Neuropathy in feet and limited toe movement?

He is the one that started treatment for severe plantar fasciitis that has lasted 20 years and began trying to several meds for neuropathy. Actually he and family doctor collaborated. After many tests and several appointments with my first neurologist, he only gave me a diagnosis and agreed with the prescriptions I was taking. A second neurologist gave me the worst medical experience that I had ever had--he was only interested in surgery. With much research and consultations, it was clear, my current doctors were just as up to date on treatments as these specialists. I started with Gabapentin, which did almost nothing for my pain, then Cymbalta , which caused severe memory issues. We finally, tried Lyrica, which helped greatly with lesser side effects--slight dizziness. My podiatrist started me on Tramadol and eventually elevated the dosage to this point--slightly over normal dose. Pain doctor tried Nucynta, which worked very well for pain--but of course the numbness was much more bothersome and very expensive. I finally decided at that time that Lyrica/tramadol left me with a lot of pain and discomfort, but it was very manageable. The pain doctor had suggested implants--but my disease has developed quickly and spread to hands so I elected not to do that--From other disease and bad joints, I have had one major surgery per years for my entire retirement, so not interested to additional ones. At this point, I am accepting being down for the worst days and getting around as well as possible for the better ones. I still cannot walk far or fast, but am able to do light workouts and ride a stationary bike several times a week. I still have seen no reason to return to neurologist.