ABSTRACT Background and Objective Amyotrophic Lateral Sclerosis (ALS) is a progressive neurodegenerative disease that impairs motor function, including oral musculature, complicating oral hygiene and care. Despite its impact, oral health in ALS patients remains under‐addressed. This personal scoping review explores oral health in ALS through the dual lens of Dr. Maurits K.A. van Selms—a dental researcher and ALS patient—highlighting care, research, and education priorities. Methods Semi‐structured interviews were conducted via email with Dr. van Selms, using a topic guide adapted from a prior personal scoping review. The interview covered personal experiences and professional insights into oral health care, research, and education in ALS. Responses were analysed and synthesised into thematic agendas. Results Dr. van Selms emphasised the neglect of oral hygiene in ALS care. He advocated for patient‐informed, tailored guidelines based on functional capacity, interdisciplinary collaboration, and improved accessibility to dental services. In research, he called for ethically sensitive, patient‐centered studies that reduce the burden of oral care. Educationally, he stressed the need for inclusive training across disciplines and stakeholder levels, promoting self‐advocacy and awareness. Instructional materials, such as videos, were recommended to support caregivers and patients. Conclusion This personal scoping review underscores the importance of integrating oral health into ALS management. Dr. van Selms' unique perspective reveals gaps in care delivery, research ethics, and education, advocating for interdisciplinary collaboration and proactive guideline development. His insights offer a roadmap for improving oral health outcomes and quality of life in ALS and similar neurodegenerative conditions.
Verhoeff et al. (Fri,) studied this question.