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.

@johnbishop

Hi @mcd123, I'm wondering if you might find the following discussion helpful - Mayo Pain Rehabilitation Program where @rwinney has shared this video from Dr. Sletten, Mayo Clinic Pain Rehabilitation Center describing Central Sensitization - https://connect.mayoclinic.org/comment/595133/

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The video was helpful. I would like to participate in the program but I understand it cost 40,000 plus staying in a hotel for three weeks. I am retired don't have that kind of cash. Than you John for your reply to me tonight.

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@windsorchris

I was very concerned about gabapentin side effects but to date, no side effects at 900mg a day and adding 100mg every week to 3600mg daily. I believe it is helping reduce the tingling of my feet and lower legs. unfortunately, the PN progresses but with less discomfort I am told. Following WinSanTor trials for pirenzepine touted as a potential reversal of PN as the nerves regrow or so described. Good luck my friend.

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What Dr would let you take 3600 MGS of gabrapentin that concerns me ?

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@johnbishop

Thank you Colleen and Mayo Connect!

@jimhd @bburleson1 @swiss @hollander @fonda @gratefulone @mikween @aliskahan @grandma41 @rabbit10 @ujeeniack @gailfaith @ridgerunner @joannem @medic7054 @fleure @beckypain66 @philio66 @peggyj4411 @16jody @twinky @martid @grandma41 @pinkmk @crystalgal @gman007 @mari @amkaloha @bobsconnect @salena54 @robertlclark @upnorthnancy @tonyc55 @painwarrior @ladyjane85 @bobe @dbentley @pgjanes @citylady @mfobrien36 @timmckinney @briansr @superwife – Welcome to our new Neuropathy Group!

Our peripheral neuropathy discussion has grown quite large making it a challenge to find the information. We hope our new Neuropathy Group will make it easier for members to find a relevant discussion to ask their questions and share information. If you don’t find a discussion that meets your need then jump right in and create a new one! Be sure to invite other Connect members to join you. Inviting is easy, just tag a member by using their Connect member name which starts with an “@” sign.

The new Neuropathy Group is your community so let’s help each other by sharing your story, asking questions, and learning while we figure out how to deal with our specific type of neuropathy.

John

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Glad to join up, thank you. Noticed a bit of numbing under the toe pads, fingers too , beginning a few months ago. Now the doctor has me on Metanx the last month. Not sure it's helping yet. It seems to be progressing a bit....ugh.

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@korgman123

Glad to join up, thank you. Noticed a bit of numbing under the toe pads, fingers too , beginning a few months ago. Now the doctor has me on Metanx the last month. Not sure it's helping yet. It seems to be progressing a bit....ugh.

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Hello @korgman123, Welcome to Connect, an online community where patients and caregivers share their experiences, find support and exchange information with others. You mentioned that you have a little bit of numbing in your toes and fingers starting a few months ago and the doctor started you on Metanx (vitamin B supplement). Here is some more information on Metanx in case you want to find out more -- Metanx Review – 8 Things You Should Consider: https://www.brainreference.com/metanx-review/

Did your doctor run any nerve conduction tests or other test and provide a diagnosis of neuropathy?

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@johnbishop

Hello @korgman123, Welcome to Connect, an online community where patients and caregivers share their experiences, find support and exchange information with others. You mentioned that you have a little bit of numbing in your toes and fingers starting a few months ago and the doctor started you on Metanx (vitamin B supplement). Here is some more information on Metanx in case you want to find out more -- Metanx Review – 8 Things You Should Consider: https://www.brainreference.com/metanx-review/

Did your doctor run any nerve conduction tests or other test and provide a diagnosis of neuropathy?

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Hello John, my doctor basically examined, no special testing

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@korgman123

He says it's neuropathy.

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Thanks, If it were me, I might be asking him why does he think it's neuropathy. Symptoms can probably be from many things. Here's some more information that might be helpful for you if you need to ask more questions if it doesn't get any better - https://neuropathycommons.org/neuropathy/tests-diagnosing-small-fiber-polyneuropathy

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Hello ~ Anyone have any tried and true treatment for swollen feet and ankles due to neuropathy? Small fiber neuropathy to be more specific. No pain, only swelling. Thank you.

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@retired123

Hello ~ Anyone have any tried and true treatment for swollen feet and ankles due to neuropathy? Small fiber neuropathy to be more specific. No pain, only swelling. Thank you.

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@retired123 I also have lymphedema and my legs and feet swell up a little during the day and I wear compression socks that help. Have you ever been tested for edema or swelling in your feet? Is it just the feet or do the legs also show swelling.

Here's some information that may give you a few things to try if you haven't already seen them.
-- Swollen Feet and Ankles: Treatments to Try: https://health.clevelandclinic.org/6-best-ways-relieve-swollen-feet-ankles-home/

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@johnbishop

Thanks, If it were me, I might be asking him why does he think it's neuropathy. Symptoms can probably be from many things. Here's some more information that might be helpful for you if you need to ask more questions if it doesn't get any better - https://neuropathycommons.org/neuropathy/tests-diagnosing-small-fiber-polyneuropathy

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Thank you John, I'll call my doctor and inquire on these tests

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