Living with Neuropathy - Welcome to the group

Welcome to the Neuropathy group.
This is a welcoming, safe place where you can meet other people who are dealing with neuropathy. Let’s learn from each other and share stories about living well with neuropathy, coping with the challenges and offering tips.

I’m Colleen, and I’m the moderator of this group, and Community Director of Connect. Chances are you’ll to be greeted by volunteer patient Mentor John (@johnbishop) and fellow members when you post to this group. Learn more about Moderators and Mentors on Connect.

We look forward to welcoming you and introducing you to other members. Feel free to browse the topics or start a new one.
Let’s chat. Why not start by introducing yourself? What concerns would you like to talk about?

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

@ubelinda

I have peripheral neuropathy and pain in legs and numbness in fingers, and would like to know try this roll on. Is this prescribed or could I just purchase and where? Thank you and blessings. Ubelinda

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I will need to ask my daughter where she purchased. I don't know about putting it on the hands. It is suggested not to rub the eyes after applying. Even when I roll it on my feet, I massage it in by just using both feet; one over and under the other one. So I never get it on my hands. I will get back with an answer about where you can purchase asap.

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@levisdad

diagnostical results from testing

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Hello @levisdad, Welcome to Connect. Am I correct that your neuropathy diagnosis was from diagnostical results from testing? Did you have an Electromyogram (EMG) Test & Nerve Conduction Study (NCS)?

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@d13

I will need to ask my daughter where she purchased. I don't know about putting it on the hands. It is suggested not to rub the eyes after applying. Even when I roll it on my feet, I massage it in by just using both feet; one over and under the other one. So I never get it on my hands. I will get back with an answer about where you can purchase asap.

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Thank you for answering! I would rub it in my legs and feet, where the pain is. Blessings.

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@ubelinda

Thank you for answering! I would rub it in my legs and feet, where the pain is. Blessings.

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She told me that she got it at a cannabis shop. So that would be the place to look for it. Dragon deep tissue salve roll up. Ingredients; cocoa butter, camphor oil, menthol, cannabis extracted oil. 3.4 oz. I don't know if you can get it online. You could google it. I sometimes wait an hour after applying and then apply again. Right before going to bed works the best for me. Good luck finding it. And hope it makes you feel better.

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@d13

She told me that she got it at a cannabis shop. So that would be the place to look for it. Dragon deep tissue salve roll up. Ingredients; cocoa butter, camphor oil, menthol, cannabis extracted oil. 3.4 oz. I don't know if you can get it online. You could google it. I sometimes wait an hour after applying and then apply again. Right before going to bed works the best for me. Good luck finding it. And hope it makes you feel better.

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Thank you! Will look for this and try it. Blessings.

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@ubelinda

Thank you! Will look for this and try it. Blessings.

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Its available online if you can’t find it locally.

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@athenalee

Its available online if you can’t find it locally.

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Thank you! Blessings.

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Hello kindred spirits. My main health concerns are all severe: pain, anxiety, insomnia and isolation.

Health was great until early 40’s, ~30 years earlier. MECFS evolved, which is neurological from stress, significant, and progressive. It is systemic, affecting multiple brain functions including cognitive,IBS and insomnia. Then Peripheral Neuropathy severely hit in feet, it too is systemic and progressive with high pain. I think these conditions are interrelated, neurologically. I’m functional but slow, getting more and more housebound.

I’m more or less tuned into the CFSME but not so much the related conditions. I’d like to see what we share in common, dealing with the symptoms et al. ✌️

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@stress

Hello kindred spirits. My main health concerns are all severe: pain, anxiety, insomnia and isolation.

Health was great until early 40’s, ~30 years earlier. MECFS evolved, which is neurological from stress, significant, and progressive. It is systemic, affecting multiple brain functions including cognitive,IBS and insomnia. Then Peripheral Neuropathy severely hit in feet, it too is systemic and progressive with high pain. I think these conditions are interrelated, neurologically. I’m functional but slow, getting more and more housebound.

I’m more or less tuned into the CFSME but not so much the related conditions. I’d like to see what we share in common, dealing with the symptoms et al. ✌️

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Hello @stress, Welcome to Connect. I think you are right in that a lot of the neurological conditions are tied together. I don't have ME/CFS but do have small fiber PN, polymalgia rheumatica, and am trying to figure out if I'm in the catagory of those with metabolic syndrome which I think is related to my neuropathy. Here's some information that I think speaks to neuropathy and ME/CFS.

Small Fiber Neuropathy (SFN) Fibromyalgia and ME/CFS Resource Page: https://www.healthrising.org/small-fiber-neuropathy-resource-page-fibromyalgia/

There are a few other discussions that you might find interesting.
-- Member Neuropathy Journey Stories: What's Yours?: https://connect.mayoclinic.org/discussion/member-neuoropathy-journey-stories-whats-yours/
-- Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) treatments: https://connect.mayoclinic.org/discussion/myalgic-encephalomyelitis-chronic-fatigue-syndrome-me-cfs-treatments/

Another connection I'm trying to understand which could possibly tie in with what you mentioned is the Metabolic Syndrome -- The Metabolic Syndrome and Neuropathy: Therapeutic Challenges and Opportunities: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3881591/

Have you tried doing any research using PubMed (https://pubmed.ncbi.nlm.nih.gov/) or Google Scholar (https://scholar.google.com/)?

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