Re: Jacobs
Luckily, my local hospital is the largest teaching hospital in Europe. That, plus a brilliant GP, I had a diagnosis within 16 months of the onset of symptoms. I've had FMS for just over three years I found out about the ulcer in November 2012 when it ruptured and I ended up in A & E, minus just short of nine pints of blood. I know what you mean about the CFS. However, the ulcer rupturing and the heavy duty antibiotics they give you to kill the bug that causes them has helped this aspect. The FMS, as it affects me, is made worse by very cold and very hot weather. The heatwave during the summer sparked off a flare that has caused further muscle wasting, meaning I have to use a motorised wheelchair if I go out anywhere. However, stress doesn't help. Also, the dreaded Fibro Fog!
Originally posted by MissiM
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