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.
The video was helpful. I would like to participate in the program but I understand it cost 40,000 plus staying in a hotel for three weeks. I am retired don't have that kind of cash. Than you John for your reply to me tonight.
What Dr would let you take 3600 MGS of gabrapentin that concerns me ?
Glad to join up, thank you. Noticed a bit of numbing under the toe pads, fingers too , beginning a few months ago. Now the doctor has me on Metanx the last month. Not sure it's helping yet. It seems to be progressing a bit....ugh.
Hello @korgman123, Welcome to Connect, an online community where patients and caregivers share their experiences, find support and exchange information with others. You mentioned that you have a little bit of numbing in your toes and fingers starting a few months ago and the doctor started you on Metanx (vitamin B supplement). Here is some more information on Metanx in case you want to find out more -- Metanx Review – 8 Things You Should Consider: https://www.brainreference.com/metanx-review/
Did your doctor run any nerve conduction tests or other test and provide a diagnosis of neuropathy?
Hello John, my doctor basically examined, no special testing
He says it's neuropathy.
Thanks, If it were me, I might be asking him why does he think it's neuropathy. Symptoms can probably be from many things. Here's some more information that might be helpful for you if you need to ask more questions if it doesn't get any better - https://neuropathycommons.org/neuropathy/tests-diagnosing-small-fiber-polyneuropathy
Hello ~ Anyone have any tried and true treatment for swollen feet and ankles due to neuropathy? Small fiber neuropathy to be more specific. No pain, only swelling. Thank you.
@retired123 I also have lymphedema and my legs and feet swell up a little during the day and I wear compression socks that help. Have you ever been tested for edema or swelling in your feet? Is it just the feet or do the legs also show swelling.
Here's some information that may give you a few things to try if you haven't already seen them.
-- Swollen Feet and Ankles: Treatments to Try: https://health.clevelandclinic.org/6-best-ways-relieve-swollen-feet-ankles-home/
Thank you John, I'll call my doctor and inquire on these tests