CFS, also known as myalgic encephalomyelitis (ME), has become a debilitating illness, which has a huge impact on the lives of children and their families.
The team from the University of Bristol in Britain found that almost 2% of 16-year-olds have CFS lasting more than six months and for nearly 3%, it lasts for more than three months. Those suffering from CFS missed, on average, more than half a day of school every week.
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“As paediatricians, we need to get better at identifying CFS/ME, particularly in those children from disadvantaged backgrounds who don’t have access to specialist care,” said senior study author Dr Esther Crawley, consultant paediatrician in CFS/ME.
The researchers looked at the condition in 5,756 participants and found that girls were almost twice as likely as boys to have the condition.
Children from families experiencing greater adversity were more likely to have the condition, dispelling the commonly held view that CFS is a ‘middle class’ illness.
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According to Sonya Chowdhury, chief executive of the non-profit organisation, Action for ME, the reality is that many young children miss more than half a day of school a week, while for the most severely affected, their disabling symptoms are compounded by the isolation and loss that comes with being indoors and/or bed-bound.
“This important study, analysing data from parent and child-completed questionnaires, highlights the increased prevalence of ME among 16-year-olds, pointing towards the even greater urgency in the need for effective treatments,” she noted.
Published in The Express Tribune, January 28th, 2016.
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