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.
Hello Donna,
I am so sorry you are going through this! You asked "can I ever feel somewhat normal again" and my answer to that is yes you can have a normal life, but it might be different than what you currently have. What I mean is you will have to learn how to manage your pain, either with medications ( as with the gabapentin that your physician has prescribed), with dietary changes, and perhaps with changes in other aspects your life. I think the worst part for me was accepting that I now have a chronic illness, but it took awhile and during this time I read and read and read scholarly articles relating to neuropathy. Physical therapy help me improve my lower extremity muscle strength, occupational therapy assisted in helping me reestablish fine motor movement of my upper extremities and Mayo clinic Connect helped me realize I wasn't alone and many people were also living with this disease. The mentors of this group frequently provide excellent website sites with helpful information and resources. One thing I can't say enough is you must be your own advocate and keep asking questions....... You will have great support with this group. Please keep us up dated on your progress.
Kim
I have neuropathy. Announced by my family doctor He tells me nothing I am learning
Donna - Just want to follow up on what John Bishop mentioned and what struck me a while back when I first came on board with Mayo Connect is what he refers to as a new normal. That stuck in my head. I have very similar symptoms to John, numbness, poor balance and I have bi-lateral drop foot and I not only found a new normal but what I find is that I must adjust to a changing new normal. My idiopathic PN is different than it was five years ago. We still travel a lot and continue doing many of the same things that we did before my diagnosis. We just do it a little differently, but we do it. Wish you the best! Ed
I would recommend that you get copies of all lab work, testing and procedures. I have 8 years worth, filed by type. It’s interesting to study them when I have a new question. For example, I was unsure about my B12 levels, and found results from a year ago, which show a normal level. I promise you any new specialist you see will be happy to see these records.
Hi Donna- welcome to the club 🙂 I second John’s mention of the Foundation for Peripheral Neuropathy’s website. I was started on Gabapentin for terrible nighttime pain (think woken up by a sledge-hammer crashing into your leg). I developed breathing problems on G. (respiratory issues are on the list of side effects). The website and the Mayo Clinic website have suggestions for mindful ways to control pain. Someone told me once the Lamaze method was basically self-hypnosis- I had two kids that way and it worked, so I decided to really try the mindful ways and they really work for me. One less medication off the list feels good. I’ve also been told the new Pain Management clinics lean heavily into the mindful ways too.
I too was very active and now have the weakness, pain, numbness, balance issues. No more badminton with the grandkids, but I can do Red Light, Green Light pretty great 🙂
Hi I'm sorry you're going through that. you seem to have acceptance which is good. Every try accupuncture? Or how about going on you tube and typing in binarual beats for PN and listen it seems to help people. Anyways I have it all over my body form drinking too much. I'm sober but my body is messed up. I'm dealing more with limitation and weakness. Try the binaural beats on you tube. Good Vibes and Ninad music help me a little. Hang in there. Tony
I was wondering if anyone has learned a way or a treatment to regain strength from nerve damage from neuropathy? When I google it, it seems pretty bleak but I still want to have some hope. Is there any supplements that could improve muscle strength? etc....
Hi Debbie you're story is inspiring. I hope you the best. I'm dealing with increased muscle weakness in my arms and body and It's very hard to come to terms with. I hope I can regain strength like you did some day. I have to get out my head because it's negative and super sad. I guess making myself think positive should be a daily practice. Anyways take care.
Thank you, Tony.
I have tried many types of medications prescribed by doctors. They do not seem to work and I do not know why I take them. I also bought massagers for hands, legs and feet to ease the pain a bit. This is the closes cure that I have for a little comfort when at home but for others I suffer as usual.
I will research binaural beats and I do have doubts for an ultimate cure.
Again, thank you.
Also, very important to check B-6 levels since a higher than normal level can result in B-6 toxicity resulting in neuropathy. Many doctors are unaware of this thinking that since B-6 is water soluble, that the excess will be eliminated naturally.