At the ME Association, we believe that research holds the key to transforming the lives of people with ME/CFS and Long Covid. Since establishing the Ramsay Research Fund in 1989/1990, we've been committed to funding high quality biomedical research into ME/CFS. So far, we’ve invested £2.6 million into research — with another £2 million planned over the next three years. None of this would be possible without your continued support. Thank you for helping us make a difference! Find out more: https
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At the ME Association, we believe that research holds the key to tran…
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This year, we are doing the BigGive to fund a new research study - but what is this study about? And how it may help the ME/CFS community? Watch our latest video to learn all about this worthwhile study, and how your donations next week will make a huge difference! Register for a reminder to donate here: https://meassociation.org.uk/big-give-2025/ #Donate #pwME #MECFS #MyalgicEncephalomyelitis #PEM #PostExertionalMalaise #MyalgicEncephalopathy #MECFSResearch | ME Association
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This year, we are doing the BigGive to fund a new research study - bu…
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Melanoma Research Foundation on Reels
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Melanoma Research Foundation on Reels
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FacebookMelanoma Research Foundation
This year, we are doing the BigGive to raise funds for a new research study, looking at what happens in the muscles, at a cellular level, when a person with ME/CFS experiences Post-Exertional Malaise (PEM). The BigGive means that all money donated during 2nd-9th December is DOUBLED - so please register to receive a reminder to donate during that week, and raise money for this potentially life-changing study. https://meassociation.org.uk/big-give-2025/ #MEAssociation #pwME #MECFS #MEResearch #Don
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This year, we are doing the BigGive to raise funds for a new research …
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How well do you know Melanoma Research Foundation ? They’re now featured in our #ReadyRaiseRise Spotlight. Take action at http://bit.ly/2ClSkjZ to help your favorite participating advocacy group be next! | Bristol Myers Squibb
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How well do you know Melanoma Research Foundation ? They’re n…
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FacebookBristol Myers Squibb
ME/CFS Research Roadmap Webinar Series: Metabolism
ME/CFS Research Roadmap Webinar Series: Metabolism
Oct 26, 2023
nih.gov
There’s still time to make a meaningful, tax-smart gift to the MRF before the year ends — and you don’t have to give cash to make a big impact. By donating cryptocurrency, contributing appreciated stock, giving through your IRA or recommending a Donor-Advised Fund grant, you can support melanoma patients while unlocking valuable tax benefits. To ensure your gift counts toward your 2025 tax return, be sure to complete it by tomorrow, December 16. Get started using our simple, secure online tools:
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There’s still time to make a meaningful, tax-smart gift to the M…
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Looking for a way to make a lasting impact on the lives of melanoma patients for generations to come? Consider contributing to the MRF’s Legacy of Progress Endowment Fund as your support will allow us to amplify our investments in critical research grants and initiatives. Watch this video below as MRF CEO, Kyleigh LiPira and Legacy of Progress Endowment Fund Founders share the immense value of this initiative. Click here to learn more: https://melanoma.org/endowment/ | Melanoma Research Foundati
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Looking for a way to make a lasting impact on the lives of melanoma p…
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Tomas et al. (2019) Assessing cellular energy dysfunction in ME/CFS using a commercially available laboratory test. Biomarker research is important because biomarkers—measurable biological indicators of disease—may help diagnose ME/CFS. This is one of several studies that needs replication before any firm conclusions can be made as to its accuracy and to ensure it is specific to ME/CFS. Read more about the study, funded by the ME Association's Ramsay Research Fund, here: https://www.nature.com/a
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Tomas et al. (2019) Assessing cellular energy dysfunction in ME/…
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The ME Association is dedicated to raising awareness and supporting the ME/CFS and Long Covid communities through its social media presence. We use our platforms to support, engage with the community, and to champion for positive change for those affected by these conditions . Follow us today: https://linktr.ee/measocials #pwME #MECFS #LongCovid #PostCovidSyndrome #PVFS #MEAssociation #FollowUs | ME Association
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The ME Association is dedicated to raising awareness and supportin…
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The UK ME CFS Biobank are offering free #MECFS samples to accelerate biomedical research for #pwME The biobank, which is funded by the ME Association, offers a range of samples including: - Mild, Moderate, Severe ME/CFS - Pre- and post-COVID including long-COVID - Multiple Sclerosis - Healthy controls Apply by 31 July: https://tinyurl.com/mp96zzwp #MECFSResearch | ME Association
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The UK ME CFS Biobank are offering free #MECFS samples to …
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• The ME Association is here for you! • Fantastic website • Expert information on ME/CFS and Long Covid • Free literature covering symptoms, diagnosis, management, benefits, and more... • Find NHS services and local support groups View our Egg-cellent website! https://meassociation.org.uk/mtec #pwME #MECFS #MyalgicE #MyalgicEncephalomyelitis #LongCovid #PostCovid #MEAssociation | ME Association
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• The ME Association is here for you! • Fantastic website • Expert i…
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We were sent this video to be shared for our #TeachMETreatME #MillionsMissing campaign. Please join us this #WorldMEDay in helping clinicians and medical students learn about myalgic encephalomyelitis (ME aka ME/CFS). You can find information at millionsmissing.org- link in our bio. Please share a video or post, email your clinicians and ask them to take the continuing medical education (we offer sample language), and/or donate to #MEAction. We need your help! You can find our full video on #MEA
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We were sent this video to be shared for our #TeachMETreatME …
2K viewsMay 13, 2024
FacebookThe #MEAction Network
Dr. Ranj Thank you so much for mentioning the ME Association as a place for information and support for people with #LongCovid & #MECFS on BBC Morning Live this morning. We truly appreciate it! EDIT: Watch the full segment and episode of BBC Morning Live on iplayer here: https://www.bbc.co.uk/iplayer/episode/m0015y9z/morning-live-series-3-30032022 #morninglive #pwME #MECFS #MyalgicE #CognitiveDysfunction #BrainFog #PoTS #LongCovid #PostCovid | ME Association
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Dr. Ranj Thank you so much for mentioning the ME Association a…
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This month, the ME Association announced the largest ever single investment in biomedical research by any charity in this field; and the largest project ever of its kind, researching the shared pathways between ME/CFS and Long Covid. But what is this ground-breaking research study that's receiving £1.1million from the MEA? Watch this video to find out, or read our blog: https://meassociation.org.uk/5n3l #MECFS #LongCovid #RamsayResearchFund #MEAssociation #ImperialCollegeLondon #RosettaStone #ME
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This month, the ME Association announced the largest ever singl…
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ME/CFS is a life altering disease. Your support will fund crucial research into the energy crash in ME/CFS, and give hope to the hundreds-of-thousands with this devastating illness in the UK. Donate now, and have your amount doubled! https://meassociation.org.uk/BigGive2025 #MECFS #MyalgicEncephalomyelitis #LongCovid #BigGive2025 #ChristmasChallenge #WhenRestIsntEnough #DoubleYourDonation | ME Association
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ME/CFS is a life altering disease. Your support will fund crucial res…
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You helped grow a global movement through your support of #MillionsMissing, BedFest, MEpedia, congressional and parliamentary outreach, and so much more! This is our vision for what comes next. Let's keep up the fight. Help us raise $100,000 to support the movement for Myalgic Encephalomyelitis equality. DONATE and SHARE: https://www.indiegogo.com/projects/meaction-2018# | The #MEAction Network
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You helped grow a global movement through your support …
85.4K viewsApr 26, 2018
FacebookThe #MEAction Network
World’s largest genetic study of ME offers hope to sufferers
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World’s largest genetic study of ME offers hope to sufferers
Apr 4, 2024
channel4.com
Karl J. Morten et al (2023) Developing a Blood Cell-Based Diagnostic Test for ME/CFS Using Peripheral Blood Mononuclear Cells In this study, funded by the ME Association's Ramsay Research Fund, researchers analysed blood cells using Raman spectroscopy and ensemble learning classification (AI technology) to try to establish a biomarker. This is one of several studies that will need replication before any firm conclusions can be made as to its accuracy and to ensure it is specific to ME/CFS. Find
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Karl J. Morten et al (2023) Developing a Blood Cell-Based Di…
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Did you know that neurological conditions affect at least 1 in 6 people across the UK and are the leading cause of ill health in the world? Despite this, there is still so much we don’t know about what causes neurological conditions, and how we might develop better treatment, care and support for those who experience them. This needs to change. The MEA states: "Currently, ME/CFS can be managed relatively well if there is an early, accurate diagnosis. However, further research is needed to find m
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Did you know that neurological conditions affect at least 1 in 6 pe…
10.4K viewsMar 12, 2025
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ME/CFS is a debilitating disease which affects hundreds of thousands of people in the UK. People with ME/CFS are often unseen and their stories remain unheard, due to the restrictive nature of the condition. Help us this ME Awareness Week, by sharing these real stories, and reminding people with ME/CFS that they are not alone. https://meassociation.org.uk/what-is-MECFS/ *If sensitive to sound, please turn down the volume as the video also has music'* #MEAW #MEAW2025 #MEAwarenessWeek #pwME #MECFS
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ME/CFS is a debilitating disease which affects hundreds of thousa…
2K views10 months ago
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We are excited to share some news about ME, and our future. We'll no longer just be ME, ME, ME – in fact, it’s going to be more of a WE. Earlier today shareholders of ME agreed to accept a proposal from Bank of Queensland (BOQ), which will see ME join their family of brands. Don't worry – we’ll still be the same old ME, and we’ll still offer the same simple, straightforward products and services we always have. BOQ and ME together – think of all the amazing things we can do; we just can’t wait t
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We are excited to share some news about ME, and our future. We'll n…
10.7K viewsFeb 21, 2021
FacebookME
Why Some People Improved… and Some Didn’t (ME/CFS Study)
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Why Some People Improved… and Some Didn’t (ME/CFS Study)
85 views3 months ago
YouTubeRe:Cognition Health
ME/CFS Research Foundation on Instagram: "Die ME/CFS Research Foundation stellt ihre Förderstrategie 2026 vor. 🎥 Im Video erklärt Jörg, warum 2026 ein wichtiges Übergangsjahr wird – und wie wir Forschung in dieser Phase gezielt stärken. Seit vier Jahren fördern wir biomedizinische Forschung zu ME/CFS & Long COVID, vernetzen Forschende und machen Forschung transparent. Die angekündigte „Nationale Dekade gegen postinfektiöse Erkrankungen“ eröffnet ab 2026 große Chancen, doch bis erste "Dekaden"-P
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ME/CFS Research Foundation on Instagram: "Die ME/CFS Researc…
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Instagrammecfs_research
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