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ME Research UK: A team of researchers in Australia – including Dr Kiran Thapaliya, Professor Sonya Marshall-Gradisnik, and Dr Natalie Eaton-Fitch who are also currently working on research funded by ME Research UK, have reviewed existing evidence relating to quality of life – the degree to...

ME Research UK: A review paper from Dr Karl Morten’s team has highlighted that “complex chronic illnesses” ME/CFS, fibromyalgia, and Gulf War Syndrome (GWS) not only have common symptoms such as fatigue and pain but also display “significant overlap in the molecular and cellular disruptions”...

Seems likely people worldwide are welcome given who she tagged in this tweet

I haven’t vetted this https://www.mecfsresearch.nz/ ME/CFS Research Kia Ora, my name is Sarah Jansen, and I am a student at the Southern Institute of Technology in Invercargill, Master of Applied Health Sciences (Wellness and Rehabilitation). I am seeking perceptions about chronic fatigue...

https://padlet.com/katha1970_/personal-collection-of-information-for-patients-with-complex-p20bhx4pb54x1may/wish/2998552241 Summary of the #UniteToFight2024 conference by @katha1970 (on Twi@er/X) First International Conference on Long Covid and ME/CFS #UniteToFight2024 marks a turning point in...

I’ve just remembered Gary Frankum, a UK speedway rider with ME, who raised quite a bit of awareness at the time. Haven’t heard anything about him in years.

Post-Covid Awareness Day in Belgium: Protest Belgian patients. Go to (Google translation from Dutch to English), https://www-bruzz-be.translate.goog/actua/gezondheid/long-covid-patienten-houden-ligbetoging-voor-betere-zorg-artsen-ontkennen-soms?_x_tr_sl=nl&_x_tr_tl=en&_x_tr_hl=en

News Release 13-Mar-2025 Symptoms of long-COVID can last up to two years after infection with COVID-19 According to a study of the COVICAT cohort, almost one in four people infected with SARS-CoV-2 suffered from long-COVID Peer-Reviewed Publication Barcelona Institute for Global Health...

Hope 4 ME & Fibro NI Two Lives – One Story is a deeply personal video that reflects the reality of those living with Myalgic Encephalomyelitis and the strikingly similar symptoms within one subset of Long Covid patients. It is an honest portrayal of loss, resilience, and the long struggle for...

Sorry to hear that. I haven't got any. They do write to me during the year by post from time to time.

Irish Independent: https://www.independent.ie/entertainment/books/book-reviews/adhd-is-a-business-as-well-as-a-medical-disorder-irish-doctor-on-the-dangers-of-overdiagnosis/a586398049.html https://archive.is/spXmx ‘ADHD is a business as well as a medical disorder’: Irish doctor on the dangers...

https://cdn.fortuneonline.org/articles/post-covid-syndrome-and-cognitive-dysfunction-ndash-aetiology.pdf Post Covid Syndrome and Cognitive Dysfunction – Aetiology and Possible Treatment Bansal CJ* and Bansal AS+ Abstract Background: Cognitive dysfunction is not infrequent after recovery...

NickyProctor ⁦‪@NickyProctor⁩ Here are slides from the talk I gave to 30+ nurses & doctors of ⁦‪@YSTeachingNHS⁩. None of this lovely group had received any training about #ME - this is not unusual. Feel free to use & share...

https://worcsmegroup.weebly.com/blog/yawn-a-play-during-mecfs-awareness-month YAWN a play during ME/CFS AWARENESS MONTH 11/3/2025 YAWN will debut at the Cheltenham Fringe Festival, at 5.00 pm, on Tuesday 27 May. Hollie Christian-Brookes, an actor-singer, with puppetry and stage combat...

https://www.openaccessgovernment.org/article/common-data-elements-to-advance-me-cfs-research/189538/ Common data elements to advance ME/CFS research First Published: 11th March 2025 Last Modified: 11th March 2025 Standardizing data collection in ME/CFS research through Common Data Elements...

https://www.linkedin.com/pulse/iacfsme-2025-conference-prepare-amazing-abstract-submission-iacfsme-vwk3c/ IACFS/ME 2025 Conference: Prepare an Amazing Abstract for Submission! International Association for Chronic Fatigue Syndrome/Myalgic Encephalomyelitis (IACFS/ME) 277 followers March 12...

https://csiro.qualtrics.com/jfe/form/SV_50apVQ5MHXTReBw Are you living with, caring for, or treating someone with Long COVID or Myalgic Encephalitis/Chronic Fatigue Syndrome (ME/CFS)? We want to hear from you! The Australian E-Health Research Centre (AEHRC) and Monash University have...

Facebook post today: - NCNED is inviting people with ME/CFS, people with long COVID and healthy volunteers to participate in ongoing and upcoming research projects at our Centre, including our clinical trial investigating Low-Dose Naltrexone (LDN) as a potential treatment for long COVID. We...

Quick extraction of text from image NATIONAL CENTRE FOR NEUROIMMUNOLOGY AND EMERGING DISEASES LOW DOSE NALTREXONE FOR THE TREATMENT OF POST COVID-19 CONDITION Project Overview Long COVID describes the presence of various COVID-19 symptoms three months after infection lasting for at least two...

Recording: According to this tweet: it covers the Lightning Process.