Help and Hope Happen Here

Laura Devita's daughter Ivy developed a back and blue eye for no apparent reason in August of 2023 when she was 2 years old and that led to her diagnosis of Stage 4 High Risk Neuroblastoma. Ivy still faces an uncertain future but has one of the best hospitals in the Memorial Sloan Kettering Cancer Center in charge of her care. Currently she is battling with a tumor which was recently found near her jaw and lymph nodes in which many doctors are looking at. Laura and her family moved to South Carolina 8 months ago but still need to travel to New...

In October of 2022 Zamara Jankowski, who was 10 months old, began to experience an odyssey that no child ever should have to go through. After being seen at 3 different hospitals, in which all of the doctors involved said that she was basically fine although perhaps suffering from some type of flu, Zamara was finally diagnosed with Neuroblastoma in late December of 2023, 14 months after her symptoms began to present themselves. Everything that could have gone wrong, did go wrong for Zamara and her mom Danielle, with the blame that should be carried focusing on the 3 hospitals that looked at her symptoms...

Loretta Brooks was diagnosed with a Head and Neck Cancer known as Nasopharyngeal Carcinoma when she was 13 years old in 1991, causing her to miss almost all of her 8th grade school year. Loretta recovered well from that form of cancer and now has dedicated her life to advocacy work for Pediatric Cancer, with a particular emphasis on the subject of survivorship, which is always a difficult issue for former Pediatric cancer patients as they move into young adulthood and then adulthood. 

Sophia Gerosa was 3 years old in April of 2025 when she was diagnosed with High Risk B Cell Acute Lymphoblastic Leukemia. After receiving great care and treatment from her caregivers at Advent Health For Children in Orlando, Sophia has completed difficult months of treatment and is now in the Maintenance program which she will complete in August of 2027.

6 year old Miriam Koska was experiencing leg pain, abdominal pain, fevers, night sweats and fatigue in the fall of 2025 when she was diagnosed with an offshoot of Neuroblastoma known as Ganglioneuroblastoma. This form of Pediatric Cancer has a similar treatment protocol to the more well known Neuroblastoma. Miriam has been through difficult treatment but is doing as well as possible as she enters her next phase of treatment at the Mayo Clinic in Rochester, Minnesota.  

Megakaryoblastic Leukemia is an even more aggressive form of Acute Myeloid Leukemia, which always is a difficult form of Pediatric Blood Cancer.  Olivia White was 15 months old in February of 2024 when she was diagnosed with this disease. After some very difficult struggles with her treatment, Olivia has been feeling much better over the past months as she approaches her 4th birthday this coming November.

For the second time in just a few months on this podcast, we heard the story of a Fungal Infection that attacked a child who was in treatment for Acute Lymphoblastic Leukemia and this infection could not be stopped for causing a child to pass away. This time it was Lola Aguilar, the 6 year old daughter of Alyssa who spoke beautifully on our podcast about what her beloved daughter had to go through after falling to the floor on Halloween in 2024, just as she was about to go Trick or Treating. 

Harper Wengrod was born on January 12th of 2024 and by the end of that year , a lump on her abdomen that her dad Joe found after Thanksgiving that was thought to be Neuroblastoma was the probable cause. That was not to be the case however as Joe and Melanie were to learn that Harper was actually suffering from Stage 3 Sertoli Cell Ovarian Cancer. This is such a rare diagnosis for a child not even a year old to receive, as Ovarian Cancer is found in women decades older than that. Harper continues to fight her battle on a daily...

After hearing the story of a friend that had a child who was diagnosed with a form of Pediatric Cancer, Mike Dechristopher got involved in this Pediatric Cancer cause in 2012 and started the Dylan Project. This Non-Profit now has helped hundreds of families in the New England area and brings joy to these kids by buying gifts each holiday season and delivering them to their homes, giving him the nickname of the Real Life Santa Claus, a nickname that is well deserved. 

Lainy Sharpe began to feel numbness in her legs, followed by paralysis when she was 12 years old in the summer of 2023. Her diagnosis was Mesenchymal Chondrosarcoma, which as rare of a diagnosis as it gets. Lainy fought as hard as possible before passing away in January of 2025 and was very much a part of the Pediatric Cancer community during her fight, which was proven by her winning the Children's Healthy Hero Award for her dedication to helping others at Banner Children's Hospital in Tucson, Arizona.

Elena Lappostato was complaining of mouth pain in September of 2025 and just a couple of weeks later, she was diagnosed with Neuroblastoma when she was 3 years old. Since that time , Elena has undergone difficult treatment including 2 autoglous stem cell transplants and is now doing well and has recently begun the next phase of her treatment which is Post Consolidation.

After winning the Vault event and finishing 2nd in the All Around Competition in the Hawaii Gymnastics Championship in November of 2017, 11 year old Kaylan Haywood competed for the first time since her winning performance in January of 2018. What resulted was Kaylan's side being weak, her foot was dragging, and her arm was hanging. In February she was diagnosed with DIPG and only was able to live for 6 more months, as she passed away on August of 2018 from this most dreaded form of Pediatric Brain Cancer.

Dana Quiroga felt a pain in her knee during her entire soccer season in 2023 and during that summer this pain did not go away, leading to her diagnosis of the Bone Cancer Osteosarcoma. Dana underwent a replacement for her knee and tibia with a prosthetic substitute and now 3 years later, Dana is feeling well and has already chosen what she plans to do with her career which will involve Pediatric Nursing.

Grace Fulcher was 16 years old in 2015 when she began to complain about double vision. Her double vision led to a diagnosis of a non curable Pediatric Brain Tumor known as an Anaplastic Astrocytoma. Grace was given 3 years to live and she did her very best in trying to make those 3 years meaningful. Grace continued with her high school studies, being a member of the National Honor Society for 3 years, and graduating Summa Cum Laude with a 4.4 Grade Point average. Because of the acceleration of her brain cancer, Grace went to college for only her first semester of freshman year...

Darline Medina's daughter Brooklyn was full of health for the 1st 2 years of her life until the winter of 2023 when Brooklyn began to experience abnormal movements in her left eye. Her eye looked okay when examined by an eye doctor but her walking did not look okay and this led to her diagnosis of DIPG. Brooklyn's diagnosis took place in April of 2023 but her life span from that day until her passing on February 17th of 2024, was just 10 months, and took place one month before her 4th birthday.

Jameson Doud was nearing his 8th birthday in August of 2024 when he was diagnosed with a Midline High Grade Glioma Pediatric Brain Cancer. In March of 2025 the Doud family got very good news that there were no signs of any cancer from the most recent scans but just a couple of months later, Jameson's scans showed that his cancer had spread to his bone and Jameson was not expected to last until Christmas of 2025. That expectation went too far unfortunately and James on passed away from this disease on August 12th of 2025.

In May of 2025, 5 year old Rosie Wittmayer was found to have a double ear infection and then began to develop fevers every 2-4 weeks. These fevers were checked out regularly but no solution was found , with one possibility floated that she had the Mumps. Finally on August 27th, Rosie and the Wittmayer family received her diagnosis of B Cell Acute Lymphoblastic Leukemia. Rosie has been through nearly 11 months of treatment and still has more than a year left as her scheduled date to end her treatment protocol will be in November of 2027. Fortunately Rosie is doing well physically .

Zach Arter had been serving youths in Omaha Nebraska for 15 years in various capacities and then decided to focus on helping Pediatric Cancer patients in August of 2024. That is when he started his HELP 1 PERSON TODAY with this non-profit which tries in a number of ways to help these kids who have to go through difficult treatment during their individual cancer battles.

As Toni and Dylan Franklin were in the playground with their children Noelle and Dylan in the spring of 2024, Noelle asked her dad to look at a bump that had formed on her leg. Withing a week Noelle was diagnosed with Osteosarcoma, a very difficult Bone Cancer. After being treated at the Pediatric Cancer hospital at Duke University which did not go well, Noelle was transferred to the Pediatric Cancer hospital at the University of North Carolina. Despite the treatment that was more to the benefit to Noelle, she was unable to recover and passed away on May 12th...

After being shuttled back and forth between her home and hospital emergency rooms for months in 2015 because of recurring fevers, Addie Stiverson received the very difficult diagnosis of Hepatoblastoma in the autumn of 2015 while visiting family in Colorado. Although her doctors were optimistic that Addie would recover from this Liver Cancer, her body said otherwise as after a Liver Transplant, Addie's cancer spread to her lungs and then her brain. Addie passed away on December 20th of 2016, having lived for only 3 years and 17 days.

A massive Malignant Rhabdoid Tumor was found on 4 month old Kinley Mercer's left kidney in the summer of 2022 and she was diagnosed with Stage 4 Kidney Cancer.  Upon undergoing chemotherapy treatment, Kinley went through scans that showed that her cancer had spread very quickly, so much so that her doctors declared that her cancer was no longer curable. Kinley passed away from this very difficult form of pediatric cancer on November 12th of 2022, only 7 1/2 months after her birth.

Andrea Wilson had two very difficult health crises on her hands, one with her younger daughter Phoenix who was diagnosed with Stage 3 High Risk  Neuroblastoma when she was 3 years old in 2017,  and one with her older daughter Liberty who contracted Septic Pneumonia while Phoenix was in treatment. Phoenix was on the 7th floor of Phoenix Children's Hospital while Liberty was on the 9th floor. Fortunately both girls are surviving and doing well and Andrea and her family are looking onto the possibility of trying to build a Western Style Ranch with horses, so that Pediatric Cancer families can have a...

The counties of Knox, Laurel, and Whitley, in Southeastern Kentucky have seen 10 DIPG diagnoses since 2024, an extraordinarily high number of cases in such a condensed area. Shay McAlister is an Independent Journalist who has been investigating this issue and will discuss the problems that are related to this most deadly form of Pediatric Brain Cancer, which normally sees 1 or 2 cases in the entire state each year. Shay has written 2 major articles on this issue and will be continuing her goal to find some answers that are needed as to why this is happening.

After experiencing a number of illness when he was 2 years old going into the spring of 2025, Caitlyn and CJ Jennings thought that their beloved son Brooks was experiencing normal illnesses that many toddlers may experience. Unfortunately that was not the case. Brooks was diagnosed with a Fusion Mesenchymal Tumor that was located in his lung and then spread to his Pelvic Bone. Brooks continued to feel well until August of last year when his health went downhill, leading to his passing on October 25th of 2025.

Shaya Rees Frum was 14 years old when her then 11 year old sister Jessie was diagnosed with DIPG on March 3rd of 2011.  Jessie passed away from this terrible Pediatric Brain Cancer on January 5th of 2012, but not before laying the groundwork for the Jessie Rees Foundation that has been directed by her father Eric for the past 14 years. I spoke with Erik about Jessie and the Foundation back in April. Shaya has taken on a major role in the Foundation, it is her full time job, and hopefully she will be the person to take on its Leadership Role, when E...

Maribeth Ditmars has suffered plenty of heartache and loss for the past 25 years, beginning with the diagnosis of Acute Lymphoblastic Leukemia in 1997 and the subsequent passing of her son Christopher at the age of 14 in 2001. This was followed by the passing of her younger son Jarrod when he was 21 years old from an accident on July 4th of 2015, which left him unconscious for the last 4 days of his life. In between those years, Maribeth successfully battled her own demons with her dependence on alcohol, to the point where she has been able to counsel many people who have had...

During Alisha Harper's pregnancy, she was told that there was a 60 percent chance that her son would be born with Down Syndrome. That statement turned out to be a correct one as Chase was born in December of 2016 with this illness and by the time Chase was 4 years old, Alisha saw that his Down Syndrome was manageable. One month after feeling as good as possible about how Chase was doing, he developed a body rash which turned out to be a symptom of Acute Lymphoblastic Leukemia. Despite having this 1-2 punch thrown at him, Chase is doing well as...

10 year old Charli Martin hurt her shoulder while competing in the New York State School Wrestling Tournament when she was in 5th grade in 2023. While going for Physical Therapy, Charli noticed a lump on her neck and after taking antibiotics and still in therapy, the pain in her shoulder did not go away. Charli then had this lump biopsied and the result was her diagnosis of High Risk B Cell Acute Lymphoblastic Leukemia. Charli has now completed her 8th grade year and at 13 years of age is back playing sports and living the life of a normal and healthy 13...

Gwen Mysiak worked in the field of Public Broadcasting for 19 years in Buffalo and during that time, her friend's cousin Andrew Pawlak was 13 years old and in 7th grade when he was diagnosed with a form of Pediatric Cancer and passed away 2 years later. Not too much time went by after that before Gwen switched carriers to become the Punt Pediatric Cancer Collaborative's Executive Director in 2012. This Collaborative focuses on 6 major programs to help families deal with a Pediatric Cancer situation, with a special emphasis on their bereavement program.

Sydney Belsher has been through a great deal in her still very young life as she is 12 1/2 years old, which started with stomach issues almost from her birth in the fall of 2013, and then her diagnosis of Infantile Acute Lymphoblastic Leukemia which came when she was 6 months old in April of 2014. Right after her diagnosis Sydney's lifespan was very uncertain as her doctors feared she would have a stroke and may not survive. This did not happen thankfully but Sydney has battled both physical and mental issues over the years . Fortunately Sydney has survived all of her issues and...

When she was 4 months old on November 14th of 2023, Kalia Arrayan was diagnosed with High Risk B Cell Acute Lymphoblastic Leukemia. This diagnosis came as a complete shock to her parents Heather and Casey who did not see any clear symptoms before a routine checkup showed a lump on her spleen. Kalia went through a very difficult treatment process for the next 8 months before she underwent a Bone Marrow Transplant with her 11 year old brother being her donor. Kalia has been doing much better over the past nearly two years as she approaches her 3rd birthday.

Marissa Metcalf does not remember many details from her treatment during her battle with Acute Lymphoblastic Leukemia which took place in 2010 when she was 3 1/2 years old. What she does know, now that she is 19 years old and looking at possible careers, is that this form of Pediatric Blood cancer has affected her in different ways as she approaches 20 years of age, and wants to help others who have been diagnosed with cancer by becoming an Oncology Nurse, which would be a great accomplishment for her and a good thing for her future patients.

Lily and Sebastian McGrath's 2 1/2 year old son Bryson was first thought to have a Wilms Tumor before his Pediatric Cancer diagnosis was changed to Stage 4 Neuroblastoma in the early days of 2023. Lily and Sebastian had to put up with a number of more than questionable medical decisions during Bryson's fight and also had to endure the final days of Bryson's life who while in Hospice Care, was  promised 24 hour round the clock availability should they be needed and when they were needed the most, they were nowhere to be found. Lily also had to watch after Bryson passed away w...

Cherie Colbom is not only an expert Nutritionist, she has written 35 books, including her Juicing For life which has sold 2 million copies and her current book which became available on April 28th entitled The Truth About Seed Oils. Cherie will talk about how Seed Oils can have negative health effects for consumers and will discuss the link between Seed Oils and Pediatric, Adolescent and Young Adult, and Adult Cancer. Cheire has been on television many times discussing this issue and has also written many articles on this subject.

Brody Bailey is one of possibly two children in the World who have been born with a Congenital Diaphragmatic Hernia and then diagnosed with Neuroblastoma. Lauren and TJ Bailey are Brody's parents and will talk about his journey with the good news being that he is more than 3 years old and is doing as well as possible health wise. The Bailey family has received great support from their Township of Deptford New Jersey community, especially from Rich Nardiello who is the head of the great Pop Pop Custom Cars Non-Profit and a wonderful advocate for the cause of Pediatric...

Jordan Belous has always had a soft spot for Pediatric Cancer Patients and when she was 16 years old in 2015 she issued a "challenge", much like the Ice Bucket Challenge, when she created a video that went viral by dancing for 14 seconds to the song WHIP/NAE NAE by Rapper Silento to either Dance or Donate. More than 7000 people took up her challenge and donated more than $100,000 to Memorial Sloan Kettering to fight the cause of Pediatric Cancer. That was the birth of her WHIP PEDIATRIC CANCER Non- Profit. Since that time Jordan has personally developed long standing and iron...

Matt Giegerich has been the Chief Executive Officer of The Matthew Larson Foundation for Pediatric Brain Tumors for the past 18 months. This foundation, also known as the Iron Matt Foundation, was started by young Matt's parents Kelly and Greg after Matt passed away from the Pediatric Brain Cancer Choroid Plexus Carcinoma in 2007, when he was 7 years old. This Foundation focuses on helping families with financial assistance as well as focusing on raising money to award Grants to researchers who are trying to help solve the many issues that are involved with Pediatric Brain Cancer.  This Foundation has now awarded o...

Mason Fox was 10 years old when he was diagnosed with Acute Lymphoblastic Leukemia in April of 2023. Mason then went through treatment and was doing very well with his recovery before a Fungal infection got the best of him quickly in February of 2024, and led to his surprising and unfortunate passing, not even 10 full months past his original diagnosis. His parents Leslie and Michael detail the amazing persona that Mason had as he was most concerned with helping others even during treatment for this blood cancer, as he bought toys with his own money and would walk down the halls...

Liam Bascle was only able to live 7 1/2 years because of an Ependymoma Brain Tumor that he was diagnosed with in April of 2015. His persona resonated with many people despite his tender age and many tributes came his way after his very unfortunate passing in November of 2021, after fighting with this Brain Tumor for 6 1/2 years . To honor the memory of their beloved son his father Nick, with support from his mom Sarah, started the Links Fore Liam Golf Tournament in New Hampshire to help raise money for the cause of Ependymoma and Pediatric Cancer. This tournament is now held in  N...

A chance phone call between Amy Davis and a friend who was taking her daughter to get checked for allergies, led Amy to take her then 2 year and 10 month old daughter Phoebe to see her Pediatrician, where shortly thereafter she was diagnosed with Acute Lymphoblastic Leukemia in June of 2010. Phoebe was in Boston Children's Hospital for 8 weeks and completed her treatment as an outpatient for the next 26 months, until she was 5 years old. From that time on Phoebe has been cancer free with no long term side effects, and is feeling great as an 18 year old. It is always...