Parliamentary Questions: support for people with fluctuating conditions who want to work, 23 May 2011
The Countess of Mar, the crossbencher who chairs the Forward […]
The Countess of Mar, the crossbencher who chairs the Forward […]
Parliamentary Question: closure of ME/CFS unit at Queen’s Hospital, Romford, 23 May 2011 Read More »
For the second time in the space of a week,
PACE Trial – text of joint letter calling for more information, 24 May 2011 Read More »
The ME Association – together with the Young ME Sufferers
From The Times, Times Money, 21 May 2011 (story by
Parliamentary Question: ESA fit to work policy for people with ME, 19 May 2011 Read More »
In a written question, Ian Swales (Liberal Democrat MP for
The difference between chronic fatigue and ME/CFS Further to a
House full for the Judy Mikovits meeting in Belfast on Sunday (May 22) Read More »
The biggest meeting room at the Holiday Inn in Belfast
Our new guidance on completing the ESA form will be ready next week Read More »
Following the introduction of a new set of Work Capability
A fortnight to go to the Liverpool ME training seminar on June 1 Read More »
With a fortnight to go before the Liverpool ME Support
Parliamentary Question: ME training for healthcare professionals, 17 May 2011 Read More »
Ian Swales, Liberal Democrat MP for Redcar and a member
Parliamentary Question: proposed closure of the ME/CFS service at Romford, 17 May 2011 Read More »
The proposed closure of the specialist inpatient service for people
New Lombardi et al paper on XMRV, In Vivo, May-June issue 2011 Read More »
From In Vivo, May-June issue 2011. Xenotropic Murine Leukemia Virus-related
Parliamentary Question: DWP and ATOS benefits guidance for ME, 17 May 2011 Read More »
In a written question, Mrs Annette Brooke, acting chairman of
The number of children and young people with ME/CFS who
In a listing on their website today (dated 18 May
‘Patients’ power and PACE’ – The Lancet editorial and nine letters, 17 May 2011 Read More »
From The Lancet online, 17 May 2011. Editorial Patients’s power
ME Association Guidelines on research, diagnosis and management translated into Dutch Read More »
Everyone attending the ME/CFS clinical and research conference in Amsterdam
Problems with life insurance – request for information Read More »
We are receiving a growing number of enquiries from people
Ellen Piro receives the King of Norway’s silver medal for services to M.E. Read More »
Mrs Ellen Piro, president of the Norwegian ME Association, has
Feedback requested on two therapies – Reverse Therapy and Somatic Experiencing Read More »
An inquirer to our email helpline has requested feedback –