Living with cystic fibrosis means living with uncertainty. The questions run quietly in the background of everyday life: Will this head cold turn into something more? Are these enough enzymes to take for this meal? Will I need IV antibiotics this time? Will I be admitted to the hospital, or can I manage this flare up at home?
Over time, these thoughts become automatic. By adulthood, most of us with CF have developed a kind of internal operating system built around vigilance, preparation, and resilience. It becomes second nature.
My journey with CF has included periods of relative stability and periods where lung infections became serious enough that transplant conversations entered the room. Through all of it, there was one constant dream that gave shape and meaning to everything else: I wanted to have a family. I’m not entirely sure where that dream came from. But somewhere deep inside, I knew motherhood was part of my path.
Before modulator therapies, that dream felt distant — something closer to hope than reality. But as new treatments emerged and I began taking modulators, something shifted. Slowly, the idea of having a family transformed from an abstract dream into a possible plan.
I met my now-husband — an experience that, for anyone dating with CF, comes with its own unique vulnerability. Finding someone who understands what CF entails and chooses to walk beside you anyway is no small thing. After we got married, we spoke with my CF care team. When they gave us the “all clear,” we allowed ourselves to imagine a future with children.
A few months later, we were pregnant.
What I expected to be a time defined purely by excitement was instead accompanied by a tidal wave of questions. CF is still relatively new territory in the obstetrics world, and while there is growing knowledge, there are also unknowns.
My “CF brain” — the part of me trained to anticipate problems and prepare for worst-case scenarios — went into overdrive. I researched, asked questions, and mentally rehearsed every possible outcome. This mindset had served me well in managing CF. It had helped keep me safe. But in pregnancy, I could feel it pulling me into a spiral of “what if” fears.
What if something goes wrong? What if my body can’t do this? What if CF changes everything?
But looking back now, after two healthy pregnancies and two beautiful baby boys — one even born at home — there is one question I wish I could have asked myself sooner:
What if it all went well?
CF had trained me to prepare for complications. It had taught me to live cautiously, to anticipate instability. That mindset is protective, and in many ways necessary. But pregnancy introduced a new and unfamiliar experience: allowing myself to witness my body doing something not defined by illness, but by creation.
This shift didn’t happen overnight. In the early months of my first pregnancy, the fear was still loud. But over time, I began to realize something important: pregnancy was not CF. Pregnancy was its own journey. While CF was part of me, it did not automatically define every outcome.
With the guidance of my medical team and careful monitoring, I slowly began to let myself experience pregnancy not just as a medical condition to manage, but as something my body was capable of doing. Appointment by appointment. Kick by kick. Breath by breath. I began to lean into this new experience and let fear slowly fade into background static.
For so long, my relationship with my body had been shaped by fragility. I had grown used to viewing my body as something that needed constant management, something that could falter without warning and required constant vigilance for when it did. But pregnancy gave me an opportunity to see my body differently — not as something working against me, but as something working with me.
That didn’t mean I ignored reality. It didn’t mean I assumed nothing could go wrong. It meant allowing space for another possibility alongside the fear.
Trust.
Trust that my body was trying. Trust that my medical team was supporting me IF anything needed addressing. Trust that both caution and hope could coexist.
Pregnancy, in an unexpected way, began to heal my relationship with my body. It helped rebuild a sense of partnership. My body was not betraying me. It was adapting, adjusting, and doing something extraordinary — even with CF.
My first pregnancy and delivery went smoothly. My second pregnancy brought a reminder that CF is always present. During that pregnancy, I needed IV antibiotics for the first time in over three years. But even then, something had shifted dramatically. Instead of fear consuming me, I felt grounded. I trusted that my body and my care team could navigate what arose. That pregnancy ended with a natural home birth that left me in complete awe.
None of this happened because I thought positively enough. CF does not work that way. Pregnancy does not work that way. Complications can happen regardless of mindset, preparation, or hope. Many people with CF experience difficult pregnancies, and their experiences are equally valid and real.
But, what mindset can shape is the emotional experience of the journey.
For so long, the only pregnancy stories I encountered in the CF community were the hardest ones — NICU stays, emergency interventions, complications, loss of lung function. These stories matter deeply, and they need to be told. But they are not the only stories of CF and pregnancy.
There is another side.
I share my story to offer representation for a different possibility. To remind someone reading this that while preparing for challenges is wise, it is also OK to leave space for hope.
You are not naïve for imagining something good.
You are not reckless for allowing yourself joy.
You are not wrong for wondering, “What if it goes well?”
No matter what your pregnancy looks like — whether it goes smoothly or has complications, whether it requires interventions or unfolds on its own — your experience is valid. Your strength is not measured by how easy or difficult your journey is, but by the courage it takes to walk it.
Living with CF requires resilience. Pregnancy requires surrender. Navigating both at once taught me that strength and softness can coexist.
If you are considering pregnancy, currently pregnant, or reflecting on your own journey, know this: there is more than one version of what pregnancy with CF can look like. There is no single story.
And sometimes, beautifully, everything goes well.
Interested in sharing your story? The CF Community Blog wants to hear from you.