How to Survive University with M.E. – The ME-friendly packing list! By Emily Bailey | 13 September 2019
Emily tell us about some of the things that have helped make her university experience more tolerable.
Emily tell us about some of the things that have helped make her university experience more tolerable.
These are the minutes from the recent Forward ME meeting in July 2019.
Emily takes us through her survival techniques and offers help and advice on how to survive at university with M.E.
We all owe an enormous debt of gratitude to Peter. He will be sadly missed and I will be attending his funeral on Friday 13th September in Edinburgh.
M.E. has taken Lorna out of the classroom but there’s more to an identity than a career.
Situations Vacant: We want to recruit a fundraiser | 06 September 2019 Read More »
We are looking to recruit someone to lead our charity fundraising efforts and public campaigns.
How to Survive University with M.E. – The First Term by Emily Bailey | 05 September 2019 Read More »
Emily takes us through her survival techniques and offers help and advice on how to survive at university with M.E.
Ewan Dale reports on a recent meeting to discuss the future of healthcare in Scotland.
Changes to Blue Badge parking criteria have come into effect making it easier for people with non-visible disabilities to get one.
MEA Website Survey: Support for M.E. in Education | 04 September 2019 Read More »
This month we’d like to hear from anyone who has experience of M.E. and education. What kind of support did you receive?
ME Association August Summary of ME/CFS Published Research | 03 September 2019 Read More »
We’ve updated the central Research Index and feature 16 ME/CFS research studies from August 2019.
NICE Guideline Review: Call for Evidence | 02 September 2019 Read More »
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.
Very Severe ME: It’s Time for Something New! By Greg Crowhurst | 16 August 2019 Read More »
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.
Top 7 Tips for Claiming Disability Benefits with M.E. by Ann Innes | 14 August 2019 Read More »
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.