Ray Hulse
Jason’s Journey was formed in 2011, when Jason was just 9 months old! Jason is 14 and enjoys mountain biking, 3D printing, Legos, and spending time with family and friends. He is living a full and healthy life. This is due to the many hours a week he spends doing treatments and also the many medications and therapies he has access to. He is thriving and we are humbled and grateful that he personally benefits from so much research and development. We want that for every person with CF.
While the CF Foundation has made incredible progress, not everyone with CF can benefit from existing therapies and we still need a cure. This will require time, funding, and persistence – but with you on our team – we are ready to go the distance.
CF is a genetic, life-shortening disease that devastates the lungs, pancreas, and other vital organs. CF makes it difficult to breathe and fight life-threatening infections, often leading to extensive lung damage and respiratory failure.
Every person born with cystic fibrosis is on a unique journey and experiences this challenging disease differently. While progress has been made, a long road lies ahead for far too many people fighting this terrible disease. We need a cure so that everyone with CF has a better chance to live a long, healthy life.
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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