Alongside our mission to ease the burden and find a cure for Parkinson’s disease through education, research and support services, Parkinson Society British Columbia (PSBC) aims to be an effective advocate for issues important to the Parkinson’s community. Through the development of a coherent provincial strategy, we believe that patient outcomes for those living with the disease can be improved. With input from our members and partners, our advocacy initiative centres around five major areas, all based on improving access to critical supports and services to deliver better care. PSBC is pleased to announce that an opinion-editorial (op-ed), co-authored by UBC/Pacific Parkinson’s Research Institute Director, Dr. Martin McKeown, and PSBC CEO Jean Blake, was recently featured in the Vancouver Sun. The op-ed outlines five initiatives:

• A provincial Parkinson’s disease strategy
• Funding to improve access to specialized staff
• Continuing education of allied health professionals
• Funding DUODOPA therapy for advanced Parkinson’s patients
• Expansion of Deep Brain Stimulation program

By taking action in these five areas, the province can help those with Parkinson’s lead independent lives for as long as possible and reduce overall impact on the healthcare system. Parkinson’s advocacy ambassadors have already contacted 28 MLAs as well as BC’s Deputy Minister of Medical Beneficiary and Pharmaceutical Services. We encourage individuals passionate about improving conditions for people with Parkinson’s to send this op-ed to your local MLA or Minister, asking for their support.

If you would like to learn more about PSBC’s advocacy initiatives, please contact Jean Blake, CEO, at jblake@parkinson.bc.ca or 1-800-668-3330.

For media inquiries, please contact Alicia Wrobel, Marketing, Communications & Events Manager, at awrobel@parkinson.bc.ca or 1-800-668-3330.