Podcasts about raise awareness

Listen and subscribe to Money Making Conversations on iHeartRadio, Apple Podcasts, Spotify, www.moneymakingconversations.com/subscribe/ or wherever you listen to podcasts. New Money Making Conversations episodes drop daily. I want to alert you, so you don’t miss out on expert analysis and insider perspectives from my guests who provide tips that can help you uplift the community, improve your financial planning, motivation, or advice on how to be a successful entrepreneur. Keep winning! Two-time Emmy and Three-time NAACP Image Award-winning, television Executive Producer Rushion McDonald interviewed Dr. Christina Dukes Brown.

Listen and subscribe to Money Making Conversations on iHeartRadio, Apple Podcasts, Spotify, www.moneymakingconversations.com/subscribe/ or wherever you listen to podcasts. New Money Making Conversations episodes drop daily. I want to alert you, so you don’t miss out on expert analysis and insider perspectives from my guests who provide tips that can help you uplift the community, improve your financial planning, motivation, or advice on how to be a successful entrepreneur. Keep winning! Two-time Emmy and Three-time NAACP Image Award-winning, television Executive Producer Rushion McDonald interviewed Dr. Christina Dukes Brown.

Listen and subscribe to Money Making Conversations on iHeartRadio, Apple Podcasts, Spotify, www.moneymakingconversations.com/subscribe/ or wherever you listen to podcasts. New Money Making Conversations episodes drop daily. I want to alert you, so you don’t miss out on expert analysis and insider perspectives from my guests who provide tips that can help you uplift the community, improve your financial planning, motivation, or advice on how to be a successful entrepreneur. Keep winning! Two-time Emmy and Three-time NAACP Image Award-winning, television Executive Producer Rushion McDonald interviewed Dr. Christina Dukes Brown.

Listen and subscribe to Money Making Conversations on iHeartRadio, Apple Podcasts, Spotify, www.moneymakingconversations.com/subscribe/ or wherever you listen to podcasts. New Money Making Conversations episodes drop daily. I want to alert you, so you don’t miss out on expert analysis and insider perspectives from my guests who provide tips that can help you uplift the community, improve your financial planning, motivation, or advice on how to be a successful entrepreneur. Keep winning! Two-time Emmy and Three-time NAACP Image Award-winning, television Executive Producer Rushion McDonald interviewed Dr. Christina Dukes Brown.

"...this old man was one of the most useful citizens of the world in his humble way. He has made a greater contribution to our civilization than we realize. He has left a place that never can be filled. Farewell, dear old eccentric heart, your labor has been a labor of love, and generations, yet unborn, will rise up and call you blessed..."Let's listen to the tribute from Sam Houston around 1847 upon Johnny Appleseed's death.Reflection questions:What approach are you taking: scattering seeds or planting seeds with intentional outcomes in mind?If you are in the pre-campaign readiness stage, have you considered the more effective ways to raise awareness in your community and brought in community leaders and potential donors to help you determine and implement those ways?Reflection on quote:Capital campaigns are like a riding a wild stallion without a saddle and one key to success is developing discipline. This series unpacks those disciplines. We've discussed how understanding our beliefs around money can assist us in creating the necessary disciplines around asking for donations. We've discussed how indecision and procrastination can steal opportunities and the importance of prioritizing tasks.  In this episode, we'll discuss the discipline necessary to successfully raising awareness for our capital campaigns through the life and work of John Chapman; otherwise known as Johnny Appleseed.  Like many, I pictured Johnny Appleseed as wandering aimlessly around the countryside, randomly sprinkling seeds that grew into trees and, against all odds, orchards.  But that wasn't the case at all.Johnny Appleseed had a purpose for apple trees. He believed that apple trees were important to cultivate as cider to be an alternative to unsafe drinking water.  He then planned the process for planting seeds to grow into trees near villages and towns in Ohio.  His labor of love had an intentional process with both immediate and generational impacts.  In the same way, during a capital campaign, we too must be intentional in how we are raising awareness. We do not simply scatter seeds and hope our communities are paying enough attention.  Instead, we consider the audiences, the people, who need to hear about our vision first.  Then, we determine how we engage those community leaders, connectors, and potential donors in the planning process for the campaign.  Further, we are intentional in what information we share with the community, information that creates confidence and excitement in the goal, and when we share that information. When we are disciplined in raising awareness, those seeds will have a greater contribution to the success of the capital campaign and a greater contribution to the small towns and rural communities we serve.      What do you think? Send me a text. To explore small town capital campaign coaching deeper and to schedule an free explore coaching call, visit ServingNonprofits.com.Music credit: Woeisuhmebop

CHAPTERS: 00:00 Introduction to Anton Newtonboom 01:11 Anton's Military Background 04:26 Anton's Role in the Military 06:17 Mental Health in the Military 08:10 Coming Down from the Adrenaline 09:47 Realizing Something Wasn't Right 11:40 Negative Self-Talk and Identity 15:24 The Sign on the Hilltop 18:00 Seeking Help and Mental Health Tools 19:08 Walking Barefoot to Raise Awareness 20:44 Walking to Everest Base Camp 23:27 Walking Barefoot Across the United States 30:04 Aligning with the Movember Movement 32:11 The Importance of Mental Health Awareness 36:30 Encounters with Wildlife 41:34 Walking Across the United States 45:18 Projected Time to Finish the Journey 46:22 Self-Care Routine and Foot Care 47:48 Walking with Anton 49:53 Supporting Movember 50:52 Greatest Piece of Advice 52:19 Finding Purpose and Gratitude 54:38 Closing Remarks

What does it look like to raise awareness from the top of the world? On the latest episode of BloodStream, Maia Meier joins our beloved hosts, Patrick and Amy, to talk about her mission to climb the Seven Summits through Project Elevate Her and bring visibility to women and girls living with bleeding disorders. From high-altitude expeditions to the everyday realities of advocacy, the conversation explores what it means to take up space in places where women with bleeding disorders have too often gone unseen. Listen now and subscribe to BloodStream Podcast wherever you get your shows.   Show Notes: Project Elevate Her   Presenting Sponsor: Takeda, visit bleedingdisorders.com to learn more. Subscribe: The BloodStream Podcast   Connect with BloodStream Media: BloodStreamMedia.com BloodStream on Facebook  BloodStream on X/Twitter  BloodStream on Instagram BloodStream on LinkedIn BloodStream on TikTok  

On this week's Headlines edition of the podcast, we discuss the latest on the Trump administration's A Home for Every Child initiative and some child welfare bills moving in Congress. We also discuss The Imprint's recent reporting on parental relinquishments, a law in Oklahoma prompted by a child fentanyl death, foster youth and chronic absenteeism, and more. Thanks to iFoster for sponsoring this episode.Reading RoomA Home for Every Child Innovation Challengehttps://acf.gov/home-every-child-innovation-challengeThe Imprint's Who Cares ProjectFosterCareCapacity.comNew Focus on Psychotropic Medication Use in Foster Care Declared at RFK ‘Overmedicalization' Summithttps://imprintnews.org/youth-services-insider/top-federal-child-welfare-official-focused-on-psychotropics/274408Trump's Planned Spending on Child Welfare and Youth Justicehttps://imprintnews.org/youth-services-insider/trumps-budget-plan-on-child-welfare-and-youth-justice/274224Federal Bill Aims to Address Sibling Separation in Foster Carehttps://imprintnews.org/top-stories/federal-bill-aims-to-address-sibling-separation-in-foster-care/274283House Committee Moves Bills to Support Current, Former Foster Youthhttps://imprintnews.org/subscriber-content/house-committee-moves-bills-to-support-current-former-foster-youth/274257Lawmakers Seek to End Ban on Medicaid Covering Foster Youths' Residential Carehttps://imprintnews.org/youth-services-insider/bill-would-end-ban-on-medicaid-covering-foster-youths-residential-care/273791Foster Care for Mental Health Treatment: Parents Surrender Thousands of Kids Each Year In Search of Helphttps://imprintnews.org/top-stories/foster-care-for-mental-health-treatment-parents-surrender-thousands-of-kids-each-year-in-search-of-help/273355Adopted and Locked Away: Kids promised ‘forever homes' instead confined in for-profit institutionshttps://apnews.com/article/adopted-children-boarding-schools-treatment-investigation-e5d8dab2e4db1f2f4c5abbfaf0d97c52At CT DCF, staff turnover is high. The costs can be devastating.https://ctmirror.org/2026/05/10/ct-dcf-staff-turnover/‘This is where they came to die': Historical marker highlights horrors at segregated reform schoolhttps://marylandmatters.org/2026/05/07/this-is-where-they-came-to-die-historical-marker-highlights-horrors-at-segregated-reform-school/Leo's Law to protect children from fentanyl approved by the Oklahoma Senatehttps://okcfox.com/news/local/leos-law-to-protect-children-from-fentanyl-approved-by-the-oklahoma-senateWhen Life ‘Explodes': New Research Explores Why California Foster Youth Miss School https://imprintnews.org/top-stories/when-life-explodes-new-research-explores-why-california-foster-youth-miss-school/274367California Lawmakers Try to Avoid Foster Youth Going Hungry Following Federal Food Stamp Cutshttps://imprintnews.org/top-stories/california-lawmakers-looking-to-avoid-foster-youth-going-hungry/274537Indigenous People Honor and Raise Awareness for Relatives Who are Missing or Have Been Killedhttps://imprintnews.org/top-stories/indigenous-people-raise-awareness-for-missing-murdered-relatives/274252‘The Little Flowers Are Me, Unbloomed:' Georgia Foster Teens Find Their Voices Through Art Exhibithttps://imprintnews.org/top-stories/the-little-flowers-are-me-unbloomed-georgia-foster-teens-find-their-voices-through-art-exhibit/274098

Sharing his empowering lived experience to raise awareness of early-onset bowel cancer, Matt Duggan is running 550km across Tasmania (for the second time!) in May 2026.Matt chats openly with Stephanie about the challenges of telling friends and family about his diagnosis and why he now wants people to recognise the signs and symptoms of bowel cancer.“Keeping my diagnosis hidden probably did more harm than good.""I wanted to do something unique to get people talking and raise awareness that bowel cancer is not an old person's disease. The two weeks I spent last year running was probably the hardest thing I have ever done but was the most rewarding.”To support Matt's amazing awareness and fundraising efforts, search Matt's Marathon Mission on Facebook and Instagram.

In this episode we are exploring  four different psychological phenomena that might just show up in the coaching room.    They are concepts that originate in the world of psychoanalysis and therapy, and whilst their presence may well have been seen as problematic, they are also commonly occurring  phenomena for ordinary people and information for us in the coaching room.     The four concepts that we discuss in this episode are transference, counter-transference, projection, and parallel processing.    Join us for this fascinating dive into some often mentioned, but poorly understood, concepts.       Enjoy the podcast? If you're enjoying the podcast it would be great if you left us a review here or wherever you listen to your podcasts.    Contact Details Find out about our Doctors' Transformational Coaching Diploma Connect with the hosts: Tom: www.linkedin.com/in/tomdillondoctorstranformationalcoachingdiploma/ Email: tomdillon@yourcoachingjourney.co.uk   Helen: www.linkedin.com/in/helenleathers/ Email: helenleathers@yourcoachingjourney.co.uk   Follow 'Your Coaching Journey' on Instagram or Linkedin: www.instagram.com/yourcoachingjourney/ www.linkedin.com/company/your-coaching-journey/   Do You Have a Question? From time to time we will have an episode where we answer listeners' questions about coaching.   If you have a question, please send it to us using one of our email addresses above and you may get a mention in a future episode. (If you want to remain anonymous, that's absolutely fine, just let us know)

“The big picture is for people in every community to have some insight into what it might be like to live even a few hours in the shoes of someone who is living in poverty,” said Bee Darrow, Virginia Cooperative Extension Family Focus coordinator.

His 13 year old son Rory passed away 7 months ago & his other son Paudie also has FA & condition is getting worse. Her wife Della, once vibrant & always the rock of the family is in advanced stages of Huntingtons disease.

Live95's Caleb Brennan spoke to Tara Hughes, who is a young Limerick student who was diagnosed with Functional Neurological Disorder or FND, and her mother, Marian, joined Caleb.Image via Live95's photo library. Hosted on Acast. See acast.com/privacy for more information.

Mark Levy has spoken to an incredible man who aims to swim for 24 hours straight in order to raise awareness for organ donation a year after a life-saving liver transplant.See omnystudio.com/listener for privacy information.

Alpha-gal syndrome, a serious allergic reaction linked to Lone Star tick bites, is driving new action in Illinois. State Representative Dan Swanson is backing legislation that would require the Department of Public Health to track cases of this meat and dairy allergy. If passed, medical providers will be required to report alpha-gal cases, giving officials a clearer picture of the syndrome's spread. Swanson emphasizes that cases are on the rise, and his focus is on raising awareness about AGS symptoms and potential dangers. The legislation aims to inform residents and better equip the state to address this emerging health threat.

Alpha-gal syndrome, a serious allergic reaction linked to Lone Star tick bites, is driving new action in Illinois. State Representative Dan Swanson is backing legislation that would require the Department of Public Health to track cases of this meat and dairy allergy. If passed, medical providers will be required to report alpha-gal cases, giving officials a clearer picture of the syndrome's spread. Swanson emphasizes that cases are on the rise, and his focus is on raising awareness about AGS symptoms and potential dangers. The legislation aims to inform residents and better equip the state to address this emerging health threat.

In this important episode of the Total Celebrity Show on the Total Education Network, host Neil Haley sits down with NFL Hall of Fame running back Barry Sanders and neurological expert Dr. Greg O'Shanick to discuss their advocacy campaign Tackle PBA, which aims to raise awareness about pseudobulbar affect (PBA)—a little-known neurological condition affecting approximately 2 million Americans, including many former football players. Dr. O'Shanick explains that PBA causes uncontrollable and unpredictable episodes of laughing and crying that are completely out of context with what the person is actually feeling or experiencing. Someone with PBA might laugh uncontrollably during a solemn church service or begin crying during a routine parent-teacher conference, leading to embarrassment, social isolation, and damaged relationships in both personal and professional settings. The condition occurs in individuals who have other chronic neurological conditions such as traumatic brain injuries, concussions, strokes, multiple sclerosis, Lou Gehrig's disease, or Alzheimer's disease. Crucially, Dr. O'Shanick emphasizes that PBA is treatable and that people don't need to suffer in silence or feel stigmatized by their symptoms.Barry Sanders shares his personal connection to the cause through his work with the Gridiron Greats Assistance Fund, which conducted a survey revealing that one-third of former NFL players exhibit PBA-like symptoms. These findings deeply resonated with Sanders, as many of these players are men he competed with and against throughout his legendary career—athletes who gave everything to the game and deserve access to proper diagnosis and treatment. Dr. O'Shanick notes that family members are often the first to recognize PBA symptoms, as affected individuals may not fully grasp what's happening to them or may attribute their emotional outbursts to grief or sadness related to their primary condition. The Tackle PBA campaign encourages anyone experiencing these symptoms or concerned about a loved one to visit tacklepba.org, where they can take a self-assessment test and find resources for discussing the condition with their physician. Both Sanders and Dr. O'Shanick stress that awareness and education are critical first steps, as PBA has been understood medically for over 100 years but often goes undiagnosed simply because patients and healthcare providers aren't familiar with it. Sanders also reflects on his life after his remarkable football career, discussing how his platform has allowed him to engage in meaningful charity work and advocacy efforts like Tackle PBA while remaining a passionate fan of the game that gave him so many opportunities.

In this segment, Mark is joined by Mark S. Allen, an Emmy Aware winning TV producer and host. Mark is also a movie reviewer with ABC 10 in Sacramento. He discusses his mission to raise awareness against driving while intoxicated.

In this uplifting episode, hosts Beth Glassman and Cathy Gildenhorn sit down with Leanna Scaglione, a powerhouse rare disease advocate and marathon runner living with NF2-Related Schwannomatosis (NF2-SWN), formerly known as neurofibromatosis type 2. Diagnosed at just 16 years old, Leanna's life changed dramatically when tumors were discovered in her nervous system, a hallmark of NF2-SWN. Many would have slowed down. Instead, Leanna sped up. Today, she has: Completed multiple marathons, including Berlin and New York City Participated in clinical trials Become an advocate and 2025 Ambassador for the Children's Tumor Foundation Set her sights on becoming the first person with NF2 to complete all 7 Abbott World Marathon Majors Her message is powerful: a diagnosis doesn't define the finish line. In This Episode, We Discuss: What NF2-SWN is and how it impacts the nervous system The emotional toll of receiving a life-altering diagnosis as a teenager Losing a dream — and finding a new one Running marathons through surgeries, treatments, and uncertainty How advocacy and visibility can change the rare disease landscape Building a life rooted in resilience, purpose, and possibility About Our Guest: Leanna Scaglione is 34 years old living with NF2-Related Schwannomatosis (NF2-SWN). Ever since being diagnosed at 16 years old, she has refused to live defined by her diagnosis. From relearning to walk, participating in immunotherapy drug trials, and going through numerous surgeries she has defied the odds against her. Most recently she has undergone surgery to remove her right acoustic neuroma. She continues to live her best life as an endurance runner, sharing her story and experiences living with NF2 in hopes to spread awareness, motivate her community and rally for a cure. Resources:  Children's Tumor Foundation NF2 Accelerator: A Strategic Portfolio Approach to End NF2 Articles Explaining NF2 MedlinePlus GeneReviews National Organization for Rare Disorders (NORD) Research from China that Leanna reference for a gene therapy for NF2 Yuan R, Wang B, Wang Y, Liu P. Gene Therapy for Neurofibromatosis Type 2-Related Schwannomatosis: Recent Progress, Challenges, and Future Directions. Oncol Ther. 2024 Jun;12(2):257-276. doi: 10.1007/s40487-024-00279-2. Epub 2024 May 17. PMID: 38760612; PMCID: PMC11187037. Additional Research Articles Alexandra K. O'Donohue, Samantha L. Ginn, Gaetan Burgio, Yemima Berman, Gabriel Dabscheck, Aaron Schindeler, The evolving landscape of NF gene therapy: Hurdles and opportunities, Molecular Therapy Nucleic Acids, Volume 36, Issue 1, 2025, 102475 ,ISSN 2162-2531, https://doi.org/10.1016/j.omtn.2025.102475. Connect With Us:   Stay tuned for the next new episode of “It Happened To Me”! In the meantime, you can listen to our previous episodes on Apple Podcasts, Spotify, streaming on the website, or any other podcast player by searching, “It Happened To Me”.  “It Happened To Me” is created and hosted by Cathy Gildenhorn and Beth Glassman. DNA Today's Kira Dineen is our executive producer and marketing lead. Amanda Andreoli is our associate producer. Ashlyn Enokian is our graphic designer. See what else we are up to on Twitter, Instagram, Facebook, YouTube and our website, ItHappenedToMePod.com. Questions/inquiries can be sent to ItHappenedToMePod@gmail.com. 

We've got an episode today that's going to stop you in your tracks. You're going to meet Joel Sheagren, an award-winning filmmaker whose story feels like a movie itself, only this one's real, raw, and full of God's fingerprints.Joel grew up in a funeral home, had demonic encounters as a kid, found himself guiding canoes in the wilderness as an agnostic teen, and somehow, through a horror movie of all things, found his way to Christ. But that was only the beginning.What happens when the bottom falls out of your career, your faith gets tested through years of anxiety, and you're suddenly raising two adopted children, one with Fetal Alcohol Spectrum Disorder (FASD), and you realize God's been writing a redemption story through it all?In this powerful conversation, you'll hear how Joel turned his pain into purpose through prayer, perseverance, and creativity. His story will help you see your own trials differently. Because sometimes, what feels like chaos is actually the setup for your calling.Chapters: [00:00] Podcast Preview[01:38] Topic and Guest Introduction[04:24] The Awakening: From Agnosticism to Faith[13:00] The Long Path: Growth Through Trials[19:48] Learning Patience When God's Timing Feels Slow[22:45] Overcoming Anxiety and Learning to Trust[25:25] The Moment Joel and His Wife Said “Yes” to Adoption[28:00] The Miraculous Two-Month Adoption Story[30:00] Recognizing Fetal Alcohol Spectrum Disorder (FASD)[34:30] Navigating Parenting Challenges with FASD[36:48] How God Used Filmmaking to Raise Awareness for FASD[40:07] Teaching Neuroplasticity and Renewing the Mind[43:05] Spiritual Breakthroughs and Mindset Shifts[47:21] About the Embracing Hope Caregiver Guide[49:35] Final Encouragement and Where to Find Joel's ResourcesResources mentioned:Embracing Hope BookGuest's bio:Joel Sheagren is an award-winning filmmaker, photographer, and storyteller whose greatest inspiration comes from home—raising two children, one of whom lives with Fetal Alcohol Spectrum Disorder (FASD).His incredible journey from agnosticism to faith began in the most unexpected places—a canoe in the wilderness and a night watching The Exorcist—moments that led him into a lifelong pursuit of telling redemptive stories through the lens of God's grace.Joel is the founder of Sam in a Can Productions (named after his son) and the visionary behind The Embrace Movement, a media-driven initiative shedding light on the hidden link between prenatal alcohol exposure and societal issues like homelessness, trafficking, and fatherlessness.Through his films, books, and caregiver resources, Joel equips families, churches, and communities to better understand and support neurodiversity while bringing hope to those navigating life's challenges.He and his wife continue to walk in faith—turning pain into purpose and using their story to help families find strength, healing, and breakthrough through Christ.Call to action:Make sure to visit yourbiggestbreakthrough.com for your FREE access to our e-book and audiobook, "Unstoppable: Divine Intervention in Overcoming Adversity," showcasing six powerful real-life stories. Get ready to be inspired by these mind-blowing breakthroughs!To learn more about Wendie and her Visibly Fit program, visit

Dana In The Morning Highlights 10/29Houston Food Bank looking to cover Houston families losing SNAP food benefitsSome families might feature different colored pumpkins to help raise awarenessAtascocita HS Lady Mustang's getting charter bus to bring support for game against Deer Park

-Ranch Adventure with Rhody (0:09) -Theft of the Crown Jewels (4:34) -Critique of Western European Governments (8:23) -Technical Issues and AI Development (14:19) -Natural Intelligence vs. Artificial Intelligence (18:19) -Impact of AI on Human Interaction (44:00) -Robots in Everyday Life (1:02:35) -Robot-Human Relationships (1:10:43) -Robots in Emergency Situations (1:16:04) -Conclusion and Future Outlook (1:16:26) -Corruption in District Courts and Department of Corrections (1:17:39) -Amanda's Investigation into Water Contamination (1:24:37) -Amanda's Efforts to Raise Awareness (1:49:31) -Jim's Perspective on the Broader Issues (1:50:04) -Call to Action and Final Thoughts (1:52:20) For more updates, visit: http://www.brighteon.com/channel/hrreport NaturalNews videos would not be possible without you, as always we remain passionately dedicated to our mission of educating people all over the world on the subject of natural healing remedies and personal liberty (food freedom, medical freedom, the freedom of speech, etc.). Together, we're helping create a better world, with more honest food labeling, reduced chemical contamination, the avoidance of toxic heavy metals and vastly increased scientific transparency. ▶️ Every dollar you spend at the Health Ranger Store goes toward helping us achieve important science and content goals for humanity: https://www.healthrangerstore.com/ ▶️ Sign Up For Our Newsletter: https://www.naturalnews.com/Readerregistration.html ▶️ Brighteon: https://www.brighteon.com/channels/hrreport ▶️ Join Our Social Network: https://brighteon.social/@HealthRanger ▶️ Check In Stock Products at: https://PrepWithMike.com

The Family Crisis Center is putting on their Purple Ribbon Run this upcoming weekend to raise awareness for domestic violence in the Rexburg area. Ally Owens, who works at the center, details the event, as well as the services the Crisis center offers to the community.

Trish Glowacki shares her journey, and what lead her to founding the Glowmedia Project and its work on youth mental health awareness.Trish, a screenwriter, playwright and producer, mother of three, lost her son Charlie in 2011 to an accidental overdose. In his honor, she started to create a musical, films and resources on youth mental health topics. The Glowmedia project has produced a musical "Warning. Take Only As Prescribed." and 9 short films on various mental health issues, with curriculum and expert input, reaching millions through partnerships with i.e. "Discovery Education". Glowmedia works with organizations, schools, educators, parents and youth. Trish emphasizes the importance of student input, self-care, and persistence on continuing the mission to reduce mental health stigma.#### On another note: I am so proud and excited to announce that SHIFT HAPPENS' Season 5 is supported by London based jewellery brand Tilly Sveaas. Its founder, Tilly Sveaas creates gorgeous, timeless pieces that have been featured in Vogue, Harper's Bazaar, Marie Claire, The Times, The New York Times etc. … Her jewellery is for women of all ages. Guess who is wearing it too: noone less then Taylor Swift. Go to www.tillysveaas.co.uk and use my code SHIFTHAPPENS to get 15% off. ####To learn more about my guest Trish Glowacki, please visit her social media page:Instagram: @glowmediafilmsWebsite: The Glowmedia ProjectYou can download all short films for free!To learn more about SHIFT HAPPENS, click here To learn more about Claudia's business Curated Conversations and her Salons in New York, Zurich and Berlin, click hereYou can also connect with Claudia on Instagram @shifthappens.podcast and LinkedIn at ClaudiaMahlerNYCThis podcast is created, produced and hosted by Claudia Mahler.

Co-hosts Ryan Piansky, a graduate student and patient advocate living with eosinophilic esophagitis (EoE) and eosinophilic asthma, and Holly Knotowicz, a speech-language pathologist living with EoE who serves on APFED's Health Sciences Advisory Council, interview three high school students who made less invasive EoE diagnostics the focus of a science fair project. Disclaimer: The information provided in this podcast is designed to support, not replace, the relationship that exists between listeners and their healthcare providers. Opinions, information, and recommendations shared in this podcast are not a substitute for medical advice. Decisions related to medical care should be made with your healthcare provider. Opinions and views of guests and co-hosts are their own.   Key Takeaways: [:51] Co-host Ryan Piansky introduces the episode, brought to you thanks to the support of Education Partners Bristol Myers Squibb, GSK, Sanofi, Regeneron, and Takeda. Ryan introduces co-host Holly Knotowicz.   [1:08] Holly introduces today's guests, three high school students from Texas who made EoE diagnostics the focus of a science fair project: Leyna, Nhu, and Jaden.   [1:47] Leyna, Nhu, and Jaden are best friends. Nhu was diagnosed with EoE last summer. Leyna said Nhu told them it took a long time for the doctors to diagnose her because they thought it could be different conditions.   [2:07] Nhu told them about her appointments and her endoscopy procedures. She had to miss school sometimes. Leyna and Jaden were concerned for her.   [2:22] Leyna took AP Bio. Her teacher was a sponsor for the science fair. Leyna thought this would be a meaningful project for the three friends to learn more about Nhu's condition.    [2:45] Holly shares that she wasn't diagnosed until her 20s, but she was sick for much of her childhood.   [3:13] Ryan shares that he was diagnosed when he was two, after two years of his parents taking him to different doctors and undergoing different tests.   [3:31] Nhu says it was hard to find a specialist. They found one and had to wait six months for an appointment. It was a long time, suffering from the effects of EoE with constant symptoms, a lot of heartburn, and painful vomiting.   [4:00] Nhu was diagnosed with EoE in her sophomore year of high school. Her friends have seen her endure a lot, but she's strong. Nhu had to miss an orchestra concert where she had a big solo, because of her EoE.   [4:32] Doctors thought Nhu could have something different, like H. Pylori or cyclic vomiting syndrome. They didn't have clear answers, which was confusing and frustrating for her family.   [4:50] Holly talks about how difficult it was for her to get a diagnosis, and how she was told she was vomiting to get attention. She shared her reaction when diagnosed. She would like someone to do a research study about the pain tolerance of people with EoE.   [5:41] Leyna says junior year is the hardest year of high school. She doesn't know how Nhu survived physics and AP classes with EoE on top of it, and making up late work.   [6:14] Nhu takes a weekly injection. Her symptoms happen almost monthly. Sometimes she misses school for two weeks and has to catch up on work. Leyna and Jaden help her with her schoolwork.   [6:47] Ryan shared how he missed a third of his senior year in high school. He's now on an injectable biologic that has helped him a lot. That treatment option wasn't available when he was in high school. Having supportive friends to send him his schoolwork and keep him up-to-date was very helpful.   [7:11] Ryan explains the esophageal string test (EST). This is a tool that was developed to help monitor eosinophilic esophagitis (EoE). The test works by having the patient swallow a capsule about the size of a Tic Tac that has a string attached.   [7:25] The capsule dissolves in the stomach while the string stays in place in the esophagus. After about an hour, it's gently removed. Along the way, the string collects samples from the lining of the esophagus, which are reviewed, similarly to a biopsy.   [7:37] Holly adds that what makes the string test unique is that it doesn't require an endoscope, anesthesia, or recovery time, things that usually come with a traditional endoscopy and biopsy.   [7:46] It's now being used with patients as young as four years old. While some people might feel some minor discomfort, it's generally much easier for regular monitoring than an endoscopy.   [7:57] Holly explains that she was involved in testing the device and developing a swallowing protocol for it at Children's Hospital of Colorado. We will talk more about this later in the episode.   [8:06] Ryan adds, to learn more about the development of the string test, listen to episode 26 of this podcast.   [8:10] The string test is one of multiple, less-invasive monitoring tools for eosinophilic esophagitis. Others include the sponge test and unsedated trans-nasal endoscopy.   [8:19] To learn more about unsedated transnasal endoscopy, listen to episodes 19 and 20, where we talk to clinicians and patients about this method.   [8:27] During that episode, we talked to the developers of the EST.   [8:38] Jaden tells how he, Leyna, and Nhu brainstormed ideas and decided to base their project specifically on how to diagnose EoE in a less invasive way than endoscopies.   [9:12] Before this project, they were not familiar with the EST. Nhu says her only option for diagnosis was an endoscopy.   [9:21] Holly says it's still like that in Maine. She came from an area of the country where the EST was researched, and it's interesting to her that she doesn't have access to it now.   [9:37] What appealed to the group about the EST as an alternative to endoscopies is that it was so different. There are so many advanced technologies, and the EST is just a capsule taped to a string. It is simple but innovative.   [10:13] Real Talk: Eosinophilic Diseases had Drs. Robin Shandas and Steven Ackerman, who were instrumental in the development of the esophageal string test, as guests on episode 26 of this podcast. Ryan encourages listeners to check out that episode at apfed.org/podcasts.   [10:42] They searched for keywords and analyzed a variety of scholarly literature. They collected a lot of data from Dr. Ackerman's papers.   [11:10] They also reached out to gastroenterologists on social media. A hard thing about science fair projects is coming up with an experiment. They didn't know what they could do just with compiled research, but they had a great sponsor who helped along the way.   [11:56] Leyna says they trusted that the doctors they reached out to on social media were competent in their understanding of different diagnostic methods. She notes that different locations may have different resources and different biases.   [12:14] Leyna says they talked to doctors in the U.S. and from different countries, including India and Mexico. She commented that communities in Mexico might not have the same resources as communities in the U.S. or India. That might change their understanding of the EST.   [12:33] We might have different biases because we don't have the same technology to research and find the same things about the EST.   [13:12] Leyna says they reached out to doctors on social media, but didn't get responses from that many doctors. Reaching out to patients would be a good thing if they want to continue the project.   [14:00] Jaden says most of the data they found was from Dr. Ackerman, including a survey he did comparing the data of the EST and the biopsies.   [14:10] They found that the EST and the biopsies were relatively similar in terms of discovering the eosinophilic count and determining whether the EoE is active or inactive.   [15:30] They found differences between ESTs and biopsies in finding how much of a certain chemical is in the patient's cells.   [14:43] Leyna comments that one of the doctors they reached out to told them about the sponge test, another less invasive method. They didn't research the sponge test, but it sounded interesting.   [15:00] Ryan says there are a lot of cool new techniques that are being researched, like the transnasal endoscopy that goes in through the nose, the string test, and the sponge test.   [15:13] Leyna says the cool thing was hearing about all these methods. They had hypothesized that there are less invasive methods that may be better than endoscopies.   [15:27] They were not able to prove their hypothesis yet. They learned a lot of different things that could be beneficial.   [15:42] Holly points out that the transnasal endoscopy is not scary. It's also known as the unsedated endoscopy. Holly has done both the EST and the unsedated endoscopy,  and they each have pluses and minuses.   [16:15] Nhu explains how the team would meet at one of their houses, usually Leyna's house. One day, they watched Interstellar together, and the “Eureka moment” scene motivated them.   [16:41] They helped each other whenever necessary. When the project board was due, they all went to Leyna's house to work on the project board. They worked together as a team.   [16:51] Jaden analyzed a lot of the data. Leyna reached out to professors. Nhu helped Jaden understand some terms. On the day they presented the project, Nhu was sick in the hospital, which made them sad. They included a photo of her on the project board.   [17:28] Holly says that although Nhu wasn't there, it may have helped people know how sick EoE can make you feel.   [18:28] Leyna says one of the doctors they reached through social media told them that endoscopies have lots of benefits. The biopsy samples give healthcare professionals a clear idea of how many eosinophils per high-powered field, a key indicator in diagnosing EoE.   [18:57] The diagnosis gives a baseline for starting treatment for the patient, monitoring how effective the treatment is. You can't count the number of eosinophils per high-powered field using the string test.   [19:11] The EST is a gelatin capsule attached to a long string that you swallow. It dissolves in the stomach. It's less expensive than an endoscopy.   [19:33] Holly says one of the big differences is that you can't diagnose EoE on a string test. It has to be diagnosed with an endoscopy.   [19:40] Leyna says they learned that from the doctors and medical students who reviewed their project board. You can't diagnose EoE with the EST, but you can monitor it.   [19:52] The string test doesn't provide a direct eosinophil count, but it reflects the level of inflammation in your esophagus, and it can measure the protein biomarkers. That correlates with the eosinophil count from a biopsy. It is good for monitoring EoE.   [20:12] Ryan says that's a great idea. In the show notes, there is a link to the diagnostic consensus guidelines. They specify that you need an endoscopy and 15 eosinophils per high-powered field to be diagnosed with EoE.   [20:28] The EST can monitor the progression of the disorder as you're trying new medicines or an elimination diet. If you need an endoscopy every three to six months, it can be taxing.    [20:49] Ryan comments on the cost. Going through anesthesia for an endoscopy is very expensive, and not everyone has the insurance to cover these diagnostic procedures. The EST is an option you can do in a doctor's office in just over an hour.   [21:16] Holly asks if Nhu has participated in a string test. Nhu has not, but she would love to do a string test if she had the chance. Whenever she sees her doctor, she brings up her condition, and what could be better for her, such as the string test.   [22:06] The science fair is a huge regional fair in Houston, called the Science and Engineering Fair of Houston (SEFH). This was their first year participating. They were regional qualifiers from their district. When they got there, everyone else had six-foot-tall printed boards. It was a shock to them.   [22:56] They hope to level up their board for next year's fair. It was cool and eye-opening to see all these student researchers and get feedback from the people who walked by their booth. They heard some interesting things to use in their next project.   [23:15] One medical student in attendance came by their project board and suggested that while the EST may not diagnose EoE, maybe it could be used as a screening tool [to help identify people who should follow up with a gastroenterologist for a diagnostic work-up]. Interestingly, this was a medical student, and she had recently scheduled an appointment with a gastroenterologist for an endoscopy to see if she has EoE.   [24:04] This student didn't seem to know much about EoE, but felt she was experiencing symptoms that might indicate EoE. She told them she had learned so much from their board. Ryan says it's great that the project was able to help this person.   [24:44] Jaden says that the students at their school didn't know much about EoE, but when they looked at the project board, they were shocked by how incredibly difficult it is to diagnose EoE and how the EST could change a lot of things as a screening method.   [25:11] Jaden says their science teacher came by to see their board and how they were doing. He liked how they included not only the research information but also the stories of why they chose their project and why they were passionate about it.   [25:34] The day of the project, Leyna and Jaden were sad that Nhu couldn't be there with them. Their sponsor, Leyna's biology teacher, was sick, but showed up at the fair to view their presentation. They raised awareness about EoE. People learned about it.   [25:54] When Nhu told Leyna about her EoE, Leyna had no idea what it was. She's glad their project brought the issue to the table. They emphasized that more research needs to be done. There is much we don't know about less invasive methods.   [26:23] Nhu has considered a career in medicine since she has been in many hospitals and talked to a lot of doctors. Jaden sees himself in the engineering field, but he enjoys researching like this and seeing things through a different perspective.   [27:05] Nhu learned a lot about herself with EoE. Leyna loves how much they learned from this project. She is interested in pursuing scientific research. She thinks it's cool that Ryan is a graduate student.   [27:24] Leyna just got back from a five-week summer research program. It was insightful. She doesn't see herself becoming a doctor, but possibly doing research and advocating for different conditions.   [27:43] When Ryan was in high school, with all his hospital time, he had an interest in medicine, then he took a turn into engineering. He enjoys research. He's passionate about engaging in patient advocacy work through APFED.   [28:10] Ryan is glad for Leyna, Nhu, and Jaden that they were able to engage with this research and do it as a group and as friends. He says it's fantastic to hear from the group about the whole process they went through.   [28:23] Holly asks, looking back on everything you guys learned and experienced in this project, what's one question or idea you would still like to explore if you had more time and resources?   [28:38] Nhu wants to research finding more ways to diagnose EoE. Testing for EoE and finding EoE are very interesting for her.   [28:53] Jaden thinks that if they had more time, they would try to create a model of the EST to show how it works. He would possibly try to improve upon the model or develop something new. Instead of just relying on the data we have, he would try to collect data.   [29:26] Leyna agrees. She would like to build a prototype, understand how the capsule works, and find out whether the string down the esophagus is uncomfortable.   [33:41] Ryan suggests there is a doctor who would let them try the string test so they could see how it feels. Holly tried the string test at a major children's hospital while it was being researched. She doesn't want to ask her patients to do something she hasn't done, since she has the diagnosis too.   [30:37] Ryan comments that he enjoyed hearing about the process of the project.   [30:51] Ryan gives a quick recap: The esophageal string test is a tool to help monitor EoE. It is not a tool to diagnose EoE. If you or a loved one has EoE or suspect that you might, ask your clinician about the string test to see if it's an option for you.   [31:03] Holly adds: School science fairs are one way to bring education about eosinophilic disorders to schools. We love hearing about community science fairs and school projects that teach others about these conditions.   [31:13] For those of you looking to learn more about eosinophilic esophagitis, we encourage you to visit apfed.org/EoE.   [31:23] For those looking to find specialists who treat EoE, we encourage you to use APFED's Specialist Finder at apfed.org/specialist.   [31:30] Ryan thanks Leyna, Nhu, and Jaden for joining us today. Holly also thanks APFED's Education Partners Bristol Myers Squibb, GSK, Sanofi, Regeneron, and Takeda for supporting this episode.   Mentioned in This Episode: Dr. Robin Shandas Dr. Steven Ackerman “Updated international consensus diagnostic criteria for eosinophilic esophagitis: Proceedings of the AGREE conference”   APFED on YouTube, Twitter, Facebook, Pinterest, Instagram Real Talk: Eosinophilic Diseases Podcast apfed.org/specialist apfed.org/connections   Education Partners: This episode of APFED's podcast is brought to you thanks to the support of Bristol Myers Squibb, GSK, Sanofi, Regeneron, and Takeda.   Tweetables:   “Nhu and Jaden are my best friends. Recently, Nhu was diagnosed with EoE. I remember her telling us about the long diagnosis process. It took the doctors quite a long time to diagnose her because they thought it could be different conditions.” — Leyna   “I thought that this would be a meaningful project for us to learn more about Nhu's condition [of EoE].” — Leyna   “The students at our school didn't know much about EoE, but when they looked at the project board, they were shocked by how incredibly difficult it is to diagnose EoE.” — Jaden   “One of the main benefits of the string test is that endoscopies can be quite expensive, especially the anesthesia. It could be beneficial for people who don't have the money for an endoscopy.” — Nhu

September 15 through 21 is Farm Safety Week in Illinois, highlighting the urgent need for caution in one of the nation's most hazardous professions. With more than 500 farming-related fatalities occurring annually across the U.S., tractor accidents top the list, alongside grain bin incidents and chemical exposures. Farmers routinely work in challenging environments and face unique risks from machinery, animals, and weather. Public awareness is equally important, as motorists often encounter slow-moving farm vehicles with limited visibility on local roads. The Governor's proclamation encourages conversations about equipment operation, health practices, and safe behaviors to avert tragedies both on and off the farm. Illinois Representative Dan Swanson, who is also a farmer, talks about farm safety week.

Alexion recently launched the second film in its Rare Connections series, Rare Connections in gMG.Managing editor Jack O'Brien talks with Lucid Diagnostics' chief technology and compliance officer Dr. Brian deGuzman about the company's nationwide initiative to provide education and testing for esophageal precancer.He explains how the NFLPA factors into the effort, which launched in Cincinnati, and how it is expanding across the country to address the heightened risk these athletes have for developing esophageal pre-cancer.Check us out at: mmm-online.com  Fast Break theme music: Mark Buergler - On The Run, Triple Scoop Music Step into the future of health media at the MM+M Media Summit on October 30th, 2025 live in NYC! Join top voices in pharma marketing for a full day of forward-thinking discussions on AI, streaming, retail media, and more. Explore the latest in omnichannel strategy, personalization, media trust, and data privacy—all under one roof. Don't wait—use promo code PODCAST for $100 off your individual ticket. Click here to register! AI Deciphered is back—live in New York City this November 13th.Join leaders from brands, agencies, and platforms for a future-focused conversation on how AI is transforming media, marketing, and the retail experience. Ready to future-proof your strategy? Secure your spot now at aidecipheredsummit.com. Use code POD at check out for $100 your ticket! Check us out at: mmm-online.com Follow us: YouTube: @MMM-onlineTikTok: @MMMnewsInstagram: @MMMnewsonlineTwitter/X: @MMMnewsLinkedIn: MM+M To read more of the most timely, balanced and original reporting in medical marketing, subscribe here.Music: “Deep Reflection” by DP and Triple Scoop Music.

A 200 Mile Journey from LA to San Diego to Raise Awareness for PH When Eric Borstein collapsed in his bedroom in 2020, doctors gave him just months to live. Instead, he fought back with walking, mental health, and the support of his community. Now, he's leading a movement, raising hundreds of thousands for pulmonary hypertension research, and walking 200 miles down the California coast to prove hope has no limits. Learn more about the 2nd Annual Where is EB? 5K Walk and Fundraiser September 7, 2025 Learn more about pulmonary hypertension trials at www.phaware.global/clinicaltrials. Follow us on social @phaware  Engage for a cure: www.phaware.global/donate #phaware Share your story: info@phaware.com @teamphhope  @where_is_eb @DJLisaFoxx  

Chicago-based emergency room physician Dr. Thaer Ahmad is one of the dozens of health care workers from the area who have traveled to Gaza to provide humanitarian aid since the October 7, 2023 attacks. Ahmad and his colleagues are sharing their experiences with Illinois lawmakers in an effort to highlight the starvation in Gaza and to stop weapon transfers to Israel. Reset hears from Dr. Ahmad, WBEZ city politics Mariah Woelfel and Ertharin Cousin, former executive director of the United Nations World Food Programme.

"For me, people say oh he's a celebrity, he's a football player, but millions of people got to see that I was going through the same struggles they were." Cam Bynum As our NFL Training Camp tour continues, we stop in Indy to sit with one of their newest additions who is making noise both on and off the field. In this upbeat and fun-filled episode of The Pivot Podcast, Indianapolis Colts safety Cam Bynum sits down with Ryan Clark, Channing Crowder, and Fred Taylor to talk about his journey from standout NFL Safety to viral sensation — and how his purpose goes far beyond football. The guys are blown away by his positive energy and contagious spirit, which truly shows why Cam is such an asset to any locker room. Now with Indianapolis, Cam reflects on leaving the Vikings, his upmost respect for Justin Jefferson and how he looks for his new defensive unit to lead the league in interceptions like he did in Minnesota. Finding a new home in Indy, he shares how he continues to grow as a leader, husband, and man of faith. Being named Captain of the Colts defense, Cam gets into what it will take to get this young team to be a competitive unit in the AFC, how to buy into new schemes and succeed under a new regime. He shares his insight around the QB competition between Daniel Jones and Anthony Richardson and how he hopes to support both by challenging from opposite side of the ball. Cam opens up about what it means to represent the Philippines on a global stage, the story behind his emotional and viral postgame celebrations waving the Filipino flag, and how he's using his platform to spotlight his heritage and his faith. He shares the deeply personal journey of helping his wife gain U.S. citizenship, giving listeners a raw look into the sacrifices, love, and cultural pride that fuel him off the field. This episode blends football, family, and purpose — showing there's so much more to Cam Bynum than what fans see on Sundays. Don't forget to like, comment and hit the subscribe button to stay up to date on our latest conversations and guests. Learn more about your ad choices. Visit megaphone.fm/adchoices

For many people, fireflies are part of the story of summer, evoking memories of lazy, hot evenings spent trying to catch them in glass jars. Now, one man is still trying to catch them — not with a jar, but with a camera — to raise awareness about the threats facing these glowing insects. John Yang reports. PBS News is supported by - https://www.pbs.org/newshour/about/funders. Hosted on Acast. See acast.com/privacy

For many people, fireflies are part of the story of summer, evoking memories of lazy, hot evenings spent trying to catch them in glass jars. Now, one man is still trying to catch them — not with a jar, but with a camera — to raise awareness about the threats facing these glowing insects. John Yang reports. PBS News is supported by - https://www.pbs.org/newshour/about/funders. Hosted on Acast. See acast.com/privacy

Guests: Kirk McLean, legendary goalie with the Vancouver Canucks Genevieve McLean, Kirk's wife and three-time cancer survivor Learn more about your ad choices. Visit megaphone.fm/adchoices

Endurance Swimmer Lewis Pugh joins Megan Lynch to talk about his latest endurance swim took place over 12 days around Martha's Vineyard to raise awareness of the shocking loss of shark populations.

National Kidney Foundation of Wisconsin CEO, Mike Crowley, is celebrating his 6 month anniversary since altruistically donating his kidney by riding his bike to all of the Wisconsin transplant clinics!

Lingam K. is a research and lens-based artist whose projects primarily focus on scientific observations. The PhD student at RMIT University in Melbourne has been working on an extensive project visualising glacial meltdown in Nepal's Himalayan region, particularly in the Khumbu area. His recent exhibition in Kathmandu, titled “Sambandh”, featured large images of glacial lakes that he had photographed during his most recent visit to the region. Our Nepal correspondent, Girish Subedi, spoke to Lingam about his findings. - मेलबर्नको आरएमआईटी युनिभर्सिटीमा पिएचडी गरिरहेका लिङ्गम के. एक अनुसन्धानकर्ता हुन्, जसले फोटोग्राफी र ध्वनिका माध्यमबाट नेपालका हिमाली क्षेत्रमा हिउँ पग्लिने समस्याको अवलोकन गर्दै आएका छन्। पछिल्लो समय खुम्बु र नोजुम्पा हिमनदीहरूमा केन्द्रित अनुसन्धान गरेका उनले गत महिना काठमान्डूमा “सम्बन्ध्” नामक एक फोटो प्रदर्शनी गरेका थिए। आफैँले खिचेका हिमनदी क्षेत्रका ती तस्बिरहरू प्रस्तुत गरेका लिङ्गमसँग हिउँ पग्लने समस्याको वास्तविकता र ती हिमाली क्षेत्रमा काम गर्दाका अनुभवबारे नेपाल संवाददाता गिरिश सुवेदीले गरेको कुराकानी सुन्नुहोस्।

More than half of Nebraska's counties, most of Kansas and all of Iowa are labeled as radon hot spots. The harmful gas is nearly undetectable and can show up in any building, including homes. Health officials and radon mitigators say it's easy to test for and fix, but harder to get the word out.

Pastor Corey Brooks, Founder and Senior Pastor at New Beginnings Church of Chicago and the Founder and CEO of Project H.O.O.D, joins John Williams to talk about the progress he’s making in the effort to build his opportunity center on the south side, and why he’s considering a walk across America to raise awareness and […]

Pastor Corey Brooks, Founder and Senior Pastor at New Beginnings Church of Chicago and the Founder and CEO of Project H.O.O.D, joins John Williams to talk about the progress he’s making in the effort to build his opportunity center on the south side, and why he’s considering a walk across America to raise awareness and […]

Pastor Corey Brooks, Founder and Senior Pastor at New Beginnings Church of Chicago and the Founder and CEO of Project H.O.O.D, joins John Williams to talk about the progress he’s making in the effort to build his opportunity center on the south side, and why he’s considering a walk across America to raise awareness and […]

American Indians in Texas at the Spanish Colonial Missions embarked on a campaign in May to highlight the disproportionate effect of violence against Native women.

Paul Byrne speaks to Detective Chief Superintendent Colm Noonan on national campaign to raise awareness around domestic violence Hosted on Acast. See acast.com/privacy for more information.

Laura Dunn, NHTSA Highway Safety Specialist. New Campaign to Raise Awareness about Hot Car Deaths

Paul McCaffrey learned he had testicular cancer in 2015. He'd been experiencing groin pain at the time, but he didn't know how to check himself for any other signs of testicular cancer. So, Paul used the Cahonas Scotland's self-check guide and found a lump in one of his testicles. In the podcast, this testicular cancer survivor shares his treatment story for cancer, as well as sepsis and avian flu. Now, he works with Cahonas Scotland as the Community Engagement Officer, where he visits schools, workplaces, and communities throughout the country to raise awareness of the signs and symptoms of testicular cancer. He and his wife are the parents of two children: a son who plays the bagpipes and a daughter who is a Highland dancer. Listen to this episode of Don't Give Up on Testicular Cancer from the Max Mallory Foundation, where you can find other episodes of the podcast. Learn more about Cahonas Scotland and the work of Paul McCaffrey to raise awareness about testicular cancer. Send us a textSupport the showFind us on Twitter, Instagram, Facebook & Linkedin. If you can please support our nonprofit through Patreon.

Show Notes: In September of 2024, 4 women kidney donors, over 4 days, biked 444 miles to promote living organ donation. We're excited to have Diane Mills, one of the four women behind the event, join us to share the story of how it all began and the incredible success it achieved. She'll talk about the supportive people they encountered along the journey and how they were able to demonstrate that living donors can lead active, fulfilling lives after donation. In our Mental Health Moment, we explore the question: Are you in control? We'll share tips on how to ease the need to control outcomes and we honor donor hero Adah McCurley.

When Oregon wildland firefighter Kevin Conley heard about the wildfires in Los Angeles, he wanted to do something to help. Conley is currently riding his bike from Astoria to Northern California to raise money for the Wildland Firefighter Foundation, which provides financial and mental health resources to those fighting the fires. We’ll talk with Conley about his ride and the importance of mental health services for firefighters.

Today’s show is about Hurricane Helene and raising awareness for those who are completely stranded and trapped in Western NC/Eastern TN. There is a blackout of information, and folks are needing to rely on social media to attempt to contact loved ones and get information and help to the people who need it. Please send […] The post Raise Awareness and Help Victims of Hurricane Helene appeared first on Radio Influence.

He was terrified for his life. There were sores all over his body - was this the new virus the CDC was warning everyone about? _____________ 2-Minute Black History is produced by PushBlack, the nation's largest non-profit Black media company. PushBlack exists to amplify the stories of Black history you didn't learn in school. You make PushBlack happen with your contributions at BlackHistoryYear.com — most people donate $10 a month, but every dollar makes a difference. If this episode moved you, share it with your people! Thanks for supporting the work. The production team for this podcast includes Cydney Smith, Len Webb, and Lilly Workneh. Our editors are Lance John and Avery Phillips from Gifted Sounds Network. Julian Walker serves as executive producer. To learn more about listener data and our privacy practices visit: https://www.audacyinc.com/privacy-policy Learn more about your ad choices. Visit https://podcastchoices.com/adchoices

June is National Men's Health Month and we're honored to feature today's guest, Robert Klein, aka "Broccoli Rob." In June of 2017, he was unexpectedly diagnosed with testicular cancer, throwing his young family and career into a tailspin.Research led him to the The China Study and the undeniable benefits of a whole foods, plant-based diet, which he adopted virtually overnight.Today, he is an avid athlete, health coach, and vocal advocate for men's health. He is a licensed Food for Life Instructor teaching and you can learn more about his upcoming classes HERE.We hear a lot about the importance of self-exams for women's breast cancer, but we just don't hear enough about men's health and prevention. Thank you, Robert, for being so open and honest with your journey. It will save lives! Episode Webpage Watch the Episode on YouTubeBroccoli Rob's Websitehttps://wholecommunities.nutritionstudies.org/tinyurl.com/PPMNY - for the June Men's Health SeriesPlant Powered Metro New York WebsiteTesticular Self-Exam Resource from The Cleveland ClinicUpcoming Events:Register for Plant-Stock August 16th-18th, 2024: https://liveplantstrong.com/ Sedona Retreat - October 8th-13th, 2024 https://plantstrongfoods.com/pages/2024-sedona-retreat COMPLEMENT: Use code PLANTSTRONG for 30% off at https://lovecomplement.com/pages/plantstrong-special-offer Leave Us a Voicemail QuestionLeave us a voicemail: https://www.speakpipe.com/plantstrong Follow PLANTSTRONG and Rip Esselstynhttps://plantstrongfoods.com/ https://www.facebook.com/GoPlantstrong https://www.instagram.com/goplantstrong/https://www.instagram.com/ripesselstyn/ Let Us Help Your PLANTSTRONG JourneyUse Code: PSSUMMER20 for $20 off Annual Subscription at https://home.mealplanner.plantstrong.com/ https://myplantstrong.com/b/trailblazer Follow the PLANTSTRONG Podcast and Give the Show a 5-star RatingApple Podcasts

In an eye-opening episode, Michael Knowles sits down with Fr. Kiely to shed light on a pressing issue often overlooked by mainstream media: 'The Hidden War On Christians Around the World.' This powerful interview delves into the harrowing stories of persecution that millions of Christians face globally, exploring the complexities and the resilience of faith under fire.   Fr. Kiely, a dedicated advocate for persecuted Christians, brings to the forefront the struggles and injustices faced by believers in various corners of the world. From the Middle East to Africa, from Asia to Latin America, this conversation uncovers the trials and tribulations of those who endure oppression for their faith.