Meet D’Ontario “Kane” Hutson, Jr.

Kane’s story with brain cancer began on what seemed like a completely normal Saturday morning. At just 7 years old, he told his mom he couldn’t see the television. Within the hour, she had him at the ophthalmologist. When Kane tried on his new glasses and his eyes immediately turned inward, they knew something wasn’t right. A trip to the children’s hospital emergency room quickly led to a CT scan, then an MRI that same night. The scans revealed a mass, and soon after surgery and pathology results, Kane was diagnosed on July 29, 2014 with Medulloblastoma — a fast-growing brain tumor.

Kane faced treatment head on. He endured six weeks of aggressive radiation, five days a week, followed by intense chemotherapy. Through it all, he fought like a warrior. He beat the odds and proved the doctors wrong in so many ways — walking, talking, and thriving in remission while continuing regular scans every three months.

In April 2022, during one of those routine scans, another mass was found. Kane was once again diagnosed with malignant Medulloblastoma. This time, his local children’s hospital in Mississippi could not treat the recurrence, so Kane and his family relocated to Houston to receive care at MD Anderson, where they remained until May 2023.

During that time, Kane faced unimaginable challenges. He lost his hearing, vision, ability to walk, talk, and the use of both hands. But Kane refused to give up.
While staying at the Ronald McDonald House, Kane discovered a love for art through one-on-one sessions with an art teacher named Mrs. Diana. With her patience, along with occupational therapy, Kane regained the use of his hands in just four months. Through physical therapy, water therapy, and the determination he shares with his mom every day, Kane worked his way out of a wheelchair after three long years. Today he walks with a walker. He has intraocular lenses to help him see and wears hearing aids for hearing loss — but none of that slows him down.
In 2023, Kane was declared cancer free once again.

But in April 2025, scans revealed the tumor had returned. This time Kane did not undergo a third surgery and is now receiving palliative chemotherapy at MD Anderson. Once again, his family had to relocate to Houston so he could receive the care he needs.

Today Kane is 16 years old, and his spirit is just as strong as ever. He’s the kind of kid who goes with the flow and refuses to let cancer define what he can or cannot do. He continues to chase his dreams and live life fully.

Kane is currently an honor roll student at his high school in Raymond, Mississippi, and on March 1, 2026, he was inducted into the National Honor Society — an incredible accomplishment that reflects his determination and heart.

Kane, we are so honored to share your story and welcome you into the All Heart Gunner family. Your strength, perseverance, and positivity inspire all of us.

You truly embody what it means to have an All Heart.

Welcome warrior Kane to the All Heart family.

Meet Ryder

Ryder is 12 years old- he just had his birthday this week — and we think he is incredibly special.

He loves to read, write his own stories, draw, and soak up knowledge of all kinds. Ryder has a particular fascination with weather and weather phenomena, and dreams of becoming a meteorologist one day. He also enjoys fishing and is known for having ALL the fun facts.

Ryder was speech delayed as a young child and didn’t begin speaking until around age four. He has been in speech therapy ever since, but it has never slowed him down or defined him. His resilience and determination shine through in everything he does.

Ryder has been diagnosed with a high-grade diffuse pediatric glioma. Through it all, he continues to show strength, curiosity, and a love for life that inspires everyone around him.

Meet Carlos

Carlos is 17 years old, and is currently receiving treatment at MD Anderson. Through every step of this journey, his mom has been right by his side—his constant source of strength, love, and support.

Carlos is a bit shy and doesn’t love the spotlight, but his bravery speaks volumes without needing the attention. His quiet strength is something truly special.

Their family is incredibly grateful for all the love, prayers, and support they’ve received. It means more than words can express.
Please continue to lift Carlos up in your thoughts and prayers as he keeps fighting.

Meet Khloe

Khloe is 6 years old and will be turning 7 this June. She is from middle Tennessee, and is currently receiving treatment at Monroe Carell Jr. Children’s Hospital at Vanderbilt after being diagnosed with DIPG.

Khloe has a beautiful smile that lights up every room she walks into. She brings joy to everyone around her. Like so many of our All Heart kids, Khloe is incredibly brave as she faces something no child should ever have to face.

Her family is walking this difficult road with strength, faith, and love as she continues treatment.

Please join us in surrounding Khloe and her family with prayers, encouragement, and support.

At All Heart Gunner, we are honored to stand beside families like Khloe’s — reminding them they are never fighting alone.

All Heart meet: Klayton

Klayton is a happy, positive 9 year old, who doesn’t let his diagnosis determine his outlook on life. Klayton has had four battles with brain cancer. One when he was 8 months old, and then reoccurences in Feb of 2023, Feb of 2024, June of 2025. Klayton is currently in remission and recieves routine MRI’s ever 3 months to check for possible Ependymoma tumor regrowth.

During his free time Klayton loves playing with hot wheels, Fortnite, Fishing, and spending time with family.
Klayton’s positivity is contagious. He smiles constantly. He uplifts all those around him. Klayton has a very strong faith and understanding of who we all lean on when faced with a storm of life. He thanks Jesus for getting him through every surgery and treatment. Klayton wants every child out there to know how strong they truly are and he wants them to know that when they get scared to pray and ask Jesus to help them and he will. As Klayton’s Journey continues, we smile and take it one day at a time. Wherever the Journey may lead we will keep our eyes on Jesus.

All Heart meet CRIMSON CHANLEE WHITE

At the beginning of September, Chanlee’s family began noticing subtle but concerning changes. When she walked, her arms didn’t swing with her legs. She complained of headaches, and soon after developed a lazy left eye. After multiple visits to a local rapid clinic, her parents continued to voice that something wasn’t right. They were told her symptoms were likely due to poor vision causing headaches. Glasses were prescribed — but the symptoms remained.

On September 18th, after coming home from work, Chanlee’s dad told his wife, Shawnta, to get her ready — they were going to the ER at Maury Regional Medical Center. After explaining everything to the ER doctor, a CT scan was ordered. That’s when their world turned upside down. A mass was found.

Within minutes, plans were made to airlift Chanlee to Monroe Carell Jr. Children’s Hospital at Vanderbilt. Shawnta flew with Chanlee while her dad drove to Nashville. The first doctor they spoke with told them her immediate goal was simply to keep Chanlee alive through the night. Their hearts were shattered.

Doctors confirmed Chanlee had a DIPG brain tumor located in her pons — inoperable and devastating in nature. The tumor measured 41mm x 46mm. Emergency surgery was performed to place a shunt to drain excess spinal fluid. After a week in the hospital, Chanlee was able to go home.

One week later, she began six weeks of radiation. Her family faithfully drove 75 miles each way, every single day. Chanlee completed treatment with remarkable strength — experiencing no major side effects other than some hair loss behind her ears.

On December 11th, an MRI brought encouraging news: the tumor had shrunk from 41x46mm to 27x32mm.

On December 28th, Chanlee began a trial medication called Modeyso, which she will continue until her next MRI on March 19th.
Through it all, this family has held tightly to their faith in God, praying together every night. Chanlee is surrounded by love — by her four sisters, Ashlee Womble, Cambrea Hanson, Zayla Hanson, and Lanee White, and her nephew, Coen Womble.

All Heart Gunner is honored to stand with and welcome Chanlee and her family as they continue this fight with courage, strength, and unwavering faith.

Meet Fabian

The All Heart Gunner Foundation is honored to introduce you to one very special young man… Fabian!
Fabian is 7 and has a BIG love for math — numbers are his thing! You’ll often find him watching Numberblocks and learning in the most joyful way. In fact, he has collected every single Numberblock plush from 1 all the way to 10 (yes, the whole set!). His passion for numbers and learning shines so brightly.

He’s also a proud big brother, and family means everything to him. With a strong faith and a family who surrounds him with love, Fabian continues to show strength and sweetness every single day.
Fabian, we are cheering you on! Your bright mind and joyful spirit inspire all of us.

Welcome Dayana

At just 11 years old, Dayana is already showing the world what strength wrapped in sweetness looks like. She is currently being treated at MD Anderson Cancer Center, and through it all, she remains beautifully and unapologetically girly.
She loves her bows, her sparkle, and all the things that make her feel confident and bright — and she wears them proudly.
Because even in the middle of the hardest fight,

Dayana is still Dayana.
Strong. Brave. Full of grace.
We are honored to stand beside her and her family. No kid fights alone.

Meet Charlotte Rose, age 2

Charlotte is the sweetest, happiest little girl. She loves music, throwing her toys, and most of all her beloved unicorn stuffy 
Finding out she had a tumor was the most terrifying moment her family has ever faced. One day, Charlotte was playing happily with her baby brother—then a sudden fall changed everything overnight.

After emergency brain surgery and a week in the hospital, Charlotte was finally able to go home. Following a month and a half of physical therapy, she took her first steps again. Hearing her laugh after an entire month brought tears of joy to everyone who loves her.

Charlotte continues to grow stronger every single day while her future includes MRIs every three months for the next ten years to ensure the cancer does not return, her family is trusting God with every step ahead. Through His grace and mercy, they are confident Charlotte will make a full recovery and thrive as she grows.

Welcome to the All Heart family Charlotte.

Meet Delaney

Delaney is a bright light with a creative soul. She loves bringing her imagination to life through drawing and painting, and when she’s not creating art, you’ll often find her in the kitchen cooking up something special.

She shares a special bond with her twin sister and looks up to her older sister, making family a huge part of who she is. Delaney’s creativity, curiosity, and gentle spirit are just a few of the many reasons she inspires everyone around her.

We are honored to introduce Delaney as part of the All Heart Gunner family and can’t wait to share more of her journey.

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 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.

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, 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!

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 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.

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.

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

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.

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.

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 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.

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 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!

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.

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!

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.

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!

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!”