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.
I have peripheral neuropathy in my hands and feet. It was diagnosed about 12 years ago. Over time it has become very painful. I was told that it usually goes along with diabetes. But I don't have diabetes.
Hello Lois (@loisogden), Welcome to Mayo Connect. We are happy you found us. Connect is a great place to share your health concerns, ask questions and learn what others are doing for treatments. I also have peripheral neuropathy. You can read my story here: https://connect.mayoclinic.org/discussion/anyone-here-dealing-with-peripheral-neuropathy/?pg=43#comment-65985
There is some information on diabetes induced neuropathy on Mayo Clinic's website here:
http://www.mayoclinic.org/diseases-conditions/diabetic-neuropathy/basics/causes/con-20033336
Can you share what you are doing to treat your neuropathy now? Also, have you met with a neurologist and had any tests for nerve damage (EMG)?
John
Welcome to Connect, Lois @loisogden . I also have peripheral neuropathy in my feet, and the pain part came on quite quickly with me, as well. I'm not diabetic, so that means they don't know the cause of the neuropathy. From all I've read, it's often not possible to pinpoint an exact cause. That's true for me.
I've tried every medication for neuropathy pain that's available, and many more that are off label, and the only one that has touched the pain is morphine.
In June, I had a spinal cord stimulator implant, and I have experienced at least 80% relief from the pain. It doesn't help numbness or pins and needles. I'm an advocate now for the Burst DR spinal cord stimulator, for sure. I know it doesn't work for everyone, but I guess I'm among the fortunate ones.
Have you looked at the various discussions in the neuropathy group? You'll find a lot of conversation and useful information that I hope will be helpful.
Jim
Thanks Jim I've never been offered this treatment.
Thank you Jim for your reply. You have shared a lot of interesting information with me, it kind of puts a new picture on it. The whole neuropathy picture is is new for me and a bit confusing with all the elements I have again not knowing what is causing it. But I'm hoping that something will be teased out in the near future with the referral to a new Dr. I'd like to look at some of the conversation that has gone on within the neuropathy group, as soon as I figure out how to find where it is.....
Lois, if you go to your home page, you should see a place to see the list of groups. Scroll down to the Neuropathy group, click on follow, and click on discussions. @loisogden
@sevey41
Boy, do I know about the shoe problem. I have enough shoes for 10 men, but I'm going through them now and getting rid of the ones that hurt my feet. I wear a pair when I have to go to town, which always means a lot of walking. That's my test. I have a lot of insoles that help cushion my feet. I've started buying shoes on the large side, to leave plenty of room for whatever insoles, or combination of insoles, work best. I keep some shoes that I know I can't walk far in, for days when I just sit in meetings or the recliner. I have one pair of slippers that have just the right amount of cushion that I put on as soon as I step in the house. I make myself only wear them indoors so they'll last longer.
Anyway, shoes become a big deal. The style now is to wear casual shoes with a suit. I haven't made that plunge yet, but I may soon.
Jim
I too know about wearing comfortable shoes. I probably have 200 or more shoes, but only can wear a few of them. I need to donate the others. I always enjoyed my beautiful shoes when I was working in an office or travelling. I'm retired now. My neuropathy in my feet is mainly on the tops and sides of my feet. I can walk fairly well if I have comfortable shoes on. I also have a pair of slippers that are well padded with memory foam. I put them on as soon as I get in the house. For my hands I have snug fitting gloves that I got from a medical supply store. I wear them at night when my hands are hurting. I have so many different problems that it is a challenge to take care of all of them. Most of my problems don't show so people don't think I am so ill. The only thing that shows is the disfiguring in my hands from the rheumatoid arthritis.
@sstouten
I wear gloves to drive. My hands ache if I don't use them. I have arthritis in my left index finger and my right thumb, and growing. So far, I can still play the piano.
Jim
Has anyone ever heard of NeuroGenx ?I received an article in a local paper that advertises, "Reversing Neuropathy".
It reads, Neurogenx is non-narcotic, non-surgical and non-invasive. The person is board certified foot surgeon with the Board of Podiatrics and wound management. I have not made an appt. but.... was wondering