“From the annual walks, to the education programs, to the vital support they provide for research, we simply can not exist as a community without Parkinson Society Southwestern Ontario.”
Meet Angela Roberts.
Angela is an associate professor of Communication Sciences and Disorders and Computer Science at Western University, as well as a clinical speech-language pathologist. Through her work, she supports individuals living with Parkinson’s disease while also contributing to research and education in the field.
When speaking with those newly diagnosed, Angela recognizes how overwhelming and frightening the experience can be. She emphasizes the importance of empowerment, reminding individuals that they have the ability to direct their care, make choices, and remain actively involved in their journey.
Angela highlights the critical role of community, noting that living with Parkinson’s is not something people should face alone. She describes the importance of building a strong support system, often referring to it as a “Parkinson’s army,” where individuals, families, professionals, and organizations come together.
She points to Parkinson Society Southwestern Ontario as a key part of that support network, connecting individuals with healthcare professionals, resources, and one another. Through conferences, education programs, and community events, the organization creates opportunities not only for learning, but for meaningful connection and shared experience.
Angela also values the unique exchange that happens within this community, where researchers and clinicians learn directly from those living with Parkinson’s, shaping better care and more relevant research.
Her perspective highlights the power of connection, collaboration, and community in navigating Parkinson’s disease.
Watch Angela’s story below.