This is topic Anyone developed motor neuropathy after having sensory for years? in forum Medical Questions at LymeNet Flash.


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Posted by chamade (Member # 11472) on :
 
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?
 
Posted by MBB3 (Member # 13459) on :
 
^UP for Chamade
 
Posted by Tincup (Member # 5829) on :
 
Yes.
 
Posted by lou (Member # 81) on :
 
me too
 
Posted by chamade (Member # 11472) on :
 
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.
 
Posted by JKMMC09 (Member # 15795) on :
 
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! [Smile]
 


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