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Well Hello There Hilary! Sounds about the same as my cute little hockers here. Color changes, pain, etc. I have a feeling this may be my fork in the road with the 3 mooseketeers. I am going to do alot of investigating. I received a pamphlet yesterday from Rush St. Lukes in Chicago, the original hospital of my diagnosis.lllll I saw a Doctor named Harold Klawans. He was in charge of the movement disorder wing. Unfortunately the doctor died 2 months after I saw him. I have this thought I would have fared better with him, much better. I need to get back there I think. Need to find rides to Chicago to see that group. They are heavy into research as Dr. Klawans wanted to find a cure in his lifetime. Thank you for your info Hilary, maybe with your help and a path I'll get back to where I should be. Thank you TTFN Gina Hugs to you Thanks to all of you PD People I have decided to contact Chicago Drs and ask for a recommendation in this area. I read books about PD and can find my problem when the 2 drs here are saying "Oh no that is not PD related. I would like to wear my shoes again some day. If my daughter gets married I would not want to wear my Garfield Slippers! Bye