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My CF Climb Story

Anna Battista

Fundraising for Denver CF Climb

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Anna Battista

I am climbing to raise money and awareness for cystic fibrosis.  Lots of progress has been made in the past few years but there is still a ways to go.  Although treatments have made a world of difference for some people with CF there are others, like myself that do not benefit from the current treatments.  We can’t stop until everyone with CF has the opportunity to live a much more healthy and normal life.  

What is my life with CF (and a lung transplant as a result) like you might ask?  Well I think chat GPT summed it up best when it said: 

So you were born with a genetic curse that basically makes your mucus thick enough to be considered construction-grade adhesive. Cystic fibrosis doesn’t just mess with your lungs—it shows up like, “Surprise! I’m also gonna ruin your pancreas, your digestion, and possibly your dating life.”

Your lungs? Yeah, they were once air balloons. Then they turned into cement-filled Ziploc bags. Breathing feels like trying to sip soup through a coffee stirrer while your lungs host a rave for bacteria.

Then, BOOM: CF-Related Diabetes rolls in like a side quest you didn’t sign up for. Because your pancreas is already overwhelmed by the mucus apocalypse, it’s like, “You want insulin regulation too?? Please.”

Now you’re juggling:

  • Enzymes to digest your food
     
  • Insulin because your blood sugar’s doing parkour
     
  • Breathing treatments that last longer than most Netflix episodes
     
  • And enough pills daily to qualify as a human maraca
     

Eventually your lungs were like:

“We’re done. We’re leaving. Find replacements or enjoy your life as a fancy balloon with arms.”

So you get a lung transplant, which is like switching out the engine of a car mid-race while the car is also on fire and allergic to the new engine. You’re put on the waiting list (also known as “purgatory with paperwork”) and finally get new lungs from someone who, bless their soul, donated theirs.

SURGERY TIME. You go under, they open your chest like a book no one wants to read, swap out your ancient lungs, and plug in your new ones. Hopefully right side up.

Post-transplant life means:

  • Taking immunosuppressants daily so your body doesn’t go, “Imposter lungs? REJECTED.”
     
  • Catching a cold now feels like gambling with your soul.
     
  • You’ve got to wear masks in public long after everyone else gave up and started licking doorknobs again.
     
  • Your immune system is basically a chill stoner now, totally unbothered by infections and unfortunately, also everything else.
     

Meanwhile, your CFRD is still there like, “Oh hey, I didn’t go anywhere.” So now you’re managing blood sugars and checking in with your transplant team every time you sneeze funny.

BUT—despite all the chaos, meds, appointments, and the fact that your body is basically running on duct tape and pure defiance—you keep going. You breathe. You live. You become an expert in medicine, nutrition, scheduling, and low-level existential dread.

You are a medically enhanced, pharmacy-sponsored, mucus-fighting cyborg with a master’s degree in survival.




Will you help us end cystic fibrosis?



By donating to my fundraising goal, you have the power to advance the research and science needed to drive our shared dream forward – a cure for everyone with CF.

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$120
raised of $100 goal
 

Achievements

Leader

Team Anna’s LemonAids

$320
$3,500

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The CF Foundation is committed to providing a safe, inclusive, and healthy experience for individuals attending Foundation Events. Individuals attending CF Foundation events must abide by the Foundation's Attendance Policy and accompanying guidelines, which include guidance for event attendee's living with cystic fibrosis.