Sophie Lecommandoux

Sophie Lecommandoux is a dedicated parent aidant and health partnership advocate, serving as the founding president of the APASC, an association for individuals affected by the rare Currarino syndrome. Currently, they are a member of the CPP Sud Méditerranée III and the review college at Inserm, contributing to the clarity of clinical research protocols. With a background in health education, Sophie is involved in standardized patient participation at the Université de Montpellier, helping to bridge the gap between medical education and patient experience. They have earned multiple degrees in health education, including the DU in Patient-Healthcare Provider Partnership and the DU in Patient Education from the University of Montpellier. Sophie is committed to enhancing health partnerships and patient education, actively participating in workshops and training sessions.