Prognosis
There is great variation in the severity and duration of symptoms and it is not possible to accurately predict recovery for individuals.
In both adults and children it appears that the prognosis is worse for the most severe cases. It also appears that early diagnosis may lessen the impact of the illness and that those with acute onset have a better prognosis than those with a gradual onset (CFS/ME Working Group 2002, p.39).
Most will improve to some degree over time and some recover well but a number of studies have indicated that less than 10% of adults regain their their pre-illness level of functioning. There is a tendency for the course of the illness to plateau from between six months and six years although some experience a fluctuating course of relative remission and relapse. Some become severely and possibly permanently disabled and some experience progressive deterioration (CFS/ME Working Group 2002, p. 7).
The prognosis for children is often better than for adults (Bell, 2001). The illness appears not to last as long and a high proportion seem to recover, though recovery may not be complete and relapse in adulthood may occur.
"Overall there is wide variation in the duration of illness, with some people recovering in less than two years while others remain ill for decades. Those who have been affected for several years seem less likely to recover; full recovery after symptoms persist more than five years is rare." (CFS/ME Working Group 2002, p. 7)
More information:
CFS/ME Working Group (2002) 'A report to the Chief Medical Officer of an Independent Working Group', Department of Health, London.
Bell, D. S. et al (2001) 'Thirteen-year follow-up of children and adolescents with chronic fatigue syndrome', Pediatrics, May, 107 (5), 223 -233.
News
![]()
Could mitochondrial dysfunction be a differentiating marker between Chronic Fatigue Syndrome and Fibromyalgia?
![]()
Daily cytokine fluctuations, driven by leptin, are associated with fatigue severity in chronic fatigue syndrome: evidence of inflammatory pathology A small pilot study of 10
Read more
Did you know?
As many as 180,000 Australians are directly affected by ME/CFS
Research
Research into ME/CFS is occuring across the globe. Follow the links below for research resources.
Alison Hunter Memorial Foundation
Australian Research Institutions
International Research Institutions
Support Organisations by State
ME/CFS Australia directs enquiries from members of the community about frontline support for people with ME/CFS to independently run state organisations.
Resources
Nutrition and ME/CFS: Download a PDF, available in the following languages:
Chinese(717 kb)Croatian(880 kb)Dutch(680 kb)French(740 kb)German(865 kb)Greek(821 kb)Italian(735 kb)Spanish(679 kb)Vietnamese(741 kb)
