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.

The vibration on feet felt good but I found no real benefit personally.

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Upcoming webinar from the Foundation for Peripheral Neuropathy...

FPN Webinar: Living Well with Peripheral Neuropathy: Q&A with Dr. Shanna Patterson
Thu, Apr 28, 2022 2:00 PM - 3:00 PM CDT

The Foundation for Peripheral Neuropathy (FPN) welcomes Dr. Shanna Patterson once again for a special webinar to answer YOUR questions on Living Well with Peripheral Neuropathy. Please join us for some first-hand answers to your questions from an expert on treatments, diet, exercise, mental health and other aspects of living with peripheral neuropathy.

Dr. Shanna Patterson, M.D., FPN’s Patient Education Advisor, is Assistant Professor of Neurology at Mount Sinai West in New York City.

Register for the webinar: https://register.gotowebinar.com/register/7607998562795615499

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Do you need to register to view the questions and answers? I am interested in the end stages of PN. Both my father and sister lost the ability to feed themselves and the ability to speak.

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@dbeshears1

Hi Beth - I had PN before chemo, and was already taking Gabapentin. The chemo made my PN worse, but only temporarily I’m glad to say. We increased my Gabapentin a little during that time, though I was already taking 3 a day. It sure helped with the night sweats and chills, and I feel it helped get my numbness and tingling back to pre-chemo levels. It took a few weeks to start working consistently though. I’ve yet to try a vibrator for numb feet.

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Have you tried Kratom? It has knocked down my pain from a 10 to a 3. Taken correctly it’s amazing and comes from the coffee family. There’s a lot of bad info out there because the Big Pharmacy folks don’t want people to stop taking their drugs. You can get more information on Kratom from the National Kratom Foundation. Is safe, non addictive and it has no side affects. My physician suggested this and I will always be thankful it’s saved my life.

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@lecowing

Do you need to register to view the questions and answers? I am interested in the end stages of PN. Both my father and sister lost the ability to feed themselves and the ability to speak.

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@lecowing - The Living Well with Peripheral Neuropathy: Q&A with Dr. Shanna Patterson webinar will eventually end up on their website but if you want to participate in the live Q&A session and ask any questions you may have via a chat window, you need to register and they will send you a link that you so that you can join the live session.

You also might want to look through the following websites to learn more about neuropathy, the symptoms, treatments, prognosis and outlook.
-- Neuropathy Commons: https://neuropathycommons.org/
-- Foundation for Peripheral Neuropathy: https://www.foundationforpn.org/
-- Resource Library - Foundatiion for Peripheral Neuropathy: https://www.foundationforpn.org/resource-library/

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Interesting but really no discussion of the end stages of PN.

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@lecowing

Interesting but really no discussion of the end stages of PN.

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I think the end stages really depend on the diagnosis and which nerves are affected. I have no medical background or training but have done a lot of research on my own condition after my neurologist basically said there are no treatments for numbness just let us know if it gets worse.

This basically sums it up... "Is neuropathy life threatening?
Symptoms can range from mild to disabling and are rarely life-threatening. The symptoms depend on the type of nerve fibers affected and the type and severity of damage. Symptoms may develop over days, weeks, or years."
--- Peripheral Neuropathy Fact Sheet: https://www.ninds.nih.gov/Disorders/Patient-Caregiver-Education/Fact-Sheets/Peripheral-Neuropathy-Fact-Sheet

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@amaze02

I'm a type 2 diabetic , I get occasional pain in my legs. Trying to increase my knowledge, for treatment and slowing its progress.

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In an ncbi.nim.nih article it says lowering triglycerides slows the progression. And also supplement ALA was the only supplement show to help.. the number of the article was PMC4239691

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@gbny1224

In an ncbi.nim.nih article it says lowering triglycerides slows the progression. And also supplement ALA was the only supplement show to help.. the number of the article was PMC4239691

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Terrible pain keeps me from sleeping. Is there anyway one with a pacemaker can have treatments for neurophy.

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I have had neuropathy in my feet for several years. I'm now 87 and recently it has spread up to near my knee. I take 1000 mcg of vitamin B-12 daily, but so far it hasn't helped. Suggestions?

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