The Parkinson’s Community Needs Your Participation
Posted Jan 29 2012 11:59am
The Parkinson Alliance is committed to helping improve the quality of life of people who have Parkinson’s disease (PD) and their care partners.
One facet of their many goals is to contribute to the improvement of quality of life through conducting survey-based research to obtain the patient perspective about the experience of PD for those with and without Deep Brain Stimulation (DBS).
Here is how you can participate: Call The Parkinson Alliance at 800-579-8440 to receive a copy of the survey. They will mail you a copy to complete and provide a self-addressed, prepaid return envelope.
You can view all their prior reports with topics like speech, gait, balance, sleep, among others at www.dbs-stn.org/survey .
Participation is valuable to the PD community, and your participation is highly appreciated.
The Parkinson Alliance is committed to helping improve the quality of life of people who have Parkinson’s disease (PD) and their care partners.
One facet of their many goals is to contribute to the improvement of quality of life through conducting survey-based research to obtain the patient perspective about the experience of PD for those with and without Deep Brain Stimulation (DBS).
Here is how you can participate: Call The Parkinson Alliance at 800-579-8440 to receive a copy of the survey. They will mail you a copy to complete and provide a self-addressed, prepaid return envelope.
You can view all their prior reports with topics like speech, gait, balance, sleep, among others at www.dbs-stn.org/survey .
Participation is valuable to the PD community, and your participation is highly appreciated.