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Height is a big contributing factor. I am 6'2", a woman, with extremely long arms and legs. My podiatrist, not my neurologist, was the first one to diagnose the PN, and to tell me that height makes it much worse. Mine is hereditary so nothing I could have done to prevent or improve it, but height still complicates matters, like trying to run a really long train set from one transformer-too much distance with all the extra resistance that implies and a weakened motor.
There are a number of research papers out there in medical journals hypothesizing that the reason more men get PN is simply because they are taller. |
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As to the height issue; several of us who are vertically challenged also have PN. I think the only benefit of being shorter is that it may take somewhat less time for the peripheral nerve re-generation to reach its ends. Best of luck with it all, Steven |
Trying to kick what was working
Hey all, at some point now I guess I need to relay what was working for me but now I'm quitting it, not so easy but making it. The what is "Suboxone", usually used to treat addicts kicking opiates. A pain clinic prescribed it and it took away 50-70% of my feet and hand neuropathy pain away, still had to be careful about how much time I spent on my feet but it got my life going again about 6 years ago. Now I'm trying to quit it due to the pain clinic causing too much trouble for me. Frequent mandatory appointments with a drug test I'd have to pay for, also forcing me to see an "in clinic" shrink before I could get a refill. OMG I feel more like an addict than someone being treated for pain! Anyway I got tired of the bother enough to now try some old alternatives. Diet, Celebrex, Neurontin high does, Cymbalta progressively increasing. I hope this all works and with some help from this forum it just might~ later ~ Raz
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