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.

I’m new to the group as of today. I have poly neuropathy. I’ve had two EMG tests, and I’ve gotten a little worse. Sometimes (right now), the pain is so bad I can’t stand it, but the main thing bothering me is loss of balance. I can be walking across the room, or even standing, and I’ll fall down. I can’t hardly get up when I fall down, which is troubling. I use a cane, except in my home, because everything is level, and I hold on to walls, furniture, etc. It started about 12 years ago as tingling in my right foot, so I went to foot doctors. The foot doctors finally said it was coming from my back, so I went to back doctors. The back doctors said, no, it was my feet. I have cervical stenosis and degenerative disk disease and other back problems, but the neurosurgeon says the PN isn’t coming from my neck or back.has anyone had luck with surgery?

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New problem: peripheral neuropathy and aching pain - arms and legs - when I lie down to try to go to sleep. This pain is directly tied to my lying down. Going to Mayo Clinic July 2021 for EMG and other tests.

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@bouf1948

I’m new to the group as of today. I have poly neuropathy. I’ve had two EMG tests, and I’ve gotten a little worse. Sometimes (right now), the pain is so bad I can’t stand it, but the main thing bothering me is loss of balance. I can be walking across the room, or even standing, and I’ll fall down. I can’t hardly get up when I fall down, which is troubling. I use a cane, except in my home, because everything is level, and I hold on to walls, furniture, etc. It started about 12 years ago as tingling in my right foot, so I went to foot doctors. The foot doctors finally said it was coming from my back, so I went to back doctors. The back doctors said, no, it was my feet. I have cervical stenosis and degenerative disk disease and other back problems, but the neurosurgeon says the PN isn’t coming from my neck or back.has anyone had luck with surgery?

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Hello @bouf1948, Welcome to Connect, an online community where patients and caregivers share their experiences, find support and exchange information with others. I have small fiber peripheral neuropathy and can understand the balance issues. I've become quite good using the senior shuffle when I first get up from sitting or start walking. So far I don't need a cane but I do use a walker when I have to get up in the middle of the night and use the bathroom.

You might find the following discussions helpful.
-- Having trouble keeping your balance?: https://connect.mayoclinic.org/discussion/having-trouble-keeping-your-balance/
-- Myofascial Release Therapy (MFR) for treating compression and pain: https://connect.mayoclinic.org/discussion/myofascial-release-therapy-mfr-for-treating-compression-and-pain/

Is your neurosurgeon recommending back surgery?

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@total99

New problem: peripheral neuropathy and aching pain - arms and legs - when I lie down to try to go to sleep. This pain is directly tied to my lying down. Going to Mayo Clinic July 2021 for EMG and other tests.

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Hello @total99, Welcome to Connect, an online community where patients and caregivers share their experiences, find support and exchange information with others. You may find the following discussion helpful.

Neuropathy Pain at Night: What helps?: https://connect.mayoclinic.org/discussion/night-pain-2/

Do you have neuropathy pain during the daytime? Can you give us an update on what you find out at your Mayo Clinic appointment in July?

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Good morning, I am new to this group and found it supportive just to open some of the posts here and see myself. This has been such a life changing experience that I knew I needed to find other people who were experiencing the same thing. I am not a patient of the Mayo Clinic and am hoping that does not matter for participation in the support group. I have Sensorimotor Peripheral Neuropathy. It is active in my arms, hands, legs and feet, bladder and I suspect digestive system. Although I have been diabetic insulin dependent for many years, I also have multiple auto immune diseases. I started falling in early December of 2020, dizziness, hands falling asleep when I would hold my cell phone, urinary incontinence and just recently bowel incontinence. I now use a walker and a wheel chair and have gone on short term disability. This came on suddenly and has progressed since it presented itself. Glad to be part of the group. LJarman

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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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I have just moved from the foot numbness/tingling stage to a point where the sharp, severe pain arrives mid-sleep hours. PCP prescribed gabapentin without much success. Now I rub capsaicin on painful areas and get enough relief to get through the night. No problem -- so far -- during the day. Any suggestions as to how to ward off increasing problems with this PN? Age 89 with routine arthritis but otherwise in OK health.

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I have noticed that I seem to have worse arm (shoulder to fingers) pain when sitting in a chair with arm rests. IOW both arms simply at my side and resting on the arm rests. I have thought that it might be related to nerve compression around the elbows, but it still happens even if I use a pillow. Obviously when we experience pain we try to figure out what is causing it and more importantly what *not* to do.

Has anyone else had this?

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@tonytrollope

I have just moved from the foot numbness/tingling stage to a point where the sharp, severe pain arrives mid-sleep hours. PCP prescribed gabapentin without much success. Now I rub capsaicin on painful areas and get enough relief to get through the night. No problem -- so far -- during the day. Any suggestions as to how to ward off increasing problems with this PN? Age 89 with routine arthritis but otherwise in OK health.

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Hello @tonytrollope, Welcome to Connect. Are you able to share a little more about your sharp, severe pain that wakes you up in the middle of the night? Is it in both legs, just one foot or both feet? It sounds a lot like it could be something similar like Tarsal Tunnel Syndrome.

"Compression of some nerves in your ankle can cause tarsal tunnel syndrome. Compression of the sciatic nerve in your back and legs can cause foot pain, too. In both cases, the pressure on these nerves tends to be worse at night, which leads to increased pain. Apr 7, 2021" -- Foot Pain At Night: 8 Causes, Treatment & Prevention: https://www.healthline.com/health/foot-pain-at-night

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@birdman518

I have noticed that I seem to have worse arm (shoulder to fingers) pain when sitting in a chair with arm rests. IOW both arms simply at my side and resting on the arm rests. I have thought that it might be related to nerve compression around the elbows, but it still happens even if I use a pillow. Obviously when we experience pain we try to figure out what is causing it and more importantly what *not* to do.

Has anyone else had this?

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I get that tingling in my arm and hands sometimes when I sleep on my side with my arm under the pillow or at the edge of the pillow. I wonder if it may just be the position of the arm and it may be compressing or stretching the nerve? Here's some info that discusses the related nerves, etc..

What to know about a pinched nerve in the arm: https://www.medicalnewstoday.com/articles/pinched-nerve-in-the-arm

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@ljarman

Good morning, I am new to this group and found it supportive just to open some of the posts here and see myself. This has been such a life changing experience that I knew I needed to find other people who were experiencing the same thing. I am not a patient of the Mayo Clinic and am hoping that does not matter for participation in the support group. I have Sensorimotor Peripheral Neuropathy. It is active in my arms, hands, legs and feet, bladder and I suspect digestive system. Although I have been diabetic insulin dependent for many years, I also have multiple auto immune diseases. I started falling in early December of 2020, dizziness, hands falling asleep when I would hold my cell phone, urinary incontinence and just recently bowel incontinence. I now use a walker and a wheel chair and have gone on short term disability. This came on suddenly and has progressed since it presented itself. Glad to be part of the group. LJarman

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Hello @ljarman, Welcome to Connect, an online community where patients and caregivers share their experiences, find support and exchange information with others. Connect is open to all who seek support and want to connect with others who share similar symptoms. I'm glad that you found Connect. It's a great place to learn what others have shared and hopefully find something that helps with your symptoms. There are many different discussions in the Neuropathy group and if you don't see what you are looking for it's easy to start another discussion.

Here are a few discussions you may want to check out and see what others have shared...
-- Generalized Sensorimotor Peripheral Neuropathy over my entire body: https://connect.mayoclinic.org/discussion/back-again-its-been-a-while/
-- Member Neuropathy Journey Stories: What's Yours?: https://connect.mayoclinic.org/discussion/member-neuoropathy-journey-stories-whats-yours/

Can you share which of your symptoms bothers you the most?

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