Put on ‘a bit of a do’ by linking up with this photo exhibition!
Put on ‘a bit of a do’ by linking up with this photo exhibition! Read More »
Local ME support groups in Essex and on the South […]
Put on ‘a bit of a do’ by linking up with this photo exhibition! Read More »
Local ME support groups in Essex and on the South […]
In a written question, the Countess of Mar asked the
New poster campaign against damaging exercise treatment for children with ME Read More »
The Young ME Sufferers Trust has this morning launched a
The Countess of Mar, who through her Forward ME Group
The Countess of Mar, the crossbencher who chairs the Forward
PACE Trial – text of joint letter calling for more information, 24 May 2011 Read More »
The ME Association – together with the Young ME Sufferers
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
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