Tuesday, November 02, 2010

Manchester

Off to Manchester for a couple of days...

On the train/Forever hypo

This morning I was reading the Independent. I picked up a copy in the lounge at Euston. I read an article by Cathy John about coming out (as an MS sufferer).

My symptoms remain mostly invisible to others: pins and needles in the hands, blurred vision, fatigue, muscle weakness and imbalance (I often give a brilliant impression of being drunk when I am not). Prior to being diagnosed the symptoms seemed so negligible, I was convinced I was a raving hypochondriac.
It caught my eye. I've been having slight problems with my vision; I have difficulty concentrating. Most telling, I often get pins and needles in my hands and lower arms.

NOTE TO SELF - must get checked out!

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