Are you living with a mitochondrial disease and interested in contributing to research and advocacy efforts aimed at improving care in Canada? If so, consider enrolling in the MitoCanada Patient Contact Registry.
The MitoCanada Patient Contact Registry is a secure medical database where patients can submit information about living with mitochondrial disease. Collected information will be used in a number of different ways to improve mitochondrial disease care including connecting participants to research opportunities and clinical trials, providing information to decision-makers on Canadians living with mitochondrial disease, and creating a better understanding of the needs of patients.
Learn more about this project here