Camden's Crusade
Follow Camden's journey and help him fight Neuroblastoma
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December 26th, 2013

12/26/2013

 
So as the excitement of a very merry Christmas is scattered throughout my house...it is hard to not think about the next step in our journey.  Camden has been such a trooper taking his pain medication 3 times a day in preparation for antibody.  This treatment is the most challenging of all~from what I have been told repetitively.  It is NOT a walk in the park and prior to starting pain medications early, you could hear the children screaming in pain from opposite ends of the hallways.  It will be hard to see him endure these next treatments, but knowing that this is going to save his life....puts a different twist on the situation.  I ask for us to join in prayer that the Good Lord and his beautiful Mother, surround Camden through each moment of our upcoming battle.  That "They" protect him, watch over him so carefully, that they see to it that the medications obliterate all of Camden's remaining cancer but spares his lungs and other organs, making sure Camden's body is strong enough to fight through without complications~which typically will lead the children to the ICU for supportive care.  Please give his nurses and doctors the insight that we know they already have~to notice unwanted events in time for rapid responses.  I ask for Ron and I to have unfailing strength that we can be at his side every second, with the faces of believe, strength, smiles, and courage.  We trust in you Lord, we believe that you will see us through this.  Please crusaders, I know you are there for us...but I ask, please wrap Camden in an armor of faith, love, and healing...in Jesus' name....

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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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