Cooper Caywood
Karen Caywood / Honor Pages
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$47,826
Raised
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$40,000
Goal
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107
Supporters
Recent Transactions
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Michelle Tibke
$50.00 / 111 days ago
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Anthony Colombini
$245.00 / 744 days ago
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Gig Harbor Heating & A/C, Inc.
$40.00 / 767 days ago
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Debbie McReynolds
$102.50 / 777 days ago
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Kimberly Carpenter
$2,274.00 / 788 days ago
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Halftime Sports, LLC
$194.00 / 788 days ago
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Marlene Caywood
$1,005.00 / 813 days ago
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Thomas and Kassandre Lyon
$500.00 / 813 days ago
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Karen and Christopher Caywood
$51.25 / 820 days ago
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Lori Schindele
$1,476.00 / 821 days ago
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Christine Carbone
$76.88 / 821 days ago
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Timothy Polen
$30.75 / 821 days ago
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Melissa Oman
$123.00 / 824 days ago
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Susan Hendrix
$61.50 / 824 days ago
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Paula McCord
$185.00 / 825 days ago
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Jim Williams
$1,090.00 / 825 days ago
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Russell Lee
$200.00 / 825 days ago
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Raymond Harvey
$945.00 / 825 days ago
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Tracy Turnbull
$80.00 / 825 days ago
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Caroline Eberhardy
$50.00 / 825 days ago
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Kristen Costing
$155.00 / 825 days ago
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Jennifer Bush Luce
$251.13 / 825 days ago
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Daniqua Carpenter
$360.00 / 825 days ago
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Harry Westcott
$235.75 / 825 days ago
About Cooper Caywood
On May 7, 2018, we were told our son, Cooper, 14.5 years old, would not be leaving the ICU. EVER. Alive anyway.
It had been over two arduous years throwing all the medical world offered at the monstrous beast of sarcomas, rhabdomyosarcoma. Neither Cooper, nor we, were going to survive this nightmare while on earth.
In the days following, I contacted Dr. Charles Keller at Children's Cancer Therapy Development Institute. I still grasped desperately to hope, was there anything else we could do?
It is an inexplicable experience to be asking and hoping for the miracle while shopping for a coffin for your child on the same day.
Dr. Charles Keller and Andy Woods jumped into action, arranging for pleural fluid to be overnighted to the Portland, OR lab where Andy spent the next 24 hours running any possible toxic combination against the mutating and multiplying cancer cells from Cooper's chest.
Dr. Keller was in constant communication with me and Cooper's oncologist. What else could be done? Was there anything known to the medical community available to buy us more time? Just a little more time.
The answer 5 years ago was that there was nothing else to stop those vulturous cells from continuing to spread. Excruciatingly, I must tell you that today is the same. Almost 1500* children’s and teen’s families will receive this news, this year, “there is ‘Nothing else’.
The team at Children's Cancer Therapy Development has been and continues to work and search for more options, any options, considering all options. But there are so many obstacles.....so, so many obstacles to saving 1500 children from dying each year.
Dr. Charles Keller and his team at Children’s Cancer Therapy Institute continue to be devoted to finding ways around these obstacles. And we must continue to HOPE.
Your kind and financial support drive the research happening in Hillsboro, OR.
Thank you for this support. All of Cooper’s honor funds are contributed to The Megan Bugg Global Rhabdomyosarcoma Research Laboratory at the Children’s Cancer Therapy Development Institute.
