I want to know more about TENS stimulation
TENS means transcutaneous electric nerve stimulation. "A transcutaneous electrical nerve stimulator (TENS) sends electrical pulses through the skin to start your body's own pain killers. The electrical pulses can release endorphins and other substances to stop pain signals in the brain. TENS can reduce pain."
This sounds good but I am still at the level of curiosity coupled with fear. Can TENS cause brain damage? And what's this about too much B6 causing more damage? I don't see how we can group everybody's metabolic systems into one clump. Can this stimulator cure PN? How long does the pain level stay at bay? How many treatments do you need and how often? I've seen the machines at Amazon. Would a neurologist have them in their office? Will this stimulator work on lumbar multilevel degenerative disc disease?
We do not have a neurologist in this whole county. And I'm not keen on traveling long distances to see one. And I just learned our Podiatrist is leaving so I need to find the new one who is replacing him. Your support is greatly accepted at all levels. Thanks. CB
Interested in more discussions like this? Go to the Neuropathy Support Group.
You have a philosophical mind. And I appreciate listening to you. Thanks for being in my corner. CB
Thanks for link, Gus. I'll look through it.
Thank you CB for your reply. I'm just a fool in constant search for wisdom in everything.
Take care.
You're most welcome.
I bought a TENS unit from Oxiline.com. It zaps quite well. It was a bit more $ than Azamon, but my DC said some of his patients were getting these and thought they were good. I may have thrown away $50 extra dollars, but so what. I think TENS and various supplements help. It takes decades to develop neuropathy, so it may take a long time to fix it. My best for you!
I was diagnosed with neuropathy last September…I’m 83..6’4” and 265 pounds..I don’t have pain..not even burning just a feeling of tightness in my feet and ankles..and I feel somewhat weak..and experience and unstable feeling and head just doesn’t feel normal. Dizzy—no….ive been taking 600mg of R-lipoic acid daily..and drastically cut back on sweets: candy, pastry, ice cream. I realize there’s not a cure—you would think in 2025 there would be medication to slow the process. Any advice from anyone..
I used the tens stimulus along with their socks for a long time and it didn’t work. I have PN but no pain, just numbness and weakness. PN is here to stay and no cure is in sight.
Yep, no cure for sure. I try all kinds of things and some do a little bit here or there. Supplements that increase nitric oxide in the blood stream seem to help, edema supplements, B12, CBD gummies, Voltaren topical gel, percussion gun vibration, walking, etc. ad in$initum. I think I'm keeping PN at bay and easing the symptoms, but no cure yet. Thanks for your reply.
Will
If you are not having pain, count yourself fortunate. The fiery, burning in my feet, ankles, thighs, buttocks has taken most activities away from me. I cannot stand very long, let alone walk very far. I will gladly trade this burning pain for tingling and numbness.
Heisenberg34…How long have you had neuropathy? Have you made major changes to your diet and exercise schedule since?? I am not diabetic…not sure if different types yield different symptoms