Podcasts about pediatric cancer

Kendel Davy is a Founding Member of the Riley Rocks Memorial Foundation and Meghan Fessenden is the Director of Social Media and Marketing for the Foundation and is Riley's sister. Together they will talk about Riley who was diagnosed with Esthesioneuroblastoma which is a Pediatric Cancer of the Nasal Cavity when she 6 years old in 2013, and battled for 3 years before her passing on July 20th of 2016 when she was 9 years old. They will also talk about their Foundation which was started by Riley's parents Kamie and Todd.

What if pediatric cancer support did not have to mean choosing between the hospital and the holistic tools that can help your child stay strong?   In this episode, Corey and Christine sit down with Season Johnson (https://www.seasonjohnson.com/), functional practitioner, founder of the nonprofit Kick Cancer (https://kickcancermovement.org/), and owner of Biodynamic Wellness (https://biodynamicwellness.com/) in San Diego, to talk about one of the most terrifying realities a parent can face: a childhood cancer diagnosis. Season shares her family's story of walking her son through acute lymphoblastic leukemia, what she learned inside the conventional system, and the practical ways parents can support nutrition, detox pathways, and quality of life alongside treatment.   Join our Patreon community! https://www.patreon.com/c/ModernAncestralMamas What you get as a member of the MAM family: -- Full Downloadable Cookbooks to help you live your ancestral life -- Full Episodes AD-FREE -- Exclusive Post-Recording Conversations with Guests -- Private Community of Ancestral Mamas   Season opens up about the shock of diagnosis as a holistic mom, the emotional whiplash of hospital life, and why so many parents feel powerless, then shows exactly where parents can take their power back. From the foods she prioritized and the hospital food she refused, to gentle at home therapies that support the liver, lymph, appetite, and nausea, this conversation is packed with tangible tools and real hope without sugarcoating how hard this road can be.  

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Gabriella and Nicholas are 22 years old, and about to graduate from Purdue University and Indiana University respectively. This fall they will enter Medical School and will likely pursue careers in the medical field that will concentrate on Pediatric Cancer. Their cousin Maddox is now 14 years and well past his battle with Acute Lymphoblastic Leukemia but Maddox's sister Maia, who was diagnosed with Ewings Sarcoma in 2022 when she was 6 years old, passed away from this Bone Cancer on November 2nd of 2025. Gabriella and Nicholas will talk about what Maia went through during her cancer battle and will also talk about their amazing Strides For Sarcoma Non-Profit which they started after Maia relapsed, which shows both their dedication to Maia and their dedication to doing what they can to help eradicate the disease that Maia was forced to go through.

After their son Christopher passed away in 1969 from Rhabdomyosarcoma, Charles and Erma Millard decided to start a Charity organization that would help Pediatric cancer patients and their families. This organization was named Four Diamonds and Suzanne Graney, who has been its Executive Director for the past 15 years, will talk about this amazing organization which pays all expenses for each child that is treated at Penn State Health's Golisano Children's Hospital that are not covered by insurance. Four Diamonds has been partnering with Penn State and their Dance Marathon known as Thon which is the largest Student Run Philanthropy in the World, with all proceeds going to Golisano Children's Hospital to fight Pediatric Cancer.  

4 year old Ava Blazis woke up on the morning of March 11th 2023 with a very unusual pain in her abdomen which continued to get worse as the day wore on. Her mother Angela brought her to UMass Memorial Medical Center and 3 days later on March 14th, she was diagnosed with Acute Lymphoblastic Leukemia. Angela and Ava then spent the next 65 days at Boston Children's Hospital while Ava was undergoing treatment. Meanwhile Angela's sister Johanna Annuziata got busy with helping to look after Ava's brother Michael, and also helping to start Team Ava, an unofficial Non-Profit, which has already raised over $300,000 to help in the cause of Pediatric Cancer. Ava is now 7 years old and is doing well physically as she has been in remission since May of 2025. 

In this episode of Ordinarily Extraordinary: Conversations with Women in STEM, host Kathy Nelson sits down with Dr. Elizabeth Mendes, a newly minted PhD and postdoctoral researcher whose work focuses on rare and aggressive pediatric cancers.Dr. Mendes recently completed her PhD at Duke University, where she spent over five years researching rhabdomyosarcoma, a rare childhood soft-tissue cancer. Her goal: identify new biological targets that could one day lead to better, more effective treatments for children. Kathy and Liz explore not only the science behind pediatric cancer research, but also the deeply human reasons that drive this work.What We Talk About in This EpisodeWhat pediatric sarcomas are—and why they're so challenging to treatLiz breaks down complex cancer biology in an approachable way, explaining how sarcomas differ from more common cancers and why their ability to “change form” makes them particularly dangerous.A non-traditional path into scienceFrom archaeology and zoology to teaching middle school math and science, Liz shares how curiosity—and not a straight line—ultimately led her to molecular biology, cancer research, and a PhD.Choosing pediatric cancer researchLiz explains why she decided to focus on rare childhood cancers that receive less funding but have devastating outcomes—and how personal experiences with cancer shaped that decision.Science close to the patientWe discuss the importance (and rarity) of researchers interacting directly with patients, families, and clinicians—and how those experiences fundamentally change how science is done.Life after the PhD: postdocs, fellowships, and moving to the UKLiz shares what it's like to finish a PhD, move countries, start a new research position, and navigate life and work during a major transition.Being your whole self in STEMFrom makeup and music to mental health and social media, Liz talks about rejecting outdated stereotypes of what scientists “should” look like—and why authenticity matters for the next generation.Representation, mentorship, and science communicationLiz reflects on why visibility matters, especially for women and first-generation students, and how platforms like social media can help make science more accessible and human.A Conversation About More Than ScienceThis episode goes beyond lab work and credentials. It's a candid conversation about grief, resilience, identity, and the responsibility scientists carry—not just to discovery, but to people. Liz's story is a powerful reminder that STEM careers don't require fitting into a mold—and that compassion belongs in science.If you enjoyed this episode:Rate and review the podcast on Apple Podcasts or SpotifyFollow or subscribe so you never miss an episodeShare with a friend, colleague, or student who might need this storyHave thoughts, questions, or guest suggestions?Email us at ordinarilyextraordinarypod@gmail.com or leave a voicemail on our website.Support the show

When Aaira Khan was in 5th grade in 2021 she and her classmates at their school in Sydney Australia received a letter from a Pediatric Cancer patient which talked about the Great Cycle Challenge. Aaira quickly decided to ride in this event to raise money for this patient and for the cause of Pediatric Cancer. Aaira has now ridden in this event each year since and in the fall of last year, started her own CAN CAMPAIGN fundraiser. This fundraiser focuses on people picking up empty cans, bringing them to get recycled, and taking the proceeds that they receive from each can and donating all of these proceeds for research, to help join in the fight for these kids who need as much help as possible as they fight their own cancer battels. This campaign was just started 3 months ago and has already raised $2600.

Dr. Armstrong is a member, St. Jude Faculty, Chair, Department of Epidemiology and Cancer Control, Co-Leader, Cancer Control & Survivorship Program and Endowed Chair in Epidemiology & Cancer Control, St Jude's Research Hospital.

Among Katie Taylor's successes as a Certified Child Life Specialist over the past 15 years have been focusing on the parents of the children that are undergoing treatment for Pediatric Cancer, and empowering these parents to help get their children and adolescents ready for upcoming doctor's appointments, which can be a tricky proposition. Katie also established a Child Life Services program at a Newborn Intensive Care Unit with an astounding 80 beds to help these critically ill newborns. These accomplishments also go along with her being an Author, Public Speaker, and Podcast Host. Katie is an extremely busy and totally dedicated professional .

When Tony Suttles heard about 9 year old Haley Chandler being diagnosed with a form of Pediatric Cancer in 2020, he decided that he needed to do something to help this girl and their family. His solution was to start a Dirt Track Car Race and decided to call it FIGHT FOR A KID. His first race in 2024 attracted 80 cars on a track that normally had 30 cars race each weekend. By 2025, 106 cars entered and over $12,000 was raised in honor of kids like Haley who were going through their individual cancer battles. Tony and James Cumby, the father of 12 year old Brailynn Cumby who I spoke with on my Podcast on Christmas Day about her Ewings Sarcoma battle, will talk about this race and the expansion plans they have for it beginning in September when their next race is scheduled.  

  For Bhavika Taunk, life took a radical turn in 2017 when her four-year-old son, Kabir, was diagnosed with acute lymphoblastic leukemia.  After a bone marrow transplant, he went on an aggressive chemotherapy regimen for two years.  Kabir relapsed twice, but has been in remission since 2020.  Bhavika tells the story of how she cared for her son and how she reaches out to other parents of children diagnosed with cancer.   Bhavika, her husband and two young sons returned from a Disney cruise in April 2017, and both sons felt sick.  While her two-year-old son soon got well, things went from bad to worse for four-year-old Kabir.  He complained of bone pain, first in his wrists, then his ankles, to the extent that he could not walk.  Then he suffered from intermittent fevers and appetite loss.   Kabir was taken to a hospital, where after blood tests, Bhavika was told that a bad virus had settled into her son's bone marrow and that he had been diagnosed with acute lymphoblastic leukemia.  She called her husband with the awful, collapsed on the floor and cried.  Bhavika said this was the most life-changing event of her life.   She went on to say the degree of helplessness accompanying such a diagnosis is overwhelming.  Up until Kabir's diagnosis, she thought she could fix anything in his life that presented a challenge.  Bhavika says the biggest lesson with a child's cancer diagnosis is the total lack of control and it is the worst imaginable feeling.   Bhavika says when caring for a child with cancer that words are very important.  She stresses that she doesn't believe in "hollow encouragement because it is very invalidating to the patient."  She says a parent cannot tell their cancer-stricken child that everything is going to be okay.   Kabir has been in remission since 2020, but still requires a great deal of attention and medical care.   Bhavika Taunk wants very much to come to the aid of parents of a child diagnosed with cancer.  She advocates for parents of Facebook and Instagram, while strenuously calling for increased funding for pediatric cancer patients.   Additional Resources:   Bhavika on Facebook: https://www.facebook.com/bhavika.v.taunk   Bhavika on Instagram: https://www.instragram.com/btaunk/   Bhavika's small business supporting pediatric cancer: Birdsong Tea – Tea With A Purpose    

In this moving conversation, Gregg-Brooke Koleno sits down with Camilla, co-founder of Mylas Beleaf, a nonprofit born from unimaginable loss and transformed into a force of compassion, advocacy, and change. After her daughter Myla was diagnosed with Wilms tumor at age six and passed at eight, Camilla refused to let grief be the end of the story. Instead, she stepped into advocacy, education, and leadership raising over $2 million, partnering with 13 Florida hospitals, and supporting 300+ families navigating pediatric cancer. Camilla shares how her journey from hospitality to real estate, to nursing school, to a master's degree in leadership shaped the organization she runs today. She opens up about the realities families face, the importance of true partnership in medical care, and the values that guide MylasBeleaf's mission. She also discusses her children's book, Who Are You, Cancer? written from Myla's perspective offering kids and caregivers clarity and courage during one of life's hardest experiences. This episode is a powerful reminder that influence isn't about authority; it's about choosing purpose over pain, standing for others when they can't stand alone, and keeping compassion alive long after the world moves on. You can learn more about Myla's Beleaf at www.MylasBeleaf.com, and follow their journey on Instagram and Facebook at @MylasBeleaf. https://www.facebook.com/mylasbeleaf/ https://www.instagram.com/mylasbeleaf/

In today's episode of Game Over: c*ncer, we explore one of the greatest superpowers in pediatric cancer research: collaboration. From co-funding grants to global scientific networks, teamwork is driving lifesaving breakthroughs, especially for the rarest and hardest-to-treat childhood cancers.Hosted by Val Solomon (Director of Program Impact) and Dana Nichols (Executive Director of CKc), this episode features an inspiring conversation with Dr. Anirban Das, a pediatric neuro-oncologist and cancer geneticist at SickKids Hospital in Toronto and assistant professor at the University of Toronto.Dr. Das is a 2024 Cannonball Kids' Cancer Young Investigator, a grant co-funded with Kindred Foundation, supporting his groundbreaking work on DNA replication repair deficiency and central nervous system tumors. His research not only spans advanced biology and immunotherapy but also reaches families across the world, including low- and middle-income countries, through the International Replication Repair Deficiency Consortium, which now includes more than 50 countries.What We Cover in This Episode:How Dr. Das unexpectedly found his path into pediatric neuro-oncologyWhy early-career funding (like CKc Young Investigator grants) is critical to innovationHow collaboration between foundations accelerates research for rare cancersThe global consortium bringing efficiency, shared data, and evidence-based care to families worldwideWhat makes replication repair deficiency tumors unique, and why they were once considered “rare”The reality of the research pipeline: grant writing, mentorship, and the challenges young investigators faceHow CKc and Kindred partnered to fuel the next generation of cancer breakthroughsWhy teamwork is not just helpful in pediatric cancer, it's essentialIf this conversation moves you, please like, comment, and share to help us educate for change. Leaving a review helps more families find tangible hope.To learn more about Kindred Foundation, visit www.kindredfoundation.caTune in to hear this inspiring and informative conversation. Don't forget to subscribe, leave a review, and join the fight to make Game Over: c*ncer a reality.----------------------------------Connect with Dana: https://www.linkedin.com/in/danaknichols/Connect with Val: https://www.linkedin.com/in/valerie-solomon/Upcoming Ckc Events: https://cannonballkidscancer.org/category/make-an-impact/events/----------------------------------Podcast Produced by Hi Hello Labs: Website: https://www.hihellolabs.com/

Grace Eline was taught values by her mom Aubrey and her father Dan at a very early age, that giving to others was far more important than wanting for yourself. Well before she was diagnosed with the Germ Cell Cancer Germinoma which took place when Grace was 9 years old, Grace had decided that rather than accepting birthday gifts, she wanted people to donate to the cause of Pediatric Cancer.  Now 16 years and completely healthy, Grace started the WITH GRACE INITIATIVE as a non-profit to help other Pediatric Cancer Warriors and their families as they go through their cancer battles. This outstanding young woman attended the State of the Union when she was 10 years old as a Pediatric Cancer Representative,  and has continued her work to help others, practicing the lessons that she was taught by her parents over 10 years ago. 

Nya Chambless is now 16 years old, has been an actor since she was 4 years old, and is the now the Award Winning 16 year old Director of the Short Film MY GUARDIAN ANGEL. Nya and her father Jerry, who is the film's producer, will talk about this film which details the true story of the friendship between Nya and Teeja Johnson, who met in pre kindergarten, became best friends , and then Teeja passed away from Neuroblastoma just 5 months later. This film was introduced to Film Festivals across the country and beyond in April of 2025, has won multiple awards, and features topics such as Inclusion, Acceptance, Love, Friendship , the scrooge of Bullying, and awareness of Pediatric Cancer. If you would like to see information on this film click on this link. http://www.griefdialogues.com/my-guardian-angel/

Imagine being told your two-year-old has cancer — and realizing the system won't fight for them the way you will.This week, Season Johnson — medical advocate, holistic nutritionist, and founder of the KickCancer Movement — joins us to expose what really goes on inside the pediatric cancer system and how her son's diagnosis pushed her to fight back. She breaks down the pushback parents face when they ask questions, how hospitals respond to holistic support, the rights families are never told about, and the simple changes that can strengthen a child's body during treatment. We also get into toxins, food as medicine, and what true parental empowerment should actually look like.Thank you to our sponsors!TAYLOR DUKES WELLNESS: Use code "ALEXCLARK" for 10% off your purchaseZEBRA: Use code "ALEX" for 10% off any orderCALIFORNIA MOBILE ACUPUNCTUREARIZONA MOBILE ACUPUNCTURECOWBOY COLOSTRUM: Use code “ALEX” for 25% offJOOVV: Get an exclusive discount on your first red light therapy orderGEVITI: Use code "ALEX" to get 20% off your first purchaseOur Guest:Season Johnson, FNTP & IHP2Season's WebsiteSeason's IGSeason's FacebookBiodynamic Wellness WebsiteBiodynamic Wellness IGThrive Through Cancer WebsiteKickcancER WebsiteKickcancer IG

Karla Gess's daughter Kadence had been limping on her right leg for several weeks, and each time Karla or Kadence's father Jarret would take her to the emergency room, her limping would be dismissed and the only thing that she was told was to take Motrin. Finally a Pediatric Nurse saw Kadence, thought her color seemed off and ordered labs, which led to her diagnosis of Stage 4 Neuroblastoma. Kadence is now 5 years old and has been battling this form of Pediatric Cancer for 17 months with at least one year of treatment on the horizon.

On Tuesday's show: Children at Risk has released its annual list of the top public schools in Houston. The organization's CEO, Bob Sanborn, walks us through the rankings.Also this hour: Houstonians played a big role in the Gemini missions, which were stepping stones in America's 1960s journey to the moon. The program that preceded Apollo is the focus of Jeffrey Kluger's new book, Gemini: Stepping Stone to the Moon, the Untold Story.Then, we visit Texas Children's Hospital to learn about the first immunotherapy center dedicated to fighting pediatric cancer.And, on Veterans Day, we hear local Air Force veteran Ty Mahany's story about an encounter with a World War II veteran and discover what he learned about engaging fellow veterans in conversations about their service.Watch

Because he was Developmentally Delayed at birth, Aliyah Vida was not that surprised when her son Joshua, who was affectionately known as Goose,  slipped while walking to the bathroom and hit is eyebrow, causing a small bump.  Unfortunately this bump continued to grow, as did his feeling lethargic, and then not eating or drinking. Goose was then diagnosed with Stage 4 Neuroblastoma in April of 2022, and this form of Pediatric Cancer led to his passing in April of 2024, before he was to turn 4 years of age. 

Medical imaging, like X-rays and CT scans, are routine, non-invasive and painless tools used by doctors to make diagnoses. But a recent study of about 4 million children published in the New England Journal of Medicine suggests that the radiation exposure from imaging could pose a risk for pediatric cancer. John Yang speaks with Dr. Rebecca Smith-Bindman, the study’s lead author, to learn more. PBS News is supported by - https://www.pbs.org/newshour/about/funders. Hosted on Acast. See acast.com/privacy

Medical imaging, like X-rays and CT scans, are routine, non-invasive and painless tools used by doctors to make diagnoses. But a recent study of about 4 million children published in the New England Journal of Medicine suggests that the radiation exposure from imaging could pose a risk for pediatric cancer. John Yang speaks with Dr. Rebecca Smith-Bindman, the study’s lead author, to learn more. PBS News is supported by - https://www.pbs.org/newshour/about/funders. Hosted on Acast. See acast.com/privacy

In episode 96 of the Summits Podcast, co-hosts Vince Todd, Jr. and Daniel Abdallah are joined by Dr. Robyn Spoon, CEO of Elevate Childhood Cancer Research and Advocacy. Tune in as Robyn shares her son's cancer story that ignited a passion for change and how Elevate Childhood Cancer Research and Advocacy is moving the needle on precision medicine for those diagnosed with childhood cancer. Learn more about Elevate Childhood Cancer Research and Advocacy at elevatechildhoodcancer.org. The Heroes Foundation Team JOEY Program proudly sponsored the 2nd Annual Indiana Pediatric Sarcoma Research & Advocacy Summit. Together, we will continue uniting Indiana against cancer.

Being put in a garbage can by a fellow classmate while in Junior High School, and having a teacher laugh at her as she was being forced to clean up the spill of a lunchroom tray which she did not cause, are just a few of the things that Mariah Forster Olson talks about in her recently published book HOPE OVER DESPAIR which details her life of the physical and mental after effects of her Neuroblastoma battle that she has lived with since her diagnosis of this form of Pediatric Cancer when she was a year old in June of 1980. Now at the age of 46, Mariah has proven without a doubt that it is possible to live a meaningful and successful life, despite being forced to endure the many unfortunate details that she describes so eloquently in her book.

Monday (3rd) Governor DeSantis and First Lady Casey DeSantis announced $30 million in grants to four Florida children's hospitals, to improve research and care for pediatric cancer patients in the state. One goal is to make sure children and families don't need to leave the state to access care. Targets include encouraging collaboration among researchers and creating a portal to help parents navigate clinical trials. We speak with Dr. Cassandra Josephson, the Hawkins Family Endowed Chair director of the Cancer and Blood Disorders Institute at Johns Hopkins All Children's Hospital in St. Petersburg. See omnystudio.com/listener for privacy information.

Jannell and Keith Royer's daughter McKenna was experiencing headaches before her Diffuse Midline Glioma diagnosis in August of 2023. This Pediatric Brain Cancer behaves in a similar manner to DIPG, leaving little room for a lifespan which is normally expected to be 9-12 months.  McKenna did not even make it that far, passing away on February 26th of 2024, 6 months after being diagnosed. Jannell and Keith will talk about how McKenna felt surprisingly well during almost all of her battle, until 8 days before her passing when she suddenly went downhill health wise. Jannell and Keith will also about their Brave Like McKenna Foundation and their advocacy work for the cause of Pediatric Cancer.

BobbiJo  Pansier met Andy Standish , the founder of the Standish Foundation For Children, at an event and just a few weeks later Bobbi Jo joined this World Wide Foundation and is now its Global Programs Manager. This Foundation works with low income and middle income countries to help children who are suffering from diseases such as Pediatric Cancer and other maladies with many aspects of healthcare. This foundation is 15 years old and is alive in 70 countries around the world, and has served 1 million children. Bobbi Jo is a Child Life Specialist and uses her background in psychosocial issues to help these kids and their families navigate what can be a very difficult path in the Healthcare world. 

Sam Taylor's daughter Ellie has been free from her treatment for Rhadomyosarcoma since April of 2023. 6 months after that, Sam started her DEEP C PODCAST which focuses on parents and how they are able to deal with their the children's Pediatric Cancer battles. This podcast is so well known that Sam hears each day from at least one parent who has listened to her podcast or knows about it, and Sam develops great relationships with all of her guests. Sam also spends a great deal of time on her Advocacy work for the cause of Pediatric Cancer, including her work with the Pediatric Oncology Group of Ontario known as POGO.If you would like to find clips of interviews that Sam has had with her guests then please go to her DEEP C PODCAST Instagram page. Interested parents would be able to see Sam and her guests interact and that is always a good thing. 

In this episode of Disruption/Interruption, host KJ sits down with Chris Cyrille, founder of SNTIMNT.AI, to discuss how he’s using data science and AI to bring clarity and confidence to crypto investing. Chris shares his personal journey, the challenges of the crypto market, and how his mission-driven approach is changing the way investors and institutions view digital assets. Key Takeaways: Personal Motivation Drives Innovation [3:52]Chris’s journey began with a personal loss, inspiring him to redirect capital toward causes like pediatric cancer and first-generation students. Crypto Volatility and Misinformation [6:25]The biggest challenge in crypto is volatility, fueled by meme coins, speculation, and misinformation, making it intimidating for new investors. Algorithmic Solutions for Peace of Mind [17:51]Sentiment AI’s algorithm “reads the room” to provide actionable signals, helping users invest with greater confidence and less stress. Staying Curious and Creative [26:34]Chris encourages listeners to maintain childlike wonder and curiosity, as unique perspectives drive creative solutions in any industry. Quote of the Show (26:54):“Keep the childlike wonder and to stay curious. I believe that's where the creativity shows itself.” – Chris Cyrille Join our Anti-PR newsletter where we’re keeping a watchful and clever eye on PR trends, PR fails, and interesting news in tech so you don't have to. You're welcome. Want PR that actually matters? Get 30 minutes of expert advice in a fast-paced, zero-nonsense session from Karla Jo Helms, a veteran Crisis PR and Anti-PR Strategist who knows how to tell your story in the best possible light and get the exposure you need to disrupt your industry. Click here to book your call: https://info.jotopr.com/free-anti-pr-eval Ways to connect with Chris Cyrille: LinkedIn: https://www.linkedin.com/in/chris-cyrille/ Company Website: https://sntimnt.ai How to get more Disruption/Interruption: Amazon Music - https://music.amazon.com/podcasts/eccda84d-4d5b-4c52-ba54-7fd8af3cbe87/disruption-interruption Apple Podcast - https://podcasts.apple.com/us/podcast/disruption-interruption/id1581985755 Spotify - https://open.spotify.com/show/6yGSwcSp8J354awJkCmJlDSee omnystudio.com/listener for privacy information.

Dr. Danielle Cameron knew that she was interested in medicine when she was a girl growing into her teenage and adolescent years while watching her father who had a career as a Cardiac Surgeon. Danielle talks about that on today's podcast as well as her many interests in the field of Pediatric Oncology, especially when it concerns solid tumors. Danielle also lends her voice as a member of a number of National committees for Organizations that are concerned with a wide variety of Pediatric Cancer issues. 

From her early years , HELPING was a word that described what Dr. Kate Lund enjoyed doing for others, and this led to her career as a Clinical Psychologist and her roles in the Pediatric Cancer World. One of these roles was as a volunteer for the Children's Brain Tumor Foundation which took place for nearly 25 years and her most recent and current role has been training her dog Wally to become a Therapy Dog who visits Pediatric Cancer patients and brings them comfort at Seattle Children's Hospital. 

In this episode of Disruption/Interruption, host KJ sits down with Jim Foote, CEO and founder of First Ascent Biomedical. Jim shares his personal journey from technology executive to cancer care innovator, after his son’s diagnosis changed his life. Discover how he’s disrupting the status quo in oncology with AI-driven, personalized medicine that’s giving new hope to patients and families. Key Takeaways: The Problem with Standard Cancer Care [3:53]The standard of care treats patients as if they are the same, but everyone is unique. This approach works two-thirds of the time, but leaves one-third of patients with few options. Functional Precision Medicine [13:04]Jim’s company tests up to 152 FDA-approved drugs on a patient’s biopsy to find the most effective treatment, providing doctors with data-driven options tailored to each individual. AI and Technology are Transforming Oncology [28:05]Advances in AI, robotics, and cloud computing have converged, making personalized cancer treatment faster, more affordable, and more effective than ever before. Impact and Future Vision [26:51]Jim’s goal is for every cancer patient to receive individualized treatment from the moment of diagnosis, improving outcomes and reducing unnecessary side effects. Quote of the Show (14:40):“I literally have gone from trying and hoping to testing and choosing.” — Jim Foote Join our Anti-PR newsletter where we’re keeping a watchful and clever eye on PR trends, PR fails, and interesting news in tech so you don't have to. You're welcome. Want PR that actually matters? Get 30 minutes of expert advice in a fast-paced, zero-nonsense session from Karla Jo Helms, a veteran Crisis PR and Anti-PR Strategist who knows how to tell your story in the best possible light and get the exposure you need to disrupt your industry. Click here to book your call: https://info.jotopr.com/free-anti-pr-eval Ways to connect with Jim Foote: LinkedIn: http://www.linkedin.com/in/jim-foote Company Website: https://firstascentbiomedical.com/ How to get more Disruption/Interruption: Amazon Music - https://music.amazon.com/podcasts/eccda84d-4d5b-4c52-ba54-7fd8af3cbe87/disruption-interruption Apple Podcast - https://podcasts.apple.com/us/podcast/disruption-interruption/id1581985755 Spotify - https://open.spotify.com/show/6yGSwcSp8J354awJkCmJlDSee omnystudio.com/listener for privacy information.

After surviving her childhood fight with Acute Lymphoblastic Leukemia, Claire Galvin has gone on to have an outstanding academic career, which has included holding a double major in Biology and Psychology which led to her receiving an Honors Bachelor Degree from the University of Toronto, a Master of Science Degree in Experimental Medicine from the University of British Columbia, and is now pursuing her Doctorate in Clinical Psychology from Concordia University in Montreal. Clair is currently working on her Dissertation which involves the study of Pediatric Cancer survivors and how they have transitioned into adulthood. Claire's dissertation is called the CHILDHOOD CANCER IDENTITY PROJECT. If you are interested in participating in this project then please email Claire at cchip.research@gmail.com

Osteosarcoma Webinar Series: Alanna Church, MD, Associate Director, Laboratory for Molecular Pediatric Pathology at Boston Children's Hospital, Assistant Professor of Pathology at Harvard Medical School, and Conference Cochair joins us on OsteoBites to discuss insights and higlights from the AACR Special Conference in Cancer Research: Discovery and Innovation in Pediatric Cancer—From Biology to Breakthrough Therapies, September 25-28 in Boston.Dr. Church is currently a Molecular and Pediatric Pathologist at Boston Children's Hospital, where she is a founder and associate medical director of the Laboratory for Molecular Pediatric Pathology (LaMPP). She is an Assistant Professor of Pathology at Harvard Medical School, the Program Director for the Harvard Molecular Genetic Pathology Fellowship, and the incoming Chair of Clinical Practice for the Association for Molecular Pathology. Her clinical and research work focuses on bringing molecular testing to the clinical care of children with cancer. Through institutional projects (the Profile study, GAIN consortium study), she has profiled thousands of children's tumors and has used these results to make real-time impacts on their diagnoses and treatments. She is involved in national initiatives to improve the quality and access to molecular testing for children with cancer, including the NCI-funded Count Me In Study (Dana Farber, Broad Institute), the National Comprehensive Cancer Network, the National Institutes of Health, and the Children's Oncology Group.

In Belf's News Gallery, Greg Belfrage goes over what's trending in the news including Trump, Democratic leaders, Mocking Democrats, Jane Goodall, Trump putting a hold on the rail tunnel project, AI, Pediatric Cancer, Military Excellence, and more...See omnystudio.com/listener for privacy information.

On this week's episode of Food Farms And Chefs Radio Show we centered our focus on a particular cause, the fast rising foodie event which benefits the Fight On Makenna Foundation. We opened the show with Chef Brian Duffy, who discussed his involvement in the Bite for the Fight Food Festival as the event's headliner celebrity chef. Our host learned that during the event, Chef Duffy performed cooking demonstrations and meet-and-greets for his fans. After sharing his background in the food industry and the significance of how much it meant to be involved with Bite for the Fight, Chef Duffy helped introduce our listeners to the event and Fight On Makenna Foundation's Co-Founder, Rich Massi.The show then focused on Fight on McKenna Foundation's mission and how they offer support for families facing the battle against pediatric cancer. Bite for the Fight Food Festival's proceeds directly impact the various programs and initiatives offered through the Fight On Makenna Foundation, a charitable organization that raises awareness of pediatric cancer and offers support for families that rely on weekly treatments from Children's Hospital of Philadelphia's (CHOP) integral cancer treatment services. The conversation concluded with details about the foundation's ongoing initiatives and opportunities for supporters to get involved through donations, social media, and future event participation.For more information on this week's guests, please follow these related links:https://www.fightonmakenna.orghttps://www.bite4thefight.comhttps://chefbrianduffy.com/about-chef-brian-duffy/https://duffifiedexperiencegroup.com

Nici and John Robinson live in England and lost their son Charlie to a Grade 3 Ependymoma in 2021, after he was diagnosed with this Brain Tumor when he was 2 years old in June of 2018. Nici and John will talk about their beloved son and will also discuss the Respite Homes that they have made available for families who are going through a Pediatric Cancer diagnosis with one of their children. The Robinson's have set these Respite Homes up through their Thumbs Up For Charlie Foundation.

Charlie Kirk shot in Utah, we analyze political violence, then talk to The Bennet Project about helping pediatric cancer- h2 full 1791 Wed, 10 Sep 2025 21:09:31 +0000 lomV2HXmGxkQ4ZOq9NQlK4FDnbfdq9Bs comedy,religion & spirituality,society & culture,news,government The Dave Glover Show comedy,religion & spirituality,society & culture,news,government Charlie Kirk shot in Utah, we analyze political violence, then talk to The Bennet Project about helping pediatric cancer- h2 The Dave Glover Show has been driving St. Louis home for over 20 years. Unafraid to discuss virtually any topic, you'll hear Dave and crew's unique perspective on current events, news and politics, and anything and everything in between. © 2025 Audacy, Inc. Comedy Religion & Spirituality Society & Culture News Government Fals

In this special episode, host Jeremy Schrand sits down with Jill Brinck, Executive Director of CancerFree KIDS, and Dr. Genevieve Kendall, a CancerFree KIDS grant recipient and pediatric cancer researcher at Baylor College of Medicine. Together, they explore the power of early-stage research funding, the challenges and breakthroughs in treating childhood cancers, and the inspiring mission behind CancerFree KIDS. Dr. Kendall shares insights into her lab's work on fusion-driven rhabdomyosarcoma and how innovative models like transgenic zebrafish are helping uncover new therapeutic targets. Whether you're a parent, a scientist, or someone passionate about making a difference, this episode offers a compelling look at how collaboration and curiosity are driving real change in pediatric oncology. Learn more - CancerFree KIDS home page Learn more about Dr Kendall's research - Kendall Lab | Nationwide Children's Hospital Learn more about CTI - CTI - CRO Specializing In Clinical Research And Consulting  02:03 Jill Brink shares her personal and professional journey that led her to become Executive Director of CancerFree KIDS.  04:02 Why funding early-stage, high-risk research is essential for pediatric cancer, highlighting the lack of profitability and federal support in this space. 05:46 Securing funding for early-stage research presents major challenges, including the need for collaboration between scientists and business leaders.  07:06 How CancerFree KIDS selects research projects, outlining the role of their Scientific Advisory Council and the grant scoring process. 09:26 Success stories driven by CancerFree KIDS funding, including early support for clinical trials and advancements in flash proton therapy. 11:22 Dr. Genevieve Kendall explains the nature of fusion-driven rhabdomyosarcoma and why its aggressive behavior and lack of targeted therapies make it difficult to treat. 13:51 How the CancerFree KIDS grant supported a new partnership and provided seed funding to test a promising research idea. 14:50 The significance of identifying HAS3 as a novel target and how it opens new possibilities for treating rhabdomyosarcoma. 16:35 Dr. Kendall describes the role of transgenic zebrafish in her research and how they help uncover therapeutic targets through comparative oncology. 19:33 Both guests share what excites them most about the future of pediatric cancer research, including innovations in CRISPR and immunotherapy. 22:32 How CancerFree KIDS measures the long-term impact of its grants, citing follow-up funding, startup companies, and FDA projects. 24:19 Jill highlights impactful partnerships and community initiatives, such as Jersey Mike's Day of Giving and the 100-Mile Challenge. 26:15 Details about the 100-Mile Challenge, including its structure and supporting events throughout September. 27:51 How CancerFree KIDS engages with families affected by cancer, ranging from support programs to events that honor children and their journeys. 29:51 The future direction of CancerFree KIDS, including expansion, collaboration, and advocacy efforts with the state of Ohio. 

In episode 93 of the Summits Podcast, co-hosts Vince Todd, Jr. and Daniel Abdallah are joined by Dr. Nur Damayanti, cancer researcher at IU School of Medicine. Tune in as Dr. Damayanti shares the personal cancer diagnosis that changed the trajectory of her career and the Heroes Foundation funding that is supporting her project to study new treatment methods for children with rare brain cancers. Learn more about recent Heroes Foundation gifts: https://www.heroesfoundation.org/the-heroes-foundation-has-awarded-nine-exciting-indiana-cancer-projects-with-223500-in-funding/

What was thought to be a stomach ailment for Meryl Summers 1st grade daughter Adelia became much more than that in February of 2023 when she was diagnosed with the Pediatric Brain Cancer Diffuse Midline Glioma. Adelia was called the Wonder Girl for so many reasons during her 15 month battle with this disease which very sadly ended with her passing on May 30th of 2024. Since that time, Meryl has become a fierce advocate for the cause of Pediatric Brain Cancer and has testified in the Massachusetts State House for a bill which recognizes the cause of Pediatric Cancer be passed and signed into law as soon as possible. 

Maria chats with elementary school teacher (30 years as an educator!) and children's book author Lori Skala about her books The Road To Rosie and The Hair Tie. Proceeds from Lori's books go to animal rescue and pediatric cancer, her two passions.Give a listen and learn about Lori and her mission.Lori can be found on IG at storyloribooks or visit her website storyloribooks.com.

Get More LVWITHLOVE Content at LVwithLOVE.com For more than a century, A-TREAT has been part of the Lehigh Valley story. The sodas and seltzers we grew up with, the flavors that feel like home. Now the brand is doing something new: using that fizz to fight pediatric cancer. In this episode of the Lehigh Valley with Love Podcast we are on site at the A-TREAT facility with Luke Jaindl, Vice President of Jaindl Companies, and Michelle Zenie Rounds, Executive Director of the Pediatric Cancer Foundation of the Lehigh Valley (PCFLV). Together they share the story behind “Fizz That Fights” Lemon Twist Seltzer, a limited edition release that puts community first. Every bottle helps raise awareness and support for PCFLV's mission to provide hope, programs, and direct assistance to more than 450 local families navigating childhood cancer. We talk about: How the A-TREAT and PCFLV partnership came to life Why local matters, from Jaindl's rescue of A-TREAT in 2015 to PCFLV's hyperlocal mission The importance of awareness initiatives like “30 Days, 30 Stories” during Pediatric Cancer Awareness Month A-TREAT's unique place in Lehigh Valley history, from Big Blue to holiday flavors, and what the future looks like Listen in for community, history, and a whole lot of fizz. Learn more about PCFLV: https://www.pcflv.org/ Watch Episode: https://youtu.be/7RpzdyyKQ_A Thank you to our Partners! WDIY 88.1 FM Wind Creek Event Center Michael Bernadyn of RE/MAX Real Estate Molly’s Irish Grille & Sports Pub Banko Beverage Company

After Megan Bugg was diagnosed with Stage 4 Alveolar Rhabdomyosarcoma in late 2014, she underwent a very difficult treatment protocol which included 150 weeks of toxic Chemotherapy , 200 Radiation treatments, 5 trips to the ICU, and 8 surgeries. Even so, Megan fought her disease every day and became an amazing and well known advocate for the cause of Pediatric Cancer before her passing on March 9th of 2022, 7 years and 2 months after her diagnosis.

Juno Wollf was born on October 11th of 2022 and was doing well until James noticed a lump under his right armpit. As happens too often, the doctors who looked at Juno did not figure out that this lump was an indication of a Malignant Rhabdoid Tumor, which was finally diagnosed on December 17th of 2022. Just 47 days after Juno's diagnosis on February of 2023, he passed away from this form of Pediatric Cancer, which is diagnosed in 20-25 kids each year. Juno only lived for a total of 114 days. 

Rewind to this year's Live Stream For the Cure event as the Last Comic Shop Podcast takes a look one of the strangest comic book mash ups of all time with "The Punisher Meets Archie"! Plus fans challenge us to come up with some of the greatest hypothetical mash ups ever! From Captain Kirk vs. Steven Seagal to Jughead vs. Wimpy, get ready for the hilarity!   Host: Andy Larson Co Hosts: Chad Smith, JA Scott & Mikey Wood Guest Host of Live Stream For the Cure: Nicholas Haskins   Special Thanks to the Live Stream For the Cure for hosting this year's event!   Support these other Cancer Fighting Charities mentioned on this week's show: The Susan G. Komen Foundation: No matter who you are or where you live, breast cancer may touch your life. Go2 for Lung Cancer: Help confront lung cancer on every front, every day, for everyone! The Prostate Cancer Foundation: Funding the world's most promising research on the biology and treatment of prostate cancer. The National Pediatric Cancer Foundation: Together, We Can Solve the Puzzle of Pediatric Cancer.  

Keith Desserich-will talk about the budget cuts from the National Insititute of Health, a huge cut from the National Cancer Institute which I just found out about and I mentioned in my outro, and other monetary losses that will have a negative affect for Pediatric Cancer patients and their families.

Being a Certified Child Life Specialist is one of the most important careers that anyone who has a passion for those that are going through a Pediatric Cancer experience can aspire to. Shani Thornton is a prototype for how important this role is and she will talk about the many things that she is involved with on a daily basis as a Child Life Specialist that helps so many people deal with the psychosocial part of dealing with a disease that no one wants or deserves. 

Susan Latta LMFT, FT is a licensed Marriage and Family Therapist and the Department Head of Clinical Services at the Austin Hatcher Foundation for Pediatric Cancer. Susan holds a Fellow in Thanatology, the study of death and dying, and received her BS from Cal Poly San Luis Obispo University and her MA from Fuller Theological Seminary. Susan brings 35 years of counseling individuals, children, and families through the many challenges that occur when a child is diagnosed with cancer, with over 23 years of experience in the medical field. Susan loves to be in nature, travel, cuddle with her 2 miniature dachshunds, Gertie and Maggie and find time to return to California to see her family and to walk on the beaches of the Pacific Ocean.Austin Hatcher Foundation's Mission: The Austin Hatcher Foundation's mission is to provide a lifetime of free, comprehensive support to childhood cancer patients and their families through mental, behavioral, educational, and social services, so they can cope in the present and thrive in the future. Austin Hatcher Foundation's Approach: Recognizing that pediatric cancer impacts every aspect of a family's life, the Austin Hatcher Foundation provides comprehensive, integrative care for childhood cancer patients, survivors, and their families — supporting cognitive development, emotional well-being, and essential life skills.Through a unique blend of therapy, education, and psychological support, the Foundation addresses each family's complex and evolving needs, helping them build resilience, restore hope, and thrive through every stage of the cancer journey.Listeners can learn more by visiting HatcherFoundation.orgGoldribbon-kids.orgNationalpcf.org Email tiffany @ info@goldribbon-kids.orgemail Kelly @ kgoddard@nationalpcf.orgSupport the show

Debi Mitchell's son Austin was diagnosed with Stage 3 Acute T Cell Lymphoblastic Non Hodgkins Lymphoma in 2021 when he was 12 years old, under the assumption that his issue before this diagnosis had to do with Asthma. Today, Austin is doing very well and is trying to establish himself as an actor. While spending her time during Austin's treatment at a Northern California Hospital which would become affectionately known as the "Kaiser Resort", Debi met other mom's who were with their children and were being treated for different forms of Pediatric Cancer. During this time in the "Kaiser Resort" these moms coalesced to form the MAMA BEARS FIGHTING CHILDHOOD CANCER Non-Profit, a Non-Profit which now has established Roots in a number of Northern California Hospitals.