ABSTRACT Background Previous studies explored information needs for carers of persons with aphasia; however, there is minimal research on information needs for carers of people with right hemisphere disorder (RHD). Carers have an important role in rehabilitation and long-term quality of life of a person with RHD. This study explores the information needs for carers throughout different periods of rehabilitation following a family member’s right hemisphere stroke. Methods/Procedures Four participants completed online surveys and a semi-structured phone interview. The interviews were transribed and analysed for emerging themes. Results Analysis revealed four themes in the onset phase including barriers to information, right versus left brain function, recovery timeline and recommendations, and information about symptoms. Three themes emerged in the rehabilitation phase including detailed impairment information, general and specific treatment information, and specificity of timeline and recommendations. The chronic phase contained five themes consisting of information on supports for carers and patients, impairment specific information, treatment and treatment options, compensatory strategies and home practice, and hope Conclusions Results suggest the importance of considering the type of information, how this information varies based on RHD, and at what point carers want to receive this information may improve the delivery of information from medical professionals to carers through the phases of recovery.