Update From our Chief Scientific Officer + Ways to Engage in Research

Every day, potentially groundbreaking Parkinson’s disease (PD) research ideas are explored in labs funded by the Parkinson’s Foundation.
What is a Facebook Fundraiser?

With the help of Facebook, it is easier than ever before to fundraise globally for the Parkinson’s Foundation.
Finding the Home You Need: Modifications for People with Parkinson’s Disease

It can be very difficult for a someone with Parkinson’s disease (PD) to find a home with accessibility features. Most real estate agents don’t have much experience dealing with accessible properties and there are few resources that can simplify the process for disabled home buyers. It takes considerable research and patience to find a property that meets your needs.
Simple Blood Draw Reveals Early Inflammation/Fatigue Connection

First described as a common symptom of Parkinson’s disease (PD) more than 20 years ago, PD-related fatigue remains an under-recognized, clinically significant, disabling symptom that can diminish quality of life (Herlofson et al., 2018; Kluger et al., 2016).
Parkinson’s Foundation to Share Research Findings at World Parkinson Congress

Every three years, the World Parkinson Congress (WPC) provides an international forum where health professionals, care partners and people with Parkinson’s disease (PD) come together to discuss the latest scientific discoveries, medical practices and caregiver initiatives related to Parkinson’s.
A Possible New Gait Way: Spinal Cord Stimulation

Many people with advanced Parkinson’s disease (PD) suffer from gait (walking) dysfunction, freezing of gait and postural instability. These symptoms can cause falling, resulting in a multitude of injuries, a loss of personal freedom, caregiver stress and a reduction in the quality of life (Pirker & Katzenschlager, 2017; Samotus, Parrent, & Jog, 2018).
GBA Mutation May Lead to Novel Therapeutics

One of the most common genetic risk factors for Parkinson’s disease (PD) is having a mutated GBA gene (which makes the enzyme glucocerebrosidase). In fact, 5 to 10 percent of people with PD have that specific GBA mutation in one copy of the gene (mutations in both copies of the gene lead to Gaucher disease).