I so wish I could take any credit at all for this… but I can’t. Kelli France, of France Photography make this killer video for me with the help of her super talented videographer because she loves me so very much. :) (I bought her dinner and fro yo… does that make up for it?) I have told her no less than 100 times that it means the world to me. It’s so priceless!!! She and Jess (videographer extrodinaire) will never know how much this means to me. It’s seriously perfect. They could not have nailed this any better!! Thank you Kelli and Jess! You talent is through the roof!!
Carter’s Cancer ~ France Photography from Kelli France on Vimeo.
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Wow. I am a puddle. This video is priceless! Love you all
I second that “Wow”.
What a beatiful gift.
Soooo sweet! What a precious video. Carter is such a brave boy. Miss you all tons!
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I got your blog from a family member who knows a friend of yours. My daughter was diagnosed with ALL at 18 months within a week or two of your sons diagnosis. This video of course was very emotional for me dealing with so many similar things. He is an amazing boy. I wish you the best on your journey! Our blog is tabnews.blogspot.com
Andrea, I can’t imagine having a baby go through this. I’m sure it’s much harder because I can reason with Carter… not so much with a baby. I hope she’s doing as well we Carter is. Good luck in this second part of DI. I am DREADING it!!! He was suppose to start it today but he bombed his counts yesterday so we’ll try again Monday.
It has certainly had it’s downs with her being so young…but kids are so amazing! She has adjusted to most things in clinic and that’s helpful. She used to SCREAM bloody murder when they took her blood pressure until her arm would turn purple and they would take it off because it couldn’t read it after 5 min. Now she just screams when they access her port…it takes me and another nurse to hold her down and one time 6 dressings because she screams until she sweats and they won’t stick. We also have to crush and compound all her drugs like the dexamethasone and chemos…and wear gloves for diaper changes for 48 hours. But we’ve been very blessed and she’s responded well to all the treatments. We just starting the steroids and Dox etc next in 11 days so we’re a few weeks behind you…I’m also dreading it but wanting it to come so it will be OVER forever. My heart and prayers are with you and your family…hope he passes counts Tuesday. If you ever need a fellow cancer Mom to vent to my email is tandreabucher@gmail.com
Holy moly, this is so sweet and beautiful and touching…he is darling; you are darling. Praying for you and yours always. {hope you don’t think it’s creepy i found your blog, and am now commenting on it…just have been thinking about you and your little guy.} xo,
Cumorah
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