Have you tried the new Protocol 525 product for neuropathy relief?

Like a lot of people on here I was first diagnosed with idiopathic neuropathy by a MD that did the Electromyography (EMG) test. I was later sent to a Neurologist at the nearby University that specializes in neuropathy. I was then told that I have neuropathy in both the large and small nerves.
I have tried a long list of supplements like those listed in the protocol 525. As well as the Neuro light that I had mentioned in my original comment. I have also used the tens machine and other vibration machines that claim to stimulate the nerves.
My apprehension with the protocol 525 is the price. When people come out the gate charging so much up front. To me that means that they know it won't work so, they try to get as much money up front as they can.
I went to a free consultation with a local chiropractor that claims a 90% success rate for neuropathy. The system included the neuro light purchase for home use and office visits for 2-3 months for tens and massage therapy. The total cost if I would have bought into the BS would have been $8000. They were even willing to fill out the paperwork to get me financing.
When I asked if I would be getting a new car at the end of the treatments? He wasn't amused.
So, if the protocol has worked for you. I am very happy to hear that and God Bless you with continued success. My radar goes up when they ask for a lot of money.

does amiodarone cause PN?

Amiodarone does seem to have a connection with PN...

"Check with your doctor right away if you have burning, numbness, tingling, or painful sensations in the arms, hands, legs, or feet. These could be symptoms of a condition called peripheral neuropathy."
--- Amiodarone (Oral Route): https://www.mayoclinic.org/drugs-supplements/amiodarone-oral-route/description/drg-20061854

"The most common amiodarone-related neurotoxicities are tremor, ataxia, and peripheral neuropathy; more infrequent neurotoxicities include myopathy, optic neuropathy, basal ganglia dysfunction, encephalopathy, and pseudotumor cerebri."
--- Amiodarone Neuropathy: https://www.medlink.com/articles/amiodarone-neuropathy

I have been on EB-6N for a year now and it has helped. It is a little pricey @159 for 90 days but continue. Foot pain and numbness has improved. I use EBM medical and no this not a paid influencer.

Hello @susiesprue, A lot of us get discouraged when looking for answers and not finding much help for the neuropathy symptoms. I hope you don't mind but I thought I would respond to your private message in the discussion I started back in 2020 on the protocol of supplements I take for my neuropathy. You may want to click the link below which will take you to the top of the discussion so that you can read through what other members have shared.
--- Have you tried the new Protocol 525 product for neuropathy relief?: https://connect.mayoclinic.org/discussion/have-you-tried-the-new-protocol-525-product-for-neuropathy-relief/

You might also find this Why the Protocol document from the FAQs on the products website helpful as it provides research links for each of the supplements in the Protocol.

I have neuropathy with no pain but can barely feel the floor. My PN has never been diagnosed so I have no idea which kind it is. The neurologists I have contacted simply tell me there is nothing I can do about it .
I gave up driving years ago because of the numbness but am being driven crazy by the lack of feeling in my feet and fear of falling. In addition, my instability seems to affect by balance system and I am frequently dizzy. I have no idea what the Protocol is and would like to know so that I can inform my neurologist that something exists that might be useful.
gloria

You can print out the "Why the Protocol" document in the post above (https://connect.mayoclinic.org/comment/1055091/) and it has a list of the protocol ingredients along with the research articles that tell you how each of the supplements helps with nerve health. I'm 81 now and have been taking it since 2016. I feel that it has kept my neuropathy from progressing and the numbness doesn't seem quite as bad as it was for me back in 2016. I think it has helped folks with neuropathy pain symptoms more than the numbness symptoms but it's not an overnight fix. I didn't notice any difference for a few months of taking it. It would be good to print out the document and discuss it with your neurologist.

You might also want to take a look at the list of complementary and alternative treatments listed on the Foundation for Peripheral Neuropathy here - https://www.foundationforpn.org/wp-content/uploads/2020/08/Complementary-and-Alternative-Treatments-Revised-2020-final.-1.pdf

You were smart to walk away from that scam. Was he going to refund your money if it didn't work? I think not! There are so many of these money-grabbing schemes out there. It's a shame that these charlatans prey on those of us stuggling with intense pain. Wouldn't it be great if we could transfer our pain to them and then say, "OK. you've got my pain. Now, let's see how well your product works for you". Of course, I would not really want anyone to have to go through what we all have to endure. I hope you are able to find something that helps you.

Mike, do you know the cause of your neuropathy? How long did you take it before you noticed improvement? Did you make any other changes such as diet etc?

I have large fiber Idiopathic peripheral neuropathy in my feet. One thing I have learned I having this for the last three years is everybody is different and reacts differently to drugs and treatment. Glad you found something works for you. Like others. I’m extremely hesitant to sell out lots of money on something that is a gamble.