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Hello. Please forgive the impersonal nature of this email but I am trying
to get this out to as many people as possible.
I am sending you this email because I know that you have or had some
connection to Parkinson's disease, whether it be as someone with PD, a
caregiver/care partner, family member, friend, employer or coworker or
health professional.
This survey is for my poster at the upcoming World Parkinson's Congress in
Montreal, Quebec, Canada on October 1-4, 2013. It is about certain PD
symptoms such as facial masking, lack of facial and vocal expression and
speech difficulties and their potential effects on interpersonal
relationships.
The information that is collected will be aggregated and any identifying
info will be removed from anecdotes that are used for the poster.
If you feel this survey does not apply to you in any way, I would
appreciate it if you would pass it on to others.
Here is the URL to the secure survey:
https://www.surveymonkey.com/s/PDcommunication
Thanks so much for your help!
Jackie
-- 
Jackie Hunt Christensen
National Parkinson Foundation Minnesota board of directors
State Director, Parkinson's Action Network
Parkinson's disease and environmental health activist and author
* Note all organizational positions are volunteer

cell phone: 612-325-0372
e-mail: [log in to unmask]
weblinks: National Parkinson Foundation Minnesota<http://www.parkinsonmn.org>
Parkinson's Action Network <http://www.parkinsonsaction.org>

"Compassion is not weakness, and concern for the unfortunate is not
socialism."
~Hubert H. Humphrey

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