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The Kansas City Foundation for Pulmonary Fibrosis

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Barbara Sloop


“Nick was diagnosed with Idiopathic Pulmonary Fibrosis (IPF) in 2016. Several years ago, his heath led  him to donate to Genesis' willed body donor program for the advancement of science.”


If you would like more information on Genesis, please visit their website at

For more information on Nick Sloop please click Tribute.

Please indicate in the PayPal note field  "in honor of Nick Sloop

2022 September Pulmonary Fibrosis Awareness Month

KC Foundation for PF lit up Union Station on September 24,2022. Watch the previous Awareness lightings slideshow

Also, Sep PF Awareness Month is to remember our friends.

Watch the 2022 In Loving Memory Tribute.

KCFPF held a Fundraising Event


Your generous gift will help us fund our mission. Together, we can make a difference!

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