A Day in the Life of Marlee – as told by Marlee Mommy gets me up at 6:25 in the morning I get dressed first, and then I have to do treatment. Mommy has already set up my vest and nebulizer on the couch for me.  I use my inhaler first, then start treatment. I will watch a show while it goes on. It takes me about 20 minutes. After that, I get to eat breakfast. I cannot eat before treatment because it will hurt my belly. My favorite breakfast is cinnamon rolls. Sometimes I eat c

Life is short…. Time is fast…. No replay, no rewind…. So enjoy every moment as it comes…. The above words hit close to the heart as we...

What a day we had! Littleton Police Department, together with several other agencies gave Marlee a day that can easily be described as...

Well, it has clearly been a few months too long since our last update. How quickly time can get away from you. First things first, Marlee...

We have shared a lot of positive news with everyone regarding Cystic Fibrosis, including all the advances we see with CF and the extended...

After a few attempts, plus a few little sister meltdowns, we were able to sit Marlee down and have her answer a few fun questions. Since...

A new season, new adventures, and a new sense of love. It has been a while since our last update, and there is so much to share! 2022...

Children's Hospital is not a place a parent dreams of visiting, let alone at least four times per year. As you walk in those main doors,...

A day in the life of Marlee is nothing short of eventful, fulfilling, and exhausting. We start early, we play hard, we don't skip a beat,...

Together in 2021, we raised over $46,000 in honor of Marlee's Magic and the Cystic Fibrosis Foundation. A special thank you to all who...