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Parkinson's Information Service
The Parkinson’s Information Service (PINS) is a service that provides people with Parkinson's disease and their families access to a team of information specialists who offer practical information and resources. The Parkinson's Disease Foundation (PDF) offers PINS as a service to the Parkinson's disease community.
PINS comprises two programs, one online and the other via telephone, where people can submit their questions. The service is managed exclusively by the Parkinson's disease Foundation and is supported by Boehringer Ingelheim.〔http://us.boehringer-ingelheim.com/newsroom/2008/10-07-08_pd_education.html〕
==Need For Resources==
In 2008, a nationwide survey in the U.S. revealed a need for increased education on key issues in the management of Parkinson's disease for patients, their loved ones, caregivers, and healthcare providers. Specifically, 93 percent of neurologists, 84 percent of people with Parkinson's, and 88 percent of caregivers expressed the strong need for resources and tools to support disease management and daily living for people with PD. The survey also found communication gaps between neurologists, people with Parkinson's disease, and caregivers.〔http://www.reuters.com/article/pressRelease/idUS125847+07-Oct-2008+PRN20081007〕 PINS and related Parkinson's educational tools seek to overcome these gaps and provide much-needed resources.
抄文引用元・出典: フリー百科事典『 ウィキペディア（Wikipedia）』
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