The Hiebert family have been long-time supporters of Parkinson SuperWalk. Al and his wife, Peggy, lived in Kelowna when Al was first diagnosed with Parkinson’s disease (PD) in 2003. Like many facing a new diagnosis, they were looking for a community of individuals on a similar journey, which they found through their local Parkinson’s support group. It was through that group they first joined Parkinson SuperWalk, beginning what has since become a family tradition that moved with them when they relocated to Vernon.
Their daughter, Sara, has cheered them on, fundraising from the sidelines for many years. More recently, she has stepped fully into the event, walking alongside her parents in 2023 and 2024, with plans to do so again this year. Her husband, Rick and their dog, Alton, are proud companions on the route. Last year, Sara led the warmup for SuperWalk, featuring high-energy movements to get the blood flowing before the walk began.
The family’s favourite part of the event is the community aspect and connecting with individuals in similar situations. It brings together people who understand what it means to live with Parkinson’s, whether firsthand, as a carepartner, or supporter. For many, it’s the first time they’ve met others who truly “get it.” That shared understanding and sense of solidarity is what keeps the Hieberts, and so many others, coming back year after year.
Funds raised from Parkinson SuperWalk help Parkinson Society BC continue to support those touched by PD every step of the way through essential programs and services. For the Hiebert family, the resources offered by the Society were instrumental in providing them much-needed knowledge about the disease and what to expect going forward.
When reflecting on how Parkinson’s has changed Al’s approach to life, he mentions that it has forced a gradual slow-down, but his faith and loving family are helping him bravely face any challenges together. The family emphasizes the importance of information and stresses that no question is too simple to remain unasked. They urge others to reach out – whether it’s to a neurologist, a support group, or the helpful programs and resources offered by Parkinson Society BC.
Sara adds that even though it is hard, feeling one’s feelings is a monumental step forward. “Don’t pretend this huge thing isn’t hard and a big deal; it is. Let yourself grieve, don’t rush yourself to just move on – even if someone else has it worse than you do, you’re allowed to feel sad about this diagnosis and the changes that will happen/are happening to your body and your life,” she says. “Find folks who will walk the journey with you.”
Join us for Parkinson SuperWalk in communities across the province on September 6 and 7. Participants will walk in solidarity to uplift the lives of over 17,500 British Columbians affected by Parkinson’s disease. Your support powers essential services, advocacy, and groundbreaking research. Register or donate today at www.parkinson.bc.ca/superwalk!