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My Great Strides Story

Kayla English
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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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$140
raised of $10,000 goal
 

Achievements

Leader

Team Kayla’s Krusaders

$867
$10,000

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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.