← Return to CIDP (Chronic Inflammatory Demyelinating Polyneuropathy)
DiscussionCIDP (Chronic Inflammatory Demyelinating Polyneuropathy)
Autoimmune Diseases | Last Active: Oct 13 3:46pm | Replies (312)Comment receiving replies
Replies to "I have a rare autoimmune neuromuscular disease that was diagnosed six years ago. Right now I..."
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?