Pippa Bennet describes her experience of ME on the We are Cardiff blog:<\/p>\n
12th May is International ME awareness day. You know ME, it\u2019s the lazy people\u2019s disease? Well, it\u2019s estimated that over 28 million people now suffer from it in the world and in the US alone, more people now have ME than AIDS.<\/p>\n
I have suffered from ME for 13 years, since I was 14. I got glandular fever and it simply never went away. Instead it mutated into a new, terrifying beast. ME is debilitating, misunderstood, confusing and unpredictable. Even the name is debated. Many people prefer the term CFS or Chronic Fatigue Syndrome over ME which stands for Myalgic Encephalomyelitis. It is pure medical semantics, but they both generally describe the same condition \u2013 depending on your doctor\u2019s preferred interpretation! The prognosis is ill-defined and unknown too. The best anyone can tell you is that if you contracted is when you were under 18 then you stand a better chance of one day getting better than if you contracted it over the age of 18…<\/p>\n
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