The Cystic Fibrosis Foundation funds millions of dollars into research for treatments for CF and working toward a cure. This research has made groundbreaking strides in improving the quality of life and life expectancy of people with CF. The life expectancy for those born in recent years (who benefit from these new treatments) has increased to 65 years! However, due to thousands of different genetic mutations causing people’s CF, and many having more rare and complex mutations, many (about 10% of those with CF) still aren’t benefitting from these new treatments, and therefore are still living with terrible realities and life shortening health issues.

When Malcolm turns 2, he is eligible to start a “modulator”, one of the new treatments, that was made possible through this research. This treatment corrects one of his mutations and should greatly improve his health outcomes. 

Please help us in donating to the Cystic Fibrosis Foundation to continue working toward treating, and eventually curing, ALL with Cystic Fibrosis. 

Love,
Caden, Kyle, and Malcolm Duff