Podcasts about pediatric cancer

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. 

Did you know that “geohealth” refers to health and disease through a geographical lens? Join Food Sleuth Radio host and Registered Dietitian, Melinda Hemmelgarn for her conversation with Alan Kolok, PhD , Professor Emeritus, Environmental Toxicology, University of Idaho, Volunteer Faculty, College of Public Health, University of Nebraska Medical Center, author of Modern Poisons: A Brief Introduction to Contemporary Toxicology, and coauthor of “Exploring the Joint Association Between Agrichemical Mixtures and Pediatric Cancer,”GeoHealth (Feb. 2025). Kolok discusses his unique research on exposure to agricultural chemical mixtures and incidence of pediatric cancers. He also describes the importance of the USGS Pesticide National Synthesis Project, and related maps in scientific research.Related Websites: https://pubmed.ncbi.nlm.nih.gov/39944898/ USGS Pesticide National Synthesis Project maps: https://water.usgs.gov/nawqa/pnsp/usage/maps/

Adolescents and young adults (AYAs) face poorer cancer outcomes and experiences compared with younger and older patients, and they historically have been lost between pediatric and adult models of oncology care. The Association of Cancer Care Centers (ACCC) is committed to providing up-to-date guidance on treating AYA patients with cancer to improve their outcomes. In this episode of CANCER BUZZ, a team from the University of North Carolina (UNC) AYA Oncology Program shares how it's meeting the unique needs of this patient population by providing developmentally appropriate cancer care through a multidisciplinary approach, including clinical trial access and interactive infusion space; sharing resources where AYAs need additional support; and developing education about fertility and the short- and long-term impacts of cancer. “We talk about things like sleep, mental health, diet, exercise, knowing all of those aspects of life have been impacted by cancer and its treatment, and in order to have the best quality of life and best outcomes, we need to pay attention to all of those aspects of an AYA survivors' life.” – Andrew Smitherman, MD, MS “We know that AYAs are one of the most underinsured or uninsured populations in the United States, and so that means often they are at least initially facing these diagnoses without any insurance at all to help defray the costs.” – Jacob Stein, MD, MPH “My approach [for talking about long term effects] is that patients want to be able to have the opportunity to receive information.” – Alison Manikowski, PsyD Read the full article here. Guests Andrew Smitherman, MD, MSc AYA Medical Director Pediatric Oncologist UNC Adolescent and Young Adult Cancer Program Lineberger Comprehensive Cancer CenterChapel Hill, NC   Jacob Stein, MD, MPH AYA Oncology Liaison Medical Oncologist UNC Adolescent and Young Adult Cancer Program Lineberger Comprehensive Cancer CenterChapel Hill, NC   Alison Manikowski, PsyDAYA Program Pediatric Psychologist UNC Adolescent and Young Adult Cancer Program Lineberger Comprehensive Cancer CenterChapel Hill, NC Resources:  UNC AYA Cancer Program ACCC AYA Resources

Dr. Andrew Y. Koh shares how he and his team are investigating how Candida colonization impacts cancer development and treatment outcomes. This line of research could reveal groundbreaking insights into the role of the microbiome in cancer. Learn more about innovative oncology research at Children's Health 

While rubbing her 3 year old daughter Chelsea's belly, Alison Hicks felt a lump which was shortly diagnosed as a Stage 4 Wilms Tumor. Chelsea fought this Pediatric  Kidney Cancer for nearly 2 years before passing away after a treatment protocol which was very difficult from the beginning to its end. As a result of Chelsea's battle and passing, Alison started the Chelsea Hicks Foundation which focuses on keeping a smile on Pediatric Cancer patients as they go through their impatient hospital treatments. 

Send us a textWe dive into the inspiring story of Aaron Norris, member of Hog Addiction Team and winner at Hogs for the Cause 2025, where they raised over $50,000 for pediatric brain cancer research while taking home the Grand Champion title.• Aaron shares his journey from growing up on an Indiana farm to launching innovative cooking equipment• Rural upbringing instilled values of faith, perseverance, and finding joy in all circumstances• Norris Thermal Technologies evolved from agricultural dryers to cutting-edge cooking equipment• The Game Changer Smoker revolutionizes commercial kitchens with its unique smoke generator technology• Participation in charitable BBQ competitions combines Aaron's competitive nature with his desire to give back• Faith serves as the foundation for Aaron's approach to business and philanthropy• Chef Paul explores culinary applications for the Game Changer in commercial kitchensFor more information about the Game Changer Smoker, visit livefireadnsmoke.com or follow @GameChangerSmoker on Instagram.Introducing the SupraCut System - the automated solution that enhances safety, quality, and efficiency, cutting up to 120 perfect citrus wedges per minute, 6 times faster than manual. Patented tech delivers uniform slices, reducing waste and eliminating plastic, while the hygienic, contactless design lowers contamination and injuries, integrating seamlessly to transform your operations and improve profitability - get started at SupraCut.com and ask about risk-free trials. Elevate your dining experience with RAK Porcelain USA! As the exclusive tableware brand for the Walk-In Talk Podcast, RAK combines exceptional craftsmanship with innovative design. Whether you're a chef, a restaurant owner, or a food enthusiast, RAK's high-quality porcelain products will enhance every meal. Discover the artistry of food presentation and make every dining occasion special. Visit rakporcelain.com today and see how RAK can transform your table The following brands and companies help us continue supporting the food industry - have a look below! Support the showThank you for listening to the Walk-In Talk Podcast, hosted by Carl Fiadini and Company. Our show not only explores the exciting and chaotic world of the restaurant business and amazing eateries but also advocates for mental health awareness in the food industry. Our podcast offers a behind-the-scenes look at the industry. Don't miss out on upcoming episodes where we'll continue to cook up thought-provoking discussions on important topics, including mental health awareness.Be sure to visit our website for more food industry-related content, including our very own TV show called Restaurant Recipes where we feature Chefs cooking up their dishes and also The Dirty Dash Cocktail Hour; the focus is mixology and amazing drinks!Thank you for tuning in, and we'll catch you next time on the Walk-In Talk Podcast. https://www.TheWalkInTalk.comLeave a review and rating, please!

Dr. John Van Doorninck is a Pediatric Cancer Hematologist and Oncologist in Denver Colorado. He is also an active member and strong supporter of World Child Cancer, an International Organization whose main focus is to help lower income and middle income countries who do not have the wealth, resources, or expertise to help the Pediatric Cancer communities, as wealthy countries such as the United States are able to do. Dr. Van Doorninck will talk about many facets of this problem, including what solutions are already in place to hopefully bring up the survival rate in these countries to 60 percent by 2030. 

The osteosarcoma community has the power to drive change in childhood cancer research! This important OsteoBites episode features Nancy Goodman, JD, Founder & Executive Director of Kids v Cancer, as she discusses how you can help advocate for the Give Kids a Chance Act—a crucial bill aimed at expanding access to novel combination therapies for kids with cancer.The Give Kids a Chance Act is bipartisan legislation that builds on the RACE for Children Act by requiring pharmaceutical companies to evaluate promising multi-drug combinations in pediatric cancers when those drugs are being tested together in adults. Since many of the most effective cancer treatments involve drug combinations, this bill is essential to improving treatment options for children with osteosarcoma and other pediatric cancers.Be a voice for change! Learn actionable ways to support this bill and ensure kids with cancer have access to more innovative therapies.

Erin Booth's son Landon was diagnosed with Acute Lymphoblastic Leukemia when he was 5 1/2 years old in March of 2021. From that time until he was in remission beginning in 2023, Landon had gone through his treatment well enough, but then after his remission started , so did his side effects . As Landon is now nearing his 10th birthday, these myriad of side effects remain an issue for him and the hope is that they will become easier as Landon moves on and approaches his Survivorship Stage.

Laura DeKraker Lang- Ree knew nothing about Pediatric Cancer when her then 3 year old daughter Cecilia was diagnosed with Acute Lymphoblastic Leukemia in 1999. Since that time, Cecilia has recovered and gone on to lead a very successful and productive life, and Laura was able to learn so much about all facets of Pediatric Cancer that she was able to write a book called THE PARENTS CANCER HANDBOOK - What Your Oncologist Does Not Have Time To Tell You which she just published several weeks ago.   

Side Effects and After Effects from any Pediatric Cancer battle can be very difficult, especially when there are so many side effects that are concerning after being diagnosed with Pediatric Brain Cancer. That is certainly the case as we just heard from Stacie Eirich in talking about her daughter Sadie who has had more than a few difficult obstacles to overcome. The hope is that she will find the right people and programs to help Sadie through her toughest times. 

In this episode of Game Over: c*ncer, hosts Dana Nichols and Val Solomon dive into the complex and emotional tightrope of balancing hope and reality in pediatric cancer.  Joining the conversation is Dr. Claire Wakefield, a psychologist, researcher, and professor specializing in pediatric psycho-oncology. Dr. Wakefield leads the Behavioral Sciences Unit at UNSW and Sydney Children's Hospital, one of the largest pediatric cancer survivorship research groups in the world.  Together, we explore the psychological and emotional challenges families face when navigating new treatment options, clinical trials, and difficult medical decisions. Dr. Wakefield shares her insights on ethical best practices, shared decision-making, and the evolving landscape of pediatric cancer care—ensuring that families receive not only medical support but also the guidance and resources needed for their well-being.  Key Topics Covered:- The intersection of pediatric cancer treatment, psychology, and hope  - How families process and make decisions about clinical trials  - The impact of new medical technologies on patient experiences  - Supporting children and parents through the hardest moments  - The global disparities in pediatric cancer treatment and efforts to bridge the gap  This thought-provoking conversation is a must-listen for anyone passionate about advancing pediatric cancer research and supporting families in the fight.  Support the mission visit us at:  https://www.cannonballkidscancer.org to make a gift and help fund innovative research.----------------------------------Podcast Produced by Hi Hello Labs: Website: https://www.hihellolabs.com/

Tay Scheibe was diagnosed with Large Cell Lymphoma when she was 10 years old and a 5th grade student on Tuesday, September 11th, 2001. Tay had 1 more cancer fight to go through and by the time she was 12, Tay was on her way to a full recovery  Tay spent much of the next years after her recovery trying to work on her own identity and in 2012, started a Toy Drive for the benefit of Pediatric Cancer patients which turned into her now Non-Profit With Love Charity in 2016. 

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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

Erica Campbell received her degree in Accounting from William and Mary and her MBA from Duke and then, years later, with advice from her mom decided to leave the business world to try and find her true passion, which turned out to be running a non-profit which concentrated on Pediatric Cancer. Since May of 2017, Erica has found this passion by being the Executive Director of the Pinky Swear Foundation which has worked with over 3000 families who are directly dealing with a Pediatric Cancer battle. 

How do you go from saying, “Somebody should do something about that,” to actually being the one to take action? In this episode of Game Over c*ncer, we dive into that exact moment—the first, scary step toward making a difference.  Hosts Val Solomon and Dana Nichols are joined by Whitney Brittain, a former CKc board member, who shares her journey from being deeply impacted by a social media post about pediatric cancer to organizing a beloved annual event, Santa Comes to Scottsdale. What started as a way to avoid long mall lines for Santa photos turned into a powerful community fundraiser that raised thousands for pediatric cancer research. Whitney's story is proof that making an impact doesn't have to be overwhelming—it can be fun, easy, and deeply rewarding. Whether you're thinking about starting your own event or just looking for ways to contribute, this episode will inspire you to take that first step.  Tune in to hear how one small idea turned into a six-year movement and why it's okay to evolve, adapt, and pass the torch when the time is right.   Like, subscribe, and share to help spread awareness about pediatric cancer research. Your action—no matter how small—can make a world of difference.  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.Learn more about Cannonball Kids' cancer Foundation at www.cannonballkidscancer.org. Like, share, and subscribe to stay informed and inspired! Together, we can make a difference.Connect with Dana: https://www.linkedin.com/in/danaknichols/Connect with Val: https://www.linkedin.com/in/valerie-solomon-516b50b8/Upcoming Ckc Events: https://cannonballkidscancer.org/category/make-an-impact/events/

When Rene Michael's 6 year old daughter Alicia was complaining of a backache in  December of 2001, little did she know that her backache would lead to a diagnosis of a Peripheral Nueroectodermal Tumor which is a Bone Cancer closely related to Ewings Sarcoma. During her inpatient treatment, her mom Rene tells the story of Alicia deciding to find a way to donate money to the Pediatric Cancer patients and their families who were on her oncology floor. Thus, the Honeysuckle Foundation was born, inspirationally started by Alicia and officially started by Rene who has been the director of this foundation since its inception in late 2002. This foundation focuses on the all important psychosocial aspects of Pediatric Cancer. Today Alicia is approaching her 30th birthday, is married, and living her best life possible.

In this episode, we're joined by Dr. Daniel Indelicato and Dr. Rohan Deraniyagala, two distinguished experts whose work is transforming the landscape of pediatric oncology. With decades of combined experience and groundbreaking research, Danny and Rohan offer invaluable insights into the world of proton therapy. Listen as they unpack the distinct advantages of proton therapy, shedding light on why this method is especially beneficial for children by minimizing harmful side effects and enhancing quality of life post-treatment.The views expressed in this podcast are those of the interviewees. By listening to this, you agree not to use this podcast as medical advice to treat any medical condition in either yourself or others, including but not limited to patients that you are treating.  Consult your own physician for any medical issues that you may be having.  This entire disclaimer also applies to any guests or contributors to the podcast.  Under no circumstances shall Ion Beam Applications SA (IBA), any guests or contributors to the podcast, or any employees, associates, or affiliates of IBA be responsible for damages arising from use of the podcast.

In this deeply moving episode of Warriors Unmasked, Chuck Thuss welcomes Laura DeKraker Lang-Ree, a mother, author, and fierce advocate for families navigating pediatric cancer. Laura shares her heart-wrenching yet empowering journey through her daughter Cecilia's leukemia diagnosis—a journey that sparked her mission to create resources and support for parents facing the unimaginable. Laura opens up about the shock and fear that consumed her when her three-year-old daughter was diagnosed with cancer. She recalls the early days of scouring the internet for guidance, only to find a lack of practical, emotional, and logistical resources for parents walking this difficult path. Determined to change that, Laura took her own experiences and turned them into something meaningful: her book, The Cancer Parent's Handbook: What Your Oncologist Doesn't Have Time to Tell You. Throughout this episode, Laura and Chuck discuss the emotional rollercoaster of being a cancer parent, the often-overlooked mental health challenges that come with the diagnosis, and the importance of building a strong support system. Laura's insights are both practical and heartfelt, offering listeners a candid look into what it's like to parent through a cancer diagnosis while continuing to nurture the rest of the family. Key Takeaways from Laura's Story: The Importance of Advocacy: Laura stresses how crucial it is for parents to become informed advocates for their children, even when the medical world feels overwhelming. Managing Emotions Amidst the Chaos: She shares strategies that helped her manage fear, grief, and anxiety during her daughter's treatments, including mindfulness, journaling, and leaning into her faith. The Power of a Support System: Laura talks about how she learned to accept help from others and how critical it was for her family's well-being. Turning Pain Into Purpose What started as a personal mission to survive the emotional toll of her daughter's diagnosis turned into a broader mission to help others. Laura created She Is You, an online community where parents can find support, share their stories, and access the tools they need to cope with pediatric cancer. Her book is packed with real-world advice, from handling medical jargon to advocating for your child's needs. Laura also reflects on the incredible strength she discovered within herself and within the pediatric cancer community. Her message is clear: no parent should walk this journey alone. Through her work, she hopes to ease the burden for others by providing the guidance she wished she had during those first terrifying days. Faith, Resilience, and Hope At the core of Laura's journey is her unwavering faith. She credits her relationship with God for giving her the strength to persevere through the darkest moments. Her story serves as a reminder that even in the face of unimaginable hardship, hope and healing are possible. Listen to the full episode to hear Laura's raw and inspiring story, and learn more about the resources available to parents navigating a child's cancer diagnosis. Stay Connected with Warriors Unmasked For more powerful stories of resilience and courage, visit Warriors Unmasked or book a coaching call with Chuck directly.   GUEST LINKS: cancerparentshandbook.com Instagram at @‌laura_dekraker_langree LINKS: www.thecompassionateconnection.com www.warriorsunmasked.com  Join Chuck's Text Community: 251-418-7966 Episode Minute By Minute: 00:00 Introduction and Welcome   03:12 Laura's World Shattered: Cecilia's Cancer Diagnosis   07:25 The Search for Guidance and the Lack of Resources   10:58 Becoming an “Expert” in Pediatric Cancer   15:14 The Emotional Impact of a Child's Diagnosis on the Entire Family   19:36 Strategies for Coping with Overwhelm and Fear   23:45 Creating The Cancer Parent's Handbook: A Guide for Parents   28:30 The Role of Faith and Community in Laura's Healing Journey   33:15 How to Advocate Effectively for Your Child's Medical Care   38:52 Laura's Tips for Maintaining Mental Health During Crisis   44:07 How the *She Is You* Community Offers Support to Cancer Parents   49:30 Words of Encouragement for Parents Facing a New Diagnosis   52:48 Final Thoughts: Finding Purpose Through Pain   55:11 How to Connect with Laura and Get Her Book 

Nancy and Richard Whipple's son Alexander spent 250 days as an inpatient at Tufts Floating Hospital for Children beginning in 2010 as a result of his Neuroblastoma diagnosis in March of 2010 when he was 8 months old.  Alexander battled for 13 months with his form of Pediatric Cancer and 2 of his stays lasted for 46 and 38 days respectively. Alexander passed away on April 1st of 2011, after a 16 hour surgery which did not work out as planned. 

Joining me today are Shawn and Sandy Smith, who I had the opportunity to meet when they attended our first While We're Waiting Weekend in Michigan a couple years ago.  Their faith has been tested in ways most of us can hardly imagine—first, when Sandy was diagnosed with breast cancer, and then, just days later, when their six-year-old son Andrew was diagnosed with DIPG, an aggressive and terminal form of brain cancer. Through every challenge, every difficult conversation, and every painful moment, Shawn and Sandy clung to their faith, trusting that God had a purpose even in their suffering. In this episode, they share how they walked through this unimaginable season with hope, how Andrew's childlike faith and joy reflected the goodness of God, and how they found peace in His promises—even when healing on this earth was not part of His plan. Their story is one of deep sorrow but also incredible trust in God's sovereignty—a story of holding fast to His Word, even when the path ahead seemed impossible. If you've ever wrestled with faith in the face of suffering, this conversation will remind you that God has not forgotten you.  Be sure and come back next week to hear more of their story!  I would love to hear your thoughts on the show. Click here to send me a message!** IMPORTANT** - All views expressed by guests on this podcast are theirs alone, and may not represent the Statement of Faith and Statement of Beliefs of the While We're Waiting ministry. We'd love for you to connect with us here at While We're Waiting! Click HERE to visit our website and learn about our free While We're Waiting Weekends for bereaved parentsClick HERE to learn more about our network of While We're Waiting support groups all across the country. Click HERE to subscribe to our YouTube channelClick HERE to follow our public Facebook pageClick HERE to follow us on Instagram Click HERE to follow us on Twitter Click HERE to make a tax-deductible donation to the While We're Waiting ministryContact Jill by email at: jill@whilewerewaiting.org

Welcome to the Change Life Destiny podcast series! In this episode, host Stephanie interviews Season Johnson, a functional nutritional therapy practitioner and a mother who shares her compelling journey through the healthcare system. Season talks about adopting her daughter, prioritizing natural health approaches, and later facing the harrowing diagnosis of her son's leukemia. Despite initial resistance, she embraced conventional treatments while integrating holistic methods. Together, they discuss the importance of advocacy, nutrition, and detoxification in pediatric cancer treatment. Season also shares inspiring stories from her nonprofit, and details her goals for impacting families affected by cancer. Tune in to explore how combining allopathic and functional medicine can foster hope and healing.00:00 Welcome to the Change Life Destiny Podcast00:44 Introducing Our Special Guest: Ms. Season Johnson01:34 Season's Journey into Health and Wellness04:19 A Mother's Battle: Facing Childhood Leukemia08:32 Advocating for Your Child's Health17:14 Supporting Families Through Non-Profit Initiatives20:50 Success Stories and Future Aspirations24:38 Envisioning the Future of Healthcare30:51 Closing Remarks and Final ThoughtsGet in touch with Season:WebsiteInstagramLinkedInChange Life & Destiny is a movement to excite, engage, and educate communities about the importance of taking control of our health and wellness. We highlight the latest and greatest technologies that can restore health, prevent disease, and promote wellness, as well as practitioners who are using cutting-edge technology to help patients take control of their health.Learn more about us here:Website: https://www.changelifedestiny.com/Instagram: https://www.instagram.com/changinglifedestiny/LinkedIn: https://www.linkedin.com/company/changelifedestiny/YouTube: https://www.youtube.com/@changelifedestinyFacebook: https://www.facebook.com/changelifedestinyWant to learn more? Visit our website or follow us on Instagram, Facebook Youtube, and LinkedIn.Want to learn more? Visit our website or follow us on Instagram, Facebook Youtube, and LinkedIn.

In this episode, we dive deep into the inspiring journey of Season Johnson. Learn how Season transitioned from being a functional nutritional therapy practitioner to becoming a beacon of hope for families dealing with pediatric cancer. She shares her personal story of her son Kicker's diagnosis with acute lymphoblastic leukemia, the challenges they faced, and the holistic approaches she adopted for his healing. Season discusses her five pillars of healing, the significance of a balanced emotional and nutritional environment, and the powerful role of community and support. Tune in for a heartwarming and educational conversation that underscores the importance of combining traditional and natural treatments in the fight against cancer. Connect with Season: Website: www.seasonjohnson.com Thrive Formula Programs: www.yourthriveformula.com Nonprofit: www.kickcancermovement.org Instagram: https://www.instagram.com/seasonjohnson/ Facebook: https://www.facebook.com/seasonmjohnson Connect with Dr. Nasha & the Metabolic Terrain Institute of Health

Trista Temimi's daughter Valeria was born on September 11th of 2023 and immediately began having health issues. It took until January of 2024 to finally receive her diagnosis of Neuroblastoma. Since that time, Valeria has been battling this pediatric cancer and today, December 16th, she is undergoing scans to see how she is doing, with the hope being that she is at least stable and hopefully the news will be even better than that for this 15 month old little girl. 

Camp Rainbow Gold was started back in the 1980's, with the goal to welcome a small amount of Pediatric Cancer patients for a week of fun and being away from their cancer issues for a short time. Now, some 40 years later, this camp has grown substantially to over 400 attendees which include not only pediatric cancer patients , but their parents, siblings, and survivors to enjoy many activities during the late spring, summer, and fall months. Chief Executive Officer Elizabeth Lizberg discusses this camp, which in reality is a 365 day a year concern for Elizabeth and her staff. 

In this episode Dr. Adewuya is joined by Dr. Heike Daldrup-Link, a Professor of Radiology at Stanford University. Our conversation explores the fascinating intersection of nanotechnology and clinical medicine, particularly its transformative role in medical imaging and its significance for pediatric oncology. We discuss how nanoparticles function within the body for imaging purposes, highlighting their advantages over traditional imaging agents. Our discussion covers the advancements in precision medicine in cancer imaging, including the reduced side effects associated with safer imaging modalities. Additionally, we will examine the ethical considerations of utilizing nanoparticles in children, explore ongoing clinical trials, and discuss potential long-term health effects on pediatric patients. Read Transcript CME Information: https://stanford.cloud-cme.com/medcastepisode94 Claim CE: https://stanford.cloud-cme.com/Form.aspx?FormID=3146

S5 E6 Tommy's Place - Creating a Healing Space to Cope with Pediatric CancerIn this episode, we interview Tim O'Connell, founder of the nonprofit “Tommy's Place” on Cape Cod, Massachusetts, which provides a week-long dream vacation home free of charge for families with children undergoing cancer treatment. Tommy's Place aims to offer a healing space to have fun and bond with loved ones on vacation despite all the life-altering challenges and burdens of pediatric cancer that affect not only the child undergoing treatment but also their families, friends, and support system. Tim shares the years-long journey of actualizing his vision for Tommy's Place, including his persistence through the roadblocks, formulation of a system that works to sustain his vision in the long term, and the importance of community members coming together to support these families through donations and volunteer work. He shares the heartwarming experience that families experience during their vacation stay and the deep and meaningful impact Tommy's Place has had on donors and volunteers. We hope this episode inspires the listener to appreciate how people can help other people in creative ways. Tommy's Place Foundation, Inc., aka "Tommy's Place", is a Massachusetts-based nonprofit corporation that owns and operates year-round magical vacation homes for kids fighting cancer in Falmouth, MA, and Centerville, MA, on Cape Cod. One family at a time, along with their extended family and friends, visits one of our two 10+ bedroom homes for one week, free of charge, dream vacation to relax, make memories, and most importantly, have FUN! Tommy's Place is open to kids aged 3-17 who are actively in treatment and living permanently and full time in New England. Tommy's Place serves 104 families yearly at our two magical vacation homes on Cape Cod in Falmouth and Centerville. Tommy's Place receives guest referrals from 10 major childhood cancer hospitals throughout New England. The first Tommy's in Falmouth officially opened to guests in July of 2021 and has been at 100% occupancy ever since. (To see more frequent updates of Tommy's Place stories and photos, please visit us on Facebook, Instagram and Twitter @tommysplacekids)Tommy's Place Foundation, Inc. is a registered 501 (c)(3), non-profit organization. All donations are tax-deductible to the extent allowed by law. Tommy's Place in Falmouth501C3 EIN: 83-1069410Be curious. Be Open. Be well.The ReidConnect-Ed Podcast is hosted by Alexis Reid and Dr. Gerald Reid, produced by Cyber Sound Studios, and original music is written and recorded by Gerald Reid.*Please note that different practitioners may have different opinions- this is our perspective and is intended to educate you on what may be possible.Follow us on Instagram @ReidConnectEdPodcast and Twitter @ReidConnectEdShow notes & Transcripts: https://reidconnect.com/reid-connect-ed-podcast

In this episode of Twenty Seven Degrees, hosts Dr. Christopher Joncas, a primary care physician, and Nancy Medeiros, an RN with an MBA, are joined by the distinguished Dr. Alvin Marcovici, a renowned neurosurgeon educated at Yale. Dr. Marcovici shares his expertise on brain tumors, shedding light on the latest research, treatment options, and the challenges patients face when diagnosed with these complex conditions. From the science behind brain tumor formation to innovative surgical approaches, this conversation offers valuable insights for both healthcare professionals and the general public. Whether you're a medical professional looking to deepen your knowledge or someone navigating a personal journey with brain tumors, this episode provides essential information on understanding, diagnosing, and treating this serious condition. Tune in for an eye-opening discussion with one of the leading experts in the field of neurosurgery.

Not only do Becca Ingersoll's twin boys Lincoln and Logan have special needs, Lincoln was diagnosed with B Cell Acute Lymphoblastic Leukemia when he was 3 years old in January of 2020. Lincoln also has Cerebral Palsy, Hydrocephalus, and Autism. Becca will talk about the very difficult and tricky road that she and her husband Josh have been navigating for the past 7 years, and will also discuss  her work as an activist and advocate in the cause of Pediatric Cancer. 

On October 24th of 2011 Reilly Cardella's best friend Kassie passed away from Leukemia when they were both 13 years old.  Reilly will discuss the relationship that they had and the inspiration that Reilly developed to become a very strong voice in the cause of Pediatric Cancer. When Reilly was 20 years old she started her non-profit Love For Lady Bug which was named after Kassie, then became a Board Member and Vice President of the Glimmer of Hope Foundation , and in 2023 was voted Miss Apopka, which is a city of 55,000 located near Orlando Florida, and recognized her for all of the advocacy work that Reilly has been involved with. Her advocacy work for the Pediatric Cancer community will undoubtedly continue for many years to come. 

On Thursday's show: A dust-up between Houston's mayor and controller seems to have escalated in recent days. We walk through what's going on with News 88.7 reporter Dominic Anthony Walsh.Also this hour: We visit an event raising funds for cancer research while celebrating children who are combatting cancer.Then, this month's installment of The Bigger Picture examines the new film Saturday Night, about the behind-the-scenes chaos leading up to the first episode of Saturday Night Live back in 1975. Joshua Zinn discusses the film and the show's affect on live sketch and improv comedy in the Houston area.And classical music meets hip hop tonight as the Energy Corridor of Houston Orchestra teams up with Houston's Fly Dance Company and Outspoken Bean.

Makenna Thomas had a back that was painful, a right arm that turned numb, and  fingers that she could not move, when she was diagnosed with Meningioma of the Spine in early 2018 at the age of 14. Makenna will talk about her battle both physically and even more so emotionally during that period and even beyond, and will also talk about her very successful recovery and life in which she is a senior at UCLA, is the President of the American Cancer Society on campus, oversees the Relay For Life Team at UCLA which is the leading fundraising college in the country for that event, and is studying neuroscience. 

If you only listen to one show this year make it this one! With Producer Sean leaving early for INTERGEO, DD was joined this week by Peta Cox for this heartfelt and inspiring story. Our guest was Claire Masikewich. Claire is a seasoned marketing and communications professional at GeoVerra with a passion for advocacy that transcends her corporate career.  In May 2023, Claire's career paused when her five-year-old daughter was diagnosed with stage 4 neuroblastoma, a rare and aggressive pediatric cancer. This life-altering event ignited a new purpose: using her marketing expertise to raise awareness and advocate for more research in the severely underfunded area of pediatric cancer. Claire's story is not only one of professional success but also of personal resilience. She has faced and overcome challenges with anxiety and depression, which once felt overwhelming. Yet, with her daughter's diagnosis, Claire channeled her strength and transformed her pain into purpose, becoming a fierce advocate while navigating her daughter's treatment. By August 2024, just before Childhood Cancer Awareness Month, the Strong Like Sloane Foundation—named in honor of her daughter—became an official charitable organization in Alberta. Since launching fundraising efforts in October 2023, the foundation has raised over $155,000 for pediatric cancer research at Calgary's Riddell Centre for Cancer Immunotherapy.  Claire is a testament to the power of resilience, personal growth, and the unwavering love of a parent. Her life's journey is an inspiration to all who face personal challenges and a reminder that, with determination and support, we can find strength and light even in the most difficult of circumstances. "You don't know what you're capable of until you're asked to be capable." Music by Zach Bryan!

Matt Kopkin, embraced the challenge of becoming a full-time grants administrator at Cannonball Kids cancer Foundation. This episode uncovers the crucial role of grant funding in pediatric cancer research, shedding light on how CKc bridges the gap in government resources to fuel groundbreaking clinical trials and support young investigators. Matt opens up about his transition from a temporary position to a pivotal role within the organization, sharing personal stories and insights into the dynamic, mission-driven environment at CKc.We invite you to experience the vibrant team spirit at CKc, where unique skills and passions converge to make a significant impact. From research to fundraising, each team member plays an essential role in advancing the mission. Our conversation highlights the camaraderie and shared enthusiasm for the cause, peppered with humorous anecdotes and reflections on the challenges of stepping out of comfort zones, especially when engaging with the community and podcasting. Celebrate the achievements in streamlining grant processes and look forward to future collaborations and growth.Join us as we explore the intricacies of the grants process with Matt, who shares his growth and adaptation to the demands of pediatric cancer research funding. He discusses the importance of simplifying grant applications and providing constructive feedback, while emphasizing the value of maintaining open communication with researchers. This episode offers a glimpse into the expanding landscape of pediatric research initiatives nationwide, and the integral role of CKc's outreach efforts. As Matt transitions to a full-time role, we anticipate a busy and rewarding grant application period, underscoring the foundation's unwavering dedication to enhancing the survivorship and quality of life for children battling cancer.For more information or assistance with grants at Ckc: grants@canonnballkidscancer.orgConnect with Dana: https://www.linkedin.com/in/danaknichols/Connect with Val: https://www.linkedin.com/in/valerie-solomon-516b50b8/Upcoming Ckc Events: https://cannonballkidscancer.org/category/make-an-impact/events/Learn more about the Cannonball Kids cancer Foundation: https://cannonballkidscancer.org/GameOverCancer. #PediatricCancer  #CannonballKidsCancer  #CancerResearch #ChildhoodCancerAwareness

Michelle Zenie's son Cole, now 26 years old , married, and a High School Biology Teacher was diagnosed with Acute Lymphoblastic Leukemia in May of 2001. Michelle was also a teacher but decided after Cole's recovery to get involved as an activist and advocate in the cause of Pediatric Cancer. This led to her becoming the Executive Director of the Pediatric Cancer Foundation of Lehigh Valley in 2014, a position that Michelle has held for the past 10 years. This foundation focuses on whatever it can do to help individual families get through their pediatric cancer struggles  during treatment , after treatment, and if there is an unfortunate bereavement situation

In this episode, we delve into a family's journey through pediatric cancer, highlighting how they supported their child through unconventional means alongside traditional treatments. Despite the financial strain and the rigorous treatment schedule, their son thrived, inspiring his parents to share their approach with other families. Now, ten years later, their son enjoys a healthy, active life, and they have helped thousands of families navigate similar challenges. Dr. Charles Penick, an MD who has shifted his perspective on medicine, discusses the importance of holistic care and critical thinking in treating cancer. We also hear from Melanie, a program member, who shares her experience implementing nutrition and other supportive therapies for her son. This episode emphasizes the power of community, the importance of supporting the body's natural healing processes, and the emotional aspects of a cancer journey. Join us as we explore creative strategies to help children thrive through cancer treatment and beyond.    Links: ● Free Weekly Info Session: https://yourthriveformula.com/weekly-sessions ● LumeBox: https://bit.ly/seasonjohnsonlume Use code seasonjohnson for $260 off ● Protocol Guide: https://yourthriveformula.com/free-protocol-guide  

After noticeably limping during a soccer game in 2019, Maggie Spada's daughter Lucy was diagnosed with Ewings Sarcoma at the age of 9. After going through a very difficult treatment protocol, Lucy is now 5 years removed from this diagnosis and is doing very well. Maggie will talk about Lucy and will also talk about her Little Warriors Foundation, which she and her husband Piero started when they learned about how little money the Federal Government was contributing to Pediatric Cancer, and also learning about the treatments that Lucy and other Ewings Sarcoma patients have to go through, which has not changed in over 40 years.

In today's episode of Camp Chaos, we give you Part 2 of one of the most IMPORTANT episodes we will ever share.  Joanna continues to share her journey of heartbreaking loss and how she even began her grief journey.  She takes us through the different stages of grief, how Will's loss affected her marriage, and how she has used various tools to help put one foot in front of the other.  She shares with us her new life mission in Will's honor, to share and fundraise for Pediatric Cancer Research through the Will Strong Foundation.  She talks us through the many ways that Will is still so present in their lives today.  We can't thank Joanna enough for bravely sharing Will's story.  Please consider donating in Will's Honor to the Pediatric Cancer Research Foundation. Join Joanna & Will in their fight against Pediatric Cancer www.willstrongteam.com @teamwillstrong Sponsors forhers.com/chaos - to start your free online visit and personalized treatment options www.bioptimizers.com/campchaos Code: CAMPCHAOS - for 10% off at checkout Follow us on Instagram: Camp Chaos Taylor Kyndra Learn more about your ad choices. Visit megaphone.fm/adchoices

Today's episode of Camp Chaos is one of the most IMPORTANT episodes we will ever share. We sit down with our friend, Joanna Irwin, as she shares the heartbreakingly beautiful story of her son Will and his journey with pediatric cancer. She takes us through the early days of her struggle to get pregnant, the joy of her pregnancy with Will, and how blissful the first few months of his life were. She walks us through the scary days of first hearing the word 'cancer' and the torturous journey she, Will, her husband, Mike, and their family went through in the following months. Joanna doesn't hold anything back and truly pulls back the curtain on what life with a child diagnosed with pediatric cancer can look like. Joanna is the strongest mother we know and we are so honored that she trusted us to share Will's story. Donate to Pediatric Cancer Research Foundation in Will's Honor: www.willstrongteam.com  Sponsors: forhers.com/chaos - to start your free online visit and personalized treatment options www.bioptimizers.com/campchaos Code: CAMPCHAOS - for 10% off at checkout Follow us on Instagram: Camp Chaos Taylor Kyndra Learn more about your ad choices. Visit megaphone.fm/adchoices

Could a simple change in diet hold the key to transforming pediatric cancer care? Today, we have a truly special guest, Season Johnson, a Functional Nutritional Therapy Practitioner dedicated to working with pediatric patients. I discovered Season on Instagram and was immediately drawn to her compelling story and expertise.  Season's own son was diagnosed with cancer at a young age, and her family's journey through this experience has shaped her mission to help others navigate the complexities of cancer treatment and nutrition.  In today's episode, we dive into Season's unique approach to nutritional therapy for children battling cancer. We'll look at rising pediatric cancer rates and how environmental factors like food toxins and EMFs might play a role. Season also shares practical tips for parents, including the benefits of sunlight, outdoor play, and a balanced diet to create a healthier environment for their children. Hit play and get inspired—because fighting cancer just got a whole lot smarter! In this episode: Season shares her son's diagnosis with acute lymphoblastic leukemia. Season talks about her initial resistance to traditional medicine and how she balanced it with alternative treatments to support her son's health.  Season opens up about the emotional rollercoaster her family experienced — from sleepless nights in the hospital to the constant worry about her son's health.  “It was a choice I had to make: am I going to let this define me, cross my arms, and sit back as a victim of our circumstances, or am I going to step up, realize I have a role to play, and not be passive?” - Season Studies show that environmental factors are a major contributor to cancer cases, including in kids, making up about 95-97% of cases. While genetics play a role in how we deal with toxins, the increased exposure to pollutants like electromagnetic fields from tech and various chemicals is a big concern. Simple steps that parents can take now to create an environment for their kids where cancer cannot survive in. How morning light affects our bodies' natural healing rhythms. Tips to manage nutrition for picky eaters during cancer treatment. How activities like bouncing on a trampoline help with detoxification and waste removal in the body. Season explains that while everyone produces cancer cells daily, whether these cells develop into tumors depends on our immune system and genetic predispositions. The good news is that 99% of these genetic variations can be influenced by our nutrition and detox efforts. Season shares some key practices to ensure our detox pathways are functioning properly, including staying hydrated, regular bowel movements, and using a sauna. Key nutritional benefits of organ meats for overall health and cancer support. Creative ways to incorporate organ meat into your family's diet, especially for kids.  What does "chemo-protective" mean in the context of foods and their effects on the body during cancer treatment? How often should you replace the things you do to effectively reduce toxins and improve overall health? How chlorella and chlorophyll protect us against radiation damage and support detoxification.  “God has given me this incredible ability, and it's deeply rewarding. The pediatric cancer field may not be lucrative, but it offers the profound opportunity to give families hope. Having walked this path myself years ago, it is an honor to turn that experience into a source of hope and support for others.” - Season Season highlights the vital role of community during cancer treatment. About Season Johnson Season Johnson is a Functional Nutritional Therapy Practitioner, Founder of The KICKcancER Movement, and a cancer mom who transitioned from having one child with cancer to supporting thousands worldwide. After her son's cancer diagnosis at age two and enduring a 3.5-year battle with daily chemotherapy and numerous surgeries, she developed an unwavering mission to help others thrive through cancer using real food, supplementation, detoxification, and environmental adjustments. She has received the Weston A. Price Foundation Activist Award and the Children's Health Advocate Award from the Nutritional Therapy Association for her work with pediatric cancer. In 2019, she earned the doTERRA Elevation Award for her commitment to aiding families through cancer via her non-profit, The KICKcancER Movement. Season has also served as the Health and Wellness Expert for the Oscars and collaborated with the San Francisco 49ers, Atlanta Braves, and Washington Nationals to integrate natural solutions into their healing protocols. Through private nutrition coaching, online programs, speaking engagements, and a podcast, she continues to educate and empower others to use real food and healthy living principles to achieve vibrant health and thrive through cancer. Links and Resources Terrasoul Superfoods Sally Fallon's Nourishing Traditions Cookbook Connect with Season Johnson Website Instagram Facebook LinkedIn   --- Wave Block DID YOU KNOW: Kids' skulls absorb 10x more radiation than adult ones? And that nurseries and Kindergarten classrooms in Europe and China have banned Wifi to protect kids.  Technology is NOT GOING AWAY, so let's figure out how to manage the risk of using it. I always have this product on my headphones! I'm not too fond of the idea of radiation going into my head, and this product from Wave Block has been tested, and it shows that it can reduce the amount of radiation by 90+%  Use the code "ENOS10" for your 10% discount. --- This episode is sponsored in part by ButcherBox. It's getting colder so no more salads for me! It's almost fall, so I'm cutting back on salads and cooking roasted and savory foods. Did you know that eating warmer foods naturally warms your body? This is why I can't eat salads in December! My friends at ButcherBox have a mind-blowing deal for this transition from August to September; choose which high-quality, lean protein you'll get for free in every order for a year—wild-caught salmon, organic chicken breasts, or grass-fed ground beef. Plus, get $30 off your first order with code "enos". That's up to $404 in savings for the year! Click Here to Purchase   This podcast is for informational purposes only and none of the information should be construed as medical advice. Listeners should seek guidance from their own medical team before making any medical or lifestyle changes.

A child's cancer diagnosis can be a family's darkest moment, but it can also unite a community. For Mollie Darby, her son's leukemia diagnosis showed her both the overwhelming challenges families face and the incredible power of community support. In this episode, she talks about her family's emotional journey that inspired the creation of JUST TRYAN IT, an organization that provides financial assistance to families with children battling cancer.-Truman Charities hosts an annual family fun event to benefit JUST TRYAN IT, and we want to see you there this year! Join us on September 15th at Knights of Columbus in Bethesda for a family-friendly event, complete with a pizza truck, moon bounce, live music and more.-You'll also hear from Jamie's sons, Zack and Dominic, about their past experience in JUST TRYAN IT's kids triathlon, and get a preview of what you can expect from this year's family fun event. Tune in to learn more about the event and how you can help make a difference! Support Dominic and his team for the JUST TRYAN IT fundraiser:https://donate.justtryanit.com/fundraiser/5524169 Register for the Truman Charities Family Fun Event:www.trumancharities.comConnect with Jamie at Truman Charities:FacebookInstagramLinkedInWebsiteYouTubeEmail: info@trumancharities.comThis episode was post produced by Podcast Boutique https://podcastboutique.com/

Teri Gaberman's son Aaron was diagnosed with a rare form of Pediatric Brain Cancer when he was 10 years old in 2005. The next year Aaron contacted former New York Yankee great Bobby Murcer who had been diagnosed with a Glioma type of Brain Cancer at the end of 2006 and that started an incredible friendship which lasted until Bobby passed away on July 8th of 2008. Teri will talk about her son's amazing life and her Berni and Mercer non- profit which has helped and is helping so many in the Pediatric Cancer community.

A special initiative and data registry at the National Cancer Institute is helping researchers understand and treat rare childhood cancers. Dr. Mary Frances Wedekind, a pediatric oncologist and assistant research physician with the Pediatric Oncology Branch at NCI, explains how the Childhood Cancer Data Initiative follows children, teens and young adults for many years to collect key information about their cancer diagnosis, imaging and treatments. She added that the initiative along with the Rare Cancer Data Registry are critical to helping researchers access and analyze the clinical and genomic data that could potentially lead to more effective targeted therapies and new drug developments that could  improve the standards of care for young patients.