Can Neuropathy be cured?

Posted by catstx @catstx, Sep 8, 2021

I’ve had P. neuropathy for 30 years. Just recently I’ve better controlled my blood sugar. So, I’m wondering if Neuropathy ever goes away, Or, if once the nerves are dead they’re just dead

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It was an IgA test. After getting its results, I am in strict adherence to gluten free diet. Not that easy to do. Today I just returned to my supermarket a bag of walnuts that I was going to use to bake chocolate chip cookies. The bag's ingredients said walnuts but when I called the customer info line, I learned it was made in a facility that processes wheat . I had to return the walnuts and so my chocolate chip cookies do not have walnuts in them. If I want walnuts, I must crack them, and almonds, out of their shells as I do like to put them in my morning oatmeal and cereal. Lots of health problems relate to our gut and what we put in it. Answers are not always found in drugs--in fact, they may cause further problems.

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Profile picture for magnum52 @magnum52

@michhino
As of January 2026 it will be 10 years since I was diagnosed with idiopathic SFN. I spent one week at the Mayo Clinic in Rochester back in June of 2021 hoping they might find a cause, they didn’t. I retired from a major pharmaceutical company and know how to research and interpret clinical trial data. I have had 2 trials of a Spinal Cord Stimulators which failed. I have taken every drug out there and every test multiple times. The only neuropathy drugs I take are pregabalin, duloxetine and Low Dose Naltrexone 4.5mg. The drug I had high hopes for was an injection called Engensis from a South Korean company called Helixmith. I have tried for several years to get an update on the drug but the company went dark. YESTERDAY, I finally received a reply from someone that used to work for the company here in the United States, and he told me they had 2 Phase III trials that did not meet the primary endpoint. They also a a money issue in continuing the research. Basically the drug is very much DEAD.
There is nothing out there that will “cure” idiopathic SFN. IF they can identify a cause, then hopefully treating the cause will cure the neuropathy. I have never heard. Of someone actually curing neuropathy. The only drugs in trial now that I know of address the pain only (palliative) and none come anywhere close to a cure. For pain, the first non-opioid pain killer invented is a drug call Journavx. It has a very unique mode of action, and can be effective in pain relief for some patients. Other drugs with a similar MOA are in research as well.
My industry has done an amazingly poor job in their approach to neuropathy. They will develop tons of me-too drugs but have failed miserably at dealing with the degeneration of nerves and reversing it.
I am not offering any medical advice, but be careful what snake oil salesmen are selling. Desperate people sometimes lose their ability to reason logically when looking for help. I will advise anyone with neuropathy to exercise AS MUCH AS POSSIBLE with aerobic and resistance training if you can. I truly believe it has he with my discomfort. Good luck to all of us.

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@magnum52 thank you I hope you’re doing good and you keep up with everything I like to follow up with you on this. Since I have the same problem and taking the same medication as well. Please stay in touch. Merry Christmas

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Profile picture for nattleu @nattleu

@magnum52 thank you I hope you’re doing good and you keep up with everything I like to follow up with you on this. Since I have the same problem and taking the same medication as well. Please stay in touch. Merry Christmas

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Hello @nattleu, I see you have been a member for awhile and this is your first post so I would like to welcome you to Connect. I'm glad to see that you have connected with @magnum52 who has shared some really good advice. In case you haven't already seen it, you might also find the Foundation for Peripheral Neuropathy helpful for suggestions on living well with neuropathy - https://www.foundationforpn.org/living-well/.

Do you mind sharing your diagnosis and what has helped you manage the symptoms?

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Profile picture for John, Volunteer Mentor @johnbishop

Hello @nattleu, I see you have been a member for awhile and this is your first post so I would like to welcome you to Connect. I'm glad to see that you have connected with @magnum52 who has shared some really good advice. In case you haven't already seen it, you might also find the Foundation for Peripheral Neuropathy helpful for suggestions on living well with neuropathy - https://www.foundationforpn.org/living-well/.

Do you mind sharing your diagnosis and what has helped you manage the symptoms?

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@johnbishop thank you so much I am so happy to be part of the group. My doctor gave me 5 mg prednisone every day and pregabalin 50 mg in the evening. It helped with burning sensation and pain. I also do legs exercises every morning and weight training twice a week. I’m 81 years old now and will be 82 in June Take Care and . Merry Christmas

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Profile picture for nattleu @nattleu

@magnum52 thank you I hope you’re doing good and you keep up with everything I like to follow up with you on this. Since I have the same problem and taking the same medication as well. Please stay in touch. Merry Christmas

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@nattleu
Reach out anytime. I am taking pregabalin 50mg twice a day; Low Dose Naltrexone 4.5mg daily which has to be compounded by a compounding pharmacy; and duloxetine 60mg daily. I also workout at the gym 5 times a week with weights and cardio. I believe this has helped me more than anything. We have to find what works for us be we cannot depend on the pharmaceutical industry for help or the various research institutions out there because they are only interested in symptom control and not finding a treatment that reverses nerve degeneration.

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Profile picture for magnum52 @magnum52

@nattleu
Reach out anytime. I am taking pregabalin 50mg twice a day; Low Dose Naltrexone 4.5mg daily which has to be compounded by a compounding pharmacy; and duloxetine 60mg daily. I also workout at the gym 5 times a week with weights and cardio. I believe this has helped me more than anything. We have to find what works for us be we cannot depend on the pharmaceutical industry for help or the various research institutions out there because they are only interested in symptom control and not finding a treatment that reverses nerve degeneration.

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@magnum52 I will check out Natrexone and thank you

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Profile picture for nattleu @nattleu

@magnum52 I will check out Natrexone and thank you

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@nattleu hope you’re doing good and staying healthy no longer using substances. Good luck and Merry Christmas

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