Take the next step toward managing Parkinson’s disease–related hallucinations and delusions
If you or the person you care for is living with Parkinson’s disease (PD)–related hallucinations and delusions, you’re not alone. Take the next step toward managing the symptoms by talking to your doctor. This guide can help.
All you have to do is answer a few questions, and a customized guide will be created.* Click the Create your guide button below to start.
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If you wish to complete the discussion guide at a later time, you can download a PDF version of it to print and fill out, and bring it with you to your next doctor's appointment.
People don’t often speak about their PD-related hallucinations and delusions, which makes these symptoms difficult to diagnose.
If you are seeing signs of these symptoms, a Parkinson’s specialist may help you find answers.
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You’ve taken an important step by learning about PD-related hallucinations and delusions.
Now plan your next move by exploring a possible treatment option. Remember, only your doctor can determine if a treatment option is right for you.
These committed organizations can give you more information about PD-related hallucinations and delusions.
The Parkinson’s Foundation makes life better for people with PD by improving care and advancing research toward a cure. In everything we do, we build on the energy, experience, and passion of our global Parkinson’s community.
The American Parkinson Disease Association (APDA) is the largest grassroots network dedicated to fighting Parkinson’s disease (PD) and works tirelessly to assist those with PD live life to the fullest in the face of this chronic, neurological disorder. APDA provides support nationally through its network of Chapters and Information & Referral (I&R) Centers, as well as a national Research Program and Centers for Advanced Research.
The Michael J. Fox Foundation is dedicated to finding a cure for Parkinson’s and to ensuring the development of improved therapies for those living with the disease today through an aggressively funded research agenda.
The Davis Phinney Foundation provides resources and connections that enable people living with Parkinson’s to take action that can immediately improve their quality of life. The organization impacts hundreds of thousands of individuals and families each year through community programs, the funding of quality of life research, and extensive online content.
Parkinson & Movement Disorder Alliance (PMD Alliance) is a community of movers and motivators working hand-in-hand with those living with a diagnosis, their care partners, adult children, and support group leaders to deliver education and connection to those impacted by movement disorders.
