10 year old Gabe Sorensen will talk about what he went through beginning in 2021 when he was diagnosed with a very rare form of Pediatric Brain Cancer at the age of 6, and how he is doing 4 years later.

Normally a diagnosis of Ovarian Cancer happens to women who are much older than 14 years old, which is what happened to Olivia Hebert in October of 2024. Olivia has been through some difficult times since her diagnosis including a temporary loss of her vision, but she was able to return to school in March, her vision has been getting better, and she is just finishing up a vacation to Disneyworld with her family. 

Kim and Trey Bowman's daughter Bella went through a long period of unexplained illnesses until she was diagnosed with an Ependymoma Brain Tumor on New Years day of 2011. During her treatment she went through a period of Proton Radiation which led to a diagnosis of Brain Stem Necrosis, which she was unable to get past. Bella ultimately passed away from this form of Pediatric Brain cancer on December 23 rd of 2011, nearly one year after her original diagnosis. 

Cedar Connell was 15 years old when he found himself on his way to Lurie Children's Hospital in Chicago to begin his treatment for B Cell Acute Lymphoblastic Leukemia in 2022. Cedar and his mom Kiki will talk about the difficult treatment that he went through, including his move from Chicago to the Dana Farber Cancer Institute in Boston in 2023. Cedar is now getting ready to do his part for the Leukemia and Lymphoma Society as TEAM CONNELLSLLS will be getting ready for a 31 day challenge beginning on July 1st and ending on August 1st to exercise 3 miles each day for that time period, in the hope that they raise 35,000.

Waiting for a proper cancer diagnosis for 9 months is something that should never happen, especially when the doctor says that the chances of cancer on a 1-10 scale were ZERO in his opinion. Unfortunately that is what happened to Jen and Will Fox in regards to their then 8 year old son who was finally diagnosed with Ewings Sarcoma in the winter of 2018, and passed away on May 25th of 2021. 

Aly Arenholz was a freshman in high school when she was diagnosed with Stage 2 Thyroid Cancer when she was 15 years old in 2021. After undergoing a very difficult battle during much of it, Aly just graduated from high school and will be attending the University of Kansas in the fall where she hopes her career path will focus on becoming a Child Life Specialist. Aly will also talk about her Non-Profit KICK CANCER LIKE A GIRL BOSS, which she started while in treatment and focuses on trying to bring a smile to the faces of Pediatric Cancer Patients. 

Alexandra Wilson passed away just 10 months after being diagnosed with Acute Lymphoblastic Leukemia in March of 2002, from this Blood Cancer that normally has a very high cure rate. Her twin sister Arianna will talk about her sister and about her role as the now official Executive Director of the Alex's Team Foundation which was named in Alexandra's honor, and helps in many ways the cause of Pediatric Cancer, with an emphasis on the Pediatric Cancer Nursing Community. 

Jennifer Vertentes was a police officer in Providence Rhode Island when she decided to go to Hasbro Children's Hospital on Thanksgiving Day of 2018 to meet kids who had to spend their Thanksgiving being treated for different reasons, including being treated for Pediatric Cancer. While she was there she met 3 year old Emerson Lucier who was going through her 3rd battle with Acute Myeloid Leukemia . This meeting inspired Jennifer to start her HERO PACKAGE FOUNDATION to help put a smile on the faces of these kids who were battling these difficult diseases. Jennifer, who in 2023 had to retire from the Police Department after suffering an injury while trying to save a person who was drowning, was also diagnosed with Ovarian Cancer that year. Fortunately for the Pediatric Cancer community, she continues to help these kids as she deals with her disease, that fortunately was diagnosed at a very early stage. 

After their 16 year old son Zach passed away from Osteosarcoma in November of 2021, Jon and Jenn Wall wanted to start a non profit focused around some type of Peer Counseling. The found it as they established ZACHS BRIDGE which partners parents who have already lost a child to Pediatric Cancer with parents who are going through their own child's pediatric cancer battle. The parents who have lost a child are there to help counsel the parents who are going through this same type of terrible experience, and trying to help them navigate this path as easily as possible. 

Kelsey Lauria began to have massive headaches early in the fall of her senior year in high school in 2014 which led to her diagnosis of Acute Myeloid Leukemia. In the later part of the winter in 2015, Kelsey experienced heart failure which led to her passing on April 18th, just 6 days after her 18th birthday and less than 6 months after her cancer diagnosis. During her treatment, Kelsey started her Bald Beauties Project to help in the fight against Pediatric Cancer and this successful non-profit has been run by her mom Maya since Kelsey's passing. 

Despite being diagnosed with a very rare form of Pediatric Brain cancer when he was 6 years old in 2021, Gabe Sorensen is living as good of a life as possible some 4 years later. Gabe was treated at St. Jude's and his goals for the future are either to become a doctor to help cure Pediatric Cancer or become a member of the Space Program.