Not The Life of Typical Terrible Two’s…….

At age 2 a child should be running wild after discovering their legs move faster than a crawling pace, but instead Mason spends his time in and out of hospital beds. This small but courageous fighter is currently taking on the biggest battle of his life and you would never know by that smile on his face. Mason was diagnosed with Stage IV Neuroblastoma in October 2013.

It began one day when Mason fell off a bike and never recovered. 3 days later his family noticed that Mason didn’t want to walk. His mother took him to the doctor and he was sent to ER where they x-ray showed an anomaly. A decision to do a CAT scan showed a tumor stretching from his diaphragm to sternum and wrapping itself around his spine. The cancer was nearly in his bone marrow and if it had been diagnosed a week later, the doctors said they wouldn’t have been able to treat him. The family was in the ER for about six hours which felt like days until they found out something was really wrong and life threatening. From that moment their lives changed forever…….

Since his diagnoses, Mason has completed 5 chemotherapy sessions and just received surgery to remove the tumor wrapped along his spine. Mason will spend 6 weeks in UCSF for a stem cell transplant followed by several additional months of chemotherapy and radiation.

“We have received assistance and support from the KRM foundation through visits, emotional support, and gifts for Mason and the family. Their touch has provided us with an extended hand of comfort and acknowledgement of the most difficult period in our life, dealing with our son’s diagnosis and treatment of stage four cancer.” – Mother of Mason

 Unfortunately Mason’s illness is not the first crisis the family has faced together. A daughter, born in 2009, died of Sudden Infant Death Syndrome.  When Mason was born, his parents were terrified for the first year of his life and relieved to make it past the SIDS stage only to find themselves face to face with another nightmare- Childhood Cancer.

 ??????????????????????????????? MasonKelly Markers2 photo 2 photo2 Pre-Surgery3 4-22-14

September is Childhood Cancer Awareness Month

September is National Childhood Cancer Awareness Month. Every 3 minutes, a family’s life is turned upside down when they hear the four devastating words, “Your child has cancer.” At Keaton’s Child Cancer Alliance, we believe that every child deserves a fighting chance – and you can help make that a reality. 

This month, we honor brave young warriors, remember our precious Angels, and stand with families fighting childhood cancer today. From fundraising events to volunteer opportunities, there’s a way for everyone to join this mission of hope.

Together, let’s Glow Gold and remind every family: you are not alone in this journey. This September, we shine a light of awareness, love, and unwavering support for every child and family facing childhood cancer.

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Families Light Up at the Descendants/Zombies: Worlds Collide Tour!

When worlds collide… the result is pure magic! Keaton families were treated to an unforgettable experience at the Descendants/Zombies: Worlds Collide Tour, and the excitement was off the charts! One parent shared, “For a moment, we weren’t thinking about treatment or next steps – we were just together, smiling, dancing, and soaking it all in. It meant the world.”

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Moment with Love for Malachi

Malachi is facing something no teenager should have to – a rare and aggressive cancer called myxoid pleomorphic liposarcoma. 
 At an age where most kids are thinking about college and their next big adventure, Malachi is thinking about treatments, hospital stays, and fighting for his future. But what’s incredible is this: Malachi is still choosing to live fully. He’s choosing joy. He’s choosing moments. 

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