News for the mito community

Momentum in mitochondrial disease (mito) research is building, and this episode brings you the February Mito Community Newsletter in a clear, listener-friendly way, from progress in clinical studies and approvals, to the practical supports and community actions that help turn momentum into access in Australia.In this episode, we share an update from Mito Foundation CEO Sean Murray, spotlight Rare Disease Day and ways to take part, and walk through key opportunities and updates including The Bloody Long Walk, an Australian clinical trial for autosomal dominant optic atrophy (ADOA), the Phase 2b PRIZM study milestone for MELAS, and a European regulatory step for KYGEVVI for TK2 deficiency (TK2d). We also cover ways to strengthen community data through the Mito Registry, a resource to help adults build a supportive care team, wellbeing and connection opportunities, and where to find Mito Foundation support services.Read the newsletter online: February NewsExplore Mito Foundation resources and events: www.mito.org.au