The Jack Strong Foundation

The Jack Strong Foundation The Jack Strong Foundation is a 501c3 non-profit organization committed to assessing and supporting financial needs of families battling childhood cancer.

Today (July 19, 2017), on the one-year anniversary of Jack’s death, we honor him with the launch of The Jack Strong Foundation. Jack had an enormous heart full of kindness. He visited and encouraged other children in the hospital, sharing smiles and delivering hope. He brought communities and thousands of people from all over the world together with his journey, and for this reason, we honor his

legacy and continue to fight. When Jack was diagnosed in 2013, we discovered the impact that treatment for pediatric cancer can cause a family emotionally and financially. Families find that their regular income has to be reallocated on things like medical expenses, medications that aren’t covered by insurance, lodging, and travel expenses. The Jack Strong Foundation seeks to continue his legacy through fundraising efforts that support families who have been impacted by childhood cancer by assessing needs and providing financial aid and awareness. When you visit, jackstrong.org, you’ll find personal stories, photos and video, coverage of families The Jack Strong Foundation is supporting, and resources on childhood cancer statistics and treatment. You can safely and securely purchase t-shirts and bracelets in our online shop, share your Jack Strong story, or donate to the foundation. The Jack Strong Foundation is a 501 c3 non-profit organization and is governed by both state and federal law. All donations are 100% tax deductible, and will help children and their families who are fighting cancer every day. We are 100% volunteer based. Each dollar that you donate goes directly into The Jack Strong Foundation to fund our programs.

  We hope that you will considerhelping us continue Jack’s legacy by making a donation this  .The Jack Strong Foundation...
12/02/2025



We hope that you will consider
helping us continue Jack’s legacy by making a donation this .

The Jack Strong Foundation is 100% volunteer based. That means that every cent of every donation goes directly to keeping our programs running.

We appreciate every donation, no matter the size, every cent helps a child fighting cancer ! 🎗

We are grateful for each and every one of you for bringing awareness to these brave faces!

https://jackstrong.org/checkout/donate?donatePageId=595ace5be4fcb5067511eaf5


Please take a moment to contact your House Representative and urge them to vote YES on the Mikaela Naylon Give Kids a Ch...
12/01/2025

Please take a moment to contact your House Representative and urge them to vote YES on the Mikaela Naylon Give Kids a Chance Act.

It only takes a few seconds, and your message will show Congress that we stand with children with cancer.

Please follow the link in the post.

Time Sensitive! Tonight and tomorrow, we have a critical opportunity to help save the lives of children with cancer.

On Monday, Dec. 1, the House of Representatives is scheduled to vote on the Mikaela Naylon Give Kids a Chance Act. Your voice can make all the difference.
This legislation is named in honor of Mikaela Naylon, a brave osteosarcoma warrior who traveled to Washington D.C. to advocate for this very bill just months before she passed away. Mikaela wanted to make a difference for other children fighting cancer, and now we have the chance to help fulfill her wish.

Here's how you can help:

Please take a moment to contact your House Representative and urge them to vote YES on the Mikaela Naylon Give Kids a Chance Act. It only takes a few seconds, and your message will show Congress that we stand with children with cancer.

Click here to write to your Representative now:

https://www.congressweb.com/KVC/14/

Let's honor Mikaela's legacy and give every child a fighting chance. Let's get this bill passed!

It is with deep sadness we share the passing of beautiful Rilyn.Her parents write: “Please keep our family in your thoug...
11/30/2025

It is with deep sadness we share the passing of beautiful Rilyn.

Her parents write:

“Please keep our family in your thoughts as we navigate this unimaginable loss. After her brave and courageous battle with cancer, heaven gained the most beautiful angel yesterday evening. Please pray for our peace as we learn to live for Rilyn and not with Rilyn. We will carry her love with us forever, but she will be deeply and endlessly missed. 💔 “

“Come on baby with me, we're gonna fly away from here. You were my best [seven] years.”

Please keep her parents, Cliff and Jamie and all those that love her; in your thoughts and prayers.
Please hold them all tightly in your hearts as they endure the very difficult days ahead.





11/28/2025





Thanks for being a top engager and making it on to my weekly engagement list! 🎉Steve Smith, Michele Brower, Dixie Armstr...
11/28/2025

Thanks for being a top engager and making it on to my weekly engagement list! 🎉

Steve Smith, Michele Brower, Dixie Armstrong

11/27/2025
❤️Please ShareAre you the parents or caregiver of a child fighting Childhood Cancer? Do you have upcoming treatments, cl...
11/26/2025

❤️Please Share

Are you the parents or caregiver of a child fighting Childhood Cancer?

Do you have upcoming treatments, clinic, surgeries or scans? Maybe your child is currently having a difficult time in treatment, and you BOTH could use some loving SUPPORT?

Let’s show the world the beautiful BRAVE faces of the many SUPERHEROES fighting childhood cancer!

❤️Please share a photo of your WARRIOR 💪 and if you choose, a little of their journey in treatment this week. We are ALL ready to send an abundance of love, prayers, support, hope, and encouragement to each of you!

WE ARE HERE‼️
WE SEE YOU‼️




This precious little face belongs to 1 yr old Kennedy Rae💕Kennedy’s parents had found a lump in her abdomen. Because of ...
11/25/2025

This precious little face belongs to 1 yr old Kennedy Rae💕

Kennedy’s parents had found a lump in her abdomen. Because of its location, they assumed it was her stomach. A few days later she awoke screaming so they immediately took her to ER. It was then, on Oct.31, 2024, her biopsy revealed it was a malignant rhabdoid tumor, which is extremely rare and aggressive.
Since that time, Kennedy endured her cancer treatment protocol, including surgeries, radiation, immunotherapy….
But even with the difficult moments and treatments that Kennedy has been through, the tumor in her liver has continued to grow, doubling in size in less than a month. The cancer has grown and spread through her little body. Kennedy Rae has been placed on hospice.

💗Her parents share: “We’re taking this time day by day, soaking in every laugh, every snuggle, every moment of Kennedy being Kennedy. Her resilience continues to amaze us. Even when she has discomfort, even when her body is fighting so hard, she still finds reasons to smile. She still tries to play. She still lights up the room. It’s a blessing we don’t take lightly.
We don’t know when things will shift or what the next weeks will look like. But we continue to trust the Lord with every step. We believe He is holding Kennedy in His hands, that her story is already known, and that her ultimate healing is secure—whether that miracle happens here with us or in heaven.”

🎗️Please join us in sending little Kennedy and her family all our love, light, comfort and support, as they walk these next uncertain steps. Please share good vibes, prayers for courage, strength, and infinite HOPE!
Sending you so much LOVE beautiful child💛

Faith Over Fear: Kennedy Rae’s Cancer Fight


The Jack Strong Foundation

💔Update on little MargarettPrecious little 3 yr old Margarett and her family received the news of her latest scan result...
11/24/2025

💔Update on little Margarett

Precious little 3 yr old Margarett and her family received the news of her latest scan results. In her momma’s words “…we received the news I have prayed I never would have to get to in all of Margarett’s journey”

Margarett’s cancer has spread all over. It has gone to her lymph nodes, ignited more in her lungs, and has returned in her liver.

Beautiful little Margarett will now continue her fight at home. Comfort, peace, family, love and making very special memories will now be their focus, as options are very limited.

Please send loving thoughts and prayers to little Margarett. Let her and her parents know they are not alone. Good vibes, prayers for courage, strength, comfort, grace and infinite HOPE! We are holding you so tightly in our hearts,and sending you so much LOVE little one💚🩷



Every warrior parent has had “that moment” when they were told “your child has cancer”. Please share a little of your st...
11/23/2025

Every warrior parent has had
“that moment” when they were told “your child has cancer”.

Please share a little of your story,
about the symptoms your child was experiencing that led you to the doctor or ER. 🎗️

is knowledge


Hello Everyone ! Please say hello to this ADORABLE SUPERHERO JACE! ❤️💙Jace just celebrated his 2nd birthday! (November 1...
11/23/2025

Hello Everyone !
Please say hello to this ADORABLE SUPERHERO JACE! ❤️💙

Jace just celebrated his 2nd birthday! (November 10th)
Happy Birthday to YOU!! 🎈

On February 25, 2025, Jace’s parents took him to the ER for stroke-like symptoms. After testing, they found a large brain tumor. Jace was diagnosed with Atypical Teratoid/Rhabdoid Tumor. AT/RT is a fast-growing, aggressive and malignant tumor. It affects your central nervous system (brain and spinal cord). It's more common among children than adults.

Jace has an older brother that he loves dearly. His name is Connor.

Let’s flood Jace and his family with encouragement, support, love, and many, many prayers. 🙏🏻

YOU’VE GOT THIS JACE‼️
YOU are so BRAVE‼️

’s Battle Buddies



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Bridgeport, WV
26330

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