My Parkinson’s Journey

The journey with Parkinson’s can be a long and frustrating one, but hang in, there are many things you can do to improve your quality of life.  One thing that has made a big impact in my life is exercise, and that’s why my wife and I have started tAPDA Larry and Ellie Headshothis website and an organization devoted to removing the barriers to vigorous exercise faced by people afflicted with Parkinson’s disease.

My primary care doctor and the first neurologist I saw first diagnosed me in 2009 with Essential Tremor and told me it didn’t matter if it was PD because there’s no cure and it was best to delay drug therapy, anyway. What inspiring news! And when the PD diagnosis was finally confirmed in late 2010, I adopted an apathetic attitude because I was not guided otherwise. In April 2012, my wife badgered me into attending an APDA support group meeting she saw noted on the calendar of our local newspaper, and my life changed.

By happenstance, a pair of wellness gurus were at that meeting pitching a free Tai Chi for Parkinson’s pilot workshop, and the organizer of the NPF’s Southeastern PD Conference was there giving away “Aware in Care” kits and urging folks to attend the Conference that October, and an animated duo of physical therapists were there urging everyone to exercise.

The Tai Chi studies cited by my gurus and the inspirational words of our now favorite PTs led me to believe there might be things I could do to slow my progression. Later, at the Southeastern Conference, Dr. Becky Farley urged us to exercise outside our comfort zone to achieve maximum benefit.

Those two events completely changed my outlook from apathy to hopefulness, and the improvement in my well-being over the past year has been dramatic.  I exercise hard and often and practice Tai Chi and Yoga daily.  I’ve been working with my Tai Chi gurus, Bob and Doris, to expand the Yellow River Center’s offerings and am about to join their Board. I’m also working with Paul “The Truth” Delgado, a retired three-time international boxing champion, to develop a boxing training program for people with Parkinson’s in a north Atlanta suburb based on the success of Punching Out Parkinson’s in Fort Worth and Rock Steady Boxing in Indianapolis.

It took me over a year to find the PD community, and as I connect with PWPs across the country at conferences and through Facebook support groups I’m learning my story is a common one. Some neurologists make their patients aware of exercise programs, support groups and clinical trials, but many – maybe even the majority – do not. PD Gladiators’ mission will be to educate the public, people with Parkinson’s disease, and the medical community about the role of exercise in slowing the progression of Parkinson’s disease and to make community-based exercise programs available to people with Parkinson’s disease and their caregivers. We are already working with our local APDA chapter on a brochure reflecting the content on this website’s home page, and we intend to proactively spread the word to practicing neurologists so that newly-diagnosed Parkinson’s patients learn about the benefits of vigorous exercise and the other things they can do now to live better with PD faster than I did.

There should be enough information on this website when it’s fully up and running to convince you to start exercising before PD stops you from moving. A body in motion tends to stay in motion, and a body at rest tends to stay at rest. The choice is mostly yours.

Larry Kahn

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