Spending summers at sleep-away camp helped me become more responsible, and allowed me to see CF clearly and accept it.
Hogan was diagnosed with cystic fibrosis at age three and has been smiling, laughing, and coughing ever since. She spreads positivity and enthusiasm wherever she goes. Raised on the coast of Maine and now living in Seattle, she finds her joy outdoors, hiking trails and exploring the mountains. She leads her Great Strides team, Hogan’s Heroes, and spends each spring fundraising for the CF community.
Blog Posts
I have had two collapsed lungs in three years. Here's what I learned.
Although packing up and moving to college is not easy for anyone, it becomes more complicated for a person living with cystic fibrosis. Not only do we have to adjust to the unfamiliar ways of college life and be entirely in charge of our health, but the group of people we trust with our life changes as well.