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Laps for Levi Cystic Fibrosis Walk T-Shirt Sales

Organized by Erin Taylor
Front large extended
Laps for Levi Cystic Fibrosis Walk T-Shirt Sales Fundraiser - unisex shirt design - front
Laps for Levi Cystic Fibrosis Walk T-Shirt Sales Fundraiser - unisex shirt design - back
Laps for Levi Cystic Fibrosis Walk T-Shirt Sales shirt design - zoomed
Gildan Ultra Cotton T-shirt

Help us beat CF by rocking this T-shirt!

Custom Ink
All funds raised will be paid directly to Laps for Levi for Cystic Fibrosis Great Strides Walk Laps for Levi Team.
$1,760 raised
116 items sold of
50 goal
Thanks to our supporters!
$25
Gildan Ultra Cotton T-shirt, Unisex - White
Gildan Ultra Cotton T-shirt
Unisex - White
Organized by Erin Taylor

About this campaign

Help support our Cystic Fibrosis Walk team, "Laps for Levi," by purchasing a shirt. Whether you walk with us in person on May 17 or in spirit, please help us raise awareness for CF by sporting this awesome shirt. We are GRATEFUL for your support. Proceeds from the T-shirt sales will go directly to the CF Foundation, an organization we truly believe will save our son's life. The rose has long served as a symbol for CF, as many children called their disease "65 roses." Levi has always loved dancing to the music of Jerry Garcia, so this shirt was specially designed forhim.By wearing this shirt, you join us in our fight to find a cure for cystic fibrosis.


In February 2014, we welcomed a very healthy baby boy into our lives.He was absolutely perfect. When Levi was just eight days old, a day after receiving a clean bill of health at his one week check up, we received a call from our pediatrician, who told us that Levi's newborn screening (routine blood draw taken while he was still in the hospital) indicated he needed further testing to rule out cystic fibrosis. After testing and two agonizing weeks of worry, Levi was diagnosed with CF at three weeks of age. While it was heart breaking news to receive, we are very thankful for the CF Foundation for implementing programs like newborn screening, which identified our son's CF well before he showed symptoms. Because he was diagnosed so young, we are able to be very proactive with his care. Today, he is a very happy, chunky one yearold. He looks and acts like other babies, but takes enzymes to help him absorb his food, takes inhaled breathing treatments2-4 timesa day to keep his lungs clear, and takes vitamin, salt and acid reflux medicine every day. As he grows older, his routine will include additional medicines. CF is a progressive disease, so we don't know what to expect, other than tohavefaith that by supporting the CF Foundation,Levi will have the drugs he needs to have a full, active life.His care takes extra work on our part, and it's definitely an emotional struggle,but we are SO THANKFUL for the CF Foundation for the advancements made in CF care that are keeping Levi healthy.He is perfect.Let's find him a cure. By purchasing a T-shirt, you are helping us raise funds to beat CF.DSC_0129JPG

Supporters

Sandy Bratton 1 item
Justin Hester 1 item
Terry and Sarah Ackerman 1 item

Way to go, Levi!!!!

Whitney Frazier 1 item
Laxmi 1 item
GraC 1 item
Traci Martin 2 items
Lisa Jewell Adkison 2 items
RD 4 items
Lori and Seth George 1 item

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