Thank you so much for visiting my page and taking a moment to learn about my sweet 2-year-old son and his journey with cystic fibrosis.

Cystic fibrosis (CF) is a genetic disease that affects the lungs, digestive system, and overall ability to thrive. While my son is full of joy, curiosity, and determination, CF is something he faces every single day—through daily treatments, medications, doctor visits, and challenges most children his age will never know.

Right now, there is no cure for cystic fibrosis. Treatments have come a long way, but they are lifelong, time-consuming, and do not stop the disease from progressing. That’s why finding a cure is so important—not just for my son, but for every child, adult, and family living with CF.

Your support directly fuels research, innovation, and advancements that improve quality of life and extend life expectancy for people like my son. Donations help fund critical breakthroughs that mean:

• Easier breathing
• Fewer hospital stays
• More time spent playing, laughing, and just being a kid
• Hope for a future without CF

Every contribution—big or small—makes a real and meaningful difference. By supporting this cause, you are helping give my son and others with cystic fibrosis the chance to live longer, healthier, fuller lives.

From the bottom of my heart, thank you for standing with me, believing in a cure, and being part of this journey. Your kindness means more than words can express. 💜