ME/CFS News
mecfsnews.bsky.social
ME/CFS News
@mecfsnews.bsky.social
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News, interesting information and commentary on ME/CFS.
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May 12 is ME/CFS Awareness Day. Speak with other people about ME/CFS today. Reject invisibility and stigma, build awarenesss and support.
Reposted by ME/CFS News
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
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
www.youtube.com
Just because China is willing to abuse relatively free flow of information doesn't mean they have the right values.
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/...
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.
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
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...
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: [email protected]
Reposted by ME/CFS News
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...
A prospective study found no relationship between joint hypermobility and ME/CFS triggered by infectious mononucleosis www.clinicaltherapeutics.com/article/S014...
You can take the FUNCAP55 questionnaire online. It is a questionnaire designed to assess functional capacity in ME/CFS.

raffbenato.github.io/funcap55/
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/...
Muscle abnormalities worsen after post-exertional malaise in long COVID

www.nature.com/articles/s41...
Heterogenous circulating miRNA changes in ME/CFS converge on a unified cluster of target genes: A computational analysis

journals.plos.org/plosone/arti...
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...
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...
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...
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...
Reposted by ME/CFS News
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
Reposted by ME/CFS News
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