Podcasts about pediatric cancer

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.

Event Objectives:Understand the role of the Children's Oncology Group in pediatric cancer research.Describe the potential for molecular profiling to guide pediatric cancer treatment and barriers to implementation.Describe barriers to new agent development in pediatric oncology.Claim CME Credit Here!

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. 

In this inspiring episode of Game Over: c*ncer, Hosts Val and Dana of Cannonball Kids' c*ncer Foundation sit down with Natasha Maio Lonbaken, chair of the Ripple Effect Luncheon. Natasha shares her personal journey from first-time volunteer to nonprofit leader all rooted in one bold decision of saying yes before she felt ready.Through honest conversations about leadership, growth, and the power of showing up, this episode explores how one woman found purpose, sisterhood, and tangible impact through CKc's Ripple Effect event. Learn how this unique event is more than a luncheon — it's a launchpad for connection, empowerment, and action in the fight against pediatric cancer.Get ready to be moved, motivated, and maybe even a little emotional as we talk about:• How to lead even when you feel unqualified• What it means to be “poured into”• Why volunteering changes more than just the cause — it changes you• How a glass of wine, a good idea, and a group of women can start a movementIf you've ever wondered what life after cancer really looks like—or how you can be part of advancing pediatric cancer research—this is the episode for you.Tune 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/

In this powerful and deeply personal episode of Game Over c*ncer, we sit down with Jasan Zimmerman—a three-time childhood and young adult cancer survivor, former molecular biologist, and now the Senior Director of Foundation Relations at the Lucile Packard Foundation for Children's Health.Jasan opens up about his lifelong journey through cancer, the mental health struggles that often follow survivorship, and his evolution from patient to patient advocate. With honesty and vulnerability, he shares what it means to process trauma, show up authentically, and build community with purpose. He also highlights the importance of patient-centered research and the critical impact of including survivors' voices in medical trials and program design.Together, we reflect on the groundbreaking research funded through CKc's partnership with Stanford, including a clinical trial showing full response in children with DIPG. This is why we do what we do.If you've ever wondered what life after cancer really looks like—or how you can be part of advancing pediatric cancer research—this is the episode for you.Tune 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/

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

Tiffany, Kelly and Steve talk about emotions associated with pediatric cancer diagnosis from the perspective of a pediatric cancer survivor, a pediatric cancer parent and a bereaved pediatric cancer parent. Reintroducing: Steve Garraty was lucky to be graduating high school. He was partying and living a lifestyle that wasn't sustainable. His priorities were upside down. He was running towards the edge of a cliff and unable to stop himself. Then God intervened. He heard the three dreaded words none of us ever want to hear: “You have cancer.”After embarking on chemotherapy and a year of hell, as all his friends headed off to college, he beat the cancer. He went from victim to victor, from asking “Why me” to “Why not me?” He ended up not only surviving but thriving.Today, Steve has been married for more than thirty years to his beautiful wife, Wendy. They have raised two incredible kids who have both graduated college and begun their own careers. Steve has had a successful career in sales and leadership. He's hired more than 250 people in his career. He's coached and developed more than a thousand sales contributors and sales leaders. He cares deeply about helping others and seeing others achieve success and accomplishing their goals.He views cancer as being the best thing to ever happen to him. It changed everything…for the better! He grew from his experience. It set the foundation to be a better husband, father, friend, and leader. He writes to share his experience to help others alter their perspective and view the glass as full!Steve resides in Tampa, Florida. He enjoys traveling, music, exercise, watching UGA football with his son, and spending as much time with family as possible.https://stevegarraty.com/https://www.instagram.com/stevegarratyauthor/If you want to donate to Gold Ribbon Kids: https://givebutter.com/gold-ribbon-kids-cancer-foundationto learn more go to:goldribbon-kids.orgnationalpcf.orgkgoddard@nationalpcf.org - Kellyinfo@goldribbon-kids.org - TiffanySupport the show

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

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

In this week's episode, Dana and Val unpack the rising concern around potential federal funding cuts and their devastating impact on pediatric cancer research. Drawing from real-time experiences with researchers and families, they discuss the challenges of navigating social media noise, burnout, misinformation, and how research cycles already measured in decades could be further delayed. With only 4% of the national cancer research budget allocated to pediatric cancers, the stakes have never been higher.This show calls for more than awareness—it calls for action. Please be encouraged to donate, volunteer, or amplify trusted organizations like CKc to ensure progress doesn't stall in the face of political uncertainty and systemic underfunding.Whether you're a donor, advocate, parent, or simply someone who cares, this podcast will equip you with truth, context, and purpose. If you're ready to go beyond the outrage and be part of real change, this is the show for you.Tune 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/

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

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

After Matt and Breanna's son 10 1/2 year old son Landon passed away from Medulloblastoma in December of 2022, Matt took up running as a way to cope with the grief from his beloved son's passing. In March of this year, Matt's running took him to Lake Folsom in Auburn California where he lives and he began a 140 mile run that honored the memory of Landon and honored 105 other Pediatric Cancer Warriors, some of whom are fighters. some of whom are survivors, and some of whom have passed away. This amazing accomplished was also captured on a 45 minute film which was put together by his "crew" of helpers who helped Matt every step of the way. 

In this episode, Doro welcomes Nicole Giroux, founder of the Lilabean Foundation. Nicole shares the journey of her daughter Lila's battle against pediatric brain cancer, and the resulting determination to contribute towards the work to fund research on pediatric cancer. The conversation explores the challenges of navigating treatment options, the need for collaboration in research, the importance of community support, and the critical role of volunteers in the foundation's mission. Nicole-and the resilient, hopeful families-encourage listeners to get involved with the foundation and lean on each other for support.

Dr. Emma Jones is a Best Selling author because of her book entitled THE PHOENIX BLUEPRINT: RISING STRONGER FROM THE BLAZE OF HEALTHCARE which details the real problem of BURNOUT in the Medical Community. Emma has been a victim of burnout twice and she will talk about her book plus her role as a Palliative Care Physician for Pediatric Cancer and Adolescent Cancer patients.

Dr. Allie Neenan became very interested in Pediatric Cancer while a student at the University of Texas in Dallas  and after getting her degree, she received her Masters and Doctorate at Eastern Michigan University, Allie is now a Doctor who focuses on Psychology and has taken her considerable knowledge and skill to the world of Pediatric Cancer where she started her CANCER CUSHION Resource Library, which has answers to so many questions which arise during an individual and family's Pediatric Cancer journey.

On Thursday's show: We learn about a $150 million donation that will create the Kinder Children's Cancer Center, a new initiative to fight childhood cancer at MD Anderson Cancer Center and Texas Children's Hospital. The gift is one of the largest such donations in the history of the Texas Medical Center and one of the largest ever given to a pediatric hospital in the country.Also this hour: Comedian Ramy Youssef performs Friday night at House of Blues, and he has a new animated series on Amazon Prime called #1 Happy Family USA! We revisit a 2019 conversation with him about how he got into comedy and about how much of his standup material and work on television has revolved around the experience of growing up Muslim in America.Then, a Houston mother lost her parental rights to her children for life because of allegations her ex-husband made in court. We learn why the Texas Supreme Court unanimously overturned that ruling and what it means for how protective orders are issued here.And Laura Walker visits a farm run by the Socialites Riding Network, a Black-owned nonprofit that teaches sustainable agriculture and an appreciation for animals.

When Brandon Cary decided to join the Idaho Pediatric Cancer Coalition as its Secretary he did not envision becoming the President of this non-profit. Since he did however, this Coalition has become the leading Pediatric Cancer non-profit in the area and has plans to expand its scope to other communities in Idaho including Boise in the near future. As part of its mission , the Coalition focuses on helping with the "little things" that the families involved with Pediatric Cancer situations can use as much help with as possible.

When 3 1/2 year old Angelina Phillips was diagnosed with Stage 4 Neuroblastoma in 2013, one oncologist actually thought that her diagnosis was so bad that her mom Danielle should consider not even giving her treatment, Angelina did receive treatment which included 3 relapses and was able to go on some memorable trips during her battle which ended with her passing just before Covid began in late February of 2020.