08/03/2025
We want to share this amazing news with you.
When Dom was born, his Dr told us that researchers were working on CF mutation corrector drugs that aim to fix the production of mucus in CF patients, basically making it normal.
The problem for Dom though is that his CF genes are very rare, so we did not have much hope that they would ever get to his specific mutation.
Well here we are, 18 years later and today Dom started his treatment on Trikafta!! This should make his mucus production normal and keep his lungs healthy!!
Thanks to everyone who has ever raised money or walked for Dommie’s dream team. This is what all our work was meant to do!!! ❤️
Dom is off to college at Stonehill in 3 weeks, seeking his degree in history and education.