Has anyone found a treatment that helps with peripheral neuropathy?

Absolutely!!!

I have recently tried Tumeric, and I am super surprised that I actually could tell a difference. It hasnt been a huge difference...but when you have diabetic peripheral neuropathy throughout your entire body, even the tiniest difference can make the biggest difference. I also basically diagnosed myself with Vitamin B, D, magnesium,and potassium deficiency because I was having these all over convulsions/jerks (they almost felt like seizures) every time I would try and relax or try and fall asleep and my daughter told me I would literally jump and twitch all night long. I went to my neurologist 3 times, the orthopedic 2 times and I can't even remember how many primary doctors I went to begging for help. That went on for almost 5 years and one day i was reading something about body jerks and the article mentioned areas of the body where spasms and twitches were more commonly happening and I thought it was worth a shot since it sounded exactly like what was going on with me and the spasms stopped the very next day and I haven't had 1 since!! I even asked the neurologist if my issues could be because of a vitamin deficiency and she said that most likely not because it is so rare. Come to find out, it's not all that rare. I'm still having the horrible neuropathy pain and sensitivity though. I feel like I'm getting bit or pinched a lot. I can scratch my arm and feel a pinch in my calf. Or I can just touch my foot and feel pins and needles pain on my head. The very worse thing I hate though is I am ALWAYS sweating! I'm always either too hot or too cold but even if I'm shivering cold, I'm STILL sweating. Does anyone else sweat like that with peripheral neuropathy?

I have not yet found a treatment that works. I did, however, (following the advice of someone else on this forum) see a podiatrist. He suggested taking 600 mg of alpha lipoid acid and 1000 mg extended release B Complex for three months. He said to take daily without fail and he will do some testing of nerve conduction when I see him in three months. I began four days ago. Has anyone tried these supplements?

Well I got my letter from the Mayo Neurologist dept. They did a “deep dive” into my medical records. I had hoped that Mayo , since they have an extensive research, I had hoped that they could provide some new research treatments. The response was due to patient capacity and that they couldn’t offer any other treatments than what I am already doing. ☹️
So I am on my own. !
What is my personal treatment : I have left leg and left foot neuropathy. ( However there are many types of Neuropothathy). I have tingling sensation , easily irratedq by pants , socks, shoes, numbness down outer thigh, outside of leg calf, around the kneecap, around the ankle bone, and diminishing sandy feeling bottom of foot under toes and along right side of left foot. My personal daily health plan. AM. Alternating days of Physical therap exercises, yoga exercises, TENS unit application ( pads in proper place), Antiflamitory fruit, Greek yogurt, cinnamon, ginger, protein powder, apple cider vinegar, etc. shake, pils: D3, multivitamin, Tumeric, Krill oil,, multi vitam B vitamin. All of good quality. ( no synthetic ). ( there is a difference !). Deep tissue massage. ( look for a massage therapist trained in deep tissue massage). It’s not Swedish massage!). It can be painful sometimes). Accupuncture for pain in back ( after extensive failed back surgery). On going Pysical therapy, magnesium lotion on leg and whole foot.
It’s time consuming. I have to balance my daily life activities and what I do for my neuropathy.
I’m currently researching studies about the Sural nerve and Tibial nerve entrapment. Thanks for listening. Watch out for scams and poor quality ingredients.

Which Mayo were you trying to get into? I was discouraged to read your post as I'm also waiting to hear from the Mayo Clinic in Rochester to see if I can get an appointment.

Mayo , Rochester, Mn. Layton phone said I should contact the Redwing mayo
office. I called Redwing. I was told I need a Dr Referral to Redwing clinic
? I’m in the process of getting my Dr referral. I don’t know if it will be
fruitful. ? ? J

That's strange because I filled out and submitted an application over a week ago. I received a phone call the next day from them with some additional questions. They also told me that the application I submitted was for neurology and that neurology had suggested my application get sent to their neuropathy group. I was told to expect a response between 7-10 business days. I'm going to remain hopeful!