Hi Everyone!
My name is Ronny Smitley. I’m 33 years old living in Cleveland, home sweet home! I was diagnosed with Cystic Fibrosis when I was about 8 months old. Obviously, I remember very little of the early years, but I can tell you what it has been like more recently.
Up until 2019, I was averaging at least one hospital admission per year for a pulmonary "tune up." That all changed in October of 2019 when the FDA approved Trikafta, the latest in a string of successful gene modulators. This new medication completely changed my life for the better. For the first time, I was able to train for and successfully run a 5k, I was able to gain and maintain a healthy weight, and I was able to begin to plan for my future with less worry that my future would be cut short.
Unfortunately, the past year has been a very humbling reminder that Trikafta is not a cure. I have been faced with some of the biggest challenges of my adult life with regards to my health. Due to some new lung bugs and new GI complications, I spent a lot of time in the hospital in the last 12 months. I was faced with difficult news and difficult decisions, including the decision to leave my full time dream job. As difficult as it was, I am now able to take the time to focus on my health and ensure I thrive. Despite these new challenges, I continue to have hope! Without Trikafta, and other new and developing treatments, the past year may have had a very different outcome, and for that I am beyond grateful.
While this new drug has been a game changer for many, it is still is NOT A CURE. There are still many CFers out there who cannot benefit from it for one reason or another. There are others still who we lost before they had the chance to see their "Trikafta Day." For this reason, we continue to fight daily. For these people, we shout even louder for a cure to be found.
I have participated in the Great Strides CF walk since I was 3 years old. That means this year will mark my 30th year of being involved! It is always a fun day to go to the zoo with your family and friends and to help try and find a cure. Rain or shine we always have fun. The walk is an opportunity to step out and show that we are better together, we fight as one for all who are affected.
Each year I participate, I am reminded that I am never alone in my fight to breathe. Events like Great Strides unite people from all walks of life who have been affected by CF in one way or another. Patients, family members, friends, and caregivers all come together to show support and raise awareness. Each year brings something new. Whether it be new research announcements or new challenges to be faced, each year is met with new faces to help offer support. I have built lifelong friendships with people that I initially met at the walk here in Cleveland. Those friends are the people I turn to when I face new struggles in my fight.
I encourage you to reach out and get involved. Remember, you are never in this battle alone. As fighters, we need each other to help make CF stand for “Cure Found” and to help make CF a thing of the past.
Breathe easy, fighters!
Ronny Smitley
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IMPORTANT NOTE ON ATTENDANCE AT FOUNDATION EVENTS:
Updated July 5th, 2023
The CF Foundation is committed to ensuring the health and wellbeing of individuals attending Foundation events. Individuals attending CF Foundation events must abide by the Foundation's Event Attendance Policy www.cff.org/attendancepolicy, which includes guidance for event attendees living with cystic fibrosis.