Truly Inspiring: Chip’s Story

My name is Chip Madren.  Along with my Mom and Dad, Lea and Ken, I have two brothers, Jack (12), and Bret (11) and two dogs.  Without much previous drama, on August 17th, 2010, my pediatrician ordered an MRI for what I thought was a concussion.   My Mom and Dad picked me up from school, took me to the appointment, and our lives went from zero to sixty in about 2.2 seconds that day.  We were immediately sent to Children’s Healthcare of Atlanta at Scottish Rite (CHOA) where, in 72 hours, I had two brain surgeries, MRI  & CT scans, followed by 14 days in PICU, and several more months inpatient.  I was diagnosed with Metastatic (spreading) Anaplastic (aggressive) Medulloblastoma (brain cancer).  Go ahead, read between the lines.  I was in school that morning.  Suddenly, words I had never heard defined our lives and people I had never met were the most important people on earth.

My diagnosis is bad.  Really bad.  There is no other way to put it into words.  As a side effect of the main tumor resection, I also suffer from a rare complication called Posterior Fossa Syndrome.  This syndrome has left me completely debilitated.  I have spent the last year attempting to relearn everything – from holding up my head, talking, swallowing, eating, sitting, walking, using my hands – everything.  I have some hearing loss and significant vision loss.  Currently, I work through about 14 home therapy sessions a week to regain my function.  I am making progress, but the road is still very ominous.  I am still completely dependent on my parents for EVERYTHING.  I have just started a rehab program at Shepherd Spinal Center where I plan to regain my life.           

On the cancer front, I underwent six weeks of cranial and spinal radiation and chemotherapy with 38 round trip ambulance rides from CHOA to Emory.  Next, came six months of intense Chemotherapy at CHOA with multiple admissions for infections, including another stay in the PICU.  I have had several surgeries to place G-J feeding tubes, two shunts and two shunt revisions, and crumbling teeth.  Over nine months, I spent over 130 nights at CHOA.  Fortunately, we live just a few miles from the hospital and could scoot home more than most!  I was able to spend the entire summer at home.  I will have MRI’s every three months for the next several years to monitor the tumors.          

With all of this being said, our family considers ourselves extremely blessed.  From the first hour of our crisis, our community has completely surrounded us.  Immediately, schedules were in place to handle everything peripheral in our lives so that my parents could focus on me.  My two brothers were driven to school each day, helped with homework, sports uniforms cleaned.  My pantry was stocked, meals delivered, laundry folded, toilets scrubbed, grass mowed, and even beds made so tight Bret found it hard to climb in at night!  The Heavens were stormed with prayers of all types.  There were Rosary groups, candles lit, little children’s bedtime prayers – Christian, Jewish, it didn’t matter.  Everyone fell to their knees for me.  I will be forever grateful.                           

The people surrounding and supporting my family have been our lifeline.  The term “lifeline” is not one I use loosely.  This support has saved all of our lives.  Jack and Bret have not missed a baseball game or a birthday party.  Dad’s friends supply the running seasonal hunting or fishing reports.  My Mom’s friends run my errands and visit frequently to chat.  Both of our families are of course helpful as well, they have to be.  It’s the friends who could have easily moved on with their own busy lives, but instead have chosen to stick around that I am so thankful.       

Before I got sick, I was a normal 13-year-old kid.  I played on my school’s baseball team, goofed off with friends and loved anything to do with the outdoors.  My main passion revolves around anything to do with hunting and fishing…..any kind of hunting and any kind of fishing!  My favorite color is Camouflage!!!  I am determined to get walking again soon so I can get back in the woods.  My Dad and I have always been partners in this passion.             

On November 30, 2011, I officially completed my chemotherapy and am considered “off-treatment” and my March 2012 MRI scans are clear.  As for now, I work hard every day at Shepherd Spinal Rehab and at home at gaining back my strength, coordination, walking, balance, speech, vision, and eating.  Everything has to be relearned.  I want to go back to school someday soon as well.  I try not to get discouraged.  This is where I am thankful for my brothers, Mom & Dad, and friends.

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About The Brain Tumor Foundation for Children

Founded in 1983, BTFC was the first nonprofit in the U.S. to focus on brain cancer in children. Our mission is to support patients and their families.
This entry was posted in Brain Tumor Awareness Month, BT Kids, BT Parents, Foundation News, People, Uncategorized. Bookmark the permalink.

One Response to Truly Inspiring: Chip’s Story

  1. Maura says:

    Chip you and you’re family are such an inspiration, so happy to hear that your latest MRI was clear, we will continue to keep you in our prayers. Maura Sandler

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