A Friday evening and Saturday Conference themed “living a full life with PSP” geared towards delivering practical value for caregivers, families and patients living with PSP, CBD and MSA. After touching on the latest updates in research and treatment advancement we’ll focus on high-impact family first issues. Advanced care-planning for all stages, Managing changes in speech, communication and swallowing, mental health for caregivers and ending with an interactive session exposing attendees to 6+ years of support group tips, tricks and resources for caregivers and patients. The PSP Society welcomes patients, families, allied health professionals and other stakeholders of the Canadian rare disease community to attend.