Seven Pairs of Hospital Socks

He woke before 6:00 -gunning for the day in general and the race tonight- prepared for occupational therapy at 9:00. He picked his own shirt (“I fight cancer – what’s your super power?“), packed his own backpack (trains, cars, and 7 pairs of hospital socks – because you never know when you might need them), and absolutely insisted that Mickey Mouse not only accompany him to therapy, but that he should most definitely be buckled into the front seat.
And why not?
It’s Chase. 

~MbM~

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Running for Gus…

One of the things that our family loves to do is promote the work of Chase’s hospital, Lurie Children’s Hospital of Chicago.  The treatment that Chase had there saved his life, and the doctors, nurses and staff of the hospital are the top in the world.

Because of this, we try to help the hospital in any way that we can.  This year, that includes dusting off my running shoes, training for several weeks using the aptly-named “Couch to 5K” app, and running in the Run for Gus, an annual fun run along the shore of Lake Michigan in Chicago.

The run was started by the family of Gus Evangelides, who lost his battle with brain cancer in 1995, just three months shy of his second birthday.  Today, his family, and dozens of other families from Lurie, run to help raise money to fund brain cancer research at the hospital.  Over the years that the Run for Gus has been going on, it’s raised millions of dollars to fund brain cancer research at Lurie.

This run has been a tremendous opportunity for our family to give back a little to Lurie Children’s.  Brain cancer is one of the leading causes of cancer deaths among children, and fatal for almost half of the kids diagnosed, but there is painfully little research being funded to help stop it.

With some exciting new developments in cancer research on the horizon (see here and here), Lurie researchers could be just a short time away from making significant discoveries toward finding life-saving treatments for kids like Chase.

I hope that some of you might be able to join us in the run on July 24 (even to cheer us on), or help me raise money for the hospital by donating toward my run.  You can do either by visiting my personal page at the Run for Gus website: http://foundation.luriechildrens.org/goto/ewoldt2014

I hope you’ll join me in supporting this worthy organization!

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Run For Gus

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Thursday, July 24th will mark the second year our family has had the pleasure of participating in Young Associates Board’s “Run For Gus” – a fundraising 5k run/1 mile walk – proceeds from which go directly to our very own Lurie Children’s Pediatric Brain Tumor Program.

This year, we were asked to share why we run (or walk):

Because he is my brother.  I held Chase when he was born, I played with him every day and early one July morning, I was the one who found him having a seizure.  Darcy, age 8

Because he was born when I was only 1 and I don’t remember a time when Chase wasn’t the brother by my side and now I know words like “cancer” and “brain tumor”.  Because I helped hold the bucket while he vomited after chemo and held his hand at his side when they took blood.  Aidan, age 5

Because I was 8 months old when my mom left me with my grandma and went to live days and nights at the hospital by Chase’s side to help him fight and I learned to walk while bringing him toys as he lay on the bed too weak to walk for himself.  Karsten, age 2

Because he is my son and I’ve carried him into operating rooms and had to leave him.  Bob, Chase’s dad

Because I gave birth to him and two years later sat in a room where they told us there was only a small percentage of survival.  Ellie, Chase’s mom

Because I fought.  And I survived.  Chase, ATRT survivor, age 4

Because Chase is where he is today thanks to the efforts of the Pediatric Brain Tumor Program at Lurie Children’s.

Because Chase is our brother and our son.  We run.

For more information on fundraising and Run for Gus, visit Bob’s page here.

Tall As The Trees

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Monday morning~

On our way to Chase’s 18-month post-radiation appointment.  18 whole months since he last whispered “I’m so brave…” and we wondered if this treatment would work and if the cancer would ever clear from his spine. 

As we drove, he stared out the car window into the cloudy morning and said: “Mom, one day, I’ll be as tall and strong as the trees.

We had a precious morning with these people who were only meant to oversee his care, but became dear friends instead.  Rejoicing in the life given…

…moment by moment.