Too often, patients do not tell their healthcare professional or Parkinson’s disease (PD) specialist about their symptoms. Initiating these conversations can be difficult, but it is important to understand that you are not alone.
From resources to community outreach and support, the patient research and advocacy groups featured here share our commitment to the Parkinson’s disease community. Together we hope to provide more information on Parkinson’s disease and to increase awareness of Parkinson’s-related hallucinations and delusions.
The first step in building your solid support system is speaking to a primary care physician who can connect you with a Parkinson’s disease specialist. Click below for more resources from More to Parkinson's.