The Spectator: John Rutter – M.E. is real. I know, I had it for seven years

[Firestormm]

http://blogs.spectator.co.uk/coffee...-m-e-is-real-i-know-i-had-it-for-seven-years/

22 March 2014

Rod Liddle may or may not be right that certain illnesses become fashionable once given a name and are illusory, as he wrote last week. But ME — myalgic encephalomyelitis, alias post-viral fatigue syndrome or yuppie flu, is not one of them.

It’s an unpleasant physical illness: it ruined seven years of my life. It probably takes a number of forms, but in my case it started with chicken pox, caught off my infant son. I seemed to make a complete recovery until a year later, when I began to experience unpleasant symptoms.

These included abnormal sensitivity to sound and light, violently inflamed eyes and blisters around the head and upper body. There was also nominal aphasia (problems recalling words). This is because the surfaces of the brain are inflamed. The mental fuzziness is compounded because the body can no longer process yeast properly.

Like malaria, it cycles on and off, and after an attack, which might last a few days, I felt terrible. I would have a week or two feeling OK, then the cycle would begin again. I’m a professional musician, and we tend not to advertise our ailments any more than journalists do, but this was real.

In the end, with an anti-yeast drug and a strict diet, the attacks grew milder and less frequent and life returned to ‘normal within limits’, but the memory remains of an awful period that was caused by a virus (identifiable by a blood test).

Sorry to spoil a good polemic with facts that don’t fit.

John Rutter is a composer and conductor. This is his letter to The Spectator, printed in the current issue.

 

[maryb]

My friend has never been the same since catching chicken pox from her grand-daughter, she had a major heart attack 9months later - I'm convinced the virus was responsible.
Even now 2yrs on many of her symptoms are still quite bad and remind me very much of ME, just different to me though. We'll never know and the medical establishment aren't helping us to.She just goes to the GP nearly every week with one symptom or other, heart-breaking really.

It just makes me wonder about those of us who came down with a virus, what if we'd had antiviral medication at the time, would we still have gone on to develop ME as we did. I don't want to discuss this further just thinking off the top of my head.