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      December 6, 2018

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      November 27, 2018

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      November 19, 2018

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      December 19, 2018

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      October 1, 2018

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      August 22, 2018

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childhood cancer

My St. Jude Moment
CharitableParenthood

My St. Jude Moment

by Jill May 12, 2016
written by Jill

When I first arrived at St. Jude Children’s Research Hospital a couple weeks ago, I heard a few employees talking about their “St. Jude Moment” and how they were excited for us to have our “St. Jude Moment.” The best I could guess was it would be this magical moment that would brand itself on my heart like a hot iron. I figured it would happen quickly. This place, after all, seemed bursting with magic and joy.

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As we toured the hospital…

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Saw the patient art…

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Talked with survivors…

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Even as we saw research in action in the labs….

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I was touched, moved, inspired, but was I having a moment? Maybe I wasn’t looking hard enough or opening my heart enough?

Toward the end of our stay, we got word at the last minute that we would be allowed to quickly walk from the Tri Delta Place,where we were serving hot food to families, to the ALSAC Pavilion, where the high school junior and senior aged patients would be heading to their very own prom that night. We could only stay for a few minutes.

I expected to see the patients, dressed in ball gowns and tuxedos, and possibly cry. And I did, in fact, catch my breath at the sight of a beautiful bald head in a pink dress escape the crowds of beaming parents and cheering doctors to step onto a luxury bus.

But it was when I turned from her to see if I could try to find her parents in the crowd that that hot iron struck my heart and the hot tears poured down my face.

So many faces of hope and joy looked on toward the children, and I couldn’t help but think what a massive moment this must have been for so many parents who heard the diagnosis of “cancer” or other life-threatening illnesses that St. Jude’s treats, and thought they might never get to see the moment that their son or daughter donned formal attire and took off in a limo for a night of dancing with their friends.

There it was. My St. Jude Moment.

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I am incredibly honored to be working with St. Jude’s Children’s Research Hospital as one of their blogging ambassadors now, and I’m looking forward to bringing you all some more stories of the INCREDIBLE things they are doing, not just for the children they treat at their hospital and clinics throughout the country, but for anyone who benefits from the protocols and research they freely share around the world.

I expected to cry many times at St. Jude’s because of sadness. In fact, all my tears were tears of joy. It is a place filled with happiness and hope, and I am a better person for having experienced it.

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May 12, 2016 13 comments
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Childhood Cancer ACTION and a #HelpSam Update
Charitable

Childhood Cancer ACTION and a #HelpSam Update

by Jill September 10, 2014
written by Jill

Last September, I read a post shared on Facebook, calling out the empty intentions behind so many “awareness” campaigns. This one was specifically addressing childhood cancer. It’s a pretty powerful read.

It was shared by Cassie Sartin, mom of Sam Sartin- a now healthy, vivacious little boy who was diagnosed with stage 4 Neuroblastoma when he was only 5 months old.

You might recall the tremendous fundraiser so many of you helped me with here over 4 years ago. We raised over $9,000 to #HelpSam.

At the time, Cassie wrote…

I hear people talk about what their kids are doing or what they hope they’ll do or become and I just desperately want him to make it there. Scraped knees, school dances, best friends, hurt feelings, swingsets and playgrounds with big slides, peeing on trees, playing in the dirt… I want him to experience it all. 

Now, 4 years later, she reports…

Sam has been off of treatment for a little over two years now. If you met him for the first time today you would never know that as a baby and toddler his tiny body had been through hell and back. He bounces off the walls, loves learning new things, tests his limits, asserts his independence, and would prefer to constantly be on the go. He can’t wait to start school next year.

(Isn’t that just the best update?! There’s more about Sam at the bottom of this post for those of you who have been interested in how he’s doing.)

When Auntie Anne’s reached out to me about the campaign they are participating in with Alex’s Lemonade Stand (a top notch charity that raises money for childhood cancer research), I jumped at the chance to collaborate, remembering how that blog post resonated with me last year.

Childhood cancer research is still tremendously under-funded. And while kids like Sam are beating it, thousands more are still fighting, like Antonio, who was diagnosed with brain cancer last year.

They all deserve the best shot at a rambunctious childhood, complete with scraped knees and school dances, right?

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So while spreading awareness is wonderful, and a great way to visibly show our support for all the fighters and survivors, it’s even more important we take action whenever we can.

That’s why I’d like to encourage you, if you are able, to please head over to the The Mighty Fight’s campaign on CrowdTilt.com and donate what you can before September 15th.

$25 funds half an hour of childhood cancer research.

If you can’t take action this way, consider hosting a lemonade stand of your own for Alex’s Lemonade Stand. Cassie also suggests signing up to donate blood or joining the national bone marrow registry at BeTheMatch.org.

I’d like to end this post with more from Cassie on how Sam is these days. 

Sam’s type and stage of cancer has about a 50-60% relapse rate (curesearch.org) so his follow-up care includes labs every month, and scans every three months to make sure he’s still in the clear. Scan time is certainly nerve-wracking, but in the day to day we are just living normal lives, whatever that means.

We had a little bump in the road when his routine scans last December showed that a spot we had been monitoring on his kidney grew larger. After surgery remove the mass it was determined to be renal cell carcinoma, a secondary cancer most likely caused from his neuroblastoma treatment.

Thankfully it had not spread to any other areas of the body, the surgery was the only treatment required. It will just be something we continue to monitor going forward. He does have some other lasting effects from treatment like high frequency hearing loss, but if hearing aids are the price we pay to have our kiddo here, we’ll gladly pay it.

I try not to tell people to “live in the now” or “cherish every second” because a.)Yuck. Cliche. And b.) Of course life and parenting aren’t without their frustrations. You don’t have to drink in every moment. But in the quiet moments, that’s what I do. I give thanks that Sam is here to challenge me and worry me sick and give me hell and grey hairs. He’s still here.

September 10, 2014 8 comments
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