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Paul continues his letter of encouragement to his younger son in the faith, Timothy.  Join us as we read and explore practical ways to lead by example in speech, conduct, love, faith, and purity.Visit: abideatascadero.orgEmail: info@abideatascadero.orgInstagram: @abide.calvary_atascFacebook: @AbideCalvaryAtascadero

Rare disease connects more people than many of us realize.  While every diagnosis is unique, the journey often includes many of the same challenges: searching for answers, navigating the healthcare system, advocating for better care, managing complex treatments, and finding hope along the way. Cystic fibrosis is considered a rare disease because it affects fewer than 200,000 people in the United States, just like mitochondrial disease. Although these conditions are different, the experiences of patients and families often have much in common. Our guest is Michael Goldberg, a rare disease patient, advocate, entrepreneur, and author. Michael and I connected on LinkedIn, and I'm so glad he reached out because his story is one that will resonate with anyone whose life has been touched by a rare disease. Michael lives with a rare mitochondrial disease and has turned his personal experiences into a mission to help others. He's the Founder and CEO of 12 Brand | MediXo, a patient-led health technology initiative focused on medication adherence, dosing accuracy, and preventive health. He also helps fund research and community programs. Right by his side is his wife Judi. We talk with her about the challenges about being a caregiver, and how that can change a marriage. They're beautiful marriage and upbeat, positive attitude will inspire you. Michael is also the author of I'll Have Mine Rare and I'll Have Mine Rare: Growing Up Different. In this episode, we talk about advocacy, caregiving, resilience, and why the rare disease community is stronger when we learn from one another. Whether your family is affected by cystic fibrosis or another rare disease, I think you'll find inspiration and encouragement in Michael's journey. To get in touch with Michael Goldberg:  info@medixo.health 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/featuredNew: Shop our merchandise! https://thebonnellfoundation.org/product-shop/Thanks to our sponsors:Vertex: https://www.vrtx.comViatris: https://www.viatris.com/enRead us on Substack: https://substack.com/@lstb?utm_campaign=profile&utm_medium=profile-pageWatch our trailer of Embracing Egypt: https://youtu.be/RYjlB25Cr9Y

Jessie Brown wanted to be a writer. She was an English major doing an MFA in creative nonfiction when she lost both of her parents and realized she had no financial safety net. So she did the practical thing and went to law school.That pattern, choosing the safe path over the one that actually fit, followed her for the next two decades. It picked her practice area. It kept her in litigation long after her body was telling her something was wrong. It even had her enrolled in a backup master's program while she was already building the business she actually wanted.Today Jessie is a coach and retreat facilitator working with attorneys at every stage, from brand new associates to partners planning their exit. She's also a trained forest bathing guide, sound healer, breathwork facilitator, and meditation teacher, and she leads nature-based retreats in Sedona.This conversation is about what it takes to finally stop letting fear pick your life for you.In this episode we cover:Why she chose law school after losing both parents and having no safety netThe senior partner who told a room of young female associates the truth about how she "had it all"The annual review where she offered to resign and was told to hire a second nannyLeaving, staying home, moving across the country, and sitting for a second bar exam on her own dimeThe deposition that made her physically ill and changed her practice areaStepping down from the partner track and taking a pay cut to do work that fit herThe Clifton Strengths result that finally explained why everything felt so hardBeing the unofficial office therapist for her entire career and what it was telling herThe safety-seeking part of her that picks every path, and how she learned to spot itWhat actually happens to a nervous system on a retreat, and why in-person still mattersConnect with Jessie Brown:Website: jessiebrown.orgEmail: jessie@jessiebrown.orgLinkedIn: Jessie BrownPodcast: AlignedWork with Erin Gerner: Erin coaches high-achieving female attorneys who are successful on paper but struggling with burnout, identity, and what's next, helping them redefine success on their own terms.

What does it really mean to be a CASA volunteer and how can just a few hours of your time make a lasting difference in a child's life?In this episode of Chamber Chat with Kate & Kat, we sit down with Happy Aldana, Executive Director of CASA of the Midlands, to learn more about the work Court Appointed Special Advocates do for children involved in the juvenile court system.Happy walks us through what a CASA volunteer does, how volunteers build relationships with children in foster care, the training involved, and why having one consistent person who continues to show up can be so important.We also talk about the need for more CASA volunteers in Saunders County, the different ways community members can support CASA even if volunteering isn't an option, and the CASA Giving Tree coming to the Wahoo Public Library this holiday season.In this episode:• What CASA stands for and who the organization serves• What a CASA volunteer actually does• Volunteer training and time commitment• The need for more volunteers in Saunders County• How CASA helps with extracurricular activities, car seats, clothing, and other needs• The CASA Giving Tree beginning November 1 at the Wahoo Public Library• Other ways you can donate and support local children and familiesInterested in becoming a CASA volunteer or supporting CASA of the Midlands?Visit casathemidlands.orgEmail: midcasadirector@gmail.comCall: 402-816-4131CASA of the Midlands serves Dodge, Saunders, and Washington Counties.This episode also features a Chamber Champion spotlight on JEO Consulting Group, a company whose roots in Wahoo date all the way back to 1937.Chamber Chat with Kate & Kat is all about the businesses, organizations, people, and stories that make the Wahoo community what it is.Keep it local, friends!

⚡️WOOHOO - within 2 days of the show being released (Sept 23-25, 2026)...guest Karina and I will personally jump into the comment section here on YouTube to answer your questions/comments. Just scroll down below the video, leave your remark, and watch for replies. Join the New Earth Evolution... engage! engage!Guest Karina La Puma doesn't just talk about manifesting... she lives in a permanent state of magnetic trust.I chat with visionary author, astrologer, and spiritual guide Karina La Puma to break down the real mechanics of manifestation... embodying the goddess, magnetic creation, and what it actually means to live in the sixth dimension. Karina has spent 40+ years exploring astrology, tarot, archetypal psychology, quantum healing, shamanic energy, and Reiki. She's the creator of the Soul Source Radiant System, author of the Toolkit for Awakening book series, and creator of the Awakening Tarot deck.Karina reveals the manifestation mistake most people don't even realize they're making... talking themselves back into lack instead of magnetizing what they want. She breaks down the difference between chasing a desire and becoming magnetic to it, and why "having" always follows "being" first.For the "New Earth Practice"... Karina leads a full quantum manifestation meditation, a guided visioning and "burying" practice designed to plant your deepest desires into the field and let them manifest magnetically.Watch this episode because you're one meditation away from becoming magnetic to everything you want... money, love, purpose... and finally understanding why it hasn't shown up yet.Timestamps:00:00 — Eden Introduces Guest & Today's Creation Adventure01:08 — Karina's Journey: From Insecurity to Spiritual Firecracker02:55 — Stepping Into the New Earth Vibe05:46 — Living as Love: Blissful States & That Elusive “Flow”08:31 — Embodied Radiance: The Simple (Not-So-Secret) Practice10:00 — Goddess Energy for All: Magnetism Beyond Gender11:17 — Turning Drama into Magnetism: Attraction Tools for Real Life14:16 — The Hero's Journey: Why Venting is Actually Expensive15:46 — Express, Release, Refocus: The Art of Non-Attachment17:48 — Working with Contrast: Sludge, Journaling & Honest Desires18:40 — Living from the End: Visualization Hacks for Manifestation22:03 — Money Magnetism25:37 — The Chi Field Trick: Creating & Infusing Your Desires29:38 — Transforming Life's Setbacks into New Earth Gold32:02 — Cosmic Curriculum: 6 Initiations for Everyday Heroes & Sheroes34:39 — Making Life Sacred: Daily Magic & Tiny Rituals36:19 — Creating Sacred Space: A Shamanic Energy Realignment39:13 — Chakras Level Up: Expanding Your Energy System42:08 — Karina Gets Real: Childhood Struggles & Becoming the Perfect Partner47:56 — Attracting Love: Unattachment, Trust, & Divine Timing50:51 — Worthiness, Co-Creation & The Magic Formula51:54 — New Earth Practice: Quantum Manifestation Meditation56:18 — Embodying Desires: Sensing, Feeling & Anchoring Your Visions1:06:00 — Eden & Karina Reflect: Integrating Practice & Human Awesomeness1:07:11 — Karina's Book Birth & Ways to ConnectKarina's Links:Website: https://www.soul-source.orgEmail: klapuma@soul-source.orgInstagram: https://www.instagram.com/karina_la_pumaYouTube: https://www.youtube.com/@karenlapuma7238LinkedIn: https://www.linkedin.com/in/karina-la-pumaFacebook: https://www.facebook.com/karina.la.puma

Come join us as we continue through Paul's letter to Timothy.  This segment opens with a recipe for apostasy, but continues in an encouragement to instead train in godliness in order to enjoy the nourishment and promise it brings.Visit: abideatascadero.orgEmail: info@abideatascadero.orgInstagram: @abide.calvary_atascFacebook: @AbideCalvaryAtascadero

I Was Wide Awake for Dr. Kimberly Canter's Presentation on Sleep and Cystic FibrosisI was wide awake during a presentation about sleep, but that's exactly what happens when you hear Dr. Kimberly Canter speak about the connection between sleep and cystic fibrosis.As the mom of two daughters with CF, I know firsthand how elusive a good night's sleep can be. For years, our nights included coughing, breathing treatments, medications, hospital stays, and the constant worry that comes with raising children with a chronic illness. Sleep wasn't simply about feeling rested it was about survival, healing, and making it through another day.That's why Dr. Canter's presentation resonated with me, and it will with you.Dr. Kimberly Canter is a pediatric psychologist, Senior Research Scientist at Nemours Children's Health, and Associate Professor of Pediatrics at Thomas Jefferson University. Her work focuses on improving the emotional and physical well-being of children and families living with chronic illnesses, including cystic fibrosis.One of the biggest takeaways? Sleep isn't a luxury, it's a critical part of CF care.Sleep Affects Every Part of LifeAs Dr. Canter explained, sleep influences nearly every aspect of our health.“Sleep impacts every single part of our life, of our health, at the physical level, at the mental level.”For people living with CF, sleep is often interrupted by persistent coughing, airway clearance treatments, sinus issues, medications, hospital routines, and the overall burden of managing a complex disease. Even when someone finally gets into bed, staying asleep can be difficult.Poor sleep doesn't just leave someone feeling tired the next day. Research shows it can affect lung health, weaken the immune system, increase the risk of infections, and contribute to anxiety and depression.New Treatments, New QuestionsOne topic I found especially interesting was Dr. Canter's discussion about CFTR modulators.These remarkable medications have transformed the lives of many people with CF, but researchers are also learning that some patients experience new or worsening sleep problems after starting these therapies. It's another reminder that while treatments continue to improve, there is still much to learn about the day-to-day experiences of people living with cystic fibrosis.It's More Than PhysicalDr. Canter also spoke about something that doesn't receive enough attention: medical trauma.Repeated hospitalizations, frightening procedures, and years of living with uncertainty can leave lasting emotional effects. For some patients, those experiences contribute to PTSD-like symptoms, anxiety, and ongoing sleep disturbances.It's a powerful reminder that caring for someone with CF means caring for both their physical and emotional health.Start the ConversationPerhaps the most practical advice Dr. Canter shared was also the simplest.“The most important initial step is to talk with your care team and make them aware that there is a problem.”Too often, families accept poor sleep as “just part of CF.” But it doesn't have to be ignored. Whether it's adjusting treatment schedules, exploring behavioral strategies, addressing anxiety, or making accommodations at school during particularly difficult periods, there may be solutions that can help.Why This MattersLiving with cystic fibrosis has changed dramatically over the past decade. People are living longer and healthier lives than ever before, thanks to extraordinary scientific advances. But quality of life matters just as much as longevity.Sleep is one of those everyday challenges that often flies under the radar, yet it influences physical health, mental health, relationships, school, work, and overall well-being.As a CF mom, I left Dr. Canter's presentation with a deeper appreciation for something so fundamental—and a reminder that sometimes the conversations we need most are about the things we rarely talk about.If you or someone you love is living with cystic fibrosis, I hope this encourages you to ask about sleep at your next clinic visit. It could make a bigger difference than you realize. Thank you. 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/featuredNew: Shop our merchandise! https://thebonnellfoundation.org/product-shop/Thanks to our sponsors:Vertex: https://www.vrtx.comViatris: https://www.viatris.com/enRead us on Substack: https://substack.com/@lstb?utm_campaign=profile&utm_medium=profile-pageWatch our trailer of Embracing Egypt: https://youtu.be/RYjlB25Cr9Y

Powerlessness can be a single sentence you learn as a kid and spend decades living out. We sit down with Haydee to talk about childhood sexual abuse, the silence that followed, and how a parent's inability to respond can quietly shape identity, relationships, and self-worth. She shares what she needed most at the moment of disclosure, how dissociation works as survival, and why the words “I believe you” can change the trajectory of a life.We also go deep on grief and the messy reality of support. During the COVID era, Haydee loses three “friends” in one week, including her first dog and two people she loves, and she describes shutting down and crying alone rather than asking for help. From there, the story turns toward resilience and meaning-making: she chooses a Lake Tahoe open-water swim as an act of remembrance and a push toward healing, tying the miles to “21 social causes” and raising funds for issues like mental health, cancer, COVID, sexual abuse, and epilepsy.Along the way, we get specific about the logistics and psychology of long-distance swimming: training plans, coaches, cold water, darkness, and the 3 a.m. start that triggers a trauma freeze. The biggest takeaway isn't just athletic grit, it's the mindset shift that comes from finally reaching out and learning to say “please help me.” If you care about trauma healing, grief support, therapy, and real-world tools for rebuilding self-trust, this conversation stays with you.Subscribe for more stories like this, share the episode with someone who needs it, and leave a rating and review to help more listeners find Multispective.Send us Fan MailSupport the showAdditionally, you can now also watch the full video version of your favourite episode here on YouTube. Please subscribe, like or drop a comment letting us know your thoughts on the episode and if you'd like more stories going forward!If you would like to offer any feedback on our show or get in touch with us, you can also contact us on the following platforms:Website: www.multispective.orgEmail: info@multispective.org Instagram: www.instagram.com/multispectivepodcast Facebook: www.facebook.com/multispectiveorgReddit: www.reddit.com/r/multispectiveSupport the show: https://www.patreon.com/multispectiveProducer & Host: Jennica SadhwaniEditing: Stephan MenzelMarketing: Lucas PhiriFatty15 promotes healthy metabolism, balanced immunity, and heart health. 2 out of 3 customers report near-term benefits, including calmer mood, deeper sleep or less snacking, within 6 weeks. 20% off on purchases link and code: ...

On this episode host Jonathan Chance talks with Michael Krachon of Theragenics about the I Know My PSA, Do You? awareness pin and why prostate cancer awareness matters. On this Jonathan and Michael talk about: ·       Why is raising awareness about prostate cancer and the PSA test is so important. ·       Why Theragenics decided to support our I Know My PSA Movement and have their employees wear our I Know My PSA, Do You?, awareness pin.·       How the pins are helping their employees start potentially lifesaving conversations.·       Theragenic's long-standing commitment to advancing prostate cancer care.·       Getting more doctors to mention the various treatment options for prostate cancer instead of just the one treatment they are most familiar with.For more information about the I Know My PSA Movement and the I Know My PSA, Do You? awareness pin, go to: www.iknowmypsa.org and Click on Join the Movement. For more information about brachytherapy and prostate cancer, visit Theragenics website at: LifeAfterSeeds.com  Prostate Cancer Aware is a copyrighted production.  No content maybe rebroadcast or reproduced without the expressed written consent of the Friedman Sidrow Foundation.  For more information about prostate cancer, the PSA test, men's health and Jonathan's inspiring new book Unaware, which is about his battle with prostate cancer.Visit our website at:  https://www.iknowmypsa.orgEmail us at:  https://www.iknowmypsa.org/contactus/Follow Prostate Cancer Aware on social media at:Facebook -  https://www.facebook.com/iknowmypsa Twitter -  https://twitter.com/iknowmypsa or @iknowmypsaThank you for listening!  Remember, Stay Aware and Stay Healthy.™

We just wrapped the 45th Annual ANMA Convention and Educational Seminar at the Westgate Las Vegas, and members are calling it one of the best years yet. In this episode, we are taking you straight to the exhibit hall floor to hear from our president and the exhibitors who make this event what it is.Attendees told us the education was insightful and spot on, the exhibit hall was fantastic, and the comment we heard most "These are my people." Among three days of speakers, CEUs, a busy exhibit hall, and our new exhibitor raffle, this year was as much about connection as it was about education. Some of the best moments happened in the hallways, over lunch, and in conversations between sessions.Voices from the Exhibit HallDr. Richard Drucker — ANMA President and founder of Drucker Labs, on a convention that exceeded expectations, Dr. Fab Mancini's banquet keynote, and his goal of filling next year's banquet room with a thousand peopleCountry Doctor Herbals & Country Doctor Academy (Cheyenne, WY) — an ANMA member since 2003 on their nutritional therapy clinic, botanical line, and the mentorship program helping practitioners turn their training into sustainable businessesBronwyn Eisen, Jigsaw Health — on their flagship Mag SRT magnesium malate with sustained-release technologyLoren Swenson, Solex & Solex School of Naturopathy — a walking tour of one of the biggest booths on the floor, featuring the Ion Rain, Infinity Mats, AO Scan, Theta Chair, and pelvic pulse chairVictoria, Apex Water Research Institute — a five-year ANMA exhibitor and past podcast guest on their structured water supplementDebbie Bailey, Bumbiotics — the most memorable conversation we recorded all weekend, on her probiotic suppository (and the nickname you won't forget)Marcelo Hamwi, VORG Superfoods — single-sourced superfoods with adaptogens and nootropics, plus the Aura O3 healing chamber parked in the middle of the hallAmeya, Health Buddha & ScaleUp42 — tech and digital marketing built specifically to help holistic practitioners acquire, manage, and retain clientsJeff, Rev222 — 12 years of ANMA conventions, their patented olive leaf extract, and why community matters when you've got a tough Monday morning caseBody Tone Wellness — 25+ years in practice and 7–8 years speaking at ANMA, with a focus on painMonica Head & Paul Burt, Austin Air Systems — first-time exhibitors from Buffalo, NY, on HEPA and activated carbon air purifiersMark Your Calendar: ANMA 2027Next year's ANMA Convention & Educational Seminar takes place in August 2027 in Las Vegas. As Dr. Drucker put it, next year is already tomorrow — and we're already working on making it even better.Visit anma.org for details as they're announced.Connect with us:Stay tuned for updates on the 45th Annual ANMA Convention at anma.orgAmerican Naturopathic Medical Association: ⁠https://www.anma.org⁠American Naturopathic Medical Certification Board: ⁠https://www.anmcb.org⁠American Naturopathic Medical Accreditation Board: ⁠https://www.anmab.org⁠Society of Complementary Alternative and Holistic Practitioners: https://www.scahp.orgEmail: admin@anma.orgThis podcast is produced by Espresso Podcast Production: https://www.espressopodcastproduction.com/Disclaimer: This podcast is for educational purposes only and should not be taken as medical advice. Consult your doctor before implementing any information shared. Views expressed are those of the speakers and do not necessarily reflect ANMA or ANMCB positions.

Hi everyone, The Bonnell Foundation's mission has always been deeply personal. As we celebrate our Sweet 16 Night of Hope Gala on September 19th, it's a perfect time to reflect on why this work matters so much.What started with a need to help families navigating cystic fibrosis has grown into a community of support, education, advocacy, and financial assistance. When Molly was diagnosed with CF, there were far fewer resources available to families. The Bonnell Foundation was created to help fill those gaps — from medical bills and hospital support bags to lung transplant grants, education scholarships, and so much more.Over the past 16 years, we've seen firsthand what that support can mean. Families have reached out to share how assistance with a bill, respiratory equipment, or a difficult hospital stay helped them get through a challenging moment. These aren't simply programs — they can be lifelines for families when they need them most.And while cystic fibrosis continues to bring enormous challenges, there is also so much reason for hope. Research, new treatments, advocacy, and the dedication of families and organizations around the world continue to move the CF community forward.At the Bonnell Foundation, that hope is reflected in every dollar raised and every family we support. Our Sweet 16 Gala is more than a fundraiser. It's a celebration of resilience, generosity, and community — and a reminder that together, we can make a difference.If you can join us on September 19th, your presence helps fuel this mission. And if you can't attend, a donation can still make a meaningful difference for a family living with cystic fibrosis.Thank you for being part of this journey, for believing in our mission, and for helping us bring more support, more resources, and more hope to families living with CF. 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/featuredNew: Shop our merchandise! https://thebonnellfoundation.org/product-shop/Thanks to our sponsors:Vertex: https://www.vrtx.comViatris: https://www.viatris.com/enRead us on Substack: https://substack.com/@lstb?utm_campaign=profile&utm_medium=profile-pageWatch our trailer of Embracing Egypt: https://youtu.be/RYjlB25Cr9Y

Join us as we continue our discussion of church leadership through 1 Timothy, this time exploring the role of a deacon.  What are the qualifications?  Can women serve?  How do we do things here at Abide Calvary?  We discuss multiple sides of this complex topic.Visit: abideatascadero.orgEmail: info@abideatascadero.orgInstagram: @abide.calvary_atascFacebook: @AbideCalvaryAtascadero

Send us Fan Mail“Gentlemen, this is a football.”Hal takes a few minutes to reflect on these famous words from coach Vince Lombardi and uses them to remind us of the “basics” of our spiritual lives.Enjoy them. To live well and finish well, discipleship is a call to do the basics well – every year we live.Remember also that September 17 is the day for our North Texas Giving Day. Your gift will help us “press on” in these critically important years.You can give NOW.Finishing Well Ministries with Hal Habecker | North Texas Giving DaySupport the show"Finishing Well Ministries aims to encourage and inspire aging Christians to understand and embrace God's calling in their later years, equipping them to actively pursue and fulfill His calling. FWM provides materials, events, and other on-line resources that provide shared insights focused on finishing our lives well. We also recruit and train volunteers who lead and encourage small groups around the world to fulfill God's mission for them in these critically important years." - Hal HabeckerWebsite: www.finishingwellministries.orgEmail us: Hal@finishingwellministries.orgFollow us on Facebook: https://www.facebook.com/finishingwellministriesSupport Our Ministry: https://www.finishingwellministries.org/donateAre there biblical principles to help us understand how to finish well?Explore the Seven Essentials for Finishing Well. Learn more.Thanks for listening as we all strive to live and finish life well!

What are the qualifications of a church elder?  If I'm not an elder, do I need to care?  How many of us can meet this standard?  How do we do things here at Abide Calvary?  Come explore these practical questions with us as we continue through 1 Timothy.Visit: abideatascadero.orgEmail: info@abideatascadero.orgInstagram: @abide.calvary_atascFacebook: @AbideCalvaryAtascadero

Friends for years and with CF as their connection, Laura and Petrina have figured out how to raise CF awareness across the world. How does cystic fibrosis care compare between Australia and the United States? Host Laura Bonnell talks with Petrina Fraccaro, CEO of CF Queensland, about her journey into CF advocacy, the mission of CF Queensland, and the support available to individuals and families living with cystic fibrosis. Laura and Petrina also discuss the global landscape of cystic fibrosis, including advocacy, carrier screening, and international collaboration. They share insights from worldwide conferences, highlight the importance of community support, and explore opportunities to improve access to care and medications for people living with CF around the globe. As cofounders of the CF Global Advocacy Alliance (CFGAA), the women talk about how organizations around the world are working together to create a brighter future for the CF community. A Personal Connection to Cystic Fibrosis Petrina's path to CF advocacy is an interesting one. With a background in public relations, education, and working to empower women, she eventually began looking for an opportunity in the not-for-profit world. She wanted to use her skills for something meaningful, particularly for a chronic illness that many people didn't understand. But CF wasn't completely unfamiliar to her. As a child, Petrina had watched a family friend live with cystic fibrosis. That early experience stayed with her and eventually helped lead her into a career advocating for people and families affected by CF. Today, that passion has grown into leadership at Cystic Fibrosis Queensland, where she works to make sure people living with CF and their families have the resources, support, and advocacy they need. Supporting Families Through Cystic Fibrosis Queensland Cystic Fibrosis Queensland provides support across Queensland and the Northern Territory, helping families navigate the financial, emotional, and practical challenges that come with CF. Petrina talked openly about the challenges the organization has faced, including financial sustainability. Rather than trying to do everything, she focused on listening to the CF community and identifying the services that were most important. Those services include: Medical subsidies to help families manage the costs associated with CF care. Specialty grants that can help provide equipment such as nebulizers and oxygen concentrators. Education scholarships that help people with CF pursue college, training, and career opportunities. Mental health support for people with CF, their families, and caregivers. What struck me throughout our conversation was how much of this work comes down to one simple idea: people should not have to navigate CF alone. Why Awareness and Education Still Matter It can be easy to look at the incredible advances in CF treatment and think that we have solved many of the problems associated with the disease. We haven't. While CF treatments have changed dramatically—and modulators have given many people with CF opportunities that previous generations never had—there are still people who are diagnosed late, people who don't have access to the newest treatments, and families who don't understand what CF means when it enters their lives. Petrina talked about the importance of reaching immigrant and multicultural communities in Australia, where cystic fibrosis may not be well understood or even recognized. That education extends beyond families. Healthcare professionals and the broader community also need to understand CF so that people can be diagnosed as early as possible and connected with appropriate care. The Importance of Carrier Screening One of the topics we discussed that I think deserves much more attention is genetic carrier screening. Cystic fibrosis is an inherited condition, and a person can be a healthy carrier without ever knowing it. In Australia, Cystic Fibrosis Australia estimates that approximately 1 in 25 people carry a CF gene change, and most carriers are unaware of their status. Research from Australia also demonstrates just how important broader carrier screening can be. In a study of 12,000 people undergoing reproductive carrier screening for CF, spinal muscular atrophy, and fragile X syndrome, 342 people were identified as CF carriers, about 1 in 34 people screened. Approximately 88% of the people identified as carriers had no known family history of the condition. That last statistic is especially important. You don't have to have a family history of cystic fibrosis to be a carrier. Australia took an important step in November 2023 when reproductive carrier screening for CF, spinal muscular atrophy, and fragile X syndrome was added to the Medicare Benefits Schedule for people who are pregnant or planning a pregnancy. Testing has increased significantly since then, although there is still a need for greater awareness and education about carrier screening. For me, this is another reminder that education can change lives. Knowing your carrier status can give people information they can use when making decisions about starting or growing their families. Mental Health Is Part of CF Care Another part of our conversation that really stood out to me was mental health. Living with CF is not just about medications, clinic appointments, hospitalizations, treatments, and lung function numbers. It can affect every part of a person's life, and it affects the entire family. Cystic Fibrosis Queensland has developed mental health programming that supports people with CF as well as their families and caregivers. Petrina also talked about mental health first-aid training, which can give people the tools to recognize when someone may be struggling and help connect them with appropriate support. We also talked about something that comes up frequently in advocacy: the power and responsibility of sharing your story. Personal stories can educate people, change hearts, raise money, and influence policy. But constantly telling your story can also be emotionally exhausting. That means we need to make sure the people sharing their experiences are supported, too. Advocacy Is About More Than Awareness One of my biggest takeaways from talking with Petrina is that advocacy isn't just about making people aware that cystic fibrosis exists. It's about changing systems. It's about making sure families can afford the care they need. It's about access to medications and equipment. It's about education. It's about mental health. It's about genetic screening. It's about making sure people in every community—including communities where CF may be less recognized—have access to knowledgeable healthcare. And it's about making sure that progress in CF doesn't leave people behind. Looking Toward the Future Petrina's journey is a great example of what can happen when someone combines professional skills with a personal passion for making a difference. Our conversation reminded me that the CF community has come incredibly far, but there is still so much work to do. The treatments may be changing. The life expectancy for people with CF is changing. The way we think about CF is changing. But the need for advocacy, education, support, and connection isn't going away. And that's why conversations like this matter. I'm grateful to Petrina—not only for the work she does every day for the CF community in Australia, but for the friendship we've built through our shared commitment to making life better for people and families living with cystic fibrosis. To learn more about CF Queensland, Australia https://www.cfqld.org.au For more about CF Global Advocacy Alliance https://cfgaa.org.au For more about the European CF Society and the conferences they hold https://www.ecfs.eu 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/featuredNew: Shop our merchandise! https://thebonnellfoundation.org/product-shop/Thanks to our sponsors:Vertex: https://www.vrtx.comViatris: https://www.viatris.com/enRead us on Substack: https://substack.com/@lstb?utm_campaign=profile&utm_medium=profile-pageWatch our trailer of Embracing Egypt: https://youtu.be/RYjlB25Cr9Y

The podcast content may contain sensitive topics. Listener discretion is advised.Sextortion has changed and parents need to know.  Today's cases almost always aren't about teens harassing teens or isolated predators seeking victims. It is estimated that more than 70% of online exploitation reports now originate overseas, where criminal networks, gangs, and cartels target high‑achieving teen males for money, power,and control. Utilizing AI, these criminals build full digital profiles of U.S. teens including their home and address, school, teams, awards, friends, parents' jobs and then pose as “friends of friends.” They can look like someone who knows them and can build a relationship quickly. With global 5G, geolocation tools, and cross‑platformmessaging, they can reach out to multiple teens anywhere at any time. If a connection is made, the criminals will move the teen across apps to avoid detection. They'll make it flirtatious, add some flattery, possibly even talk about a relationship. They'll send an explicit image, often fake or taken fromsomeone else, and ask for one in return.Once they obtain even a partial image, AI tools allow them to fabricate explicit content and launch brutal, nonstop blackmail campaigns. Organized groups often work inteams, sending hundreds of threatening messages. This new form of sextortion has already led to devastating loss of life among young males. This episode helps families understand:·      How overseas criminals impersonate teens·      Why “friend of a friend” is no longer safe·      How cross‑platform grooming works·      The red flags teens must recognize·      Why parents must create a crisis plan before something happensFinancial sextortion is preventable but only if families talk about it early and often. Listen to this P3 Kids podcast as it gives parents and teens the knowledge, language, and tools to stay safe, stay aware, and stay connected.For more info and to donate to this 501(c)3 charity, you can reach Million Kids at:Website: https://MillionKids.orgEmail: info@MillionKids.orgBe sure to follow and like our posts on: Facebook: iemillionkidsInstagram: millionkidsteen

Join us this week on a deep dive into the book of Luke as Jesus brings salvation to a demon possessed man.  We explore the theme of Jesus being King over all, a fact even a legion of demons must acknowledge.Visit: abideatascadero.orgEmail: info@abideatascadero.orgInstagram: @abide.calvary_atascFacebook: @AbideCalvaryAtascadero

The podcast content may contain sensitive topics. Listener discretion is advised.If you think your child is safe because they're in your home… think again! Criminals from across the world can reach them instantly through the device you probably bought for them. Let's candidly talk about the danger no one wants to face.Parents today are raising kids in a world no generation has ever faced. It is a world so vast, so fast, and so dangerous that most adults can't even picture it.It's no longer enough to teach kids the basics of life. Today's parents must prepare their children to live in a globallyconnected digital universe where every swipe, click, andmessage can open the door to 5.5 billion people including criminals, cartels, extortion networks, and extremist groups operating from countries many of us have never even heard of.Seventy percent of the planet is now online with high‑speed 5G. That means your child can be contacted instantlyby anyone, anywhere. Criminals in the poorest corners of the world now have direct access to the most private moments of your child's life.And they're not just looking for money. They're looking for nudes, deepfakes, crypto payments, emotional control, and indoctrination into some of the darkest online communities ever created. Here's the part no one wants to talk aboutbecause they think: It's terrifying. It's negative. It's overwhelming. So parents avoid it, schools avoid it and teens think they are invincible.Yet here's the truth: How can you teach your child to protect themselves if they don't recognize the danger?This episode of P3 Kids, presented by Opal Singleton, the President and CEO of MillionKids.org, breaks down the realityevery family must understand:None of us have lived in this world before. There is no rule book.Teens are more tech‑savvy than parents but far morenaïve.Parents are even less informed than their kids aboutglobal online crime.Criminals can enter your child's life through their deviceat any moment.Teens believe they're invincible: “It won't happento me.”AI lets predators study your child and mimic someonethey trust.Kids will do anything to keep their device whichincludes hiding danger.The greatest risk to families is being uninformedabout how the online world really works.This podcast isn't about fear, it isabout truth, empowerment, and giving parents the education and tools to protect their kids in a world that has changed faster than anyone expected. Talk to your kids, as this is one conversation you can't skip.For more info and to donate to this 501(c)3 charity, you can reach Million Kids at:Website: https://MillionKids.orgEmail: info@MillionKids.orgBe sure to follow and like our posts on: Facebook: iemillionkidsInstagram: millionkidsteen

#HealingJourney #GriefSupport #BrwnGrlzCollectiveFrom Rosie with Love | Finding Strength Through Grief with Janine Ryans | BrwnGrlz CollectiveGrief changes us, but it does not have to define us.In this heartfelt conversation, we sit down with Janine Ryans, founder of Rosie with Love, to explore what it means to navigate loss, honor the people we love, and continue moving forward with purpose. Together, we discuss healing, resilience, the power of community, and why having honest conversations about grief can help others feel less alone.Whether you're grieving a loved one, supporting someone through loss, or simply looking for a conversation filled with compassion and hope, this episode reminds us that healing is not about forgetting. It's about learning how to carry love with us as we move forward.At BrwnGrlz Collective, we believe that meaningful conversations create meaningful connections, and this episode is a reminder that even in life's most difficult moments, there is still room for healing, growth, and community.

Maria Owl joins us to talk about her Channeling Mediumship and Indigenous Initiations. She shares wisdom from Grand Master Qi, Lakota Hopi, and others. She discusses her experiences and what she learned from communicating and swimming with Dolphins for six years in Hawaii. Maria conducts Cacao ceremonies Maria, and she explains the significance and ceremonial use of this ancient ritual. #Channeling #mediumship #cacaoceremony #swimmingwithdolphins #indigenousmedicine Maria Owl CONTACT:Website: https://sacredfuture.orgEMAIL: contact@sacredfuture.orgFOLLOW US ON FACEBOOK: http://www.facebook.com/ASMALPodcastVISIT OUR WEBSITE: http://www.asmallmediumatlarge.coEMAIL: asmallmediumatlargepodcast@gmail.com Show Produced by Green Valley Production StudioMusic by DJ Booda: http://www.djbooda.com

Join us as we explore this complex passage that illustrates the complimentary roles men and women play in the church.Visit: abideatascadero.orgEmail: info@abideatascadero.orgInstagram: @abide.calvary_atascFacebook: @AbideCalvaryAtascadero

On this episode host Jonathan Chance gets personal and talks about the test that helped save his life. Jonathan talks about: ·       How a simple blood test, the PSA test, helped save his life..·       Why early detection tests like the PSA test is so important.·       Why prostate cancer is known as the silent killer.·       Why an elevated PSA does not always mean prostate cancer.·       The importance of talking with your doctor about prostate cancer and getting a PSA test.·       How podcast listeners can help start conversations about prostate cancer and by joining the I Know My PSA Movement.Prostate Cancer Aware is grateful to the Jevan and Ruzanna Chimayan Foundation for their generous donation, which helps fuel our podcast and website to raise critical awareness about prostate cancer and the PSA test around the world.Prostate Cancer Aware is a copyrighted production.  No content maybe rebroadcast or reproduced without the expressed written consent of the Friedman Sidrow Foundation.  For more information about prostate cancer, the PSA test, men's health and Jonathan's inspiring new book Unaware, which is about his battle with prostate cancer.Visit our website at:  https://www.iknowmypsa.orgEmail us at:  https://www.iknowmypsa.org/contactus/Follow Prostate Cancer Aware on social media at:Facebook -  https://www.facebook.com/iknowmypsa Twitter -  https://twitter.com/iknowmypsa or @iknowmypsaThank you for listening!  Remember, Stay Aware and Stay Healthy.™

In S8E10 I sit down with he visionary team behind Custodia Borealis: Melissa Seims, Dr. Sue Terry, Alexandra Stockdale-Haley, and Toby Norman-Wright to discuss their respective roles and shared vision for the future of the project, mission, current acquisitions, and much more!Custodia Borealis:Become a member (includes goodies) https://ko-fi.com/custodiaborealisHelp us through our Crowdfunder: https://www.crowdfunder.co.uk/p/help-establish-an-occult-museum-in-the-north Follow our Facebook page: https://www.facebook.com/groups/custodiaborealisCheck out our Website: www.custodiaborealis.orgEmail us at: custodiaborealis@gmail.comSUBSCRIBE to the ARCANVM Newsletter:⁠⁠https://ikebaker.com/newsletter⁠⁠For all things Ike be sure to visit/message him at: https://ikebaker.com⁠⁠SUPPORT ARCANVM for $5/MONTH: https://patreon.com/arcanvm   ⁠ FOLLOW on Facebook: https://facebook.com/arcanvvm   ⁠ FOLLOW on Instagram: @a.r.c.a.n.v.m#magic #magick #spirituality

Join us this week in celebrating the grace of Jesus, who not only mediates on our behalf, but takes on the sentence, and through his desire to see all saved, challenges us, in turn, to pray that all will come to this same truth.Visit: abideatascadero.orgEmail: info@abideatascadero.orgInstagram: @abide.calvary_atascFacebook: @AbideCalvaryAtascadero

The podcast content may contain sensitive topics. Listener discretion is advised.The hideous tragedy of financial sextortion is that many THINK they know about it. The reality is that sextortion has changed dramatically in the past couple of years because of artificial intelligence and global internet connection. This is a continuation of exploring the impact of criminals around the world as they have learned they can destroy our kid's lives while so many of adults believe we have good kids who won't ever become victims. The reality: “you be careful online“ is not enough to protect you or your child. Ask a teen and they'll insist, “I know, Mom/Dad. I'm careful. I only talk to people I know, who know me, or who know a friend.” But that confidence is exactly what predators exploit.This episode of the Protect & Prevent Podcast, P3Kids, is designed to bring urgency to parents, teachers, counselors, pastors, first responders, and teenagers themselves about financial sextortion.These criminals reach our kids anywhere. Their bedroom, at a basketball game, the backseat of a car, the school gym. They use AI to gather everything about their targets: their achievements, their friends list, their home, their parents, their school. They look like someone who knows your child.And here's the part no one wants to believe: 1 in 6 teen boys and 1 in 7 teen girls have sent a sext. To them, it may seem like no big deal. In addition to that, any image, even if fully clothed, can be manipulated with AI and used to shame, threaten, and destroy a child's life. Once criminals have an image, the torture is relentless.Please listen to this PODCAST and share it with everyone you know. No family should ever lose a precious child because they didn't know about financial sextortion. Not one more. Not ever again.For more info and to donate to this 501(c)3 charity, you can reach Million Kids at:Website: https://MillionKids.orgEmail: info@MillionKids.orgBe sure to follow and like our posts on:Facebook: / iemillionkidsInstagram: / millionkidsteen

Your skin changes every week of the month — and your skincare routine has no idea. This month's guest explains why.Kari Collins spent decades in the beauty industry — salons, med spas, skincare with plastic surgeons — before a health crisis in her late 30s forced her to stop and listen to what her body had been saying all along. Now a board-certified holistic health practitioner with the ANMCB and co-founder of True Femme Collective, she's on a mission to change how women think about their skin, their cycles, and the "types" the beauty aisle has been selling them.In this episode:Why "no woman can ever say I just have oily skin" — and the four phases your skincare routine is ignoringThe menstruation research that convinced Kari most skin issues trace back to one root causeWhat happens to your skin when estrogen shows up (and the ancient wisdom behind Kari's "wise era")The 5-minute habit that starts decoding what your skin is telling you — this monthThe family healing story behind True Femme CollectivePlus: this month's Practice Pointer on two words that sound interchangeable but define your entire professional relationship. Which one are you using?Explore Kari's work, Sacred Silk, and her research library at truefemmecollective.comANMA 45th Annual Convention & Educational SeminarAugust 28–30, 2026 — Westgate Las Vegas Resort & CasinoJoin the natural health community for education, connection, and professional growth. Hear from leading voices in natural health, explore the exhibit hall, earn CEUs, and connect with professionals from across the country. Register and book your room at anma.org/conventionConnect with us:Stay tuned for updates on the 45th Annual ANMA Convention at anma.orgAmerican Naturopathic Medical Association: ⁠https://www.anma.org⁠American Naturopathic Medical Certification Board: ⁠https://www.anmcb.org⁠American Naturopathic Medical Accreditation Board: ⁠https://www.anmab.org⁠Society of Complementary Alternative and Holistic Practitioners: https://www.scahp.orgEmail: admin@anma.orgThis podcast is produced by Espresso Podcast Production: https://www.espressopodcastproduction.com/Disclaimer: This podcast is for educational purposes only and should not be taken as medical advice. Consult your doctor before implementing any information shared. Views expressed are those of the speakers and do not necessarily reflect ANMA or ANMCB positions.

Join us for a two-part exploration of both the mercy granted Paul (the “chief of sinners”), and his encouragement to Timothy to remain in place despite difficult tasks ahead.Visit: abideatascadero.orgEmail: info@abideatascadero.orgInstagram: @abide.calvary_atascFacebook: @AbideCalvaryAtascadero

The podcast content may contain sensitive topics. Listener discretion is advised.The tragedy is this: parents may THINK their kids understandsextortion. Ask a teen and they'll insist, “I know, Mom/Dad. I'm careful. I only talk to people I know, who know me, or who know afriend.” But that confidence is exactly what predators exploit.This episode of the Protect & Prevent Podcast, P3Kids, is designed to bring urgency to parents, teachers, counselors, pastors, first responders, and teenagers themselves about financial sextortion. Most families don't realize more than 80% of onlinesexual‑exploitation reports now come from overseas. Andsince global 5G connected the world, 45 successful boys, ages 13 to 17, have died by suicide after being targeted in financial sextortion scams.These criminals reach our kids anywhere. Their bedroom, the backseat of a car, the school gym. They use AI to gathereverything about their targets: their achievements, their friends list, their home, their parents, their school. They look like someone who knows your child.And here's the part no one wants to believe: 1 in 6 teen boys and 1 in 7 teen girls have sent a sext. To them, it may seem like no big deal. In addition to that, any image, even if fully clothed, can be manipulated with AI and used to shame, threaten, and destroy a child's life. Once criminals have an image, the torture is relentless.Please listen to this PODCAST and share it with everyone you know. No family should ever lose a precious child because they didn't know about financial sextortion. Not one more. Notever again.For more info and to donate to this 501(c)3 charity, you can reach MillionKids at:Website: https://MillionKids.orgEmail: info@MillionKids.orgBe sure to follow and like our posts on:Facebook:   / iemillionkidsInstagram:   / millionkidsteen 

While the law reflects back to us the temptations of sin, the Holy Spirit gives us the strength to resist those temptations!  Join us as we explore the role of the Old Covenant law in our New Covenant lives with Jesus.Visit: abideatascadero.orgEmail: info@abideatascadero.orgInstagram: @abide.calvary_atascFacebook: @AbideCalvaryAtascadero

People don't pick and choose when they die, and that one fact changes everything about the people who respond when a life ends. We sit down with a funeral service operative to talk about the deathcare work most of us never see: the 3 a.m. callouts, the constant on-call rotation, and why the hours burn through staff even faster than the sight of a dead body ever could. If you've ever wondered who actually arrives, what they do first, and how they keep functioning, this conversation goes there with honesty and detail. We walk through the real chain of events from the first phone call to transport and mortuary care, including the difference between an expected death at home and a sudden death under a coroner's contract that requires police presence and a post-mortem. He explains the roles inside funeral services, why evidence matters at murders and serious collisions, and how celebrity deaths can turn a scene into a public spectacle thanks to cameras and social media. We also talk about presentation, how families choose clothing, why the face can look unfamiliar after death, and what those changes make him believe about the soul and consciousness. Then the conversation turns to the hardest calls: severe decomposition, violent scenes, and the quiet tragedy of someone being left unnoticed for months. We explore compartmentalizing, what it takes to comfort families in shock, and how religion and cultural expectations can clash with urgent government timelines when time is not negotiable. If death scares you, you're not alone; we end with a candid answer to whether he fears death and why. Subscribe for more human stories, share this with someone who avoids the topic, and leave a rating and review so more listeners can find the show.Send us Fan MailSupport the showAdditionally, you can now also watch the full video version of your favourite episode here on YouTube. Please subscribe, like or drop a comment letting us know your thoughts on the episode and if you'd like more stories going forward!If you would like to offer any feedback on our show or get in touch with us, you can also contact us on the following platforms:Website: www.multispective.orgEmail: info@multispective.org Instagram: www.instagram.com/multispectivepodcast Facebook: www.facebook.com/multispectiveorgReddit: www.reddit.com/r/multispectiveSupport the show: https://www.patreon.com/multispectiveProducer & Host: Jennica SadhwaniEditing: Stephan MenzelMarketing: Lucas PhiriFatty15 promotes healthy metabolism, balanced immunity, and heart health. 2 out of 3 customers report near-term benefits, including calmer mood, deeper sleep or less snacking, within 6 weeks. 20% off on purchases link and code: ...

In this episode of MHD Off the Record — South LA Highlights, host Chavonne Taylor sits down with Coach Dominic "Nick" Haider, founder of Guardian Project Los Angeles and Omni Jiu-Jitsu Academy. Coach Nick shares his personal journey from a bullied mixed-race kid who found refuge in martial arts through a scholarship, to a professional fighter, to a chef-turned-jiu-jitsu instructor dedicated to serving South LA youth.The conversation explores how Guardian Project LA provides free jiu-jitsu training, mentorship, meals, and wellness resources at Harvard Park, South Park, and Algin Sutton Park through the LAPD's Community Safety Partnership (CSP) program. Coach Nick explains his philosophy of creating a safe, non-militarized space where kids can build confidence, resilience, and agency — drawing on lessons from his own childhood and his years running restaurant kitchens with a culture of care.ResourcesWebsite: guardianlosangeles.orgEmail: nickh@guardianlosangeles.org or nick@omnijiu-jitsu.comCommunity AnnouncementMetro Vermont Transit Corridor Project — South LA, help shape the future of transit on Vermont Avenue. Metro's Vermont Transit Corridor Project is moving toward construction, and the decisions made now will affect how families, workers, students, and seniors travel for years to come. Join a community meeting August 10–15, in person or online, and make sure our neighborhoods are heard.

The podcast content may contain sensitive topics. Listener discretion is advised.Every parent knows the goal: To raise a child who can make good (even great) choices. But today's digital world isn't the neighborhood we grew up in. It's a maze of AI‑generated identities, animated avatars, chatbots that feel human,and platforms like Discord and Roblox where strangers can slip into a child's life disguised as “just another kid.”So what happens when your child makes one impulsive choice, has one moment of curiosity or feels one moment of pressure and suddenly finds themselves trapped in the cul‑de‑sac of life? A place where they feel stuck, scared, and unsure how to get out?This episode of P3 Kids tackles the conversations every parent needs to have before that moment ever arrives.We explore how the global internet connects your child to millions of people, including extremist groups, pedophiles, and criminal organizations who use psychological manipulation, AI‑altered images, and emotional pressure to break down a young person's defenses. These predators don't just want attention; they want influence, control, and leverage.And when a child is targeted, they face a terrifying choice: Do they comply and risk having their life changed forever? Ordo they reach out to a trusted adult who can help them navigate the crisis?This podcast gives parents the tools to make sure their child chooses the second option.Never in history has this conversation been more urgent. By talking with your child now, before they're in trouble, you give them the strength to make the right choice when it matters most. You help them understand that asking for help isn't failure, it is the most powerful choice they can make.This episode is not just information. It's prevention. It's empowerment. And it might be the conversation thatprotects your child when they need it most.Sign up for the free weekly MillionKids.org eblast with REAL stories, REAL trends, REAL tactics, and REAL ways to protect your family.Website: https://MillionKids.orgEmail: info@MillionKids.orgBe sure to follow and like our posts on:Facebook: https://www.facebook.com/IEMillionKidsInstagram: https://instagram.com/MillionKidsTeen

n this episode of the Fearless Happiest Podcast, host Max speaks with Helen Malinowski, a trauma therapist specializing in clinician burnout. Helen shares her journey into therapy, the challenges she faced, and the importance of self-care and community support for clinicians. They discuss the impact of burnout, the discovery of somatic therapies, and practical strategies for maintaining mental health in the helping profession. The conversation emphasizes the need for clinicians to prioritize their well-being to effectively support their clients. In this conversation, Helen Malinowski discusses the irreplaceable role of human connection in therapy, emphasizing that while AI can assist, it cannot replicate the emotional presence of a therapist. The importance of self-care for clinicians is highlighted, as they often prioritize their clients' needs over their own. Helen also shares insights on fearlessness and happiness, suggesting that true contentment comes from being present in the moment. The discussion concludes with a focus on the wisdom of listening to one's body and the significance of integrating personal experiences into therapeutic practices.Website: https://somaticintegratedinstitute.orgEmail: info@somaticintegratedinstitute.orgInstagram: https://www.instagram.com/somaticinformedtherapies/?hl=enSpecial offer: https://www.flourishingpractice.org/fearlesshappynessFor More From Sober Coach/Substance Abuse Counselor Max Njist, visitMaxNijst.org

What would you do if you didn't know what your future held? For people living with cystic fibrosis, uncertainty is often a constant companion. Inka Nisinbaum faced one of the biggest unknowns of her life as she waited 15 months for a double lung and liver transplant. Every day brought the same question: Would she survive long enough to receive the gift of new organs? Rather than let fear define her, Inka prepared for every possibility. She created a list of dreams she would pursue if she lived and a bucket list in case she didn't. Then she did something even more powerful—she fought. She refused to give up, pushed through impossible challenges, and ultimately built a life beyond what anyone thought possible. Her story is a reminder that while we can't always control the future, we can choose how we face it. Born with cystic fibrosis and given just four years to live, Inka Nisinbaum defies every expectation. At 22, she survives a rare double lung and liver transplant after waiting more than a year for a donor, beginning a long and difficult recovery that eventually gives her nearly 17 years of stability. But in 2019, she's hit again with chronic lung rejection—what she calls a “second death sentence.” With her lung function rapidly declining, she fights back the only way she knows how: by running. Starting from just one minute at a time—even while hospitalized with a PICC line, she slowly rebuilds her strength and goes on to complete a half marathon. Against the odds, her lung function stabilizes and she regains her life again. Her journey becomes even more extraordinary as she moves to the U.S., gets married, and becomes the first woman known to have a baby after a double lung and liver transplant. To buy her book: https://read.amazon.com/sample/B0H1SFYZCH?clientId=share 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/featuredNew: Shop our merchandise! https://thebonnellfoundation.org/product-shop/Thanks to our sponsors:Vertex: https://www.vrtx.comViatris: https://www.viatris.com/enRead us on Substack: https://substack.com/@lstb?utm_campaign=profile&utm_medium=profile-pageWatch our trailer of Embracing Egypt: https://youtu.be/RYjlB25Cr9Y

Join us as we begin Paul's first letter to his dear son in the faith, a letter of encouragement and instruction to the young pastor of the church in Ephesus, Timothy.Visit: abideatascadero.orgEmail: info@abideatascadero.orgInstagram: @abide.calvary_atascFacebook: @AbideCalvaryAtascadero

The podcast content may contain sensitive topics. Listenerdiscretion is advised.This may be the most important digital‑safetyconversation you may ever have with your teenager.  Artificial intelligence and global internet access havecompletely changed sexting, online relationships, and the risks young people face when sharing images, whether “partial” nudes, full nudes and even fully clothed images. Before parents can guide their teens, they must understandthese changes themselves.A recent research study from the University of Wisconsin–EauClaire revealed a sobering truth: 1 in 4 teens have received a sext, and 1 in 4 have sent one. At the same time, the United States has now seen approximately 44 cases of financial sextortion involving boys ages 13 to 17 who died bysuicide after being targeted by overseas criminal organizations. These criminals, operating from places like Nigeria and Myanmar, pose as a “cute girl,” send a photo, and coax a teen into sharing a nude. It doesn't takemuch. Once they have even a fragment of an image, blackmail can begin. The threats are relentless. The psychological torture isunimaginable. And our kids are not prepared for it.When you hand your child a phone, you're not just givingthem a device, you are connecting them to 5.5 billion people, including cartelsand organized crime groups who use AI to look exactly like your teen's new bestfriend.This P3Kids Podcast episode gives you the tools, language,and confidence to have a healthy, enlightened, and protective conversation with your family. You'll learn how to explain the new digital risks in a way your teen can understand and be able to act on it.An informed teen is far less likely to fall prey to sextortion but that starts with an informed parent.Your child's safety begins with your knowledge.This episode helps you start the conversation that couldsave their life.Sign up for the free weekly MillionKids.org eblast with REAL stories, REAL trends, REAL tactics, and REAL ways to protect your family.Website: https://MillionKids.orgEmail: info@MillionKids.orgBe sure to follow and like our posts on:Facebook: https://www.facebook.com/IEMillionKidsInstagram: https://instagram.com/MillionKidsTeen

This week Gary Mansfield speaks Helen Downie aka Unskilled Worker (@unskilledworker) Helen is a self-taught artist and has been painting for just seven years, in that short time, she has amassed over 280,000 Instagram followers, under the Moniker Unskilled Worker and has become one of the country's most sought after painters.Helen wanted her Unskilled Worker to be anonymous, sexless, ageless and colourless. She wanted it to be anyone. As her popularity grew, as did the viewer's curiosity as to whom this person was, that created such stand-alone artwork. To Helen's amusement, the most popular belief was that it was a 24 year old male behind this name. This podcast was recorded via the video meeting app, ZOOM; during social distancing, using the built-in software. For full line up of confirmed artists go to https://www. ministryofarts.orgEmail: info@ministryofarts.orgSocial Media: @ministryofartsorg Hosted on Acast. See acast.com/privacy for more information.

When you think of worship does your mind automatically think of music or or song? Join us today as we explore how worship has more to do with how we live our daily lives than with the songs we sing at church.Visit: abideatascadero.orgEmail: info@abideatascadero.orgInstagram: @abide.calvary_atascFacebook: @AbideCalvaryAtascadero

On this episode host Jonathan Chance talks with his guest, renowned Interventional Radiologist Dr. Aaron M. Fischman about the benign side of prostate health. On this episode Jonathan and Dr. Fischman discuss: ·       What is BPH or an enlarged prostate.·       BPH treatment options like PAE.·       Urinary symptoms men should not ignore.·       What could cause a rising PSA level.·       How an elevated PSA does not always mean prostate cancer.Prostate Cancer Aware is grateful to the Jevan and Ruzanna Chimayan Foundation for their generous donation, which helps fuel our podcast and website to raise critical awareness about prostate cancer and the PSA test around the world.For more information about Dr. Fischman, visit his website at: https://drfischman.com/Prostate Cancer Aware is a copyrighted production.  No content maybe rebroadcast or reproduced without the expressed written consent of the Friedman Sidrow Foundation.  For more information about prostate cancer, the PSA test, men's health and Jonathan's inspiring new book Unaware, which is about his battle with prostate cancer.Visit our website at:  https://www.iknowmypsa.orgEmail us at:  https://www.iknowmypsa.org/contactus/Follow Prostate Cancer Aware on social media at:Facebook -  https://www.facebook.com/iknowmypsa Twitter -  https://twitter.com/iknowmypsa or @iknowmypsaThank you for listening!  Remember, Stay Aware and Stay Healthy.™

Luck of the Irish.   Irish international amateur golfer David Howard  doesn't seem to need luck with all the talent he has. We had an inspiring conversation about chasing big dreams while living with cystic fibrosis. When we recorded this podcast David had not yet qualified for the Open Championship.  He did qualify just after we recorded and went on to play. Quoting from the Open Championship paper, "On the course, Howard more than held his own alongside the world's best. He started with a four-over-par 74 before finding his groove on Friday. A birdie at the 11th was his fourth of the day and took him to +2, within sight of the cut line. Howard ultimately missed out, dropping a shot at 14 to finish three-over for his week, but took heart from his display." Bravo David!  You're an inspiration.  David shares his journey growing up in Cork, Ireland, where he was diagnosed with CF at the age of seven and learned to balance daily treatments, hospital stays, and the demands of competitive golf. He also explains how his golfing journey began with Pitch and Putt, a sport similar to golf that features shorter holes and requires just a few clubs. The game helped him develop his skills and passion before transitioning to competitive golf. David talks about how advances in CF care have transformed his health, allowing him to compete at the highest levels of amateur golf while representing Ireland on the international stage. The conversation explores David's breakthrough victories, including winning the prestigious East of Ireland Amateur Championship, his ambitions of turning professional, and the discipline and mental resilience required to compete in elite sports. He also shares practical tips on how he stays mentally focused during a golf tournament, manages pressure, and keeps his confidence throughout competition. David reflects on the important role his family, coaches, and teammates have played throughout his journey. Beyond golf, David opens up about the emotional side of living with cystic fibrosis, the importance of talking openly about chronic illness and mental health, and why he is passionate about raising awareness through fundraising and advocacy. He also shares his hopes of writing a book one day and inspiring the next generation of young people living with CF to believe that their diagnosis does not have to define their future. Whether you're a golf fan, part of the cystic fibrosis community, or simply love stories of perseverance, this episode is a reminder that determination, support, and advances in medicine can make extraordinary dreams possible. David is an ambassador for Cystic Fibrosis Ireland. https://www.cfireland.ie Thanks to Nicola Delaney-Foxe for connecting us! 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/featuredNew: Shop our merchandise! https://thebonnellfoundation.org/product-shop/Thanks to our sponsors:Vertex: https://www.vrtx.comViatris: https://www.viatris.com/enRead us on Substack: https://substack.com/@lstb?utm_campaign=profile&utm_medium=profile-pageWatch our trailer of Embracing Egypt: https://youtu.be/RYjlB25Cr9Y

The podcast content may contain sensitive topics. Listener discretion is advised.Every year, thousands of Americans fall in love online and some lose everything. In 2025 alone, the FBI reported over $1.3 billion stolen through online romance scams, most targeting women ages 40 to 69. These crimes don't just breakhearts but they destroy lives.Romance scams often seem to begin innocently enough: a message on Facebook, a match on Tinder, a charming stranger on Hinge or OK Cupid. But behind the screen, many victims are being groomed by criminals (sometimes even criminal networks) that know exactly how to weaponize loneliness, grief, and hope. They study emotions, mirror empathy, andbuild trust until the victim believes they've found “the one.” Then comes the manipulation. Requests for money, offering investment “advice”, or excuses for why they can't meet in person.In this episode of the P3Kids Podcast (Protect & Prevent), Opal Singleton shares with you how these scams work and how to protect  yourself or a family member. You'll learn:·       How to verify who you're talking to online·       The red flags that signal emotional grooming and “love bombing”·       Why a reverse‑image search or private investigator can save you from financial ruin·       And how to protect yourself and your loved onesbefore affection turns into exploitationThis isn't just about money, it's about reclaiming trust, dignity, and safety in a digital world where love can be dangerouslymanipulated.Sign up for the free weekly MillionKids.org eblast with REAL stories, REAL trends, REAL tactics, and REAL ways to protect your family.Website: https://MillionKids.orgEmail: info@MillionKids.orgBe sure to follow and like our posts on:Facebook: https://www.facebook.com/IEMillionKidsInstagram: https://instagram.com/MillionKidsTeen

We talk with Luna Westish about growing up in The Way International and how it shaped money, relationships, and control over her body. We trace what it takes to leave a high control religion and rebuild boundaries, community, and a sense of self. • growing up with questions that get shut down • learning later that the group is widely labeled a cult • recruiting tactics, love bombing, and financial manipulation • sexual coercion, abuse, and the danger of offshoot fellowships • boundary violations in childhood and how they echo into adulthood • the “coffee” invitation moment that clarifies danger • leaving as a decision that takes years to form • responsibility versus culpability for adults who choose the system • rebuilding life through work changes, mutual aid, and self-trust • healing in phases, chronic illness limits, and listening to the body If you enjoyed the episode and would like to help support the show, please follow and subscribe. You can rate and review your feedback on any of our platforms listed in the description. Send us Fan MailSupport the showAdditionally, you can now also watch the full video version of your favourite episode here on YouTube. Please subscribe, like or drop a comment letting us know your thoughts on the episode and if you'd like more stories going forward!If you would like to offer any feedback on our show or get in touch with us, you can also contact us on the following platforms:Website: www.multispective.orgEmail: info@multispective.org Instagram: www.instagram.com/multispectivepodcast Facebook: www.facebook.com/multispectiveorgReddit: www.reddit.com/r/multispectiveSupport the show: https://www.patreon.com/multispectiveProducer & Host: Jennica SadhwaniEditing: Stephan MenzelMarketing: Lucas PhiriFatty15 promotes healthy metabolism, balanced immunity, and heart health. 2 out of 3 customers report near-term benefits, including calmer mood, deeper sleep or less snacking, within 6 weeks. 20% off on purchases link and code: ...

"Can I come home with you?" It's not a question you'd expect from a nutritionist, but it's the one that launched an entirely new profession.This month on the ANMA Podcast, we sit down with Anne Masri, founder of MediChefs, whose own health crisis 30 years ago set her on a path she never saw coming. What she discovered along the way exposed a blind spot in nearly every wellness practice — and her answer to it has physicians, patients, and chefs lining up.Anne Masri is a board certified nutritional chef and nutritional consultant. She is the founder of MediChefs, a private cheffing service that uses nutritional therapy to prevent and reverse disease. MediChefs bridges the gap between diagnosis and food on the table. Anne, like many in the health and wellness space, found an answer to her own health challenges through integrative health practices. She has been walking the talk for 30+ years and is helping others reach their optimal health with years of curated wisdom.Tune in to hear:The moment Anne realized why even the most motivated clients fail to follow their eating plans — and what she did about itHow chefs, caregivers, and home cooks are turning a passion for food into a credentialed career in health and wellnessAnne's simplest tip for using food more intentionally, starting with your very next mealPlus, this month's Practice Pointer: the one set of documents every natural health practitioner should review right now — and the questions to ask when you do.Connect with MediChefs:Website: medichefs.comAbout Anne & the MediChefs philosophy: medichefs.com/about-usBoard Certification Program: medichefs.com/become-a-medichefHire a MediChef: medichefs.com/contactPhone: (833) MED-CHEFEmail: info@medichefs.comANMA 45th Annual Convention & Educational SeminarAugust 28–30, 2026 — Westgate Las Vegas Resort & CasinoJoin the natural health community for education, connection, and professional growth. Hear from leading voices in natural health, explore the exhibit hall, earn CEUs, and connect with professionals from across the country. Special room rates start at just $55/night.Registration and room rate deadline: August 1, 2026 Register and book your room at anma.org/conventionConnect with us:Stay tuned for updates on the 45th Annual ANMA Convention at anma.orgAmerican Naturopathic Medical Association: ⁠https://www.anma.org⁠American Naturopathic Medical Certification Board: ⁠https://www.anmcb.org⁠American Naturopathic Medical Accreditation Board: ⁠https://www.anmab.org⁠Society of Complementary Alternative and Holistic Practitioners: https://www.scahp.orgEmail: admin@anma.orgThis podcast is produced by Espresso Podcast Production: https://www.espressopodcastproduction.com/Disclaimer: This podcast is for educational purposes only and should not be taken as medical advice. Consult your doctor before implementing any information shared. Views expressed are those of the speakers and do not necessarily reflect ANMA or ANMCB positions.

Dreams and Determination: Meet four Inspiring students, Living with cystic fibrosis. One of the greatest joys of The Bonnell Foundation is helping young adults living with cystic fibrosis pursue their educational dreams. Every year, we award scholarships to students attending universities, trade schools, and community colleges. While these scholarships help with tuition and expenses, they also send an important message: we believe in these students and in the futures they are building. Living with cystic fibrosis often means balancing classes, careers, friendships, and family life alongside daily treatments, medications, and frequent medical appointments. For many families, the financial burden of CF can make the cost of higher education even more challenging. That's why our scholarship program is so meaningful. Each year, our top recipients receive $2,500 to help them continue their education and pursue their goals. The thank-you notes we receive from recipients are heartfelt reminders that a scholarship is about much more than money. It is about hope, opportunity, and encouragement. On this week's podcast, we are honored to introduce four remarkable scholarship recipients whose determination and resilience inspire us. Serena Scillia is a 20-year-old from Westerville, Ohio, attending Bowling Green State University. Serena is studying Early Childhood Education and hopes to become a teacher. When she's not focused on her studies, she enjoys coaching volleyball, reading, and spending time with her family and beloved dog. Serena's passion for helping others shines through in her career choice, and she's determined to make a difference in the lives of children. Jayla Jacobs has been living with cystic fibrosis since she was diagnosed at age five. Now 18 years old, she has already become a powerful advocate for the CF community. Jayla has spoken at multiple fundraising and awareness events, including the Cystic Fibrosis Foundation's Guys and Dolls Auction Gala, where she helped raise an incredible $2.2 million for CF research. This fall, she will begin studying English at North Carolina State University. Jayla loves outdoor adventures, drawing, and writing stories. She also understands the impact of CF on families, with two of her brothers living with the disease as well. Isabella Banaszynski is preparing for an exciting new chapter as she heads to Drexel University in Philadelphia this fall. An accomplished club wrestler and aspiring architect, Isabella has already demonstrated the discipline and determination needed to succeed in demanding environments. She plans to major in Architecture while continuing to pursue her athletic interests. Isabella's journey is proof that living with CF does not define what is possible. Ben Ferguson attends Taylor University and is majoring in Finance. Originally from Columbus, Indiana, Ben comes from a large family with four brothers and one sister. While he is the only member of his family living with cystic fibrosis, he has never allowed the disease to limit his ambitions. Ben is focused on building a successful future while managing the daily challenges that come with CF. These four young adults represent the strength, perseverance, and optimism that define so many people in the cystic fibrosis community. Their stories remind us that while CF can create obstacles, it does not determine a person's potential. Join us on this week's podcast as Serena, Jayla, Isabella, and Ben share their experiences living with cystic fibrosis, pursuing higher education, and what receiving a Bonnell Foundation scholarship means to them. Their stories are inspiring, their goals are ambitious, and their futures are bright. This is exactly why The Bonnell Foundation continues its scholarship program year after year: to invest in dreams, support determination, and help the next generation of leaders living with cystic fibrosis reach their full potential. 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/featuredNew: Shop our merchandise! https://thebonnellfoundation.org/product-shop/Thanks to our sponsors:Vertex: https://www.vrtx.comViatris: https://www.viatris.com/enRead us on Substack: https://substack.com/@lstb?utm_campaign=profile&utm_medium=profile-pageWatch our trailer of Embracing Egypt: https://youtu.be/RYjlB25Cr9Y

On this episode host Jonathan Chance talks with his guest, respected clinical researcher and consultant Bill Cavanagh talk about how there is hope for patients because of the research being done on prostate cancer and what this means for men battling the disease. On this episode Jonathan and Bill discuss: ·       What is the biggest misconception people have about break through cancer treatments?·       How researchers and the work they do provides hope for people who are fighting prostate cancer.·       What motivates researchers like Bill in the fight against prostate cancer?Prostate Cancer Aware is grateful to the Jevan and Ruzanna Chimayan Foundation for their generous donation, which helps fuel our podcast and website to raise critical awareness about prostate cancer and the PSA test around the world.For more information about Bill Cavanagh and his research, visit his website at: https://www.abscopalevents.com/blog  Prostate Cancer Aware is a copyrighted production.  No content maybe rebroadcast or reproduced without the expressed written consent of the Friedman Sidrow Foundation.  For more information about prostate cancer, the PSA test, men's health and Jonathan's inspiring new book Unaware, which is about his battle with prostate cancer.Visit our website at:  https://www.iknowmypsa.orgEmail us at:  https://www.iknowmypsa.org/contactus/Follow Prostate Cancer Aware on social media at:Facebook -  https://www.facebook.com/iknowmypsa Twitter -  https://twitter.com/iknowmypsa or @iknowmypsaThank you for listening!  Remember, Stay Aware and Stay Healthy.™

I thoroughly enjoy doing my podcasts. It's the one thing I truly miss from my television news reporting days — interviewing extraordinary people every single day. Through The Bonnell Foundation, I now host a weekly podcast, and honestly, I wish I could do them daily. Not only does it bring me so much joy, but it also gives me the opportunity to share the stories of the incredible people I meet along the way. Kate O'Donnell is one of those people. Kate was inspired by a brother she never met. Her brother Joey died from cystic fibrosis just three months before she was born. CF is a brutal disease, but the community that rises from this tragedy is filled with some of the most inspiring, compassionate, and courageous people you will ever meet. Kate's father, Joe O'Donnell, became one of the cystic fibrosis community's most influential volunteer leaders and fundraisers. Together with his wife Kathy, he founded The Joey Fund in memory of Joey. Today, Kate is helping carry that legacy forward and bringing new energy and passion to the mission. And trust me — by the end of this podcast, you're probably going to want a Joey hat of your own. You can support The Joey Fund here: https://joeyfund.org/donate-1 Kate is smart, fun, energetic, and deeply committed to making a difference in the CF community. I know you'll be inspired by everything she continues to do. 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/featuredNew: Shop our merchandise! https://thebonnellfoundation.org/product-shop/Thanks to our sponsors:Vertex: https://www.vrtx.comViatris: https://www.viatris.com/enRead us on Substack: https://substack.com/@lstb?utm_campaign=profile&utm_medium=profile-pageWatch our trailer of Embracing Egypt: https://youtu.be/RYjlB25Cr9Y

Feeling “emotionally left” can mess with your whole life, even when nothing looked obviously wrong from the outside. Danica joins us to talk about complex trauma through the lens so many people recognize: caregivers who were physically present, but emotionally misattuned. That chronic gap can teach a kid to overfunction, stay hyper aware, and believe they have to handle everything alone.We dig into what complex trauma actually means, how it differs from complex PTSD symptoms, and why survivors often become brutally hard on themselves. We connect the dots between self blame, people pleasing, perfectionism, and repeating the same relationship with a “new actor.” Danica breaks down the nervous system piece in plain language, including why ambiguity can feel dangerous and why “control” is often a request for something healthier: containment, regulation, and the ability to come back to baseline after stress.You'll also hear practical, grounded approaches from somatic therapy and trauma informed care: meeting basic needs as real nervous system work, rebuilding hunger and thirst cues, and learning to describe emotions as sensations instead of getting trapped in a single story. We also talk attachment adaptations, titration, and why going low and slow in dating can be a powerful way to build earned security.If you've been wondering whether healing is possible after childhood emotional neglect, this conversation offers both clarity and hope. Subscribe to Multispective, share this with someone who needs it, and leave a rating and review so more listeners can find these trauma healing tools.Send us Fan MailSupport the showAdditionally, you can now also watch the full video version of your favourite episode here on YouTube. Please subscribe, like or drop a comment letting us know your thoughts on the episode and if you'd like more stories going forward!If you would like to offer any feedback on our show or get in touch with us, you can also contact us on the following platforms:Website: www.multispective.orgEmail: info@multispective.org Instagram: www.instagram.com/multispectivepodcast Facebook: www.facebook.com/multispectiveorgReddit: www.reddit.com/r/multispectiveSupport the show: https://www.patreon.com/multispectiveProducer & Host: Jennica SadhwaniEditing: Stephan MenzelMarketing: Lucas PhiriFatty15 promotes healthy metabolism, balanced immunity, and heart health. 2 out of 3 customers report near-term benefits, including calmer mood, deeper sleep or less snacking, within 6 weeks. 20% off on purchases link and code: ...

Jon Gay and I had a great time recording this podcast because we not only talked about podcasting, but also reflected on our years in the broadcast business and what people should know before starting a podcast of their own. There's a lot of laughter, behind-the-scenes stories, and practical insight for anyone curious about the world of audio storytelling. Jon and I go way back to our radio days. We worked at different stations in the same building, crossing paths in a fast-paced world built on deadlines, storytelling, and finding the right words at the right moment. Radio teaches you quickly how to think on your feet, write with purpose, deliver information clearly, and connect with people through your voice. What's interesting is that neither of us spent much time trying to “sound like radio people.” We focused on being authentic, credible, and conversational. The voice came naturally because the storytelling mattered more than the performance. For me, podcasting became a natural extension of the work I do with my Foundation. It gave me a platform to continue having meaningful conversations, telling important stories, and creating a space where people feel comfortable enough to share their experiences honestly. That's one reason I was thrilled to eventually hire Jon as my podcast editor. I already knew his professionalism, creativity, and work ethic from our radio days, and he understood the heart behind what I was trying to create. Jon has a real talent for shaping conversations into stories that people genuinely connect with. In this episode, we talk about the evolution from radio to podcasting, the art of authentic storytelling, and why genuine connection matters more than ever in today's media landscape. And finally, Jon, it seems like everyone wants to start a podcast these days. I can't tell you how many people ask me where to begin, and honestly, I don't always have the time to walk everyone through it. So when someone comes to you and says, “I want to start a podcast,” what's the very first thing you tell them? If you want to talk with Jon you can contact him here: jag@jagpodcastproductions.com 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/featuredNew: Shop our merchandise! https://thebonnellfoundation.org/product-shop/Thanks to our sponsors:Vertex: https://www.vrtx.comViatris: https://www.viatris.com/enRead us on Substack: https://substack.com/@lstb?utm_campaign=profile&utm_medium=profile-pageWatch our trailer of Embracing Egypt: https://youtu.be/RYjlB25Cr9Y

In this REWIND episode Gary Mansfield speaks to Rob Munday (@mundayspace)Rob Munday is a World renowned Holographic artist, who has produced commissioned portraits of [among many others] HM Queen Elizabeth II, Angelina Jolie and Karl Largerfeld.His Portrait of HM Queen Elizabeth II was later used on Jersey's £100 banknote and postage stamp.His latest series ‘Naturaliaum' is a set of large-scale individual lenticular flower portraits, produce in such a way that they are 3D to the naked eye. Munday is just in the final stages of creating a ‘mobile' camera set-up, enabling him to take lenticular portraits outside of the studio with much more ease. For full line up of confirmed artists go to https://www. ministryofarts.orgEmail: info@ministryofarts.orgSocial Media: @ministryofartsorg Hosted on Acast. See acast.com/privacy for more information.

A mother tells her child that one “impure” thought could mean eternal fire and she claims she can read minds. That fear becomes the fuel for a family-run, high-control religious group where confession lasts until 3 a.m., “demons” explain every human impulse, and doubt is treated like a moral failure. Peggy, author of *Surviving the Family Kingdom* and a psychotherapist, unpacks what it's like when the cult leader is also your parent. Peggy walks us through the early chaos that made her mother vulnerable to extreme beliefs, the Pentecostal influence that normalized spiritual spectacle, and the slow shift from searching for faith to building a closed system of control. We talk about coercive control tactics like sleep deprivation, isolation, punishments, the “hot seat,” and how love bombing can flip into fear the moment someone stops complying. Then we follow the moment everything breaks open: motherhood. Peggy describes how parenting clarified what she could no longer accept, how she stopped policing her own mind, and why leaving required a strategy that protected her from manipulation. We also explore the harder, less-discussed part of cult recovery and religious trauma: rebuilding identity, living with triggers, and navigating a complicated relationship with an aging parent who never offers acknowledgement. Peggy shares how EMDR helped neutralize the images and body memories that kept her feeling haunted. If this conversation helps you, subscribe, share it with someone who needs it, and leave a rating and review so more listeners can find stories of survival and recovery.Send us Fan MailSupport the showAdditionally, you can now also watch the full video version of your favourite episode here on YouTube. Please subscribe, like or drop a comment letting us know your thoughts on the episode and if you'd like more stories going forward!If you would like to offer any feedback on our show or get in touch with us, you can also contact us on the following platforms:Website: www.multispective.orgEmail: info@multispective.org Instagram: www.instagram.com/multispectivepodcast Facebook: www.facebook.com/multispectiveorgReddit: www.reddit.com/r/multispectiveSupport the show: https://www.patreon.com/multispectiveProducer & Host: Jennica SadhwaniEditing: Stephan MenzelMarketing: Lucas PhiriFatty15 promotes healthy metabolism, balanced immunity, and heart health. 2 out of 3 customers report near-term benefits, including calmer mood, deeper sleep or less snacking, within 6 weeks. 20% off on purchases link and code: ...