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Like the title says, did anyone developed weakness/tremors (not twitches, which I have plenty) after having neuropathic pain(burning, tingling) for a few years?
-------------------- Why me? Well, why not me??? Posts: 411 | From San Francisco, CA | Registered: Mar 2007
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May I ask about some details, was the preceding sensory neuropathy symmetric or unilateral/patchy? How long before the motor symptoms started and did it eventually improve?
thanks.
-------------------- Why me? Well, why not me??? Posts: 411 | From San Francisco, CA | Registered: Mar 2007
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My daughter began with the tingling, shooting pains, numbness, and a skin biopsy showing small fiber nerve damage and neuropathy. Months later she had an EMG and Nerve Conduction study showing Demeylinating polyneuropathy.
A few months down the road, she began having twitching, shaking, and eventually full blown myoclonus.
It progressed (for her) into full blown Grand-Mal seizures due to mis-diagnosis of the under-lying case (Which was, obviously, Lyme disease and Co-infections).
Hopefully you're on antibiotics and your disease progression will be halted, or very minimal! Posts: 371 | From CT | Registered: Jun 2008
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