There is currently no cure for cystic Fibrosis! My son, Matthew was diagnosed at 8 weeks old in 1992 and life expectancy was 27. With advances in care and treatments, he has exceeded his life expectancy. In January he turned 33 years old, an age we never thought we would see for him. Yes, he has endured quite a bit in these years, but his strength, determination and courage have brought him to this point. Especially knowing that because he has two nonsense mutations he does not qualify for the life changing modulators. He is in the last 10% that has no available modulator treatments. He works hard in taking care of himself and says daily exercise is key to good health.