Living with Neuropathy - Welcome to the group

John thanks for the information.
My son has Peripheral Neuropathy and he also has Planter Facscitis. I thought all his issues were neuropathy. After talking to him again my symptoms might be fascitis. It feels like stones in my shoe at times and is strictly on the sole of my foot. He said to stretch that area by rolling them on a ball several times a day. I will try that first before rushing to the doctor.

There is a another discussion you might find helpful if you have plantar fasciitis.
-- Plantar Fasciitis: How did you get rid of it?: https://connect.mayoclinic.org/discussion/plantar-fasciitis-1/

Sounds like your son shared some good info with you. Hope you can give us an update if it helps you.

Hello @brklimeks, I just responded to another of your posts and was reviewing your story. I really am shocked that you were taken off Gabapentih and Cymbalta totally by your provider before starting medical cannabis. I have been using both of those medications for quite some time along with the cannabis. I need Gabapentin for the tingle tangles in my hands. I need the Cymbalta to help control my anxiety level. Anxiety creates pain. Neither interferes with my "marijuana" program for pain control. MJ is not a be all end all option, in my opinion in that it doesn't take care of every neuropathic symptom.

I am so sorry about your psychotic episode. That had to be very frightening. I understand what it feels like to be on that hamster wheel. Do you feel mentally safe now?

Chris

Yes I’m fine now. Thank you for your understanding. After two years since my psychiatric hospitalization, I’m just putting the pieces together. I asked to be taken off or titrated down on my meds so I could use MJ and he was not happy. He was as not clear on a schedule/dosage for reducing my meds, only the order in which I was to stop them. I was on Cymbalta for pain as well as the Gabapentin and Norco (PRN). I’m not sure if that was reported back to him or the practice owner by the psych department. I’m on so many meds I keep thinking that I should see someone at to just go over all of them. Thanks again!

Ooops! I just saw this now after I already started talking about what I am calling my peripheral neuropathy! I think I pretty much introduced myself in the comment I wrote.

After 2 1/2 years of lower leg neuropathy and having a lot of physical therapy, blood tests, spinal MRI, x rays, ultrasound, and EMG, massage, massagers, nerve stimulators, the next suggested test is a nerve biopsy. How is a nerve biopsy going to help or what is it going to rule out?

Hello @nft, Welcome to Connect, an online community where patients and caregivers share their experiences, find support and exchange information with others.

"Nerve biopsy is the removal of a small piece of nerve for examination. Through a small incision, a sample of nerve is removed and examined under a microscope. Nerve biopsy may be performed to identify nerve degeneration, identify inflammatory nerve conditions (neuropathies), or to confirm specific diagnoses." -- Nerve biopsy Information: https://www.mountsinai.org/health-library/tests/nerve-biopsy

Are both legs affected?

Hello everyone. I’m 35 years old and have SFN. It is painful and awful. I am wondering if people here with idiopathic small fiber neuropathy are able to still have good quality of life. Which is my main concern. I just don’t want to live a life of chronic pain that is not well controlled. Wondering how people cope with this illness and maintain everything else life has to offer. Wishing all of you well.

Any one else with severe nerve damage ..from Cipro ?ive been totally incapacitated for 8 yrs since my 3rd day of Cipro ..i was a healthy 47 yr old since im now a55 yr old invalid w 0 quality of life and drs shrug n do nothing ..

My neuropathy is affecting my balance. I have fallen which really concerns me. Is there any help for these issues that I'm haing.