23/10/2025
Multiple System Atrophy (MSA) is a rare, progressive neurological disorder affecting approximately 5 in every 100,000 people. It impacts both the motor system, which controls movement and balance, and the autonomic system, which regulates involuntary functions such as blood pressure, heart rate, and bladder control.
Our client, Barry, was diagnosed with MSA in 2022. Since then, he has shown remarkable determination, commitment, and positivity in the face of ongoing challenges. Barry attends hydrotherapy sessions four times a week to maintain his strength, mobility, and quality of life. His perseverance and spirit make him an inspiration to others living with MSA and similar neurological conditions.
Together with his wife, Nola, Barry is passionate about raising awareness of MSA. By sharing their journey, they hope to help others better understand the condition and the importance of early diagnosis, community support, and ongoing therapy. Read the below article to learn more about Barry’s story and how he continues to make every day count.
Diagnosed with rare neurological disorder Multiple System Atrophy (MSA), Barry and his partner Nola faced delays, missteps and mounting challenges in finding the right support. Read their story of resilience, regional challenges and finding support through community neurological care.
