The Parker Evans Osteosarcoma Fund

Parker

Parker Kenneth Evans was 15 years old, a beloved son, brother, and friend to all. He was a bright light in this world with a smile that could fill a room, a heart that loved deeply, and a joyful spirit that made everyone around him feel seen and loved. To know Parker was to love him.

Before cancer, Parker was a typical teenager. He loved his family, his friends, Disney, video games, theater, and making people laugh. He had the most unique personality and a way of bringing happiness wherever he went. We never imagined that what seemed like normal growing pains would be something that would forever change our lives.

In November 2025, Parker was diagnosed with high-grade osteosarcoma in his left femur that had already metastasized to his lungs. What started as leg pain, something so easy to explain away in a growing teenager, became the beginning of a fight no child should ever have to face. From the moment Parker was diagnosed, he showed strength and courage far beyond his years. He endured chemotherapy, surgery, countless appointments, hospital stays, and challenges that most people will never experience, yet he continued to be the same Parker we always knew and loved. Even on the hardest days, he found reasons to smile, loved others deeply, and continued to shine his light.

Parker showed us the true meaning of bravery, facing every challenge with strength, courage, and a spirit that refused to give up. On February 19, 2026, Parker passed away peacefully surrounded by love. In just 112 days, we went from hearing the words “your child has cancer” to saying goodbye to our firstborn son. No family should have to watch their child fight so hard and still be left wishing for more time. While our hearts will forever ache for more memories, more moments, and more chapters in the story we were writing together, we find peace knowing Parker’s fight did not end in defeat. When his earthly fight was finished, we can only imagine him ringing the bell in Heaven, whole, healed, and victorious, the loudest and most beautiful celebration.

We are incredibly proud of the way Parker faced this battle, the courage he showed, and the impact he made during his 15 years. Through Parker’s journey, we saw firsthand the devastating reality of metastatic osteosarcoma and how desperately more research is needed. Treatments for osteosarcoma have seen very little advancement in decades, and children fighting this disease deserve better. Families need more options, more hope, and most importantly, more time.

The Parker Evans Osteosarcoma Fund was created to continue Parker’s fight by supporting research that leads to new treatments, better outcomes, and ultimately a cure.

Parker’s light also continues through Parker’s Fight Pals, a mission created in his honor. During his hardest days, Parker found comfort in his Squishmallows. They brought smiles during long hospital stays, comfort during painful moments, and a little bit of joy when he needed it most. Through Parker’s Fight Pals, we donate Squishmallows to children battling cancer so they can feel that same comfort and encouragement Parker felt. Our mission is to continue spreading Parker’s light and love, one smile and one hug at a time.

Parker’s courage, kindness, faith, and the way he loved others continue to inspire us every single day. His light continues through every life touched by his story, every child comforted through Parker’s Fight Pals, and every step taken toward a future where children diagnosed with osteosarcoma have a different ending.

Parker, we will continue your fight. We will continue spreading your light. We love you so BIG.

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Our Mission

MIB Agents Is A Leading Pediatric Osteosarcoma Nonprofit Dedicated To Making It Better For Our Community Of Patients, Families, Medical Professionals, Researchers, And Industry Partners Through Programs, Education, And Research.
Supporting Doctors, Researchers, and the Medical Community
FACTOR Osteosarcoma Conference

FACTOR brings together the leading researchers, clinicians, surgeons, together with patient families and OsteoWarriors to Make It Better for those battling this disease.

Annual OutSmarting Osteosarcoma Grant

Each year a grant of $100,000 is awarded to a project that will focus on moving research forward for osteosarcoma patients.

Osteosarcoma Resources for you to give to patients

Browse our extensive list of osteosarcoma resources from MIB Agents and our partner organizations.

OsteoBites Weekly Webinar

OsteoBites is a weekly webinar and podcast where we invite Osteosarcoma Experts and OsteoWarriors to share their research, hope, and innovation.

Supporting Kids and Young Adults with Osteosarcoma
Gamer Agents

Agent GAMERS game with their fellow OsteoWarriors and OsteoSiblings.

Ambassador Agents

Ambassador Agents are certified peer visitors who provide hope, understanding, and resources.

Warrior Mail

OsteoWarriors receive monthly letters of hope and cheer from MIB Agent Writers around the world.

Missions

When an OsteoWarrior transitions to hospice care, MIB Agents provides an experience or an item of comfort and entertainment.

HQ at FACTOR Osteosarcoma Conference

The OsteoWarriors HQ (headquarters) brings kids and young adults who have a connection to osteosarcoma together and It. Is. Awesome!

Vision

A world with less toxic, more effective treatments and a cure for osteosarcoma.

Values

We are devoted to creating and instilling hope with and for our inclusive and collaborative osteosarcoma community. We do this through mutual trust, transparency and compassion.