Mark Levine

Help and Hope Happen Here

Health EN ↓ 556 episodes

This Podcast is going to be about Pediatric Cancer and the need to keep the awareness of this terrible disease in the public eye. My plan is to be able to interview a wide spectrum of people who all have a passion and a stake in finding a way to make the lives of these Pediatric Cancer Patients easier. I will interview oncologists, nurses, recovered patients, parents who have had to oversee their children's cancer fight, heads of Pediatric Cancer Foundations and Organizations , and others who would like to use this forum to advocate for these children.

Author

Mark Levine

Category

Health

Latest episode

Jul 9, 2026

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Episodes

Toni and Dylan Franklin will talk about their daughter Noelle who was diagnosed with Osteosarcoma in May of 2024 and was only able to survive this Bone Cancer for 1 year, as she passed away in May of 2025 09.07.2026

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 Can...

Christina Stiverson will talk about her daughter Adelaide ( Addie) who was diagnosed with the very rare Liver Cancer known as Hepatoblastoma as she approached her 2nd birthday in the fall of 2015 and passed away in December of 2016 06.07.2026

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, Ad...

Tristin Mercer's daughter Kinley was diagnosed with Stage 4 Kidney Cancer in the summer of 2022 when she was 4 months old. Kinley's cancer spread very quickly and she passed away on November 12th of 2022, just 7 1/2 months after her birth. 02.07.2026

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 diffi...

Andrea Wilson will talk about her daughter Phoenix who was diagnosed with Neuroblastoma in 2017 when she was 3 years old and her older daughter Liberty who's own life was in the balance while Phoenix was in treatment. 29.06.2026

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. F...

Shay McAlister is an Independent Journalist who has been investigating the Cluster of DIPG diagnoses that have surrounded 3 counties in Southeastern Kentucky. Shay will talk about this problem and what the powers that be in Kentucky are doing about it 25.06.2026

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 entir...

Caitlyn and CJ Downings 2 year old son Brooks was diagnosed with a Fusion Mesenchymal Tumor in his lung in the spring of 2025, and passed away on October 25th of last year, just 8 months ago. 22.06.2026

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...

Shaya Rees Frum will talk about her beloved sister and best friend Jessie who passed away after a 10 month battle with DIPG that ended with her passing on January 5th of 2012. Shaya is now very involved with the Jessie Rees Foundation. 18.06.2026

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 Apri...

Maribeth Ditmars will talk about her son Christopher who battled Acute Lymphoblastic Leukemia before his passing when he was 14 in 2001, successfully battling her own demons, and the loss of her other son Jarrod in July of 2015 15.06.2026

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 h...

Alisha Harper will talk about her son Chase who was diagnosed with Down Syndrome officially when he was born and 4 years later was diagnosed with Leukemia. Chase is going strong as he is now 9 years old 11.06.2026

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 d...

Kayla and Charli Martin will talk about Charli's diagnosis of High Risk B Cell Acute Lymphoblastic Leukemia when she was 10 years old and in 5th grade in 2023. Charli is now doing well as she has just completed her 8th grade year. 08.06.2026

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...

Gwen Mysiak became the Executive Director of the Punt Pediatric Cancer Collaborative in 2012. This Collaborative was started by former Buffalo Bills Punter Brian Moorman and his wife Amber in 2004 and focuses on 6 major programs. 04.06.2026

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 Directo...

Carla and Sydney Belsher will talk about Sydney's battle with Infantile Acute Lymphoblastic Leukemia which she was diagnosed with in April of 2014 when she was 6 months old and how she is doing now at the age of 12 1/2. 01.06.2026

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 h...

Heather and Casey Arrayan will talk about their daughter Kalia who was diagnosed with High Risk B Cell Acute Lymphoblastic Leukemia in November of 2023 and her recovery is now going well after her Bone Marrow Transplant in July of 2024. 28.05.2026

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 Ma...

Dale and Marissa Metcalf will talk about Marissa's successful fight with Acute Lymphoblastic Leukemia when she was 3 1/2 years old in 2010 and her goal to become a Pediatric Cancer Oncology Nurse 25.05.2026

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 ha...

Lily McGrath will talk about her son Bryson who had a very difficult path to navigate during his 1027 day fight with Neuroblastoma that began in early 2023 and ended with his passing on September 26th of 2025 when he was 5 years old. 21.05.2026

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...

Cherie Calbom is a well known Nutritionist who will talk about the negative health effects that Seed Oils can have on consumers and the link that exists between these Oils and Pediatric, Adolescent and Young Adult, and Adult Cancer. 18.05.2026

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 Adu...

Lauren and TJ Bailey will talk about their son Brody who was born with a Congenital Diaphragmatic Hernia in early 2023 and then just after his first birthday he was diagnosed with Neuroblastoma. 14.05.2026

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 Townshi...

Jordan Belous will talk about her spectacular connections that she has made with so many pediatric cancer patients and their families through her WHIP PEDIATRIC CANCER Non-Profit 11.05.2026

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 Memo...

Matt Giegerich will talk about his role as CEO of the Matthew Larson or Iron Matt Foundation for Pediatric Brain Tumors which was started by young Matt's parents Kelly and Greg after his passing from a form of Pediatric Brain cancer in 2007 07.05.2026

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 fa...

Leslie and Michael Fox will talk about their son Mason who was diagnosed with Acute Lymphoblastic Leukemia in April of 2023, was doing well, and then was attacked by a Fungal infection that led to his passing in February of 2024. 04.05.2026

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 am...

Nick and Sarah Bascle will talk about their son Liam who was diagnosed with an Ependymoma Brain Tumor when he was 10 months old in April of 2015, and lived his best life possible before his passing on November 23rd of 2021 30.04.2026

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 suppo...

Amy and Phoebe Davis will talk about Phoebe's battle with Acute Lymphoblastic Leukemia which she was diagnosed with just before her 3rd birthday in 2010 and how well she is doing now as a thriving 18 year old. 27.04.2026

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...

Amy and Matt Cisneros will talk about their son Cullen who was diagnosed with Acute Myeloid Leukemia when he was 3 years old in 2012, gained remission quickly, was in good health for the next 8 years, and then was diagnosed with Ewings Sarcoma 23.04.2026

After being diagnosed with Acute Myeloid Leukemia when he was 3 years old in 2012, Cullen Cisneros was able to live the next 8 years of his life free of cancer until 2020 when leg pain during a baseball game led to a diagnosis of Ewings Sarcoma. Cullen's parents Amy and Matt will talk about their beloved son, who fought from 2020 until May of 2025 to try and do everything he could to stay ali...

Amelia Mijach will talk about her son Hayes who was diagnosed with High Risk Acute Lymphoblastic Leukemia when he was 2 years old in 2024 and after very difficult treatment, he is finally feeling better and is back to being an active little boy. 20.04.2026

Amelia Mijach's then 2 year old son Hayes was diagnosed with High Risk Acute Lymphoblastic Leukemia when he was 2 years old in August of 2024 and the reason for his high risk status was because of his extraordinarily high white blood cell count at diagnosis. Hayes then contacted a serious fungal infection during his consolidation phase of his treatment and during the next year and a half of t...

Erik Rees will talk about his daughter Jessie who was diagnosed with DIGP on March 3rd of 2011 and passed away only 10 months later on January 5th of 2012 when she was 12 years old. Jessie was the inspiration behind the Jessie Rees Foundation. 16.04.2026

Erik Rees became an amazing Cancer Dad and Pediatric Cancer advocate during and after his daughter Jessie battled with and passed away from DIPG at the age of 12 in January of 2012. Erik talks about his beloved daughter and then details the Jessie Rees Foundation which was started because of Jessie's wish to help Pediatric Cancer patients who were at Children's Hospital of Orange County...

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