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.

Hi I suffer like most of us on here with Peripheral neuropathy. I Am just starting on Gabapentin. and if that doesn't work Dr. say Lyrica?? Don't know what else to say. Hope we all find a miracle to help us with this pain.

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@grammlyn

Hi I suffer like most of us on here with Peripheral neuropathy. I Am just starting on Gabapentin. and if that doesn't work Dr. say Lyrica?? Don't know what else to say. Hope we all find a miracle to help us with this pain.

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@grammlyn Lyrica helps many people. I started taking it a couple of years ago, and it was really working for me. Unfortunately, I had a serious reaction to it and spent 3 days in the hospital. I was really disappointed that I couldn't take the only medication that relieved my neuropathy pain. I hope that you will find the one that works for you.

Jim

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@catro

I have a form of PN that causes pain in my feet and lower legs and recently in my hands. But I can be pain free all day, go to sleep and three hours later wake up in pain. Has anyone given you an explanation for what happens after you go to sleep that causes the pain to come on?

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@catro I have the same problem. The pain level during the day seems to have no connection to my pain in the prone position. Within a few seconds after lying down my feet start hurting. Same thing in my recliner. I'm going to show my pain specialist the article @steeldove posted and see if it's something I should try.

Jim

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@jimhd

@grammlyn Lyrica helps many people. I started taking it a couple of years ago, and it was really working for me. Unfortunately, I had a serious reaction to it and spent 3 days in the hospital. I was really disappointed that I couldn't take the only medication that relieved my neuropathy pain. I hope that you will find the one that works for you.

Jim

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A lot of us are like you! Drug s, shots, ! You have to do some type of exercise if your neuropathy is from spinal stenosis! Gabapentin, lyrica and back shots didn’t help me! Maybe they will help you! Good luck!

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@jimhd

@grammlyn Lyrica helps many people. I started taking it a couple of years ago, and it was really working for me. Unfortunately, I had a serious reaction to it and spent 3 days in the hospital. I was really disappointed that I couldn't take the only medication that relieved my neuropathy pain. I hope that you will find the one that works for you.

Jim

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Hi John,. You do just a wonderful job and I know all of us are grateful and very appreciative. I use a very inexpensive tens machine and it does wonders.🙂 Perhaps it can help others as well. Rose

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@johnbishop

@helennicola I think the link provided by @steeldove sheds some light on your question about feeling pain more at night. Here's the link mentioned in the earlier post - https://www.healthline.com/health-news/this-is-the-worst-time-of-day-for-pain-sensitivity

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Thanks John, I found it very helpful. Helen

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The Foundation for Peripheral Neuropathy kicked off a new series of patient education webinars that I think might be interesting for those of us with peripheral neuropathy.

Webinar: Living Well with PN: Session 1: Managing the Symptoms of PN with Dr. Shanna Patterson
-- https://www.foundationforpn.org/living-well/fpn-media-center/webinar-managing-symptoms-of-pn/

They also have some more on their latest news page here: https://www.foundationforpn.org/news/

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@johnbishop

The Foundation for Peripheral Neuropathy kicked off a new series of patient education webinars that I think might be interesting for those of us with peripheral neuropathy.

Webinar: Living Well with PN: Session 1: Managing the Symptoms of PN with Dr. Shanna Patterson
-- https://www.foundationforpn.org/living-well/fpn-media-center/webinar-managing-symptoms-of-pn/

They also have some more on their latest news page here: https://www.foundationforpn.org/news/

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@johnbishop Thank you for sharing John!

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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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Please respond does the injection of Wharton's Jelly cure Neuropathy?

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