2016 Rallying Survey: Data, Data, Data - Cure Parkinson's

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2016 Rallying Survey: Data, Data, Data

CPT_Helen profile image
CPT_HelenPartner
3 Replies

This year we want to understand what information people with Parkinson's share and how that information can influence decision making in healthcare and research.

Your views are extremely important to us. We will use the information gathered from this survey to form the basis of the focused discussions at the "Rallying to the Challenge" meeting this September. The survey should take 15-20 minutes to complete.

If you would like to share your views, please click the link below to complete the survey.

surveymonkey.co.uk/r/2016Ra...

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CPT_Helen profile image
CPT_Helen
Partner
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laglag profile image
laglag

Is this just for the UK folks?

CPT_Helen profile image
CPT_HelenPartner in reply to laglag

Thanks so much. A survey for people living with people with Parkinson's will be posted early next week. And we would love to hear from you wherever you are in the world. Your views are very important. Many thanks. Helen

soup profile image
soup

Hi Helen, can we companions/partners/caregivers have a survey entry point please. My husband gathers information one way and I use social media and forums to add to the decision making.

We are both part of the information gathering and decision making team sitting on the patien't side of the consulting room.

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