Cost-effectiveness of Interventions for Chronic Fatigue Syndrome or Myalgic Encephalomyelitis: A Systematic Review of Economic Evaluations.
Cochrane M et al. (2021) Cost-effectiveness of Interventions for Chronic […]
Research Papers
Understanding the economic impact of myalgic encephalomyelitis/chronic fatigue syndrome in Ireland: a qualitative study.
Cullinan J et al. (2020) Understanding the economic impact of
The Development of a Consistent Europe-Wide Approach to Investigating the Economic Impact of Myalgic Encephalomyelitis (ME/CFS): A Report from the European Network on ME/CFS (EUROMENE).
Pheby D et al. (2020) The Development of a Consistent
The Role of Prevention in Reducing the Economic Impact of ME/CFS in Europe: A Report from the Socioeconomics Working Group of the European Network on ME/CFS (EUROMENE).
Pheby DFH et al. (2021)The Role of Prevention in Reducing
Factors associated with work status in chronic fatigue syndrome.
Factors associated with work status in chronic fatigue syndrome. Read More »
Stevelink S et al. (2019) Factors associated with work status
Updated ME/CFS prevalence estimates reflecting post-COVID increases and associated economic costs and funding implications.
Mirin AA et al. (2022) Updated ME/CFS prevalence estimates reflecting
Hidden from Sight: Why the complexity of ME/CFS needs to be recognised by policy makers.
Hidden from Sight: Why the complexity of ME/CFS needs to be recognised by policy makers. Read More »
Űstűnkaya T and Machin R (2021) Hidden from Sight: Why
Work Rehabilitation and Medical Retirement for Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Patients. A Review and Appraisal of Diagnostic Strategies.
Vink M and Vink-Niese F (2019) Work Rehabilitation and Medical
Inaugural meeting to re-establish APPG led by Carol Monaghan MP with Dr Charles Shepherd and the MEA providing secretariat.
All-Party Parliamentary Group on ME. (2020) Inaugural meeting to re-establish
Inquiry into NHS Service Provision for ME/CFS.
Inquiry into NHS Service Provision for ME/CFS. Read More »
All-Party Parliamentary Group on ME. (2010) Inquiry into NHS Service
Shadow Burden of Undiagnosed Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) on Society: Retrospective and Prospective-In Light of COVID-19.
Araja D et al. (2021) Shadow Burden of Undiagnosed Myalgic
24 January. Appropriate ME Treatment. Led by Carol Monaghan, MP. Hansard transcript:
24 January. Appropriate ME Treatment. Led by Carol Monaghan, MP. Hansard transcript: Read More »
House of Commons (2019) Debate . 24 January. Appropriate ME
Subjective and objective cognitive function in adolescent with chronic fatigue following Epstein-Barr virus infection.
Oie MG et al. (2022)Subjective and objective cognitive function in
Co-morbid conditions in children with chronic fatigue syndrome/myalgic encephalomyelitis (CFS/ME) – a retrospective case note review of a large cohort.
Oliver L and Patel K . (2012) Co-morbid conditions in
Developing and pretesting a new patient reported outcome measure for paediatric Chronic Fatigue Syndrome/ Myalgic Encephalopathy (CFS/ME): cognitive interviews with children.
Parslow RM et al. (2019) Developing and pretesting a new
Development of a conceptual framework to underpin a health-related quality of life outcome measure in paediatric chronic fatigue syndrome/myalgic encephalopathy (CFS/ME): prioritisation through card ranking.
Parslow RM et al. (2020) Development of a conceptual framework
Sleep-wake rhythm disturbances and perceived sleep in adolescent chronic fatigue syndrome.
Pedersen M et al. (2017) Sleep-wake rhythm disturbances and perceived
Stress vulnerability in adolescents with chronic fatigue syndrome: experimental study investigating heart rate variability and skin conductance responses.
Rimes KA et al. (2017) Stress vulnerability in adolescents with
Impaired Health-Related Quality of Life in Adolescent Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: The Impact of Core Symptoms.
Roma M et al. (2019) Impaired Health-Related Quality of Life