Here's a webinar from my MDS at Cedars Sinai. I have personally received great relief from some of the treatments he describes in this presentation. https://davisphinneyfoundation.org/events/dystonia-in-parkinsons-what-it-is-and-how-its-treated/
I just read this article and found it helpful in that I have been frustrated at exercising daily and not feeling like I'm experiencing any increase in strength or stamina. This article explained that a recent study has determined that "physical activity, although beneficial, does not fully compensate for the deficits arising from the neurodegenerative mechanisms inherent to the disease." This SUCKS, but it helps me not feel quite so frustrated. Any thoughts?
This is being presented by the Davis Phinney Foundation (dpf.org) on July 14, 11am PT. The presentation is being done by my MDS, Dr. Michele Tagliati from Cedars Sinai in LA. He has really helped me with all manner of my symptoms of my disease, and I recommend him highly. Register now.
https://davisphinneyfoundation.org/events/dystonia-in-parkinsons-what-it-is-and-how-its-treated/