Podcasts about disabled

Seattle man buys billboards shaming city’s progressive politicians, ‘I shouldn’t have to’: Disabled veteran spends $3,000 on billboard calling out Seattle on crime, drugs, Seattle councilmember says sex trade, gun violence problems continue, John and Joe debate the safety of Seattle, Deborah Juarez chastises John for speculating about the Mayor Recall petitioners’ motivations, 69 Seattle cops quit as SPD heads for worst year since 2023 // Pierce County Sheriff Swank launches podcast, takes aim at law targeting elected sheriffs in debut episode, Pierce County Sheriff Keith Swank claims Shon Barnes challenged him to a fight // LETTERS

Sometimes pushing forward looks like going faster. And sometimes it looks like recording a podcast from bed. In Episode 155 of Pushing Forward with Alycia, Alycia Anderson welcomes her husband, Marty Anderson, back to the microphone for one of their most personal conversations yet. Over the past several months, Alycia and Marty have found themselves navigating an unexpected medical journey that has included multiple hospitalizations, a bowel obstruction, a uterine embolization and the placement of a nephrostomy tube to protect Alycia's functioning kidney while her body heals. But this episode is not simply a medical update. It is a conversation about aging with disability, something Alycia and Marty are discovering requires continuously getting reacquainted with bodies that change over time. Both are wheelchair users. Both live with different disabilities. And after nearly fifteen years of marriage, the couple is experiencing one of those seasons when the vows “in sickness and in health” become very real. When the Body Changes the Plan Alycia has spent a lifetime adapting. Born with a congenital disability, she describes herself in the episode as a “science project that's gone right.” From the outside, people may simply see a wheelchair user. Internally, however, her anatomy and health are far more complex. Now, aging, disability and perimenopause are colliding in ways she could not have predicted. The physical challenges have also introduced something emotionally difficult for a lifelong achiever: being forced to slow down. Alycia admits that one of her greatest fears has not simply been the medical uncertainty. It has been losing momentum. After an incredibly successful Disability Pride Month, nine events, the company's first live webinar and Alycia's Pitch Perfect competition win at Disability:IN, suddenly the body demanded something completely different. Rest. Running a Business When Life Says Stop Being self employed might seem like it would make dealing with illness easier. Alycia and Marty explain why the opposite can be true. There is no traditional medical leave. No department waiting to absorb the workload. No manager to tell that you will be unavailable for the month. When one partner becomes sick, the other is balancing caregiving, household responsibilities, client needs and the business itself. It has forced Marty into an even larger role while simultaneously asking Alycia to release control over work she deeply cares about. And for a self described Type A personality, that surrender has not come easily. When Both Partners Have Disabilities One of the most compelling parts of the conversation explores a question people have asked Alycia and Marty throughout their relationship: How will two disabled people take care of each other? Their answer is beautifully simple. They adapt. When Alycia became unable to transfer as easily after her hospitalization, Marty drew from years of disability experience and ordered a transfer board. They modified routines. They used equipment differently. They accepted home healthcare. They figured it out together. And while their disabilities can create additional logistical complications, Alycia says they also create something extraordinarily valuable within their relationship: understanding. Marty does not need an explanation of what it feels like when the body suddenly stops cooperating. Alycia does not need to translate disability for him. That shared understanding creates an intimacy rooted in lived experience. “I Don't Have to Be the Strongest Person in the Room Every Day” Perhaps the most vulnerable moment comes when Marty asks Alycia what this season is teaching her. She does not manufacture an inspirational answer. Instead, she admits that she does not know yet. She is still inside it. But she is beginning to understand something important. It is okay to rest. It is okay to say she is too tired. It is okay to receive help. And it is okay not to be the strongest person in the room every single day. For someone whose career has been built around resilience, achievement and pushing forward, that may be one of the biggest adaptations of all. Love as an Accessibility Tool There is also a love story woven quietly through this episode. Alycia talks about lying in bed while recovering, looking over at Marty and feeling safe. She describes this medical season as a reminder of the depth their marriage has developed over time. Not because everything has been easy. Because it has not. But because when things become difficult, they know how to turn toward one another. Their marriage becomes another form of adaptation. Another form of access. Another reminder that independence does not have to mean doing everything alone. Episode Themes ♿ The Things Disability Keeps Teaching Us ♿ Aging with disability and adapting as bodies and needs change ❤️ Disabled love and marriage through unexpected medical challenges

Try Mars Men https://mengotomars.com #ad #sponsored Follow the boys! @bradleyjohnson @realiswill Support the Podcast! https://www.patreon.com/theleoanddannyshow Subscribe to the Crew! Danny's Channel ▶ / @dannymullenofficial Follow the Crew! Leo's IG ▶ / leofdot Danny's IG ▶ / dannymullen Leo's Twitter ▶ @Leodottavio Danny's Twitter ▶ @DannyMullenfts

Phamaly Theatre Company is the longest-running theater company in the U.S. dedicated to performers with disabilities. Managing Director Corinne Melon and blind actor Romy Lopez share behind-the-scenes challenges, hilarious moments, and the empowering ways that humor, camaraderie, and creativity break down stereotypes.

Disability Advocate Shane Hryhorec joined Will and Stacey. See omnystudio.com/listener for privacy information.

New Childrens Commissioner Jane Searle sets out her agenda for the role in her first media interview since beginning the job two weeks ago.

What if the trip you thought was impossible was simply waiting for the right access? For many disabled travelers, dreaming about a destination comes with an immediate second thought: But can I actually go there? In Episode 154 of Pushing Forward with Alycia, Alycia Anderson sits down with Karen Morales, luxury travel advisor, speaker, wheelchair user, disability travel advocate, and leader within Fora Travel's accessibility initiative, for a conversation that may completely change the way you think about accessible travel. Karen lives with limb girdle muscular dystrophy and began using a wheelchair full time in 2020. But losing mobility did not mean losing her identity as a traveler. Instead, it pushed her to rethink what independence, adventure, and possibility could look like. And she went exploring. Japan. Morocco. Sicily. Costa Rica. France. Canada. Africa. Karen discovered that some of the destinations disabled travelers assume will be impossible can deliver extraordinary experiences when the right people, information, creativity, and hospitality come together. Her work is also proving something the travel industry cannot ignore. Fora's accessibility initiative has been associated with $75 million in accessible travel sales, showing that accessible hospitality is not merely about regulations or checking an ADA box. It represents a significant and underserved business opportunity. Karen's philosophy is refreshingly simple: Travel is travel. Hospitality is hospitality. Whether someone needs a roll in shower, a specific bed height, allergy accommodations, a medical refrigerator, sensory support, a service animal accommodation, or simply a different pillow, great hospitality begins by understanding what that traveler needs before they arrive. This conversation goes far beyond accessible hotel rooms. Alycia and Karen talk about accepting mobility devices, reclaiming independence, traveling with progressive disability, universal design, raising expectations, the power of lived experience, and why disabled people should not have to beg to participate in life's most beautiful experiences. And Karen leaves us with one invitation: Stop assuming the world is closed to you before you explore what might actually be possible.

Hosted on Acast. See acast.com/privacy for more information.

People Magazine recently published a list of more than 60 celebrities who have publicly shared their abortion stories. The article claims these stories can help erase abortion stigma—but when we actually read what many of these celebrities said, we found something very different.In this episode of the Pro-Life Podcast, we unpack People Magazine's list, talk about what these stories reveal about the culture surrounding abortion, and discuss how we can respond with compassion instead of simply telling women that abortion is their only option.We also discuss New York's new physician-assisted suicide law and the slippery slope of euthanasia.If you or someone you know is facing an unexpected pregnancy, you are not alone. Find a Pro-Life pregnancy resource center near you using our Pregnancy Resource Map.And join us at the Texas Right to Life Life Gala on September 26 to hear Rebekah Hagan share her powerful story.Like, follow, and share this episode with a friend!--Sources: Celebrities Who Have Shared Their Abortion Stories to Help Women Feel Less Alone https://people.com/celebrity-abortion-stories-12027981New York Assisted Suicide Law Goes Into Effect Killing the Elderly and Disabled https://www.lifenews.com/2026/08/04/new-york-assisted-suicide-law-goes-into-effect-killing-the-elderly-and-disabled/Pregnancy Help https://texasrighttolife.com/pregnancy-assistance/--Follow us: ⁨@TexasRightToLife⁩Join Patriot Mobile: https://patriotmobile.com/texasrighttolife/ Get a FREE MONTH when you use the offer code TRTL.Find your favorite Pro-Life gear at Store.TexasRightToLife.com and use code PODCAST at checkout for 15% off. You can subscribe to the ProLife Podcast at:Apple Podcasts: https://podcasts.apple.com/us/podcast/prolife-podcast/id1612172721Spotify: https://open.spotify.com/show/3povSwEEJ37aESIoeqPx2qCastbox: https://castbox.fm/channel/id4813902?country=usRadioPublic: https://radiopublic.com/prolife-podcast-6rmx3NAmazon Music: https://music.amazon.com/podcasts/1dea935a-608a-4fed-8174-427f256e9d72/prolife-podcastiHeart Radio: https://www.iheart.com/podcast/269-prolife-podcast-105028810/And Pocket Casts: https://pca.st/9gmni47j FOLLOW US:Facebook - https://www.facebook.com/TexasRightToLife/Instagram - https://www.instagram.com/txrighttolife/X - https://x.com/txrighttolifeWebsite - https://texasrighttolife.com

Disability Issues Minister Louise Upston has announced amendments to the Disability Support Services Bill, but some say the bill is still harmful. New Plymouth mother Victoria Coleman has a young son with complex disabilities. She spoke to Ingrid Hipkiss about her concerns.

Watch the video version on YouTube: https://youtu.be/INRjvz4emc4 Hosts Jodi and Keith interview documentary filmmaker Reid Davenport about his film "Life After," which revisits the 1983 case of Elizabeth Bouvia to examine ongoing debates about assisted dying, autonomy, and systemic abandonment of disabled people. Reid explains he was drawn to tensions between nondisabled and disabled progressives and to how media framed Bouvia's desire to die as caused by disability while ignoring factors like divorce, miscarriage, discrimination, isolation, poverty, and inadequate healthcare. He argues bodily autonomy is shaped by surrounding conditions and that people need the right and support to live as they choose before the right to die. The discussion highlights medical and state ableism, misjudgments about disabled quality of life, the need to center disabled voices, and concerns illustrated in the film about assisted suicide access in Canada amid poor support and care. Watch "Life After" on PBS Independent Lens: https://www.pbs.org/independentlens/documentaries/life-after/ "Life After" website: https://www.lifeafterfilm.com/ Reid Davenport's website: https://www.reiddavenport.com/

It's feared Clare's disabled drivers will be left worse off under a new vehicle adaption scheme due to be rolled out. The Government is currently progressing a grant programme which will cover minor adaptations to cars for people with mobility needs. The coalition is also reviewing the existing disabled drivers and passengers scheme which offers VAT and VRT reliefs, sparking concerns from industry leaders that it may be phased out. Clare Aontú Representative June Dillon says clarity is urgently needed.

It's feared Clare's disabled drivers will be left worse off under a new vehicle adaption scheme due to be rolled out.   The Government is currently progressing a grant programme which will cover minor adaptations to cars for people with mobility needs.   The coalition is also reviewing the existing disabled drivers and passengers scheme which offers VAT and VRT reliefs, sparking concerns from industry leaders that it may be phased out.   Clare Aontú Representative June Dillon has been telling Clare FM's Daragh Dolan that clarity is urgently needed. To discuss this further, Alan Morrissey was joined by Desmond Lillis, a disabled driver. Photo (c) YAROVA from YAROVA via Canva

Taylor Farms, F Them too! - Ninja Slam Dance - Everybody Thinks She's a SPY - 6 Dollar discount at Best Buy??? - The R Word, Hire the Disabled. Fuck the Man!! - When People in the Media F Up - The Body Parts Admission

Ableism favors the non-disabled at any cost. That is the powerful phrase that resonates after my conversation with India Harville, an exceptionally talented dancer, educator and disability justice advocate. It conveys that ableism is structural, embedded in government systems and in our cultural norms, which limit the access of disabled people to resources, opportunity and agency over their own lives. This reality, although exacerbated in this toxic political climate is not new. It has taken fearless organizing by generations of disabled activists to forge game changing policy breakthroughs, including passage of the now embattled Americans for Disabilities Act and Fair Housing Laws. So, it is not surprising that for India, advocacy is an everyday necessity. She is active in legislative policy campaigns that advance disability justice and she uses her voice and expertise to support her fellow dancers in securing housing and attendents. At Embraced Body, the nonprofit she founded, India makes self-expression accessible to dancers with disabilities and other marginalized identities. As a consultant, she coaches organizations in taking the steps needed to create inclusive workplaces where everyone is seen and heard. We can all learn from India and for our collective humanity, we must.  

Welcome to a new episode of A Friend for the Long Haul - A Long Covid Podcast! Claire Jones, co-founder of Sista Creatives Rising and creator of Musings of a Black Disabled Elder, is a repeat guest of the pod. She has developed a five-part framework for navigating life's chaos: Clarity, Awareness, Presence, Acceptance, and Gratitude. In this episode, Claire and I talk about what it means to build a life when illness, disability, trauma, grief, and change knock us sideways.We talk about:Learning to live and resist within your capacity, and why your contribution doesn't have to look like anyone else'sClaire's experience with cancer and how it changed her relationship with self-love, joy, and worthinessWhy acceptance isn't the same thing as forgivenessGrieving the life you thought you would have while still making room for a different kind of joyThe cognitive cost of constantly trying to manage other people's experience of youLiving a COVID-conscious life without allowing other people's perceptions to define what makes a life rich or fulfilling"Getting ahead of life before life gets ahead of you”Claire reminds us that life will always contain suffering, disruption, and uncertainty. The goal isn't to become so grounded that nothing ever knocks us off course, it's to develop a way back to ourselves.Read Sista Creatives Rising and Musings of a Black Disabled Elder on Substack.A Friend for the Long Haul is a podcast about chronic illness, disability, Long COVID, community, and the messy business of building meaningful lives when our bodies and circumstances don't cooperate with the plans we made.If this conversation resonates with you, subscribe/follow the podcast and share it with someone who might need it.#LongCOVID #ChronicIllness #Disability #DisabilityCommunity #ChronicIllnessCommunity #Acceptance #Grief #SelfLove #SistaCreativesRisingFind Claire and Amaranthia's Instagram account for Sista Creatives Rising here: https://www.instagram.com/sistacreativesrising and their website is: https://www.sistacreativesrising.com/ Follow A Friend for the Long Haul - A Long Covid Podcast on Instagram: https://www.instagram.com/afriendforthelonghaulpodcast/A Friend for the Long Haul is a one disabled woman produced podcast. If you'd like to support my work, you can:Check out my shop, full of snarky long covid and chronic illness shirts, mugs, and bags. Any proceeds from the shop go right back to the podcast, or community care/mutual aid.I have an Amazon gift registry focused on back to school and things that would help at home. We're a family of 6 neurodivergent and disabled baddies. All 4 kids are heading back to school next week, and any help is always appreciated.Venmo me at: afriend4thelonghaulOr, just listen, review, and share this podcast! Thank you!

It takes a lot of effort to hide one's disability, and it all comes down to internalized ableism.Support the showWebsite: badattitudespod.comBad Attitudes Shop: badattitudesshop.etsy.comBecome a Member: ko-fi.com/badattitudespod Follow @badattitudespod on Instagram, Facebook, Threads, and BlueSkyBe sure to leave a rating or review wherever you listen!FairyNerdy: https://linktr.ee/fairynerdy

Today I am joined by Suyapa Ulloa, where we discussed how belonging to an immigrant family can shape how disability is talked about and handled within the family. We explored how caregivers/parents can support the mental health of non-disabled siblings, navigating moments of resentment without shame, and resources to support disability justice and inclusion. Suyapa shares her immigrant family's journey navigating their dynamic with a disabled child and reflects on her experience as a non-disabled elder sibling.  About today's guest: Suyapa Ulloa is a Licensed Clinical Social Worker licensed in CA, NV, and FL who can be found on the Latinx Therapy directory.  Practice website:  https://www.suyapasutherapist.com/  Find Suyapa in Our Directory: https://latinxtherapy.com/therapists/suyapa-ulloa-lcsw/  Resources:  https://sinsinvalid.org/  https://dredf.org/   https://awnnetwork.org/  https://ncil.org/   

On the High Seas, Pirates roam the waters. But one Pirate Captain in particular has a mission, a vendetta to take on the biggest monster that has been terrorizing the world, and he will stop at nothing to make sure that monster burns.Welcome back to Dungeons and Disabled as we kick off Smoke On The Water, a DnD 5.5e actual play where disabled players play disabled characters. In this first episode, Loam Tidepool and Squiggly Squenton meet in the Sunken Ship Tavern, get pulled into trouble with the crew of the Bad Moon Rising, and uncover a dangerous connection to a mysterious patron.Cast:  @MikeTheQuad   @TheThormungandr  and  @SteveSaylor  as the Game MasterFollow Dungeons & Disabledshttps://dungeonsanddisableds.com Subscribe on Apple Podcasts: https://podcasts.apple.com/us/podcast/dungeons-disableds/id1736626889Subscribe on Spotify: https://open.spotify.com/show/1I1Fz50aSFVZEdC31a3Tck?si=6b5c3e27313d47f3Twitter: https://twitter.com/dndisabledsInstagram: https://instagram.com/dndisableds

Am I the Jerk? is the show where you can confess your deepest darkest secrets and be part of the conversation.

Hello Brave Friends! I'm so excited for our very first Thriving Disabled Adults episode, #187. This is a new episode that we are doing for Season 7 of Brave Together Parenting Podcast, and our first guest is a radiant soul. I could feel his energy and his vibrance, just reading about him. So I cannot wait for you to hear this conversation with Cam Calkoen.Cam Calkoen is from New Zealand and he says that his life, defined by cerebral palsy, ambition and service above self, embodies resilience and determination. He defied expectations by mastering running and speaking, achievements once deemed impossible for him. Cam is thrilled to share his journey on Brave Together Parenting, celebrating his parents nurturing and his own mindset as he prepares for parenthood himself.Cam's story reflects values of courage and limitless potential as a full professional, inspirational speaker. He delivers a powerful message worldwide, inspiring others to surpass perceived limits and embrace their unique abilities. Please enjoy my conversation with Cam Calkoen. Find out more about Cam Calkoen here.Find more information about Life Coach, Susanna Peace Lovell here.Find Susanna's book, Your True Self is Enough here.Find our first book from We Are Brave Together, Becoming Brave Together here.Find our second book from We Are Brave Together, Suddenly Brave Together here. Find FULL episodes and clips of our podcast on Youtube here.Brave Together is the podcast for We are Brave Together, a not-for-profit organization based in the USA. The heart of We Are Brave Together is to strengthen, encourage, inspire and validate all moms of children with disabilities and other needs in their unique journeys. JOIN the international community of We Are Brave Together here. Donate to support all of We Are Brave Together's programs and offerings here. Can't get enough of the Brave Together Podcast? Follow us on Instagram , Facebook and Youtube. Feel free to contact Jessica Patay via email: jpatay@wearebravetogether.org If you have any topic requests or if you would like to share a story, leave us a message here.Please leave a review and rating today! We thank you in advance!Disclaimer

A shorter episode this week. There are only so many ways to say disability ≠ sickness.Support the showWebsite: badattitudespod.comBad Attitudes Shop: badattitudesshop.etsy.comBecome a Member: ko-fi.com/badattitudespod Follow @badattitudespod on Instagram, Facebook, Threads, and BlueSkyBe sure to leave a rating or review wherever you listen!FairyNerdy: https://linktr.ee/fairynerdy

On this episode of Crying Out Cloud, Eden Koby Naftali & Amitai Cohen sit down to unpack the wildest cloud security news of the month: from AI chatbots going rogue to massive supply chain battles.What's Inside:- The WP2Shell vulnerability and why 60% of WordPress instances were at risk- GitHub's aggressive mitigations to combat TeamPCP's supply chain attacks- Why 20-year-old vulnerabilities like SquidBleed are suddenly being unearthed by AI- The Klue hack and the hidden dangers of over-privileged AI agents in Salesforce- How attackers bypassed Meta's security using VPNs, deepfakes, and a gullible AI support bot

Luke Tarrant left a great job in finance and walked away from the corporate world, knowing he didn't want to spend his life stuck in an office. He sold everything he owned and spent years riding his motorcycle across the world, chasing the kind of adventure few people ever experience.On a ride through Colombia, everything came to a screeching halt when he was involved in a motorcycle accident that left him fighting for his life. After weeks in a Colombian hospital, Luke ultimately had his leg amputated.Since then, he's grown a massive global social media following by sharing his journey, inspiring millions with his adventures, resilience, and outlook on life.In Chapter 413, Jase and Luke dive into the motorcycle crash that changed everything, the incredible strangers who came together to help save his life, crossing the Darien Gap by boat, ending up at a cartel party in Mexico, learning to walk and ride again with a prosthetic leg, and why he refuses to move on until he returns to Colombia to finish the ride.CHAPTERS:00:00:00 Intro00:03:45 A week together at the Isle of Man TT00:12:41 Cardo Ad00:16:30 The start line, the goodbyes and the cemetery00:20:15 Racing a car at the TT with half a leg00:22:30 Two crashes in one day on the mountain road00:27:27 Back to the start00:29:19 The London School of Economics and the Wolf of Wall Street00:32:02 Walking into his boss's office and quitting00:33:45 Landing in the US with no plan and a Suzuki DR65000:36:00 Buying a house versus buying freedom00:40:30 Ten days in the dirt and how little you need00:44:15 The present self and the remembering self00:48:00 The post that blew up by accident00:52:08 AG1 Ad00:53:06 How he got into motorcycles00:55:30 His dad gets a bike licence and a tattoo01:01:25 The Vietnam tour company that changed both their dads' lives01:04:30 The Ho Chi Minh trail and the bomb craters01:07:48 Venezuela, the caravans and the Darien Gap01:12:49 Selling the American dream01:17:15 Why he would choose Mexico over the US01:20:15 Why it has to be a motorcycle01:25:49 The crash01:29:28 No memory and no vision attached to it01:31:30 Waking up in a different part of Colombia01:33:33 The leg comes off or you die01:34:29 The Instagram story that got him out01:36:00 Sepsis01:41:15 A month of deciding how much more to cut off01:45:05 The air ambulance and the prince's plane01:48:45 Going back to find out what actually happened01:57:48 Motosport Ad01:58:30 Coming home in a wheelchair02:02:59 The night he realised he had become disabled02:07:30 The beach in Mexico02:10:41 The prosthetic, and what is actually left02:14:56 Kurdistan and back in a wheelchair02:18:45 Disabled, and who actually is02:22:30 Jase on the bike he could never have as a kid02:29:15 Half a million followers and the dopamine02:36:45 Losing the warehouse in the fire02:42:04 FIST Ad02:45:00 Why he turns down most brands02:50:56 Mexico, and why he keeps going back02:53:15 The night he followed a stranger to a cartel party03:03:00 Corrupt police and the fake driving licences03:10:25 Devil's breath and getting roofiedSee Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

Paid work can be a pathway to independence, purpose, and connection — but Australians with disability are far less likely to be employed than everyone else, especially those with high support needs. Many who do work are paid well below the minimum wage, some as little as $3.31 an hour. How do we build a system for disabled workers that opens up better jobs and fairer wages? In this podcast, Grattan Associate Ben Jefferson talks to Grattan Disability Program Director Sam Bennett and Senior Associate Owain Emslie about our report, Opening doors: Better jobs and fairer wages for disabled workers, which sets out a pragmatic path to better employment outcomes for disabled people with high support needs — while ensuring no one is left behind. Read our report: https://grattan.edu.au/report/opening-doors-better-jobs-and-fairer-wages-for-disabled-workers/ Thanks for listening to the Grattan Podcast. Our research, reports and analysis are freely available thanks to the donations of listeners like you. Please consider making a regular or one-off donation at grattan.edu.au/donate. You can follow us on LinkedIn and Instagram, and sign up to our newsletter on our website to stay up to date with Grattan's news. Thanks again for listening. Instagram: www.instagram.com/grattaninstitute/ LinkedIn: www.linkedin.com/company/grattan-institute/

July 27, 2026- Legislation awaiting the governor's signature would require municipal social workers have panic buttons when making a home visit. We consider this safety proposal with Sharon McLennon Wier, executive director of the Center for Independence of the Disabled, New York.

Are we ready to have a disabled person in a position of power? Trick question! We already have.Support the showWebsite: badattitudespod.comBad Attitudes Shop: badattitudesshop.etsy.comBecome a Member: ko-fi.com/badattitudespod Follow @badattitudespod on Instagram, Facebook, Threads, and BlueSkyBe sure to leave a rating or review wherever you listen!FairyNerdy: https://linktr.ee/fairynerdy

Donate (no account necessary) | Subscribe (account required) Join Bryan Dean Wright, former CIA Operations Officer, as he dives into today's top stories shaping America and the world. In this episode of The Wright Report, Bryan breaks down Secret Service warnings that threats against President Trump's life have reached unprecedented levels, plus confirmation that Russia is feeding Iran the intel it needs to kill CIA officers in the Middle East. Bryan covers the widening fallout from the war, including destroyed CIA safe houses across the region, Saudi oil tankers turning back from the Red Sea, and Speaker Mike Johnson's blunt admission that it's time to wind the war down. He also breaks down a landmark nuclear energy deal between the US and Saudi Arabia, plus a scrappy American startup helping close the drone gap with China. Plus, Bryan covers a failed House GOP effort to lock in Trump's transgender military ban, a shocking study on Oregon's soaring rates of youth hormone treatments, record fines the Trump administration is levying against illegal aliens, and promising new medical research linking oral health to arthritis and repurposing a familiar drug to fight cancer. "And you shall know the truth, and the truth shall make you free." - John 8:32   Keywords: Wright Report, Bryan Dean Wright, Secret Service, assassination threats, Trump, Russia, CIA, Iran war, Red Sea, Saudi Arabia, nuclear deal, drones, Neros, transgender military ban, Oregon, gender dysphoria, ICE fines, cancer research

What happens when you finally meet someone who understands how your body works? For Alycia Anderson and Karen Tamley, a LinkedIn introduction became the beginning of a powerful disability sisterhood. Both women were born with sacral agenesis, a rare congenital disability affecting the lower spine. They grew up using wheelchairs during a time when disabled children were routinely underestimated, accessibility was rare, and doctors placed devastating limitations on their futures. Then they met and immediately began comparing notes: “Wait, your body does that? Mine does too.” In Episode 151 of Pushing Forward with Alycia, Karen Tamley, President and CEO of Access Living, joins Alycia for an honest conversation about rare disability, peer support, leadership, aging, Disability Pride, and the urgent fight to protect disability rights. Finding Someone Who Understands Karen did not meet another person with sacral agenesis until her twenties. Before social media, finding others with the same disability was incredibly difficult. Meeting Alycia gave both women a rare opportunity to talk openly about their bodies, mobility, health, childhoods, and aging without having to explain every detail first. Karen describes that connection as a security blanket and safety net. Their friendship reflects the importance of peer support within the independent living movement. Disabled people hold knowledge that cannot always be found in medical offices or textbooks, and that lived experience can help others navigate healthcare, access, identity, and everyday life. Growing Up Before Accessibility Alycia and Karen remember life before the Americans with Disabilities Act. They recall inaccessible buses, oversized wheelchairs, buildings with stairs, restaurants without accessible bathrooms, and being carried into spaces. Karen shares that her mother carried her up four stairs every morning to reach a summer job in an inaccessible building. She also remembers putting flip flops on her hands so she could crawl across public restroom floors. Alycia had done the same thing. Their stories reveal how exclusion becomes normalized when disabled people are not protected by enforceable civil rights. Community Living Is a Disability Right Karen explains the importance of the 1999 Olmstead decision, which affirmed that unnecessary institutionalization and segregation can be discrimination under the Americans with Disabilities Act. The decision helped establish that disabled people have the right to receive services and live within their communities. Through Access Living and partner organizations, disabled people are supported as they transition from nursing facilities and institutions into their own homes. Karen warns that Medicaid reductions, weakened enforcement, and renewed conversations about institutionalization threaten decades of progress. Disabled people are asking for the right to live in their own homes, make decisions about their lives, and participate fully in their communities. Advocacy Belongs to Everyone Karen reminds listeners that advocacy is not limited to policy experts. People can make a difference by learning from trusted disability led organizations, sharing accurate information, contacting elected officials, submitting public comments, telling personal stories, amplifying disabled advocates, and connecting with a local Center for Independent Living. Her message is clear: Do not assume your voice will not be heard. Speak up anyway. Leadership Begins in the Deep End Karen credits her parents and mentors with encouraging her to take risks. Her mother often said they were going to throw Karen into the deep end of the pool and let her figure out how to swim. That mindset followed her throughout her career. Mentors including Judy Heumann, Ed Roberts, Wade Blank, and Marca Bristo recognized Karen's potential and placed her in leadership roles before she always felt ready. Karen later served as Commissioner of the Chicago Mayor's Office for People with Disabilities, was appointed to the U.S. Access Board, and became President and CEO of Access Living. Her journey demonstrates the power of leaders who believe in someone before that person fully believes in themselves. Disability Pride and Aging For Karen, Disability Pride means community, visibility, self worth, and being okay with who we are. It does not mean loving every part of disability every day. Pride can exist alongside pain, fear, frustration, internalized ableism, and uncertainty. Alycia and Karen also discuss the realities of aging with a rare disability, including concerns about mobility, transfers, travel, health, and future independence. Both women were given frightening medical predictions as children. Decades later, they are still here, leading, traveling, advocating, creating community, and celebrating every year they were told they might never have. Aging with disability can be uncertain. It is also a privilege. You Deserve to Be in the Space Karen's Pushing Forward moment is a challenge to step outside your comfort zone. Attend the event. Accept the opportunity. Enter the room, even when you do not know anyone. Leadership does not eliminate fear or imposter syndrome. You deserve to be there. You deserve to be in that space. Two Women, One Rare Disability, and a Movement to Protect

When Qudsiya spoke with Cheryl Green and Thomas Reid back in Season 4, they were on the precipice of launching a new project with the support of our beloved disabled ancestor, Alice Wong to bring more disabled creatives into the world of podcasting. Since then, Thomas and Cheryl launched Pod Access, a hub for disabled podcasters, including a library of disabled led podcasts, a skill share platform, a podcast featuring insights about how to launch and grow a podcast specifically designed for disabled podcasters, and many other resources and opportunities for collaboration.  In this episode, you'll get a firsthand window into Cheryl and Thomas's podcasting origin stories, their creative process, and why they believe disability isn't a specialty topic—it's an essential lens for telling stories about everything from culture, to climate, to the economy. Nearly six years ago, Alice Wong introduced Qudsiya to Cheryl Green, who then introduced her to Thomas Reid. Alice began a chain of connections without which Down to the StrutsWould never have been born. This is a testament to the power of disability community, and the magic that spreads when we help each other share our stories --Let us know what you think with a comment or review!Visit our website⁠ ⁠for⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ transcripts⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠.⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Subscribe to Qudsiya's Substack, ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Getting Down To It⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Support the team behind the podcast ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠with a donation⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠

President of 'Riding for the Disabled' Liz Dwyer told Ross Stevenson and Russel Howcroft a lot of the items stolen are fundamental to their existence, and they can not afford to replace them.See omnystudio.com/listener for privacy information.

Link Up w/The Morning Sickness Digitally All Over:Instagram: @hms_98_official, @bosskupd, @bretvesely, @dickToledoX/Twitter: @HMSon98, @DickToledo, @bretveselyFacebook: @HMSKUPDYouTube: @hmspodcast9320, @98kupdRequest/Call in/Wakeup Song line:(IN AZ) 602.585.9800More HMS: holmbergpodcast.com, 98kupd.comEmail: dtoledo@98kupd.com, bvesely@98kupd.com, bbogen@98kupd.comSee Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

Link Up w/The Morning Sickness Digitally All Over:Instagram: @hms_98_official, @bosskupd, @bretvesely, @dickToledoX/Twitter: @HMSon98, @DickToledo, @bretveselyFacebook: @HMSKUPDYouTube: @hmspodcast9320, @98kupdRequest/Call in/Wakeup Song line:(IN AZ) 602.585.9800More HMS: holmbergpodcast.com, 98kupd.comEmail: dtoledo@98kupd.com, bvesely@98kupd.com, bbogen@98kupd.comSee Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

A call to place disability at the center of climate and disaster responsesEvery disaster is a disability disaster, argues Angela Frederick. Disabled Power: A Storm, A Grid, and Embodied Harm in the Age of Disaster (NYU Press, 2025) tells the stories of Texans with disabilities who endured the 2021 Texas power crisis, which forced millions of Texas residents to endure a dayslong winter storm without heat or water. Based on 58 in-depth interviews with disabled Texans and parents of disabled children, Frederick highlights how disabled people and those with chronic health conditions are uniquely harmed when basic infrastructure such as power and water systems fail. She argues that the vulnerability people with disabilities experienced during this disaster was not an inevitable consequence of individual disabled bodies. Rather, disability vulnerability was “produced” by policies that “disabled” vital infrastructure.Frederick also emphasizes another meaning of the phrase “disabled power:” the individual and collective resilience and creativity Texans with disabilities exercised to survive the disaster. Despite common perceptions of people with disabilities as passive victims, Frederick shows how many found strategies to survive and to provide and receive care within their communities. Ultimately, the implications of this disaster extend far beyond Texas and underscore our increased vulnerability to infrastructural failures as extreme weather events become more common. Disabled Power offers a blueprint for reimagining vulnerability and resilience to center people with disabilities in disaster research and emergency response. Learn more about your ad choices. Visit megaphone.fm/adchoices Support our show by becoming a premium member! https://newbooksnetwork.supportingcast.fm/environmental-studies

A call to place disability at the center of climate and disaster responsesEvery disaster is a disability disaster, argues Angela Frederick. Disabled Power: A Storm, A Grid, and Embodied Harm in the Age of Disaster (NYU Press, 2025) tells the stories of Texans with disabilities who endured the 2021 Texas power crisis, which forced millions of Texas residents to endure a dayslong winter storm without heat or water. Based on 58 in-depth interviews with disabled Texans and parents of disabled children, Frederick highlights how disabled people and those with chronic health conditions are uniquely harmed when basic infrastructure such as power and water systems fail. She argues that the vulnerability people with disabilities experienced during this disaster was not an inevitable consequence of individual disabled bodies. Rather, disability vulnerability was “produced” by policies that “disabled” vital infrastructure.Frederick also emphasizes another meaning of the phrase “disabled power:” the individual and collective resilience and creativity Texans with disabilities exercised to survive the disaster. Despite common perceptions of people with disabilities as passive victims, Frederick shows how many found strategies to survive and to provide and receive care within their communities. Ultimately, the implications of this disaster extend far beyond Texas and underscore our increased vulnerability to infrastructural failures as extreme weather events become more common. Disabled Power offers a blueprint for reimagining vulnerability and resilience to center people with disabilities in disaster research and emergency response. Learn more about your ad choices. Visit megaphone.fm/adchoices Support our show by becoming a premium member! https://newbooksnetwork.supportingcast.fm/new-books-network

A call to place disability at the center of climate and disaster responsesEvery disaster is a disability disaster, argues Angela Frederick. Disabled Power: A Storm, A Grid, and Embodied Harm in the Age of Disaster (NYU Press, 2025) tells the stories of Texans with disabilities who endured the 2021 Texas power crisis, which forced millions of Texas residents to endure a dayslong winter storm without heat or water. Based on 58 in-depth interviews with disabled Texans and parents of disabled children, Frederick highlights how disabled people and those with chronic health conditions are uniquely harmed when basic infrastructure such as power and water systems fail. She argues that the vulnerability people with disabilities experienced during this disaster was not an inevitable consequence of individual disabled bodies. Rather, disability vulnerability was “produced” by policies that “disabled” vital infrastructure.Frederick also emphasizes another meaning of the phrase “disabled power:” the individual and collective resilience and creativity Texans with disabilities exercised to survive the disaster. Despite common perceptions of people with disabilities as passive victims, Frederick shows how many found strategies to survive and to provide and receive care within their communities. Ultimately, the implications of this disaster extend far beyond Texas and underscore our increased vulnerability to infrastructural failures as extreme weather events become more common. Disabled Power offers a blueprint for reimagining vulnerability and resilience to center people with disabilities in disaster research and emergency response. Learn more about your ad choices. Visit megaphone.fm/adchoices Support our show by becoming a premium member! https://newbooksnetwork.supportingcast.fm/american-studies

A call to place disability at the center of climate and disaster responsesEvery disaster is a disability disaster, argues Angela Frederick. Disabled Power: A Storm, A Grid, and Embodied Harm in the Age of Disaster (NYU Press, 2025) tells the stories of Texans with disabilities who endured the 2021 Texas power crisis, which forced millions of Texas residents to endure a dayslong winter storm without heat or water. Based on 58 in-depth interviews with disabled Texans and parents of disabled children, Frederick highlights how disabled people and those with chronic health conditions are uniquely harmed when basic infrastructure such as power and water systems fail. She argues that the vulnerability people with disabilities experienced during this disaster was not an inevitable consequence of individual disabled bodies. Rather, disability vulnerability was “produced” by policies that “disabled” vital infrastructure.Frederick also emphasizes another meaning of the phrase “disabled power:” the individual and collective resilience and creativity Texans with disabilities exercised to survive the disaster. Despite common perceptions of people with disabilities as passive victims, Frederick shows how many found strategies to survive and to provide and receive care within their communities. Ultimately, the implications of this disaster extend far beyond Texas and underscore our increased vulnerability to infrastructural failures as extreme weather events become more common. Disabled Power offers a blueprint for reimagining vulnerability and resilience to center people with disabilities in disaster research and emergency response. Learn more about your ad choices. Visit megaphone.fm/adchoices Support our show by becoming a premium member! https://newbooksnetwork.supportingcast.fm/public-policy

As our disabled and medically complex children grow and mature, caring for and navigating their sexual health can be a tricky topic. From appropriately navigating sexual activity, consent, basic hygiene and even more complicated topics like birth control and how puberty can bring about new health complications, we're breaking down a ton of different sexual health aspects in this episode.A huge thank you to our sponsor for this summer season, Real Food Blends! Real Food Blends are the only 100% real food meals thatare ready-to-feed for people with feeding tubes. Offering 8 different meals and1 snack for adults & kids, it's the closest thing to homemade blenderized tube feeding. Learn more at realfoodblends.com!Links:Fill out our contact form to join upcoming discussion groups!Join The Rare Life newsletter and never miss an update!Follow Amanda on Instagram @amanda.griffith.atkins!Follow Jill on Instagram @jill.arneson!Follow us on Instagram @the_rare_life!Donate to the podcast or Contact me about sponsoring an episode.

Her latest book, Out of the Box, Trish Harris shines a light on 25 deaf and disabled artists, activists and adventurers.

Watch the video version on YouTube: https://youtu.be/DoefSSe9QW0 Hosts Keith and Jodi interview the married writing team behind the pen name Sebastian Grey about their debut novel, "Merry Band of Misfits," a heist story centering disabled characters as protagonists, including Vinnie, a man with Down syndrome, and his chosen family planning a bank heist to protect their home. They discuss their film/TV background, their goal to counter "inspirational side character" tropes, and why the heist genre highlights capability, moral ambiguity, and agency. The authors describe barriers in Hollywood and why they created their indie press, Bastion House, to control the message. They detail a Kirkus Review they call an "erasure" for centering the non-disabled brother Nicholas and mislabeling or omitting key disabilities, prompting them to speak publicly. In the "Deep Cut" segment, the hosts analyze the book's themes of autonomy, caregiving, ableism, community living, humor, and low expectations. Sebastian Grey: https://sebastiangreytheauthor.substack.com/ Bastian House Publishing: https://bastianhousepublishing.com/ Purchase "Merry Band of Misfits": https://books2read.com/merry-band-of-misfits

John Hinderaker of the Power Line Blog joins Howie to discuss his new article on the number of Americans claiming to be "disabled".  Visit the Howie Carr Radio Network website to access columns, podcasts, and other exclusive content. See Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

Democracy Docket founder Marc Elias breaks down Trump's firing of the remaining commissioners at the Election Assistance Commission, the federal agency that certifies voting equipment, administers a national backup voter registration form and provides expertise and training to state election officials. It's now legally paralyzed months before the 2026 midterms. Marc argues Trump likely has two main motives: sidelining nonpartisan election expertise (as he's done with vaccines, food safety and the military) and deliberately degrading state election administration to manufacture a post-election narrative. He also warns that without commissioners, the White House may try to pressure EAC staff directly.

In June, the DOJ issued a memo that should sound alarm bells for every disabled person in the United States.Support the showWebsite: badattitudespod.comBad Attitudes Shop: badattitudesshop.etsy.comBecome a Member: ko-fi.com/badattitudespod Follow @badattitudespod on Instagram, Facebook, Threads, and BlueSkyBe sure to leave a rating or review wherever you listen!FairyNerdy: https://linktr.ee/fairynerdy

This podcast and YouTube episode features an in-depth conversation with Anthony David Vernon, a philosopher and educator, exploring the intersection of disability studies, left-wing politics, and the systemic failures of accessibility in a post-pandemic world. The discussion challenges the "normative" framework of society, examining how both civic institutions and political movements often fail to truly incorporate the voices and needs of the disabled community.Key Discussion HighlightsThe ADA and the "Checkmark" Problem: Vernon argues that because the ADA is enforced primarily through personal lawsuits and remains largely unfunded, it often results in "checkmark" compliance rather than true accessibility.The Post-Pandemic Erasure: The conversation explores how the rush to move past COVID-19 safety measures has prioritized "normative desires" over the accessibility needs of high-risk and disabled individuals.Multimodality as Justice: Implementing "ready-made" scaffolding and multiple points of entry into education and digital spaces benefits all learners, not just those with a formal diagnosis. Referenced Works (APA Format)Albers, B. (2022). Able-bodied leftists cannot abandon disabled solidarity to move on from COVID. Truthout. https://truthout.org/articles/abled-bodied-leftists-cannot-abandon-disabled-solidarity-to-move-on-from-covid/Data for Progress. (2023, October 3). Disabled voters do not believe politicians care about disabled Americans. https://www.dataforprogress.org/blog/2023/10/3/disabled-voters-do-not-believe-politicians-care-about-disabled-americansHryhorec, S. (2025, October 26). LET ME IN: Mark Butler's office isn't accessible [Video]. YouTube. https://www.youtube.com/watch?v=DEfbZzCspDkIacoboni, G. (2023). Why politics is failing disabled people and what to do about it. Independent Social Research Foundation (ISRF). https://isrf.org/blog/why-politics-is-failing-disabled-people-and-what-to-do-about-itRotarou, E. S., & Sakellariou, D. (2024). Neoliberalism and disability: The systemic erasure of access. Social Science & Medicine. https://www.sciencedirect.com/science/article/pii/S0277953623007189University of Hawaiʻi at Mānoa. (n.d.). Disability studies and political theory: A framework for inclusion. https://scholarspace.manoa.hawaii.edu/server/api/core/bitstreams/425af050-0220-49dc-b28d-f86d976dcf02/contentVarn, C. D. (2023, October). Multimodal availability for those with learning disabilities. PeerCentered. https://www.peercentered.org/2023/10/multimodal-availability-for-those-with.htmlVernon, A. D. (2023, December). Silence: Non-verbal communication in philosophy. Activated Thinker. https://medium.com/activated-thinker/silence-non-verbal-communication-in-philosophy-d5d148ba8a1dWillies, E. (2025, June 16). Anthony David Vernon advocates for social democracy as a tool of rebellion against fascism [Video]. YouTube. https://www.youtube.com/watch?v=Rs7l6jNGDzwSend us Fan Mail Musis by Bitterlake, Used with Permission, all rights to BitterlakeSupport the showCrew:Host: C. Derick VarnIntro and Outro Music by Bitter Lake.Intro Video Design: Jason MylesArt Design: Corn and C. Derick VarnLinks and Social Media:twitter: @varnvlogblue sky: @varnvlog.bsky.socialYou can find the additional streams on YoutubeCurrent Patreon at the Sponsor Tier: Jordan Sheldon, Mark J. Matthews, Lindsay Kimbrough, RedWolf, DRV, Kenneth McKee, JY Chan, Matthew Monahan, Parzival, Adriel Mixon, Buddy Roark, Daniel Petrovic,Julian, Drea, Free Beer 

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For most of us, traveling with medically complex and disabled children can feel daunting, scary, or maybe even impossible. But while not necessarily easy or simple, if travel is a priority for your family, it is possible with the right planning and preparation.In today's episode, we share the best tips and tricks from The Rare Life community. We cover everything from general planning to airplane specific tips (there are a ton!) to finding the best accommodations and more. We even have a few tips for camping with medically complex kiddos!Plus, we also dive into the big feelings that can come up for us around traveling with our kids and why it's okay if that's not a priority for your family right now. If you really want to take your disabled children on a trip, there are many ways to do it, but we also recognize that travel still isn't feasible or accessible for many.Thank you to everyone who submitted tips, tricks, hacks, and ideas to this episode! And don't forget to check our website and YouTube channel (linked below) for articles linking our favorite travel items, carriers, and tips, plus images of all the setups and devices parents in our community use.Links:Visit our Youtube channel to see thevideo version of this episode with photos of all the items mentioned and captions so you can read along!Listen to Ep 118: Organization Hacks for helpful devices when packing andtraveling.Listen to Ep 66 with Falesha Johnson on how she travels with her daughter Cali, who was machine dependent at the time.Follow us on Instagram @the_rare_life!Fill out our contact form to join upcoming discussion groups!Join The Rare Life newsletter and never miss an update!Donate to the podcast or Contact me about sponsoring an episode.

Independent investigative journalism, broadcasting, trouble-making and muckraking with Brad Friedman of BradBlog.com

Disabled people are the most unfairly treated minority in Germany, according to one former member of parliament. This is especially true in the world of work. The unemployment rate among disabled people is twice that of people with no disability. When they do find work, it's often in an institution where they are paid less than the minimum wage and where they do not have the usual rights and protections enjoyed by most employed people. Yet they are often producing goods for big companies with well-known brand names. Amy Zayed, one of very few disabled journalists working in Germany, asks what can be done to make Germany more inclusive.

A New York mother is suing a hospital for the homicide of her disabled 28-year-old daughter, who was admitted with a mild cough and died 41 days later after being intubated, sedated, and given Remdesivir, Propofol, Precedex, and Fentanyl — despite never having a COVID-19 diagnosis. Rebecca Charles says her daughter Danielle arrived at Northwell Hospital in Glen Cove with normal vitals, normal oxygen, and no pneumonia, sepsis, or respiratory distress. Records the family later obtained showed she could have been monitored or sent home. Instead, she was admitted on August 27, 2021 and died on October 6, after the hospital billed roughly $650,000. Rebecca and Free Now Foundation's Alix Mayer lay out the documents, the drug protocol, and the litigation now moving forward with a team of attorneys. Plus: Eric Bolling on the 14-point US-Iran framework, the Strait of Hormuz, election security, and the midterms; and the hosts of the Wise Nuts podcast on the Iran deal, Lebanon, voter ID, and California's election fallout. Rebecca Charles is suing a New York hospital for homicide in the death of her disabled 28-year-old daughter, Danielle, who died over 41 days, killed allegedly by narcotics and other medications “during COVID” although she did not have a diagnosis of COVID-19 at the time. Learn more at https://freenowfoundation.org Alix Mayer, MBA, is Board Chair and President of Free Now Foundation, California's leading medical freedom law non-profit. In 1996, while running a worldwide research group for Apple Inc., six vaccines for a vacation left her disabled and brain-damaged, ending her career. Now substantially recovered, she formerly served on the Children's Health Defense board and RFK Jr.'s presidential campaign finance committee. She holds degrees from Duke (BA) and Northwestern (MBA). Follow at https://x.com/freenowusa Armond Garibyan and Arno Akhverdyan are the hosts of the WiseNuts Podcast, a channel for unfiltered conversations, trending topics, and exclusive interviews, bringing in-depth discussions on topics across culture, business, sports, fatherhood, and entertainment. Follow at https://x.com/wise_nuts 「 SUPPORT OUR SPONSORS 」 • FATTY15 – The future of essential fatty acids is here! Strengthen your cells against age-related breakdown with Fatty15. Get 15% off a 90-day Starter Kit Subscription at ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠https://drdrew.com/fatty15⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ • PALEOVALLEY - "Paleovalley has a wide variety of extraordinary products that are both healthful and delicious,” says Dr. Drew. "I am a huge fan of this brand and know you'll love it too!” Get 15% off your first order at ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠https://drdrew.com/paleovalley⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ • THE WELLNESS COMPANY - Counteract harmful spike proteins with TWC's Signature Series Spike Support Formula containing nattokinase and selenium. Learn more about TWC's supplements at ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠https://twc.health/drew⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ 「 ABOUT THE SHOW 」 This show is for entertainment and/or informational purposes only, and is not a substitute for medical advice, diagnosis, or treatment. Executive Producers • Kaleb Nation - ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠https://kalebnation.com⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ • Susan Pinsky - ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠https://x.com/firstladyoflove⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ Content Producer • Emily Barsh - ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠https://x.com/emilytvproducer⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ Learn more about your ad choices. Visit megaphone.fm/adchoices

Evil MSI Background: BASE64 Statistical Analysis https://isc.sans.edu/diary/Evil%20MSI%20Background%3A%20BASE64%20Statistical%20Analysis/33072 Cisco Catalyst SD-WAN Manager Arbitrary File Write Vulnerability https://sec.cloudapps.cisco.com/security/center/content/CiscoSecurityAdvisory/cisco-sa-sdwan-arbfw-c2rZvQ TSME/SME not activating on Ryzen 7 9700X https://github.com/AMDESE/AMDSEV/issues/292 Deep-Research Agents Can Be Poisoned via User-Generated Content https://arxiv.org/pdf/2605.24245 My Upcoming Classes https://www.sans.org/profiles/dr-johannes-ullrich