If You Keep the Patient First, You'll Never Go Wrong

For parents living with mitochondrial disease, one of the hardest conversations to navigate is how—and when—to talk to your kids about your diagnosis. In...

Patient-Focused Drug Development (PFDD) meetings are one of the most powerful advocacy tools available to rare disease communities—but most patients have never heard of...

ENERGY IN ACTION - EPISODE 110 MitoArtisian’s   Welcome back to our fellow mito warrior, Christine Knox, who's here to talk about a new program...