Lucas, an eight-year-old boy diagnosed with a rare genetic disease that causes extreme skin fragility, lives with joy and courage despite the daily pains and challenges, while his parents share the struggle for proper treatments and the importance of raising awareness for Epidermolysis Bullosa. #EpidermóliseBolhosa #SaúdeInfantil #Sensibilização (translated)
observador.pt
Lucas, o menino com uma doença rara que gosta da vida como é
