Katie and the bumblebee Aidan's Avengers




Our Mission: 

“Understanding the devastating effects of pediatric brain cancer, Aidan’s Avengers™ strive to raise awareness and funding for research programs that focus on pediatric brain cancers such as DIPG and to provide financial peace of mind for families affected by pediatric brain cancer.”  


Become Aware 

Aidan was a happy, healthy and energetic 3-year old little boy…up until diagnosis. Read Aidan’s story here.


Support Our Cause

Aidans Avengers

Support Aidan’s Avengers by making a tax-deductible donation or by purchasing gifts and apparel.


Join Us


Join us in the battle! Learn what you can do to make a difference. We will NOT stop until a cure is found!


St. Jude describes DIPG perfectly…

Aidan and Mommy

Aidan and Mommy

DIPG children must move from one experimental protocol to another, enduring treatments with side-effects unacceptable with any other diagnosis. The cruelty of this disease cannot be denied!

DIPG spares the child of their cognitive abilities, while slowly robbing them of their motor functions resulting in partial paralysis, inability to walk, loss of voice & sight and finally ending with an inability to eat and breathe.

It is both heart wrenching and painful as these children are fully aware of their decline often until their last day.”



In the News

Aidan & Mommy

What I Wish More People Understood About Losing A Child

I read this article and felt it was a perfect share for our family and friends… I know it can be hard for others to know what to say or do when they see us — this article is spot on! “Four and half years after the death of my oldest son, I finally went to…

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The black box of DIPG

Overturning dogma to open the black box of DIPG  by TOM ULRICH on JANUARY 12, 2015 You can’t advance the care of a disease that you can’t study. And for 40 years, that was the case with a rare, uniformly fatal pediatric brain tumor called diffuse intrinsic pontine glioma, or DIPG. DIPG isn’t like most brain…


Meet Buzz ~ Aidan’s Gift

It’s been awhile since we have posted. Things here are as expected, good moments and of course many sad days. The holiday season has been especially difficult for the whole family as we get closer to our first Christmas without Aidan 😥 . Aidan gave us a beautiful gift this past weekend and we wanted to…


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We are heartbroken!! NO parent should be faced with this pain.
The last several months I got to know Dylan's loving mother Amanda. I wish we would have been brought together because our boys, Aidan and Dylan were having a play date, but instead I met Amanda because of the monster called DIPG.

Dylan's fight with cancer - DIPG -->We are sharing in your sorrow and hoping you will find comfort in the wonderful memories you shared with Dylan.

“If ever there is tomorrow when we're not together... there is something you must always remember. You are braver than you believe, stronger than you seem, and smarter than you think. But the most important thing is, even if we're apart... I'll always be with you.” A.A. Milne - Winnie the Pooh
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At 2am this morning Dylan gained his angel wings. He did not suffer long once his progression started. And for that I am thankful. He was courageous in his fight against DIPG. He absolutely loved h...

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If you ever wanted to try Painting with a Twist - Royersford, PA -- Sun, Aug 7th @ 2:30 is your chance & ALL sales benefit Aidan's Avengers! Caitlin and I tried it out in May, we had a lot of fun (oh & I can't draw) If you are local - hope you can join us for a fun time and a good cause. We will be painting - **Summertime Wishes** - Please register here: tinyurl.com/hr3p7y3 [PLEASE SHARE] ... See MoreSee Less

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Please keep this handsome superhero, Dylan and his loving family in your thoughts & prayers. They're heading to DC in hopes of being accepted in a new trial for DIPG. THIS IS WHY WE FIGHT!! Dylan's fight with cancer - DIPG ... See MoreSee Less

Dylan loved his trip to Clyde Peeling's Reptiland! We had a personal tour guide that gave us the best experience! Thank you to Tara O'Neil Dunion and family for giving us this experience. It was all ...

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