Watch a panel of experts discuss COVID-19 vaccines through the lens of cystic fibrosis.
Blog Posts
Feb. 21, 2021|
4 min read
Living with cystic fibrosis, I owe gratitude to the friends, family, and care team members who love me, support me, and make my life easier. Join me in letting those who support you know how much you appreciate them.
April 21, 2020|
4 min read
I am thankful for the relationships I have online with other people with cystic fibrosis. But the flip side of using social media is that I open myself up to the possibility of unkind words or feelings of sadness whenever I log in.
Jan. 8, 2019|
4 min read
At the third plenary at this year's North American Cystic Fibrosis Conference, we explored what it means to partner in care and how to do it better.
Oct. 20, 2018|
4 min read
When it comes to my cystic fibrosis care team, I've learned that it's often the little moments that matter most.
June 23, 2017|
5 min read