UK CFS News

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Helping to make the UK a better place for people with ME/CFS. ME/CFS is hard to accept. And those » Helping to make the UK a better place for people with ME/CFS. ME/CFS is hard to accept. And those who do not accept their illness rarely recover. So we help people understand and come to terms with their illness.

The aims of ME Research UK are to advance scientific knowledge by funding biomedical research » The aims of ME Research UK are to advance scientific knowledge by funding biomedical research into the causes, consequences and treatment of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS), and to provide high quality information on all aspects of the disease for a wide range of audiences. Follow to get information on all researches on CFS/ME.

I am Suzan Jackson. I have had Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) since » I am Suzan Jackson. I have had Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) since March 2002. Both of my sons also got ME/CFS at ages 6 and 10. This blog is about how our family lives with chronic illness, with a focus on living and enjoying our lives in spite of these challenges.