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Understanding Cystic Fibrosis: Challenges and Hope
Cystic Fibrosis (CF) is a genetic condition that affects the lungs, digestive system, and other organs. It is caused by mutations in the CFTR gene, which disrupts the body’s ability to regulate the movement of salt and water in and out of cells. This leads to thick, sticky mucus building up in the lungs and digestive tract, creating a breeding ground for infections and making it difficult for affected individuals to breathe and digest food properly.
For many, CF is a lifelong journey that begins in childhood. Symptoms often include persistent coughing, frequent lung infections, poor growth, and difficulty gaining weight. Children with CF may experience fatigue and shortness of breath that can interfere with school, play, and everyday activities. Families often find themselves managing complex treatment routines, from inhaled medications to enzyme supplements and physiotherapy sessions to clear mucus from the lungs.
Living…