCarlasLife docs.google.com/document/d/1Ny…
This is absolutely horrifying. PSYCHIATRY HAS NO PLACE IN TREATING ME! #SaveCarlasLife
This is absolutely horrifying. PSYCHIATRY HAS NO PLACE IN TREATING ME! #SaveCarlasLife
Living with very severe ME is an ongoing daily grieving process. Grieving all the things you have lost, the things you are slowly losing and the things you know you are about to lose.
PROTEST #SaveCarlasLife #ExposeMENow Carla is extremely ill in West Middlesex Hospital. Doctors are ignoring NICE guidance on severe ME & ignoring her severe POTS You know what to do THURS 18 APRIL 11am-1pm BST EVERYONE ONLINE USE THE HASHTAGS We'll be at the hospital too 1/
Kirstie Sivapalan @KirstieSivaP
3K Followers 2K Following Making a noise about the injustices & lack of support for #pwME #LongCovid 💙 @[email protected] 🐘 @KirstieSivap 🐳 @kirstiesivapalan 🧵Tara Foti, PhD MPH @TaraFotiPhD
810 Followers 771 Following Perinatal health researcher, Adjunct @usfcoph | Former @kpdor Postdoc, @usfcoph PhD, @URMC MPH | Now #disabled #LongCovid #PostVax #MECFS @RemissionBiome #R50Rachel 44 @RachReynolds510
90 Followers 809 Following ME/CFS/Long Covid campaigner |Coeliac awareness| Get Tories OutPhil Prydderch 🏴�.. @PJPrydderch
1K Followers 2K Following Dad of two | EVs | Born at 332 ppm CO2 | ME, FMS, POTS | @wrexham_AFC ex part-owner⚽️ | M.CIWEM | Flood Defence & Hydrometryinnocent @innocent1915968
816 Followers 2K Following Nothing interesting about me just living life 🤛Fabi @8gfz4ht
85 Followers 249 Following in my dreams with bell 100 on a sailing boat, eating pizza and enjoying the sunset #LongCovidFighter #NichtGenesen #TheLastMasked #NotRecoveredGwenny @Gwenny264486
1 Followers 23 FollowingRoyal Free 1955 @RFH1955
2K Followers 2K Following ME/CFS archive, especially RFH 1955. For education, not profit. Research @CiaranJ_Farrell & @Needles_Toosay. https://t.co/bYPmViWQCG.Emma 🛌♿🌱☮�.. @emma_vegan_mua
1K Followers 3K Following She/her. Severe ME, CCI/AAI, hEDS & co, AuDHD. Ex makeup artist, ethical vegan, socialist. #BlackLivesMatter #TransRightsAreHumanRights Support striking workersDr LG @subversivepsych
4K Followers 5K Following 🇮🇪➡️🇪🇸Dr(MD/MRCPsych) BSc(Hons)Pharmacol. Not medical advice. Life on hold. SARSCoV2 04/20 #LC #MECFS #CH #coagulonaut p/t #sloth 🦥 #endmedicalgaslightingChronically Illumise .. @ChronIllumise
22 Followers 239 Following Lily. #pwME, pwPOTS, Pokémon fan (she/her).Bo @BoJamilla
6 Followers 15 Following chronically ill 🫂 spoonie 🥄 ME/CFS 💙 artist 🦋 mama 💖 cats 🐈 cosy gaming 👾 reading and audiobooks 📖Long Covid Patient Ac.. @LC_UK_Action
4K Followers 2K Following @[email protected] https://t.co/DlgXF9BQSeM @maryhum82842507
84 Followers 1K FollowingN.Crawford 🐈⬛.. @Caitshith
282 Followers 1K Following eco-socialist. disabled with moderate viral ME, neurodivergent with adhd + autism.Lou MacGregor @cutpriceguignol
4K Followers 4K Following Author, horror fanatic, cat staff. Check out my short horror collection at the link below!CHRONIC Campaign @chronic_action
1K Followers 5K Following Arts Comedy & Science Social Justice Campaign • Chronic Illness & Disability • Science page ⬇️ Arts page: https://t.co/E2qSDNLEdQ🙏🏷️☕️ https://t.co/fosjDeOMYPJessica @mamaoftwinsRN
683 Followers 2K Following feisty lifelong liberal 💙 🚫DM 🚫MAGAts #bluewave2024 🌊#votebluenomatterwho #FBR #bidenharris2024 #WOKEaf #nomorebookbans #proudally 🏳️🌈🌈R. @chronicsheepe
1K Followers 2K Following Hi. severe #MEcfs #longcovid #MCAS #POTS ♿️ | Ex-Film industry worker📽 | they/them | mstdn: [email protected]Syd @fcknsyd
2K Followers 1K Following 24 year old who’s life is currently on pause because of #LongCovid since April 2022 #POTS #Dysautonomia #MECFS #hEDS @CadAgainstLCjess @jessicaliu35752
10 Followers 121 Following 18 yr old w very severe me/cfs and long covid. been lurking for a while.Michelle McParlin @MAC4U25
1K Followers 1K Following “People Problems call for People Solutions” Recovering the long tail #longcovid #countlongcovid #pwlc now also interested #MECFS #PoTs Mother, Dog lover #FBLCPauline boyd @princesspenny62
416 Followers 4K Following Busy trying to save my life from a Fatal disease from Toxic mold in my Rental home. Owner fatally poisondd me and Retailiaton horroibly for the last 5 yearsAbolition @forAbolition
0 Followers 2K FollowingCease Fire Now @HeidiHeatherH
138 Followers 1K Following https://t.co/7lBlTAtOgc All humans deserve safe housing, food, education & healthcare. I’m severe me/cfs/lc for over 2 years #millionsmissing #absurdismTim @TimofejM77894
130 Followers 236 Following Severe myalgic encephalomyelitis triggered by mild COVIDEmy with ME @EmyWithME
162 Followers 239 Following BME PhD student, lover of nature. Learning everything about #ME/#LC/#POTS/#MCAS/#hEDS in hopes of recovering+helping others. She/her. #ActuallyAutistic 🖤🩶🤍💜Life Is A Mirage; Let.. @liamliago427
737 Followers 5K Following It's about the blood. ____________ Trump is the forerunner antichrist. I mute Magats.Lena Lund @LenaLenaLund
33 Followers 185 FollowingStephjdk @stephjdk79452
1 Followers 24 FollowingMichelle Miyagi @MichelleMiyagi
250 Followers 1K Following Former RN. Feminist. LGBTQIA Empowering us to choose self-compassionate boundaries. LOVE 🌈✌🏽🤗 The Logical Heart Knows Best #LongCOVID #MdDSLilly @Lillymaxx
1K Followers 2K Following MOI+BiblioBenevole+Outlander +🏴+📚reader+🥃+ ✨dreamer #5VAX #N95 #LongCovid #CleanAirVeronica Cane @VeroCane25
15 Followers 175 FollowingJesusIsComing @JesusIs91940818
88 Followers 386 Following Mat 24:7 For nation shall rise against nation, and kingdom against kingdom: and there shall be famines, and pestilences, and earthquakes, in divers places.Albert @mkklmlc
3 Followers 58 Following 26. Designer. Thought I would make an account to keep up with all things LC and connect with other long haulers 🙇♂️❤️ #longcovidStripy Lightbulb CIC @StripyLightCIC
2K Followers 2K Following Evidence-based #CPD 3 credits #mecfs #etraining for #employers, #healthcare and #education professionals and their organisations.Thea @TheaKnudsen4
151 Followers 339 FollowingEdna, M.E.Advocate �.. @EdnaMacNamara
699 Followers 1K Following 💙 M.E.Carer & Advocate of son aged 30, ME for 10yrs 💙. RaisingAwareness for #PwME. #Carers #LC #findAcureMEJess T @jesst914
1K Followers 3K Following Row row row your boat, Gently down the stream... Merrily merrily merrily merrily Life is but a dream. Life is short and sweet. Be kind to everyone No lists plzCoolerKing @MEcoolerking
99 Followers 98 Following 2022 is year 25 of being 90-95% bedbound in a darkened room with ME. I finally accessed medical treatment for POTS in 2020, 22 years after becoming ill.Amar Sharif @AmarSharif11
481 Followers 476 Following Consultant Physician Gastroenterologist and Hepatologist MBBS, MRCP, MD, FRCP.Debbie Filippaki, BSW.. @filippakid
812 Followers 2K Following Teacher & social worker: environmental & health humanities, community development, linguistics, queer & disability pride. Workplace violence survivor.plague rat 🐀 @x3r0gxx
8K Followers 7K Following federation of plague rats against forced mass infection 🐀 🐀 🐀 🏴Dianna Cowern @thephysicsgirl
214K Followers 2K Following Science Video Creator, Currently #LongCOVID, MIT Physics, Forbes 30u30 https://t.co/BT5fDLw3NOProf Gemma Carey, PhD.. @gemcarey
26K Followers 2K Following Public admin, social policy, public health. Lots of NDIS @UNSW. PROVAX, vax injured - in severe ME recovery. (And non aca-author). Views are my ownSteve Topple @MrTopple
33K Followers 5K Following Journalist @TheCanaryUK | Journalist @BywireNews | Vibes @Reggaeville @PauzeRadio | Contrib @RadArtReview | Project lead @ #CanaryAmplify | Views my own etc.E ❀ @farbeyondtired
360 Followers 262 Following Severe ME for 13 years, hEDS and co• 26y/o • somewhere to share my thoughts when I have enough energy/brain power to do so.Royal Free 1955 @RFH1955
2K Followers 2K Following ME/CFS archive, especially RFH 1955. For education, not profit. Research @CiaranJ_Farrell & @Needles_Toosay. https://t.co/bYPmViWQCG.Nicola Jeffery @NicolaCJeffery
5K Followers 5K Following 'Behind that loud-mouthed journalist @MrTopple is an even louder-mouthed woman!' Mum, Activist, #ChronicIllness warrior! #BLM! Standing up to #Classism!Autisdick ☭ 😷 �.. @hiimjakekthx
1K Followers 2K Following @Remissionbiome n=50 Participant🍳🧠 🏳️🌈. Disabled by SARS2, Marxist, jew-ish. @hiimjakekthanks priv altMark Rober @MarkRober
509K Followers 505 Following Former NASA and Apple engineer. Current YouTuber and friend of science. CrunchLabs founder- https://t.co/3UMhZ5kV9hDaisy @daisy_court75
832 Followers 430 Following Severe Myalgic Encephalomyelitis | Dysautonomia | MCAS | Trying to navigate chronic illness with perseverance, an open heart, and a dose of humor 🐳Sabrina Poirier (On H.. @Sabrina_Poirier
6K Followers 6K Following Community Builder / Passionate Collaborator / Chair - #MedicalEducation Group / #ResearchPartner / #MECFS #LongCovid Advocate / #PwME / #MCAS / #POTS / #FibroRhi @RhiaRhiaRhi
1K Followers 722 Following Any pronouns. Bsc, PgDip Molecular Biology. Neuroscience Nerd & Science Communicator. Eternally trapped at VUW.#MEAction Network UK @MEActNetUK
7K Followers 610 Following UK branch of global grassroots movement @MEActNet. Empowering patients to fight for the #MillionsMissing with ME. Health equality & biomedical research now!miss m @FatiguedStill
2K Followers 381 Following Long Covid since September 2022 | ME | chronic fatigue | POTS | MCASDealWithM.E. @me_dealwithme
670 Followers 266 Following One voice wanting to make the lives of M.E. patients better.CrunchME @wecrunchme
764 Followers 34 Following Mapping the scientific, tech & advocacy ecosystem around #MECFS, #LongCovid, and other infection-associated chronic illnesses 🗺️ | Organised by @rorprestonUniteToFight2024 @U2Fight_World
3K Followers 121 Following 100% crowdfunded LC & ME/CFS conference project. community-driven. independent. global.Ror Preston @RorPreston
2K Followers 555 Following Lead Data Scientist @visible_health 💙 | Organiser @wecrunchme 🗺️ | #MECFS since 2018 | Own OpinionsMeriam Rllb @lowbatterydream
550 Followers 409 Following PharmD, 26, Long Covid March 2020 | ME/CFS | POTS | Personal IG : meriamrhallab | Chronic illness IG : lowbatterydreamsplague rat 🐀 @x3r0gxx
8K Followers 7K Following federation of plague rats against forced mass infection 🐀 🐀 🐀 🏴Elly Bailey @ellbail
1K Followers 2K Following 🇵🇸 Welcome to the Recumbent Renaissance. Freedom’s just another word for nothing left to lose. Amor fati. Dercum’s/ME/longcovid. Remission Biome R50🌻Kirsty @Kirstycfsmelife
586 Followers 708 Following CFS/ME 15+ years and POTS 🐼 trying to improve my health and one day fully recoverEtta Loveday @EttaLovedayME
351 Followers 169 Following She/Her, Rising awareness for people living with severe/very severe ME! #ME #SevereMEStripy Lightbulb CIC @StripyLightCIC
2K Followers 2K Following Evidence-based #CPD 3 credits #mecfs #etraining for #employers, #healthcare and #education professionals and their organisations.Dress for ME Charity .. @DressFor_ME
3K Followers 5K Following I am @JenGovey & use my powers of #cosplay to raise money for @invest_in_ME Take the #DressForME challenge! https://t.co/jOqrVcbVKb 😍 #pwME She/theyEndMalnutritioninME @MalnutritionME
233 Followers 296 Following Campaign for improvements in medical care for ME patients with gastrointestinal symptoms. https://t.co/fOkzoiJqv2Alexis @alexis___me
197 Followers 176 Following Consultant in Health Protection (Public Health) | Severe ME, Long Covid and POTS patient | Advocate | Father | Husband to @clglbrtLindsey 🩵🇨🇦 @LindseyMarie_xo
1K Followers 721 Following Life | Empathy | Love | Meditation | Health&Fitness | Music Festivals | Travel. MUA | Web/UX Designer. Disabled by #LongCovid & #MECFS since Jan/22 💔Erin Tarantino 🇨�.. @erincandy
10K Followers 3K Following 🇨🇦SPORTS/#LeafsForever•Movies/History/Gaming/Politics/Creator/Cat Rescuer• Anti-disinfo activist. Leukaemia cancer survivor! #LongCovid since March 2022 ♑️britt 🎀 @reneeswilder
41 Followers 51 Following 17yo w/ sjorgens, hEDS, POTS, moderate ME — my own safe space 🤍 — regina george hyperfixationJoshua Leisk @joshual_tm
4K Followers 43 Following Coach, author, researcher. Currently focused on unifying theory for ME/CFS, Long Covid and “Long Haulers”.Dr. Deepti Gurdasani @dgurdasani1
143K Followers 6K Following Clinical epidemiology, machine learning, NLP, global health. Intersectional feminist. she/her. Also on @[email protected] @dgurdasani1.bsky.socialDebbie Seymour @debbie_seymour
2K Followers 779 Following This account can no longer be managed at this time due to Debbie's deteriorating condition. She is okay, but not improving. #LongCovid #MECFS #POTSSarah Mac @grannyash510
928 Followers 3K Following M.E for 19 years. Views of fairness and equality for all. Here to learn and to be kind (usually 🙃). NHS supporter. Pro Science and knowledge.Arlette @ArlettePoolen
1K Followers 863 Following I am one of the #MillionsMissing since 2005 - 30 jaar - She/herSStyles @StylesSa191919
592 Followers 1K Following Loved running, cycling, swimming & living life to the full until #LymeDisease #MECFS 🕷💚#bethelightinthedarkness🕯 #schnauzerlover 🐾 #LoveNotHate ❤Neurologist Mom @NeurologistMom
5K Followers 263 Following A neurologist, M.D. a mother of a 15-year-old girl with severe neuroCOVID/ME/CFS who has been managing her daughter's treatment at home since October2022it's ME Ingrid @MElotje99
733 Followers 4K Following Carpe diem and take no shit 👊 One of the #MillionsMissing due to #MEcfs #PAISBateman Horne Center @BatemanHorne
6K Followers 1K Following Bateman Horne Center is a non-profit medical, research, and education center devoted to eradicating ME/CFS, FM, Long COVID, and related conditions.Helen Goss @HelenMMGoss
2K Followers 953 Following 🏴 @longcovidkids ❤️🔥 Parent/carer #LongCovidKids 🤘🏼 Advocate #LongCovid 🐾 Cat spam 🪐 Space nerd 🌪️ Chronically persistent force of natureKirstie Sivapalan @KirstieSivaP
3K Followers 2K Following Making a noise about the injustices & lack of support for #pwME #LongCovid 💙 @[email protected] 🐘 @KirstieSivap 🐳 @kirstiesivapalan 🧵Venlafaxine withdrawa.. @TalkVenlafaxine
326 Followers 565 Following Iatrogenic harm from VenlafaxineKate Stott @K8Stott
4K Followers 3K Following Tech Founder, Previous Scottish Business Woman of the Year. #Longcovid since Mar 20. #Crohns Confirmed Microclots & endothelial damage. #LongCovidKids advocateoliver benson @olliebenson_
670 Followers 650 Followingmarkmooch @MarkMooch
1K Followers 1K Following Elder Millennial & Social Justice Warrior. ME Patient. Drummer. Northerner. Pontificate a lot. Cannot read research papers due to fatigue. Dry Humour. 🌱Timo Strotmann @TimoStrotmann
4K Followers 280 Following Tech Enthusiast - Software Engineer - Health Advocate Co-Founder of https://t.co/0klWgSEzbpEmily Johnson (is on .. @emily_rj
8K Followers 6K Following Digital journalism. Design, news/book edits, linguistics, data, tech. Medical + academic research. Disability in news consults. @the_dailydis. #CripTheVoteEmma 🦋 @Emma40025133
2K Followers 986 Following Chronically ill with MCAS, POTS & ME/CFS. All brought on by covid infection in January 2021.Phi @phi_psd
5K Followers 931 Following Australian/Greek/Cypriot nerdy visual designer, living in Berlin. 🇨🇾🇬🇷🇩🇪 end #prescribedharm #longcovid & #mecfs @berlinbuyersI feel like a newborn baby sometimes, with this brain injury. Nothing makes much sense anymore and I have to reorganize my entire brain and refamiliarize myself with everything.
If you have had a "remission event" (defined as suddenly feeling remarkably better to the point of almost like a 'normal healthy' person over a period of a few HOURS) what was the trigger? Please describe your experience in comments. If you choose 'other' i.e. probiotics, diet…
UPDATE: #SaveCarlasLife - it seems the hospital are finally doing something positive - but still not quite enough - plus #BringMillieHome FYI transcript of the video in reply below:
Disabled people, do you prefer: vouchers instead of cash, getting reimbursed after showing receipts, or (my favourite) getting treatment INSTEAD of money to survive?
Be nice today to do anything today without bursting into tears at the sheer cruel, vindictive & sadistic unfairness of it all. What do I say to my disabled daughter about her future? What do I say? How do I tell her the future under this government is one they don’t want her in?
Reciting the mantra that recovery is possible, delegitimises and gaslights pwME who have been sick past the point where recovery is possible. I know some need to believe this to stay mentally afloat but the fact is recovery is not possible for the majority after 5 years of #mecfs
Hilarious that so many politicians are yapping about ‘supporting people into work’ after they bitched and moaned for the last 4 years about people working from home and successfully pushed so many people back to city centre offices, thus excluding many disabled ppl from work. 🤨
I'll shortly be starting stage 1 of the bornfree protocol Its gonna be a heck of a rollercoaster so please bear with me. I plan on writing it all down when I have more energy and probably won't be up for answering many qs during. 🤞🤞🤞🤞🤞🤞🤞🤞🤞🤞
Update about Millie Petition change.org/p/save-millie-… #MillieSevereME #SevereME #pwME #saveMillie #BringMillieHome #DontLetMEDie #ExposeMENow
Where are the urgent #LongCovid treatment trials? The immunotherapies? Every man & his dog seems to understand the desperate need for them but year after year, they never really materialise, save a few scraps. Millions suffering yet still so pathetically little real-world action.
They’re diagnosing people with Long Covid as depressed and then throwing everyone out the window. This is a reason for building solidarity with mad people: not bc LC is a form of madness but bc we are subjected to a similar treatment by the state
Steve is currently at West Middlesex Hospital speaking to Carla's family and will be giving a full update on Carla and her situation this evening. #SaveCarlasLife
All it takes is a healthy-looking person with a stupid smile on their face holding literally *anything* and I’m ready to buy it now like a dog after a chew toy hoping it will make an impact on my health. And Instagram knows it! 😂 #mecfs #SevereMECFS #pwME #LongCovid
GP said today his preferred reference source is CKS (Clinical Knowledge Summaries). CKS covers 370 topics with a 'focus on the most common & significant presentations in primary care'. There's no CKS for ME - not important or prevalent enough to be listed in an index used by GPs?
Long Covid day 465. I just left my doctor’s office, and she doesn’t think I’ll ever recover. She only has one Long Covid patient who has 100% recovered. So yeah, I guess that was my life, done at 32, lol—so much for those super mild variants. Thanks for nothing, public health.
I got a letter. So now that I'm 99% bedbound and can't even sit or leave the house, I finally qualify for free public transportation by bus. Lol. Those things are always too little too late. Help is always 1000 steps behind your basic needs when you're disabled/chronically ill.
@Naomi_D_Harvey @inadarkroom247 Common in EDS to have young looking skin on face but old hands. I have this.
Past me was a fool. Learn from me. Don’t take constipation lightly, especially if you’re near or in the Severe end of ME. Take proper steps to prevent it worsening when the first signs show. Don’t be me 😖😭
Should M.E be treated as a Mitochondrial Disease? Just had a discussion on this, it is classed as a secondary mitochondrial disease. No real treatment for primary, apart from diet, supplements & wild card... 'exercise' even though it damages muscle fibre.
I was just thinking how f*cked all those with #Longcovid would be if #MECFS did not exist. Read this ridiculous title. Who is paying for this misinformation? We need to follow the money. This needs to be exposed. Imagine a world where the covid pandemic lead to a severe…