Hello to my sensory ganglionopathy pals. I want to thank all the people in the group that responded to my last post last year. Just to give you an update. I am no longer on gabapentin. Which I found out after teetering down most the side effects were what I had going on. I am now on savella and it helps just a little bit. I'm also using a compound cream that my neurologist prescribed. Once the cream is on. It's relief for 10 minutes. My balance issues are still there and using a walker permanently. Also still using the wheelchair for long distances. Thank you all for giving me some hope. Knowing that I'm not alone with this disease. I am going to have more faith in my abilities to be able to handle this disease. Thank you all again.