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

2 weeks, 3 days later

5/25/2013

 
Day 5 chemo complete! We remain here at CCMC for a few more days in an effort to wean Cam from IV nutrition and IV medications. The other piece that will keep us here is his nightly fevers. Fevers are a big concern and even if he gets one at home, its a ED visit or readmission to hospital. Hoping those subside now that chemo is complete for cycle 1. We are getting restless here and anxious to return home! Rest assured we are in caring hands as all of the doctors, nurses, and everyone else here has been nothing but wonderful!!
Jodie
5/25/2013 02:16:38 am

So glad he's completed day 5 and round 1!!! Hope those fevers get under control fast!!

Tina Neborsky
5/25/2013 03:03:03 am

So happy to hear Round One is complete. Praying like crazy Camden, Jess and Ron will get to go home ASAP!!

Laura Rose
5/25/2013 05:07:54 am

We are praying hard & hope you all can come home soon!

Sky's mommy
5/25/2013 07:13:08 am

Good job kiddo! Camden's mommy...it is a hard road to travel down when your child is sick. Life turns upside down and everything changes in the blink of an eye. You will have days when you feel defeated and annoyed at doctors and nurses, the hospital will become your home away from home and you may even want to bang on god's door and demand answers. This journey will make you and your family so close and you will quickly learn how important the small stuff is and how much courage, strength and patience you an your son have. The heart of a fighter is a beautiful thing and the love of a mother is truly unconditional. You are going to become a nurse quickly and without any experience but you will get the hang of it. Things that seem so scary at first will come second nature soon enough. There are times when you will want to break down and it's okay...just cry your heart out and wipe off your face and put your armor back on to fight this battle with your son. Most of all, keep hope. That's what will get you through the day. Time is what you make of it...make it count.

Mary Anne Culhane
5/25/2013 09:32:57 am

Go Camden! The Caped Crusader is a 4 year old boy named Camden and he is made of the toughest stuff!

Sandra Wilson
5/25/2013 11:44:45 am

Camden is such a strong little man, with a great big smile and heart to go with it. We are so touched with your smiles and hugs for mom, your sister and dad. May the sun shine in your room and bring you rays of God's Hope...

Amber
5/25/2013 01:04:38 pm

We are praying for your family .... Stay strong !


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.