Camden's Crusade
Follow Camden's journey and help him fight Neuroblastoma
  • Home
  • Mommy’s Message
  • Neuroblastoma
  • Donate
  • 2015 Cancer Sucks Lemon Challenge
  • 2014 Whipping Childhood Cancer
  • Fundraisers
  • Camden's Challenge
  • Cam's Candids
  • CC Videos & Articles
  • About Us
  • Contact Us
  • Raise Awareness & Get Involved
  • Guestbook
  • Camden's Celebration & Charity Challenge

Home Sweet Home

6/7/2013

 
Camden is doing amazing at home; running, playing, and jumping!! Despite he still limps some and displays weakness in his left leg...he is back to himself (minus some hair). Yesterday he was riding his bike in the driveway, which was awesome to see! Round 2 of chemo starts Tuesday after a clinic appointment to check on lab values! Keep praying, still have a long road ahead of us!!!
noni
6/7/2013 07:32:21 am

I am so happy that Camden is having a good week at home. it will help him be stronger for his next round of chemo. Everyone please keep praying!!!!! I love you so much Camden. Noni

Milaana
6/7/2013 08:54:15 am

That's so good. I hope he gets even better!!!!!! Let's go Camden!

Tara
6/7/2013 09:18:05 am

"A child's laugh could simply be the most wonderful sound in the world." So glad he is smiling and playing, although I bet your smile was wider :-) Keep it up, Cam!! You got this!

Justin Brooks
6/7/2013 10:26:28 am

SO INSPIRING! Man that gets me pumped!! Good for him! Enjoy the sunshine, when it comes back out :)

Aunt Diane, Uncle Rich, Memere, Grampy Roger & the gang from Texas
6/8/2013 02:52:59 am

So glad to hear Camden is doing well at home!! We are all praying for you. We love you Camden and believe you will beat this because you are strong and are OUR Super Hero.

Memere & Grampy Roger are sending good thoughts from Texas.

Lily and Kyra say they love you and hope you are feeling better soon.


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!

    Archives

    December 2019
    November 2019
    September 2019
    August 2019
    April 2019
    June 2018
    February 2018
    September 2017
    August 2017
    May 2017
    April 2017
    February 2017
    January 2017
    November 2016
    August 2016
    July 2016
    June 2016
    May 2016
    February 2016
    January 2016
    December 2015
    November 2015
    October 2015
    September 2015
    August 2015
    July 2015
    June 2015
    May 2015
    April 2015
    March 2015
    February 2015
    January 2015
    December 2014
    November 2014
    October 2014
    September 2014
    August 2014
    July 2014
    June 2014
    May 2014
    April 2014
    March 2014
    February 2014
    January 2014
    December 2013
    November 2013
    October 2013
    September 2013
    August 2013
    July 2013
    June 2013
    May 2013

    RSS Feed

    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

Powered by Create your own unique website with customizable templates.