Prayer Requests

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  Two-year-old Timmy was diagnosed with Pontocebellar Hypoplasia 2A (PCH2A) — a rare neurological condition that affects brain development, muscle tone, movement, and more.

Timmy’s journey involves feeding tubes, therapies, hospital stays, specialists, and equipment…

But it also includes smiles, strength, resilience, and a spirit that shines brighter than any diagnosis. In fact, despite many struggles, Timmy continues to exceed all doctors' expectations.

Seven-year-old Reese has DIPG and additional tumors on his brain, the same inoperable brain cancer Owen had.  

He suffers from headaches and has had surgery to remove one of the operable tumors on his brain.

He continues to be high functioning, and he is bravely fighting every day to overcome this disease.

Two-year-old Elijah is battling ETMR (Embryonal Tumor with Multilayered Rosettes), an extremely rare and aggressive pediatric brain cancer. 

He has undergone surgery, radiation, blood platelet therapy, and he has high dose chemotherapy and additional surgeries in his future.

Learn more about Elijah's journey as well as how you can help them below.

Aug. 20, 2018 - Oct. 14, 2026

In November 2025, Eight-year-old Huddy was diagnosed with Diffuse Intrinsic Pontine Glioma (DIPG). He faced unimaginable challenges with courage that earned him the name Super Huddy. But cancer never defined him. He was defined by his laughter, kindness, faith, and love.

Very sadly, Huddy passed away October 14, 2026.

Huddy’s eight years were nowhere near enough, but the love he gave will last forever. His family will carry his laughter, hugs, courage, and faith in their hearts until they meet again.

Please keep Huddy's family in your prayers.

Josh has been battling brain cancer for quite some time. Although he is not a young child; he has been on our prayer list for more than a year, so we are including him here.

Josh and his wife, Lauren, became parents in early 2026, and they are in a continuous search for the treatments that will eliminate his brain cancer.

Thank you for keeping Josh in your prayers.

Levi’s parents need to have his story shared and shared again in order to reach the right doctor, researcher, scientist, hospital, or person who may know something they haven’t been offered yet.

Levi is only 3 months old and is fighting congenital melanoma. Because cancer like this in a newborn is so incredibly rare, there are essentially no clinical trials designed for babies like him, and the options available are extremely limited.

They are desperately trying to explore every possible avenue that could help cure his melanoma including additional treatments, innovative therapies, research protocols, and other medically guided approaches. But over and over, they are told no because of his age, because there isn’t enough pediatric data, or because existing trials simply were never designed for infants.

Levi's parents understand why doctors have to be cautious. But it is devastating to know there may be possibilities out there and still feel like their baby is too young to access them.

They are asking everyone who sees this: PLEASE SHARE Levi’s story. Share it with oncologists, melanoma specialists, pediatric cancer researchers, pharmaceutical researchers, scientists, advocacy organizations, and anyone who may be able to connect us with the right person.

They are not asking for false hope. They are asking for knowledge, options, collaboration, and a chance.

There has to be someone out there who has seen something similar, is researching something relevant, or knows a team willing to look at Levi’s case differently.

Please help us get his story in front of them.

WE KNOW PRAYER WORKS.

We have many prayer requests- some are private, and some we share with permission of the individuals/family.

If you have a prayer request, we would love to pray for your family member or friend.  We will keep your request private, or we can share your request with your permission.

Fill out our contact form to add your prayer request.