Bicycling helping people with Parkinson’s curb their symptoms

Image Credit: Matt McClain/Washington Post

As its title suggests, a January 10, 2012 feature article in The Washington Post (Bicycling and other exercise may help people with Parkinson’s curb their symptoms,) states “while it cannot cure Parkinson’s, heavy-duty exercise shows promise for countering, even delaying, the inability to move that the disease causes.”

In her article, Post reporter Alice Reid details results that medical researchers and Parkinson’s patients are seeing from regular, intense exercise (such as rowing and cycling)

The article notes that the National Parkinson Foundation “emphasizes exercise as an important tool to fight the disease,” and “The Michael J. Fox Foundation for Parkinson’s Research has funded close to $3 million in exercise research.”

Jay Alberts, the Cleveland Clinic researcher best known for his landmark work on “Forced Exercise” (cycling for Parkinson’s therapy) is quoted throughout the piece. A ‘just-completed study’ conducted by Alberts in which patients rode indoor bikes for exercise benefits is featured prominently.

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Art & Laughter as Parkinson’s Therapies

Anne's "Painting with Parkinson's" Group

Innovative therapies for people with Parkinson’s disease are originating and being practiced all over the world. From Australia via the Pacific Northwest comes this write-up “Art, laughter are therapy for PD group.” Written by Anne Atkin — volunteer, public speaker, ambassador and librarian with Australia-based Parkinson’s Victoria. as well as author of a new book: “Living and Laughing with Parkinsons”

Anne began her first “Painting with Parkinson’s” group in 2007, parlaying her love of art and experience as a teacher into benefit for others with Parkinson’s. Anne’s article was orginally published in the Nov/Dec 2011 issue of The Parkinson’s Post, bi-monthly newsletter of the Northwest Parkinson’s Foundation (www.nwpf.org). The mission of this Seattle-based organization is “to establish an optimal quality of life for the Northwest Parkinson’s community through awareness, education, advocacy and care.”

Special thanks to Ruth Egger of the NWPF for permission to reprint the article.

Here’s Anne Atkin’s article “Art, laughter are therapy for PD group”

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Parkinson’s Nutrition: Concerns & Recommendations

The Holiday Season is over!   With the New Year, it’s time to get back to healthy eating!

Proper nutrition for people with Parkinson’s disease is a recurring theme here at The Theracycle Blog.  Thus we’re glad to post a very informative write up on concerns and recommendations for Parkinson’s nutrition, courtesy of the California Parkinson’s Group (www.calparkinsons.org), whose mission is to “foster support and collaboration among friends and families with young onset Parkinson’s Disease through dialogue, education and involvement in the medical research community.”

Be sure to visit the CPG for a collection of useful PD materials and to participate in their forums: www.calparkinsons.org

Don't forget to eat your prunes!

Your mother always told you to “EAT YOUR PRUNES!” Read on to learn why and other helpful insights in “Significance of Nutrition in Parkinson’s” from our friends at the CPG.

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Contact Congress Today to Save SBIR

Call or Email Congress NOW to Save SBIR

If you’ve been following the Theracycle Blog, you may know that we recently received a hard-to-land NIH-SBIR grant to fund research and product development of new Theracycles to benefit people with Parkinson’s disease..

What you may not know (but should)–  is that the 30 year old SBIR (Small Business Innovation Research) program is a political hot potato on Capitol Hill in Washington, D.C. Of real concern to us is the possibility of the expiration of SBIR programs on December 16, 2011!!

For all of you who share our belief in the importance of continued federal funding of SBIR, please read this urgent appeal from U.S. Senator Mary Landrieu with her clarion call for us to call or email our U.S. Representative to express our strong support to save SBIR…

Please Tweet this message to “Contact Congress Today to Save SBIR”  http://bit.ly/v01T87

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Theracycle: Part of Boston’s Leadership in Life Sciences

Theracycles "Made in Massachusetts" Help Drive Life Sciences Innovation

An 11/29/11 article in Mass High Tech titled “Report: Boston area is top U.S. life sciences hub” cites research from real estate services firm JonesLaSalle that
rates the metropolitan Boston area as the #1 region for established and emerging life sciences businesses (in comparison to other parts of the United States).

An excerpt from the JonesLaSalle 2011 Global Life Sciences Cluster Report reads “The [Boston] area enjoys seven times the number of workers in biotech R&D than the national average.” The area has more than 85,000 high-tech research employees and more than 340,000 hospital and medical employees.

The Mass High Tech article notes the Report “also highlights Massachusetts as the recipient home of 13 percent of all National Institutes of Health funding, with five of the top eight NIH-funded hospitals in the U.S. and the top five NIH-funded universities.”

As an NIH-funded Massachusetts small business, The Exercycle Company is proud to be part and parcel of the Boston-area’s preeminence as the top region for life sciences in the country.  While our operations might be considered small in comparison to some of the med-tech giants that operate in the Bay State — growing demand for our Theracycle (which powers proven exercise therapy for Parkinson’s disease), shows that we’re movin’ up!

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.

November is “National Family Caregivers Month”

In case you didn’t know it— November is “National Family Caregivers Month”.

According to the National Alliance for Caregiving, more than than 65 million people (29% of the U.S. population), provide care for a chronically ill, disabled or aged family member or friend during any given year and spend an average of 20 hours per week providing care for their loved one.

For 15 years, the National Family Caregivers Association (NFCA), has recognized and celebrated family caregivers. Identifying Family Caregivers! is the theme for National Family Caregivers Month 2011.

Theracycle is an ardent supporter of “National Family Caregivers Month,” and we hope you’ll join us in supporting the mission of the NFCA to educate, support, empower and speak up for the millions of Americans who give so much of themselves to provide for the health and well-being of a beloved family member.

To join or donate to the NFCA visit: http://www.nfcacares.org/join_nfca/

“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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Free eBook for People with Parkinson’s Disease

If you or someone you care about has Parkinson’s disease, you’ll be interested in reading a free new eBook on a successful new therapy that is helping people with PD substantially reduce their symptoms.

Entitled “How a New Therapy Brings Hope & Results to People with Parkinson’s Disease” click here to download the Free eBook from the Theracycle website.