There are 4 types of registries for Parkinson’s (PD):

  1. PD Initial –
    Parkinson’s initial registry is our way to collect baseline information regarding people living with Parkinson’s.
    Patients voluntarily register for the registry and enter their health information.
    Click here to access the registry.
  2. PD Follow-up –
    Parkinson’s follow-up registry is our way to continue collecting information regarding people living with Parkinson’s.
    We recommend to fill out the registry on a monthly basis. You can add a reminder to your calendar.
    Click here to access the registry.
  3. PD Prevention Initial –
    Parkinson’s initial registry is our way to collect baseline information regarding people without Parkinson’s, who want to prevent it (such as healthy people, people with Parkinson’s in the family, genetically diagnosed to have one of the PD/Gaucher genes). Patients voluntarily register for the registry and enter their health information.
    Click here to access the registry.
  4. PD Prevention Follow-up –
    Parkinson’s follow-up registry is our way to continue collecting information regarding people who want to prevent Parkinson’s.
    We recommend to fill out the registry on a quarterly basis. You can add a reminder to your calendar.
    Click here to access the registry.