We’ve updated the central Research Index and feature 12 ME/CFS research studies from September 2019.
News | The ME Association- Part 18
This month we’re all about Pets and how much they can mean to someone who is not in the best of health.
The influential Cochrane organisation has published an updated review and issued a statement following concerns expressed by the patient community.
We’ve updated the central Research Index and feature 16 ME/CFS research studies from August 2019.
NICE is asking stakeholders for evidence to support the ongoing review. The deadline is 4th October by 5pm.
It is estimated that more than 580,000 Canadians live with myalgic encephalomyelitis (ME), formerly known as chronic fatigue syndrome.
Physios 4 ME report on the results from the MEA website survey that took place in July.
Dr Morten provides additional comment on the recent validation attempt of the Acumen test and we include a detailed report.
I have cared day and night for my wife who has lain in unspeakable torment, torture and agony, for twenty-six years.
Dr Sarah Jarvis talks The Sun through the main signs your exhaustion could actually be a symptom of ME/CFS.
The MEA’s Welfare Rights Adviser provides her top-tips for people with M.E. when applying or renewing ESA and PIP.
All women are invited to cervical screening, and all women should be able to have access to a test.
The long-awaited independent assessment of Dr Myhill’s mitochondrial function test was published earlier this week.
Anonymity is a cover for the disappointment that is only overwhelmed by the relentless exhaustion of M.E.
Laura, now 25, has chosen to lay bare the brutal reality of life with M.E. – which affects 250,000 people in the UK.
The nursing home was accommodating at first. However, they didn’t have any experience caring for M.E patients and I don’t think they fully realised the extent of the situation.
Day after day this fragile hope is crushed, shattered, ground down like broken glass. Monotony, drudgery, despair! How can I escape?
The impact of these last three decades of attempts to bury the serious disease M.E. under a sea of unrelated and vague “fatigue conditions” has been catastrophic for patients.
“Many only succeed in obtaining the benefits they should be entitled to after going through a long and stressful appeal process.” Dr Charles Shepherd.
We are delighted that Gary Burgess has recorded a special episode that considers the Real impact of Severe M.E. with Jo Moss and Ann Innes.