The life of the Baigorri family with Steinert's disease, Murphy's Law turned into pathology: "It's a sinister lottery"

Myotonic dystrophy type 1 (DM1) is a genetic disorder causing muscle weakness and various systemic issues. Patients face challenges in daily activities, speech, and swallowing. Symptoms can include respiratory infections, heart problems, and early cataracts. María Baigorri, diagnosed at 16, experiences significant disability and societal misunderstanding. Her father, also a carrier, reflects on the generational anticipation phenomenon, where symptoms worsen in successive generations. Despite challenges, María engages in theater and mobility exercises to improve her condition. The disease's complexity highlights the need for awareness and understanding of rare conditions.