Foot neuropathy: What gives you relief?
It seems if I get enough activity/exercise daily I don’t have pain; if not, am awakened from sleep and must get up (even in the middle of the night). What’s going on & what more should I do to avoid rest-disruption?
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Please post the pics or link from Amazon on these 2 oils. Thank you.
That is the way I feel too bc I don't want to come out worse.
Best of luck to you.
Hi
I just read your email.
Thank you very much for taking the time to inform me about your experience.
I guess I should look up the video & see.
I was at the dr. in Vegas yesterday to find out about my shoulder & this dr. said he only fixes them but does not do reconstructive.
So, you say they can do a reverse & that would be better?
I have back problems too. Scoliosis & the neck so that is why I am hesitant on everything.
Plus with this Neuropathy, it is killing me.
I guess I will just try & wait it out but just afraid it will get worse with time & then I will need to do it anyways.
Thank you so much for sharing. I am going to watch the videos.
God bless you
Genie
I still take care of myself too & do my housework, but I tire easily & my legs give out on me.
I do something & sit down & then get up & do something else.
Oops! I used the wrong word. I posted IMAGES….not a video. Sorry.
Chris
Gabapentin...beware!!! Yes it really helped me with my Neuropathy and spasming, but it really messed with my cognition. I had wean off of it. Now I'm trying Pregabalin, which is providing relief without the confusion.
Exercise has made a huge difference in my physical and mental states. Once I got back to classes (finally, after COVID prevented all gatherings for me), my nightly leg muscle spasms totally stopped and I was able to get off of the muscle relaxers. I also have a Spinal Cord Stimulator which has made a big difference. Treatment for my condition seems to be a big science experiment. My docs and have tried one thing after another, observing results and moving on. I think the biggest key to finding relief is to have a good relationship with a doc who takes you seriously and gives you the time to fully discuss your situation.
What is the name of the device you use that’s similar to a tens unit?
Do you need a prescription to get it? Thank you for the info!
I'm not sure that mine is comparable as my unit is implanted whereas the Tens is used outside of the body...but anyway, mine is an Abbott Spinal Cord Stimulator https://www.nevrohfx.com/why-hfx/overview/ here's a link. I'm on Medicare with a supplemental policy...it was 100% covered by insurance.