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.
(2)

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.

❤️Please ShareAre you the parents or caregiver of a child fighting Childhood Cancer? Do you have upcoming treatments, cl...
03/18/2026

❤️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 beautiful and brave superhero is Lilah! 💕She is scheduled for her 3 month MRI  tomorrow. Please pray for everything...
03/18/2026

This beautiful and brave superhero is Lilah! 💕

She is scheduled for her 3 month MRI tomorrow. Please pray for everything to be clear.

Her Momma writes:

“Please Lord hasn’t she been through enough? Please. Please just let me have more time with her. Just a little bit more time. Even if she’s not healed please don’t let her leave me this soon. Please let me get to know her a little bit more. I’ve only had 2.5 years with her. It’s not enough Lord. Please I need more time. Please.
Lilahs MRI is tomorrow. A very high emotion day for us. I’m trying not to think too much about what I can’t control.”

Let’s flood Lilah and her beautiful family with encouragement, support, love, and many, many prayers. 🙏🏻

WE’RE WITH YOU LILAH ‼️
Sending many, many prayers




03/17/2026
💔Update on CylusIt is with the heaviest of hearts that we share with you the passing of the very brave Cylus. His mother...
03/14/2026

💔Update on Cylus

It is with the heaviest of hearts that we share with you the passing of the very brave Cylus.

His mother shares:

“No more pain. No more pokes. Our sweet angel stormed the gates of heaven at 1:00 pm today. I told him it was okay to go to Jesus & he went. Cancer didn’t win. You did, Cy. I look forward to the day I am with you again. Warrior Cy reigns in Heaven. I will never be the same.

“My beautiful son, you are healed now. You fought so hard & the war is over.

Cylus Kade Gamel
12/04/15 - 03/14/26

🎗️We are so very sorry. Though Cylus’s time here was heartbreakingly short, legacy of empathy, wonder, and unfiltered joy will live on in every act of kindness done in his name.
🙏🏼Please keep Cylus’s parents, family, and all who loved him in your thoughts and prayers. Please hold them each tightly in your hearts as they endure the very difficult days ahead.

Rachael Lee
Brandon Ty Gamel


♥️Update on JazzyJazzy will be having scans this afternoon. Her sweet Momma updates: “ As of now, she will be getting bo...
03/13/2026

♥️Update on Jazzy

Jazzy will be having scans this afternoon.
Her sweet Momma updates:

“ As of now, she will be getting both her MRI and CT scan sometime this afternoon. While she is sleeping, they will also remove the drain tube and change her port. She does have a cut on the inside near her ear that is causing some drainage, but they believe that along with the air pocket will resolve on its own — they will continue to monitor her closely.

“The good news is that her head is looking so much better tumor-wise. There are no large visible bumps anymore, which is such a relief to see.

“She was also fitted for her helmet today — we’re hoping it will be pink 💗. Overall she is doing okay, and now we are just waiting on scan results to know more. This is such a long and emotional road, and the waiting is one of the hardest parts.

🎗️Jazzy’s perseverance is awe inspiring, her emotional resilience, and her positive attitude is unmatched. Sending light, love, positivity and prayers for continued progress towards being cancer free and healing.
Watch out little one, BIG ((hugs)) coming your way♥️

♥️Precious Baby Hazel is having a surgery this morning to place a G-Tube. This is a tube that goes directly into her sto...
03/13/2026

♥️Precious Baby Hazel is having a surgery this morning to place a G-Tube. This is a tube that goes directly into her stomach from the outside of her belly. Hazel hasn’t been eating, and continues to lose weight. The G-Tube will enable her mother to insert real food, meds, and vitamins.
Her momma shares:

“Her procedure started at 8:25. The first part was diagnostic testing to make sure they could do the surgery laparoscopically. Soon after it started, Dr Danzer called and let me know that she has way too much scar tissue and that her liver is adhered to her abdominal wall.

“They will need to make an abdominal incision instead. 😔.

“Not sure what this means for recovery, but ... just means more complex, taking more time and more risk for complications.”

🎗️Please send all forms of healing energy, loving prayers, and positive vibes for Baby Hazel💛 Hold her tightly in your hearts and thoughts today.
We see you too dear momma♥️



♥️This beautiful, brave little boy is Cylus. He is 10 years old, and just recently reached his one year mark since his d...
03/12/2026

♥️This beautiful, brave little boy is Cylus.
He is 10 years old, and just recently reached his one year mark since his diagnosis with High Risk Neuroblastoma Cancer.

Cylus’s family has received the results from his latest CT scans.
His father shares:

“I’m sorry everyone.

“To all of you that I haven’t been able to text or call about this who love and care so deeply for Rachael, Greyson, myself and especially Cylus that you have to read this here. And to preface everything, I will continue to fight and pray for a miracle. I hope and pray for it every second. I have not given up, nor has Rachael, Greyson, or Cylus.

“However we have now needed to consider the worst and most inexplicable of pain.

“Originally we were hoping to contain the cancer that has recently flared up in Cylus’s body so we could potentially get to Penn State for a clinical trial consultation. Unfortunately, Cy’s cancer has “exploded” beyond control and we were advised that travel is extremely dangerous and may limit the time we have remaining with him.

“This morning we received the results of the CT scans done last night after worries arose from two X-rays done. We were admitted the day before needing to leave for Penn State due to pnematosis. The X-rays done were to at the time tell us how bad that was but the doctors were afraid it may also be his disease spreading rapidly after looking at them. The CT scans confirmed that nightmare is a reality.

“His cancer has spread explosively all over his lungs and other areas of his body. We have asked if we can continue looking at things safely to try and slow the disease down and even alternate options outside of normal care and while the answer is yes, it is something that we have been told and pled to not go far to get. As this may leave us with less time than we already have.

“As I write this with tears in my eyes and feeling as broken as I have ever felt I ask that you please continue to pray for my little family. Our sunshine is setting once again. Our rainbow baby after Scarlett will soon join his big sister in heaven. We were originally given 1-2 months left, but that time is very likely much less now.

“We ask that in that prayer you ask for our family to be given comfort, peace, and Christs guidance.

“I told my wife months ago that I wanted to be as strong in my faith in the bad as it is in the good. I am unwavering in that sentiment. Where as Jesus did perform many miracles, he also asked some to remain faithful and still give glory and praise while going through the most difficult of things.

“So I say to all of you now, all glory to God. His path is greater than anything I can fathom. And of course while I wish Cylus and all of us never had to face this reality, I know that God love and strength will hold us up. We may not have received the miracle of healing, but we have received the miracle of ten years of the most beautiful, strong, and incredible little boy. His incredible fight and resolve will never leave me. I couldn’t be more proud as a father.

“Cancer dies. My son will not. He will live in Rachael Lee Greyson Gamel and my heart forever. Free from pain or sadness.

“God bless all the little children in their fight. Thank you all so much for your love and support for us. I pray for all of you daily.

“With love,
“A broken dad.

🎗️Please send your loving thoughts, good vibes, prayers for courage, strength, comfort, and infinite HOPE! Mom and Dad…you are not alone. We stand strong beside you.

We are holding you so tightly in our hearts precious child, and sending you bundles of ((hugs)) and so much LOVE♥️

Rachael Lee

🎗️

We love seeing how far our community reaches.  From small towns to big cities, every one of you makes a difference in th...
03/05/2026

We love seeing how far our community reaches. From small towns to big cities, every one of you makes a difference in the fight against childhood cancer.

One of the most powerful things about this page is YOU! ❤️
The incredible people who show up with love, hope, and strength for children fighting some form of childhood cancer.

Drop your city or country (if outside the USA), in the comments and let’s see how far our childhood cancer warriors support network stretches! ❤️🎗️

Extra fun if you can add a fun emoji that represents your spot!





This handsome and brave superhero is Aiden!❤️💙❤️💙He is scheduled for scans tonight and tomorrow!Let’s flood Aiden and hi...
03/04/2026

This handsome and brave superhero is Aiden!❤️💙❤️💙

He is scheduled for scans tonight and tomorrow!

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

YOU’VE GOT THIS AIDEN ‼️



HAPPY 5th BIRTHDAY WAYLON!!🎉🎈🎉🎈Please join us in wishing SUPERHERO WAYLON a VERY  HAPPY BIRTHDAY‼️🎈🎉We hope your day is ...
03/02/2026

HAPPY 5th BIRTHDAY WAYLON!!🎉🎈

🎉🎈Please join us in wishing SUPERHERO WAYLON a VERY HAPPY BIRTHDAY‼️🎈🎉

We hope your day is overflowing with everything that you L♥️VE!! 🎈



Address

Bridgeport, WV
26330

Alerts

Be the first to know and let us send you an email when The Jack Strong Foundation posts news and promotions. Your email address will not be used for any other purpose, and you can unsubscribe at any time.

Contact The Practice

Send a message to The Jack Strong Foundation:

Share

Share on Facebook Share on Twitter Share on LinkedIn
Share on Pinterest Share on Reddit Share via Email
Share on WhatsApp Share on Instagram Share on Telegram