Interventions to treat pain in paediatric CFS/ME: a systematic review.
Interventions to treat pain in paediatric CFS/ME: a systematic review. Read More »
Ascough C et al. (2020) Interventions to treat pain in […]
Research Papers
Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: When Suffering Is Multiplied.
Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: When Suffering Is Multiplied. Read More »
Komaroff AL (2021) Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: When Suffering Is
Questioning Biomedicine’s Privileging of Disease and Measurability.
Questioning Biomedicine’s Privileging of Disease and Measurability. Read More »
Kroll C (2021) Questioning Biomedicine’s Privileging of Disease and Measurability.
Impacts of online support groups on quality of life, and perceived anxiety and depression in those with ME/CFS: a survey.
Morehouse S et al. (2021) Impacts of online support groups
The functional status and wellbeing of people with myalgic encephalomyelitis/chronic fatigue syndrome and their carers.
Nacul LC et al. (2011) The functional status and wellbeing
Chronic fatigue syndrome: Patients’ experiences, clinical practice and epistemic justice.
Oter-Quintana C et al. (2021) Chronic fatigue syndrome: Patients’ experiences,
Quality of life in chronic fatigue syndrome.
Quality of life in chronic fatigue syndrome. Read More »
Schweitzer R et al. (1995) Quality of life in chronic
Living with M.E.: the chronic/post-viral fatigue syndrome,
Living with M.E.: the chronic/post-viral fatigue syndrome, Read More »
Shepherd C. (1999) Living with M.E.: the chronic/post-viral fatigue syndrome,
Health-related Quality of Life in Norwegian Adolescents Living With Chronic Fatigue Syndrome.
Simila W et al. (2020) Health-related Quality of Life in
Pain is associated with reduced quality of life and functional status in patients with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome,
Strand EB et al. (2018) Pain is associated with reduced
An exploratory study of discrepancies between objective and subjective measurement of the physical activity level in female patients with chronic fatigue syndrome.
Vergauwen K et al. (2021) An exploratory study of discrepancies
Impact of myalgic encephalomyelitis/ chronic fatigue syndrome (ME/CFS) on the quality of life of people with ME/CFS and their partners and family members: an online crosssectional survey.
Vyas J et al. (2022) Impact of myalgic encephalomyelitis/ chronic
Dietary supplements, daily nutrient intake, and health-related quality of life among people with myalgic encephalomyelitis/chronic fatigue syndrome.
Weigel B et al . (2022). Dietary supplements, daily nutrient
Comparing Operationalized Approaches for Substantial Reduction of Functioning in Chronic Fatigue Syndrome and Myalgic Encephalomyelitis.
Wiedbusch E and Jason LA (2022) Comparing Operationalized Approaches for
Health related quality of life in adolescents with chronic fatigue syndrome: a cross-sectional study.
Winger A et al. (2015) Health related quality of life
Life-Threatening Malnutrition in Very Severe ME/CFS.
Life-Threatening Malnutrition in Very Severe ME/CFS. Read More »
Baxter H et al. (2021) Life-Threatening Malnutrition in Very Severe
Ensuring the Voice of the Very Severely Affected Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Patient Is Heard in Research – A Research Model.
Baxter H (2022) Ensuring the Voice of c�� the Very
Comprehensive Examination of Severely Ill ME/CFS Patients.
Comprehensive Examination of Severely Ill ME/CFS Patients. Read More »
Chang C-J et al. (2021) Comprehensive Examination of Severely Ill
Extremely Severe ME/CFS- A Personal Account.
Extremely Severe ME/CFS- A Personal Account. Read More »
Dafoe W (2021) Extremely Severe ME/CFS- A Personal Account. Healthcare