Anyone here dealing with peripheral neuropathy?

Hi - I am very new to this site.
I have idiopathic sensorimotor peripheral neuropathy, got official dx at Mayo in MN in Feb 2020 but been dealing with this since 2016. Started with numbness both feet 2015, drop foot in both 2017, about 70% numbness shins down to toes. Since Aug 2020, unusual sweating upper part of body. I do not have dry eyes, mouth. Small amounts of neuropathy in finger tips. I've heard pinched nerve from a fall can trigger neuropathy.

Hi every one! New to site. 6/25/2022. I had neck surgery in April 2021. Over a year ago. Now I have the two fingers on my right hand, that I cannot use. I went to an neurological Doctor Who gave me a EMG test. Then, she diagnosed me with having a ALS. She referred me to another doctor to confirm her findings. But, the next doctor felt that he could not say one way or the other whether I had ALS or not. So, that doctor said that because of prior surgeries to my spine and cervical spine, he cannot say for sure. Now they have sent me to an ALS specialist. So far, I have had one blood test, and I'm waiting to have two MRIs. One of my cervical spine and another of my thoracic spine. None of these doctors are close to my home. I live in New Jersey near the Atlantic ocean. And they sent me to an ALS specialist in Philadelphia. We will see what happens. I am certainly getting fed up with this runaround. I had, like I said, next surgery in April 2021.

And like they say, if it looks like a duck, if it acts like a duck. It must be a duck. It had only been one month since my neck surgery, when the third and fourth digit on my right hand acted up.
Remarkable!

Hi @njed, Welcome to Connect. I think you are right, a pinched or compressed nerve can cause nerve pain and other symptoms. It sounds like you don't have any pain with your diagnosed idiopathic sensorimotor peripheral neuropathy, just the numbness.

Did your Mayo Clinic neurologist suggest or start any treatments?

Yes I’m dealing with it and it’s very painful on a daily for me mine started with a shingle on my arm that the doctors thought was a spider bite later I found out it was shingles and I had nerve damage from shoulder to finger right arm I was told by several doctors to get the vaccine since then I did. I had it injected into the left arm now the left arm has just as much nerve damage as the right arm I’m also experiencing nerve damage in my left leg none of this happened prior to me taking this vaccine. My auto immune system is also off and they don’t know why I am so depressed and I cry on a daily due to the pain I really wish I could find help an explanation for this. 😰

Hi @lesterjo, Welcome to Connect. It can be quite discouraging when trying to get a diagnosis and a treatment that helps. There is another discussion you might find helpful --- Neuromuscular Testing and Waiting for ALS confirmation: https://connect.mayoclinic.org/discussion/neuromuscular-testing/.

When is your appointment with the ALS specialist in Philadelphia?

Hi every one! New to site. 6/25/2022. I had neck surgery in April 2021. Over a year ago. Now I have the two fingers on my right hand, that I cannot use. I went to an neurological Doctor Who gave me a EMG test. Then, she diagnosed me with having a ALS. She referred me to another doctor to confirm her findings. But, the next doctor felt that he could not say one way or the other whether I had ALS or not. So, that doctor said that because of prior surgeries to my spine and cervical spine, he cannot say for sure. Now they have sent me to an ALS specialist. So far, I have had one blood test, and I'm waiting to have two MRIs. One of my cervical spine and another of my thoracic spine. None of these doctors are close to my home. I live in New Jersey near the Atlantic ocean. And they sent me to an ALS specialist in Philadelphia. We will see what happens. I am certainly getting fed up with this runaround. I had, like I said, next surgery in April 2021.

And like they say, if it looks like a duck, if it acts like a duck. It must be a duck. It had only been one month since my neck surgery, when the third and fourth digit on my right hand acted up.
Remarkable!

Welcome @daphnebattle, I can't imagine the pain you must be in from the shingles. Was it the Shingrix vaccine that you got?

If I am fortunate about anything involving this, I do not have pain. No treatment plan other than to do physical therapy if possible and walk flat surfaces when possible. The thinking in 2020 by Mayo was that my issue could be genetic related which does often appear in 6th generation of life, I was 64 when this started. Went to Johns Hopkins in Baltimore, they came up with the same thinking, genetic. I've had blood work done in Phila for a variety of possibilities, all came back normal. My suspicion is that without a cause, a treatment plan is difficult, I am not diabetic. I do wear walk-on-flex which helps with balance.