What We Do

• We average hundreds of phone call hours each month from Parkinsonians (“people with Parkinson’s”) and their care partners and family members and from the general public.
• Each month, we conduct several Support Group meetings for Parkinsonians and their care partners.
• We distribute monthly summaries of the latest Parkinson’s research.
• We provide several hours of Parkinson’s education each month through meetings and seminars.
• Our volunteers make home and hospital visits and provide countless hours of service each month to our Parkinson’s community.
• Through our Summer Forum and our participation in community events, we take every available opportunity to advocate for our local Parkinsonians.