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Single and widowed moms often hear well–meaning phrases like, “Your daddy is now your guardian angel.” In this episode, Lori gently unpacks what Scripture really says about angels, clarifies common misunderstandings, and offers comforting, hope–filled truth you can share with your children. Key Takeaways for Moms:1. Do our loved ones become angels when they die?2. Angels in Scripture3. Angels in our lives today4. How to teach our children about angelsScriptures Mentioned:Psalm 34:7, 91Matthew 18:10, 22:30Luke 2:8–20, 20:35–362 Corinthians 5:8Hebrews 1:14Revelation 5:11–12; 7:11–12Connect with Lori and Perspective Ministries:Website: perspectiveministries.orgEmail: lori@perspectiveministries.orgSubscribe to the Raising Fatherless Kids podcast and YouTube channel, and share this episode with a mom who is wondering how to talk with her children about angels and their loved ones in heaven.

As we start the book of Colossians, we see that Christ alone is sufficient for salvation from our sins and the source of all our hope.Visit: abideatascadero.orgEmail: info@abideatascadero.orgInstagram: @abide.calvary_atascFacebook: @AbideCalvaryAtascadero

Join the community of believers seeking to hear God: https://receiveacademy.com/Connect with Christina:Website: www.terebinth.orgEmail: terebinthministries777@gmail.comChapters:00:00 Introduction04:58 Balancing Career and Faith06:37 Discovering Her Role in the Body of Christ17:47 The Spirit Growth Sheet27:32 Practical Steps for Spiritual Growth33:46 Hearing God's Voice39:33 The Call to Japan43:36 Cycling Through Japan50:59 The Call to Full-Time Missionary Work58:50 Living Without a Plan01:00:21 Final Reflections and Prayer

Join us as we learn more about contentment, which is a continuing process of trusting and relying daily on God's sufficiency. Visit: abideatascadero.orgEmail: info@abideatascadero.orgInstagram: @abide.calvary_atascFacebook: @AbideCalvaryAtascadero

What does it mean to live with cystic fibrosis (CF) in Amish and Mennonite communities, where many families don't use phones, computers, or even electricity? For some, this means relying on handwritten letters for communication, trying herbal remedies before conventional medicine, and declining treatments like lung transplants or in vitro fertilization because of cultural and religious beliefs.Update State CF Center (Syracuse, NY) Social Worker Lejla Bush, who has worked with the CF community for over a decade, shares how Amish and Mennonite families navigate CF while staying true to their traditions. She explains the unique challenges, from financial hurdles without health insurance, to hospital care that must adapt to cultural practices, and the vital role of community support in helping families face this disease.Most importantly, Lejla reminds us that while the cultural context is different, Amish and Mennonite parents hold the same hopes, fears, and love for their children as any other family affected by CF.This episode opens a window into the powerful intersection of culture, medicine, and resilience.We did a Q and A with some people in the Amish and Mennonite communities. Thanks to Lejla for sharing so much information about the Amish and Mennonite communities.To see a letter of Q and A with one of the Amish patients click here: https://thebonnellfoundation.org/wp-content/uploads/2025/09/AmishLetter.jpg Please like, subscribe, and comment on our podcasts!Please consider making a donation: https://thebonnellfoundation.org/donate/The Bonnell Foundation website:https://thebonnellfoundation.orgEmail us at: thebonnellfoundation@gmail.com Watch our podcasts on YouTube: https://www.youtube.com/@laurabonnell1136/featuredThanks to our sponsors:Vertex: https://www.vrtx.comViatris: https://www.viatris.com/en

If not attended to, our worry and  disagreements can grow. Listen as we learn how God can refocus us on His goodness and bring us peace.Visit: abideatascadero.orgEmail: info@abideatascadero.orgInstagram: @abide.calvary_atascFacebook: @AbideCalvaryAtascadero

Hominins and feathered dinosaurs get all the publicity, but what even is a non-mammalian synapsid? They are some of the weirdest and coolest fossils in the fossil record, and they get almost no attention! Join Todd and Paul as they chat with paleontologist Matt McLain about these weird fossils. Do they really prove mammal evolution, or is there much more to the story? Find out on this episode of Let's Talk Creation!Episodes mentioned in this episodeEpisode 8Where is My Missing Link?https://youtu.be/KlHuBactLEEEpisode 42Why are Horse Fossils Important to Creationists?https://youtu.be/ZtDvd7mcAQgPlaylist of Paleoanthropologyhttps://www.youtube.com/playlist?list=PLOzn-NecEi8EQEPL-CsmVZRo--osOXXFfMaterials Mentioned in this EpisodeThe origin and evolution of mammalsTS Kemp https://global.oup.com/academic/product/the-origin-and-evolution-of-mammals-9780198507611?cc=us&lang=en&von Baer, Karl Ernst. Über Entwickelungsgeschichte der Thiere. Beobachtung und reflexion. [On the Developmental History of the Animals. Observations and Reflections]. Königsberg: 1828. http://www.biodiversitylibrary.org/item/28306Written in GermanBiography on von Baer.https://www.britannica.com/biography/Karl-Ernst-Ritter-von-Baer-Edler-von-HuthornKemp, TS. 2009. Phylogenetic interrelationships and pattern of evolution of the therapsides: testing for polytomyhttps://www.tskempoxford.com/_files/ugd/0c689e_1b3b7fcb16b4447e848ad84a1362b1f6.pdf

Delivering Hope across Continents. The why and how Summer Bauder got involved with CF Vests Worldwide.Summer Bauder is a remarkable woman whose story embodies compassion, perseverance, and global impact.Summer's journey began as a stay-at-home mom managing a bustling household a life filled with love, chaos, and purpose. But everything changed when her brother-in-law's daughter was diagnosed with cystic fibrosis (CF). What started as a family connection to CF grew into a calling that now spans continents.Today, Summer serves as a key volunteer for CF Vest Worldwide, a nonprofit that provides life-changing airway clearance vests to people with CF who can't afford them. Her days are filled with cleaning, sorting, and shipping donated vests to families across the globe, and sometimes, personally delivering them.From India to Colombia to Ecuador, Summer has met families whose gratitude reminds her daily why this work matters. She shares powerful, heartwarming moments, like watching a child take easier breaths for the first time, and the challenges of navigating logistics, language barriers, and limited resources.Next up? Honduras, where Summer delivers 10 vests to families in need.Balancing her large family and international volunteer work hasn't been easy, but Summer says her experiences at home prepared her for the organizational and emotional demands of this mission. Her story is a reminder that one person — one family — can make a global difference.This episode shines a light on the power of community, family support, and the ripple effect of kindness.If you'd like to support Summer's efforts, CF Vest Worldwide is currently accepting donations of child-sized garmentsused to distribute vests to children with CF around the world.What's her connection? Her why?  It's her brother, Josh Bauder.To see more about Summer's work, watch her video: https://youtu.be/sHSB9kIp060To contact CFVWW: rod@cfvww.org Please like, subscribe, and comment on our podcasts!Please consider making a donation: https://thebonnellfoundation.org/donate/The Bonnell Foundation website:https://thebonnellfoundation.orgEmail us at: thebonnellfoundation@gmail.com Watch our podcasts on YouTube: https://www.youtube.com/@laurabonnell1136/featuredThanks to our sponsors:Vertex: https://www.vrtx.comViatris: https://www.viatris.com/en

In this passage, God calls us not to live in regret over the past or in worry about our future, but to live in the moment by His truth. Listen in as we explore the practical application of this concept. Visit: abideatascadero.orgEmail: info@abideatascadero.orgInstagram: @abide.calvary_atascFacebook: @AbideCalvaryAtascadero

Jennifer McKinnon is fierce. Doctors said Jennifer wouldn't live past the age of three.Today, she's a single mom of twins, an unstoppable advocate who's raised over a million dollars for cystic fibrosis research, and the founder of Just One More Breath. Her story is proof that while CF is tough, Jennifer is tougher, and that hope, when held fiercely, can change everything.Jennifer was born in the 1970s with cystic fibrosis, a time when the disease was still cloaked in uncertainty and fear. Few children with CF lived to see adulthood, and the treatments that exist today were still decades away. From the very beginning, every breath she took was a small act of defiance. Hospital rooms became her playgrounds, IV poles her silent companions, and the steady rhythm of nebulizers the soundtrack of her childhood.But even in those sterile rooms filled with machines and medicine, Jennifer's spirit burned bright. She refused to let CF define her — or defeat her. Through endless hospital stays, setbacks, and the exhausting daily grind of treatments, she found reasons to laugh, to dream, and to keep fighting. Every milestone, every birthday, every deep breath, became a victory.Then came 2019, a year that would rewrite her story once again. With the arrival of Trikafta, the groundbreaking CF modulator, Jennifer's world shifted. Suddenly, life felt lighter — her lungs stronger, her body more capable. For the first time, she could picture a future not limited by her disease but expanded by possibility. She could plan, imagine, and live, truly live, in ways she once only dreamed of.Yet Jennifer's story isn't just about survival; it's about transformation. Rather than turning inward, she turned outward — channeling her strength into action. She's raised over a million dollars for cystic fibrosis research, driven by the belief that every dollar brings us closer to a cure. She became a mother to twins through the extraordinary gift of her sister, proving that family and love can find a way even when the odds seem impossible.Today, Jennifer stands as a single mom, a tireless advocate, and the voice behind Just One More Breath, a platform dedicated to raising awareness, sharing stories, and inspiring others to keep pushing forward ... one breath at a time.Her journey is a powerful reminder that life with cystic fibrosis is unpredictable, yes, but it is also breathtakingly beautiful. It's a life lived with intention, courage, and grace. Jennifer's story teaches us that even when the odds seem insurmountable, resilience can turn pain into purpose, and hope can carry you through the darkest storms.Because for Jennifer, every breath is more than survival.It's a celebration of strength, of love, and of the limitless power of the human spirit.Jennifer on IG: https://www.instagram.com/just.onemorebreath/?hl=enWebsite: https://jennifer-mckinnon.com/?  Please like, subscribe, and comment on our podcasts!Please consider making a donation: https://thebonnellfoundation.org/donate/The Bonnell Foundation website:https://thebonnellfoundation.orgEmail us at: thebonnellfoundation@gmail.com Watch our podcasts on YouTube: https://www.youtube.com/@laurabonnell1136/featuredThanks to our sponsors:Vertex: https://www.vrtx.comViatris: https://www.viatris.com/en

What do you value in this life? In this passage, Paul says nothing compares to the worth of His relationship with Christ.Visit: abideatascadero.orgEmail: info@abideatascadero.orgInstagram: @abide.calvary_atascFacebook: @AbideCalvaryAtascadero

Did God really make a man and name him "Dirt?" He sure did! Todd and Paul talk about creationist beliefs in Genesis chapter 2. They cover all the basic creationist beliefs from the creation of Adam (AKA "Dirt") to the planting of the Garden of Eden to the naming of animals and the creation of woman. Also: Did it rain before the Flood? (*SPOILER* YES.) Where is Eden? (*SPOILER* It's gone now.) And what's up with all the agricultural hints in this chapter? Check it out in the latest episode of Let's Talk Creation! Episodes mentioned in this episodeEpisode 79: Creationism 101: In the Beginninghttps://youtu.be/2SZWrYad2lwEpisode 83: Creationism 101: Creation Weekhttps://youtu.be/R6lv-BFlQr0Episode 86: Creationism 101: Do we really need Genesis 1https://youtu.be/ha8-mm06cKEEpisode 90: Creationism 101: The Days of Creationhttps://youtu.be/sMu9pY9WWcIEpisode 121: Creationism 101: Does Genesis 1 contradict Genesis 2https://youtu.be/WJE7ysOAls0

The Triple Threat to the Rare Disease Ecosystem — A Conversation with Dr. Wendy ChungSometimes you come across someone whose work changes the way you think about an entire field. That's exactly what happened when I read about Dr. Wendy Chung in Rare Revolution Magazine.Dr. Chung is one of those rare people who stands at the intersection of science, medicine, ethics, and humanity. She's a clinical and molecular geneticist, the Chief of Pediatrics at Boston Children's Hospital, and the Mary Ellen Avery Professor at Harvard Medical School. She leads NIH-funded research into the genetics of conditions like pulmonary hypertension, autism, birth defects, and a wide range of rare diseases. She's advanced newborn screening for life-threatening disorders like spinal muscular atrophy and Duchenne muscular dystrophy — work that means the difference between life and death for many families. She's been recognized with the Rare Impact Award from NORD, is a member of the National Academy of Medicine, and is a leading voice on the ethics of genomics.But titles and accolades only tell part of her story. What stands out most is her deep commitment to the people behind the science, the families living day in and day out with conditions that most of the world has never heard of.When we spoke, Dr. Chung described what she calls the “triple threat” to the rare disease ecosystem:Misinformation in health that spreads faster than facts and erodes trust in science.Lack of access to healthcare, leaving too many without the treatments they need, when they need them.Insufficient investment in research, slowing the pace of discovery and delaying life-saving therapies.Each of these challenges is daunting on its own, but together they create a fragile and often hostile environment for progress in rare disease research and care.She pointed out that while most genetic conditions are rare individually, collectively they are surprisingly common — affecting millions worldwide. That's a staggering thought, especially considering how little public awareness and funding rare diseases often receive.We also talked about autism, a condition she has studied extensively. She emphasized that autism is a spectrum, with multiple causes, the majority of which are genetic. Understanding that complexity is crucial, not only for advancing science but also for helping families cope and make informed decisions.One of the threads running through our conversation was the urgent need for better communication in science. In an age where misinformation spreads in seconds, the ability to convey facts clearly and accessibly isn't just a nice skill — it's a necessity. Miscommunication or confusion doesn't just impact public opinion; it influences policy decisions, research funding, and the direction of healthcare itself.Dr. Chung stressed that advocacy matters at every level — from the conversations parents have with their children's doctors to the policies shaped in Washington. Community engagement isn't just a feel-good idea; it's one of the most effective ways to accelerate progress. Patients, families, scientists, and policymakers all have a role to play, and collaboration among them is where breakthroughs happen.In the end, our conversation left me with two truths. First, that rare disease progress depends on persistence from so many people. The researchers who refuse to give up, from families who continue to fight for answers, and from advocates who push for change. Second, that truth itself is a kind of medicine. The more accurately, compassionately, and consistently we can communicate about rare diseases, the better chance we have at building a healthcare ecosystem that works for everyone.Dr. Wendy Chung is leading that charge, not just in the lab, but in the public square. And in this fight, both matter equally. Please like, subscribe, and comment on our podcasts!Please consider making a donation: https://thebonnellfoundation.org/donate/The Bonnell Foundation website:https://thebonnellfoundation.orgEmail us at: thebonnellfoundation@gmail.com Watch our podcasts on YouTube: https://www.youtube.com/@laurabonnell1136/featuredThanks to our sponsors:Vertex: https://www.vrtx.comViatris: https://www.viatris.com/en

It is a challenge to place others interests above our own. Listen in as Paul explains why this is an important factor in the way God wants us to encourage one another. Visit: abideatascadero.orgEmail: info@abideatascadero.orgInstagram: @abide.calvary_atascFacebook: @AbideCalvaryAtascadero

Our Harvest of Hope Gala was unforgettable—so much love, energy, and sparkle! The theme this year was Diamonds and Denim, and the outfits did not disappoint.Huge thanks to our co-chair, Heather Trammell. Heather is not only a CF mom but also a source of wisdom and support in our community. She did an amazing job organizing the Gala and has already committed to leading again in 2026. Heather and her husband Chris (who, fun fact, is now best friends with Joe Bonnell) bring so much heart to our mission.We were also grateful to have Tara Fahrner with us. Tara is a CF mom to 2½-year-old Beau, who was diagnosed at birth through newborn screening. Tara describes the diagnosis as a shock, but she's thankful for the strong CF community that has surrounded her family. She and Heather both serve on the Quality Improvement Team at the University of Michigan as well as our Advisory Board.And a big shout-out to Dave Ingraham, who traveled three hours from Lake City, Michigan, to be at the Gala. Dave's truck is wrapped with The Bonnell Foundation logo and QR code, and he drives it in parades to spread awareness. He's fully embraced his granddaughter Briar Lynn's journey with CF, supporting both her and his daughter, a single mom. His dedication is inspiring. Please like, subscribe, and comment on our podcasts!Please consider making a donation: https://thebonnellfoundation.org/donate/The Bonnell Foundation website:https://thebonnellfoundation.orgEmail us at: thebonnellfoundation@gmail.com Watch our podcasts on YouTube: https://www.youtube.com/@laurabonnell1136/featuredThanks to our sponsors:Vertex: https://www.vrtx.comViatris: https://www.viatris.com/en

God wants to work an on-going process of faith in us, by His power. This week's passage highlights some specific ways God can help us reflect His character more.Visit: abideatascadero.orgEmail: info@abideatascadero.orgInstagram: @abide.calvary_atascFacebook: @AbideCalvaryAtascadero

Were the Flood waters filled with chemical contamination? Did Noah and company leave the ark to find a world poisoned with toxic sludge? In their latest episode, Todd and Paul chat with chemist Aaron Hutchison about the toxic elements arsenic and mercury. Dr. Hutchison explains his research on these dangerous elements and what would have happened to them during the Flood. Listen in and find out how the Lord preserved us from toxic contamination!Materials mentioned in this episodeHutchison, A.R. Mercury and the Genesis Flood: a response to Morton, pp.31-33 in: Hutchison, A.R. and J.H. Whitmore (eds), Proceedings of the First Conference on Creation Geology (Creation Research Science Education Foundation, Columbus, OH).Hutchison, A.R. 2009. Mercury toxicity and the Genesis Flood, pp.29-44 in: Oard, M.J. and J.K. Reed (eds), Rock Solid Answers (Master Books, Green Forest, AR). https://assets.answersingenesis.org/doc/articles/am/v5/n2/rock-solid-answers-ch3.pdfHutchison, A. 2010. Did mercury poisoning create a toxic Flood? Answers 5(2):70-73. https://answersingenesis.org/the-flood/did-mercury-poisoning-create-a-toxic-flood/Hutchison, A.R. and C. Bortel. 2018. The fate of arsenic in Noah's Flood, pp.229-237 in: Whitmore, J.H. (ed), Proceedings of the Eighth International Conference on Creationism (Creation Science Fellowship, Pittsburgh, Pennsylvania).https://digitalcommons.cedarville.edu/cgi/viewcontent.cgi?article=1037&context=icc_proceedingsHutchison, A. 2021. A Flood of arsenic. Answers 16(2):30-32. https://answersingenesis.org/chemistry/flood-arsenic/

If you've ever been part of the cystic fibrosis community, you've probably heard of the sweat chloride test, maybe you've even had one yourself. But what does that test really measure, and why does it still matter in the age of CF modulators?Laura talks with Dr. Patrick Sosnay, Vice President and Head of CF Development at Vertex Pharmaceuticals. Before joining Vertex, Dr. Sosnay was a clinician and researcher at Johns Hopkins, where he helped define the genetic criteria for diagnosing CF and co-founded the influential CFTR2 database.Dr. Sosnay brings his expertise, and a gift for explaining complex science.  He unpacks the real story behind sweat chloride testing. Together, we explore:* What the sweat test actually measures — and how it connects to the CFTR protein.* Why sweat chloride is still vital long after diagnosis.* How researchers use it to track CF progression and measure treatment success.* What all this means for people living with CF and their families today.This episode redefines the sweat chloride test as more than just a diagnostic number, it's a powerful marker of health, innovation, and hope for the future.Listen now and gain a fresh perspective on one of the most familiar, yet evolving  parts of cystic fibrosis care.(Vertex is a sponsor of this podcast. The Bonnell Foundation remains committed to transparent, balanced conversations that serve the CF community first.)Additionaly we explore:What the sweat test measures and how it's tied to the CFTR protein (cystic fibrosis transmembrane conductance regulator).Why sweat chloride remains important well beyond diagnosis.How researchers use it to understand CF progression and evaluate new treatments.What this means for families and patients living with CF every day.This episode shares the reframing of the sweat chloride test, not as a simple number, but as a meaningful marker of health, research, and hope for the future. Please like, subscribe, and comment on our podcasts!Please consider making a donation: https://thebonnellfoundation.org/donate/The Bonnell Foundation website:https://thebonnellfoundation.orgEmail us at: thebonnellfoundation@gmail.com Watch our podcasts on YouTube: https://www.youtube.com/@laurabonnell1136/featuredThanks to our sponsors:Vertex: https://www.vrtx.comViatris: https://www.viatris.com/en

To celebrate the 400th episode of the SFN Dad To Dad Podcast, David Hirsch, founder of 21st Century Dads Foundation and host of the SFN Dad To Dad Podcast offers his heartfelt thanks to all those who have been involved with and supported 21CD & SFN.  He reflects on:addressing the issue of father absence in society,his journey as a fatherhood advocate,starting the Illinois Fatherhood Initiative, making an appearance on the Oprah Winfrey Show, starting the 21st Century Dads Foundation, Dads Honor Ride 2015 from Santa Monica to Chicago, 2,325 miles in 21 days, giving a TEDx Talk entitled: Why We Need To Break The Cycle Of Father Absence, writing the book: A Father's Journey To Break The Cycle Of Father Absence, Dads Honor Ride 2016 from Boston to Chicago, 1,400 miles in 21 days, Creating the C2EFA (Cycle To End Father Absence) indoor riding events, Dads Honor Ride 2017 Around Lake Michigan, 958 miles in 9 days, creating the Special Fathers Network Mentoring Program, starting the SFN Dad To Dad Podcast, recording 24 bi-weekly Zoom calls on various topicscreating the 21CD YouTube channel,holding annual SFN Dads Virtual Conferences, creating the SFN audiobook series, creating the weekly virtual SFN Mastermind Group experience, andholding annual SFN Mastermind Group weekend retreatsSpecial thanks to all the individuals, businesses, and foundations that have financially supported 21CD, the growing list of partners and affiliates, all the individuals who have volunteered, especially the 21CD board of directors: Tom Costello, Rich Gathro, Gary Grube, Chris Hunter, Shane Madden, Wayne Messmer, Brian Page and John Shouse.  Special thanks to Shane Madden for creating the SFN fathers jingle at teh beginning and end of this episode.  And last but not least, Tom Couch of Couch Media, who has produced the past 398 episodes of the SFN Dad To Dad Podcast. Show Notes –   Email - david@21stCenturyDads.orgEmail - tcouch2501@gmail.comWebsite - https://21stcenturydads.org/  TEDx Talk -  https://www.youtube.com/watch?v=7CDeMgmeb94Special Fathers Network - SFN is a dad to dad mentoring program for fathers raising children with special needs. Many of the 500+ SFN Mentor Fathers, who are raising kids with special needs, have said: "I wish there was something like this when we first received our child's diagnosis. I felt so isolated. There was no one within my family, at work, at church or within my friend group who understood or could relate to what I was going through."SFN Mentor Fathers share their experiences with younger dads closer to the beginning of their journey raising a child with the same or similar special needs. The SFN Mentor Fathers do NOT offer legal or medical advice, that is what lawyers and doctors do. They simply share their experiences and how they have made the most of challenging situations.21CD YouTube Channel: https://www.youtube.com/@21stcenturydads58/videosClick Here to donate: https://21stcenturydads.org/donate/Special Fathers Network: https://21stcenturydads.org/SFN Dads Mastermind Group - https://21stcenturydads.org/sfn-mastermind-group/

Our attitude is a crucial part of allowing God's love to work through us to help us in our human relationships, even in the church. Listen to hear how Paul instructs us to live like Christ in this.Visit: abideatascadero.orgEmail: info@abideatascadero.orgInstagram: @abide.calvary_atascFacebook: @AbideCalvaryAtascadero

When Pete Proimos decided to share his cystic fibrosis story at 40, after decades of silence , it marked a turning point. That decision, guided by his philosophy “Out at 40,” sparked a movement built on honesty, empathy, and empowerment.Today, as CEO of the Filotimo Foundation, Pete is redefining what it means to thrive with an invisible illness and helping others find strength in their own stories.Pete is a tireless advocate for people living with cystic fibrosis. Diagnosed at birth, Pete has spent his life navigating the challenges of CF—while rewriting the narrative of what it means to truly thrive with a chronic, invisible illness.Through the Filotimo Foundation, Pete has built a strong network of support for individuals and families—while breaking down the stigma surrounding conditions you can't always see.Whether you live with CF, love someone who does, or simply care about creating a more compassionate world, Pete's story will inspire you.To learn more about Pete's Foundation; https://filotimofoundation.org  Please like, subscribe, and comment on our podcasts!Please consider making a donation: https://thebonnellfoundation.org/donate/The Bonnell Foundation website:https://thebonnellfoundation.orgEmail us at: thebonnellfoundation@gmail.com Watch our podcasts on YouTube: https://www.youtube.com/@laurabonnell1136/featuredThanks to our sponsors:Vertex: https://www.vrtx.comViatris: https://www.viatris.com/en

The Education Concierge Podcast - Season 10Stop Being a Fire Extinguisher: How School Pulse is Building Mental Fitness in SchoolsHost: Benita G.Guest: Yuri, Founder of School PulseAfter witnessing seven student suicides in his community, clinical social worker Yuri created School Pulse to shift schools from reactive crisis mode to proactive prevention. In this conversation, we explore why mental fitness matters more than crisis intervention and how text-based support with real people is transforming student wellbeing.You'll hear about:Why waiting for crisis isn't working and how to build protective factors insteadThe 5:1 ratio: students need 5 positive interactions for every 1 negative to thriveHow School Pulse sends proactive texts twice weekly with live support respondingNavigating cultural barriers to mental health in ethnic communitiesThe "two-touch" solution that helps schools without adding educator workloadKey Quote: "Your psychology is everything. The way you perceive things matters more than the things themselves."Connect with Yuri:>Here is a  2-minute video that quickly summarizes service and how schools deploy our incredible strategiesHere is a link to all of our extraordinary VIDEOS that listeners can use with their teensHere is a link to the most comprehensive MENTAL HEALTH RESOURCE PAGE in the country, that we created and deliver to every school, parent, and student.Links to my books: SchoolPulse: www.schoolpulse.orgKnow Thy Selfie - t.ly/juUMBMind Over Grey Matter - t.ly/SxNUUWebsite: schoolpulse.orgEmail: yuri@schoolpulse.orgConnect with Benita: Follow The Education Concierge Podcast on all platforms Season 10: Legacy in ProgressDon't forget to like, share, subscribe, and most importantly - go do something.Tags: #MentalHealth #StudentWellness #SchoolCounseling #PreventionMatters #EducationInnovation #MentalFitness #ProactiveSupport

Everyone says that Genesis 2 contradicts Genesis 1! Could everyone be wrong? Join Paul and Todd as they discuss the alleged problems with Genesis 2 in this latest episode in our Creationism 101 series. From the name of God to the creation of birds, Todd and Paul take on eight contradictions and find most of them wanting. The detailed creation of Adam is definitely different from the creation week, but rumors of contradiction are greatly exaggerated.Materials mentioned in this episodeCameron, N.M. de S. 1980. The unity and harmony of Genesis 1-3. Biblical Creation 6: 37-44. https://biblicalcreationtrust.org/pdf/biblical-creation-02-06_the_unity_and_harmony_of_genesis_1-3_37-44.pdf

Turning Diagnosis into Purpose: Deana and Liam's MissionWhen Liam was diagnosed with cystic fibrosis (10 years ago) at just three weeks old, Deana's world shifted overnight. What began as one mother's fight for her child has grown into a movement empowering families, educators, and kids facing chronic illness, all through courage, creativity, and hope.From bestselling advocacy workbooks to emotional wellness initiatives, Deana and Liam are transforming personal challenges into meaningful change. You'll hear how storytelling became their most powerful tool, and why their message, hope is louder, is resonating far beyond the CF community.In this episode, we talk about:How The Ultimate CF Family Workbook came to lifeThe importance of storytelling in chronic illnessTheir upcoming children's book and animated series, Liam's ChroniclesHow they're changing the conversation around invisible illnessLearn more about their work or grab a workbook: [Insert Website or Linktree]Available on Amazon + EtsyFeatured by hospitals like SickKids and CHEOConnect with Deana & Liam:FB: Facebook.com/liamsmission00To order: www.liamsmission.ca IG: Instagram.com/liamsmission Please like, subscribe, and comment on our podcasts!Please consider making a donation: https://thebonnellfoundation.org/donate/The Bonnell Foundation website:https://thebonnellfoundation.orgEmail us at: thebonnellfoundation@gmail.com Watch our podcasts on YouTube: https://www.youtube.com/@laurabonnell1136/featuredThanks to our sponsors:Vertex: https://www.vrtx.comViatris: https://www.viatris.com/en

God wants to equip us in our faith by being in unity with other believers, standing together without fear when we encounter those who oppose us. Please join us as we listen to some of the ways He wants to help us to do this.Visit: abideatascadero.orgEmail: info@abideatascadero.orgInstagram: @abide.calvary_atascFacebook: @AbideCalvaryAtascadero

I had the joy of meeting Heather Ashle in person at a Family Night hosted by Children's Hospital of Michigan a couple months ago. Her energy lit up the room as she spoke—honestly, nervously, and beautifully, about what it means to live with cystic fibrosis (CF). It was her first time speaking at a CF event, and you could feel how much it meant to her.Heather grew up finding refuge in fantasy, books filled with dragons, magic, and faraway worlds. While CF demanded hours of treatment each day, her imagination offered something far more powerful: freedom. “Fantasy wasn't just fun—it was survival. In worlds of dragons and magic, I could breathe easier.” — Heather AshleNow, with two English degrees from Oakland University, Heather continues crafting those very stories. She writes with the hope of giving others what fantasy once gave her: wonder, empathy, and a temporary escape from the weight of reality.You can find Heather wherever imagination thrives—on the page, on stage, at Ren Fests, or in magical corners of our community like Witches' Bazaars. She is pure magic.Fantasy Author of the Realm Riders Series www.heatherashle.comFor links to Heathers author social media and where her books are available: www.heatherashle.com/linktree Publishing via HB Ink, LLC www.hbinkllc.com  And https://www.facebook.com/HBInkLLC/Also: https://www.instagram.com/hbinkpublisher/ Please like, subscribe, and comment on our podcasts!Please consider making a donation: https://thebonnellfoundation.org/donate/The Bonnell Foundation website:https://thebonnellfoundation.orgEmail us at: thebonnellfoundation@gmail.com Watch our podcasts on YouTube: https://www.youtube.com/@laurabonnell1136/featuredThanks to our sponsors:Vertex: https://www.vrtx.comViatris: https://www.viatris.com/en

God wants to grow our faith even in difficult circumstances. This week's passage shows how He works this transforming process in us, with a balance of love, knowledge and discernment. Visit: abideatascadero.orgEmail: info@abideatascadero.orgInstagram: @abide.calvary_atascFacebook: @AbideCalvaryAtascadero

We often hear the claim that creationism is a recent theological error, but there have been young age creationists for most of the history of the church. In this episode, Todd and Paul chat with Warren Johns about the Scriptural Geologists, a group of creationists active during the earliest growth of the science of geology. Back before geologists were geologists, there were still creationists holding the faith! Learn all about them in this week's episode of Let's Talk Creation!Materials mentioned in this episodeJohns, Warren H. “Scriptural Geology, 1820-1860: An Essay and Review.” Origins, no. 62 (Jan. 1, 2008). Online link: https://www.grisda.org/origins-62042Johns, Warren H. “Scriptural Geology, Then and Now.” Answers Research Journal, vol. 9 (2016). Online link: Scriptural Geology, Then and NowMortenson, Terry. 2004. The Great Turning Point. https://a.co/d/9xeZ6i2Young, George, and John Bird. 1822. A Geological Survey of the Yorkshire Coast. http://www.biodiversitylibrary.org/title/44925.Haber, Francis. 1959. Age of the World: Moses to Darwin. https://a.co/d/hMgPjS4The list of Terry Mortenson's articles on the scriptural geologists are found at the bottom of his biography hosted by Creation Ministries International.https://creation.com/en/people/dr-terry-mortensonNelson, Byron. 1931. The deluge story in stone: A history of the flood theory of geology. https://creation.com/en/people/dr-terry-mortensonMcIver, Tom. 1992. Anti-Evolution: A Reader's Guide to Writings Before and After Darwin. https://a.co/d/h0sFClc

The unstoppable Jennifer Dunlea is an advocate, a fighter, and an all-around powerhouse. Born with Cystic Fibrosis, Jen has faced more medical battles than most people do in a lifetime, including surviving a rare cancer at just 23 years old. She's a two-time double lung transplant recipient, living with diabetes and gastroparesis, and still somehow finds the energy to raise her voice, and awareness, for the CF and transplant communities every single day. You might know her from social media, where she shares her journey with honesty, humor, and heart under the handle @jencantbreathe on TikTok, Instagram, YouTube, and Facebook.Trust me, you're going to be inspired by this conversation.To follow Jen: @jencantbreatheCOTA health fundraising campaign: https://cota.org/cotaforjenslungs/our-story/The Sick Chick Hour: https://open.spotify.com/show/7eegd1SwLueAnrxueC7VVeYoutube for Jen: https://youtube.com/@jencantbreathe?si=QXrvZniAYTwjmv2v     Please like, subscribe, and comment on our podcasts!Please consider making a donation: https://thebonnellfoundation.org/donate/The Bonnell Foundation website:https://thebonnellfoundation.orgEmail us at: thebonnellfoundation@gmail.com Watch our podcasts on YouTube: https://www.youtube.com/@laurabonnell1136/featuredThanks to our sponsors:Vertex: https://www.vrtx.comViatris: https://www.viatris.com/en

Hard circumstances are common in this life and the Philippian church was in need of God-given encouragement and direction. Paul gives these and all believers reasons to trust a faithful God to supply the joy and contentment needed to navigate any trial.Visit: abideatascadero.orgEmail: info@abideatascadero.orgInstagram: @abide.calvary_atascFacebook: @AbideCalvaryAtascadero

As member firm activity increases in blockchain and crypto assets, FINRA is launching a Crypto and Blockchain Education Program designed to empower member firm compliance and combat crypto fraud by broadening the knowledge base of member firms and associated persons. On this episode, FINRA's Crypto Hub Chief Jason Foye, Director of Critical Skills and Capabilities Training Rowan Job-White and Director of Continuing Education Services Genay Glasgo delve into the program's self-paced e-learning courses and an upcoming in-person training.Resources mentioned in this episode:FINRA Crypto and Blockchain Education ProgramFinancial Learning ExperienceEmail: cryptoed@finra.orgEmail: flex@fina.orgKey Topics: Crypto AssetsSEC Crypto Task ForcePodcast: An Introduction to FINRA's Crypto Asset Work and the Crypto HubCertified Regulatory and Compliance Professional ProgramBlog Post: FINRA Forward Find us: LinkedIn / X / YouTube / Facebook / Instagram / E-mailSubscribe to our show on Apple Podcasts, Google Play and by RSS.

The Chosen Part 5: God's TimingBill CorleyOriginal Air Date: 2025.09.14Thanks for checking us out!Join us and invite a friend for our new series, “The Chosen”.Service TimesSaturday Night: 5:30pmSunday Morning: 10:30amSunday Morning Bible Study: 9:30amWatch Service the Following Week Via: App, Website, or YouTubeChristian Education for Our KidsPromiseland: Sunday 10:30amYouth Sunday School: 10:30am 6th and upOffice HoursClosed Monday and TuesdaysWednesday 10am - 1pm and 2pm -4pm and Thursday and Friday 10am – 4pmDo You have questions about God, the Bible, church? How about a question about our current series? Text your question in to 760-301-4840 and we may be able to answer them during our next message. You can even text in during our Saturday night service and we will answer them.We provide free counselling: marriage, family, financial, and pre-marital, Homeless assistance, fuel cards, and family support. Please contact our office at 760-384-3333 for any questions.Visit and explore our website: www.crossroads-ridgecrest.orgEmail us: ccc@ccc-rc.org

Prayer is a topic easily misunderstood but is a huge part of our spiritual life. In this passage, Paul encourages us to act in the discipline of prayer allowing God to rejuvenate our faith.Visit: abideatascadero.orgEmail: info@abideatascadero.orgInstagram: @abide.calvary_atascFacebook: @AbideCalvaryAtascadero

The challenges and triumphs of living with a rare disease. Leslie Baldwin shares her personal journey with Common Variable Immune Deficiency and Ehlers-Danlos Syndrome. You'll hear what fueled her passion for advocacy and the creation of Michigan Rare (MI-RARE). Together, they discuss the power of community, the importance of patient empowerment, and how collaboration with policymakers can expand access and resources for those living with rare conditions.TakeawaysAdvocacy is essential for the rare disease community.Building connections provides vital support.Patients should feel empowered to speak up for their health.Collaboration with policymakers can drive positive change.Storytelling inspires and unites the community.Engagement raises awareness and strengthens support networks.Advocacy days introduce rare disease issues to lawmakers.Recognizing unique challenges leads to better understanding.Coalitions amplify the collective voice of rare disease advocates.Empowering patients and caregivers enhances quality of life.About Leslie BaldwinA Michigan native now living in Holt, Leslie is a rare disease advocate. She co-founding MI-RARE, a foundation uniting rare disease voices across Michigan, alongside Kayla Miller, Kathi Luis, Kortney Lee, Chris Draper, and Laura Bonnell.Her advocacy experience is wide-ranging: she has worked with Autism Speaks, National Organization for Rare Disorders (NORD), The EveryLife Foundation, NIH, CMS, and the FDA. As Director of Strategic Advancement with Texas Rare Alliance, she helped pass key legislation that earned her national recognition as a finalist for the 2023 Rare Voice Award in State Advocacy.On September 30th, MI-RARE will host the Michigan Rare Disease State Advocacy Day at the Capitol, a powerful opportunity for patients, families, and caregivers to share their stories with lawmakers and demonstrate that while each condition may be rare, together we are many.To connect go to: MI-rare.org Register for Advocacy Day opens August 4th and ends September 12th, 2025.  There is a travel stipend too. Go to the MI-Rare website.To connect with Leslie Baldwin: leslie@mi-rare.org Please like, subscribe, and comment on our podcasts!Please consider making a donation: https://thebonnellfoundation.org/donate/The Bonnell Foundation website:https://thebonnellfoundation.orgEmail us at: thebonnellfoundation@gmail.com Watch our podcasts on YouTube: https://www.youtube.com/@laurabonnell1136/featuredThanks to our sponsors:Vertex: https://www.vrtx.comViatris: https://www.viatris.com/en

The Chosen Part 4: Jesus is a Real PersonDionne SalmondsOriginal Air Date: 2025.09.07Thanks for checking us out!Join us and invite a friend for our new series, “The Chosen”.Service TimesSaturday Night: 5:30pmSunday Morning: 10:30amSunday Morning Bible Study: 9:30amWatch Service the Following Week Via: App, Website, or YouTubeChristian Education for Our KidsPromiseland: Sunday 10:30amYouth Sunday School: 10:30am 6th and upOffice HoursClosed Friday – MondayTuesday and Thursday 10am – 4pmWednesday 1pm & 2pm – 4pmDo You have questions about God, the Bible, church? How about a question about our current series? Text your question in to 760-301-4840 and we may be able to answer them during our next message. You can even text in during our Saturday night service and we will answer them.We provide free counselling: marriage, family, financial, and pre-marital, Homeless assistance, fuel cards, and family support. Please contact our office at 760-384-3333 for any questions.Visit and explore our website: www.crossroads-ridgecrest.orgEmail us: ccc@ccc-rc.org

Miss America 2025 Abbie Stockard: A Champion for Kids, Health, and Cystic FibrosisAbbie Stockard, Miss America 2025, joins us to share her incredible journey, from Auburn University nursing student and Tiger Paws dancer to national advocate and role model. At just 22, Abbie has earned over $89,000 in scholarships through the Miss America Opportunity and is using her platform to promote pediatric health, women's leadership, and awareness for cystic fibrosis (CF).Inspired by her best friend Maddie, Abbie has raised over $200,000 for CF research and was honored as the Cystic Fibrosis Foundation's “2024 Hero of Hope.” She also created High Five for Kids, a wellness program that empowers children—including those with chronic illnesses, to build healthy habits for life.In this episode, Abbie talks about balancing school, service, and advocacy, and how she's using her voice to drive real change in healthcare and beyond. Don't miss this inspiring conversation with a young woman leading with heart, purpose, and unstoppable energy. Please like, subscribe, and comment on our podcasts!Please consider making a donation: https://thebonnellfoundation.org/donate/The Bonnell Foundation website:https://thebonnellfoundation.orgEmail us at: thebonnellfoundation@gmail.com Watch our podcasts on YouTube: https://www.youtube.com/@laurabonnell1136/featuredThanks to our sponsors:Vertex: https://www.vrtx.comViatris: https://www.viatris.com/en

This week, God reminds us that we are not left to live the life of faith in our own strength. Through His Holy Spirit given at salvation, He equips and protects us, to give us everything we need to stand in the truth of His word.Visit: abideatascadero.orgEmail: info@abideatascadero.orgInstagram: @abide.calvary_atascFacebook: @AbideCalvaryAtascadero

Obedience is difficult for all of us when someone asks us to do something, but what about when it is God asking? In this week's message, we learn some of the reasons & benefits to obey God.Visit: abideatascadero.orgEmail: info@abideatascadero.orgInstagram: @abide.calvary_atascFacebook: @AbideCalvaryAtascadero

Dean Dayna Bowen Matthew, legal scholar, author, and Dean of The George Washington University Law School, delivers a compelling examination of how bias, both implicit and structural, continues to shape health outcomes in America. Drawing on decades of work at the intersection of civil rights and healthcare, she explains how inequities in housing, education, and employment are compounded by biases in medical decision-making, access, and policy enforcement.From the legacy of redlining to the subtle ways patient care can be influenced by race, ethnicity, and socioeconomic status, Dean Matthew makes the case that health equity cannot be achieved without confronting bias head-on. This episode is a call to action for healthcare providers, policymakers, and community leaders to recognize their role in dismantling these barriers and to commit to systemic change. As our Season 3 opener, it sets the tone for a series dedicated to breaking down inequity at its roots.-AT L.A.S.T.Website: WeAreATLast.orgEmail: adam.cady@weareatlast.orgSupport: https://secure.givelively.org/donate/athletic-trainers-leveraging-activism-for-social-transformationLinkedIn: https://www.linkedin.com/company/at-l-a-s-tInstagram: https://www.instagram.com/atlastpod35% OFF Thorne Products compliments of http://raincrosshp.com/ go to https://thor.ne/Ch2Uc20% OFF Xcelerated Recovery products: Code Rain20: https://xrscience.org/-Artwork by Jason Eisenberg Instagram: https://www.instagram.com/dots_and_squares/LinkedIn: https://www.linkedin.com/in/jasoneisenberg00/-Music by Willie B the Ichiban DonInstagram: https://www.instagram.com/ichibandon/LinkedIn: https://www.linkedin.com/in/william-brown-25945b168/-Production / Engineering / Editing / by Gerson SandovalWebsite: www.davyrover.comInstagram: https://www.instagram.com/davy.rover/LinkedIn: https://www.linkedin.com/in/gersonsandovalengineer/Music Credits: Davy Rover, West Coast Bop-GuestWebsite: https://www.law.gwu.edu/dayna-bowen-matthewLinkedIn:

The Chosen Part 3: Real PeopleBill CorleyOriginal Air Date: 2025.08.30Thanks for checking us out!Join us and invite a friend for our new series, “The Chosen”.Service TimesSaturday Night: 5:30pmSunday Morning: 10:30amSunday Morning Bible Study: 9:30amWatch Service the Following Week Via: App, Website, or YouTubeChristian Education for Our KidsPromiseland: Sunday 10:30amYouth Sunday School: 10:30am 6th and upOffice HoursClosed Friday – MondayTuesday and Thursday 10am – 4pmWednesday 1pm & 2pm – 4pmDo You have questions about God, the Bible, church? How about a question about our current series? Text your question in to 760-301-4840 and we may be able to answer them during our next message. You can even text in during our Saturday night service and we will answer them.We provide free counselling: marriage, family, financial, and pre-marital, Homeless assistance, fuel cards, and family support. Please contact our office at 760-384-3333 for any questions.Visit and explore our website: www.crossroads-ridgecrest.orgEmail us: ccc@ccc-rc.org

What if a scan could do more than show you a picture, what if it could tell you a story about what's happening inside a child's body, in real time?That's exactly what Dr. Chris Flask is working to make possible.Dr. Flask is a Professor of Radiology, Biomedical Engineering, and Pediatrics at Case Western Reserve University and University Hospitals of Cleveland. He's at the forefront of an exciting transformation in medical imaging, one that could change the way we care for children with rare genetic diseases like cystic fibrosis (CF) and polycystic kidney disease (PKD).“Our goal is to turn imaging, instead of just image creation, into data,” says Dr. Flask. “We want to create numbers. So we can say, this is what's going on in the lungs. And when we put these patients on modulator therapies, we can see a 10 percent improvement in their lung disease. And similar responses in the pancreas, the liver, and the gut. That's our goal—quantifying it through this fingerprinting methodology.”This approach, MRI fingerprinting, is a revolutionary leap forward. Developed over the past decade at Case Western's MRI center, it's fast, accurate, and most importantly for kids: it requires no sedation, no radiation, and no contrast agents. Each image slice takes just 15 seconds, making it safer and more accessible for the most vulnerable patients.Dr. Flask's work is supported by the NIH, the Cystic Fibrosis Foundation, and an extraordinary 42-year collaboration with Siemens MRI. Together, they're paving the way for multi-center clinical trials using this technology to better understand disease progression and therapy outcomes.This episode is all about the intersection of science, innovation, and compassion, and the powerful impact of data-driven care.We're honored to welcome Dr. Flask to the show, although he prefers we call him Chris. You won't want to miss this deep dive into what's next for pediatric imaging and precision medicine.Share with anyone who's passionate about medical innovation, pediatric health, or rare disease research. Please like, subscribe, and comment on our podcasts!Please consider making a donation: https://thebonnellfoundation.org/donate/The Bonnell Foundation website:https://thebonnellfoundation.orgEmail us at: thebonnellfoundation@gmail.com Watch our podcasts on YouTube: https://www.youtube.com/@laurabonnell1136/featuredThanks to our sponsors:Vertex: https://www.vrtx.comViatris: https://www.viatris.com/en

The Chosen Part 2: I Choose YouBrad HarlowOriginal Air Date: 2025.08.24Thanks for checking us out!Join us and invite a friend for our new series, “The Chosen”. Service TimesSaturday Night: 5:30pmSunday Morning: 10:30amSunday Morning Bible Study: 9:30amWatch Service the Following Week Via: App, Website, or YouTube Christian Education for Our KidsPromiseland: Sunday 10:30amYouth Sunday School: 10:30am 6th and up Office HoursClosed Friday – MondayTuesday and Thursday 10am – 4pmWednesday 1pm & 2pm – 4pmDo You have questions about God, the Bible, church? How about a question about our current series? Text your question in to 760-301-4840 and we may be able to answer them during our next message. You can even text in during our Saturday night service and we will answer them.We provide free counselling: marriage, family, financial, and pre-marital, Homeless assistance, fuel cards, and family support. Please contact our office at 760-384-3333 for any questions.Visit and explore our website: www.crossroads-ridgecrest.orgEmail us: ccc@ccc-rc.org

What purpose does Christ have for marriage? We learn that through the earthly example of marriage, Jesus wants to show us the relationship He desires with each of us.Visit: abideatascadero.orgEmail: info@abideatascadero.orgInstagram: @abide.calvary_atascFacebook: @AbideCalvaryAtascadero

In this episode Gary Mansfield speaks to Helen Starr (@themechatroniclibrary) Helen Starr, a Trinidadian artist and activist, is known for blending digital technology with cultural storytelling. She explores identity, indigeneity, and spirituality through immersive art, often using virtual and augmented reality. Helen advocates for inclusivity in the arts, challenging colonial narratives and amplifying marginalised voices. Her work connects Caribbean heritage with future-facing media, fostering dialogue on community, environment, and social justice while reimagining how technology shapes human experience. To Support this podcast from as little as £3 per month: www.patreon/ministryofarts For full line up of confirmed artists go to https://www.ministryofarts.orgEmail: ministryofartsorg@gmail.comSocial Media: @ministryofartsorg Hosted on Acast. See acast.com/privacy for more information.

The Chosen Part 1: We Are All ChosenBill CorleyOriginal Air Date: 2025.08.16Join us and invite a friend for our new series, “The Chosen”.Service TimesSaturday Night: 5:30pmSunday Morning: 10:30amSunday Morning Bible Study: 9:30amWatch Service the Following Week Via: App, Website, or YouTubeChristian Education for Our KidsPromiseland: Sunday 10:30amYouth Sunday School: 10:30am 6th and upOffice HoursClosed Friday – MondayTuesday and Thursday 10am – 4pmWednesday 1pm & 2pm – 4pmDo You have questions about God, the Bible, church? How about a question about our current series? Text your question in to 760-301-4840 and we may be able to answer them during our next message. You can even text in during our Saturday night service and we will answer them.We provide free counselling: marriage, family, financial, and pre-marital, Homeless assistance, fuel cards, and family support. Please contact our office at 760-384-3333 for any questions.Visit and explore our website: www.crossroads-ridgecrest.orgEmail us: ccc@ccc-rc.org

“I always say that singing and performing was as much a part of my DNA as cystic fibrosis.” Julia RaeFrom the moment Julia Rae could speak, she was singing, and from the moment she could dream, she was already imagining a bigger stage. As her mother fondly recalls, at just two years old, Julia was watching Barney on TV and asked, “How do I get in there and do that with him?” That instinct, that pull toward performance, was never just about the spotlight. For Julia Rae, the stage became her sanctuary, and later, her platform for purpose.Diagnosed with cystic fibrosis at birth, Julia's life has never followed an easy script. But instead of letting a chronic illness limit her, she embraced the full range of her voice, as a singer, actress, writer, and advocate. She didn't just want to perform; she wanted to make a difference.At 16, Julia founded Singing at the Top of My Lungs, a nonprofit inspired by her own hospital experiences. Initially, the organization supported both CF research and creative therapies at children's hospitals. But as larger institutions took a stronger lead in research, Julia saw a growing gap elsewhere.“I've decided to devote all of Singing at the Top of My Lungs to music and creative art therapies... They are significantly underfunded, not covered by insurance, and they are often, honestly, the unsung heroes of children's hospitals.”Julia's foundation now champions music and art therapies — the very programs that once transformed her own stays in sterile hospital rooms into spaces of joy and creativity. She knows firsthand that healing isn't just about medicine — it's also about expression, play, and being seen as more than your diagnosis.Her own career blossomed when a YouTube performance caught the attention of a Beverly Hills record producer, leading to her single “Be That Girl” being featured in the film The Greening of Whitney Brown. She's since performed the national anthem at major sports arenas, starred in national commercials, and most recently, in the 2024 film Playing Through. Her appearance on ABC's Listen to Your Heart introduced her to a national audience, but she never let fame outshine her mission.In parallel with her artistic pursuits, Julia has become a tireless advocate. She co-created and hosted Making It Matterwith the Boomer Esiason Foundation, currently leads Uncommon Lungs with Vertex Pharmaceuticals, and recently launched a podcast called A Deeper Look, spotlighting bold, thoughtful conversations with inspiring women.Julia Rae is more than a performer, she's a force. Her life is a testament to what happens when passion meets purpose, and when a voice refuses to be silenced by circumstance.For the chronic illness community, and for anyone who's ever been told “you can't” — Julia's story sings a different tune.She's not just making music. She's making it matter. Please like, subscribe, and comment on our podcasts!Please consider making a donation: https://thebonnellfoundation.org/donate/The Bonnell Foundation website:https://thebonnellfoundation.orgEmail us at: thebonnellfoundation@gmail.com Watch our podcasts on YouTube: https://www.youtube.com/@laurabonnell1136/featuredThanks to our sponsors:Vertex: https://www.vrtx.comViatris: https://www.viatris.com/en

In this episode Gary Mansfield speaks to Graeme Messer (@GraemeMesser) Graeme Messer is a London-based multidisciplinary artist whose work spans assemblage, photography, text, and performance. Originally from South Africa, he moved to the UK in the 1980s and built a successful early career in theatre, directing works by Shakespeare and Tennessee Williams, and founding the award-winning company Out of Bounds.Since 2010, Messer has focused solely on visual art, bringing his theatrical flair into the gallery space. Messer's work is often autobiographical, exploring themes such as identity, shame, self-worth, and the complex interplay between vulnerability and resilience. He is known for his distinctive mirror pieces—vintage mirrors etched with bold, confrontational or affirming text, illuminated with LED lighting. These works prompt viewers to reflect—both literally and metaphorically—on themselves and the world around them. Messer continues to push boundaries, using art as a means to question, provoke, and connect. For more information on the work of Graeme Messer go tohttps://www.Graeme Messer.com To Support this podcast from as little as £3 per month: www.patreon/ministryofarts For full line up of confirmed artists go to https://www.ministryofarts.orgEmail: ministryofartsorg@gmail.comSocial Media: @ministryofartsorg Hosted on Acast. See acast.com/privacy for more information.

Never Just Surviving: Sophie Holmes on Running 36 Marathons with Cystic FibrosisDespite a schedule packed with training, advocacy, and breaking world records, Sophie Holmes of the U.K. always makes time to share her story, and we're so grateful she did.Diagnosed with cystic fibrosis at just four months old, Sophie was told she might not live past her teens. But rather than letting that define her, she's spent her life rewriting the narrative. Her latest, jaw-dropping accomplishment? Running 36 marathons in 36 days. That's right—36 consecutive days, 26.2 miles each day, driven by pure determination and an unshakable belief in what's possible.Sophie is not only an elite athlete and personal trainer, she's a powerful advocate for chronic illness awareness. In this episode of the Living with Cystic Fibrosis podcast, she talks about what fueled her through each grueling mile, how she manages the intense physical demands of endurance sports while living with CF.“Mindset is everything.” – Sophie HolmesIt's easy to say that exercise is one of the best things someone with CF can do. But Sophie reminds us: that doesn't mean it's easy. Her story is a powerful example of grit, strength, and living fully—even when the odds are stacked against you.Sophie's Story:Diagnosed with cystic fibrosis at four months oldTold she might not live past her teenage yearsRan 36 marathons in 36 days, demonstrating her extraordinary enduranceSet a Lake Cuomo Ultra Ironman World RecordBelieves mindset is the key to overcoming life's toughest challengesWorks as a personal trainer and chronic illness advocateRedefines resilience—not just surviving, but thrivingInspires runners, athletes, and anyone living with chronic illnessLives with relentless drive and purposeShows us what's possible when you push beyond the limits others set for youYou can find Sophie Holmes on IG: https://www.instagram.com/sophiegraceholmes/ Please like, subscribe, and comment on our podcasts!Please consider making a donation: https://thebonnellfoundation.org/donate/The Bonnell Foundation website:https://thebonnellfoundation.orgEmail us at: thebonnellfoundation@gmail.com Watch our podcasts on YouTube: https://www.youtube.com/@laurabonnell1136/featuredThanks to our sponsors:Vertex: https://www.vrtx.comViatris: https://www.viatris.com/en

➡ CLICK HERE to send me a text, I'd love to hear what you thought about this episode! Leave your name in the text so I know who it's from! Today on the podcast, I'm talking with Rita Bertrand and Marjorie Moon, the founding members of Milwaukee's very own Threshold Choir. These two women, along with eleven other members of the Milwaukee chapter's choir sing soft, quiet and calming songs, in harmony, in the rooms of people who are on the threshold. Mostly these are people who are at the threshold of death, but they've also been invited to other thresholds as well, as we talk about on the pod. You might imagine this kind of work as somber or sorrowful, but what we found was something far more hopeful: connection, compassion, and yes — JOY. These women aren't afraid of silence. They bring presence, patience, and the kind of care that asks for nothing in return.

Jeff Cook is a professor of philosophy and co-host of the Around the Circle podcast. He lives in Greeley, Colorado, and is the author of three books, including Around the Circle | An Enneagram Book, available HERE. www.aroundthecircle.orgORDER OUR Hunter, Farmer, and Teamer BOOK: HERE Get Enneagram Certified HERE.www.theartofgrowth.orgEmail us your thoughts and questions! Follow us on Instagram at ArtofGrowth for more on this subject this month and let us know what you are doing. Go to our website to sign up for:Corporate Training  One-on-one coaching  Enneagram Certification    AND MORE...Support the showhttps://www.theartofgrowth.org/Support the showhttps://www.theartofgrowth.org/