The Cystic Fibrosis Foundation is committed to advocating for the rights and well-being of individuals living with cystic fibrosis (CF) at both the federal and state levels. Our advocacy efforts are rooted in our mission to ensure that everyone affected by CF has access to the highest quality of specialized care. Through a dedicated lens, we meticulously evaluate policies and legislation to identify opportunities for meaningful change and improvement in CF care and treatment. By engaging with lawmakers, policymakers, and government agencies, we strive to shape healthcare policies that prioritize the needs of the CF community, advocating for increased access to innovative treatments, comprehensive healthcare coverage, and robust research funding. Through our unwavering advocacy efforts, we remain steadfast in our commitment to championing the rights and well-being of individuals with CF, working tirelessly to enact positive change and improve outcomes for all those affected by this challenging disease.