Close

In Honor of Cannon

Just as you've rallied around Cannon, please support CaringBridge — the home for Cannon's community of support.

Donate Now in Honor of Cannon

Cannon’s Story

Welcome to our Cannonball's Page! Cannon Wiggins is so lucky to be loved by so many people that we wanted to create a page for everyone to keep updated on his progress. Cannon is a very special boy and he needs all of your prayers to fight this nasty disease of neuroblastoma cancer.Please pray for our son. He is our world.Facts:

Cannon was born on August 10, 2011
and was diagnosed at 20 months
old on April 19, 2013 with
Stage 4 Neuroblastoma:
Nymc-amplified, poor histology,
COG protocol at Arnold Palmer Children's Hospital, Resection surgery by Dr. Michael Laquaglia at Memorial Sloan Kettering Hospital scheduled August 2, 2013
Stem cell transplant after 6 rounds of chemo at CHOP
Proton radiation at CHOP
Antibody therapy completed 4 rounds to date at APH Orlando
Tumor: in abdomen, both legs, armpit - bone marrow and lymph nodes
Prognosis: will cannonball this cancer out and be cancer free

Latest Journal Update

A Dead Dog...A Dead Son...

A Dead Dog... A Dead Son


Crazy title, I know. But you see, sometimes my head is a little crazy... sometimes a lot crazy.


As I type I'm sitting on a late night flight from Alabama to Orlando (home). I spent the weekend in parent orientation for my daughter who is about to be a freshman at the best university in the country (winky face). University of Alabama will be her new home for the next four years.


As I reflect as I often do I look out the window in this almost empty plane and see speckles on the ground. Tiny, tiny spots - I'm thousands of feet up high in the sky floating in the air. I bet people never thought that would happen... but it did.


Many people don't think pediatric cancer can be cured. It can! It will! Perhaps not in my lifetime, but it will. Although Cannonball Kids' cancer is a small fish today in the beating kids' cancer world - we are proud to be part of the movement to change the face of kids' cancer!! Nothing is impossible!!


William Becker said: "The difficulties and struggles of today are but the best price we must pay for the accomplishment and victory of tomorrow."


I believe we can victor over children's cancer. I just do! Others disagree but if you allow people's words to stop you, they will!


I won't stop all my days from TRYING!!


Coincidentally, (I don't believe in coincidences and many of you have read me write - "God incidences") a Martina McBride song played on my iPhone - "I'm Gonna Love You Through It". If you aren't familiar, it's about a woman who has cancer and she says "cancer doesn't discriminate if you're 38". Instantly I changed the song. cancer is a life sucker, that's a fact!! It wants every piece of you - your kid, your marriage, your health. It will take every ounce of you if you allow it. Sometimes you don't even see it happen.


Tonight I texted with my friend whose child is fighting neuroblastoma like Cannon, but my dear friend's daughter is fighting a relapse. To say she and her family are living in Hell doesn't quite cover it. So tonight when I got to the airport and they told me the flight was very delayed and I wouldn't get into Orlando until 12am, I told them "There are bigger problems. I can handle a delayed flight." All I could think of was my friend and her baby girl! Today the reality is my life, my marriage, my relationship with my four kids, our Foundation - all of it can be what I want it to be! If I allow cancer to keep sucking me dry then it will. That means turning off cancer songs and not listening to them with tears rolling down my face. I'm getting better - I'm a work in progress!


Oh, the title - I almost forgot!!! Exhaustion is kicking in now. Olivia and I were walking and I said "You will miss Winston our dog when you move here. I am not sure how much longer he will last." In part I was preparing her and me. Olivia was like "You have Winston dead and he is only 5." You see our last mastiff only lived until he was 4 and on average his breed lives until 8. I'm very attached to Winston - really attached. I mean, he was my first baby. I have raised him from 6 weeks old. Olivia and I named him. Statistics are a funny thing - whether it's for cancer or your dog we shouldn't allow them to rule our thoughts. I often do and I am working on doing a better job at that!! Experience has shown me living in today saves me amongst other things gray hairs and worry lines. ;)


The mind is a very powerful tool and I've had a dead dog in mine and a dead son. The reality is only I can control my mind. I want Winston to live forever just like I want Cannon too. But the truth is neither will. But if I think about what COULD happen tomorrow I can't possibly enjoy TODAY. Today my dog loves me like crazy and is very much alive and so is my son. Today both are alive!!! TODAY! I need to remind myself of this!


Today! This weekend!


I had one of the best weekends since Cannon was diagnosed. My sister and Olivia and I teased each other all weekend and laughed so hard for three days that I'm not sure but I think I may now have abs. I allowed my control freak self to let go and enjoy the moments. When I sat in the airport tonight I prayed and I thanked God - "Thank you for giving me this amazing weekend with my daughter and sister - two of the most important people in my life. I would lay down my life for them both!" A truly special weekend that I will never forget!


A high-five to dad who stayed behind and did swimming, park play, ice cream and Chick-Fil-Ai with the three crazy sons of ours with no help whatsoever and better still, zero complaining! I'm pretty proud that my husband leaves the house with three under four, perhaps too much information but that's what I call sexy!!! You're one of a kind Michael Wiggins - I am so thankful you're my teammate in LIFE! What you do with a smile on your face is amazing!


I am

I continue to be

Thankful For The Fight


Purchase our Book - "Thankful For The Fight" - all proceeds to research

https://www.createspace.com/5409855 />

Make a donation to our pediatric cancer research projects

https://secure.squarespace.com/commerce/donate?donatePageId=5403bb30e4b0a7034afbc6dd />

Host a card club event

Melissa.m.wiggins@cannonballkidscancer.org


Written by Mumma-Bear


Cannonball Kids' cancer


www.cannonballkidscancer.org


Thankful For The Fight


Pray Hard

Pray Big


1 year and 2 months No Evidence of Disease


No Relapse Ever

heart
22 people hearted this

Comments

3 Comments

Jodie Redman-Barrett
By Jodie Redman-Barrett
Love, {{{HUGS}}}, and prayers...as always! <3
Sue Koslovsky
By Sue Koslovsky
Love reading your posts. Congratulations on reaching another milestone in yours and Olivia' s life. Her life will change and so will yours. The boys and you will miss her being around. Just know that you are giving her a terrific opportunity that many young people do not have. She will not disappoint you! Congratulations on another milestone! 14 months with no evidence of disease in Cannon' s body is wonderful! Our little granddaughter, Kate Koslovsky, goes in for scans and a bone marrow aspiration the end of July. Please pray that good results are on the horizon. We continue to pray for your family. May GOD keep you wrapped in love and give you the peace that allows you to live in the moment. Love and hugs, Kate's grandparents
e welk
By e welk
I admit your title threw me, but reading your explanation brought tears. I know in a way what you mean.(With elderly parents I have feared them leaving me all too often - I finally told myself "They are HERE, stop mourning them while they are alive!") How much greater your fear for your young son must be, and how much greater your wisdom and bravery by living each day with joy. You are an inspiration Melissa.