About Michelle Herpolsheimer
Michelle has participated in CF Foundation events locally for years, served on committees, and fundraised. She is a member of Community Voice and a facilitator for Teen Connections. In addition, Michelle is a member of the CF Community Blog editorial board, her CF clinic's patient and family advisory council, and CF advocate for Congressional Captains (Heart of America Chapter). A resident of Wichita, Kan., Michelle holds BA in human services/psychology. She enjoys writing, including a blog about her life since starting Trikafta®, cooking, riding my bike, gardening, music, singing, and spending time with her husband and their two bird dogs.
This site contains general information about cystic fibrosis, as well as personal insight from the CF community. Opinions and experiences shared by members of our community, including but not limited to people with CF and their families, belong solely to the blog post author and do not represent those of the Cystic Fibrosis Foundation, unless explicitly stated. In addition, the site is not intended as a substitute for treatment advice from a medical professional. Consult your doctor before making any changes to your treatment.