What do you need to know?
* Any individual diagnosed with PD is eligible to enroll.
* Participation in the registry is voluntary, confidential and free of charge.
* Eligible participants will be notified about opportunities to participate in clinical trials, though they are under no obligation to enter.
* Participants will need to complete an updated questionnaire every six months.
* Participants may also be asked to complete additional surveys for PD research projects.
* Any data provided will be used in scientific publications in summary form only.
* Participant names will not be released to anyone outside the Parkinson's disease Registry management team without written authorization, nor will names be sold for advertising or fund-raising purposes.
