Camden's Crusade
Follow Camden's journey and help him fight Neuroblastoma
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Day -2

9/22/2013

 

Day -2 is a day of rest!  No chemo today.  Camden is disconnected from his IV pole and roaming freely within his room.  He is still eating and drinking (which has slowed down some).  The transplant doctor suspects within a few days he will require a feeding tube....Praying we prove them wrong, but realistic too!!  I am okay with whatever Camden needs to get him through this with the least amount of pain and the most amount of support!  I cannot praise the staff enough....it takes a special person to be an children's oncology nurse and we are thankful to have so many on our side...from Boston to Hartford!!  Chemo resumes tomorrow and then transplant 24 hrs after....

Gramma Nanc
9/22/2013 05:45:39 am

Yes thank God for all those special people that help with Cams treatment !!, ,Super Hero Camden we all are praying for you , we know you are Boston strong !! Love & big hugs

AUNT DONNA
9/22/2013 08:29:58 am

I am so glad that you are surrounded by such wonderful people. Mom and dad were telling me about all the nice things Boston . does for the children and the parents. We are praying for the stem-cell transplant to go well and he doesn't need a feeding tube. Stay strong and remember we are all praying for a complete healing and EXPECTING THAT MIRACLE. We love you very very much.

Jean Vince link
9/23/2013 03:15:42 am

Sending all my love and prayers to Camden!! God Bless all the family......
Infinite love to Jessica, Ron, Emma Rose, Alan & Patrice
Again More Love and Prayers
Auntie Jean
Much xoxo


Comments are closed.
    Picture
    Mommy & Me

    Mommy

    She's going to keep everyone up to date about my progress.  Isn't she the best mommy ever?

    Mommy thought long and hard about my new website.  She thought about protecting me and not putting my hospital pictures online.  But my mommy wants everyone to know that Neuroblastoma isn't just another illness, that it's scary and very serious.  My mommy wants to make sure that other kids don't go through this and that their parents know what to look for.  My cancer is very mean, and I'm scared, but I have my mommy - and daddy - to rub my belly and hold me tight.  I love them so much!

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    Diagnosis:  May 9, 2013
    Surgery:     September 2013
    Transplant: September 2013
    STRICT ISOLATION UNTIL
              January 2014
    Radiation:   November 2013
    Antibody:    January 2014
    END OF TREATMENT                
              June 9, 2014    
    DFMO Trial:  June 2014
        (27 months of DFMO)
    **FINISHED ALL TREATMENT
    JULY 25, 2016


    5 years from diagnosis!!
    May 9, 2018
    ​
    5 years from frontline!! 
    June 9, 2019

    IN REMISSION:  pending
    (waiting for 5 year mark from maintenance). 

    Benign Tumor:  June 2019

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