We have been conducting a nationwide study on the experiences of women with Tourette's Syndrome (TS) across the lifespan. Extant research has heavily focused on the experiences of males with TS with little investigation into the differences in physiology and sociocultural experiences that affect women. This study has been collecting information from participants who were Assigned Female at Birth and self-identify as women ages 18 years and up. We have specifically collected information pertaining to women's physiological experiences across the lifespan (menses, pregnancy, perimenopause, menopause, etc.) and how tic symptoms may change during these events. In addition to collecting information via three surveys, participants were also invited to participate in an optional remote interview with the research team to learn more about their experiences, concerns, and things they wish to learn more about. Many women do not receive a TS diagnosis until much later in life, after which they have already carried a substantial burden of symptoms associated with TS without any explanation or targeted treatment. This study aims to improve that experience.