Category Archives: News

#WAMES_800 – Donations ‘In lieu of gifts’

Give donations ‘In lieu of gifts’ – to aid our #WAMES_8oo Fundraising Journey   Why not celebrate your next special occasion by asking your friends and family to lend support to people with ME/CFS? By asking your friends and family … Continue reading

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World ME Alliance asks WHO to recognise ME

World ME Alliance calls on WHO Director General to recognise ME alongside Long Covid   On Wednesday 12th October Dr Tedros Ghebreyesus, Director General of the World Health Organization, wrote an op-ed in the Guardian. In it, he lays clear … Continue reading

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Research: DNA changes during a relapse and recovery cycle in ME/CFS

Dynamic epigenetic changes during a relapse and recovery cycle in Myalgic Encephalomyelitis/ Chronic Fatigue Syndrome   Epigenetics is the study of how your behaviors and environment can cause changes that affect the way your genes work. Unlike genetic changes, epigenetic … Continue reading

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Volunteers invited to join WAMES communications team

Can you help WAMES keep the ME community informed?   Are you social media savvy & want pwme to receive the right info at the right time so it makes a real difference to people’s daily lives? Can you help … Continue reading

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Research: Orthostatic Intolerance & neurocognitive impairment overlap in ME/CFS

Orthostatic Intolerance & neurocognitive impairment overlap in ME/CFS   Prof Jason Leonard and US colleagues investigated the relationship between Orthostatic Intolerance and neurocognitive impairment in ME/CFS Orthostatic intolerance (OI) is the development of symptoms when standing upright that are relieved … Continue reading

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Research review: Genetics of COVID-19 & ME/CFS

Genetics of COVID-19 and ME/CFS: a systematic review   Greek researchers found 71 studies for COVID-19 and 26 studies for ME/CFS that looked at genes. They concluded: “In spite of the fact that COVID-19 and ME/CFS present with some similar … Continue reading

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Research: Fitbit trackers & PROMs help monitor ME/CFS activity

Activity monitoring and patient-reported outcome measures in ME/CFS patients A small Norwegian study from the team led by Prof Olav Mella and Dr Oystein Fluge trialled wearable activity trackers and questionnaires to monitor heart rate and activity to aid pacing … Continue reading

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Do I need a formal diagnosis of ME/CFS?

Do you have a diagnosis of ME or CFS from the NHS?   For decades many people with suspected ME have not been able to find an NHS professional to confirm their diagnosis. As the NHS has had nothing to … Continue reading

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Understanding ME (and Long COVID)

Understanding Myalgic Encephalomyelitis – Myalgic Encephalomyelitis and Long COVID have overlapping presentation   Dr Sonya Marshall-Gradisnik and Dr Natalie Eaton-Fitch from Griffith University, on the Gold Coast in Australia, say there is a significant overlap in symptoms and possibly the … Continue reading

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Respect and include unpaid carers for people with ME/CFS

Prioritising unpaid carers in new approaches to ME/CFS   Dr Siobhan O’Dwyer, a Senior Lecturer in Ageing and Family Care at the University of Exeter Medical School, consulted carers of people with ME/CFS and concluded they had a key role … Continue reading

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