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Anyone here dealing with peripheral neuropathy?

Neuropathy | Last Active: 5 days ago | Replies (2974)

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@jakedduck1

@golfgame
If I were reading a book I’d like to know why they wrote it and when the author is selling products that could cure/help Neuropathy I think I found the answer and would immediately put it where it belongs, in the garbage or a roaring fire.
I’d give more credence to your doctor's opinion than a couple people selling products under the guise of being physicians. The only help they probably gave you was how to disconnect from your money. There are new books, pills, and other money separation devices coming out daily with many ready to hand over their hard-earned money to them. Depending how much vitamin E are in those pills, perhaps the author will have a cure for whatever bleeding disorder or other problem you may have or be able to cure you of your hemorrhaging stroke that may be lurking. Sometimes neuropathy gets better like mine did. My neuropathy was most likely caused by seizure medication. That medication became unstable, and regardless of my dose was always at a toxic level so I had to switch seizure medications. Sometime later, the horrible, painful sensations went away and were replaced with numbness. I think it would be better to spend money on trying to find what actually caused the neuropathy, than try to cure it with some magic pill. I’m not about to spend my money to line someone else’s pockets, whose intention it was to cheat me.
Just my 2 cents worth.
Take care,
Jake

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Replies to "@golfgame If I were reading a book I’d like to know why they wrote it and..."

Thanks for your reply and thoughts. What you say has merit and makes sense to me. Being new to PN makes it very hard to find substantive, reliable information and direction.
Any direction or links would be appreciated. I am non-diabetic or even pre-diabetic. I actually believe that the series of COVID shots may have been the trigger as the timeline lines up.

There are articles on you tube by a research neurologist Dr Anna Outlander google her. Her research starts back before 2018 into neurology. One of the things my neurologist has banged into my head is if you can’t find the etiology (cause) you can’t find out how to treat the neuropathy. I believe mine is due to hypothyroidism but when I talked to my neurologist and pain management doctor in Texas they had heard of her research and have decided to refer me. Mine is progressiving really fast.
Theee is additional testing she does that my doctors have not done. I am hoping to find out more