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Living with Neuropathy - Welcome to the group

Neuropathy | Last Active: Oct 27 5:51pm | Replies (6152)

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@summertime4

@johnbishop Hi everyone. I see the subject is the Protocol. I had seen your post several months ago about the Protocol. At first I thought it was exercises or other therapy or vitamins. Yes, I found it is actually vitamins of sort and as reading more found it was also a "Product" and had it's own website and all. I was taken back by the price of these products and how long you would have to use them before you saw some relief or what. I cannot afford their product even for short time. I cannot spend much money for over the counter products either. I do take vitamins and am prescribed Vitamin B12 shots. Even with this I am told my neuropathy has progressed and this is the reason for constant, awful numbness of legs and feet. I used to have the tingling and feelings of little bugs crawling on my legs. I was told I have progressed past that the numbness and will stay with me. I go off the chart with anxiety. I constantly feel like my legs and feet are encased in cement or I have to take heavy socks off that I do not have on. I am frightened as I was just told that information yesterday by my physical therapist. I will say that the water therapy feels good and I am fortunate that I can have this even with the shut downs. Can I get more information from the group in regards to progression and where I might be going from here. Thank you. If I were able to I would certainly look into trying the "Protocol" I also get desperate for relief.

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Replies to "@johnbishop Hi everyone. I see the subject is the Protocol. I had seen your post several..."

@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