When I was diagnosed with peripheral neuropathy about 10 years ago I had never heard of it and went to the web for information. That was fruitless. My big question was what is going to happen to me. How do I prepare for the future. To not get any answers has been very frustrating. I was able to find and join a support group that met monthly and was coordinated by a hospital provided social worker. The sense of not being alone was amazing. Every member of that group was somewhat sad and very frustrated. Most suffered from diabetes which I don’t have, and the members were in a great deal of pain and on gabapentin and other drugs. Covid ended the support group.