Parliamentary Question (Scotland): Scottish Good Practice Statement on ME/CFS – 17 January 2011
Elaine Murray, Labour MSP for Dumfries, tabled two questions about […]
Physiotherapy journal urges gentle approach to prescribed exercise for people with ME – 19 January 2011
From ‘Frontline’ magazine, journal of the Chartered Society of Physiotherapy,
‘XMRV: testing the blood supply’ – Wall Street Journal health blog, 20 January 2011
‘XMRV: testing the blood supply’ – Wall Street Journal health blog, 20 January 2011 Read More »
From the Wall Street Journal health blogger, Amy Dockser Marcus,
Parliamentary Questions: Research into ME, 18 January 2011
Parliamentary Questions: Research into ME, 18 January 2011 Read More »
Two MPs tabled separate questions about ME research and received
Research abstract: Group CBT and Graded Exercise versus “usual treatment”
Research abstract: Group CBT and Graded Exercise versus “usual treatment” Read More »
Health-related quality of life in patients with chronic fatigue syndrome:
‘Sufferer’s plea for more research rebuffed by Health Secretary’ – The Press, York, 14 January 2011
From The Press, York, 14 January 2011 (story by Richard
Wellcome Trust researchers reply to XMRV criticism – ‘Scicasts’ blog, 13 January 2011
Wellcome Trust researchers reply to XMRV criticism – ‘Scicasts’ blog, 13 January 2011 Read More »
From “Scicasts”, a life sciences research blog, 13 January 2o11
Pathology of ME/CFS: pilot study of four autopsy reports
Pathology of ME/CFS: pilot study of four autopsy reports Read More »
Below is the conference abstract for a presentation given by
Disability benefits cuts ‘could breach law’ – BBC News, 8 January 2011
Disability benefits cuts ‘could breach law’ – BBC News, 8 January 2011 Read More »
From BBC News Online, 8 January 2011. Plans to cut
‘Hurricane force’ debate about XMRV findings – ‘Science’ magazine, 7 January 2010
‘Hurricane force’ debate about XMRV findings – ‘Science’ magazine, 7 January 2010 Read More »
From ‘Science’ magazine (“News of the Week”), 7 January 2010.
Ethics committee finally approves controversial ‘SMILE’ pilot study into Lightning Process and children with ME/CFS
In a letter received today, the ME Association was informed
‘Where do we go from here?’ – answer from the Whittemore Peterson Institute, 1 January 2011
Statement issued by the Whittemore Peterson Institute, 1 January 2010
‘Exhausted by illness and doubts’ – New York Times, 3 January 2011
‘Exhausted by illness and doubts’ – New York Times, 3 January 2011 Read More »
From the New York Times website, 3 January 2011 (story
Use of the term myalgic encephalopathy on the new MEA website
Use of the term myalgic encephalopathy on the new MEA website Read More »
Medical conditions of uncertain or unknown causation often accumulate a
The Lightning Process and SMILE trial is an “unethical” study involving children | 20 September 2010
A plan to recruit children with ME/Chronic Fatigue Syndrome to