Newly expanded to include partners, Caregiver-to-Caregiver allows husbands, wives, partners or companions of people with young onset Parkinson’s Disease to develop the same kind of unique, personal support their partners have enjoyed through Person-to-Per

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Dance for Parkinson’s is modeled after a national dance program designed to empower participants to explore movement and music in ways that are refreshing, enjoyable, stimulating and creative.

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While living with PD can be challenging there is hope. Hope in the fact, that there are things you can do to maintain your quality of life and live well.

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The APDA National Young Onset Center offers Parkinson’s Disease programs and services that focus on education, wellness and building a strong support base. Provides personalized and confidential one-to-one service.

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Calls are generally answered live, and messages returned within 24 hours. Discuss Parkinson’s and it’s effects on the individual and family, make home visit requests, and well as community resources.

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Have you or a loved one been recently diagnosed with Parkinson’s disease (PD)? Are you adjusting to life several years into PD? Do you need help finding a physician or a support group or managing your medications? Ask the experts at PDF your questions.

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PSCKY is a statewide resource offering assistance and education to Parkinson patients and their families after diagnosis.

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PDF keeps an unpublished listing of Parkinson’s support groups and we would like to invite you to be a part of the list or to call us to find a group in your community.

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Gain access to a comprehensive listing of articles, checklists, books, DVDs, videos, webcasts and web sites to help you learn more about PD.

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Critical information for both persons with Parkinson’s and their caregivers to help them understand the disease, know what to expect and where to go for additional assistance.

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Providing innovative care and services to support, educate, and inform the region’s 25,000 individuals diagnosed with Parkinson’s disease to maximize wellness and quality of life.

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Annual workshops to provide latest information on new research, treatments and resources for people with Parkinson’s and their caregivers.

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Attendees participate in one hour of seated Parkinson’s exercise, followed by lunch and games. Caregivers are encouraged to use this time respite.

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The mission of The Parkinson’s Institute (The PI) is to provide comprehensive patient care, while discovering new treatment options to improve the quality of life for all Parkinson’s disease (PD) patients.

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