Recommended literature/de

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Empfohlene Literatur zu ME/CFS auf Deutsch[edit | edit source]

  • BLEIJENBERG, Gijs, Jos W. M. VAN DERMEER (2016) 464e. CHRONISCHES FATIQUE SYNDROM. Für die deutsche Ausgabe Patricia Grabowski und Carmen Scheibenbogen. Aus: Harrisons Innere Medizin Abschnitt 4 • 19. Auflage, deutsche Ausgabe • In Zusammenarbeit mit der Charité • Herausgegeben von N. Suttorp, M. Möckel, B. Siegmund, M. Dietel • © ABW Wissenschaftsverlag GmbH, Altensteinstraße 42, D-14195 Berlin • www.abw-verlag.de https://eref.thieme.de/images/supmat/9783940615503_464.pdf (abgerufen 26. August 2019)
  • FENNELL Patricia A. Die Erfahrung, an CFS/CFIDS erkrankt zu sein. DAS VIER_STADIEN MODELL. Übersetzung durch Petra Dönselmann, Anne Fink, Andrea Noll. Fatigatio Schriftenreihe Heft 4. Original: "A Systematic, Four-Stage, Progressive Model for Mapping the CFIDS Experience" In: "The CFIDS Chronicle", 1993 https://www.fatigatio.de/fileadmin/user_upload/07/docs/3.04_Auszug_Fennell.pdf (abgerufen 26. August 2019)
  • HARTLIEB Christine (2019) Psychotherapeutisch orientierte Behandlungen beim Krankheitsbild ME/CFS. Hinweise für TherapeutInnen. https://www.hartlieb.top/psth-cfs.pdf (abgerufen 27. August 2019)
  • SCHEIBENBOGEN, C. , H.-D. Volk, P. Grabowski, K. Wittke, C. Giannini, B. Hoffmeister, L. Hanitsch (2014) Chronisches Fatigue-Syndrom: Heutige Vorstellung zur PATHOGENESE DIAGNOSTIK THERAPIE In: tägliche praxis – Die Zeitschrift für Allgemeinmedizin, Heft 55, 2014, S. 567–574, PDF (abgerufen 25. Oktober 2016) https://www.fatigatio.de/.../user_upload/07/docs/cfs_cs.pdf

Zu Pacing (auf Deutsch)[edit | edit source]

  • DIE BALANCE HALTEN TROTZ CFS! Übersetzung von "COPING SKILLS: How to Maintain Your Equilibrium in the CFS Balancing Act" von National Chronic Fatigue Syndrome and Fibromyalgia Association, P.O. Box 18426, Kansas City, Missouri 64133, USA. Übersetzung durch Petra Dönselmann, Sande, Anne Fink und Theres Jeanrenaud für Fatigatio https://www.fatigatio.de/leben-mit-cfs/balance-halten/ (abgerufen 26. August 2019)

Einzelnachweise[edit | edit source]

  1. Scheibenbogen, Carmen; Wittke, K.; Hanitsch, L.; Grabowski, P.; Behrends, U. (2019). "Chronisches Fatigue-Syndrom/CFS. Praktische Empfehlungen zur Diagnostik und Therapie". Ärzteblatt Sachsen. 2019 (9). 

ME/CFS - An acronym that combines myalgic encephalomyelitis with chronic fatigue syndrome. Sometimes they are combined because people have trouble distinguishing one from the other. Sometimes they are combined because people see them as synonyms of each other.

Myalgic encephalomyelitis (ME) - A disease often marked by neurological symptoms, but fatigue is sometimes a symptom as well. Some diagnostic criteria distinguish it from chronic fatigue syndrome, while other diagnostic criteria consider it to be a synonym for chronic fatigue syndrome. A defining characteristic of ME is post-exertional malaise (PEM), or post-exertional neuroimmune exhaustion (PENE), which is a notable exacerbation of symptoms brought on by small exertions. PEM can last for days or weeks. Symptoms can include cognitive impairments, muscle pain (myalgia), trouble remaining upright (orthostatic intolerance), sleep abnormalities, and gastro-intestinal impairments, among others. An estimated 25% of those suffering from ME are housebound or bedbound. The World Health Organization (WHO) classifies ME as a neurological disease.

Myalgic encephalomyelitis (ME) - A disease often marked by neurological symptoms, but fatigue is sometimes a symptom as well. Some diagnostic criteria distinguish it from chronic fatigue syndrome, while other diagnostic criteria consider it to be a synonym for chronic fatigue syndrome. A defining characteristic of ME is post-exertional malaise (PEM), or post-exertional neuroimmune exhaustion (PENE), which is a notable exacerbation of symptoms brought on by small exertions. PEM can last for days or weeks. Symptoms can include cognitive impairments, muscle pain (myalgia), trouble remaining upright (orthostatic intolerance), sleep abnormalities, and gastro-intestinal impairments, among others. An estimated 25% of those suffering from ME are housebound or bedbound. The World Health Organization (WHO) classifies ME as a neurological disease.

The information provided at this site is not intended to diagnose or treat any illness.
From MEpedia, a crowd-sourced encyclopedia of ME and CFS science and history.