
Using Social Connection as “Medicine” in Parkinson Disease Care: Robert Cochrane, PhD
The CEO and founder of Yes, And...eXercise (YAX) discussed how support groups, psychosocial connection, and hybrid telehealth models can complement pharmacologic treatment in Parkinson disease. [WATCH TIME: 3 minutes]
WATCH TIME: 3 minutes | Captions are auto-generated and may contain errors.
"We accept now that exercise is medicine with Parkinson disease. If we can accept that connection is medicine, therefore support groups that provide that connection, we can do a lot with that."
Connection and psychosocial support have become increasingly recognized as critical components of comprehensive care for individuals with Parkinson disease (PD), complementing pharmacologic and rehabilitative interventions. Beyond managing motor symptoms, clinicians and care teams are tasked with addressing the emotional, social, and relational challenges that can contribute to isolation, reduced quality of life, and diminished adherence to therapy. Emerging models of care emphasize that structured support, peer engagement, and regular contact can function as an important “therapeutic dose” alongside standard treatments.
At the 5th Annual
In a follow-up interview with NeurologyLive®, Cochrane, CEO and founder of Yes, And...eXercise, expanded on these themes, describing how support groups, improvisation, and storytelling can positively influence patients’ lived experience with PD. Throughout the interview, he detailed the role of technology in sustaining meaningful connections between patients, care partners, and communities, and discussed ongoing gaps in how clinicians recognize and “prescribe” connection as part of routine care.














