All Heart Families

Callan Plumley

Callan is the newest and smallest warrior to join the All Heart Gunner family—and he’s already stolen our hearts. With his bright smile and big personality, Callan is approaching his 2nd birthday in just a few short weeks, a milestone worth celebrating in a big way.

Callan is currently receiving care at Children’s Health in Dallas, surrounded by an incredible medical team and the even more incredible love of his family. He is the baby brother to two proud older brothers, and together they are being raised by parents who work tirelessly to support their family—his mom, a dedicated realtor, and his dad, who owns and operates a landscaping company.

Like so many families we serve, Callan’s journey has brought unexpected challenges, but also undeniable strength, faith, and resilience. We are honored to walk alongside Callan and his family, lifting them up with support, prayer, and love every step of the way.

Welcome to the All Heart Gunner family, Callan. We are so glad you’re here—and we’re cheering you on always!

Kylie Mills

Kylie Mills is a 16 year old brain cancer warrior. Diagnosed with an inoperable brainstem tumor in July 2024, she has inspired thousands during her fight. Before cancer, Kylie was an avid tennis player and traveler.

Kylie has been on the cutting edge of treatment, even electing to become the first pediatric patient in the country for a vaccine trial at Nationwide Children’s Hospital in Columbus, Ohio. That trial worked for a while before she elected to undergo a second round of radiation. We believe she is the first US patient on what is now her second clinical trial. Throughout each step she has chosen to be a trailblazer in a search to help find cures for all kids facing brain cancer.

Kylie is the best big sister and a wonderful daughter. She is a hero to all of her cousins and friends. Most importantly, she is a child of Jesus. Kylie and her family have taken the fight head on with Grace, determination, and a lot of faith, as they have lived their motto of #faithoverfear
Merry Christmas Kylie and welcome. Our prayer warriors have you covered.

Bennett Pattison

After three years in the adoption process, this family welcomed Bennett at birth, and he quickly became the perfect addition to their home. As they were settling into life as a family of four, everything changed when Bennett was diagnosed with ATRT at just eight months old.

In the beginning, Bennett was given only a 15% chance of survival. Several of his doctors later shared that when they first met him, they didn’t believe he was going to make it. But Bennett had other plans. He defied the odds, completed his intensive treatments with very few complications, and is now working hard to catch up on his milestones. To help prevent recurrence, he continues with a year of maintenance chemotherapy.

Through it all, Bennett remains incredibly happy and full of joy. His bright spirit has made him a favorite among hospital staff, leaving a lasting impression on everyone he meets. As this family looks ahead, they are hopeful the new year will bring opportunities to reconnect, grow stronger together, and experience moments of normalcy that mean so much after such a long journey.

Welcome to the family Bennett!

Landon Nickerson

Landon is a loving, kind-hearted soul who makes friends wherever he goes. He’s the child who always looks for the one left out and welcomes them in. Full of nonstop energy, Landon loves riding his scooter, racing his BMX at Baker Creek Preserve, and building anything he can imagine at home. His laughter is contagious, and his joy leaves a lasting impression on everyone he meets.

On October 18th, Landon’s world changed when imaging at East Tennessee Children’s Hospital revealed a midline brain tumor. Emergency surgery was performed to remove as much of the tumor as possible, restore fluid drainage, and obtain a biopsy. He was diagnosed with Glioma H3K27, Grade IV.

After surgery, Landon experienced weakness on his left side, but through daily therapy, he regained full mobility in just two and a half weeks—an incredible display of strength and determination.
Landon began proton radiation therapy on November 13th. When swelling caused complications, he bravely underwent a second surgery on November 24th for shunt placement and was home the very next day.

Landon continues radiation treatments as his care team works to determine the next steps, including chemotherapy and possible treatment at St. Jude. His resilience, courage, and joyful spirit continue to inspire all who follow his journey.

Please keep Landon and his family in your prayers and hearts as they continue this fight. Welcome to the family Landon!

Laila Deleon

Laila, age 7, continues to shine as a bright, funny little girl who lights up every room she walks into. Everyone who meets her says the same thing — even one encounter with Laila leaves a lasting impact.

She loves art, creating anything her imagination dreams up, gymnastics, and every kind of animal. When she was younger, she proudly declared she wanted to be a zoologist. But above everything else, she absolutely adores her three younger brothers.

This September, everything changed when Laila began having headaches and just wasn’t herself. A CT scan at the children’s hospital in Knoxville revealed a tumor the size of an orange on her cerebellum. She underwent a six-hour surgery, and doctors were able to remove almost all of it. Shortly after, she was diagnosed with medulloblastoma.

Laila bravely completed six weeks of proton radiation therapy, and now begins nine rounds of chemotherapy. Each month, she’ll spend four days inpatient — with her first round starting December 22nd.
Through it all, Laila continues to show the world her strength, her light, and her incredible spirit. Please pray for a easy first chemo so she can get home and enjoy Christmas!

Welcome to the All Heart Gunner family Laila!

Hunter Sargent

All Heart meet Hunter!

Hunter is 15 yrs old. He was diagnosed with a rare aggressive glioma on October 16th 2025. Hunter has had 2 brain surgeries and has been doing daily radiation and taking chemo pills. After being in the hospital for over a month Hunter got to go home for Thanksgiving!

Hunter loves the outdoors, fishing, riding 4 wheelers, motor bikes, and hunting. He loves to play his bass guitar in church. Hunter loves GOD, JESUS, and THE HOLY GHOST and his family, friends, and the Church. He does a reenactment of JESUS’s life at Easter. He loves talking with people about the LORD and praying with them. He is always finding a way to make people laugh and always trying to help others. He loves everyone, never meets a stranger. He has always been a very loving, caring, and outgoing person. He worries about others before himself. Hunter, his brothers, Dad and cousins are always playing pranks on each other. Hunter is just a wonderful person inside and out. Please remember him when you pray, we know GOD is able.

Welcome to the family Hunter

Ethan Guzman

Four-year-old Ethan Guzman from Kansas City is as brave as they come.

Full of energy and a huge Spider-Man fan, Ethan has taken on more in his young life than most of us ever will. We were so lucky to get to meet up with the family at the “Phog” and introduce Ethan to the team, along with giving him our All Heart package.

Ethan was diagnosed with stage three ependymoma, a rare and aggressive brain cancer. He’s already undergone two brain surgeries and completed 33 rounds of radiation. Chemotherapy isn’t an option for his type of cancer — but that hasn’t stopped him from fighting with everything he has.
He has two older siblings and is the sweetest big brother to a newborn baby sister. 

This December, Ethan will undergo scans to determine if his cancer is still stable. We ask our community to lift him and his family up in prayer, love, and strength as they face this next step.

Alex Hudson

Alex is a joyful 2-year-old who is full of life — obsessed with Lightning McQueen, loves being outside, and has a laugh that fills every room with smiles.

In early July 2025, Alex woke up from his nap at daycare with a limp and was unable to walk in the 4th of July parade. His family took him to the doctor, who noticed that he was favoring his left eye. After a weekend of worsening symptoms, a CT scan on July 7th revealed a large mass on Alex’s midbrain, near and on the brain stem. An MRI at Novant Health Hemby Children’s Hospital in Charlotte confirmed the diagnosis, and the following day, Alex and his family were on their way to St. Jude Children’s Research Hospital.

Alex spent nearly three months at St. Jude, enduring a roller coaster of challenges — multiple brain surgeries, hydrocephalus, steroid withdrawal, and a shunt placement — which led to a two-week inpatient stay where he lost much of his mobility and control over the left side of his body.
Because of the tumor’s size and location, surgery remains risky. Thankfully, Alex’s family was able to enroll him in a trial medicine targeting the genetic makeup of his tumor. He will continue this treatment for at least two years.

Despite everything he’s faced, Alex continues to smile, laugh, and inspire everyone around him. He’s regained much of his strength and now has one big goal — to be walking again by Christmas! 🎄
Every day is a blessing, and while some are more difficult than others, Alex’s family shared how thankful they are for the generosity of the All Heart Gunner Foundation and the community of families who have walked this road before them.

We are also so grateful for Sara, who had the honor of meeting Alex and his family on our behalf. Sara represents the heart of this foundation — showing up for this family with love, compassion, and a true servant’s heart. We couldn’t be more thankful for her dedication and the light she brings.

Waylon Rich

Meet Waylon

Waylon is a bright and brave 5-year-old who is facing an incredibly tough journey with Large Cell/Anaplastic Medulloblastoma (grade 4, stage M2) along with a low-grade glioma. He has already endured two brain surgeries, completed radiation, and is now on his second round of chemotherapy.

But Waylon is so much more than his diagnosis. He’s the youngest of five, a sweet little brother who fills his family’s world with joy. He loves Mickey Mouse, The Grinch, Bluey, and video games. He enjoys music, helping in the kitchen, and making every moment count. 

Waylon’s courage and smile remind us why we fight for kids like him every single day. Please join us in sending love, encouragement, and prayers to this amazing little warrior.

Yusuf Safa

All Heart, please welcome Yusuf onto our family!

Yusuf, now seven years old, is one of those children who carries joy with him wherever he goes. Bursting with energy, he’s always ready for a soccer match, a round of Uno, an adventure in Roblox, or a game of PlayStation with friends and family. As he steps into 2nd grade, his fun-loving spirit and radiant smile make every moment spent with him a gift.

In March of this year, Yusuf’s world—and his family’s—shifted when he was diagnosed with medulloblastoma, a type of brain tumor. Yet in the face of this life-changing news, Yusuf has shown a bravery beyond his years. Currently receiving radiation and chemotherapy treatment at St. Jude Children’s Research Hospital, he continues to shine with resilience, teaching everyone around him what true courage looks like.

The love and support surrounding Yusuf has been a blessing beyond measure. From family and friends to compassionate organizations, an entire community has come together to lift him and remind his family they are not walking this journey alone.

Yusuf is a fighter, a playful soul, and a light that continues to shine even in difficult times. His story is one of joy, gratitude, and unshakable hope—proof that love and togetherness can carry us through the hardest battles.

Yusuf’s father wanted to also express -the difference the All Heart Gunner Foundation is making with its mission to stand beside families fighting childhood cancer has touched Yusuf’s heart in countless ways. With compassion, care, and unwavering love, All Heart Gunner has been a source of comfort and strength—helping to remind Yusuf and his family of the power of community.

Walter "Wally" Davis

Please welcome Wally (Walter), he was so viberant and fun and loved his Special Aflac duck!

Here is a little about him from his momma: “Meet Wally (Walter) our beloved 8 year old boy with joyful eyes and a flashy smile that lights up every room he enters. Walter is a kind, empathetic and funny boy- I wish everyone could get to know him. He can be a wise guy and has playfully teased all the nurses, doctors and staff that care for him- laying claim to the titles “the popularest boy” and “King Wally”.

On May 23rd 2025 (opening day), we went to the theater to watch “The Last Rodeo” with our kids. It was a movie about a family’s fight and love for their child who was diagnosed with a brain tumor. This was not a movie we would have chosen to watch with our children but upon the repeated insistence of both our children, we agreed. It was very strange to us that they wanted to watch this movie but we now see how God was preparing us as a family for what was to come.

On June 12th 2025, we were shocked to learn that Walter had a 4 cm growth in his brain. We went to the ER because of some sudden double vision he was having after experiencing transient headaches for a few weeks. He had tested for a senior level martial arts belt the previous week and was swinging on monkey bars like the little monkey he is the day before- just a testament to how none of us are guaranteed tomorrow but are given the gift of today to love and make memories with those around us – especially our family .

Walter was immediately transferred to the ICU unit by the ER doctors and shortly after this, an external drain was placed in his head to drain fluid build up and relieve pressure on his brain. After the neurosurgeon viewed the spinal scans she was surprised that he wasn’t already paraplegic by the time he had come in – soon it was confirmed that he had an aggressive form of Medulloblastoma. About a month after the tumor removal surgery, Walter started a 5 day per week combined proton radiation and chemotherapy treatment plan. His oncologist said that he is making this look easy – We see God’s protection over him and undeniable strength from above. He will get a few weeks to recover once he completes this phase and will then start a 6 month maintenance chemotherapy plan. We have been deeply supported by our church, family and friends who are journeying alongside us.

Walter wants to be a builder, Air Force pilot and artist when he grows up! When I asked him yesterday, he also wanted to be a pizzeria waiter so that’s a maybe. He became a born again Christian on 7/11/2023 and was baptized last year along with his sister Emmalynn and his best friend Hunter. This gives us immeasurable hope and certainty for his future!

“We are praying for complete and permanent healing for this very special son of ours – please join us in these prayers in name of Jesus! Thank you.”
-Much love from the Davis Family

Ayevn Dennis

All Heart Family, meet Ayven!

Ayven is a vibrant 5-year-old boy, bursting with energy, love, and personality. He loves his family with everything he has—and his dance moves are just as fierce as his loyalty. With a curious spirit and ever-evolving interests, Ayven finds joy in all kinds of adventures. From Pokémon and Minecraft to Hot Wheels, Magna-Tiles, coloring, and painting—his imagination knows no bounds.

He’s a fan of rollercoasters, Snake.io, Dinosaur Universe, Steve and Maggie, Among Us, and Spider-Man. He loves collecting gemstones, hiking, and is known for hoarding everyone’s spare coins.
On May 13, 2025, Ayven was diagnosed with DIPG—Diffuse Intrinsic Pontine Glioma—a rare and aggressive brain tumor located in the pons. The prognosis for DIPG is devastating, with limited treatment options available. Ayven bravely completed 30 rounds of radiation by July 15, and there was hope he would stabilize for a while.

Sadly, on July 27, he developed hydrocephalus and required emergency placement of a VP shunt the following day. He returned home on July 29, but was soon readmitted with worsening symptoms on July 30. His shunt was adjusted, and he is currently stable in the hospital.

Ayven is scheduled for an updated MRI on August 7, and his family is hopeful he’ll be eligible for a clinical trial. He is surrounded by love—an older brother who postponed starting college to be by his side, and a mom and dad who would give anything to trade places with him. Ayven deserves a fighting chance.

Mirabella "Bella" Ward

Help us welcome Bella into the All Heart family.

Bella is 11 years old—a cheerleader, pageant girl, travel basketball player, and softball star. Raised on a farm, she’s a true country girl at heart. She loves Jesus, sings Anne Wilson with passion, and radiates kindness wherever she goes.

Bella isn’t just active—she’s deeply caring. She prays for everyone she meets, always putting others before herself. Her faith is unwavering.

On May 14, Bella was diagnosed with diffuse midline glioma, an aggressive form of brain cancer that has now spread to her spine. But even in the face of this heartbreaking diagnosis, Bella’s faith remains unshaken. She believes God has a bigger plan for her—even if it’s not the one anyone expected.

Her hope? That her journey brings people closer to Jesus. Because to Bella, that’s what matters most.

Please keep her in your prayers and help share her story.

Taylor Carroll

All Heart Family meet Taylor.

Taylor is a 10 year old artsy, animated, and downright silly kid like she’s always been—even after everything she’s been through. She’s the kind of child who fills a room with energy and imagination. She loves to draw, paint, and sketch, and if she’s not doing that, she’s making TikTok videos with her Calico Critter toys like she’s directing her own little movie.

One thing she says all the time is, “So what are we going to do today?” It’s her little way of reminding her mom and all of us that she’s full of life, curiosity, and hope. She doesn’t take a single day for granted, and that’s something to admire. Her mom tells her she has a different kind of strength—one that’s quiet but fierce.

Her world changed in an instant when she was diagnosed with medulloblastoma, a type of brain cancer. Taylor went from living our normal life to being admitted to the hospital in February and not going home until May. Everything shifted. It was hard, scary, and heartbreaking—but through it all, Taylor never stopped being Taylor.

Just recently, she got to ring that beautiful bell after completing her radiation treatments, and now in full-on rehab and recovery mode. She calls it “Taylor 2.0”—because this next version of her is just as creative, strong, and full of life, but with a story of survival and courage.

Caleb Caesar

All Heart meet Caleb.

Caleb Caesar is a 14-year-old with a huge personality, a sharp sense of humor, and a love for life that shines through everything he does. He’s the youngest of two brothers and recently graduated from middle school, ready to take on the world in his own unique way.
Caleb is a gamer at heart—whether he’s racking up wins in Call of Duty, breaking ankles in NBA 2K, or running the field in Madden, he brings the same competitive energy and focus every time. While he used to spend a lot of time on the basketball court or working out, his journey with brain cancer has shifted how he moves through the world. But it hasn’t changed his spirit one bit.
These days, Caleb channels his energy into the things he loves most—gaming, connecting with friends, and expressing himself through fashion. Shoes and clothes are more than just style for him—
Despite the challenges he faces, Caleb lives with courage, humor, and heart. He’s a reminder that strength comes in many forms—and his just happens to come with a killer sense of style and a controller in hand. Welcome to the All Heart Family Caleb!

Elspeth Kenney

All Heart Family, please join us in giving a big All Heart welcome to Elspeth!

Elspeth is 12 years old and just wrapped up her 6th grade year—way to go, Elspeth! She’s a creative soul who loves painting and drawing, and when she’s not making art, you can often find her gaming on Roblox, especially in her favorite world, Adopt Me.

She’s also a big fan of Bluey (who isn’t?) and jamming out to Sabrina Carpenter. Elspeth has her heart set on getting a dog soon, and we are totally rooting for her—paws crossed!

Welcome to the All Heart family, Elspeth!

Jayden Polinsky

Jayden David Polinsky was born May 23, 2007, in Oconomowoc, Wisconsin.
Three words that describe Jayden from the moment he was born up through his almost 18 years of life: Humble, Angelic, Valiant.
Jayden grew up in Watertown, Wisconsin with his mother, father and 3 sisters. He always was surrounded by family as his grandparents lived next door and he had cousins in every direction of the town. From spending time in a small Catholic school during his early years of education to taking advantage of the online education route when covid started. He spent his high school career taking classes at home and at school. He has 9 classes left to complete his high school diploma. Unfortunately, due to his short-term memory issues he can’t complete it at this time. He worked his first job starting at 14 years old as a dishwasher and prep cook. When our family moved to Tennessee in August 2023 Jayden’s love for nature exploded and his appreciation for family evolved even more.
Jayden played his first video game at about 2-3 years old. He was hooked. He’s spent hours and hours enduring in the thrill of gaming. From his PC, PS5, Nintendo Switch he’s excelled at any game he’s taken on. During his radiation treatment at St. Jude in Memphis he participated in two Nintendo Smash Brother competitions and took 1st place in both. The joy of gaming captured his imagination which has opened his talents to music, drawing and being a creator.
Jayden is a person who savors the simple pleasures in life. This could be going for a walk, eating dinner with his family, playing a video game with his dad. He has a passion for God’s beauty on this Earth and dreams of exploring as many states as possible, including other countries. He dreams of seeing skyscrapers in New York City to the wildlife in the Yellowstone National Park. He dreams of experiencing the culture of Japan and eating pasta in Italy. About a month ago Jayden and I were on a walk down a nature trail in Knoxville, TN. We stopped at a bench, and he said to me, “Mom, if Earth can be this beautiful can you imagine what Heaven has to be like.”
Jayden has the heart that doesn’t just shine-it warms. His selfless love comes from somewhere beyond this world. Jayden doesn’t get discouraged, he doesn’t get angry or let his emotions stop him from getting up every day and making the most out of the life God has blessed him with.

Kinsley Marcum
All Heart family meet beautiful Kinsley!

Kinsley is a bright loving girl full of smiles and always happy. She is 7 years old. Born on August 30, 2017. Kinsley was diagnosed when she was 3 years old with autism. Kinsley loves her family, puppies, her teachers and friends. She loves to jam out to music and watch her tv shows and special movies. Kinsley is full of light.

She had gotten sick the end of January and continued to get sick with different symptoms. Her momma had a gut feeling that something wasn’t right and kept on taking her to different doctors searching for an answer. In March their world would be turned up side down. She was put into Johnson City Children’s Hospital for a few days looking for an answer still. Then came more bad news.

Kinsley, their beautiful daughter had a MRI done, they said she had an infection disease or a type of cancer. Come to find out, she had a brain bleed and the doctors had to work fast. Kinsley was med lifted to Knoxville Children’s hospital. From there, did multiple CT scans and MRI’s. Kinsley was diagnosed with a diffuse midline glioma, a brain tumor. Worse still – it was a high grade cancer. Kinsley went through chemo treatments and radiation while at Knoxville Children’s hospital.

We will wrap this family up in our prayers! Welcome to an incredible army of prayer warriors with All Heart Gunner!

Hudson Roberts
All Heart family please meet Hudson. Hudson and his family are “All Heart” and we were so thankful to get to meet them!

Hudson is 12 years old, his first year of middle school is not at all what he had hoped it would be. After months of symptoms like morning vomiting, headaches, and dizziness… he was diagnosed with a brain tumor on December 19th after passing out walking in the hallway at school the previous day. He had surgery to remove almost all of the tumor on December 23rd, but his surgeon knew that it was cancerous before he even got an official diagnosis from pathology. He has gone through an intense phase of proton therapy + chemotherapy. And is now in maintenance chemo for the next 5 months.

Hudson is one of the most amazing boys, mature beyond his years, a very smart kid, a kind and genuine friend to many. His steadfast faith and belief that God is with him every minute has been an inspiration to many. Hudson has a story to tell and we will continue to pray for miraculous healing. The family said they are so thankful for the community that has rallied around Hudson to support them even in the darkest days.

Welcome to the All Heart family!

Nate Trinca
We are so excited to introduce you to Nate of “Keep Nate Great.”

Nate is 18 and a true warrior, he has been fighting brain cancer since he was 5 years old.

When we met Nate he was so kind and welcoming toward us. The thing that touched us and stood out the most was his incredible fighting spirit that just leapt out! He is courageous, strong, loving, and steadfast. Nate is what we all strive to be. Please join us in prayer as he could use some prayer warriors to stand with him right now. Follow him and his journey at Keep Nate Great.

Welcome to the All Heart Family Nate! We got you!

Cynthia Reyes

Please help us welcome Cynthia!

Cynthia is 17 now and seemed to be okay until age 5. She had a tumor in her brain pressing on her optic nerve. It needed radiation she ended up getting radiation and seemed to be okay. In 2020 Cynthia was getting migraines and was given all kinds of medications, but then she started having seizures. She had a tumor that was quite large, it hadn’t spread but it was cancer.

In 2021 Cynthia was having pain in her neck and shoulder and had difficulties raising her arm. The doctors discovered she had a cluster of 12 tumors and had to have surgery. Cynthia was 14 and she was losing weight. Everyone thought it was because she wanted to fit into a nice quinceanera dress for her 15th birthday.

Long story short, Cynthia ended up at MD Anderson for what seemed to be an enlarged kidney. However, it ended up being stage 4 renal cell carcinoma. Brain cancer alone wasn’t enough. They allowed her to start any and all treatments after her quinceanera. Two weeks after her quinceañera she started chemo and had a lot of complications.

Cynthia is a senior this year. This has been her first year she has been able to go a whole year with no hospital stays. She’s in culinary class and loves her teacher and the class. She would like to do something with animals, maybe a veterinarian tech or something in that realm. Her dad calls her the animal whisperer. She’s so good with animals and training her own animals. When she is home her animals are her safe place.

Cynthia is the youngest of 3 girls, she has vision issues, she still suffers from seizures from the brain cancer, balance issues and depression.
They say they think it’s easier to count their blessings than good or bad days. The family says their faith has gotten them this far and will continue to get them through. As of now Cynthia is in remission from both the brain and the kidney cancer. That’s the biggest of blessings.

Welcome Cynthia and family. We will wrap you all in prayer.

Melvin Macklin
Meet Melvin!

Melvin is 17 years old and was diagnosed in July 2022. Melvin loves football, playing video games, horse back riding, and the Astros.

He is such an amazing kid and he keeps everyone in good spirits. Melvin is strong and resilient with the happiest disposition despite everything. Thankfully Melvin is a competitor and won’t let cancer win. Prayer warriors add Melvin to your prayer list.

Christopher Thomas
All Heart Family please meet Chris!

Chris is 4 years old. He was diagnosed with ependymoma grade 3 brain cancer in January. After 5 ER visits they finally did a CT scan, and found a “large mass”, in his brain. That night they were transported 3.5 hours to another hospital where he had brain surgery the very next day. Since then he has went through another brain surgery & is waiting to start his treatment with St. Jude in Memphis, TN. Chris has not missed a beat yet!

He enjoys riding his 4-wheeler, playing soccer, and basketball. His favorite team is the Lakers, and favorite prayer is Lebron James. He really loves cars and trucks! He has a mass collection of hot wheel that he races daily. He also enjoys spending time with his two sisters (ages 8 and 7 months). His dream car is a Grey mustang. The prayers are one day he’s able to ride through town in his Mustang!

Hailey Marrylees
We want to introduce our #33 All Heart Family to you!

We absolutely could not have picked a more precious girl to be the recipient. She and Gunner are the same age with a spirit that rings true – a warrior with a big heart. All Heart.

Hailey Merrylees is a vibrant and strong 17-year-old that is battling brain cancer. If you can spare a moment, we would love to share Hailey’s story with you.

Hailey is a Grade 12 student at South Secondary School in London, Ontario, Canada and has been passionate about dance since she was just 3 years old. She has spent countless hours training and performing at Absolute Dance in Kilworth, Ontario and always lighting up the stage with her energy and smile. Her dream is to attend university and become a teacher, but right now, her focus is on beating brain cancer.

On October 18, 2024, her world changed when her parents, Damen and Ly, received a phone call that no parent is ever prepared for. After undergoing an MRI to investigate hormonal issues, the results revealed two brain tumors. They were instructed to bring Hailey immediately to the emergency department at the Children’s Hospital in London, Ontario.

Following several weeks of hospital stays and numerous tests, Hailey underwent brain surgery to obtain biopsies of the tumors. Thankfully, the surgery went well, and two weeks later, the results came in—Hailey’s tumors were confirmed to be cancerous – germinoma tumours near her pituitary gland.

Her doctors developed a comprehensive treatment plan consisting of four months of chemotherapy, followed by one month of radiation. Hailey has completed her fourth round of chemo, and we are incredibly grateful that the tumors are responding positively and shrinking.

However, due to the nature of her cancer, Hailey requires a specialized form of radiation called Proton Beam Therapy, which is not currently available in Canada. To receive this critical treatment, Hailey and her family must travel to the University of Florida Health Proton Therapy Institute in Jacksonville, Florida, on Feb. 18, 2025. While the radiation treatment itself will be covered by Ontario Health, the associated costs—such as travel, accommodations, meals, and lost income—are not totally covered.

Hailey’s mother, Ly has been off work to care for her throughout this journey and will continue to be by her side for the months ahead. The funds raised through Hailey’s GoFundMe will help cover the significant costs of travel and living expenses in Florida, as well as support the family during this difficult time. Hailey’s younger brother Conrad who is 12 years old has also been very brave and supporting his sister through all of this.

Hailey is a fighter, full of courage, grace, and determination. She has inspired all of us with her strength and positivity, and we are determined to give her every possible chance to recover fully and live out her dreams.

From the bottom of our hearts, thank you for being part of Hailey’s journey. Together, we can help her win this fight.

With love and gratitude,

The Merrylees, Heeney, and Nguyen family

Welcome to the All Heart Family.

Preston Minnich
All Heart Gunner family allow us to introduce Preston!

Preston is one and a half and currently living at St. Jude’s while undergoing treatment. His dad is still in Virginia and comes on the weekends to visit Preston and his mom. Preston is expected to be at St. Jude’s another two years undergoing treatment.

Due to his brain tumor, he hasn’t been able to physically meet some major milestones such as crawling and walking. However, he has started pulling himself up and is trying to get back on track. He is a happy little guy who loves his momma, dad, grandma and all of his kitties back home.

We are so glad to get to be apart of his journey. Preston, just know that the All Heart family has you in our prayers. Always.

Elaina Smith

All Heart family… meet Elaina!

Elaina is about to celebrate her 10th birthday! Double digits! She is also a big sister to her 4 year old brother. She is a fighter, firecracker, gymnastics loving girl. However, her very favorite thing to do is to travel – she has more stamps in her passport than her mom can remember!

Elaina was diagnosed in 2016 and is being treated at St. Jude’s currently. Elaina and her family have such big hearts and are always meeting and encouraging other newly diagnosed families with insider tips on how to navigate this difficult world. They are cut from our same cloth!

Welcome to the All Heart Family Elaina!

Peyton Smith

Meet our first little one from Colorado … Miss Peyton!

A bit about her family… they are a family of 7. The children from oldest down Ethan just turned 21 he is in college in Kansas, Avery is 15, Camdyn is 11, Peyton is 10, and Rylee is 9. They have always been a very close family and enjoy each and every day together. This year has been a very challenging time. It started out just regular week – working to raise animals with the children for 4-h projects and to show them at our local fair. Midway of the fair week August 5th – 11th we noticed Peyton wasn’t her self but assumed it was due to the long days and heat, as the week progressed it became clear she needed to go to the doctor. The local hospital ran a few test for several things like west Nile, and a few other illnesses but no results.

She went to her first day of school and became very sick and had to come home early. They ended up at a children’s hospital and did a MRI . Our world stopped. She has a large tumor in the center of her brain . She was progressing very fast and soon had several severe seizures and had to be sedated, in the process due the pressure in head she lost her sight , speech , and ability to walk or move her arms. The medical team in Denver had to install a drain in her head to relieve the pressure as well as take a biopsy. The results came back many days later. It was the worse thing I have ever heard. She has no option for surgery and she has (K27M midline diffuse glioblastoma).

The prognosis was very grim as there are no known cures and its aggressive nature leaves very little time . She went through a very strong pen point radiation for several weeks. She started to speak again and then gradually started regaining motor skills Thankfully Peyton met the criteria to be in a clinical trial at St Jude’s. A short time later November 18th they headed back to Memphis to start her treatments finishing on December 23rd.

From Peytons Dad: “I know this sounds like a very rough time you’d be right nearly or impossible . The only way we are still going is through our Lord and Savior Jesus Christ, wonderful family, friends, and complete strangers that are amazing and Christians all over the world praying, we are doing our part to have faith in what we pray for and staying positive.”

Peyton has the warmest heart and loves animals and especially bugs! Her favorite meal is either steak or Italian – we say have both! She leans on her favorite bible verse Philippians 4:13 and was excited for the Bible books we sent. Welcome to the All Heart Family Peyton!

Dash Johnson

Meet Dash!

In April of 2024, Dash, a vibrant and energetic seven-year-old boy became very ill. Little did he or his family know that they were about to start a journey into uncharted territory. A 7cm tumor was discovered in his brain, leading to an emergency craniotomy surgery to remove the tumor. The pathology of the tumor led to a devastating diagnosis, cancer.

Despite the challenges, Dash has shown incredible courage, resilience and determination. He has undergone 30 treatments of intensive Proton Radiation therapy, a highly specialized treatment designed to target the tumor while minimizing damage to healthy tissue. These treatments were administered at The Ohio State University’s The James Outpatient Treatment Center. Dash and his family live in Georgia and travel back and forth to Columbus, Ohio for his ongoing immunotherapy at Nationwide Children’s Hospital.

As Dash continues his journey, his family remains hopeful and optimistic for a full and speedy recovery. Dash continues to remind everyone “God’s got this!”

Creed Thacker

Meet Creed Thacker!

Creed is 15 year old and he has so much Courage. He was diagnosed with a “Germinoma” brain tumor on July 10th. He had what was going to be a “routine” CT scan on July 2nd, however his family was called into the doctor’s office that afternoon and informed that he has a mass on his Pineal Gland. He had an MRI which determined that the “mass” was not allowing his spinal fluid to drain from around his brain. They preformed brain surgery on July 5th to relieve the pressure and made a new canal for the fluid to drain away from his brain.

Creed is such a courageous young man and has a strong faith in God. He enjoys spending time with his large, loving family, attending services at his little, loving country church. He also enjoys playing video games, collecting his hundreds of stickers, Putt Putt, bowling and working his magic on his many Technic Lego sets that he has been gifted throughout his journey.

Avery Espinoza

All Heart family, please welcome Avery!

Avery was diagnosed with a PXA grade 2 thalamic brain tumor at the age of 11. They were able to successfully remove 49% of her tumor and it was deemed benign. Once released from the hospital and inpatient physical therapy center, she celebrated her 12th birthday and began 2 oral chemos shortly after. Her chemo treatments have had to change multiple times over the years because they would stop working at a point.

Her quality of life had been good until this year. In June 2024, we discovered Avery’s tumor had spread to her lower spinal cord. Her new chemo she began in June led to an extreme loss of weight for her due to terrible nausea. In August, she was admitted with gallstones and underwent a procedure to relieve them. She was switched to a new chemo and steroids and was improving, but her pain began to get worse. During her clinic visit on 9/17/24, she was admitted to the PICU at MD Anderson. She was admitted for pain management and kidney stones. She had a stent placed on 9/18 and an ng tube as well. On 9/20 she began throwing up consistently and on 9/21 she coded 3 times and was intubated.

Over the next few days she was extubated and coded for the 4th time on 9/28. She was intubated again and now suffered from a pneumothorax as well. She has since received a tracheostomy and GJ tube and is making progress daily. She still has a long road ahead to begin radiation and relearn how to walk and use her limbs, but we believe she is a miracle and God can do all things!

This girl is a fighter and she’s so very brave!

She is the youngest of 4 children and before cancer she loved volleyball, spending time with her friends, playing with her dogs, listening to music and movie/game nights with her family.

She is known for her face making and sassy attitude.

Follow her journey here: Avery’s Fight Against Childhood Cancer

Quindarian McGuire
All Heart family, our hearts just grew by one more!

Quindarian has joined our family. He is a quiet little guy and loves Chucky Cheese more than just about anything.

Quindarian is the youngest of 5 children and not only has been diagnosed with brain cancer, but his family has recently lost their home due to a dangerous situation. Because of our help they have been able to now secure a safe place to live while trying to get Q healthy again. He is being treated at MD Anderson in Houston, Texas and we know he is in good hands.

Welcome to the All Heart family Quindarian!

Karter Jones
Meet Karter!

Karter is 6 years old and was diagnosed with mudullablastoma in July 2024. He is currently being treated at MD Anderson in Houston, Texas. Karter was very excited to receive his own Bible and books to read while at treatment daily.

Karter’s past few months have been extremely difficult, not only on him but his entire family. While going through treatment Karter has not lost his sweet smile! We know with the All Heart team behind him, we will pray him through the rest of treatment while keeping his spirits high and his smile bright.

Follow Karter’s journey: Karter’s Journey

Zayden Rose
We would like to introduce you to Zayden Rose.

This beautiful boy was diagnosed with brain cancer at 3 months old. Zayden is now a strapping 4 year old and still fighting!

Zayden is battling at MD Anderson and as always could use some more people in his corner! Don’t worry little guy… we are all here for you!

Welcome to the All Heart Family Zayden!

Arnetris Cole

Meet Arnetris!

Arnetris is 14 year old from Miami who has been fighting brain cancer since March 2023. Her tumor was found one month to the day after losing her dad to cancer. She is the youngest of 6 children.

We will be praying for her and her family as they fight through this battle. Her most recent scans showed her tumor was stable. Scans again in three months.

Welcome to the All Heart Family Arnetris!

Leighton Boynton

We had the privilege of meeting Leighton, her Mom and her Nana this week while at clinic in Knoxville. Leighton smiled, gave us “knuckles” and flirted with Brandon from afar –  She didn’t like it when he got to close!

Leighton is a 15 month old that was diagnosed with a low grade glioma in December 2023 when she was just 7 months old. After almost two months of complications with her shunt surgery, she began chemo with the most wonderful team at Children’s Healthcare of Atlanta. She currently receives chemo in Atlanta and at ETCH.

Leighton loves music, puppies, and wearing her pearls. Her family has seen the Lord work in so many ways through their girl and the community around them. Remember to pray for Leighton every time you wear your pearls!

Welcome to the All Heart family Leighton and family. We love you and your bright smile so much already!

August Olenski

Let us introduce our first Texan to the All Heart Family, August.

August is a playful, wise kid who is over-the-moon excited to start kindergarten this fall at the same school his older brother attends (he’s spent the last three years in another school for deaf education). August loves playing with his siblings – whether it is building a city with MagnaTiles or going to the pool. He is a kind, gentle boy who has the most positive, uplifting spirit. As an example, he recently spilled soup all over the table while out at a restaurant with the family. His immediate response to the incident was, “Hey guys! Hey guys. It’s okay. We’ve got this!” His attitude is humbling and has been a major factor in his survivorship.

August is now a three-time brain cancer and stroke survivor. As a result of complications from treatment, August has been diagnosed in the past five years as clinically trach-dependent, gtube-dependent, deaf, and visually impaired. Despite those obstacles, he’s defied all odds – so you can imagine the celebration around mainstream kindergarten.

We know that August will continue to battle with that same ALL HEART mentality and warrior spirit. We are so glad to have been able to be a part of his journey and ask that you keep August and his family in your prayers.

Swayze Happney

Smiling Swayze

We were honored to get to meet this precious baby. She is a happy little thing despite everything she is going through. She smiles and absolutely lights up when her big brothers talk to her – she thinks they hung the moon.

Swayze Jane is a 13 month old baby girl who was diagnosed with a brain tumor back in March 2024. Swayze had surgery and then underwent 2 rounds of induction chemotherapy at East Tennessee Children’s Hospital in Knoxville and multiple rounds of high dose chemotherapy with stem cell transplant at Tri Star Centennial in Nashville.

Swayze is the youngest of three siblings, but is not afraid to let her big brothers know that she’s the boss! She is the smiliest little girl and loves all things pink.
Her favorite movies are The Little Mermaid and Trolls, and of course she is Ms.Rachel’s #1 fan.

Follow her – 🎀 Saving Swayze🎗️

Welcome to the All Heart Family!

Jolee Manis

Meet our new friend Jolee!

Jolee was diagnosed June 1, 2018 with medulloblastoma at the age of 2. She was transferred from ETCH to Vanderbilt due to the size of her tumor. She underwent surgery and spent three weeks recovering before inpatient chemo began. She completed three rounds of chemo before it was stopped in September due to infection. She remained inpatient until November and was finally able to go home and that’s when outpatient chemo was started. Scans in January 2019 showed disease progression so it was decided that proton radiation was needed. She did 6 weeks of radiation while getting chemo at ETCH. She was NED (No Evidence of Disease) after completion in April 2019.

Routine scans in April 2024 showed a new tumor and she underwent surgery again at the age of 8 and it was a relapse of medulloblastoma.
Jolee is the happiest girl. She loves being a big sister to Amelia, her dog Daisy and being with her family. She loves going to church, especially Sunday School where her Aunt Jess is the teacher. She loves all things Disney. She is in the second grade.

Welcome to the All Heart Family Jolee 

Hensen O'Quinn

Meet our friend Hensen.

Hensen is a 3 year old little guy from Virginia who is being treated in Knoxville. He has two older sisters who love him dearly and can’t wait to come to Knoxville when school is out for the summer.

Hensen was released from the hospital after a 33 day stay. Please keep Hensen and his family in your thoughts and prayers.

Follow his journey Hope For Hensen

Frank Chupko

Meet Frank!

Frank is 16 and has recently relapsed with his brain tumor. Frank is being treated at CHOP (Children’s Hospital of Philadelphia) where he was told his tumor is inoperable.

Frank is the oldest of 5 children and was so excited to receive the Bible and the grant we sent. He wants to get an air conditioner for his bedroom and some new clothes.

Please join us in prayer for Frank and his battle through cancer.

Timothy Hindermyer Jr.

Meet our friend Timothy!

Timothy is being treated at CHOP (Children’s Hospital of Philadelphia). He is currently undergoing both chemo treatment and proton radiation.

Timothy loves video games, legos, drawing and of course watching YouTube. Timothy is currently inpatient and could use all our love and prayers.

He is a fighter and knows our All Heart community is fighting!

Josie Vicker

We want to introduce you to Josie!

Josie is a 9 year old girl from Alabama  and wise beyond her years. She is compassionate, empathetic, and has a presence about her that people say give them such a peace. She hasn’t ever complained and almost acts like she just knows this is part of her journey.

She loves to stitch and she has been an amazing artist since she was about 3 years old. She loves to sketch more than anything but is talented at anything artistic. She loves her stuffies (stuffed animals).

Before becoming sick she was an All Star cheerleader at her school and was working on her back tuck. Her goal is to start back in the next few months as well as playing softball.

She is selfless and worries more about her mom and dad than she does herself. Josie is the very definition of All Heart ❤️

Welcome to our All Heart Family Josie.

Rhonan Malpass
Meet Rhonan from New York!

She was first diagnosed May 2022 just after her 16th birthday. She’s had brain surgery, radiation and is currently undergoing chemo. Rhonan is a typical 17 year old girl. Loves are current rap music, fashion, make up, warm weather, jewelry, shopping and spending time with her little sister Quinn and her pets.

She is an adventure loving girl and wise beyond her years. Rhonan likes movies and relaxing, and board games, slime and anything with fun textures. She’s polite but advocates for herself with no problem. She has a sense of humor like none other and loves to help others through their problems. She’s brutally honest and has no problem telling others whats on her mind. Shes makes everyone want to be the best version of themselves.

Rhonan says “Thank you so much for your support. I’m happy to find such amazing people in my corner.”

Welcome Rhonan to our All Heart Family

Colson Keller

Meet Colson!

Colson is 10 years old and has been battling brain cancer since he was 1 year old. Due to the location of Colson’s tumor he has very minimal eye sight, but that doesn’t change his happy disposition.

When we first met Colson he told us that he loves to sing and his favorite song to sing right now is “O Little Star of Bethlehem”. Colson is an old soul with a big heart for his family and was a joy to talk too. He told us all about making videos of himself singing and how one day he will be famous for it.

Colson is filling everyone that he meets with love and hope for the future. Welcome into the All Heart family Colson.

Kallie Reese

All Heart Team meet Kallie!

Kallie is 16 and has been a brain cancer warrior since she was 10 years old. She has the strongest spirit and softest smile. Despite all of the chemo over the past decade she is excelling in high school and as per a typical teenage girl – she can’t wait to go shopping!

Kallie is being treated at both Vanderbilt and ETCH by some of the same doctors we know. It is a small world after all. Please keep her in your prayers as she continues her battle with brain cancer.

Welcome to the All Heart Family!

Abraham Tolley
Meet Abraham!

Abraham was diagnosed with a brain tumor in March 2023 from noticeable right sided weakness. He began treatment at Vanderbilt University Children’s Hospital and has since transitioned to ETCH to receive weekly chemotherapy.

Abraham loves his toys, animals and family! He is a happy little guy and has the best imagination.
A few of his favorite things are Batman, Transformers and cooking!

Welcome to the All Heart Family Abraham!

Kane Bollinger

All Heart Family meet Kane!

Kane is 4 years old and has a birthday coming up the week of Christmas. Kane’s brain tumor was found last December and he has been battling all year! Right now, Kane is off treatment and working on gaining some strength and weight back.

Kane loves to go to the park, Target, and Five Below. His drink of choice is chocolate milk and he absolutely loved his chocolate ice cream cone! We were so excited to get to talk Paw Patrol and Bluey.

Please show Kane and his family some of that All Heart love!

Nora Brannon
Meet Nora!

She turned 1 in May, not even a month after, Crossville Hosptial and Children’s Hospital diagnosed her with “bells palsy”. Steroids helped for a little bit but the 2nd round of steroids didn’t help.

Her family took her to Children’s in Knoxville, they scanned her head said she was fine. That’s when she got her 2nd dose of steroids which didn’t help. All it took was for her to have a seizure sometime in August. She had surgery in September.

Then her tumor came back and they started chemo in October 3rd. Chemo is ending the last Thursday of April in the clinic! Then probably radiation.

Nora unfortunately passed away on November 17, 2023 but our hearts are always with Nora and her beautiful family.

Matthew Hart
All Heart Family meet Matthew!

Matthew is 11 years old and has been beating brain cancer since he was 2! He lives in Georgia with his mom, dad, brother, and sister.
Matthew loves trains, black holes (like outer space), and making his Yummy Jars!

Matthew has a huge sweet tooth  and him smiling when he ordered a cinnamon roll cake was one of our favorite moments!

To follow Matthew check out: Yummy Jars for Matthew

Isaiah Deal
Meet Isaiah.

He lives in Farmington, New Mexico and we connected with him from Knoxville, Tennessee! It really is a small world.

Isaiah was diagnosed at age 6 with a brain tumor in the middle of his brain stem. He’s had 3 brain biopsy surgeries, but the surgeons were unable to debulk any of the tumor. He underwent weekly chemo for 1 year. The chemotherapy unfortunately was a fail. He is now in a drug trial that will hopefully keep his tumor stalled. Isaiah is helping cure brain cancer in other children by being in this drug trial at St. Jude’s.

Isaiah is almost 9 and loves music, especially Elvis! He tries to visit Graceland each time the family travels to St. Jude. Isaiah is a master of jokes and always has a smile on for everyone he sees. In spite of only attending 80 days of school last year, he excelled and is in the gifted and talented program in 3rd grade.

Isaiah always has a joke to brighten your day:

What does a snow man eat for breakfast?

Frosted flakes!

Follow his journey Isaiah’s cancer fight and keep him and his family in your prayers.

Jayla Cantrell

Allow us to introduce you to Jayla!

Jayla turned 3 in June and was diagnosed with a brain tumor in July 2023.

Jayla loves Play-Doh and cooking in her play kitchen. She also loves Barbie, Cocomelon, and Bluey. Jayla, the baby of the family, has a big brother and a big sister who love her so much.

This precious family from Knoxville is planning on spending the rest of the year in Nashville for stem cell treatments and a trial chemo. Please be in prayer for them as they undergo this trying process.

Hayley Geren
All Heart Family please meet Hayley and her beautiful family!

Hayley is 15 and is undergoing treatment now. She in fact received chemo today and was still happy and gracious to meet us at the park. Hayley wants to be a 4th or 5th grade teacher when she grows up. She and London became fast friends. Hayley is a beautiful example of being a warrior and fighting her battle with the “All Heart” mentality.

Thank you to our All Heart Family that has made it possible for us to help families like this. We couldn’t do this without all your love and support.

Tillery Phillips
Meet Tillery!

Tillery and her family have been fighting brain cancer since she was 15 months old. This brave little warrior has now been fighting for 8 years!

Because of the success of our All Heart Prom this past April we were able to give Tillery and her family a donation yesterday while she was busy raising money for Alex’s Lemonade Stand. Tillery was a perfect host and brought us all an ice cold lemonade complete with a lemon slice on the cup!

Once you are in the pediatric cancer world, the world becomes very small and the smallest acts of kindness and love mean the most. In this world, everyone is battling, everyone is raw, and being able to give truly is the greatest gift. Gunner was smiling as we were all loving and bonding with each other yesterday.

Please follow her incredible fight on her page Tillery is Loved.

AJ Cucksey
All Heart family, we would like to introduce you to AJ!

AJ is 12 years old and is battling brain cancer, again. AJ has an older brother and little sister and when he talks about them he lights up. He loves football and was able to play for his middle school team this past fall.

He is starting a new treatment this week and the plan is to do this treatment is for 42 weeks. It is a long road and we are so happy to connect with them and introduce him and his family to all our prayer warriors.

Please follow his story at Prayers for AJ Cucksey.

Wyatt Crippen
Meet Wyatt!

We were honored to meet Wyatt and his mom, Kristi Hardin Crippen, and share some of the All Heart Gunner love. It means so much during the week of Christmas to give, to love, and to cover this boy and his family in prayer.

Wyatt is 18 years old and was diagnosed with a brain tumor at the age of 7. Wyatt loves old cars and wants to buy one to fix up. He loves music and his favorite band is Metallica. He is a senior this year and is excited to graduate, but is somewhat reluctant about becoming an adult. (We can’t say we blame him!)

Welcome to the All Heart Family!

June Lanham
Our first child we helped. 

It was a year ago today Gunner left us. Thanks to the All Heart Gunner Foundation and most especially, the ones who came and supported the All Heart Prom!  We were honored to get to help a family in the same battle against brain cancer.

Please meet the first child we have been able to make a donation to, June.

 June is 6 years old and was first diagnosed February 2020. June is the middle child in her family, she has an older sister and younger brother. June loves music, her favorite singer is Elvis, and her favorite song is Teddy Bear. She just graduated Kindergarten and loved school.

Please follow June on her page June’s Fight to keep updated.

There is absolutely nothing more beautiful than getting to share Gunner and the All Heart family with someone new. We know Gunner would be so proud to help and would’ve loved to be here focused on others walking in this pediatric brain cancer world.

Welcome to the All Heart Family June!

Thank you all so much to the All Heart Family for making this donation possible.

All our love
Brandon, Brittany, London and Gracelyn