My name is Elizabeth, and I am the mother of a 10-year-old boy diagnosed with Cystic Fibrosis (CF). I reside in Cuba—a country where, regrettably, patients suffering from this disease lack access to the medications and essential supplies necessary for their treatment.
My son carries the F508del genetic mutation, inherited from both parents, and is currently colonized by bacteria such as *Pseudomonas* and *Staphylococcus*, according to his treating pediatrician. This situation makes the need for appropriate medications to control the disease and improve his quality of life all the more urgent.
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