CF Community Blog

Jacqui Sjoberg

Adult with CF

Learn more about Jacqui Sjoberg

  1. Understudied Areas in CF Get Extra Attention at NACFC

    By Jacqui Sjoberg January 14, 2021

    I could fill a book with all the things I learned at the virtual North American Cystic Fibrosis Conference this year, but I am especially glad that there was a focus on diversity, gender health, and sex-based differences in CF.

  2. What I’ve Learned From 11 CF Care Centers in 21 Years

    By Jacqui Sjoberg June 18, 2020

    As a military spouse who makes frequent moves, I have had to transition to new cystic fibrosis care centers 11 times in 21 years. Here are three things I have learned to make each changeover work.

About Jacqui Sjoberg

Jacqui was diagnosed with cystic fibrosis at birth. She has participated in numerous clinical trials to further advance CF care. Jacqui is serving as a patient advocate on the CF Women's Health Research Working Group and as a clinical research community reviewer. You can find Jacqui in her kitchen, cooking for her husband and two boys or walking along the beach and trails near her home in southern California. She can be reached at entertain365@gmail.com.

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.