Living with Neuropathy - Welcome to the group

@summertime4 Have you asked your neurologist for supplement/vitamin recommendations? Outside of B vitamins, Stabilized R Alpha Lipoic Acid and Acetyl L Carnatine are thought to be most helpful to neuropathy. Even if you can just afford those, it may help you. There are others and each person may have specific needs based upon their health issues and diagnosis. Just like certain protocol supplements may not be suited for everyone and should always be presented to your Dr before beginning.

Progression is a touchy, unknown area, unfortunately, and noone can exactly pinpoint what's next for you personally. I was petrified last spring when my first signs of leg decline began. It continued with various side effects, sensations and weaknesses that alarmed me into thinking a permanent wheelchair was in my future. Well, it was and still is, for distant walking. Ex: grocery stores, department stores, hospitals, airports. I can however have days when I can walk around my back yard (under 1/4 acre) slow and steady, then days when I cant. Gone are the days of running, jumping, skipping or even a normal paced walk. My legs debilitate me some days... I struggle with a slow stride room to room and am down with heat for the day but, I'm not in a wheelchair permanently and that is huge. It's heavy stuff and confusing to me many of days. I have polyneuropathy so legs are just one example.

As for the hopeful stuff...I have sensations that are much better managed now between lyrica, supplements, eating better. I've documented every symptom from day one and I. able to look back and see what things have worsened, improved, gone away or return. When there is so much happening inside your body (like a hostile take over), it's mentally helpful to find anything, any small thing that is hopeful.

I hope that you keep working your body as best you can and dont give up on it or yourself ever. Keep researching, learning and asking. A relentless disease deserves a relentless response.

My best to you.
Rachel

Rachel, I have polyneuropathy, too. Without the pain. Do you have pain or just weakness/numbness. Mine is hereditary. Is yours?
Steph

@albiet, @rwinney, @jeffrapp, @mikeoc, @cwallen9, @dazzah1234, and @cloudnine -- I just created a new discussion for the Protocol 525 product for the treatment of the pain & discomfort for neuropathy. I thought you might want to follow it. I'm hoping any other members who have tried the 525 or the original protocol will share their experience in the new discussion here:

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/

Hello Steph @stefspad. I was B12 deficient and I have pain, weakness, burning and intervals of numbness.

@summertime4 Have you asked your neurologist for supplement/vitamin recommendations? Outside of B vitamins, Stabilized R Alpha Lipoic Acid and Acetyl L Carnatine are thought to be most helpful to neuropathy. Even if you can just afford those, it may help you. There are others and each person may have specific needs based upon their health issues and diagnosis. Just like certain protocol supplements may not be suited for everyone and should always be presented to your Dr before beginning.

Progression is a touchy, unknown area, unfortunately, and noone can exactly pinpoint what's next for you personally. I was petrified last spring when my first signs of leg decline began. It continued with various side effects, sensations and weaknesses that alarmed me into thinking a permanent wheelchair was in my future. Well, it was and still is, for distant walking. Ex: grocery stores, department stores, hospitals, airports. I can however have days when I can walk around my back yard (under 1/4 acre) slow and steady, then days when I cant. Gone are the days of running, jumping, skipping or even a normal paced walk. My legs debilitate me some days... I struggle with a slow stride room to room and am down with heat for the day but, I'm not in a wheelchair permanently and that is huge. It's heavy stuff and confusing to me many of days. I have polyneuropathy so legs are just one example.

As for the hopeful stuff...I have sensations that are much better managed now between lyrica, supplements, eating better. I've documented every symptom from day one and I. able to look back and see what things have worsened, improved, gone away or return. When there is so much happening inside your body (like a hostile take over), it's mentally helpful to find anything, any small thing that is hopeful.

I hope that you keep working your body as best you can and dont give up on it or yourself ever. Keep researching, learning and asking. A relentless disease deserves a relentless response.

My best to you.
Rachel

@albiet, @rwinney, @jeffrapp, @mikeoc, @cwallen9, @dazzah1234, and @cloudnine -- I just created a new discussion for the Protocol 525 product for the treatment of the pain & discomfort for neuropathy. I thought you might want to follow it. I'm hoping any other members who have tried the 525 or the original protocol will share their experience in the new discussion here:

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/

@rwinney Thank you I am listening to everyone and so thankful you are all here. I need to do more for myself. I do need more vitamins. I take Vit D daily. I tested low on that. I am also prescribed B12 injections. Since the shutdown I have not had one. A friend was giving me the shot and with not being able to have visitors and me not being instructed as how to do it, I have not been getting one. I have to do better.

Sorry to hear about the pain and burning. The more I read the more I consider myself lucky, even though I am now using a walker a lot of the time.