Salt Fest for Cystic Fibrosis

Salt Fest for Cystic Fibrosis

From Julie Freeland Goodrow

I'm Elena Goodrow, a 15 year old with Cystic Fibrosis living life to the fullest. I've created a magical concert experience to showcase new musicians AND fundraise for the Cystic Fibrosis community. Support the cause!

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Greetings! My name is Elena Goodrow and I am a 15 year old living life to the fullest despite having Cystic Fibrosis.  Together with a group of teens, I am working to create a magical concert experience to showcase new musical talent while raising funds and awareness for the Cystic Fibrosis community at SALT FEST 2019!!  As we prepare for SALT FEST on July 13th, 2019 at the Social Circle Theater,  we are gathering donations and selling original designed shirts promoting and commemorating our event!  We expect at least 200 concert goers to show up for the event.

Our fundraising efforts and sponsorship dollars will benefit Miles for Cystic Fibrosis (M4CF).   Miles for Cystic Fibrosis honors children and adults living with cystic fibrosis (CF), a life shortening disease that affects 30,000 people in the United States, as they make their own marathon efforts every day to maintain their health.  They do this by raising awareness and funds, aiding CF families in need, supporting research to find a cure, and promoting a physically active lifestyle for individuals with CF and their local communities. My family has been actively involved in this organization since its inaugural year over 10 years ago!

I am passionate about making a difference in the Cystic Fibrosis community.  My involvement and the help of my family has helped me to raise over $300,000 for the CF community.  Help me and my super talented friends keep that number growing by making a donation towards our event, SALT FEST 2019!   Your donation would act as a catalyst to help us reach our goal.

For more information about Salt Fest 2019 visit our Facebook page @Salt.Fest or Instagram @salt_fest.  Learn about our funds recipient organization --Miles for Cystic Fibrosis-- on their website www.milesforcysticfibrosis.org.

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