ME/CFS South Australia Inc supports the needs of sufferers of Myalgic Encephalomyelitis, Chronic Fatigue Syndrome and related illnesses. We do this by providing services and information to members.
ME/CFS South Australia Inc aims to keep members informed of various research projects, diets, medications, therapies, news items, etc. All communication, both verbal and written, is merely to disseminate information and not to make recommendations or directives.
Unless otherwise stated, the views expressed on this Web site are not necessarily the official views of the Society or its Committee and are not simply an endorsement of products or services.
ME/CFS Costs The UK Economy £3.3 Billion A Year
Monday 2 October 2017
Chronic Fatigue Syndrome/ Myalgic Encephalomyelitis (CFS/ME) costs the UK economy £3.3 billion a year
Today, the Optimum Health Clinic (OHC), a charity specialising in the research into CFS/ME, launches in conjunction with the think tank 2020health, ground-breaking research assessing the costs of CFS/ME to the UK economy. This study entitled “CFS/ME: counting the cost” is the first study to assess both the direct and indirect cost of this illness.
This illness costs the UK economy at least £3.3 billion each year.
David Butcher, chairman of the OHC said:
“For too long there has been too much argument about CFS/ME which has not translated into effective treatments for sufferers. The cost of this illness to our country shows that the time has come for a comprehensive research strategy into the bio medical causes of and effective treatments for this appalling illness. We commissioned this research into the cost of CFS/ME to the economy because we want to improve awareness of this poorly understood illness in order to argue for greater funding of research”.
Julia Manning, Founder Director of 2020health, the health think tank who carried out this research, said:
“2020health was very keen to undertake this research because we are acutely aware that there is a lack of understanding about CFS/ME in both the NHS and society, and that the economic implications of the condition were unknown. We are especially pleased to have shone a spotlight on the previously underestimated costs of CFS/ME to society, as this should provide a real incentive for more support and research into this illness”.
CFS/ME devastates the lives of sufferers, their families and their carers and destroyed lives deserve attention. “The only way we will put an end to the needless waste of lives and money is to develop a better understanding of this illness and finding more effective treatments, and the only way we will achieve that is by funding research into both bio medical causes and treatments”, said David Butcher.
blog comments powered by Disqus