Latest Posts

YOUR voice: Sophie Wardle

Diagnosed with Young Onset Parkinson’s in 2008 after years of unexplained symptoms, artist Sophie Wardle shares the shock of diagnosis, the impact on work, family life and independence, and how creativity, travel, movement and community have helped her keep saying yes to life. Her story is honest, funny, resilient and full of hard-won perspective.

August 1, 2026

Patron Viewpoints: July 2026 Newsletter

Nose to diagnose! Patron viewpoints and CEO Update - read our July 2026 newsletter.

July 30, 2026

YOUR voice: Ellie Finch

Diagnosed with Young Onset Parkinson’s at 29, Ellie Finch Hulme shares her journey through symptoms, diagnosis, work, treatment, DBS, motherhood and finding strength through friendship, therapy and the Parkinson’s community. Her story is honest, moving and full of resilience, showing how connection, advocacy and staying active have helped her keep focusing on what matters most.

July 1, 2026

YOUR voice: Barrie Smith

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.

June 1, 2026

YOUR voice: Gina Walter

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.

May 6, 2026

YOUR voice: Rose Donaldson

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.

April 22, 2026

YOUR voice: Wendy Noble

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.

April 15, 2026

YOUR voice: Sarah Sykes

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.

April 8, 2026

YOUR voice: Paul Morris

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.

April 1, 2026

YOUR voice: Snehal Amembal

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.

March 8, 2026

YOUR voice: Rebecca Jones

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.