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

Posted by John, Volunteer Mentor @johnbishop, Apr 21, 2020

I have used the original version of the Protocol 525 product (https://theprotocolworks.com/) since 2016. I have idiopathic small fiber peripheral neuropathy with the only symptom being numbness in both legs. When I started taking the protocol, the numbness was just below my knees. After 2 months, the numbness seems to be just above the ankles which is subjective on my part with no additional testing. I do feel it is a win-win for me as my neuropathy has not progressed like I was told it would by the neurologist. I have continued taking the protocol in hopes that it may continue to roll back the numbness symptoms. I have noticed some new feeling in my feet in the last 2 months. Some feeling has returned to me feet and they seem to feel better lately although I still have the numbness – hard to describe the difference.

The Protocol 525 is not a cure for neuropathy. It treats the pain and discomfort symptoms of neuropathy without the drugs which have their own side effects. Have you tried the Protocol 525 or the original protocol? Did it help? If yes, how? If no, please share.

Note: I have no commercial investment in the protocol and I am sharing this information as someone who has found some degree of relief using this combination of supplements. I also discussed these supplements with my Mayo primary care team before I started taking them. The care team sent them to the pharmacist for review who did not have any major concerns for me taking them.

*** Edited Oct 3, 2023 ***
For more information and a list of the ingredients, please see the frequently asked questions on the Protocol's website here - https://theprotocolworks.com/faq/.

Interested in more discussions like this? Go to the Neuropathy Support Group.

Has anyone tried the cream? Surterra tincture oil.

REPLY
@jeffrapp

Thanks for the info about the protocol, @johnbishop.
You've reported that since starting the protocol. you think your symptoms have leveled off, and may have begun to get better (new feelings in your feet).
Since you have SFP, and therefore an anatomic deficit which can be proven with a biopsy, have you ever considered getting another biopsy done, which may show an increase in nerve fibers, and therefore confirm your subjective feelings.
As you know, this disease is particularly difficult to manage, in part because symptoms are the result of so many variables, including mood. It would be wonderful to be able to demonstrate improvement based on an objective test.
What do you think?

Jump to this post

Hi Jeff @jeffrapp, I had thought about getting retested for my neuropathy but did not follow through. My Mayo neurologist didn't use a punch biopsy for my diagnosis. I had a couple of EMGs and some labs along with a physical exam when he diagnosed me with idiopathic small fiber PN. I did think about seeing if I could get another EMG to see if there was some difference but it's a matter of paying for the tests and getting one scheduled so I haven't pursued it anymore. I agree that it would confirm my subjective feelings quite a lot if the test confirmed improvement. After this COVID-19 situation improves I may talk to my primary care doc to see if I could schedule something that would be covered by my insurance. I missed my annual exam due to COVID so will add it to my list of questions for my doctor. Thanks for the suggestion!

REPLY
@johnbishop

Hi Jeff @jeffrapp, I had thought about getting retested for my neuropathy but did not follow through. My Mayo neurologist didn't use a punch biopsy for my diagnosis. I had a couple of EMGs and some labs along with a physical exam when he diagnosed me with idiopathic small fiber PN. I did think about seeing if I could get another EMG to see if there was some difference but it's a matter of paying for the tests and getting one scheduled so I haven't pursued it anymore. I agree that it would confirm my subjective feelings quite a lot if the test confirmed improvement. After this COVID-19 situation improves I may talk to my primary care doc to see if I could schedule something that would be covered by my insurance. I missed my annual exam due to COVID so will add it to my list of questions for my doctor. Thanks for the suggestion!

Jump to this post

Hi John, I was under the impression that SFN was not detectable by EMG; that is what I was told since my 2 EMG tests were negative. Further tests showed nothing so my neurologist assumed by my symptoms I had idiopathic SFN, stating that the treatment would be the same no matter what. Do you know which test specifically showed you to have SFN? I did forego the skin biopsy which she has since offered to do.

REPLY

Hi Helen @helennicola, Actually the EMG is one of the tests for diagnosing peripheral neuropathy. I had nerve damage for 20+ years before seeking a diagnosis because I only had numbness and then when talking with the doctors early on I was told if they ran tests and found I had nerve damage there was nothing they could do. Then when I finally "needed" to know and setup an appointment with a neurologist, he setup several appointments including labs, MRI and EMG then he examined me and diagnosed me as idiopathic small fiber PN. And confirmed my biggest fear...there was nothing he could do for the numbness. He also took pictures (with my permission) of my "hammer toes" which he said were typical of someone with peripheral neuropathy. That's what brought me to Connect and learning how to advocate for my own health and learn as much as I can about my health conditions.

Neuropathy Commons has some good information on diagnosing neuropathy and the different tests here:
-- https://neuropathycommons.org/neuropathy/tests-diagnosing-small-fiber-polyneuropathy

Matthew B. Jensen. Assistant Professor of Neurology, University of Wisconsin has a YouTube channel with a lot of really good information in easy to understand language in most of his videos: https://www.youtube.com/channel/UCJaXGRxxjnF2mvLiOFmmHLQ

REPLY
@cmartinjr

I have Experienced small fiber peripheral neuropathy for about 4 yrs with mostly pain in my feet with minor numbness. The pain on some days limits my activities to none.. I have the worst pain when standing. I tried the protocol for about 1 1/2 yrs and saw no improvement in the pain, however I still take the R alpha lipoid acid, heavy levels of Omega-3, and magnesium along with my gabapentin and cymbalta. I continue my research and discuss my condition with my pain Doctor, although she is not much help. I plan to try and reduce or eliminate the gabapentin due to the impact it has on my memory. The foundation for peripheral neuropathy has a lot of information that I am trying right now along with all the good information I read on this forum. I know every person is different and I keep trying different things to try what will work the best for me.

Jump to this post

Great Picture with horse ... I am former senior equestrian.
I am having a terrible time with neuropathic/neuralgia pain of right superficial abdomen adjacent to umbilical area and going laterally. I went through this 10 years ago on the left side. I tried Lyrica and gabapentin ... in a fog. I tried amitriptyline ... in a fog... not much help if at all. I am using lidocaine 5% patches bid and ice packs. What is the difference in ALA and R-ALA. I am under care of Endo MD for diabetes, Primary care MD, and whole regimen of doctors. Just seeking comments and ideas.

REPLY
@alglenn

Great Picture with horse ... I am former senior equestrian.
I am having a terrible time with neuropathic/neuralgia pain of right superficial abdomen adjacent to umbilical area and going laterally. I went through this 10 years ago on the left side. I tried Lyrica and gabapentin ... in a fog. I tried amitriptyline ... in a fog... not much help if at all. I am using lidocaine 5% patches bid and ice packs. What is the difference in ALA and R-ALA. I am under care of Endo MD for diabetes, Primary care MD, and whole regimen of doctors. Just seeking comments and ideas.

Jump to this post

R ALA stand for R Alpha Lipoic Acid. Here is what it says on the first website I looked at:

R-Lipoic Acid Details
Alpha-lipoic acid occurs naturally as a 50/50 mixture of R-lipoic acid (R-ALA) and S-lipoic acid (S-ALA). R-lipoic acid by itself functions as an essential cofactor for many enzymes involved in energy production.* It also has characteristics, including significant antioxidant effects, that contribute to liver, brain, nerve, and eye health.* Studies indicate that supplements containing only R-lipoic acid appear to be better absorbed than supplements containing both R-lipoic acid and S-lipoic acid, with results showing twice as much ALA appearing in the bloodstream after an oral dose of R-Lipoic acid.* Because R-Lipoic acid is the form best utilized by the body, Thorne provides R-lipoic acid bound to sodium, providing it in its most stable, absorbable form.*

Alpha-lipoic acid, also known as thioctic acid, was discovered in 1951 as a molecule that assists in acyl-group transfer and as a coenzyme in the Krebs Cycle. In the 1980s, the scientific community realized that alpha-lipoic acid is also a powerful antioxidant.* What sets ALA apart from other fatty acids is that it's an antioxidant in both fat- and water-soluble environments, and it's also an antioxidant in both its oxidized and reduced forms.* This is unlike vitamin C, for instance, which is a water-soluble antioxidant, as well as vitamin E, which is a fat-soluble antioxidant. ALA also increases intracellular glutathione and CoQ10 levels.* Its other mechanisms of action include promoting normal protein glycosylation and inhibiting the enzyme aldose reductase, which in turn inhibits conversion of glucose to sorbitol.*

REPLY
@alglenn

Great Picture with horse ... I am former senior equestrian.
I am having a terrible time with neuropathic/neuralgia pain of right superficial abdomen adjacent to umbilical area and going laterally. I went through this 10 years ago on the left side. I tried Lyrica and gabapentin ... in a fog. I tried amitriptyline ... in a fog... not much help if at all. I am using lidocaine 5% patches bid and ice packs. What is the difference in ALA and R-ALA. I am under care of Endo MD for diabetes, Primary care MD, and whole regimen of doctors. Just seeking comments and ideas.

Jump to this post

Hello @alglenn, Welcome to Mayo Clinic Connect. You ask a great question about the difference between ALA and R-ALA. The R-form of alpha-lipoic acid is the active, natural form. If you look closely at the ingredients for most ALA supplements you will find that they contain a large amount of S-ALA (synthetically manufactured and inactive form of ALA). Here are a few references that you might find helpful for learning more about ALA and R-ALA.

ConsumerLab.com - R-Form Alpha-Lipoic Acid & S-Form Alpha-Lipoic Acid:
-- https://www.consumerlab.com/answers/i-heard-the-s-form-of-alpha-lipoic-acid-is-bad-for-me-why-is-it-in-my-supplement/S-Alpha-Lipoic-Acid/
(R)-Lipoic Acid: Unique ‘Mitochondrial Antioxidant’ Fights Premature Aging:
-- https://nutritionreview.org/2019/07/r-lipoic-acid-unique-mitochondrial-antioxidant-fights-premature-aging/
Linus Pauling Institute » Micronutrient Information Center -- Lipoic Acid:
-- https://lpi.oregonstate.edu/mic/dietary-factors/lipoic-acid

Here is some information that I found on that may provide information to help.
Abdominal Wall Pain: Clinical Evaluation, Differential Diagnosis, and Treatment: https://www.aafp.org/afp/2018/1001/p429.html

There is also another discussion on Connect you may want to read through where other members are discussing similar symptoms.
Has anyone been diagnosed with Abdominal Wall Pain: https://connect.mayoclinic.org/discussion/has-anyone-been-diagnosed-with-abdominal-wall-pain/

You mentioned the abdominal pain - neuropathic/neuralgia. Did the doctors give you a specific diagnosis?

REPLY

Can you explain the 525 protocol?

REPLY
@bustrbrwn22

Can you explain the 525 protocol?

Jump to this post

@bustrbrwn22, The 525 Protocol is a product that includes different supplements packaged together by a non profit 501c3 group to help treat the pain symptoms of peripheral neuropathy. I have been taking the original protocol since 2016 and switched to the new 525 when it became available early this year. I only have numbness but feel it has helped me some and has slowed or stopped the progression of my idiopathic small fiber PN.

You can learn more about it and get support for the 525 Protocol on their Facebook page. There is a link to join the Facebook group on their website to order the product here: https://solutions2pnpd.com/ There is also an instruction sheet in PDF format that compares the old protocol with the new 525 - https://solutions2pnpd.com/wp-content/uploads/2020/07/NEW-Instructions-525.pdf

There are members taking some or most of the supplements included in the 525 Protocol who can share what they take.

REPLY
Please sign in or register to post a reply.