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Parker's Platoon
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Parker's Platoon

Hi Friends and Family,




Parker's Platoon is back for our 12th year of raising money for Cystic Fibrosis, CF. As most of you know, our son Parker was diagnosed at birth with Cystic Fibrosis. Everyday our family wakes up hoping for a cure for this life shortening disease. The fact is, there has been amazing progress in medicine allowing several with CF to live longer fuller lives, but that is only for some, not all. We still have a long way to go!!! There are just over 30,000 people living with Cystic Fibrosis in the United States, more than 700 living in Indiana. We fight every day for a cure and we need your help to get it done!




Parker is now 12 years old and is growing so fast and changing everyday, but what hasn't changed is Cystic Fibrosis. Every day Parker still has to take 18 pills just to digest what he eats, complete a 30 minute session with his therapy vest (jiggles), take vitamins and takes his new medicine, Kalydeco. Parker doesn't have to do all of these things because he is sick, this is the life of a healthy person with CF. If someone with CF gets sick, a lot of these medications and therapies triple and may include being confined to a hospital bed.




This year we invite you to walk with us for our annual Great Strides Walk. We will be walking again at the beautiful Victory Field in Indianapolis! The walk will be held on April 27th. Will you join us this year?




Will you consider making a donation and/or walking with us on April 27? If so, you can click on the link below.


Your gift is 100-percent tax deductible! If you plan to walk with us, please register as a walker.




fundraise.cff.org/IndyGS2025/ParkersPlatoon




Thank you for your continued support,


Jeremy, Sandy and Parker Ware
$1,000.00
$250.00
$0.00

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$1,250
raised of $5,000 goal
 

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3 Participants

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Attendance Policy

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.