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Monday November 29th 2021 This 30-minute webinar will provide information about Sexuality, Romance and Gender when you have Cerebral Palsy and Complex Communication Needs, and What Ableism has to do with CP, AAC, Romance and Sex. The session will be followed by a joint Q&A session. Megan Walsh is a speech pathologist completing her PhD at Deakin University. She attended Northwestern University in the United States for her Bachelor’s and Master’s degrees before moving to Victoria in 2007 and working as a clinician. Her clinical focus has always been on working with people who use Alternative and Augmentative Communication (AAC) and their families, and she is currently involved in research around parent capacity building and AAC. She is currently bridging clinical knowledge and research for better outcomes for young people with cerebral palsy with the CP-Achieve research team. FAQ: What is CP-Achieve? The Centre of Research Excellence: Australian Centre for Health, Independence, Economic Participation and Value Enhanced Care for adolescents and young adults with cerebral palsy (CP-Achieve). CP-ACHIEVE is a five year, NHMRC funded Centre of Research Excellence project that supports collaborative research and development in cerebral palsy research. The team consists of a multidisciplinary group of adolescents and young adults with cerebral palsy, families, clinicians, researchers and students that are all working together to fulfil CP-Achieve’s aims. CP-Achieve commenced in February 2020 and will finish in 2025. What does CP-Achieve do? CP-ACHIEVE fosters health care access and promotes healthy lifestyle interventions to improve community participation. Two overarching aims guide the research program: to improve physical and mental health, and to build supportive family, community and health service environments. The outcomes of CP-Achieve are to establish rigorous population-based data about the scope of health and participation problems, best practices and guidelines for health and disability service providers, means to empower adolescents and young adults with cerebral palsy to use health and community services, and models of cost-effectiveness to inform policy and practice, and drive value-enhanced care.