The "Giving Train" is a platform designed to give back and pay it forward.
Our Amazing Owen is a 501c3 non-profit foundation dedicated to providing support to local Southern Arizona children and families that have been diagnosed with Pediatric Cancer.
03/19/2025
Harper and I participated in a Sip & Paint fundraiser last night. This fun event was hosted by our friends at Butterfield RV park benefiting Owen’s foundation. Thank you Beth, with Southern Gypsy Artist for guiding us through the artistic process and nurturing our creativity. We had such a great time with this great group. Thanks Butterfield!
04/15/2024
Owen’s foundation was selected as the recipient of Butterfield RV Resorts annual fundraising efforts. A culmination of auctions, estate sales and donations by seasonal guests and year round residents of the park. Together they raised over $6,000 dollars to benefit “The Giving Train” and support our efforts to provide comfort and support to the pediatric cancer community throughout Southern Arizona. A special thank you goes out to Park Managers Tammy and Jeff Madden and all the residents of Butterfield RV resort. We would also like to thank the family and friends of Tom Colwell for their generous donations and Richard Anderson for all his hardwork and efforts in honor of Tom. Thank you all so very much. We appreciate each and every one of you.
04/10/2024
A special Thank you to Ron McLaughlin of Benson AZ, for his donation of a mobility scooter to Apryl Hunter and her mother Deanna Hernandez. The scooter will provide this family with much needed transportation to and from appointments. We are so thankful or these opportunities to facilitate connections and assist families in the cancer community. Thank you Ron for your generous donation.
03/02/2024
Last week, the Benson AZ employees of Sulphur Springs Valley Electric Cooperative, graciously selected Our Amazing Owen Foundation as the recepiant of their fund raising efforts. Made in honor of Chase Manzo. A huge Thank You goes out to Ashton Thomas, Dylan Layton and all the employees of SSVEC for their generous contribution in honor of Chase Manzo.
12/03/2023
Tonight the girls and I were honored to ride in the Benson Christmas parade to represent Owens charity and the wonderfully supportive community of Butterfield RV resort. Thanks Chuck, we loved the cool ride (1928 Ford model A) Merry Christmas Benson! Love- Taillie Family
10/01/2023
A SUPER BIG THANK YOU to Cindy Allen and the generous folks at Benson Clean and Beautiful for their donation to our foundation. Frank stopped by on route to pick up the check himself.
Every penny helps us to continue our mission of providing comfort kits to the family’s of children who are receiving treatment at Diamond Children’s Medical Center in Tucson. Thank you for your continued support Benson. ❤️
04/28/2023
We are so grateful to our friends at Butterfield RV Resort in Benson for selecting our foundation as a recipient of their fundraising efforts. Thank you Butterfield! 🩵🎗
04/23/2023
To follow Mia's journey and show your support please check out her page below.
Mia was born w/ a rare bone marrow failure syndrome called: Diamond Blackfan Anemia. Her body DOES NOT produce any red blood cells. Please Donate Blood! (Over 235 blood transfusions)
04/23/2023
Received this heartfelt email from the parent of child who received one of our comfort kits during her stay in the hospital last month. Messages like this mean everything to us. Thank you to everyone who continues to support the foundation. Your donations really DO make a difference in the lives of these families.
(Mia's family gave us permission to share her letter and photo)
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12/18/2022
Kartchner Wonderland was a great success! A BIG thank you to everyone who worked so hard to put this event together and to everyone who came out to enjoy it. We had such a fun time visiting with people who stopped by our booth; we are so grateful for your generosity. Many pediatric cancer families will benefit from the funds we raised tonight. 🥰❤️🎗 Merry Christmas!
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As the baby of our family, Owen was born at 37 weeks gestation along side twin sister Kate. He was a sweet, gentle and loving baby with a beautiful smile and infectious laugh. Most of his early months were spent at home growing, learning and playing with his older siblings. Owen loved being part of his family. Whether it was playing Legos with his big brother Nathan, dress-up with big sister Harper or dancing to the Wiggles with Kate he just wanted to be included.
Two months prior to his 2nd birthday Owen started showing signs of concern. High unexplained fevers, absent gazing, trouble balancing and eventually daily throwing up led us to an early Monday morning check up with our pediatrician. After a short evaluation she could see that something was definitely wrong. She suspected intercranial pressure and sent us directly to our local hospital. After blood work and a CT scan the results revealed a large mass in the center of Owens brain. He was air lifted to a children's hospital 3 hours from home. Additional testing, MRIs and biopsies would identify his brain cancer as Pineal Blastoma. This extremely rare and aggressive tumor was already stage 4. A resection to remove the mass was our first plan of action. But, we almost lost our son the day of his surgery. This incredibly vascular tumor bled and bled as it was removed piece by piece. The blood loss could not be stopped. The resection to remove the tumor was successful but the operation almost cost Owen his life.
Weeks of recovery and rehabilitation led us to the next phase of his protocol, chemotherapy. Whatever cancer was left behind had to be dealt with, or at the very least slowed down. For the next 3 months Owen was inpatient every 3 weeks for treatment. During this time his stem cells were harvested and another central line placed in his chest. After the holidays Owen began another series of high dose chemotherapy treatments followed by three rescue stem cell transplants meant to boost his immune system and help his counts to recover. These high dose, toxic chemicals would prove effective against his cancer but only for a little while. Only 7 weeks after Owen was declared “no evidence of disease” following a clear MRI, his cancer came BACK. What began as one solid mass tumor in his brain, was now 10-12 small and large tumors throughout his brain and spine. This, just 48 hours after our son, an ambassador for the Relay for Life (an American Cancer Society fundraiser) had been honored and celebrated as a “survivor”. Owen had relapsed.
The morning the cancer revealed itself to us again was just like any other. Coffee, news, breakfast, cartoons.... But Owen had slept in. He was tired we thought from playing at the park the day before. But when he finally awoke and got out of bed, he couldn't walk. He was shaky and unstable. I remember my husband calling out to me from the bedroom. The sound of worry and urgency in his voice. I stopped what I was doing in the kitchen and headed towards the hall. That's when I saw him. Owen was struggling to stand. I stopped there in the doorway and sat down on the floor and sobbed. I knew what had happened. My instincts hadn't failed me before although, I prayed desperately that this time I was wrong. We called the hospital to report his symptoms to his doctors, they told us to come in immediately. We packed in slow motion. We didn't want to go back. We knew what this meant. Couldn't we have just one more day of innocent optimism? But the testing began again. ID bracelets, white sheets, lines accessed and fluids started. Weight and height measured, blood drawn and vitals recorded. It had only been 7 weeks? The news of our admission started to travel. At first down the halls and out the doors but then to our hometown to neighbors, family and friends all across the country. We had always kept everyone “in the loop”. It was a careful but conscious decision we made early on in Owens diagnosis to share his journey with the everyone. To share our good days and our bad. What started off as just a few followers quickly grew. We knew we would need their prayers and they would need our updates. But no one was prepared for this news. We had all fought so hard to beat this awful disease, especially Owen. And now it was back.
From the Sunday he relapsed to the Sunday he passed was three weeks. Just three short weeks to wrap our minds around the idea that our beautiful, precious, amazing son was sick again. We had to prepare ourselves for the idea that we weren't going to be able to “fix it” this time. And we would very possible have to say goodbye to our child. No time is ever enough to prepare for the loss of a loved one, especially a child. Now, don't get me wrong, we didn't just give up and give in. Every minute of everyday was a desperate search for answers and options. We called and emailed and researched, doctors, treatments, trials and alternative medicines...… We began palliative radiation the very week he was admitted; requiring him to be put under general anesthesia every single day. We played, we ate, we slept, we laughed, we cried and we prayed to the very fullest extent of every moment we had together. It was beautiful and gut wrenching all at the same time. Everyday was full of love and light and sadness and fear, a roller coaster of emotions. But, eventually we would come to the end of his treatment. What could be done, had been done. And once the tough decisions were made we were left with no other choice but to take our amazing Owen home. It is after all what we wanted from the very beginning. And he knew this time was different. But as always he did his best to protect us. Often sharing a soft smile, gentle fist bump or wave with his visitors. His final gift to us was a wonderful and unforgettable trip with our family to the Grand Canyon by train. Owen and his Dad always loved trains and it seemed fitting that we take that final ride together.
After returning home Owen began to decline. What we thought might take weeks or even months was only days. His system had begun shutting down and the tumors on his brain stem were causing a lot of problems. Eventually his body gave way to an infection and within hours he was gone. In our arms and surrounded by his loved ones Owen slipped gently from this world to the next. And moments later a beautiful double rainbow appeared in the sky over our home. A reminder of Gods promise. It was the most awful and incredible day of my life. And, it was a gift and an honor to be there with him through it all. I was truly blessed by the beauty of his life. We all were. Owen was a strong, smart, brave and loving child. I still don't understand why he had to leave us so early on his journey but I do trust in Gods promise that we will meet again. So until then, I just keep looking up, waiting for the clouds to part and for the rainbow to appear. We continue his work, spreading his joy and sharing his light. Because that's what this life is really all about- “Giving”.