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My Breathe Team Story

Kevin Vargo

Fundraising for BMW Berlin Marathon 2026

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Kevin Vargo

I’m attempting to raise $4,000 for cystic fibrosis research in honor of my granddaughter, who was diagnosed with CF before she was born. She’ll be three years old soon, and like every child with CF, her life already includes daily challenges no child should have to face. There is no cure for cystic fibrosis, and many people with CF are still waiting for the breakthroughs that will allow them to live longer, healthier lives. This fall, I’ll be running the Berlin Marathon as part of the 2026 Breathe Team to support the scientists working toward a cure. 🫁💛🏃‍♂️


Cystic fibrosis is a genetic disease that affects long-term health and quality of life. It primarily impacts the lungs and pancreas, but it can affect multiple organs throughout the body. In the lungs, CF causes thick, sticky mucus that is difficult to clear, trapping bacteria and leading to frequent infections and ongoing inflammation. Over time, this can reduce lung function and make breathing more difficult, requiring consistent daily treatments and medical care. 🫁

CF also affects the pancreas and digestive system. Thick mucus can block digestive enzymes from reaching the intestines, making it harder for the body to absorb key nutrients—especially fats, proteins, and fat-soluble vitamins. Even with a healthy appetite, many people with CF rely on enzyme supplements and carefully managed nutrition to support growth, strength, and immune function. 🍽️

Because nutrition plays such a critical role in overall health, people with CF often need to closely monitor their diet and energy intake throughout their lives. CF can also affect other areas of the body, including the sinuses, liver, and reproductive system, and it increases the risk of conditions such as CF-related diabetes and bone disease. Daily life often includes airway clearance, medications, enzyme therapy, and regular medical visits—all part of managing the condition over the long term.


While research breakthroughs have brought meaningful progress, continued scientific advances are essential. By donating toward my fundraising goal, you help advance the research and science needed to move us closer to a world where every person with cystic fibrosis has the chance to live a long, healthy life. Thank you for taking the time to read this and for supporting cystic fibrosis research in any way you can. Every bit of awareness and support truly matters. 🌍🙏

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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.