I'm still stuck in limbo land, though its offs own choosing since a former neuro ticked me off telling me nothing was wrong while handing me a scrip for neurontin for my supposedly imaginary symptoms. He then wrote in my records "probable multiple sclerosis".
Fast forward to 2013 where I start getting new and disturbing and/or very painful symptoms with my annual relapse. The worst being spasms in my foot, hand and leg. Pain doc referred me to ms specialist 6 months ago and my appointment is finally soon. I'm in my second flare. Waking up to these spasms which lessen but continue through the day sucks. Walking through Walmart or at work and they suddenly common sucks. That and the heavy legs and cognitive stuff I'd making work, and life, hard. Ugh. Hoping for final answers soon...and some steroids which I'm used to having for flares but pai doc won't RX because she doesn't want y symptoms masked.
Fast forward to 2013 where I start getting new and disturbing and/or very painful symptoms with my annual relapse. The worst being spasms in my foot, hand and leg. Pain doc referred me to ms specialist 6 months ago and my appointment is finally soon. I'm in my second flare. Waking up to these spasms which lessen but continue through the day sucks. Walking through Walmart or at work and they suddenly common sucks. That and the heavy legs and cognitive stuff I'd making work, and life, hard. Ugh. Hoping for final answers soon...and some steroids which I'm used to having for flares but pai doc won't RX because she doesn't want y symptoms masked.
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