#JoeStrong71

Joe had his whole life in front of him—plans, goals, and a future that should have been his to shape. Joe loved deeply—his family, his friends, football, hockey, and every moment of life he was given. He was the kind of person who embraced it all, who looked forward to what came next with excitement and purpose.Joe didn’t want to leave. He wanted to go to college, build a career, get married, have children, and grow old surrounded by the people he loved. He had dreams just like anyone else—dreams that were unfairly taken from him.On 3/23/23 the angels came to take him home - the reality remains difficult to accept. Years of missing his laughter, his presence, and the milestones he should be living. Years of connecting with other families facing the unimaginable. Years of witnessing both heartbreak and incredible resilience. And still—there is no cure.But there is progress. And there is hope.Each year, more than 400 children and young adults in the United States are diagnosed with DIPG, and treatment options remain heartbreakingly limited.We cannot accept this as the status quo.We are asking you to stand with us—to turn compassion into action. Your support helps fuel critical research and provides resources to families navigating this devastating diagnosis.Thank you for standing with us, for remembering Joe, and for helping us continue this fight.

C.A.T.S.

Our hearts are torn knowing Teegan Cannon (almost age 8) from O’Fallon, MO won her battle in Heaven on Thursday morning as the sun began to rise. She was one month shy of turning 8 years old. A big sister to brother Mickey, age 6, and the only daughter of Hannah Cotner and Alexander Cannon. Teegan loved blue and purple and sparkles. She loved every animal and especially kitty-cats. Teegan was a friend to everyone — weekly giving away her treasures to those she knew would enjoy them. She was a happy, kind and curious little girl who dreamed of owning a candy store and having lots of pets. She also had the misfortune of developing DIPG in 2024. Please keep her family in your hearts and prayers. Hannah has stayed home caring for Teegan and the family could use immediate help with Teegan’s final expenses and current bills. If you are a foundation and would like to help please contact Debbie.carver@tough2gether.org who is coordinating with Teegan’s parents. Fly high sweet Teegan. You have been so courageous against this awful disease. Run and play with the most beautiful children we know, love and truly miss.Donations made to Tough2gether Foundation are tax-deductible to the extent allowed by law. While funds raised in connection with this family will directly support them, all donations are made to Tough2gether Foundation and may also be used to support other families facing pediatric cancer, related programs, and charitable initiatives at the Foundation’s discretion.

David Turner Jr. Fund

Make a donation in David Jr’s honor for Christmas this year. Every dollar supports DIPG research and families.#makeeverydaythebestdayever #davidsadventureWe accept donations in other ways:Venmo - PaypalMail checks to Tough2gether Foundation: 2201 Columbian Rd, Wamego, KS 66547Tax-Deductible Giving Notice:Donations made to Tough2gether Foundation are tax-deductible to the extent allowed by law. While funds raised in connection with this family will directly support them, all donations are made to Tough2gether Foundation and may also be used to support other families facing pediatric cancer, related programs, and charitable initiatives at the Foundation’s discretion.

Lauren Kate Costanzo

Lauren Kate Costanzo, 20, of Congers, passed away at home surrounded by her family on April 16, 2024 after a courageous year and a half long battle with Diffuse Intrinsic Pontine Glioma (DIPG). Lauren graduated from Clarkstown North High School with honors and was studying to become an ESL teacher at SUNY Cortland when she was diagnosed. She was a proud member of the Sigma Delta Tau sorority. Lauren loved spending time with her family which consisted of her parents, Steven and Eileen, and her three sisters. She was a wonderful younger sister to Jill and Holly, and a loving and protective big sister to Faith. When they were all together, the laughs never stopped. Lauren had a great sense of humor, a beautiful smile, and a bright and sunny personality. She made friends everywhere she went. Lauren will be deeply missed by all who were blessed to know and love her. As heartbreaking as Lauren’s passing is for her family and friends, she would love to be remembered with a smile.

Long Live Leo

Leo was pure light. The kind that walked into a room before he did. The kind that made people feel safe, seen, and loved without him ever having to try.He was brave in ways no child should ever have to be. He fought battles that most adults could not imagine, and even in the hardest moments, Leo’s heart stayed gentle. He smiled through pain, cracked jokes through fear, and reminded all of us what real strength looks like.This fundraiser isn’t just about remembering Leo. It is about carrying him forward.It’s about turning unimaginable loss into purpose. Turning grief into fuel. Turning love into action.By supporting this fundraiser for Tough2gether, you’re helping families who are walking the same road Leo once walked. You’re funding research. You’re supporting children who deserve more time, more options, more hope. You’re standing in the gap when families feel like the ground has disappeared beneath them.Leo loved making people smile. He loved helping others. This is his legacy.If his story touches your heart, please give.If you’ve ever loved a child, please share.If you believe no family should fight this alone, please stand with us.Together, we fight.Together, we remember.Together, we make sure Leo’s light never fadesDonations made to Tough2gether Foundation are tax-deductible to the extent allowed by law. While funds raised in connection with this family will directly support them, all donations are made to Tough2gether Foundation and may also be used to support other families facing pediatric cancer, related programs, and charitable initiatives at the Foundation’s discretion.

Love for Logan

Logan was a bright and adventurous 13-year-old from California who had a deep love for the outdoors, nature, and all animals—even the ugly ones. He found joy in exploring the world around him, whether it was being outside, observing wildlife, or simply appreciating the beauty of nature. Logan’s curiosity, kindness, and unique spirit left a lasting impression on everyone who knew him.Logan is survived by his loving father, Matt; his devoted mother, Kasey; and his older sister, who meant the world to him. He will always be remembered for his gentle heart, his sense of wonder, and the way he embraced life with courage and authenticity.This memorial fund is intended to provide support for Logan’s family and families like Logan’s, research funding, special experiences for young teens like Logan through Memories and Magical Moments, and other projects as determined with the input of Logan’s family. The family thanks you for your support now and throughout Logan’s battle.We accept donations in other ways:Venmo - PaypalMail checks to Tough2gether Foundation: 2201 Columbian Rd, Wamego, KS 66547Tax-Deductible Giving Notice:Donations made to Tough2gether Foundation are tax-deductible to the extent allowed by law. While funds raised in connection with this family will directly support them, all donations are made to Tough2gether Foundation and may also be used to support other families facing pediatric cancer, related programs, and charitable initiatives at the Foundation’s discretion.

Maddox Express

Hop aboard the Maddox Express towards a cure for DIPG.Maddox was the light of our lives and he deserved a chance to grow old, he deserved the chance to just be a kid, but DIPG stole that.Together we can do so much more, together we can fight. In Maddox's memory we are devoted to helping other families in the fight as well as helping parents during the grieving process and with your help we can continue to spread a little Maddox Magic where ever it is needed.Forever and Always Full Steam Ahead 🚂We accept donations in other ways:Venmo - PaypalMail checks to Tough2gether Foundation: 2201 Columbian Rd, Wamego, KS 66547Tax-Deductible Giving Notice:Donations made to Tough2gether Foundation are tax-deductible to the extent allowed by law. While funds raised in connection with this family will directly support them, all donations are made to Tough2gether Foundation and may also be used to support other families facing pediatric cancer, related programs, and charitable initiatives at the Foundation’s discretion.

Madeline Remy Fund

Marguerite's Miracles

This page is for supporters of the mission of Marguerite Chenier's family. Marguerite was a kindergartener at Mandeville Elementary diagnosed with a terminal brain tumor. The Chenier family now fight for others in her honor, providing support to families facing unimaginable challenges.Marguerite's Miracles is a fund of Tough2gether Foundation.Donations made to Tough2gether Foundation are tax-deductible to the extent allowed by law. While funds raised in connection with this family will directly support them, all donations are made to Tough2gether Foundation and may also be used to support other families facing pediatric cancer, related programs, and charitable initiatives at the Foundation’s discretion.

Noah Halek Strong

We accept donations in other ways:Venmo - PaypalMail checks to Tough2gether Foundation: 2201 Columbian Rd, Wamego, KS 66547Tax-Deductible Giving Notice:Donations made to Tough2gether Foundation are tax-deductible to the extent allowed by law. While funds raised in connection with this family will directly support them, all donations are made to Tough2gether Foundation and may also be used to support other families facing pediatric cancer, related programs, and charitable initiatives at the Foundation’s discretion.

Ryan's WAG

Ryan Tyler Kirkby had a contagious laugh and a sophisticated sense of humor with a heavy reliance on sarcasm and comedic timing. He loved music with meaningful lyrics (Imagine Dragons was his favorite band), chess, reading, swimming, and his friends. Ryan was known for his insightful and sometimes cheeky remarks and his HUGE LOVE of animals (3 cats and hundreds of stuffies for whom he cared were meticulously catalogued by name, birth date, photo and occupation in his iPad contact list, requiring special birthday desserts with little notice). Ryan dreamt of becoming a veterinarian but soon after his DIPG biopsy/diagnosis in December 2022, he could no longer attend his cherished school (SSSAS) and instead watched YouTube and played Roblox as best he could with one working hand.An only child, Ryan’s constant companion was his stuffy, Foxy. Their adventurous spirits drove them to explore new foods, experiences, 4 countries, and 25 states together. Ryan fought DIPG for 18 months with Foxy by his side- Foxy had MRIs, his own AFOs, and was regularly caught giving himself medical assessments, messing with computers, and using hospital equipment. Once Ryan was confined to a wheelchair, Foxy and his gang formed Ryan’s Warrior Animal Guard (WAG) to guard against scary things.Ryan, age 9, passed away on June 13, 2024, leaving a Ryan-sized hole in our hearts. Ryan continues fighting through his post-mortem tumor donation… and Ryan’s family and Ryan’s WAG won’t give up the fight until a cure is found.DIPG is a terminal-upon-diagnosis brain cancer with no known treatment and no known cure with a life expectancy of 6-12 months. The standard of care has not changed in over 60 years and includes only palliative brain radiation meant to extend life. Clinical trials in all pediatric cancers is significantly underfunded by the government (approximately 5%...

Sweet ZoeJane

Our Sweet Zoe Jane was given 6-9 months to live when she was diagnosed with DIPG brain cancer. She battled for almost six years and was one of the first children to participate in the ONC201 clinical trial in New York City, Not only was she a pioneer, but she was one of the longest surviving patients on the trial. Zoe Jane fought as hard as she possibly could while she was here with us, and even in death she kept fighting by donating her tumor to DIPG research.We will continue this fight in honor of our sweet girl! She did not die in vain!Childhood cancer gets about 4% of government funding for research and less than 1% of that goes to DIPG!It is families like ours, who have lost our babies, and families in the battle who are terrified of losing theirs that can stand up and make a difference with YOUR help! Without private fundraising for research, we do not believe Zoe Jane would have had the chance to participate in the ONC201 trial. These efforts blessed us with over 5 years more than Zoe Jane was given at diagnosis and ONC201 became the first FDA approved drug to be specifically used towards DIPG.Our mission is to raise funds as a founding family of the Tough2gether Foundation in honor of our Sweet Zoe Jane. All funds raised will go to DIPG research, helping families currently in the battle, and serving others in honor of our baby girl.We need a cure! Like yesterday! Help us! Share Zoe Jane's Story. Donate if you can so we can help end DIPG. Don't wait for childhood cancer to affect your family before you choose to help.In the words of another amazing DIPG Warriors mother, "DIPG, We are coming for you!"To learn more about...

TaterTough

Keeping Our Promises and Living TaterToughTate lived life with a spirit, dignity, and smile that taught us and so many that odds are meant to be overcome and we do not have to be defined by the challenges and situations that are put in front of us. If you were blessed to know Tate, you know what he meant to you and for those that were not able to meet him in person we hope that be being a part of our mission you understand who he was and how he continues to impact so many. Your support of TaterTough will help us continue to fund research, building and support our cancer communities, live by Tate’s example and inspire everyone to live TaterTough.The TaterTough Foundation was started to honor Tate and our commitment to keep the promises we made to him. The promise to defeat the monster that is DIPG so that no other child would have to fight the fight he did. And the promise to support, take care of and uplift families just like so many took care of us. The goal of TaterTough is to financially support pediatric cancer patients of DIPG and other cancers, their families, and foundations and organizations that work to improve their quality of life and medical care. We accept donations in other ways:Venmo - PaypalMail checks to Tough2gether Foundation: 2201 Columbian Rd, Wamego, KS 66547Tax-Deductible Giving Notice:Donations made to Tough2gether Foundation are tax-deductible to the extent allowed by law. While funds raised in connection with this family will directly support them, all donations are made to Tough2gether Foundation and may also be used to support other families facing pediatric cancer, related programs, and charitable initiatives at the Foundation’s discretion.

Team Tyler

Donations made to Tough2gether Foundation are tax-deductible to the extent allowed by law. While funds raised in connection with this family will directly support them, all donations are made to Tough2gether Foundation and may also be used to support other families facing pediatric cancer, related programs, and charitable initiatives at the Foundation’s discretion.

Abigale Vanhoosier

On 12/13/2024 Our sweet Abigale was diagnosed with an inoperable, terminal brain cancer, DIPG. Diffuse Intrinsic Pontine Glioma. Within a few days, Abby had lost her ability to walk independently, barely able to talk, and was not able to swallow without choking unless given bites of food smaller than your fingertip. Abby underwent 30 rounds of Proton Radiation to the brainstem, participated in a clinical trial and later was approved for the Expanded Access Program of the newly FDA Approved Onc201, Modeyso.Abby had great success with the Proton Radiation, as it shrunk her tumor about 50% and she was able re-gain all of her abilities and returned to normal daily living, like school, playing and just getting to be a child! On 10/14/25, her symptoms re-appeared within a few days. She had an MRI, with the results being either Radiation Necrosis or possible tumor progression. She went back on Steroids and started Avastin treatments to lessen the symptoms and this seems to be helping, however she is still having some difficulties and is unable to completely wean from the steroids at this time.We have put this off as long as we could, however we are now needing more financial help. There are several holistic and alternative treatments that are out of pocket and pricey that we are interested in pursuing, as well as her already astronomical medical bills. Her doctor has given us a timeline of a "few months at the most" and while we refuse to accept that and believe in a earthside healing miracle, we are also painfully aware of the expenses we may have in the next "few months." We just want to be prepared ahead of time and not drowning in financial stress during this very hard and unpredictable time.Donate, share, and most importantly, PRAY! With...

Benjamin Stein-Lobovits

Cora Hopf

Cora is a loving 9-year-old who was diagnosed with DIPG in October of 2025. She has a heart overflowing with love and shares it so freely with everyone she meets. Cora loves Jesus, fiercely cherishes her family, and finds joy in animals, nature, and art—seeing beauty in the little things that many might overlook.Even through the hardest days, Cora continues to shine. She remains joyful, holding tightly to her faith and trusting in Jesus’ plan, believing with all her heart that His plan is always good.Cora is currently enrolled in a clinical trial and travels often for treatment. Despite everything she faces, she continues to smile, to love deeply, and to find goodness wherever she goes. Her strength, faith, and light inspire everyone around her—reminding us all what it means to live with courage, hope, and unwavering love.Donations made to Tough2gether Foundation are tax-deductible to the extent allowed by law. While funds raised in connection with this family will directly support them, all donations are made to Tough2gether Foundation and may also be used to support other families facing pediatric cancer, related programs, and charitable initiatives at the Foundation’s discretion.

Dalton Close

Dalton Close is a vibrant 16 year with the brightest smile that will light up the room. He loves to spend time with his family, siblings, friends, church, and golf is one of his favorite pastimes. Recently he was diagnosed with a Diffused Midline Glioma (DMG) Stage IV aggressive brain cancer which is not operable.Update on Dalton (3/7/2026):We made it successfully through and the first week is done with minimal side effects. He is really missing his siblings and was a sad (down day) about it. He has been super fatigued sleeping a lot this week but pushed through to get out of the house today.We hit up the Traders Joes for some good healthy food and then walked a few blocks to have Mexican!!On Monday, he will have infusion #2 where they will increase the amount of T cells from 10 million to 50 million which means he could have more of a reaction but 50 million will be his dose going forward. Keep up those prayers and good vibes!!!Folks have reached out about sending a card to Dalton. If you feel so inclined and would like to send an encourage or fun cards you may send them to the address7450 Woodlawn Ave NE Seattle WA 98115Donations made to Tough2gether Foundation are tax-deductible to the extent allowed by law. While funds raised in connection with this family will directly support them, all donations are made to Tough2gether Foundation and may also be used to support other families facing pediatric cancer, related programs, and charitable initiatives at the Foundation’s discretion.

Daniel Childress

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David Pottroff

Destiny Miniard

My name is Destiny Miniard I’m 9 years old I’m from London Ky! I was diagnosed with dipg in January when I was 8 years old! But that does not define me! I’m blessed to be here for the ones we lost the ones in the fight and the ones that will diagnosed after me! I’m a child of god and will spread his light no matter my situation! My biggest hope is that dipg didn’t exist or that there was a for sure cure! because I have gone through a lot of painful things having dipg. That no kid should go through for example I went through a shunt placement on my 9th birthday and also had 6 weeks radiation i’ve had to have a mild surgery, not put to sleep!that’s why I’m grateful that god chose me out of a million kids because I’m strong and brave enough to take the treatments that a lot of people would be scared of because I know god only knows what will happen and it is left up to him! I’m proud to be apart of a great and very supportive community! And I’m lucky to have my family fighting beside me! Cuz when one person gets cancer we all fight it! Thank you!Donations made to Tough2gether Foundation are tax-deductible to the extent allowed by law. While funds raised in connection with this family will directly support them, all donations are made to Tough2gether Foundation and may also be used to support other families facing pediatric cancer, related programs, and charitable initiatives at the Foundation’s discretion.

Ezra Talkington

This is ezra journey! hepatoblastoma hepatocellular neoplasm nos liver cancer stage 4 terminal. May 20th 2024 we started our cancer journey with the simple words... its cancer. From that day forward it was my mission to let the world know who ezra is! After countless pokes, 12 surgeries, too many infusions to count. We have made the decision to just make memories with ezra. Our goal is to complete a small buckets list for him, see the ocean, got on a boat, see real snow, and see the mountains! Ezra is so strong and brave with every poke he gets he is our families hero/Spider-man.Donations made to Tough2gether Foundation are tax-deductible to the extent allowed by law. While funds raised in connection with this family will directly support them, all donations are made to Tough2gether Foundation and may also be used to support other families facing pediatric cancer, related programs, and charitable initiatives at the Foundation’s discretion.

Grace Wethor

Grace Wethor is an award-winning actress, director, bestselling author, & brain cancer legislation advocate. After being diagnosed with an untreatable brain tumor at age 13, she moved to Los Angeles and began pursuing her dreams in film with full force. She gave her first TED Talk at age 15, released her first bestselling book at 16, spoke at the United Nations at 17, and released her first docu-series at 18. In 2024 she was honored with a United Nations Global Impact Award. She is now a brain cancer/pediatric health legislation advocate and has made her way to the White House & Capitol Hill while spearheading bills that would bring over $250m in funding to youth healthcare. Ten years later and still fighting, she hopes to use film to tell unseen stories & show other young people that they can pursue their dreams despite their circumstances or illness.

Izzy Cashion

On August 13th, 2025, I took my perfectly healthy 4-year-old daughter, Isabella, to the ED for abnormal movements of her eyes. What I thought, or hoped, was going to be a diagnosis of a lazy eye, turned into my worst nightmare come true. The next day, Isabella, or “Izzy” as we call her, was diagnosed with DIPG, an inoperable brainstem tumor, which has a median survival of 9-11 months. As a pediatric oncology NP, my first instinct was to assume Izzy had a brain tumor, and I had to actively talk myself out of jumping to the worst case scenario, as I often did.Isabella loves princesses and unicorns. She learned to swim this summer, all while this monster of a tumor was growing inside of her little head. Izzy played t-ball this fall. She just went back to gymnastics classes. She loves preK. She is adored by her two younger brothers. She’s at an age where she talks about the future, “when I become a Mommy”, “when I turn 5”, “when I can drive a car”. It makes my heart sink every time, because the chance of a future is statistically unlikely. DIPG is a disease that has been ignored for many decades. Right now, Izzy’s only chance at extending her life lies in clinical trials — phase 1 studies that exist to test safety, not to cure. There are treatments being developed that are significantly shrinking tumors in some children. But we need to accelerate this research, so treatment modalities can be combined together into treatment protocols. Cancer is not cured with one therapy alone. In pediatrics, research moves painfully slow, much slower than for adults, due to lack of funding, lack of the ability of drug companies to profit off of pediatric cancer treatments and government regulations in place for...

Jake Mendez

Jasper Rodriguez

We will never forget the day that we received the news. Our world shattered when last summer we were told that our sweet Jasper had DIPG (diffuse intrinsic pontine glioma) a terminal brain cancer, primarily affecting children.Jasper, now 5 years old, is full of love, life and laughter. He loves spending time with his family—especially his older brothers. He loves being silly and his giggle fits make everyone laugh. He is obsessed with Spidey, trains, airplanes, building forts, and creative dancing for the family. He is hoping to play tee-ball in the Spring.We never thought we would have a child with cancer. We were devastated to learn there is no cure for DIPG. How could that be with all the supposed advances in medicine? We were told that beyond radiation there was no standard of care for DIPG and that we should focus on making memories. As we talked at length to his doctors, we were so discouraged to know how few clinical trials were available for our son, especially at one of the best children’s hospitals in the country. Of the clinical trials that existed, most were full, far way, or for older children, and only in stage one.After careful consideration, we enrolled in a clinical trial that has shown to give time to patients but has not proven to be a cure. Jasper was in this trial for 14 months, until in December 2025, when his tumor was found to be in progression. He completed a second round of radiation in January 2026. We pray for a miracle and try to be optimistic that we can find another clinical trial that will be a good fit for Jasper that give him enough time for a cure to be discovered. Each day with Jasper is a blessing and a miracle...

Jen Thomas

John Paul Macri

John Paul’s storyOn March 21, 2025, our healthy, joyful 8‑year‑old son John Paul was diagnosed with an inoperable, incurable brain tumor called DIPG (Diffuse Intrinsic Pontine Glioma) after episodes of tripping and double vision. We looked to the doctors for answers, only to be told his life expectancy was 2–11 months and that there was no cure, only six weeks of palliative radiation and the possibility of entering a Phase 1 clinical trial. While the doctors informed us about the trials, we had to choose on our own which one to try – no one would tell us what the best option would be. Today, we travel across the country every three weeks so John Paul can receive CAR‑T immunotherapy in Seattle, doing everything possible to save his life.John Paul loves to learn and approaches the world with a curiosity far beyond his years, asking questions about everything and everyone he meets. He is a walking encyclopedia of Star Wars knowledge, has the best sense of humor, and finds ways to make people laugh even on hospital days. He finds joy in helping others, sharing his faith, cheering loudly for James Madison University sports, and his genuine interest in people means he makes friends everywhere he goes—from school to airplanes to clinic waiting rooms.​ He dreams of serving in the US Military when he grows up as well as being a mental health doctor.What makes DIPG so devastatingDIPG tumors grow inside the brainstem, which controls vital functions like breathing and movement, making surgery impossible in most cases.​DIPG is one of the deadliest brain tumors, with a median survival of about 9-11 months from diagnosis. Fewer than 5% of children survive two years after diagnosis despite decades of research.Children with DIPG slowly lose the ability to move, talk, eat and smile, all while their...

Kalvin Lynch

Kalvin Lynch is a vibrant, funny, and incredibly courageous 16-year-old who was recently diagnosed with DIPG — an aggressive and fast-growing brain tumor located on the brain stem. Because of its location, it is inoperable, and the prognosis is devastating.With the time we have, our focus is simple: make every moment count.We are trying to fit years of memories into a handful of months.Kalvin wants nothing more than to feel like himself again - to drive, to play his drums, to laugh with friends, and to lead his school in his natural, lighthearted way. That's who he is.Even now, he continues to joke through the hardest days, somehow working harder to comfort us than himself.He is deeply loved by his family, his church, and his friends. If you know Kalvin, you know his joy is contagious. You would be hard-pressed to find a more remarkable young man.Kalvin will undergo intensive radiation treatment five days a week for six weeks. The treatment center is two hours away - each direction.The travel, lodging, and associated expenses add up quickly, and we are asking for help to ease that burden so his parents' focus can remain where it belongs: on Kalvin.If you feel led to give, pray, or share, we are profoundly grateful.Life is short. Hold your people close.Don't let the small things steal your joy.Donations made to Tough2gether Foundation are tax-deductible to the extent allowed by law. While funds raised in connection with this family will directly support them, all donations are made to Tough2gether Foundation and may also be used to support other families facing pediatric cancer, related programs, and charitable initiatives at the Foundation’s discretion.

Kaylee Gibbs-Starnes

Kaylee, my 17-year-old daughter, was diagnosed with a rare and very aggressive type of brain tumor in her spinal cord. The tumor has taken away her ability to move from the chest down, and now it’s growing into her brain stem, causing her to lose use of her arms. There is no treatment or cure for this disease in the United States, and there is very little research or funding available. I have spent countless hours researching and making thousands of calls, desperate to find hope for Kaylee. During her make a wish trip that didn’t get to happen she was hospitalized due to a blood clot. We are in the process of getting Kaylee accepted into a program that could help save her life .The funds raised will help us cover travel expenses, and Kaylee’s treatments, and anything extra she may need while we’re away from the rest of our family. We are extremely grateful for everyone who has supported us through this tough and trying battle. We have so many people on our side, loving, praying, and supporting us—we couldn’t have done it without you all. We’re hoping this fundraiser reaches enough people so we can afford to pay for Kaylee to make this scary journey and, in hopes, receive what could be life-saving treatmentsDonations made to Tough2gether Foundation are tax-deductible to the extent allowed by law. While funds raised in connection with this family will directly support them, all donations are made to Tough2gether Foundation and may also be used to support other families facing pediatric cancer, related programs, and charitable initiatives at the Foundation’s discretion.

Liliana Holland

Donations made to Tough2gether Foundation are tax-deductible to the extent allowed by law. While funds raised in connection with this family will directly support them, all donations are made to Tough2gether Foundation and may also be used to support other families facing pediatric cancer, related programs, and charitable initiatives at the Foundation’s discretion.

McLaren Grimes

In the fall of 2025, McLaren started getting headaches. At first, we thought it was just part of growing up. Three weeks later, after the pain continued, a CT scan showed nothing abnormal — we were so relieved.But two days later, everything changed. McLaren began having severe headaches and lost motor function on her right side. On October 1st, 2025, an MRI revealed a mass in front and beside her brain stem.A biopsy was done on October 3rd, and it confirmed our worst fear — the mass is cancerous. We’re waiting for the full diagnosis and treatment plan next week.Through every appointment, every hard moment, McLaren has been strong, sweet, and full of light. She’s showing us what real courage looks like.We’re deeply grateful for all the love and prayers coming our way.Donations made to Tough2gether Foundation are tax-deductible to the extent allowed by law. While funds raised in connection with this family will directly support them, all donations are made to Tough2gether Foundation and may also be used to support other families facing pediatric cancer, related programs, and charitable initiatives at the Foundation’s discretion.

Meadow Carmody

Nicole Puglisi

Olivia Giacone

Olivia is a joyful girl diagnosed with DIPG, a rare pediatric brain tumor. With limited treatment options, funding for research is crucial. Organizations like ChadTough Defeat DIPG Foundation are dedicated to advancing research and clinical trials to find better treatments. Donations support critical research, offering hope for Olivia and other children facing DIPG. Contributions to Tough2gether Foundation are tax-deductible and may also assist families and charitable programs related to pediatric cancer.

Paislee Porod

Support Paislee and her family as they navigate DIPG by donating to the Tough2gether Foundation. Donations are tax-deductible and aim to assist them as well as other families facing pediatric cancer.

Pavle Radic

That smile, that wonderful, beautiful and infectious smile that is always there, that instantly tells you what kind of person Pavle is like.Pavle Radic is just starting his teenage years in 2026 and being intelligent, thoughtful, caring and truly invested in his faith, family and friends, has had a great start to being a teenager. Unfortunately, January 2026 after going to the ER, then having a biopsy we were told that he has a Diffuse Midline Glioma (DMG) brain tumor.Pavle, because of his wonderful positive personality, did not let that get him down. He has a get things done, looking forward to the next day attitude. He loves to play on his computer and with his dog Dunja, checking out the latest cars and loves to read A LOT. He studies his faith in depth and still worries about his friends and family more than himself.Pavle has responded well to experimental off label use of treatments for his original tumor. Unfortunately, a recent MRI showed 3 new tumors in areas separate from the original tumor.Pavle has been accepted to the Seattle Children's Hospital Brainchild 4 clinical trials, which offer the best chance to treat all of his tumors. This requires 8 weeks of staying in Seattle and then returning once monthly for numerous months. The multiple times flying to Seattle will be extremely expensive and our family asks if you please could help Pavle get this treatment. We know that in a world such as it is, more people like Pavle in it can make the difference.Our family greatly appreciates and thanks you for your caring and generosity.Donations made to Tough2gether Foundation are tax-deductible to the extent allowed by law. While funds raised in connection with this family will directly support them, all donations are made to Tough2gether Foundation and...

Randy Craig

My name is Randy Craig. I have DMG and I was diagnosed with it in August of 2023.You can also purchase Randy's Shirt to show your support!We accept donations in other ways:Venmo - PaypalMail checks to Tough2gether Foundation: 2201 Columbian Rd, Wamego, KS 66547Tax-Deductible Giving Notice:Donations made to Tough2gether Foundation are tax-deductible to the extent allowed by law. While funds raised in connection with this family will directly support them, all donations are made to Tough2gether Foundation and may also be used to support other families facing pediatric cancer, related programs, and charitable initiatives at the Foundation’s discretion.

Raymond Dejillas

Raymond is 17 years old, a junior in high school in Modesto, CA, originally from the beautiful island of Saipan. A true lover of soccer, wearing his school’s JV and Varsity jerseys had always been his dream. In March 2025, he was diagnosed with DIPG — a life-changing diagnosis that took away his ability to play the game he loves.Yet DIPG has never taken away who Raymond is. He is kind, gentle-hearted, and full of warmth. He spends his time making others laugh, reading to his little sister, and helping her master her latest Minecraft creations. His strength shines far beyond the soccer field — in his courage, his compassion, and the joy he brings to everyone around him.In January 2026, recent scans showed that his tumor has grown and spread into his spine. Raymond is currently undergoing re-radiation at Stanford and has enrolled in a new clinical trial, ONC206, through UCSF.At this stage, our focus is on providing Raymond the best possible quality of life and cherishing every moment together as a family. Funds raised will help with travel, lodging, medical expenses, and allow his mom, Marylou, and dad, Alex, to take time away from work to care for him — creating meaningful memories, surrounding him with love, and walking this journey together.Donations made to Tough2gether Foundation are tax-deductible to the extent allowed by law. While funds raised in connection with this family will directly support them, all donations are made to Tough2gether Foundation and may also be used to support other families facing pediatric cancer, related programs, and charitable initiatives at the Foundation’s discretion.

Sarah Basore

Addison Bell

Aria Pitre

Aria Pitre of Youngsville, Louisiana was 6 years old.She loved all things rainbow and sparkles. Her favorite animal was a cat and even when her tumor took her ability to speak, we were able to communicate with her sweet “meows” Her favorite color was rainbow and loved eating spaghetti and tacos. Her favorite hobbies were dancing and doing arts and crafts. She had a determination like no other child I have ever known. She never let this disease define her and DIPG never broke her spirit. Aria was the best big sister to Ethan and the absolute pride and joy of her mom Katelyn Pitre and dad Logan Pitre. This fund will assist the Pitre family, and families fighting DIPG like Aria. The family hopes to continue Aria’s legacy of love for others in her Louisiana community and among those fighting this horrific tumor type. We accept donations in other ways:Venmo - PaypalMail checks to Tough2gether Foundation: 2201 Columbian Rd, Wamego, KS 66547Tax-Deductible Giving Notice:Donations made to Tough2gether Foundation are tax-deductible to the extent allowed by law. While funds raised in connection with this family will directly support them, all donations are made to Tough2gether Foundation and may also be used to support other families facing pediatric cancer, related programs, and charitable initiatives at the Foundation’s discretion.

Braylon Hodgeson

Brooklyn Medina

Charlie Poole

Grace Simoes

Hadley Schmidt

Harley Rockind

Ike Bauer

Ike is 20 (turning 21 on Monday). He was first diagnosed in 2017 at age 12 with ALL. He received treatment until 2020 and was in remission until March 2025 when he was diagnosed with therapy induced AML.While they were not certain they could get him into remission, he achieved complete remission after 3 rounds. Then he had a stem cell transplant of from an unrelated donor. That went well. After 2 rounds, his count would not recover and was confirmed to have relapsed via a bone marrow biopsy. Within a week, we moved his care to MD Anderson. He has qualified for a clinical trial and should start next week. The goal is remission with a likely second stem cell transplant.Ike loves to be with his buddies, fishing, hunting, or just hanging out. He tracks and watches all kinds of sports. Loves the Chiefs and KU basketball.We accept donations in other ways:Venmo - PaypalMail checks to Tough2gether Foundation: 2201 Columbian Rd, Wamego, KS 66547Tax-Deductible Giving Notice:Donations made to Tough2gether Foundation are tax-deductible to the extent allowed by law. While funds raised in connection with this family will directly support them, all donations are made to Tough2gether Foundation and may also be used to support other families facing pediatric cancer, related programs, and charitable initiatives at the Foundation’s discretion.

Jace Ward

Jace Ward was a young man with a fierce spirit. At just 20 years old, he was building a life: working at a law firm, studying business, making friends, dreaming about his future. But in May 2019, something unexpected happened: he noticed a change in his peripheral vision. What seemed like a small symptom soon became a life-changing diagnosis — DIPG, Diffuse Intrinsic Pontine Glioma, a devastating and terminal brainstem cancer. When the doctors told him, “You have 6-9 months,” his response was both heartbreaking and powerful: “I’m not afraid to die; I’m afraid I won’t make an impact before I do.” That became not just his mindset, but his mission. A Man on a Mission Rather than retreat, Jace pushed forward. He didn’t just fight for himself — he fought for every child, every family, every person who would come after him facing DIPG or similar brain cancers. On the Tough2gether “Meet Jace” page, his mantra is clear: “I can’t die, I’m busy.” He traveled, advocated, learned, and connected. He researched clinical trials and asked hard questions: when he had a biopsy, he didn’t just accept pain and prognosis — he pressed: “Which trial should I do next?” He realized that many families don’t have the infrastructure, the support, or the resources to navigate complex cancer trials. So he turned his energy toward building something bigger than himself — a system to help others. Building Something Bigger: Legacy Through Action Jace channeled his vision into concrete, systemic change: He helped launch a patient navigation continuum, bridging gaps in access to care for DIPG/DMG (diffuse midline glioma) patients. He co-founded the Tough2gether Foundation (along with his parents), to support research, clinical trials, and most importantly, other families fighting. He insisted on sharing data: in his final wishes, he asked that his brain tissue be donated — “If you don’t [share what you learn from it], I’ll haunt you.” He advocated at the national level — from Congress to the NIH, he raised his voice. He wanted lawmakers, scientists, and clinicians to see DIPG, to feel urgency, to make the circle bigger. Even as his own body weakened, he continued: through CAR T-cell therapy trials, he saw improvements, shared everything he experienced with doctors, and helped future patients benefit. Legacy & Impact Jace passed away on July 3, 2021, but his mission did not end. Through his vision, My DIPG Navigator was created — a resource to help families access treatment, understand trials, and navigate complex systems. The Tough2gether Foundation continues to raise funds, support research, and provide emotional and financial help to families. Each year, people gather in his memory (for example, the “Live Free” event on June 29) to celebrate his life, his spirit, and his fight. His family, especially his mother Lisa Ward, continues to advocate fiercely — making sure that Jace’s dream of a future “when a child hears they have DIPG, it won’t mean a death sentence” continues to drive progress. In His Own Words One of Jace’s most defining moments was when he asked his doctor how long he had to live — not out of fear, but out of purpose. He recognized that time was a gift, and he refused to waste even a minute. The way he lived those months showed courage, clarity, and a deep commitment to others.

Jacob Mann

Jaxson Rand

Shop the Jaxson Collection: https://tough2gether.givecloud.co/product/JAXMERCH/the-jaxson-collection

Jayana Gonzales

Many have followed Jayana Gonzalez from San Jose over the last two years as she met every challenge with such grace and bravery. Nothing was fair about Jayana’s battle over the last year. Rhino virus caused inflammation, she was intubated and relied on steroids to reduce inflammation. No matter what her team and parents tried, her body never fully recovered which kept Jayana in ICU for most of 2025. She lost her ability to walk, talk, swallow, and no longer could use her hands. Most recently she could not move her eyes, yet deep within, her love radiated through the entire room touching all who cared for herJayana’s parents stayed by her side 24/7, filling Jayana’s days with love and joy. Jayana’s sister, Janaya, was born in the hospital last July and continued to live in ICU with mom and dad by Jayana’s side until January 2nd when Jayana passed peacefully through Heaven’s gates.Jayana was a beautiful, sweet girl that loved her mom and dad and five siblings. She was so funny, sassy and full of life. The strongest lil fighter ever. She never gave up, all the way to the end.Mariah and Johnny, her parents from San Jose, CA, are planning a celebration of life later this month. As a young family raising six children, they would appreciate any help to cover the cost. We’re committed to see Jayana’s life celebrated. Please consider donating a tax deductible contribution to this page or by check with memo “Jayana” to Tough2gether Foundation, 2201 Columbian Rd, Wamego, KS 66547.Every bit given assures Mariah and Johnny that Jayana’s journey was seen, her life mattered far beyond those who were directly blessed by her laughter and many were inspired by her love for her family even in her hardest days.We accept donations in other...

Jesselyn Silva

Joe Smeeding

Kaia Abernethy

Kinleigh Connelly

Lacey Breech

Lev Schissler

Lily McKinstry

Londyn Buss

Maddie Moore

McKinli Bauer

McKinli Anne BauerNovember 5, 2019 – January 25, 2026McKinli was the only child of Dustin Tatar and Brae Bauer from Sulphur, LA.She loved the colors pink and purple, princesses, mermaids, unicorns, dancing, gymnastics, cheerleading and animals.McKinli had a dog and a cat, and her mother describes her as loving, feisty and sweet.This fund support McKinli's family and families like them as they navigate these new steps.We accept donations in other ways:Venmo - PaypalMail checks to Tough2gether Foundation: 2201 Columbian Rd, Wamego, KS 66547Tax-Deductible Giving Notice:Donations made to Tough2gether Foundation are tax-deductible to the extent allowed by law. While funds raised in connection with this family will directly support them, all donations are made to Tough2gether Foundation and may also be used to support other families facing pediatric cancer, related programs, and charitable initiatives at the Foundation’s discretion.

Peyton Valiquette

Rosalie Cano

In Loving Memory of Rosalie CanoFrom the very beginning, Rosalie’s journey was surrounded by love. On May 6th, 2024, she was diagnosed, and from that day forward, so many of you stood with us—through prayers, messages, visits, and generous support.We witnessed an outpouring of love that carried us through some of the hardest moments of our lives. Your prayers gave us strength, your kindness gave us comfort, and your presence reminded us that we were never alone.Rosalie was the most loving, caring, and beautiful girl. She touched so many hearts in a way that will never be forgotten. Her strength and spirit were truly remarkable.Today, we find peace in knowing that Rosalie rests in God’s presence and is no longer battling this ruthless disease.“He will wipe every tear from their eyes. There will be no more death or mourning or crying or pain…” — Revelation 21:4We want to sincerely thank each and every one of you who prayed, supported, and walked alongside us during this journey. We will never forget the love you showed our family.Thank you for continuing to honor her memory.Donations made to Tough2gether Foundation are tax-deductible to the extent allowed by law. While funds raised in connection with this family will directly support them, all donations are made to Tough2gether Foundation and may also be used to support other families facing pediatric cancer, related programs, and charitable initiatives at the Foundation’s discretion.

Seana Isaac

Sidrah Roan

Teddy Kelly-Clark

Waylon Richmond

Xavier Tan

Zoe Ward