GBS and Complex Regional Pain Syndrome Type II?

After approximately 6 months recovery from the AMSAN variant of GBS, my pain became significantly worse, I developed red/violet feet and hands, swelling, and my nails stopped growing. I had also started to develop hammer toes on both feet.

I recently saw a neurologist in Leeds, UK, after my GP suspected CIDP. He suggested the trophic changes in my hands and feet were due to Complex Regional Pain Syndrome (CPRS) Type II.

Has anyone else with GBS been diagnosed with this condition and what treatment did you receive or how has it progressed?