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Relevant bibliographies by topics / Myalgic encephalomyelitis

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Academic literature on the topic 'Myalgic encephalomyelitis'

Author: Grafiati

Published: 4 June 2021

Last updated: 30 July 2024

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Journal articles on the topic "Myalgic encephalomyelitis"

1

Maros, Kathleen. "Myalgic encephalomyelitis?" Medical Journal of Australia 148, no. 8 (April 1988): 424. http://dx.doi.org/10.5694/j.1326-5377.1988.tb115981.x.

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Lev, M. "Myalgic Encephalomyelitis." Journal of the Royal Society of Medicine 82, no. 11 (November 1989): 693–94. http://dx.doi.org/10.1177/014107688908201127.

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Rosen, S. D., J. C. King, and P. G. F. Nixon. "Myalgic Encephalomyelitis." Journal of the Royal Society of Medicine 83, no. 3 (March 1990): 199. http://dx.doi.org/10.1177/014107689008300336.

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Hodson, A. D. "Myalgic Encephalomyelitis." Journal of the Royal Society of Medicine 83, no. 3 (March 1990): 199–200. http://dx.doi.org/10.1177/014107689008300337.

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Wessely, S. "Myalgic Encephalomyelitis." Journal of the Royal Society of Medicine 84, no. 3 (March 1991): 182–83. http://dx.doi.org/10.1177/014107689108400338.

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Gordon, Neil. "Myalgic Encephalomyelitis." Developmental Medicine & Child Neurology 30, no. 5 (November 12, 2008): 677–82. http://dx.doi.org/10.1111/j.1469-8749.1988.tb04808.x.

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Hartnell, L. "Myalgic encephalomyelitis." BMJ 298, no. 6687 (June 10, 1989): 1577–78. http://dx.doi.org/10.1136/bmj.298.6687.1577-b.

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Wookey, C. "Myalgic encephalomyelitis." BMJ 298, no. 6687 (June 10, 1989): 1578. http://dx.doi.org/10.1136/bmj.298.6687.1578.

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Walker, R. G. "Myalgic encephalomyelitis." BMJ 298, no. 6687 (June 10, 1989): 1578. http://dx.doi.org/10.1136/bmj.298.6687.1578-a.

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Staines, Donald. "Myalgic encephalomyelitis hypothesis." Medical Journal of Australia 143, no. 2 (July 1985): 91. http://dx.doi.org/10.5694/j.1326-5377.1985.tb122819.x.

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Dissertations / Theses on the topic "Myalgic encephalomyelitis"

1

Wolfe, Patricia Jean de. "I'm really ill, I've got M.E. : bodily disorder and the quest for disease." Thesis, Goldsmiths College (University of London), 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.298292.

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De, Wolfe Patricia Jean. "'I'm really ill, I've got M.E.' : bodily disorder and the quest for the disease." Thesis, Goldsmiths College (University of London), 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.287740.

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Horton-Salway, Mary. "Mind and body in the discursive construction of M.E.: a struggle for authorship of an illness." Thesis, Loughborough University, 1998. https://dspace.lboro.ac.uk/2134/6982.

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This thesis is an analysis of the discursive construction of a controversial medical condition (Myalgic Encephalomyelitis) and how it has been made sense of, in and through the discourse of medical scientists, general practitioners, and M E sufferers. Various kinds of text and talk are analysed from the perspective of discursive psychology, arguing that versions of reality are a product of participants' constructive and dialogical practices. (I include my own text as an example of this.) The analysis of scientific texts, illness narratives, diagnostic narratives, and M E self-help group discussions, show how explanations about the status of M E and its causes are embedded in accounts of the identity of sufferers, the nature and status of medical explanation, and the competencies of medical practitioners. There is a sense in which the controversial topic of this thesis provides an ideal forum for examining both lay and professional reasoning practices about illness, in a context where the 'objective' world of 'medical facts' threatens to disintegrate into merely subjective points of view. One of my concerns has been to show how the participants themselves orient to, and manage this 'reality disjuncture' by means of a variety of discursive devices. The main body of the thesis addresses this problem through issues such as: the significance of diagnostic labels, different models of medicine, and the relevance of mind and body in explanations for illness. Finally, there is an analysis of the narrative constructions of M E sufferers and GPs, to show how psychosocial 'evidence' is used to warrant the speaker's interpretation of illness as either a mental or physical phenomenon.

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Procter, Charlotte Anne. "The post-viral fatigue syndrome." Thesis, Durham University, 1990. http://etheses.dur.ac.uk/6221/.

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Post-viral fatigue syndrome (myalgic encephalomyelitis) is a physically debilitating disorder associated with chronic disabling fatigue. This thesis presents two studies which look at the impact of illness from a personal-psychological and from a family perspective. The first investigates the psychological features of the syndrome. The prevalence of psychiatric disorder in 20 patients with the PVFS was determined. Sixty percent satisfied criteria for a current psychiatric disorder. Diagnoses were of neurotic depression and other neuroses. Only 25 % of a comparatively disabled group of 20 arthritis sufferers received similar diagnoses. Diagnoses did not substantially differ in type from a group of 20 subjects with major depressive disorders, although selected differences in symptom profile and the role of previous life-time psychiatric episodes, suggest that the PVFS cannot be regarded as a variant form of depressive disorder. A logistic regression analysis achieved a satisfactory separation of the two disorders on the basis of psychiatric symptoms. The second study investigates 9 school-aged children with mothers suffering from the syndrome, and 9 children with healthy parents. The children in the PVFS group had been exposed to their mother's illness from between 18 months and 14 years. They were found to have significantly more problems in the school environment in comparison to controls, rated as more shy and anxious, less assertive and with more relationship problems with peers. General family orientation was less active with fewer out-of-home family pursuits. Family interactions were somewhat more negative. Child adjustment is discussed in terms of the linkages between family, school and peer-group in the lives of these children. Investigations into the adaptive potential of such linkages and the permeability of the boundaries between the spheres raise important questions for ameliorative work in the counselling of PVFS sufferers and their families.

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Jaffray, Penny. "Society, the body and pain : sociological factors in assessing the meaning and experience of pain in myalgic encephalomyelitis ("yuppie flu") sufferers." Thesis, Rhodes University, 2002. http://hdl.handle.net/10962/d1008381.

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This thesis explores the meaning and experience of the bodily states associated with the condition referred to as myalgic encephalomyelitis (ME). It uses as a theoretical point of departure an understanding of the body as a socially constructed phenomenon and, in so dOing, offers an interpretation of illness that is seen to differ markedly from those offered by the medical and behavioural sciences. Using descriptive narrative research analysis, the thesis attempts to elicit personal trajectories of illness experience. In contrast to biomedical and social trajectories of illness, in which the interpretation and meaning given to the condition are imposed externally, personal trajectories are seen to provide unique subjective accounts of illness experience. And the value of using narrative accounts of illness is seen to lie in their ability to bring to light these individualised versions of illness experience. It is shown, in addition, that these narrative accounts of illness are also valuable in exposing the culturally shared knowledge that is employed in the process of assigning meaning to illness experiences. The aim of the thesis, then, in employing the descriptive narrative research method is to describe these shared cultural schemas. It is suggested that this approach leads to an interpretation of illness experience which sheds light on important links between the body, self and society. It is argued, more specifically, that Western capitalist society is associated with the creation of an "unnatural" environment and social context which is perceived to be inherently damaging and threatening to the well·being of those living in it; and that this assumption is pivotal to the interpretation of the illness experiences narrated and analysed for the thesis. This sociological reading of embodiment provides a basis for understanding the experience of illness, as not one simply embedded in the body or mind of the individual, but as one laden with personal meaning assimilated from, and hence revealing of, the social context in which the illness is experienced. As such, an attempt is made to provide an account of illness experience distinct from the dominant biomedical and behavioural accounts of ME.

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Goudsmit, Ellen Marianne. "The psychological aspects and management of chronic fatigue syndrome." Thesis, Brunel University, 1996. http://bura.brunel.ac.uk/handle/2438/4283.

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Chronic fatigue syndrome (CFS) describes a condition characterised by severe fatigue of at least six months' duration. In this thesis, it is argued that the complexity of CFS with respect to other symptoms, the patients' response to their illness and the determinants of emotional distress, has yet to be fully recognised. This may have narrowed the focus of research and limited the range of treatments available. The first of the three studies investigated CFS from the patients' perspective. The findings challenge some of the generalisations concerning CFS, particularly those relating to the patients' attributions and their choice of coping strategies. They also suggest that the effects of the condition may have been underestimated and that certain influences on emotional distress may have been overlooked. The second study assessed a number of variables thought to be associated with emotional distress and psychological adjustment. The results show that uncertainty and lack of social support were significantly correlated with anxiety and depression while functional impairment was more closely linked to cognitive difficulties and other illness-related measures. The third study evaluated a management programme which acknowledges the complexity of CFS. After six months, significant differences between the treated patients and waiting-list controls were found for a number of variables, including fatigue, somatic symptoms, anxiety and perceived self-efficacy. However, many patients continued to record high levels of emotional distress, showing that the programme was not sufficient to deal with all the problems experienced.

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Ramsden, Rebecca Mary. "Narratives of partners of individuals affected by Chronic Fatigue Syndrome/Myalgic Encephalomyelitis." Thesis, University of Hertfordshire, 2016. http://hdl.handle.net/2299/17195.

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Background and Aims: Chronic Fatigue Syndrome/Myalgic Encephalomyelitis (CFS/ME) remains a poorly understood condition, shrouded in uncertainty and dispute. Research suggests this context to have a profound bearing on those touched by the condition, impacting significantly on their experience and the narratives constructed thereof. However, no studies examining the narratives of partners of individuals affected by CFS/ME appear to have been carried out to date. Based upon this gap in the literature, this study sought to hear the narratives of partners of adults living with CFS/ME, giving particular consideration to the ways in which these narratives were told to an outsider, and how the outsider may have influenced the narrative. Methodology: This study drew on a qualitative approach. A purposive sample of six partners of adults affected by CFS/ME (4 men and 2 women) was recruited. Individual interviews were conducted that were audio-recorded and transcribed. Narrative analysis was used to analyse the transcripts, focusing principally on how participants narrated their accounts, as well as on the content of narratives and the narrative and discursive features that shaped the telling of the accounts. Analysis and Findings: Multiple readings of the narratives identified two areas of collective focus within participants' accounts - 'stories from then' and 'stories from now'. Some similarities in how 'stories from now' were told were seen to emerge down gender lines. Notably participants' storytelling could be seen to represent a form of response to wider narratives that purvey around CFS/ME, with participants' being observed to construct particular meanings around CFS/ME, as well as particular 'identities' of themselves, their partner, their relationship and 'others' who had played a key role in their story of living with the condition. The findings are discussed in terms of their potential bearing for clinical practice and future research endeavours. In addition, the strengths and the limitations of the research are considered.

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Barcroft, Rachel. "Chronic fatigue syndrome/myalgic encephalomyelitis and fibromyalgia : a social model of disability perspective." Thesis, Lancaster University, 2017. http://eprints.lancs.ac.uk/87165/.

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This thesis is composed firstly of a literature review focusing on the attitudes of health professionals towards chronic fatigue syndrome/myalgic encephalomyelitis (CFS/ME) and fibromyalgia. Secondly, a research paper explores the ways in which people living with CFS/ME have experienced psycho-emotional disablism. Finally, a critical appraisal discusses the process of conducting the research as well as its strengths and limitations. The literature review takes the form of a meta-synthesis regarding the attitudes of healthcare professionals towards CFS/ME and fibromyalgia. A meta-ethnographic approach was used with reciprocal translation producing the following themes: “Feeling hopeless and more hopeless”: psychological effects of lack of knowledge; “Your heart sinks when they come in the room”: stigma and stereotypes; and “I’m going to be with you through thick and thin”: management of the condition. The review highlights the difficulties faced by health professionals regarding the management and diagnosis of both conditions, as well as possible reasons for the negative attitudes held by some professionals. The research paper, which employed thematic analysis, explores the ways in which people living with CFS/ME have experienced psycho-emotional disablism. Three overarching themes were identified: “fighting to be heard”; “lack of legitimacy” and “feeling invisible”. Participants described the discrimination and stigma that they had encountered from many areas of society. Ideas for future research are proposed. The critical appraisal presents the author’s reflections on the research process as well as its strengths and limitations, and the five stages of the process are described as follows: choosing a thesis topic and designing the project; recruitment and research interviews; the interview process; analysis and writing up of the data; and the author’s reflections on the project.

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Hardcastle, Sharni Lee. "Examination of Innate and Adaptive Immune Cells in Chronic Fatigue Syndrome/Myalgic Encephalomyelitis Patients with Varying Degrees of Symptom Severity." Thesis, Griffith University, 2015. http://hdl.handle.net/10072/367042.

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The immune system has a critical influence on the maintenance of physiological homeostasis. To date, immunological dysfunction, particularly reduced natural killer (NK) cell cytotoxic activity in Chronic Fatigue Syndrome/Myalgic Encephalomyelitis (CFS/ME) patients has been consistently observed. CFS/ME is a severely debilitating illness, with no known pathomechanism and diagnosis is made according to symptom specific criteria. CFS/ME is characterised by persistent and unexplained fatigue, alongside a range of symptoms, including: post-exertional neuroimmune exhaustion, neurological, immune, gastrointestinal, genitourinary and energy metabolism impairments. However, a symptom specific criterion provides complications for diagnosis, particularly as symptoms may be qualitative. CFS/ME is also a heterogeneous illness, with patients experiencing moderate to severe symptoms. CFS/ME patients with moderate symptoms are those who have reduced mobility and ability to perform their routine daily activities. CFS/ME patients with severe symptoms are usually homebound and/or restricted to a wheelchair. The debilitating nature of CFS/ME creates an economic burden and contributes largely to health resources, affecting CFS/ME patients as well as the wider community. In Australia, the annual cost to the community per CFS/ME patient, with a prevalence rate of 0.2% is $729.3 million (based on 2012 estimates and earlier prevalence studies).
Thesis (PhD Doctorate)
Doctor of Philosophy (PhD)
School of Medical Science
Griffith Health
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Lynch, Sean Patrick Jeremy. "The nature of fatigue in the chronic fatigue syndrome : a longitudinal study." Thesis, Imperial College London, 1996. http://hdl.handle.net/10044/1/7496.

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Books on the topic "Myalgic encephalomyelitis"

1

Great, Britain Parliament. Myalgic encephalomyelitis Bill. London: H.M.S.O., 1991.

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White, Erica. M.E. sailing free: Nutritional answersto chronic fatigue. Leigh-on-Sea: White, 1996.

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Midgley, Michael. A life worth living: A practical guide [to living with myalgic encephalomyelitis (ME)]. Colwyn Bay: Overton Studios Press, 1995.

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Ho-Yen, Darrel O. Better recovery from viral illnesses. 3rd ed. Inverness: Dodona, 1993.

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Dr, Murphy Gabrielle, ed. Coping better with chronic fatigue syndrome/myalgic encephalomyelitis: Cognitive behaviour therapy for chronic fatigue syndrome/myalgic encephalomyelitis (CFS/ ME). London: Karnac Books, 2009.

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O, Behan Peter, Goldberg D. P, and Mowbray J. F, eds. Postviral fatigue syndrome. Edinburgh: Churchill Livingstone, 1991.

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Shepherd, Charles. Myalgic encephalomyelitis: Post-viral fatigue syndrome : guidelines for the care of patients. 2nd ed. Stanford-le-Hope: M.E. Association, 1995.

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Shepherd, Charles. Myalgic encephalomyelitis: Post-viral fatigue syndrome : guidelines for thecare of patients. Stanford-le-Hope: M.E. Association, 1994.

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9

Great Britain. Department of Health. Chronic fatigue syndrome/myalgic encephalopathy (CFS/ME). London: Department of Health, 2004.

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Youngman, Chris. Holiday in Hell. Bradford: Harvestime, 1988.

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Book chapters on the topic "Myalgic encephalomyelitis"

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Oette, Mark, Marvin J. Stone, Hendrik P. N. Scholl, Peter Charbel Issa, Monika Fleckenstein, Steffen Schmitz-Valckenberg, Frank G. Holz, et al. "Myalgic Encephalomyelitis." In Encyclopedia of Molecular Mechanisms of Disease, 1393. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-29676-8_8006.

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Costa, D. C., and A. Greco. "Chronic Fatigue Syndrome/Myalgic Encephalomyelitis." In Nuclear Medicine in Psychiatry, 289–300. Berlin, Heidelberg: Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/978-3-642-18773-5_17.

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Puri, Basant K. "Do Modern Western Diets Play a Role in Myalgic Encephalomyelitis?" In Modern Dietary Fat Intakes in Disease Promotion, 345–49. Totowa, NJ: Humana Press, 2010. http://dx.doi.org/10.1007/978-1-60327-571-2_21.

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Sarzi-Puttini, Piercarlo, Alberto Batticciotto, Rossella Talotta, and Fabiola Atzeni. "Differential Diagnosis of Vasovagal Syncope: Myalgic Encephalomyelitis/Chronic Fatigue Syndrome." In Vasovagal Syncope, 197–211. Cham: Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-09102-0_16.

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Wicks, Sally. "Chronic Fatigue Syndrome/ Myalgic Encephalomyelitis in Children and Young People." In Child and Adolescent Mental Health, 366–73. 3rd ed. Third edition. | New York, NY: Routledge, 2021.: CRC Press, 2021. http://dx.doi.org/10.4324/9781003083139-55.

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Glaudemans, Andor W. J. M. "PET and SPECT Studies in the Chronic Fatigue Syndrome/Myalgic Encephalomyelitis." In PET and SPECT in Psychiatry, 743–58. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-40384-2_33.

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Wallis, Amy, Melinda L. Jackson, Michelle Ball, Donald P. Lewis, and Dorothy Bruck. "Sleep, Cognitive and Mood Symptoms in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome." In The Handbook of Stress and Health, 501–22. Chichester, UK: John Wiley & Sons, Ltd, 2017. http://dx.doi.org/10.1002/9781118993811.ch31.

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Watanabe, Yasuyoshi. "PET/SPECT/MRI/fMRI Studies in the Myalgic Encephalomyelitis/Chronic Fatigue Syndrome." In PET and SPECT in Psychiatry, 985–1001. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-57231-0_32.

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Löfgren, Monika, Marie-Louise Schult, Ann Öhman, Per Julin, and Jan Ekholm. "Fibromyalgia Syndrome or Chronic Fatigue Syndrome/Myalgic Encephalomyelitis and Factors Influencing Work Disability in Women." In Handbooks in Health, Work, and Disability, 459–80. Boston, MA: Springer US, 2016. http://dx.doi.org/10.1007/978-1-4899-7627-7_26.

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Maes, Michael. "Inflammatory and Oxidative and Nitrosative Stress Cascades as New Drug Targets in Myalgic Encephalomyelitis and Chronic Fatigue Syndrome." In Inflammation in Psychiatry, 162–74. Basel: S. KARGER AG, 2013. http://dx.doi.org/10.1159/000343982.

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Conference papers on the topic "Myalgic encephalomyelitis"

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Borsting, Jorun. "SUPPORTING RELAXATION: SLOWBREATH FOR PEOPLE WITH MYALGIC ENCEPHALOMYELITIS." In International Conference on e-Health 2019. IADIS Press, 2019. http://dx.doi.org/10.33965/eh2019_201910l019.

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Zupanc, Timon. "Myalgic Encephalomyelitis/Chronic Fatigue Syndrome – Etiology, Pathophysiology, Diagnosis and Treatment." In Socratic lectures 10. University of Lubljana Press, 2024. http://dx.doi.org/10.55295/psl.2024.ii1.

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Abstract: Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is a complex condition characterized by a broad spectrum of overlapping symptoms and manifesting in multiple systems of the body. Patients experience symptoms such as profound fatigue, post-exertional malaise (PEM), unrefreshing sleep, and cognitive impairments. It affects millions worldwide, yet much is still unknown about its etiology and pathophysiology. The condition's onset is frequently linked to infectious triggers, including viral infections, suggesting a dysregulated immune response as a central component. Diagnosing ME/CFS poses significant challenges due to many unspecific symptoms that overlap with various other conditions. Current treatment strategies focus primarily on symptomatic relief and lifestyle modifications to manage disease impact. The COVID-19 pandemic has further spotlighted ME/CFS, drawing parallels between long COVID and ME/CFS symptomatology and underscoring the urgent need for comprehensive research. Keywords: Myalgic Encephalomyelitis, Chronic Fatigue Syndrome, Infectious trigger, Post-Exertional Malaise, COVID-19, Post-COVID syndrome

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Pearce, Mark, Emma Slack, Katrina Pears, Julia Newton, and Judith Rankin. "OP72 Myalgic encephalomyelitis/chronic fatigue syndrome and pregnancy: a mixed-methods systematic review." In Society for Social Medicine Annual Scientific Meeting Abstracts. BMJ Publishing Group Ltd, 2022. http://dx.doi.org/10.1136/jech-2022-ssmabstracts.71.

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Squires, Johanna, Sarra Al-Zayer, Peng Li, Wenzhong Xiao, and David Systrom. "Investigation into the Plasma Proteome Signature in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS)." In ERS International Congress 2023 abstracts. European Respiratory Society, 2023. http://dx.doi.org/10.1183/13993003.congress-2023.pa2960.

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Domingues, Tiago Dias, Helena Mouriño, and Nuno Sepúlveda. "A statistical analysis of serological data from the UK myalgic encephalomyelitis/chronic fatigue syndrome biobank." In INTERNATIONAL CONFERENCE OF NUMERICAL ANALYSIS AND APPLIED MATHEMATICS ICNAAM 2019. AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0026633.

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Squires, Johanna, Sarra Al-Zayer, and David Systrom. "Exercise capacity in myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) treated with long-term pyridostigmine." In ERS International Congress 2023 abstracts. European Respiratory Society, 2023. http://dx.doi.org/10.1183/13993003.congress-2023.pa4639.

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Wichmann Madsen, K., J. Squires, M. C. Stovall, S. Al-Zayer, C. J. Chang, W. Xiao, R. Pari, P. Joseph, and D. M. Systrom. "Sex Differences in Hemodynamic Response to Exercise in Patients With Myalgic Encephalomyelitis: Insights From Invasive Cardiopulmonary Exercise Testing." In American Thoracic Society 2023 International Conference, May 19-24, 2023 - Washington, DC. American Thoracic Society, 2023. http://dx.doi.org/10.1164/ajrccm-conference.2023.207.1_meetingabstracts.a2995.

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Stovall, M. C., P. Joseph, R. Pari, A. Warren, S. Miller, J. Squires, W. Xiao, A. B. Waxman, and D. M. Systrom. "Acute Effect of Pyridostigmine in Exertional Intolerance in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS): A Randomized Placebo-Controlled Clinical Trial." In American Thoracic Society 2022 International Conference, May 13-18, 2022 - San Francisco, CA. American Thoracic Society, 2022. http://dx.doi.org/10.1164/ajrccm-conference.2022.205.1_meetingabstracts.a2063.

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Neale, FK, TY Segal, and DS Hargreaves. "G13 Prevalence and correlates of low mood, poor quality of life and high symptom impact in adolescents attending a tertiary service for chronic fatigue syndrome/myalgic encephalomyelitis." In Royal College of Paediatrics and Child Health, Abstracts of the Annual Conference, 13–15 March 2018, SEC, Glasgow, Children First – Ethics, Morality and Advocacy in Childhood, The Journal of the Royal College of Paediatrics and Child Health. BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health, 2018. http://dx.doi.org/10.1136/archdischild-2018-rcpch.13.

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Ayadi O’Donnell, N., A. McCourt, and T. Segal. "G531(P) A cohort study of whether parental separation and lack of contact with a parent predicts disease severity at diagnosis in young peoples chronic fatigue syndrome/myalgic encephalomyelitis." In Royal College of Paediatrics and Child Health, Abstracts of the RCPCH Conference–Online, 25 September 2020–13 November 2020. BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health, 2020. http://dx.doi.org/10.1136/archdischild-2020-rcpch.449.

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Reports on the topic "Myalgic encephalomyelitis"

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Jindal-Snape, Divya, Chris Murray, Rebecca Camilleri, Ruth Debono, Maria Gauci, Damon Herd, Steven Affleck, Rebecca Elise, Tasha Leah Santiago, and Marilyn Mintoff. Living With MYALGIC ENCEPHALOMYELITIS: An Invisible Disability. University of Dundee, May 2022. http://dx.doi.org/10.20933/100001243.

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Contents: Living with Myalgic Encephalomyelitis (ME) and Post-exertional Malaise - page 3 Story: Rebecca Camilleri; Script: Divya Jindal-Snape; Art: Steven Affleck Living with ME: A New Reality - page 4 Story: Rebecca Camilleri; Script: Divya Jindal-Snape; Art: Steven Affleck Working and Living with Myalgic Encephalomyelitis - page 7 Story: Maria Gauci; Script: Divya Jindal-Snape; Art: Rebecca Elysium Grocery Shopping: Myalgic Encephalomyelitis and Post-exertional Malaise - page 8 Story: Rebecca Camilleri; Script: Divya Jindal-Snape; Art: Tasha Leah Santiago Mysterious Pain - Invisible Disability - page 9 Author: Ruth DeBono; Art: Tasha Leah Santiago

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Smith, M. E. Beth, Heidi D. Nelson, Elizabeth Haney, Miranda Pappas, Monica Daeges, Ngoc Wasson, and Marian McDonagh. Diagnosis and Treatment of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome. Agency for Healthcare Research and Quality, December 2014. http://dx.doi.org/10.23970/ahrqepcerta219.

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Vahratian, Anjel, Jin-Mann S. Lin, Jeanne Bertolli, and Elizabeth R. Unger. Myalgic Encephalomyelitis/Chronic Fatigue Syndrome in Adults: United States, 2021-2022. Hyattsville, MD: National Center for Health Statistics (U.S.). National Health Interview Survey (NHIS), December 2023. http://dx.doi.org/10.15620/cdc:134504.

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