My Cystic Fibrosis Story
Nicole nicole@factoryfive.com
Fundraising for BMW Berlin Marathon 2026
Nicole nicole@factoryfive.com
My sister, Jennifer, was diagnosed with a fatal lung disease called Cystic Fibrosis as a baby. I remember being told she might not live to see eight years old.
Because of the incredible work of the Cystic Fibrosis Foundation, life saving treatments now exist and real progress is being made toward finding a cure. But this progress only continues if we keep showing up.
Cystic Fibrosis is a rare orphan disease, and research depends heavily on fundraising and community support. My sister and so many others living with CF are counting on people like you and me to keep fighting for better treatments and a cure.
Too many people with CF still die young. I am running to help change that.
Every stride reminds me how fortunate I am to breathe freely, while for my sister, breathing can be a daily battle.
By donating to my fundraising goal, you are helping advance the research and science needed to bring us closer to a cure for everyone with Cystic Fibrosis.
Thank you for being part of this fight. 💙
Because of the incredible work of the Cystic Fibrosis Foundation, life saving treatments now exist and real progress is being made toward finding a cure. But this progress only continues if we keep showing up.
Cystic Fibrosis is a rare orphan disease, and research depends heavily on fundraising and community support. My sister and so many others living with CF are counting on people like you and me to keep fighting for better treatments and a cure.
Too many people with CF still die young. I am running to help change that.
Every stride reminds me how fortunate I am to breathe freely, while for my sister, breathing can be a daily battle.
By donating to my fundraising goal, you are helping advance the research and science needed to bring us closer to a cure for everyone with Cystic Fibrosis.
Thank you for being part of this fight. 💙
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