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Dysphagia, or difficulty swallowing, is a common consequence of head and neck cancer (HNC) and its associated treatments. Speech-language pathologists (SLPs) often play an integral role in the rehabilitation of swallowing difficulties for people with HNC. In clinical speech pathology, it is of utmost importance to base treatment decisions on high-quality evidence. One key tenant of evidence-based practice that is often overlooked is the client perspective. To date, limited research has explored the perspectives of individuals with HNC who have received treatment for dysphagia, especially HNC survivors living in the United States (U.S.). To close this gap, the aim of this project is to establish an increased comprehension of the perspectives of individuals with HNC who have been treated for dysphagia. Specifically, the project explores participant perceptions of which elements of dysphagia care led to positive clinical experiences and which elements created barriers to positive experiences. Six individuals participated in individual, semi-structured interviews to share their experiences with HNC and dysphagia treatment. Using interpretative phenomenological analysis, the interview data were coded and analyzed. A set of themes emerged from the recurrent and substantiated ideas within the data. The ability to participate in dysphagia therapy was limited by the physical effects of cancer treatments. Swallowing difficulties caused the participants to experience psychological and emotional reactions. Participants revealed that they had no concerns with accessing treatment financially. However, several individuals were not provided with a speech therapy referral until significant swallowing difficulties developed. Generally, the participants found value in their dysphagia treatments and faced no difficulty accessing speech therapy once they were referred. Future research directions and clinical implications were provided to improve patient-centered care for individuals with HNC and dysphagia.