A belated thank you for your reply. They say "Better late than never".
Has any progress been made in treating patients with PD induced Camptocormia in the past year?
My neurologist, who in the past had ruled it out, is now suggesting that I may want to consider it. He was very specific that there was no guarantee, but the odds of success have improved to 50%. He cited recent discussions of DBS as an early intervention tool and overall better outcomes of DBS. Unfortunately for me, there are no specific studies of DBS for Camptocormia, that he can reference.
Are you aware of any? Has your thinking changed from the earlier reply you gave to my post?