• Help us to support others – donate now and change a life

    Donate now


  • A
  • A
  • A
Text size

Calling all knitters – gift an angel this Christmas

September 02, 2019

You may have heard of our annual project “Christmas Angels” which supports people with M.E. to share Christmas cards with each other via our office. Some are very isolated, so these…

Involving young people in the NICE guideline development

August 13, 2019

We are pleased to announce that Action for M.E. will be working with Oxford Brookes University to gather the experiences of children and young people with M.E. to develop a new guideline…

"Great misery has been inflicted" says UN reporter

May 23, 2019

“Great misery has been inflicted unnecessarily, especially on the working poor, on single mothers struggling against mighty odds, on people with disabilities who are already marginalized,”…


May 22, 2019

M.E. is a largely misunderstood and unrecognised illness, not only nationally but also globally. As a result, it is easy to see how isolation and ignorance become common themes experienced…

Are you missing M.E.? - Naomi's story

May 10, 2019

Hi, my name is Naomi and I have a condition called M.E. Before I became ill, I was at university studying nursing. Then I started to experience more symptoms and would get frustrated…

A day in the life of Ev

May 09, 2019

As part of our M.E. awareness month campaign, Action for M.E. handed over our social media pages to Ev - a person with M.E. She spent the day posting about her condition, experiences…

Are you missing M.E.? - Martin's story

May 01, 2019

I was diagnosed in April 2018 after forcing my GP to correctly diagnose me. However I believe I have had M.E since I was 18/19 years old. Over the last three years it has become severe…

May is M.E. Awareness Month

May 01, 2019

For M.E. Awareness Month 2019, we are asking professionals, planners and policy-makers: "Are you missing M.E.?"Many children and adults with M.E. tell us they feel missed out, and left…

Our staff Walk with M.E. team – in honour of the SAMS

April 23, 2019

As part of Walk with M.E. 2019, ten members of Action for M.E.’s staff are taking part. In preparation for the campaign, we all had many ideas about how we would make our team special.Our…

M.E. in Sunday Times: "I've been made to feel a burden"

March 24, 2019

Responding to the hundreds of comments it received following Rod Liddle's comment piece on M.E. last weekend, the Sunday Times has published an article highlighting the reality of M.E.…

#ShareGoodScience in response to The Sunday Times

March 18, 2019

A number of you have contacted us about the awful story by Rod Liddle in yesterday’s Sunday Times. Given the stiff competition to get a response published in the paper itself, we have…

Fundraiser of the week - Nick West

March 15, 2019

Our fundraiser of the week has quite a unique story. Nick West has been a collector for over 42 years and has amassed a collection of over 9300 different British beer cans. His hobby…

Patients and researchers moving M.E. research forward

March 14, 2019

Yesterday, you may have seen a story published by an international news agency about some M.E. researchers facing online abuse and harassment. We cannot condone any behaviour that…

M.E. inspiration on International Women's Day

March 08, 2019

International Women’s Day celebrates women all over the world and the amazing work they have done. Whether they are politicians, doctors, campaigners, carers, friends, or family members,…

Scottish Parliament discussion of M.E. during Petitions Committee

January 30, 2019

Thursday 24 January was a busy day for the M.E. community with debates being held in both UK and Scottish Parliament. The Scottish Petitions Committee was attended by Scotland’s Chief…

Parliamentary debates on M.E. on 24 January

January 25, 2019

"It’s actually quite remarkable to consider how little is being sent on research, it's something like 0.02% of all active grants given by mainstream funding agencies going to support…

Scottish government launches National Action Plan

January 16, 2019

The Scottish Government has published a draft National Action Plan on Neurological Conditions. It sets out the vision of improving diagnosis, treatment and care of people with neurological…

LGO ruling on access to education

January 15, 2019

Action for M.E. has been working with 16-year-old Maddie, who lives in Hayle, Cornwall, where the Local Government and Social Care Ombudsman (LGO) has made a ruling against the Council…

Fundraiser of the week: Notts County FC

September 14, 2018

Congratulations to Notts County FC, our Fundraiser of the Week! As part of our one-month sponsorship of the club, generously donated to us by one of our supporters, Notts have kindly…

Join us at Notts County FC this month

September 03, 2018

Are you a football fan? Do you or a keen supporter in your family struggle to attend games because of M.E.? As part of Action for M.E.’s September sponsorship of Notts County FC,…

M.E. on BBC Radio London Drivetime show today

August 23, 2018

Making M.E. the focus of his Drivetime show today on BBC Radio London, Eddie Nestor MBE will hear from people living with M.E. about the impact of the condition on school, work and…

"I was desperate to talk to someone who understood"

April 17, 2018

"When my son Lewis, now 11, caught a bug he seemed unable to shake off in 2016, his symptoms seemed worryingly familiar. Although I tried to convince myself he would soon be back to…

Unrest screening plus Q&A in Bath on 14 November

November 03, 2017

As charity partner of the award-winning M.E. documentary Unrest, Action for M.E. is delighted to support a community screening in Bath later this month, where our Chief Executive, Sonya…

Double your donation: the Big Give Christmas Challenge

November 01, 2017

The children and adults that Action for M.E. supports rely on services funded by your generous donations. We are absolutely thrilled that, for one week only, those donations will be…

See award-winning M.E. doc Unrest at our events

October 18, 2017

Action for M.E. is thrilled to be partnering with award-winning documentary Unrest to raise awareness and understanding of M.E. and its impact. Working with the team behind the film,…

SMILE Trial results published: Action for M.E. comment

September 20, 2017

Results of a trial published today show that a small cohort of young people with mild or moderate M.E. report improvement in their symptoms after undergoing the Lightning Process in…

M.E. in Northern Ireland: our NVTV interview

August 17, 2017

Less than half of UK NHS boards commission a specialist service for M.E., and Northern Ireland has no provision at all, leaving thousands of desperately ill people unable to access…

Sonya Chowdhury responds to ‘psychosomatic’ comment

October 10, 2016

Action for M.E. Chief Executive Sonya Chowdhury has challenged a comment posted on the British Medical Journal (BMJ) website which suggested that for M.E. patients, the condition is…

M.E. in the media: new challenges for Jude and Beth

September 20, 2016

In the news this month are two women with M.E. celebrating their achievements. Jude Adams, who has lived with M.E. for seven years, has released her first album, supported by Arts Council…

Millions missing: add your voice to the campaign

September 07, 2016

A global M.E.-awareness event is planned for Tuesday 27 September, and you can get involved. Building on the success of protests that took place across the world in May and June, the Millions…

Ministers answer parliamentary questions on M.E.

June 14, 2016

This week, two written parliamentary questions have been answered on M.E. The first was tabled by Alex Cunningham MP, and arose as a result of Mr Cunningham attending the recent APPG…

Taking care of carers: Carers Week 2016

June 06, 2016

“My husband’s life has had to change as drastically as my own in order to accommodate my condition, and over the years he has often had to act as my carer. Our life as a couple has…

M.E. in the media: the double whammy of isolation

June 02, 2016

“I only see one or two people for an hour or two at most – I can't cope with any more than that,” says Tisha Bratt, who has had M.E. for 22 years. “My husband is wonderful. We met after…

M.E. in the media: raising awareness, reducing isolation

May 16, 2016

We’re just over half way through M.E. Awareness Month 2016, and are delighted that so many local and regional newspapers are helping to spread our message: don’t ignore M.E.Our media…

M.E. in the media: M.E. Awareness Month so far

May 10, 2016

Already this M.E. Awareness Month our media case studies have appeared in the local press and on newspaper websites across the UK. This year our media work is focusing on the isolation…