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for diagnonsense
diagnonsense it sounds like you suffer from HMSN Type 2 (Heriditory Motor Sensory Neuropathy Type 2 Axonal) Hope thats helps.
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This may be a dumb question, but, are EMGs abnormal in any of the CMTs? Or is it strictly small fiber and only found on skin biopsy?
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My PN is apparently hereditary since my mother has it too, although the nature of our pain is different. At Mayo they diagnosed me with small-fiber sensory neuropathy. I have no motor involvement. It sounds like CMT (Charcot-Marie-Tooth disease) generally has motor involvement. Does it always? Is it still possible that I have CMT with no motor involvement. The pain started slow and has progressed over 7 years.
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http://www.charcot-marie-tooth.org/a.../diagnosis.php |
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http://www.charcot-marie-tooth.org/a...t/symptoms.php Symptoms of CMT vary greatly even within the same family. The same type that is diagnosed in a family member is what the rest would have if they do inherit it. Symptoms can become evident when you are young, old, or in-between. Or they might not ever be that evident. CMT is a complicated syndrome. |
At the top of the forum
there is a thread concerning PN, tips, etc. In that thread I have information concerning CMT.
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According to Mayo, this is what I have: "Length-dependent sensory axonal peripheral neuropathy due to #2 and #3" Unfortunately, I don't have a clue what any of that means. -sigh- I just want a simple explanation that I understand without words like axonal and sheaths--I have NO idea what those are and as much as I have researched them, I can't comprehend it.
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Yeah, that's what I'm talking about. Thanks... those are simple terms. I want so badly to understand exactly what my diagnosis means... but I can't break it apart and figure it out because it just doesn't make any sense... PN is so complex compared to all the other medical problems I have--I have no trouble understanding those.
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