Added: 4 years ago
From: robmoff2
Views: 10,050
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  • I know Jake's family and they are the nicest people in the world....love and miss you Jake!!

  • my heart breaks for your family. my daughter has hepotoblastoma stage 4, she is 6yo, we have just started our fight, thank you for sharing your story, so much of what you have shared rings so true with us. my daughter is like Jake, always smiling no fear of death, and is a shining light to us. God bless

  • This a wonderful thing they are doing. I have a 15 month old little boy and another boy due in January. The thing that surprises me the most is that Stacy is so giving. I say this because I knew her in high school and she was not a very nice person and looked down on alot of people. Glad to see she has matured and my heart goes out to her and her husband.

  • this is so sad my friend masie is i think related to him in some way and it is still so sad

  • omg i am crying omg !! i didnt even know him and i love him!

    ♥hayley =*[[

  • Jake is my retired assistant principal's grandson. Today we watched a video about him that she had brought by the school. Currently we are having a can food drive to help raise money for children with cancer.

  • I stumbled across Jake's site when my son was first diagnosed. It was about 1.5 years ago. I have followed his courageous battle and kept him in my daily prayer. This video is a beautiful tribute to an incredible boy and his family.

    Thank you for opening up your hearts to the world to further awareness of the horrible beast robbing us of our precious children!!

    May God continue to bless you all

  • I went on Jakes website everyday to see how he was doing. When i went on and it said he earned his wings i burst into tears, im so glad he isn't suffering anymore but, he was so young. I love yo Jake and your forever in my heart!

  • Not sure how this happened,Sorry Albert.

    Here's my post under my own name:

    You all have been and still are in my prayers. I have been keeping up with Jake's story on the Recipezaar website. It is easy to see what a special little boy Jake was throught the pictures & videos, even for those of us who didn't "really" know him. What a wonderful way you have choosen to honor Jake. I wish much,much success to the Jake Owen Raborn Foundation.

    God bless you all.

    Hugs,

    Islandgirl77551

  • Thank you for sharing your story. It hit really close to home. My 2-year old son was diagnosed with Hepatoblastoma in November of 2005. The end of August will mark 1.5 years of remission.

  • My 2 yr old son was diagnosed with stage 4 hepatoblastoma with pulmonary metastisis just this past June. He's now on his second round of chemo. We are being treated at MD Anderson in Houston TX.

    The reality of this kills me, but I thank you for sharing your story.

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