← Return to CIDP (Chronic Inflammatory Demyelinating Polyneuropathy)
DiscussionCIDP (Chronic Inflammatory Demyelinating Polyneuropathy)
Autoimmune Diseases | Last Active: Feb 11 11:30am | Replies (349)Comment receiving replies
Replies to "I have a rare autoimmune neuromuscular disease that was diagnosed six years ago. Right now I..."
I have just started to get a vitamin and lidocaine IV and it helps with the nerve burn and pain. It lasts for about 10 days. I get them every 2 weeks. It is worth trying. I now have scheduled it every 10 days and will post an update in a couple weeks.
Hello @txamo, Welcome to Mayo Clinic Connect. You will notice that we have moved your post to an existing discussion "CIDP (chronic inflammatory demylinating polyneuropathy)" so that you can meet other members with similar symptoms and learn what they have shared helps them. If you click the VIEW & REPLY button at the bottom of the email notification, it will take you to the discussion.
You may also be interested in the following related discussions:
- Ketamine for chronic pain: https://connect.mayoclinic.org/discussion/ketamine-for-chronic-pain/
- Ketamine Infusion: https://connect.mayoclinic.org/discussion/ketamine-infusion/
Have you been able to discuss ketamine as a possible treatment with your doctor or care team?