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My Great Strides Story
Kayla English
As most of you all know, I am 37 years old living with cystic fibrosis. CF is a rare genetic disease that affects many different parts of the body but really focuses on the lungs and digestive system. Because of that, I take medicine every time I eat and do breathing treatments and take other meds to assist with my breathing symptoms. The research and treatments have come a long way since I was diagnosed at 6 years old, but we still don’t have a cure yet.
Because CF is so rare, there is no government funding for research to find a cure. It is due to this, that we work so hard to fund raise. We have made so much progress, but we aren’t done yet! There is still work to do!
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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