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ME/CFS News

@mecfsnews.bsky.social
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News, interesting information and commentary on ME/CFS.

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ME/CFS News @mecfsnews.bsky.social · 12/05/2024
May 12 is ME/CFS Awareness Day. Speak with other people about ME/CFS today. Reject invisibility and stigma, build awarenesss and support.
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Tom Kindlon @tomkindlon.bsky.social · 29/03/2024
This is not what many people would like to hear I suspect but is important to take on board: "The majority of research funding [in general] comes from charities, with only a small percentage coming from the government for other diseases" From: www.youtube.com/watch?v=W3Ji... #MEcfs #CFS #PwME
youtube.com
Who Funds Research? | Why The Charity Sector is Vital For Long Covid & ME/CFS
In this conversation, we discuss the importance of funding for research in the charity sector, specifically for ME, CFS, and long COVID. The majority of research funding comes from charities, with only a small percentage coming from the government for other diseases, hence the need to emphasise the power of an established and reputable organisation in the charity sector. The example of the Cystic Fibrosis Trust is an inspiring case of how focused efforts and resources can lead to significant improvements in a niche illness. We compare the fundraising efforts for ME/CFS with other diseases like MND and Parkinson's, noting the disparity in funding despite the lower number of people affected by ME/CFS. Hopefully this provides an overview of why the charity sector is so important, and inspiring that even diseases with low numbers of people were able to drive such huge change! Apologies that my camera dies right at the end of the call, but Peter wraps up the discussion for us. Hope you enjoy! TIMESTAMPS 00:00 Intro 03:15 Importance of Funding for Research 04:13 Sources of Funding for Medical Research 09:02 Funding for Parkinson's Disease Research 11:10 Funding for Cystic Fibrosis Research 15:22 Funding for Motor Neuron Disease Research 23:31 Funding for ME/CFS Research 26:07 Need for Fundraising and Driving Cash into ME Research 30:14 Harnessing the Engaged Patient Community 32:15 Comparison of Fundraising in ME Charities 34:23 Sources of Funding 35:11 Legacy Giving and Challenges 36:35 Spending on Fundraising, Support, Research, and Advocacy 37:57 Comparison with Other Diseases 40:46 Fundraising Strategies and Professionalism 44:12 Importance of Fundraising Spend 46:05 Lessons from Successful Charities 48:16 Overcoming Stigma and Misconceptions 51:48 Long-Term Trends in Income 56:09 Challenges and Overlapping Issues 58:47 Learning from Other Disease Charities 01:02:21 The Impact of Legacy Giving 01:06:58 Targeting People Close to Those with the Disease 01:08:24 Engaging Community and Faith Groups 01:09:38 Involving Community Groups in Fundraising 01:11:12 Engaging Companies and Offices 01:14:40 Learning from Other Charities: Parkinson's UK 01:15:28 Customer Journey: First Awareness of the Disease 01:16:13 Customer Journey: Joining the Charity 01:17:18 Customer Journey: Getting Involved 01:18:23 Search Engine Optimization and Visibility 01:23:42 The Customer Journey 01:32:19 Key Takeaways OTHER LINKS: 💌 Newsletter - https://harryboby.substack.com/ 🐦 Twitter - /harryboby4 🎤 TikTok - /harryboby2
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ME/CFS News @mecfsnews.bsky.social · 14/03/2024
A review that focuses on the pathophysiology of skeletal muscle in ME/CFS. The authors believe that skeletal muscle tissue offers opportunities for diagnosis and treatment. onlinelibrary.wiley.com/doi/10.1111/...
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ME/CFS News @mecfsnews.bsky.social · 12/03/2024
You don’t want to get better’: the outdated treatment of ME/CFS patients is a national scandal by George Monbiot www.theguardian.com/commentisfre...
theguardian.com
‘You don’t want to get better’: the outdated treatment of ME/CFS patients is a national scandal | George Monbiot
The notion that this illness is psychosomatic is having devastating effects, says Guardian columnist George Monbiot
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ME/CFS News @mecfsnews.bsky.social · 08/03/2024
Talking with normal people about my ME/CFS can be frustrating. Some people are like "I've listened to you for two minutes, and now I'm going to give you advice that will cure your illness after 20+ years." It makes me feel misunderstood and like my time has been wasted.
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ME/CFS News @mecfsnews.bsky.social · 07/03/2024
The DecodeME study has been delayed. It was due to be completed by August of this year. The sample collection has taken longer than anticipated. The results will be released as soon as possible, before August 2025. www.decodeme.org.uk/study-extens... ME/CFS
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ME/CFS News @mecfsnews.bsky.social · 29/02/2024
Heterogeneity in Measures of Illness among Patients with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Is Not Explained by Clinical Practice: A Study in Seven U.S. Specialty Clinics www.mdpi.com/2077-0383/13...
mdpi.com
Heterogeneity in Measures of Illness among Patients with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Is Not Explained by Clinical Practice: A Study in Seven U.S. Specialty Clinics
Background: One of the goals of the Multi-site Clinical Assessment of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (MCAM) study was to evaluate whether clinicians experienced in diagnosing and c...
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ME/CFS News @mecfsnews.bsky.social · 28/02/2024
A recent opinion piece questioned the validity of the NICE guidelines for ME/CFS. NICE has now published a rebuttal titled: NICE guideline on ME/CFS: robust advice based on a thorough review of the evidence (not open access at the time of writing) jnnp.bmj.com/content/earl...
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ME/CFS News @mecfsnews.bsky.social · 21/02/2024
Deep phenotyping of post-infectious myalgic encephalomyelitis/chronic fatigue syndrome. This is the publication of the NIH's intramural study on ME/CFS. www.nature.com/articles/s41...
nature.com
Deep phenotyping of post-infectious myalgic encephalomyelitis/chronic fatigue syndrome - Nature Communications
Post-infectious myalgic encephalomyelitis/chronic fatigue syndrome (PI-ME/CFS) is a disabling disorder, yet the clinical phenotype is poorly defined and the pathophysiology unknown. Here, the authors ...
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ME/CFS News @mecfsnews.bsky.social · 17/02/2024
The National Institute for Neurological Disorders and Stroke is collecting feedback from the public on the research priorities for ME/CFS. You can view and submit feedback here: ninds.ideascalegov.com/c/campaigns/... Alternatively you can submit feedback here: MECFSResearchRoadmap@ninds.nih.gov
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Tom Kindlon @tomkindlon.bsky.social · 13/02/2024
NINDS will be hosting a webinar on March 4, 2024, 11-12pm ET to provide updates on the ME/CFS Research Roadmap. Speakers: Vicky Whittemore, Maureen Hansen, and Lucinda (Cindy) Bateman. Links in image: www.ninds.nih.gov/about-ninds/... nih.zoomgov.com/webinar/regi... support.zoom.com/hc/en/articl...
News from NIH: Webinar on March 4 about the ME/CFS Research Roadmap

NINDS will be hosting a webinar on March 4, 2024, from 11-12pm ET to provide updates on the ME/CFS Research Roadmap. Speakers will include Vicky Whittemore, Ph.D., NINDS program director; and Research Roadmap co-chairs Maureen Hansen, Ph.D., and Lucinda (Cindy) Bateman, M.D. Please register for the webinar in advance.


During the webinar, attendees will have the opportunity to ask questions out loud or to submit written questions in the Zoom Q&A box. For those on the phone, please dial *9 to raise/lower your hand and *6 to mute/unmute. Additional instructions for joining by phone are on the Zoom support website. We regret that we may not be able to respond to all questions that we receive, but we will try to answer as many as possible in the time allotted.


Regards,

The Trans-NIH ME/CFS Working Group
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Tom Kindlon @tomkindlon.bsky.social · 28/01/2024
An EU-funded, multi-million Euro project investigating the impact of infectious diseases on the development of immunological diseases (including #MECFS, #MS, #RA, #IBD & #LongCovid) is being launched. Across many countries Info in English: www.s4me.info/threads/news... #CFS #PwME #PostCovid
s4me.info
News from the Visegrád Countries - Czech Republic, Poland, Slovakia and Hungary
Two abstracts from the 32nd International Congress of Clinical Neurophysiology (ICCN) of the IFCN, September 4-8, 2022, Geneva, Switzerland. The...
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ME/CFS News @mecfsnews.bsky.social · 19/01/2024
A prospective study found no relationship between joint hypermobility and ME/CFS triggered by infectious mononucleosis www.clinicaltherapeutics.com/article/S014...
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ME/CFS News @mecfsnews.bsky.social · 14/01/2024
You can take the FUNCAP55 questionnaire online. It is a questionnaire designed to assess functional capacity in ME/CFS. raffbenato.github.io/funcap55/
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ME/CFS News @mecfsnews.bsky.social · 05/01/2024
Dysregulation of extracellular vesicle protein cargo in female myalgic encephalomyelitis/chronic fatigue syndrome cases and sedentary controls in response to maximal exercise isevjournals.onlinelibrary.wiley.com/doi/10.1002/...
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ME/CFS News @mecfsnews.bsky.social · 05/01/2024
Muscle abnormalities worsen after post-exertional malaise in long COVID www.nature.com/articles/s41...
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ME/CFS News @mecfsnews.bsky.social · 02/01/2024
Heterogenous circulating miRNA changes in ME/CFS converge on a unified cluster of target genes: A computational analysis journals.plos.org/plosone/arti...
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ME/CFS News @mecfsnews.bsky.social · 29/12/2023
Identification of CD8 T-cell dysfunction associated with symptoms in myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) and Long COVID and treatment with a nebulized antioxidant/anti-pathogen agent in a retrospective case series www.sciencedirect.com/science/arti...
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ME/CFS News @mecfsnews.bsky.social · 16/12/2023
Disease severity and cerebral blood flow reduction during tilt testing are highly associated in ME/CFS: a more severe disease is related to a larger cerebral blood flow reduction. www.mdpi.com/1648-9144/59...
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ME/CFS News @mecfsnews.bsky.social · 16/12/2023
Microvascular Capillary and Precapillary Cardiovascular Disturbances Strongly Interact to Severely Affect Tissue Perfusion and Mitochondrial Function in ME/CFS Evolving from the Post COVID-19 Syndrome www.preprints.org/manuscript/2...
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ME/CFS News @mecfsnews.bsky.social · 15/12/2023
PrecisionLife, Action for ME, and the MRC Human Genetics Unit have been awarded an Advancing Precision Medicine grant by Innovate UK to improve diagnosis & treatment of ME/CFS and Long Covid. precisionlife.com/news-and-eve...
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Andromeda Yelton @thatandromeda.bsky.social · 14/12/2023
They...cured lupus??? www.nature.com/articles/d41... I mean. It's a hella intense, sci-fi treatment, and we're talking only a dozen or two patients, but they have actually knocked down four different autoimmune diseases here and it...works??
nature.com
‘It’s all gone’: CAR-T therapy forces autoimmune diseases into remission
Engineered immune cells, most commonly used to treat cancers, show their power against lupus and other immune disorders. Engineered immune cells, most commonly used to treat cancers, show their power ...
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Tom Kindlon @tomkindlon.bsky.social · 14/12/2023
New from China: A cross-sectional study exploring the relationship between symptoms of anxiety/depression and P50 sensory gating in adult patients diagnosed with #chronicfatiguesyndrome / #myalgicencephalomyelitis Abstract: www.frontiersin.org/articles/10.... #MEcfs #CFS #PwME
Screenshot of abstract
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Tom Kindlon @tomkindlon.bsky.social · 11/12/2023
New UK #MEcfs research: "Compelled loneliness and necessitated social isolation: 'It’s like being on the other side of a mirror, just looking in'” Free onlinelibrary.wiley.com/doi/10.1111/... #MyalgicEncephalomyelitis #ChronicFatigueSyndrome #MEcfs #CFS #PwME
Abstract
This article develops the conceptualisation of loneliness by drawing on 42 accounts of myalgic encephalomyelitis (ME). While illness experience is a central concern of the sociology of health and illness, experiences of loneliness alongside contested and chronic illness have received less attention. The analysis illustrates how loneliness can be an integral part of living with ME and offers two novel conceptual contributions - necessitated social isolation and compelled loneliness. Necessitated social isolation concerns how ME symptoms can make social lives increasingly restricted. Compelled loneliness highlights how the combined experiences of both stigma and contested illness can lead to social withdrawal and rejection, which create a sense of loneliness. The article argues that loneliness and social isolation can be conceptually distinct yet recursive and overlapping. With the worsening of ME, the participants experienced a cycle of loneliness, in which social isolation and
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ME/CFS News @mecfsnews.bsky.social · 10/12/2023
Preprint: Mechanisms underlying exercise intolerance in Long COVID: an accumulation of multi-system dysfunction www.medrxiv.org/content/10.1...
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ME/CFS News @mecfsnews.bsky.social · 09/12/2023
Post-COVID exercise intolerance is associated with capillary alterations and immune dysregulations in skeletal muscles actaneurocomms.biomedcentral.com/articles/10....
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ME/CFS News @mecfsnews.bsky.social · 08/12/2023
Naltrexone 6 mg once daily versus placebo in women with fibromyalgia did not improve pain but might improve memory. www.thelancet.com/journals/lan...
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ME/CFS News @mecfsnews.bsky.social · 05/12/2023
Preprint: Immunological Patient Stratification in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome The study identified two subgroups, one with immunodeficiency (reduced complement protein C4a levels), and one with mucosal barrier leakage. www.preprints.org/manuscript/2...
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ME/CFS News @mecfsnews.bsky.social · 04/12/2023
Full article. Post-exertional malaise in daily life and experimental exercise models in patients with myalgic encephalomyelitis/chronic fatigue syndrome www.frontiersin.org/articles/10....
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ME/CFS News @mecfsnews.bsky.social · 30/11/2023
DNA Methylation Changes in Blood Cells of Fibromyalgia and Chronic Fatigue Syndrome Patients www.dovepress.com/dna-methylat...
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Tom Kindlon @tomkindlon.bsky.social · 29/11/2023
New: Brain-regional characteristics and neuroinflammation in ME/CFS patients from neuroimaging: A systematic review and meta-analysis Free fulltext: www.sciencedirect.com/science/arti... #MyalgicEncephalomyelitis #ChronicFatigueSyndrome #MEcfs #CFS #PwME 1/
Highlights
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Neuroinflammation is the most convincing hypothesis for ME/CFS pathophysiology, explaining its multifaceted symptoms and pathological features.

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Across various neuroimaging techniques, including MRI, MRS, PET, and EEG, the frontal cortex was the most frequently observed region.

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Our meta-analysis data showed that not only the insula and thalamus showed significant hypoactivity, but also the limbic system.

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Cortical-limbic disconnection leads to the abnormalities of metabolite and brain waves, which eventually contribute to main symptoms of ME/CFS.
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ME/CFS News @mecfsnews.bsky.social · 28/11/2023
Dysregulation of the Kynurenine Pathway, Cytokine Expression Pattern, and Proteomics Profile Link to Symptomology in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) link.springer.com/article/10.1...
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ME/CFS News @mecfsnews.bsky.social · 28/11/2023
Catalytic Antibodies May Contribute to Demyelination in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome pubs.acs.org/doi/10.1021/...
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ME/CFS News @mecfsnews.bsky.social · 25/11/2023
Are you suffering from loneliness? What helps you as ME/CFS patient feel less lonely?
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David Tuller @davetuller1.bsky.social · 25/11/2023
Here's my interview with @betsyladyzhets.bsky.social and @mileswgriffis.bsky.social about their new online publication @thesicktimes.bsky.social: virology.ws/2023/11/24/t...
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Tom Kindlon @tomkindlon.bsky.social · 24/11/2023
New: In Memory of Professor Derek Pheby Free full text: www.clinicaterapeutica.it/ojs/index.ph... Obituary of this sympathetic researcher active in the ME/CFS field over many years (he had a personal connection) #MyalgicEncephalomyelitis #ChronicFatigueSyndrome #MEcfs #CFS #PwME #MyalgicE
Photo of Prof Pheby
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Tom Kindlon @tomkindlon.bsky.social · 19/11/2023
From ME Research UK: Today is International Men’s Day. Read more about ME/CFS in men, and the challenges men with the disease face on our website: bit.ly/imd2023a #InternationalMensDay #InternationalMensDay2023 #IMD2023 #MEcfs #CFS #MyalgicE #PwME #MyalgicEncephalomyelitis #ChronicFatigueSyndrome
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ME/CFS News @mecfsnews.bsky.social · 19/11/2023
A structural genetic variant affecting AKR1C1 and AKR1C2 was identified in a patient with a complex illness resembling ME/CFS. This discovery was possible because the authors used long read sequencing instead of short reads. translational-medicine.biomedcentral.com/articles/10....
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ME/CFS News @mecfsnews.bsky.social · 17/11/2023
Today, the European Medicines Agency is holding a workshop on generating clinical evidence for the treatment and prevention of long COVID. Live broadcast from 13:00 - 18:00 Amsterdam time (CET). www.ema.europa.eu/en/events/wo...
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ME/CFS News @mecfsnews.bsky.social · 17/11/2023
The ME Association (MEA) is pleased to announce that the Ramsay Research Fund will be providing some further funding to Dr Karl Morten et al in Oxford to continue their research involving Raman spectroscopy to find a diagnostic biomarker for ME/CFS. meassociation.org.uk/2023/11/rama...
meassociation.org.uk
Raman research set to continue thanks to Ramsay Research funding from the ME Association - The ME As...
The ME Association (MEA) is pleased to announce that the … Raman research set to continue thanks to Ramsay Research funding from the ME Association Read More »
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ME/CFS News @mecfsnews.bsky.social · 16/11/2023
Dysautonomia and small fiber neuropathy in post-COVID condition and Chronic Fatigue Syndrome Findings suggest damage to unmyelinated fibers and non-length dependent SFN. translational-medicine.biomedcentral.com/articles/10....
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ME/CFS News @mecfsnews.bsky.social · 16/11/2023
The Workwell Foundation has announced a collaboration with STAT Health to test a new in-ear wearable device that measures cerebral blood flow. Changes in cerebral blood flow in will be tracked during a 2-day CPET. ME/CFS, Long Covid. workwellfoundation.org/workwell-tea...
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The Sick Times @thesicktimes.org · 14/11/2023
"If our medical and public health institutions fail to understand how [infection-associated] diseases work and come up with solutions now, they are doomed to repeat their mistakes of the last three years when future pathogens hit," writes @betsyladyzhets.bsky.social in her editorial letter.
thesicktimes.org
Welcome to The Sick Times, a letter from our co-founder, Betsy Ladyzhets
The story sounds familiar, but Long Covid is different: this time, the number of sick people is too big to ignore. People with Long Covid are making their voices heard everywhere from their doctors…
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ME/CFS News @mecfsnews.bsky.social · 12/11/2023
Simmaron Research has announced a treatment study of rapamycin for ME/CFS. It will not be placebo controlled but track levels of ATG-13 during treatment. www.simmaronresearch.com/rapamycin-tr...
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ME/CFS News @mecfsnews.bsky.social · 11/11/2023
Small intestinal bacterial overgrowth is highly prevalent in patients with ME/CFS referred for breath testing. journals.lww.com/ajg/fulltext...
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Tom Kindlon @tomkindlon.bsky.social · 11/11/2023
New pre-print: #MyalgicEncephalomyelitis / #ChronicFatigueSyndrome (Me/Cfs): The Biology of a Neglected Disease Free fulltext: papers.ssrn.com/sol3/papers.... #MEcfs #CFS #PwME
Screenshot of abstract
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ME/CFS News @mecfsnews.bsky.social · 11/11/2023
The economic burden of myalgic encephalomyelitis/chronic fatigue syndrome in Australia. The conclusion is that ME/CFS poses a significant economic burden in Australia. #MECFS www.publish.csiro.au/AH/justaccep...
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ME/CFS News @mecfsnews.bsky.social · 11/11/2023
I have often thought that I needed a guide for living well with ME/CFS (to the degree that is possible). What are some lessons you have learned?
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ME/CFS News @mecfsnews.bsky.social · 10/11/2023
A short overview of post-exertional malaise by Rob Wüst et al, with a focus on long covid. www.scienceopen.com/document/rea...
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ME/CFS News @mecfsnews.bsky.social · 09/11/2023
Dr Nath on the NIH's intramural study of ME/CFS: "we think all our findings suggest persistent antigen leads to immune dysfunction and microbial dysbiosis in GI tract. Neuroimmune axis gets dysregulated, contributing to metabolic abnormalities." x.com/oslersweb/st...
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