Is Exercise the New Drug for Parkinson’s Disease?

 In our earlier post, “Delay the Disease – Exercise to Fight Parkinson’s Symptoms” you met David Zid and Jackie Russell, the founders of Delay the Disease—an exercise program developed specifically for people with Parkinson’s disease.

Here in her first guest post for the Theracycle Blog, Jackie Russell provides her expert opinion on the topic “Is Exercise the New Drug for Parkinson’s Disease?”

 

 

 

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Delay the Disease – Exercise to Fight Parkinson’s Symptoms

Delay the Disease is a fitness plan and community-based exercise program designed to empower people with Parkinson’s disease (PD) to optimize their physical function.  Originating in Columbus, Ohio in 2007, Delay The Disease is quickly becoming a national phenomenon in the Parkinson’s prevention field, and is starting to become internationally acknowledged.

Delay the Disease founders (David Zid BA, ACE, APG and Jackie Russell, RN, BSN, CNOR) have expertise in working with individuals diagnosed with PD and offer training to other health care professionals nationally.  This program is based on current evidenced-based research, and Zid’s extensive experience with one/on/one training of people with PD.  Their goal is to demonstrate how exercise can change symptoms, foster optimism and allow individuals to maintain independence.  They believe that fighting this disease with hope is the key.

David and Jackie have spoken to over 20,000 People with Parkinson’s (PWP) and their families— at symposia, continuing education courses, and PWP workshops.

As PD affects the entire family, their programs focus on helping the individual, caring for the caregiver, and educating other healthcare professionals about the importance of Parkinson’s–specific exercise and therapy. They are passionate and enthusiastic that PD does not need to define a person; it can be managed with the appropriate “tools in the tool box of treatment”. And, as Jackie comments regularly “exercise is a very important tool.”

Delay the Disease is available in a book, and 2 DVDs. Learn more about Delay the Disease at www.delaythedisease.com.  Books and DVDs can be ordered from the website, or through Amazon.

“Parkinson’s isn’t my life. I have Parkinson’s. Why does it have to have to be my life?”

Here’s another post from our friend and Guest Blogger Marc Sherman, who regularly chronicles what he calls his “journey and struggle through the life changes attributed to the onset of Parkinson’s Disease.” in his “But This is the Hand That I Shoot With” blog.

“Parkinson’s isn’t my life. I have Parkinson’s. Why does it have to have to be my life?

By Marc Sherman

The quote comes from the movie, “Love and Other Drugs.”  The movie was both fluff and at times true to life.  The quote “Parkinson’s isn’t my life. I have Parkinson’s. Why does it have to be my life?”  stuck with me, and made me wonder, is it my life?  If so, is it possible for it not to be my life?

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Help support “Ride With Larry” (A film of one man’s Parkinson’s journey)

A team of filmmakers, who all have loved ones with Parkinson’s, are creating the first film for the Parkinson’s community, by the Parkinson’s community that will help spark an international movement for research, awareness, and inspiration.

The film, Ride with Larry, follows Larry Smith, a retired police captain, now beloved small town baker, as he rides his bike across South Dakota, pushing his limits and expanding the boundary of possibilities for those with Parkinson’s disease. Weaved amongst the progress of Larry’s ride is an intimate portrait of the every day battle against Parkinson’s, the great minds working to find a cure, and the community love of Vermillion, SD that makes joined together to give Larry Smith one great ride.


The Exercycle Company (makers of the Theracycle) is a proud sponsor of Ride with Larry (including having furnished this Theracycle for Larry to work out on). We hope that readers of the Theracycle blog and others will join us in supporting this important film by contributing to the next state in its creation…

Read this message from Team Larry on how YOU can help!

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Groucho Marx: Parkinson’s Specialist

 

Marc Sherman is a 54 year old attorney who lives in Forrest Hills, NY. He describes himself as I “someone who loved childhood, and in a sense, never really left it.”

Diagnosed with Parkinson’s disease in 2006 (an event that Marc says “should have caused me to leave childhood and become an adult,” Marc Sherman puts his legal expertise to work for The People with Parkinson’s Advisory Council of the National Parkinson’s Foundation. Marc is also the host of the Living with PD blog where he discusses his experiences living with Parkinson’s, often through witty parodies…

Forget the Mayo Brothers… Marc turned instead to The Marx Brothers for their diagostic and clinical expertise in treating his Parkinson’s disease, as you’ll read in his latest post:

A Night At The Doctors

 

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Mariana: My Theracycle Story

One of the key components of the new Theracycle Blog is the inclusion and contribution of personal stories and advice from individuals who live with mobility issues and whom we know and respect.  We’re calling these posts “Theracycle Stories”

Our first contribution for Theracycle Stories is from our friend Mariana from northern New England, who was diagnosed with Multiple Sclerosis several years ago. While MS might slow others down, Mariana’s a spirited and tireless advocate for regular and vigorous exercise as something that’s helped her “feel more alive.”
Mariana’s writing up another article for The Theracycle Blog on her other favorite exercise passion: Weight Lifting. Stay tuned.

Here’s Mariana’s story…

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