From meassociation.org.uk
'From ME to You' – help us find the unsung heroes who care for you - The ME Association
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Two years ago, we ran a campaign offering our members […]
#mecfs #carers #LongCovid #unsungheroes #myalgicencephalomyelitis
22h ago
From meassociation.org.uk
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Today (13.11.24), the Telegraph reports on the Perrin Technique with […]
#pwme #mecfs #myalgice #myalgicencephalomyelitis
22h ago
From meassociation.org.uk
Survey: 2024 Autumn Covid and Flu Vaccinations - The ME Association
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We are launching this website survey to gather information on […]
#cfs #pwme #mecfs #chronicfatiguesyndrome #myalgicencephalomyelitis
22h ago
From meassociation.org.uk
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This week (5th-7th November) in Holyrood, MSPs are passing an […]
on Nov 6
From meassociation.org.uk
ME/CFS: Watch Dr Shepherd's presentation to the Stockport ME Group - The ME Association
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Recently, Dr Charles Shepherd gave a presentation to Stockport ME […]
on Nov 2
From meassociation.org.uk
Template: Covid Autumn Booster Vaccine (2024) - The ME Association
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This template letter can help you obtain a Free NHS […]
on Nov 2
From meassociation.org.uk
Recognise ME – Raising Awareness in GP Practices - The ME Association
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The ME Association is committed to improving healthcare for people […]
on Oct 6
From meassociation.org.uk
Update on a new All-Party Parliamentary Group (APPG) on ME - The ME Association
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Action for ME and the ME Association are keen to […]
on Oct 6
From meassociation.org.uk
News Medical: Cardiovascular risks of COVID-19 antivirals - The ME Association
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Emerging evidence reveals that COVID-19 antiviral therapies may pose severe […]
on Sep 17
From meassociation.org.uk
Writing a children’s book featuring a protagonist who has ME - The ME Association
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Sally Doherty talks about her new book – Max and […]
on Sep 16
From meassociation.org.uk
Research: Myalgic Encephalomyelitis is clear to see in the blood - The ME Association
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Simon McGrath provides a summary of important research from Edinburgh.
on Sep 10
From meassociation.org.uk
Norwegian team of researchers are presented with the Howes-Goudsmit Award - The ME Association
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The ME Association are pleased to announce we have awarded […]
on Sep 9
From meassociation.org.uk
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From Fatigue: Biomedicine, Health & Behavior, 7 July 2016. EDITORIAL […]
on Aug 11
From meassociation.org.uk
Severe M.E Awareness Week: Sally Doherty - The ME Association
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I’ve been ill with ME for over fifteen years now […]
on Aug 8
From meassociation.org.uk
Disability Classification - The ME Association
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How does the government define a disability? Does the government classify ME/CFS as a disability? I ask because I assume that this could have important implications for people who are having problems with benefits, education or work.
on Jul 30
From meassociation.org.uk
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Pauline Ovenden was a patient advocate and veteran of the Royal Free outbreak. She will be sadly missed.
on Jul 26
From meassociation.org.uk
Building an NHS that's there for people with Long Covid and ME - The ME Association
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#ThereForME is a patient- and carer-led campaign calling for an […]
on Jul 25
From meassociation.org.uk
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**Trigger Warning: Upsetting Content** Listen to Sean O'Neill (senior writer […]
on Jul 25
From meassociation.org.uk
A new support pack for anyone with ME/CFS going to hospital - The ME Association
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The pack aims to address the many issues facing people with ME/CFS when they attend hospital.
on Jul 21
From meassociation.org.uk
BBC News: Father of woman with ME/CFS scared she will 'die in hospital' - The ME Association
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**Trigger Warning: Upsetting Content** A man says he is terrified […]
on Jul 12
From meassociation.org.uk
Science Alert: Long Covid: Full-Body Scans Reveal Long-Term Immune Effects - The ME Association
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Long Covid is a brutal illness without a known mechanism […]
on Jul 4
From meassociation.org.uk
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We hope the protocol when implemented will bring relief to the hundreds of thousands of people who suffer from these very debilitating symptoms
on Jun 26
From meassociation.org.uk
The ME Association: Pregnancy Study: Would you like to take part? - The ME Association
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We are pleased that the faMEly study is now starting […]
on Jun 26
From meassociation.org.uk
The ME Association Template Letter: General Election - The ME Association
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You can write to your general election candidates with our […]
on Jun 26
From meassociation.org.uk
New York Times: New report underscores the seriousness of Long Covid - The ME Association
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An important report from the National Acadamies in America with comparisons to ME/CFS and FM.
on Jun 9
From meassociation.org.uk
NHS England Launches New E-learning Module on ME/CFS! - The ME Association
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The new e-learning module was launched at the BACME conference...
on May 27
From meassociation.org.uk
The ME Association - The ME Association
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The ME Association provides support, research, advice and a helpline for the community of people affected by ME/CFS
on May 20
From meassociation.org.uk
Research: Working together to find answers to ME/CFS! - The ME Association
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There are 4 workshops taking place this summer for researchers, clinicians and people with ME/CFS.
on May 18
From meassociation.org.uk
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The ME Association is committed to working with the NHS and social care providers to improve healthcare for people with ME/CFS and Long Covid.
on May 18
From meassociation.org.uk
Parents of children with Long Covid accused of making it up - The ME Association
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“There is a cultural problem that is ingrained within medicine to not believe patients if we can’t explain their symptoms..."
on May 18
From meassociation.org.uk
Free Booklet: The Importance of Early & Accurate Diagnosis in ME/CFS - The ME Association
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We are pleased to announce that this very popular free […]
on Mar 15
From meassociation.org.uk
MAGENTA Trial: GET is not an effective treatment for ME/CFS - The ME Association
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Graded exercise therapy is not an effective treatment for chilren and young people with ME/CFS.
on Mar 8
From meassociation.org.uk
ME/CFS Research Published 6 – 12 February 2024 - The ME Association
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The weekly research round-up includes all recent publications about ME/CFS and Long Covid, which includes the key terms: Myalgic Encephalomyelitis, Chronic Fatigue Syndrome, ME/CFS, Long Covid and Post Covid syndrome.
on Feb 17
From meassociation.org.uk
ME/CFS Research Published 30 January – 5 February 2024 - The ME Association
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The weekly research round-up includes recent publications about ME/CFS and Long Covid. We highlight studies that have particularly caught our attention.
on Feb 11
From meassociation.org.uk
ME/CFS Research Published 23 – 29 January 2024 - The ME Association
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The weekly research round-up includes recent publications about ME/CFS and Long Covid. We highlight studies that have particularly caught our attention.
on Feb 2
From meassociation.org.uk
ME/CFS Research Published 16 – 22 January 2024 - The ME Association
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The weekly research round-up includes recent publications about ME/CFS and Long Covid. […]
on Jan 27
From meassociation.org.uk
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From the British Medical Journal, 8 November 2011 (story by […]
on Jan 19
From meassociation.org.uk
ME/CFS and Long Covid Research: 5 – 11 December 2023 - The ME Association
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The weekly research round-up includes recent publications about ME/CFS and Long Covid.
on Dec 23
From meassociation.org.uk
ME/CFS Research Published 12 – 18 December 2023 - The ME Association
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The weekly research round-up includes recent publications about ME/CFS and Long Covid. We highlight studies that have particularly caught our attention.
on Dec 23
From meassociation.org.uk
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Research evidence shows that the presence of PEM cannot be disputed and is not due to inactivity or deconditioning.
on Dec 23
From meassociation.org.uk
In the world Beyond Closed Doors, this girl tells it like it really is! - The ME Association
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In our world, Jessica Taylor-Bearman has celebrity status. She’s got … In the world Beyond Closed Doors, this girl tells it like it really is! Read More »
on Dec 23
From meassociation.org.uk
When Sally met Toby, you got fireworks! - The ME Association
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“Flapping fluttermice!” You fear for young Toby Bean as he … When Sally met Toby, you got fireworks! Read More »
on Dec 23
From meassociation.org.uk
ME Connect - The ME Association
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ME Connect is here to support people with ME/CFS and their carers make informed choices. It is here to listen and try to understand the issues they are facing. It is available 365 days a year!
on Dec 15
From meassociation.org.uk
Rapamycin Pilot Treatment Trial for ME/CFS - The ME Association
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Rapamycin therapy inhibits mTOR and reduces autophagy disruption. We believe … Rapamycin Pilot Treatment Trial for ME/CFS Read More »
on Dec 11
From meassociation.org.uk
ME/CFS Research Published 27 November – 4 December 2023 - The ME Association
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The weekly research round-up includes recent publications about ME/CFS and Long Covid. … ME/CFS Research Published 27 November – 4 December 2023 Read More »
on Dec 9
From meassociation.org.uk
ME/CFS Research Published 21 – 27 November 2023 - The ME Association
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The weekly research round-up includes recent publications about ME/CFS and Long Covid. We highlight the studies that have particularly caught our interest and follow these with the full list of publications together with their abstracts (summaries).
on Dec 1
From meassociation.org.uk
A new radical approach needed for Long COVID research - The ME Association
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With no treatment or cure in sight for Long Covid patients, who is really to blame for 3 years of disappointing clinical research results?
on Nov 25
From meassociation.org.uk
Living with M.E. A Photographic Study by Jeremy Jeffs - The ME Association
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Photographer Jeremy Jeffs is looking for more people to take part in a project that aims to give identity and visibility to people who are living with M.E.
on Nov 24