About Jenavese Armstrong
Jena was diagnosed with cystic fibrosis at 2 years old while living overseas. Despite facing several obstacles, she obtained her bachelor's degree in psychology and master's in social work. Her career has been focused in community mental health and crisis. She received a lung transplant on May 19, 2017, which allows her to continue service in her community. She is passionate about family, food, travel, and humanity.
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.