Younger Parkinsonís Patients Get Website And New Book

Top Quote Parkinsonís disease affects an estimated four million people worldwide, with as many as one million in the US alone. End Quote
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  • (1888PressRelease) May 09, 2009 - (Springfield, GA)óParkinsonís disease affects an estimated four million people worldwide, with as many as one million in the US alone. But itís estimated that fewer than twenty percent of people with Parkinsonís are diagnosed before the age of fifty, and even fewer before the age of forty.

    Now, new efforts are being made to reach out to these young-onset patients and the young children they often care for.
    The American Parkinsonís Disease Association recently launched the website, which caters to young-onset patients as well as their family members, friends and healthcare providers.

    Author and Parkinsonís patient Kay Mixson Jenkins has also worked to help early-onset Parkinsonís disease patients and their children with her new book, Who Is Pee Dee? Explaining Parkinsonís to a Child.

    Ms. Jenkinsí book is the story of a boy named Colt and his toy panda bear, Pee Dee. Coltís mother has Parkinsonís disease and he doesnít understand why she has the symptoms she does. The book is a deeply personal endeavor for Ms. Jenkins.

    ďI was diagnosed with Parkinsonís disease when I was thirty-four, so I know what itís like to be a young person and be told that you have this disease,Ē says Ms. Jenkins, ďParkinsonís carries with it a great deal of predictability. I know what will happen to my body as I degenerate, but I canít stop it.Ē

    In Who Is Pee Dee?, Ms. Jenkins addresses some of the more startling aspects of young-onset Parkinsonís, including:
    ē By the time symptoms develop, eighty percent of the chemicals that control movement are gone.
    ē Many children will grow up having never seen their parents without Parkinsonís.
    ē The medications that Parkinsonís patients use to treat the disease can have side effects that make parenting even more difficult.
    ē Parents with Parkinsonís often have to plan their schedules around the medications they take.

    Ms. Jenkins has been active in raising awareness about the disease and is the founder of Parkinsonís in the Park, a charity organization that raises money for research. She is also active in lobbying her state representatives to provide for funding for cutting-edge research techniques.

    ďI think this is a great resource for people who want support and tips on how to handle this disease and the effects it might have on others,Ē says Ms. Jenkins of the APDA website. ďI hope that Who Is Pee Dee? will do the same.Ē

    Kay Mixson Jenkins is the Georgia state co-coordinator for the Parkinsonís Action Network, leads the Effingham County Parkinsonís support group and was selected as a Parkinsonís patient advocate for UCB, Inc.

    For more information, contact the author directly via kmj ( @ ) ParkinsonsInThePark dot org dot

    (Who Is Pee Dee? Explaining Parkinsonís Disease to a Child by Kay Mixson Jenkins; illustrated by Richard Morgan; ISBN: 978-0-9819129-0-5; $12.95; 33 pages; 8Ē x 8Ē; hardcover; UCB, Inc.)

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