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.
@helennicola, Thanks for your reply. I don't know if it makes a difference to know whether it is SFN and idiopathic. Obviously, you do not have diabetes nor have you been through chemotherapy. Those pre-conditions are treated somewhat differently.
Gabapentin at 300 mg in the evening is the very minimum dosage. Are you struggling with that in terms of sleeping or feeling stressed? You mentioned that you have less patience? Do you now practice yoga, meditation, and mindfulness? I just returned from my annual 3-day retreat where I learned the things I need to do based upon where I am with SFN.
And this time there were new opportunities. For example, I belong to a sangha. Tonight the sangha is coming to my house to take a walking meditation along the Mississippi River and then some mindful meditation and homemade treats around the fire-pit. So, as the hostess, I can feel the stress building. My head is dancing with little zappers. I will do some pre-event meditation. Hopefully, that will calm me down. Just being with these ladies for their love and support is amazingly helpful.
And then, if you are comfortable sharing.....do you use medical cannabis? If so, how has that experience been for you? Do you live in a state with access?
Bye for now, I need to get to work on the fruit for the sangria. Let us know how we can help you. Just make sure you are showing self-compassion and putting yourself first. We cannot care for others until we care for ourselves. We need to feel what that is like.
May you feel safe and protected today. Chris
Hi Jeff, So you tapered off the Lyrica and then resumed? Did you ever take Gabapentin?Is your pain such that you thought you could do without the Lyrica? Since my pain is at its worst at night I don’t think I could get through the night without gabapentin but have been wondering if I should try switching to Lyrica. Have you experienced any side effects? Have you tried taking it just at night before bed? My dr. originally prescribed gaba to me 3xday but it really affected my co-ordination and memory. Perhaps that would have gotten better in time but since I play golf and bridge I just tried taking it at night only which works ok for now. (fingers crossed) Good luck to you too!
Hello! Im sorry tp hear of ypur pain. Skin punch biopsy is a simple and factual determination for SFN. Tests for underlying causes include genetic testing, multiple blood draws and spinal tap. I have full body SFN caused by B12 deficiency. Outside of Gabepentin, Lyrica is one to try. I have benefited from the controlled release version of it. I also take Cymbalta for anxiety due to the complexity of the disease and receive lidocaine infusion therapy. A multidisciplinary approach is typically used for SFN. I wish you well and hope you continue to communicate with your neurologist and find what may be able to help you.
Just wanted to be clear that the Lyrica CR (controlled release) is only once a day and does a great job with my pins and needles, zaps etc...
How high can you safely go in daily amount of Lyrica?
Hi @rwinney. Just out of curiosity, does your insurance cover LyricaCR? Mine doesn't. It's very expensive.
Thank you Chris for your thoughts and good wishes. I try meditating (my version) but not too good at it; too many stressful things going on right now, husband having (2)much- needed spinal surgeries coming up, my dog’s heart murmur very bad and me possibly needing another hip replacement. I have not tried med. can. it is not legal in my state but would if I could! I can’t even drink any alcohol because it does have a very negative effect on my pain at night. I do exercise which helps and have taken up painting again so that helps. Have fun with your friends, “laughter is the best medicine” so they say!
The usual dose of Lyrica for peripheral neuropathy is 50-100 mg 3x daily. Maximum dose is 600 mg per day, but that doesn't mean it's safe for you, or any the random person.
I take 300mg of Gabapentin and just started 60 mg of Cymbalta at bedtime . I haven’t found any topicals for stinging.
Actually reading many of the posts are scaring me . Does PN always progress ? Hoping mine would remain
stable . Thanks for your help.
I used to take gabapentin in fairly large amounts. I never really experienced any side effects, but then I have always been an expensive date. I also never knew if it was doing anything, as my symptoms progressed while I was on it. Of course, they may have progressed more it I weren't on it.
I switched to Lyrica just to try it. There doesn't seem to be any difference.
I find that my feet feel much better in warm weather, which it is now. There are so many variables as to how I feel, including emotional ones. It makes it very hard to decide what is working or not, as you probably know by now.
I don't get the sense that that either of them work right away. In my case, if they work at all, it seems to be a cumulative effect over many days. You may have a different result.
Keep experimenting.