We are interested in understanding the symptom and side effect terminology used by people with Parkinson's and their family members and how this might be similar or different from the language used by healthcare professionals.
If you are interested in sharing your experiences, please complete one of the two surveys available:
1. For people with Parkinson's - surveymonkey.co.uk/r/descri...
2. For the family/partner/spouse of PwP - surveymonkey.co.uk/r/PDsymp...
Both surveys consist of 6 key questions and should take no longer than 5-10 minutes to complete.
Thank you!