- To increase the awareness of neuropsychiatric and non-motor issues in Parkinson’s disease (PD)
- To provide education, support, and resources for people with PD and their care partners, specifically focused on those PD features often considered “taboo” or not often discussed
- To improve the quality of life of people with PD and care partners and decrease caregiver burden of those caring for people with PD
Who Can Participate
Anyone diagnosed with PD or who is a care partner of someone with PD.