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Grand Magnate
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Join Date: Jan 2008
Location: Red Wing, MN
Posts: 3,166
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Grand Magnate
Join Date: Jan 2008
Location: Red Wing, MN
Posts: 3,166
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Quote:
Originally Posted by lady_express_44
I'm losing track of people's stories now, Polar.  You are on 4.5mg, right?
Have you had any attacks . . . are you RRMS, SPMS, or PPMS? How long have you had MS?
How have you progressed over this 3 yrs, if you don't mind me asking?
Cherie |
4mg is my limit, I've found..My bladder starts doing somersaults when I try 4.5..I was dx'd as PPMS, the progression is mostly cognitive, with numbness in hands and buzzing in both legs..Balance has become more of a problem, slowly but steadily..Still walking though! I had an MRI a couple months ago, and it showed new and active brain lesions..My thyroid went completely wonky on me at about the same time (hypothyroid), going from 1.5 to 19.8 in a matter of a few months..All this sounds bad, but considering alternatives, I'm happy with where I'm at!
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