progression of sensory polyneuropathy - vibrating/buzzing
Hello, is your progression fast or slow?
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Mine crept up slowly. I started noticing symptoms- almost 2 years ago and then it got very bad last summer. I seem to be stabilizing now to at least a more manageable situation.
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Mhm and the whole body or just some parts=
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Mine was pretty sudden. Everything at the same time - feet, hands, hot/cold spots, dizziness etc. It has waxed and waned depending on the week but I haven't gotten better or worse since it started. Would say the vibrating is much less than before but the pain and fasciculations are more frequent.
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Mine is sensorimotor axonal polyneuropathy.
The "sensations" had started in limbs, approx. 33 years ago. They were very mild then. It's gotten progressively worse over these 33 years... slowly. I did a lot to try to intervene and sensory nerve regrowth had been noted on skin punch biopsies. However, at this point, the sensory nerve die-off is greater than any regrowth. It's likely the rate of progression is multi-factorial in nature. I am sure there are individual differences. Warmly, DejaVu |
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Mine started about 7 years ago in my feet. Within a few weeks it was everywhere but the left side of my face.
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Mhm, thanks. In my case it was also a rapid onset. Do you get also tingling or numbness in your tongue occasionely? On one side of the tongue
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