Note: This column describes the author’s own experiences with using masks during nebulizer treatments. Not everyone will have the same response to treatment. Consult your doctor before starting or stopping a therapy. I haven’t dealt with many sinus issues in my lifetime. At age 17, I had a nasal polyp…
Living Beyond — Jennifer Cogliano

Jennifer Cogliano, diagnosed with cystic fibrosis in her first few days of life, has been defying the odds of her disease for the majority of her life. She has a daughter, worked as a nurse for 20 years, and then received the gift of life through a bilateral lung transplant in 2020 during the pandemic. Jennifer is the self-published author of a children’s picture book, “The Friendship Umbrella,” which teaches about being kind, helping others, and appreciating each other’s differences. Jennifer loves dogs and music, has a strong faith in God, and has always chosen to count her blessings instead of her struggles.
February has always been a complicated month for me. The holidays are over, spring feels impossibly far away, and here in the Northeast, the gray skies and frigid temperatures seem to stretch on endlessly. And with cold and flu season raging, this time of year presents its own unique challenges…

I live in southeastern Pennsylvania, where the trees and flowers bloom in April and May. In my early adult years, May was usually the month when I’d be hospitalized with a cystic fibrosis (CF) pulmonary exacerbation. Many times, I chalked it up to being run-down after leading a team…
I was extremely active growing up. I was the point guard on my elementary school’s girls’ basketball team and the catcher on the softball team. I had no problems playing entire games and participating in multiple practices each week. My cystic fibrosis (CF) physician always encouraged my mom to…
I recently agreed to facilitate one of the Cystic Fibrosis Foundation’s CF Circles, which are virtual small-group discussions about a specific topic. The focus of this particular gathering was “Living with cystic fibrosis (CF) over 40.” After my double-lung transplant in 2020, I decided to take a…
To follow my column last week about the rate of divorce after surviving advanced cystic fibrosis (CF) and double-lung transplant, this week I’ll focus on the intricate balance of living while dying. Don’t get me wrong, the improvement in my lung health since my transplant four years ago…
In a private Facebook group for adults living with cystic fibrosis (CF), a post jumped out at me asking if anyone had gone through a divorce after their double-lung transplant. The post instantly caught my attention because that’s my current situation. What disturbed me was the number of responses…
In the first few days after my double-lung transplant in 2020, I was looking at a hand-held mirror and saw a central venous catheter protruding from the left side of my neck. A large, bulky bandage covered the right side. Little did I know then that the bandage represented something…
The power of water is underrated. If you Google it, you’ll see you can delve into multiple aspects of water’s properties, including how it supports thermal energy, hydropower, transportation, and anti-erosion efforts. It’s a universal solvent (because of its molecular structure), it’s often symbolic (as in the Bible), and…
Is it just me, or did January feel like an entire year all on its own? From drastic political shifts to devastating wildfires, extra-cold temperatures to egg shortages, a surge in influenza activity to outbreaks of tuberculosis, 2025 has been exhausting so far. On top of everything, I feel a…
This month, my beautiful daughter, Claudia, will celebrate her 29th birthday. I was 24 and living with cystic fibrosis (CF) when I became her mother. It’s now been four years since my double-lung transplant, and I’m currently fighting COVID-19 for the fourth time in four years. As the…
The end of 2024 is upon us, which means it’s time to reflect on the past year and evaluate ourselves and our decisions. It’s also a time for resolution — the promise to implement positive life changes in the new year. Many New Year’s resolutions focus on exercise, with goals…
They say that the older you get, the faster time passes. At 53 years old, I completely agree. As I look back at the columns I’ve written in the past, I can’t believe we’re approaching the holiday season again. Don’t get me wrong — I’m thankful for it.
Your CF Community

Visit the Cystic Fibrosis News Today forums to connect with others in the CF community.
Recent Posts
- It’s time to stop obsessing over life expectancy in CF
- Handgrip test reflects breathing muscle strength in adults with cystic fibrosis
- Enjoying life amid the noise and rules of cystic fibrosis
- Air pollution spikes pose risk of delayed lung issues in CF patients: Study
- Using Trikafta may shield CF patients from lung damage: Study