Background: Cerebral palsy (CP), a neurological disorder affecting movement and posture, poses significant challenges for affected individuals and their families. Awareness and early intervention play a pivotal role in improving outcomes, yet public knowledge about CP remains limited, particularly in rural areas. In Hamirpur, where access to specialized healthcare services is constrained, understanding the community’s awareness of CP is crucial to addressing misconceptions and promoting timely diagnosis and management.Material and Methods: This descriptive, cross-sectional study assessed the knowledge and awareness of CP among 400 residents of Hamirpur, Himachal Pradesh, from August to October 2024. Participants were selected through stratified random sampling and completed a structured questionnaire capturing socio-demographic details and knowledge of CP, including its symptoms, causes, management, and social implications. Data were analyzed using descriptive statistics, and knowledge levels were categorized into four grades: very good (>80%), good (60–79%), fair (41–59%), and poor (<40%).Results: The study revealed a foundational awareness of CP among participants, with 74% correctly identifying CP as a neurological disorder and 81% recognizing its management potential through therapies. A majority (80%) understood the importance of early intervention, while 78.5% were aware of the role of inclusive education. However, gaps in knowledge were evident, particularly regarding the hereditary aspects of CP (71%) and socio-cultural barriers to care (70%). Knowledge scores classified 28% of participants as having very good knowledge, 34% good, 28% fair, and 10% poor. Rural residents and those with lower education levels demonstrated significantly lower awareness, highlighting disparities in information dissemination.Conclusion: While the general public in Hamirpur exhibits a basic understanding of CP, significant knowledge gaps persist, especially in technical and social aspects of care. Targeted educational programs, community-centered interventions, and advocacy efforts are essential to improve awareness, reduce stigma, and enhance early diagnosis and management of CP. Prioritizing CP as a public health concern can foster inclusive policies and improve quality of life for affected individuals and their families.