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Cait's Honor Page
Dyan Naylor / Honor Pages
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Cait bravely battled Rhabdomyosarcoma from 2019 through 2023. Help us carry on her legacy as we fundraise cuttting-edge research in hopes that families like ours have safe and effective treatment options.
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$29,812
Raised
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$50,000
Goal
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187
Supporters
Recent Transactions
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Elizabeth Quayle
$51.25 / 167 days ago
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Nicole Merrill
$102.50 / 209 days ago
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Marcus D Goodie Goodloe
$128.13 / 247 days ago
We love you Cait Naylor and the entire Naylor family. #CaitStrong Goodloe’s
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Doug & Ellen Peters
$100.00 / 251 days ago
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Michael Webb
$205.00 / 252 days ago
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Anonymous
$102.50 / 252 days ago
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Anonymous
$102.50 / 252 days ago
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Kimberly Fowler
$50.00 / 253 days ago
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Christine Klein
$200.00 / 256 days ago
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Shawn Freeman
$102.50 / 261 days ago
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Mario Fizulich
$102.50 / 303 days ago
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Athena Chakiris Hogue
$50.00 / 369 days ago
No child should ever have to endure what Cait did, and her family right along with her. What a beautiful and courageous young lady, such an extraordinary soul. PLEASE DONATE AND SHARE SO OTHERS CAN DO THE SAME. HELP END THIS VILE ILLNESS SO IT CAN NO LONGER STEAL OUR LOVED ONES FROM US. THANK YOU!!!
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M L
$150.00 / 412 days ago
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Kimberly Green
$20.00 / 472 days ago
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Chung Shin
$100.00 / 472 days ago
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Perry Lynn
$50.00 / 472 days ago
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Zoe McCook
$102.50 / 479 days ago
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Joe and Deane Naylor
$400.00 / 486 days ago
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Rich Sigler
$102.50 / 497 days ago
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Valerie Sampson
$102.50 / 498 days ago
Hoping for a cure so others do not have to endure the pain like your family has.
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Lynne Naylor
$50.00 / 504 days ago
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Anonymous
$1,110.00 / 505 days ago
Color Street Fundraiser to Honor Cait Naylor💛 It was an honor and a privilege to help and contribute. Thank you
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Anonymous
$51.25 / 510 days ago
About Cait's Honor Page
Cait Naylor was diagnosed with a rare pediatric cancer in 2019 called Rhabdomyosarcoma. As a result of this disease she endured countless needle pokes, blood transfusions, PET Scans, overnight hospital stays and eleven various types of chemotherapies, inhibitors, supplements, nearly 50 sessions of radiation and five surgeries. Sadly, very little research is conducted on Rhabdomyosarcoma because of its rarity. Much of the research that has been conducted has been financed through donations and grants from philanthropic foundations. Very little government funding is utilized to research treatment options for rare cancers like Rhabdomyosarcoma. Cait was told, early on in her diagnosis, that keeping a positive outlook would help her in beating this cancer. Nearly every day Cait demonstrated her commitment through grace, courage and humor. Her drive motivated so many to share her outlook on living with purpose and that “There is always something to be thankful for”. Cait passed away on January 16th, 2023. Her death has left us utterly heartbroken. As her family we are committed to doing our part and upholding Cait's legacy. Please join us in raising money to research treatment options for Rhabdomyosarcoma. We know that there is a cure around the corner, and with your help, we will get there faster. All money donated will directly support the Megan Bugg Global Rhabdomyosarcoma Research Laboratory within the Children’s Cancer Therapy Development Institute (cc-TDI). cc-TDI is a non-profit biotech focused on developing safe, effective and less-toxic treatment options for underserved childhood cancers.