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.
Do you think boron might help with neuropathy pain or does anyone in the group have experience with this?
@jimhd Last month I underwent a 7-day trial with a Medtronic SCS and found that it helped some, particularly in my back and my nighttime foot pain, but didn't offer relief for bilateral miralgia paresthetica and knee pain. I researched more about lateral femoral nerve, and thought that could be the issue. I've messaged my doc at Mayo and asked if it's possible to insert SCS leads at two different locations on my spine, and if so, might he be willing to try to insert one in my very scoliotic lumbar spine. Here's hoping!
@faithwalker007 I can't find any of your books in my local library system or on Mobius. Being a gypsy and knowing how expensive it is to move books overseas, I gave up buying books a long time ago.
Thank you Colleen! I hope to learn a lot here!
My name is Renee Blare
You have to spell the last name right lol. I have an author page on Amazon.
As for library? Not sure
I have neuropathy in my feet, only at night. Drs. have me on pregabalin 75 mg. I'm suppose to take it 2x a day, but I can't due to it making me drowsy, so only at night do I take it. I have started with Acupuncture and a massage called Tunia. Both have helped me tremendously. Has anyone else ever used an alternative way besides drugs?
Hi greeneyes55. What does the neuropathy in your feet feel like?
My husband describes it as take a flat board and slap it on the bottom of his feet and the result is the pain... stinging, burning, numbing at first, and cold and hot at the same time.
His words, not mine.