Help and Hope Happen Here
Episodes
546 episodes
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.
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 yea...
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.
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 ...
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.
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 befo...
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
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 possibl...
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.
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 ...
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.
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...
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.
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 ne...
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
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...
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
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 ...
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.
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 o...
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
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 unfortun...
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.
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 wi...
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
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...
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.
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...
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.
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 Jes...
Ben Shroyer will talk about his now 10 year old daughter Hannah who is a survivor of Stage 4 Neuroblastoma and Histiocytosis and will talk about his Casting For The Kids Foundation which he started to help families financially and emotionally.
Ben Shroyers then 2 year old daughter Hannah was diagnosed with Stage 4 Neuroblastoma in 2018, then was diagnosed with Histiocytosis which ended up in her brain before she became cancer free in 2021. Now 10 years old and in 3rd grade, Han...
Kelly DiGiammo and her son Brayden will talk about Brayden's battle with Acute Myeloid Leukemia which Brayden was diagnosed with in late February of 2024. Brayden is now just one month away from the second anniversary of his remission and is doing well
When Kelly DiGiammo's son Brayden was 13 years old in early 2024 he developed troubling health symptoms, including going from being one of the fastest runners in the school to losing his breath and running very slowly, experiencing continuing c...
Mary Kemp and Kaitlyn Lee will talk about the Society For Emerging Leaders organization which Mary co-founded in 2022 and which Kaitlyn is its Executive Director. This organization is made up by over 350 students..
The bill AB 703 which was signed into law by California Governor Gavin Newsom and which I talked about with Sahil Metha on my podcast a few weeks ago is just one of the important accomplishments that was led by the Society Of Emerging Leaders, ...
Jacob Orlick was 11 years old when he was diagnosed with Ewings Sarcoma in 2019. Now 18 years old and doing well, Jacob will talk about his roles as A Motivational Speaker and his podcast, Motvational Mic.
Jacob Orlick is now a senior in High School and making plans to attend Penn State University in the fall. Jacob was 11 when he was diagnosed with the Bone Cancer Ewings Sarcoma, had his right leg amputated, but has been able to live a fulfillin...
Dr. Katerina Levy is a Pediatric Psychologist who has written a book entitled THE HEALING GARDEN. This book is fiction but gives great strategies to kids and families who are trying to cope with a Pediatric Cancer diagnosis.
Dr. Katerina Levy decided to write her book THE HEALING Garden while she was a resident at the Broward Medical Health Center in South Florida. This book was based on the Healing Garden that she saw while at that Medical Center and is full of st...
Meghan Macantee was diagnosed with Acute Myeloid Leukemia as a sophomore at SUNY Potsdam where she originally hurt her hamstring during swimming practice. Meghan is fine now but went through some terrible times before her diagnosis .
Being treated terribly by her swimming coach and eventually belittled and made fun of by her teammates, Meghan Macantee was diagnosed with Acute Myeloid Leukemia in the fall of 2023, during her sophomore year at SUNY Potsdam where she was a mem...
Kim Alexander will talk about her daughter Payton who was 15 years old when she was diagnosed with Ewings Sarcoma in January of 2018 and fought bravely for 3 1/2 years until her passing in November of 2021 at the age of 19
Payton Alexander was living a healthy and normal life for a 14 year old until late in 2017 when she began experiencing symptoms that needed to be checked out. These symptoms led to her diagnosis of Ewings Sarcoma in January of 2018. Payton cont...
Tamy Bell will talk about her son Griffin who was diagnosed with Neuroblastoma when he was 16 months old in September of 2018, and had his 3rd relapse in April of 2023, leading to his passing at 6 years old in March of 2024.
Tamy Bell's son Griffin was born 3 months prematurely in June of 2017 and 16 months later was diagnosed with Neuroblastoma in September of 2018. Griffin relapsed on two occasions after that but then in April of 2023, had a 3rd relapse that was ...
Sahil Mehta will talk about the amazing and far too short life of his older brother Ronil who passed away from DIPG in 2018 and what Sahil did subsequently in Ronil's honor and memory to greatly affect the cause of Pediatric Cancer.
Sahil Mehta's older brother Ronil wanted to donate his brain to Stanford University after his passing from DIPG in 2018 in the hope that it would help another DIPG Victim in the future. Sahil took this request as his personal responsibility and...
Carrigan Nelson's mom Tammy, her Aunt Bonnie, and closest friends Devean Piermont, Hannah Nasser, and Madison Quinn will join in a tribute to a true Icon, who passed away from Osteosarcoma on Christmas Day of 2025.
Carrigan Nelson was diagnosed with Osteosarcoma in March of 2019 and fought for the next 69 months with this form of Pediatric Bone Cancer until her passing on Christmas Day in 2025 when she was 24 years old. Carrigan was a truly Iconic young w...