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.

@mznecie

My name is Charlotte, and I have been with a disease that is causing my neoraphy issue from my waist, to my feet. the flare up sometimes are unbearable.

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I understand what do you do to ease the neuropathy?

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@twobrooklyn

If it’s legal i your state give it a try, some people get decent relief,

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It's legal in NJ just don't know where to begin since I'm not sure where to go or how much to take seeing I'm on a lot of medication.

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Hi my name is Diane and I have autonomic small fiber neuropathy. I started having motility issues since 2014. I was recently diagnosed with mild esophageal dysmotility. Has anyone else ever been diagnosed with this and if so what was the treatment.

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@dianecostella

Hi my name is Diane and I have autonomic small fiber neuropathy. I started having motility issues since 2014. I was recently diagnosed with mild esophageal dysmotility. Has anyone else ever been diagnosed with this and if so what was the treatment.

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Hello @dianecostella, There is another discussion you might find helpful that includes esophageal dysmotility as one of the pieces of CREST Syndrome - https://connect.mayoclinic.org/discussion/crest-syndrome/. @jimhd may also be able to share some information or suggestions with you.

Until others are able to respond to your question, here is some information I found that might be helpful.
"What is the treatment for esophageal dysmotility? Achalasia may be treated with drugs that relax smooth muscle and prevent spasm, such as isosorbide dinitrate or nifedipine. Pneumatic dilation is a procedure that dilates the LES with a high-pressure balloon." --- FAQs about Swallowing Disorders | Johns Hopkins: https://www.hopkinsmedicine.org/gastroenterology_hepatology/diseases_conditions/faqs/swallowing_disorders.html

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@faust73

Morning Chris I never had neuropathy before until I got my Pfizer COVID shots but getting the booster really got the neuropathy to be much more intense. My symptoms are bottom of my feet go numb my legs burn - tingling and pins and needles. I take diazepam for the nerves and it helps some but wears off quickly as seeing I can only take 2 pills a day. I haven't been diagnosed by a doctor per say going to see a new neurologist end of January. I go for pain management and between having issues with my back and the neuropathy (which the Pain Management told me I have) it's been a nightmare for me. Having all these issues have caused me to not be able to do anything can't go for long walks with my pups and an effort sometimes just to function. I've been working out over 30 years I have a full gym in my house but some of the machines I can't use because it causes the neuropathy to increase. I'm going for physical therapy this month and hope that will help. As far as cannabis I know people who have highly recommended using it for pain relief but I take so much medication I have no idea what I should do. I wouldn't know where to begin or how to use cannabis everything just confuses. I'm getting more and more depressed and very frustrated. Any information you can give me would be much appreciated. Jo

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I had a similar experience with the Pfizer vaccine. I won't be getting the booster. My blood work indicates an immune-mediated peripheral neuropathy. The good news is that the symptoms improved substantially about 9 months after the last vaccine. There is a Facebook group for vaccine-injured people called Neuro V Long-Haulers. Everyone there reports about a 9 month timeline for substantial improvement of the peripheral neuropathy symptoms. You could receive advice and support by joining that group. I suggest asking the neurologist to check your autoimmune antibody titer and also your alpha-2-globulin levels. (These are not routinely measured.) My titer increased but then increased again substantially about 8 months after the vaccine. I discovered in the earlier months, that I could control the pain by avoiding sitting completely. Apparently, my sciatic nerve and/or spinal chord was inflamed. My tolerance for sitting is now much improved.

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@centre

I can’t recommend enough to call around until you find a PT practice that does computerized Gait Analysis. The PT puts what looks like a gel orthotic with an ankle attachment in each shoe and has you walk while they view what’s happening on the laptop screen. The graphs that come up in “real time” show where you are putting pressure on each part of the soles of your feet as you walk (now able to compare the affected and unaffected leg).
With me- I have (R) lower leg neuropathy with weakness, numbness and tingling. The graphs showed that I was getting very little “push-off”” from my toes and the ball of my foot as I stepped through each step. The PT made a metal rocker and embedded it in the shoe, so now I get a mechanical push off, rather than landing flat. The graphs also showed that I was tending to walk on the outer edge of my foot (my sole has very little feeling), so he added built-up to the inside of my shoe so my ankle is positioned in much better alignment, which has caused my knee to be in better alignment, which has led to markedly diminished knee pain from just being up and about. He did recommend I shorten my walk (used to do 3-4 miles/day) and keep it to around the block twice, paying attention to good form (with the affected leg- concentrating on exaggerated heel strike and active push-off, shortened step length). It’s made such a difference!!
The left shoe sole was built up so the shoes are the same height. You can’t tell they are adaptive shoes- the PT recommended lace-ups, I bought Brooks sneakers as they have a mesh top to accommodate comfortably the hammertoes I’m now getting on the affected foot due to the imbalance of muscle tone, due to the neuropathy (the gift that keeps on giving!). I bought two pairs at Dick’s Sporting Goods, so I could be sure to always have a pair to wear.
I understand John recommending a podiatrist but I would strongly vote for a PT practise for the computerized gait analysis- not just someone watching from behind as you walk, but actual data to address the specific problems that can be addressed with specific adaptions. If none of the PTs do the shoes themselves, they will know someone who does and will give them specific instructions, then have you return for PT follow-up to see if the adaptions need to be adjusted.
Good luck and don’t be discouraged if takes a lot of calls. I drove two hours each way four times to get these shoes and they have made an incredible difference in my life- I can enjoy walking again, my knee doesn’t hurt, I’m not being nudged off-balance, I could go on and on!!!

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Good information. In what state did you find your specialized PT?

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@kwfinnie

Good information. In what state did you find your specialized PT?

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PA, but I think if you call a large practice or a Rehab Hospital, if the person who answers the phone has no idea what you’re talking about, then ask to speak to the PT director or leave a message for that person to call you back or do they have a work e-Mail address you can write to? The director will know exactly what you’re looking for and either they have it or they’ll know a practice that does. Can you tell I got waylaid at the receptionist level? 😂 But we neuropathy folks are good at perseverance, aren’t we?!

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@faust73

Morning I have Neuropathy in both my legs and feet. Tried multiple medications and even massage therapy. Nothing seems to work some days are better than others but when it's bad it's bad. I never had this problem before and not sure what started this Neuropathy. I'm inclined to think that I got my Pfizer booster shot and ever since then I've had these symptoms. I also had back surgery 2 years ago with a fusion on L4/L5 and have never been the same. It's been up and down with P/T and medications but nothing helps. Thinking about marijuana. Any thoughts would be appreciated. Thank you JoJo

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Cut out sugar in all forms ( including bread,) use almond flour. No diet drinks. I did a strict diet plus red light therapy. One can get a good light at sgrow they are on Amazon. I use a lot of natural supplements. Try Mega Benfototiamine & Optimized Carnatine the first is a form of B-1 but can penetrate.bllod/ brain barrier the latter is a amino acid. If you are interested private msg me I will be glad to tell.you where I get mine from and why

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Hello I've had neuropathy in my ' and legs For will more than 10 years. But about 2 months ago, Tingling and a sensation of numbers started in my hands. My MRI shows Degenerative disk disease and osteoarthritis from lumbar to cervical. This sensation in my hands has become unbearable and cruel. Pain is horrible, especially at night. There is nerve impingement at C6-7. My left hand is awful but now it has begun in my right. Pain management did a cervical epidural at that location a out two weeks ago. The pain has only grown worse. What do I do? To make matters worse, I'm a painter. Please help. I am in CT. I can't put the degree of pain into words. Please excuse errors as I have dictated this. I am 75.

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@gladrag

Hello I've had neuropathy in my ' and legs For will more than 10 years. But about 2 months ago, Tingling and a sensation of numbers started in my hands. My MRI shows Degenerative disk disease and osteoarthritis from lumbar to cervical. This sensation in my hands has become unbearable and cruel. Pain is horrible, especially at night. There is nerve impingement at C6-7. My left hand is awful but now it has begun in my right. Pain management did a cervical epidural at that location a out two weeks ago. The pain has only grown worse. What do I do? To make matters worse, I'm a painter. Please help. I am in CT. I can't put the degree of pain into words. Please excuse errors as I have dictated this. I am 75.

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Hello @gladrag, Welcome to Connect. I know it's difficult when the pain keeps getting worse and you haven't found anything that helps. I also have degenerative disc disease and osteopenia but so far my pain is mostly limited to my lower back and it's more of an ache. I also have idiopathic small fiber peripheral neuropathy with just numbness in the feet and some in the legs. I shared my story and what helps me along with other members in the following discussion.

Member Neuropathy Journey Stories: What's Yours?: https://connect.mayoclinic.org/discussion/member-neuoropathy-journey-stories-whats-yours/

You mentioned you are seeing a Pain management doctor and had a cervical epidural about two week ago. Have you told the doctor the treatment hasn't worked and the pain is worse?

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