YOUR voice is a series of personal stories from people living with young onset Parkinson’s. Each piece shares one person’s lived experience, in their own words, reflecting the realities of balancing work, family, health, and identity at a life stage where Parkinson’s is least expected.
Together, these voices build understanding, connection, and visibility – reminding us there is no single YOPD story, only real lives being lived.
YOUR voice: Barrie Smith
June 3, 2026
Diagnosed at 49 after decades of unexplained symptoms, Barrie shares his determination to be heard, stay himself and support others. Through advocacy and community building, he reflects on trusting your instincts, living authentically and finding strength in the Parkinson’s community.
YOUR voice: Gina Walter
May 6, 2026
After a long and difficult path to diagnosis, this story reflects grief, determination and unexpected growth with Young Onset Parkinson’s. From becoming a fitness instructor to building community and embracing family honesty, it’s a journey about living in the present and finding purpose beyond the condition.
YOUR voice: Rose Donaldson
April 22, 2026
Diagnosed just before 50, Rose shares her journey from early symptoms and shock diagnosis to building community, creativity and confidence. Through hiking, dance, choir and her podcast, she reflects on positivity, peer support and the importance of staying active with Young Onset Parkinson’s.
YOUR voice: Wendy Noble
April 15, 2026
Diagnosed with Young Onset Parkinson’s at 51, Wendy shares how she continues working, performing music and travelling a decade later. Through research involvement, community support and careful routines, she reflects on adapting expectations, staying connected and choosing to live fully despite uncertainty.
YOUR voice: Sarah Sykes
April 8, 2026
A careers adviser diagnosed with Young Onset Parkinson’s at 46 shares how empathy, volunteering and creativity reshaped her outlook. From supporting students and running peer groups to poetry and family walks, she reflects on pacing life, accepting help and finding strength through community.
YOUR voice: Paul Morris
April 1, 2026
Diagnosed with Young Onset Parkinson’s at 32, Paul shares how life continued through career, marriage and parenthood before Deep Brain Stimulation changed his journey. From adapting hobbies and exercise to finding purpose through community and volunteering, his story reflects acceptance, resilience and connection.
YOUR voice: Snehal Amembal
March 8, 2026
A writer and poet living with Young Onset Parkinson’s shares her diagnosis journey, the role of creativity in coping, and how routine, exercise and advocacy have helped her build a hopeful and purposeful daily life.
YOUR voice: Rebecca Jones
February 20, 2026
Rebecca was diagnosed with Young Onset Parkinson’s at 41 while balancing NHS leadership, motherhood and a busy family life. She shares the difficult decision to retire, how creativity and routine help her manage symptoms, and why openness, community and purpose have become central to living well with YOPD.
YOUR voice: Samantha Cole
January 31, 2026
Samantha Cole is a Consultant Clinical Health Psychologist, NHS leader, parent, and CEO of Spotlight YOPD, living with young-onset Parkinson’s. In this reflective and honest piece, she shares how she continues to work full-time, adapts her routines, and stays active while living with YOPD. Samantha offers thoughtful insights on medication, family life, identity, and advocacy, giving a calm, human perspective on balancing health, leadership, and everyday life.