CFS Movement

As a parent and carer for a teen with chronic fatigue syndrome / myalgic encephalomyelitis (CFS/ME), I was often puzzled by how wiped out he would become after we’d been to a medical appointment, tried to keep up with his studies or sat up for a few hours when weContinue Reading

Once you are interested in a particular topic, you seem to develop a sensitivity to it. Last week I came across an interview with Andrea Wool, the topic was, ‘Everything You Need to Know About Exercise and Chronic Illness’. How I wish I had this information at hand when myContinue Reading

Being a carer often means you are time poor and exhausted, so why would you introduce more activities into your busy day? Part of the carer’s role is to ensure they are well enough to be there for their loved ones. Your good health is important, one of the factorsContinue Reading