We Need To Hear From You!
Srinivasa Subramaniam, PhD, associate professor of neuroscience at Scripps Research, Florida found that “after a decade, about 95 percent of Parkinson’s patients will experience some degree of involuntary dyskinesia”. We know that people with Parkinson’s, as well as their care partners, both experience the impact of dyskinesia on everyday life. Consistent with the unique service model you have come to expect from PMD Alliance, this survey is designed to not simply gather data, but to understand the experience of dyskinesia on your life.
Please take 5-8 minutes to complete this survey and share the impact of dyskinesia with us.
We value everyone’s input, even if you do not currently experience dyskinesia, as is it tied to addressing OFF time, which is also explored in this survey.
There are two different surveys – one for people living with Parkinson’s and one for Care Partners. We encourage each of you to take the time to complete the survey designed just for you!
Your voice is directly used when conceptualizing and creating new programs and services that not only educate, but generate resilience and improved connection for you, especially in this unique time period.
Let your voice be heard!