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 @janicemjackson, Welcome to Connect. Since you mentioned you also have sciatic pain, I'm wondering if you might find the following discussion helpful:
--- Peripheral neuropathy and sciatica: What helps with the pain?: https://connect.mayoclinic.org/discussion/peripheral-neruopathy-injections-not-working-tramadol-to-control-pa/.
Some people have found that Myofascial Release Therapy (MFR) has been helpful for sciatic pain. There is another discussion on the therapy here:
--- Myofascial Release Therapy (MFR) for treating compression and pain:
https://connect.mayoclinic.org/discussion/myofascial-release-therapy-mfr-for-treating-compression-and-pain/.
Have you heard of Myofascial Release Therapy?
I have been making numerous attempts to JOIN but there is NO 'JOIN' in
the upper right corner of my screen!! AD, when I put i my e-mail and
password~~~NA, except I am not enrolled. I cannot get in to reply to
johnbishop or retrieve other messages . Janice M Jackson
Hi Janice @janicemjackson, You were able to reply to my post so I'm pretty sure that means you are logged into Connect and you don't have to Join. Did you see my previous message? If you click the VIEW & REPLY button at the bottom of this email notification, it takes you to this post. Then if you just scroll up a little you will see my reply to your previous post with a couple of links to other discussions. Since you are already logged in you don't have to join or login to reply to my post or post a new comment/question.
Hi. Thanks for the responses to my message. I'm sorry it has taken me so long to reply. I don't know much about my neuropathy. A Podiatrist did a biopsy on my feet and it indicated that the nerves are healthy. A few years ago a Neurologist conducted electrical tests of the nerves in my legs and feet. I can't remember what he said about the results. They weren't too encouraging. He told me if I started to have pain, to contact him. I need to talk to him again. I'm going to continue monitoring the forum to learn about neuropathy. I have spinal stenosis. Lumbar surgery about 6 years ago, and neck surgery 5 years ago. glen g
Oh, let me see~~~My Neurologist asked if I had ever taken Tramadol & I did have it when I had the broken Tibia. I tolerated it well & was dependent on it during the extreme Physical Therapy sessions. I had a real hummer for a Therapist but after many tearful sessions she was able to get me walking & the balance in tact. Now, however the balance is shot to~~~~! You know, I have other complications like Degenerative Disc Disease. Had a heart attack in 2010, no one in my family had that heart issue. I had the 2nd heart attack in the ICU, had stent and then emergency surgery to correct a faulty connection. I was hospitalized in theDenver/Wheatridge area for 8 days. I have had NO heart issues since!! I also have had Melanoma (1999) with a large biopsy in the middle of my forehead. NOW I have a peculiar mole that has manifested itself smack in the middle of the old scar~all these years later. I always attributed it to High Altitude living and a heavy ski schedule in my 30's, 40,s & 50's. HHHHHMMMM isn't this interesting? NO~~~ My Mother always said "No one cares to hear about our ailments &, you know, she never complained about anything. I know she suffered terribly with osteoporosis! BTW, I have that too! Have lost 4"'s. Aging has not been fun & yet I have so much to be grateful for~~~I live in one of the most beautiful places in the world (Rocky Mountain Nat'l. Park ) is just outside my door and I overlook Fall River. I do have caring family members. Regards, Janice P.S. More than you wanted or needed to know.
what was the dosage fo the tramadol
hello. have been using tramadol 50 mg since the beginning. for a few years only needed 1 a day then had to up it to 3 a day for many years. only about 18 months ago have had to take up to 5 or 6 a day, some 2 at a time depending on the level of pain. during the day I can kind of ignore the pain if it's not too bad by keeping busy and my mind off it so as not to have to take so many pills but sometimes that backfires on me and have to double the pills to dull the pain. can't win. lol.
I am looking for help with foot peripheral neuropathy guessing would be the term. I have been to many doctors but only a band aid. I am on gabapentin 300 mg 3 times a day for 8 years. I am wondering or looking for advice on maybe a surgery which could help me out instead of adding more pain medicine. Any suggestions?
Hello @rez2019, Welcome to Connect. I'm not knowledgeable about any surgery that can provide relief for peripheral neuropathy. The only situation I can think of is if you have a specific compressed nerve issue somewhere and surgery can relieve the nerve compression.
I have idiopathic small fiber PN and shared my story in another discussion here: Member Neuropathy Journey Stories: What's Yours?: https://connect.mayoclinic.org/comment/310341/.
The Foundation for Peripheral Neuropathy has a list of complementary and alternative treatments if you are trying to avoid more pain medication: https://www.foundationforpn.org/wp-content/uploads/2020/08/Complementary-and-Alternative-Treatments-Revised-2020-final.-1.pdf.
Have you looked into any complementary or alternative treatments for neuropathy?
Hi,
My name y it a Marg and I’ve been diognosed with orthostatic tremors. I can’t stand for ant length if time and if I try to do too much my legs feel like I’ve just completed a 10 km run. I feel unbalanced in open spaces. I’m much better if someone is walking on my right side or even a building etc. I’ve researched a bit and as far as I can see everyone has different symptoms. Walking across roads or car parks us a nightmare. Does anyone else have these symptoms and if so how do you deal with it?