Camden's Crusade
Follow Camden's journey and help him fight Neuroblastoma
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Round 4, Day 2

7/23/2013

 

Days are going by slowly, 2 more to go! Camden is doing an amazing job. I know you all would be just as proud of him as me and Ron. Treatments are long...one medication runs 24 hrs for 3 days, another is 6 hrs (requiring premedication before and at hour 4 and 8) for 4 days. 3rd chemo med is a slow push through an IV. Camden has developed an amazing tolerance to the hospital setting...my little warrior!! We are thinking more and more about our "make a wish" options, any suggestions? We are certain of our idea, but open to other thoughts! Keep us in your prayers....much love!!

Pam Howe
7/24/2013 01:05:24 am

Glad to hear Cam is such a warrior...Ian was our little trooper when he went through treatment. We went to Disney for Ian's Make-a-Wish...staying at Give Kids the World Village..amazing and special..we did not want to leave the Village..it was so fun and you guys will enjoy it especially after all you are going through now

Erica Hunt
7/24/2013 11:11:26 am

Don't know what your plans our...if he is able Disney does amazing work with Make a Wish...but if he can't travel what about something with superheros. Maybe a huge party with friends and family and people who come dressed as super heroes for him to hang out out with for the day.

So glad to hear that your little hero is doing so well. Always praying for him and your family.


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    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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