Podcasts about disability advocates

The curtain rises on another powerful episode, spotlighting incredible stories and inspiring voices in the world of disability inclusion.

We're back with more incredible stories and inspiring voices in the world of disability inclusion.

Tune in to hear from Scott Ford, camp director of Michigan Blind Athletic Association's Sports camp! Give it a listen and be sure to visit https://buff.ly/sgpc3k2 for more information and camp registration!

In this episode, host, Phil Tower speaks with David Bulkowski, executive director, Disability Advocates of Kent County.Disability Advocates' mission is “to work alongside persons with disabilities as they seek to lead self-directed lives.” They provide a wide array of services throughout Kent, Mecosta, Ionia, Montcalm, and Osceola counties to individuals with physical, cognitive, mental, and sensory disabilities and their families.Dave spoke with us about their upcoming Disability Awareness Day on Saturday, March 28, at The Salvation Army Kroc Center, 2500 Division Ave in Grand Rapids.The event runs from 9 AM to 2 PM.Disability Awareness Day is designed for connection, empowerment, and action. Dave encouraged, “Whether you're an advocate, an organization, or someone navigating life with a disability, this event offers resources, strategies, and community support to help you thrive. The event will feature a Keynote Speaker: Dr. Melba Velez-Ortiz. Registration for Disability Awareness Day Online: DAKC online 

In this episode in our Allocator's Edge mini-series we welcome Craig Thomas, Chief Investment Officer of Verger Capital Management. In this role, he oversees all aspects of the firm's investment process, including asset allocation, portfolio construction and manager selection. Prior to co-founding Verger, Craig spent ten years performing similar investment duties for Wake Forest University's Office of Investments where he most recently served as Director of Investments. He also serves as a mentor with Girls Who Invest, is a board member of Disability Advocates of Northwest North Carolina, and has also served as an Advisory Board member to a number of investment partnerships. And if the name Verger Capital Management is ringing bells, it may be because the firm's CEO Jim Dunn was a guest on the podcast last year. In the episode we chat with Craig about putting Verger's 3 Ps into practice; the importance of portfolio diversification and liquidity in uncertain times; dealing with higher inflation and maintaining a focus on absolute returns; and finally, reasons to select and change fund managers. Enjoy! NEW EPISODES: We release main series episodes every two weeks on Mondays. You can subscribe via Podbean or use this feed URL (https://tvpschroders.podbean.com/feed.xml) in Apple Podcasts, Spotify, Google Podcasts and other podcast players. GET IN TOUCH: send us a tweet: @TheValueTeam  Important information. This podcast is for investment professionals only. Marketing material for Financial Professionals and Professional Clients only.  The material is not intended to provide, and should not be relied on for, accounting, legal or tax advice, or investment recommendations.  Reliance should not be placed on any views or information in the material when taking individual investment and/or strategic decisions.  Past Performance is not a guide to future performance and may not be repeated.  Diversification cannot ensure profits or protect against loss of principal.  The value of investments and the income from them may go down as well as up and investors may not get back the amounts originally invested.  Exchange rate changes may cause the value of investments to fall as well as rise.  Investing in emerging markets and securities with limited liquidity can expose investors to greater risk.  Private assets investments are only available to Qualified Investors, who are sophisticated enough to understand the risk associated with these investments.  This material may contain “forward-looking” information, such as forecasts or projections. Please note that any such information is not a guarantee of any future performance and there is no assurance that any forecast or projection will be realised.  Reliance should not be placed on any views or information in the material when taking individual investment and/or strategic decisions. The views and opinions contained herein are those of the individuals to whom they are attributed and may not necessarily represent views expressed or reflected in other Schroders communications, strategies or funds.  Any reference to regions/ countries/ sectors/ stocks/ securities is for illustrative purposes only and not a recommendation to buy or sell any financial instruments or adopt a specific investment strategy. Any data has been sourced by us and is provided without any warranties of any kind. It should be independently verified before further publication or use. Third party data is owned or licenced by the data provider and may not be reproduced, extracted or used for any other purpose without the data provider's consent. Neither we, nor the data provider, will have any liability in connection with the third party data.

Listen every weekday for a local newscast featuring town, county, state and regional headlines. It's the daily dose of news you need on Wyoming, Idaho and the Mountain West — all in four minutes or less. 

The Americans with Disabilities Act has done a lot to improve accessibility in public spaces, but people with physical disabilities still encounter barriers every day.

Australia's Parliament has approved new laws that govern the operation of the National Disability Insurance Scheme. Minister Bill Shorten has also published a list that outlines what NDIS funding can and cannot be spent on from now on. But disability advocates say all of this has been "rapidly" developed with next to no engagement with the sector - and it might not even solve the problems it's supposed to address. In this episode of the Too Hard Basket, we take a closer look at what the changes are, and why disability groups are so concerned.

In Episode 23 of True Tales by Disability Advocates, hosts MsBoye, Jennifer McKinney, and Adam Griebel welcome storyteller, actor, dancer, and friend Juan Munoz. Juan shares with MsBoye touching and humorous stories about his friendships, his childhood, and his enduring love with his late wife Susie. They discuss his journey as a dancer and his involvement with Actual Lives Austin Theater Group.  Juan's reflections on love and loss offer a poignant exploration of his life and relationships. He opens up with vulnerability & honesty,  about the challenges and blessings he encountered in his life.  Listen to hear how Juan's radical decision to embrace dance and his unwavering bond with Susie shaped his extraordinary journey and have become the foundations for his future adventures. Guest BioJuan Munez, born in Santa Maria, California, is a storyteller, actor, and certified dance instructor. Passionate about inclusive dance, Juan initially focused on teaching dance to individuals of all abilities. His journey later took him to Austin, Texas, where he performed with the Actual Lives Austin Theater Group and shared poignant, often humorous stories about his experiences. A devoted person of faith, Juan advocates for religious communities to be inclusive and accessible. His life reflects a deep commitment to community, connection, and creativity, showing how challenges can spark advocacy and the desire to build empathy and understanding through storytelling. His enduring dedication to his late wife Susie and their shared adventures exemplify a life richly lived with love and resilience. LinksArt Spark DanceBody Shift CollectiveDanceAbility InternationalClick here to listen with the full transcript.For more details about our programs go to Art Spark Texas, True Tales Podcast Page.Segments of this podcast were read by an automated voice. Inconsistencies in pronunciation and tone may occur.

The All Local Morning for Monday, September 30th 2024

Originally recorded in October 2021. n this special replay, we revisit one of my favourite conversations with Carly Findlay. Carly's journey as a writer, speaker, and activist has not only shaped disability advocacy in Australia but also inspired countless people globally. If you missed this episode the first time, now's your chance to hear how Carly uses her platform to challenge perceptions and break down barriers for people with disabilities. Listen in for powerful reflections on advocacy, identity, and the power of storytelling.   Connect with Carly:  Instagram: https://www.instagram.com/carlyfindlay/?hl=en  Website: https://carlyfindlay.com.au Carly's Books: Growing Up Disabled in Australia: https://www.blackincbooks.com.au/books/growing-disabled-australia Say Hello: https://www.booktopia.com.au/say-hello-carly-findlay/book/9781460755037.html Connect with Peta: Instagram: @petahooke Website: www.icantstandpodcast.com Email: icantstandpodcast@gmail.com Episode Transcript:https://www.icantstandpodcast.comSee omnystudio.com/listener for privacy information.

Disability advocates say they are concerned that reforms to the National Disability Insurance Scheme will make life more difficult for people with disabilities, their families and those in the sector. The new legislation – called Getting the NDIS Back on Track - contains the most significant changes to the scheme since it started a decade ago. - नेस्नल डिसएबिलिटी इन्स्युरेन्स स्कीम (एनडीआइएस) भनिने राष्ट्रिय अपाङ्गता बिमा योजनामा गरिएका सुधारले अपाङ्गता भएका व्यक्तिहरू, तीनका परिवार र यो क्षेत्रमा रहेकाहरूको जीवनयापन झन् गाह्रो बनाएको अपाङ्गता अभियन्ताहरू बताउँछन्।

Disability advocates say they are concerned that reforms to the National Disability Insurance Scheme will make life more difficult for people with disabilities, their families and those in the sector. - Para pendukung disabilitas mengatakan mereka khawatir bahwa reformasi Skema Asuransi Disabilitas Nasional akan membuat kehidupan lebih sulit bagi penyandang disabilitas, keluarga mereka, dan mereka yang bekerja di sektor tersebut.

Disability advocates say they are concerned that reforms to the National Disability Insurance Scheme will make life more difficult for people with disabilities, their families and those in the sector. The new legislation – called Getting the NDIS Back on Track - contains the most significant changes to the scheme since it started a decade ago.

The Minister for Disability Issues Louise Upston wants to strip Whaikaha or the Disability Ministry, of its role in delivering support services, and instead shift it to the Minstry of Social Development, but the backlash has been swift and scathing. Some disability advocates said the community wasn't consulted and said the ministry played an important role in giving them control over decisions that affect their lives, Director of Advocacy for IHC Tania Thomas speaks to Lisa Owen.

The National Disability Insurance Scheme ((NDIS)) has long been the subject of debate and controversy. - Skema Asuransi Disabilitas Nasional (NDIS) telah lama menjadi subjek perdebatan dan kontroversi.

This week on the Live to Walk Again Podcast we were lucky enough to visit with Carson Pforsich and Desi D'Ancona who are an Interabled Couple, Disability Advocates, and Carson also does the public speaking. We talked about how Carson suffered a spinal cord injury, how Carson and Desi met and then reconnected after Carson's SCI, how the couple are planning on raising money to help others dealing with disabilities, and what their future plans are. Follow along on their journey and connect with Carson and Desi at the link to their Instagram page below!! Please listen, like, rate, review, and share the podcast!! We're just trying to find a cure for paralysis!! Carson and Desi: IG: @carsonanddesi LTWA: IG: @livetowalkagain FB: @livetowalkagain Twitter: @Livetowalk1      

Laughter, Legacy, and New Voices"Who Will Remember Us? The Warrior Spirit of Disability Advocates" is the kickoff episode of Season 3 of the True Tales by Disability Advocates Podcast, coming to you during Disability Pride Month. The new host team of MsBoye, Jennifer McKinney, and Adam Griebel bring fresh energy and humor to the show. Together, they introduce listeners to the impactful legacy of early advocates celebrating the legacy of early disability advocates with heartwarming and playful storytelling. Featuring guest Chris Strickling, one of the original creators of Actual Lives Austin, the episode shares engaging and humorous stories about advocates who have passed, like Terrell and Felix Briones. Their personal narratives provide a raw and honest glimpse into their lives, highlighting the power of storytelling as an advocacy for the right of people with disabilities to live full adult lives. Produced by Art Spark Texas' Speaking Advocates Program, the podcast highlights the importance of humor and authenticity in advocacy through storytelling while underscoring the importance of reclaiming lost voices and celebrating the contributions of those who have paved the way for future generations. Introduction to True Tales by Disability Advocates​Welcome to True Tales by Disability Advocates Podcast, authentic voices of people thriving with disabilities, where individuals use the art of storytelling to change the world....Meet the Hosts of Season 3Hello, everyone, I'm MsBoye....Honoring the Pioneers of Actual Lives AustinWe are starting Season 3 by looking back at folks who have paved the way for us ....Chris Strickling on the Power of StorytellingTell us a little about those early days and the power of storytelling as a form of advocacy....Terrell's Morning RoutineIf you're ready, let's hear the first story. " Morning Routine" by Ter-rell...Felix Briones' Speed and HumorThe next, uh, stories are from Felix....Memories and Impact of Actual Lives AustinChris, do you have a favorite memory or story from your time with Actual Lives Austin?...Final Thoughts and FarewellWell, you know, this has just been so great....Closing Remarks and Call to ActionThank you for listening to episode one of the third season of True Tales by Disability Advocates Podcast....Click here to listen with the full transcript.For more details about our programs go to Art Spark Texas, True Tales Podcast Page.

Nova Scotia has missed its deadline to stop admitting people with disabilities into large institutions, but an official says work is still underway. The lawyer who represents the Disability Rights Commission of Nova Scotia says the missed deadline is a failure by the province. The CBC's Jean Laroche reports.

Disability advocates celebrated rare wins at a meeting of the Virginia Disability Commission Thursday afternoon. Brad Kutner has more from those who helped make the changes happen. 

More and more, it feels like our country is offering its citizens the care they need to survive, but not to thrive. At the same time, we're witnessing an increase of attempts to repeal health coverage laws like the Affordable Care Act, and privatize programs like Medicaid. This has left the disability community at the forefront of the fight to protect and expand our governments' care resources. So, what happens when you get tired of waiting around for change and you decide to take matters into your hands? We'll hear from a disability justice advocate who decided to run for office to bring awareness to the care crisis. As well as a mother of a medically complex child who founded her own lobbying organization aiming to influence healthcare policies in Congress. In our final episode of the season, we're talking about care access, disability justice and the political power of the disability community.Learn more about how you can build change at actblue.com/buildthechange or follow us on Instagram and TikTok.

Tuesday's federal budget included news that the "Canada Disability Benefit Act" will only amount to about $200 per month at maximum, and many advocates across the country are sharing concerns. The executive director of the Coalition of Persons with Disabilities Newfoundland and Labrador Nancy Reid joined us today to discuss.

Haley Flaro is the Executive Director of Ability New Brunswick.

all local 6a 2.23.24

Disability rights advocates in Connecticut are demanding better medical access. And this legislative session, they're pushing lawmakers to pass two bills. Both aim to improve medical equipment and training, and access to better care when examining, diagnosing and treating patients with disabilities. We hear from one advocacy group involved in this effort, the Citizens Coalition for Equal Access, or CC=A. Public Health Committee Co-Chair and State Sen. Saud Anwar also shares his hopes for the pair of bills — one focused on medical diagnostic equipment, the other on lifts — which he helped to draft after an informational hearing with disability rights advocates across Connecticut last September. Where We Live heard from eight members of CC=A prior to this program, who talked about some of their negative experiences in the medical setting. As Jamie Mosier shared, "Something has to be passed to make sure we get what I need, that we get what everybody needs, before we're all dead." Plus later today, wheelchair users and advocates across the state will gather at the State Capitol. They plan to rally in support of the "transformational recommendations by the legislative Wheelchair Repair Task Force to tackle the absurd delays faced by 90% of roughly 5,000 CT consumers." Task Force member and consumer advocate Jonathan Sigworth joins us to discuss this legislative push. GUESTS: Dr. Cindy Miller: Member, Citizens Coalition for Equal Access; Former Associate Professor, Yale University Ruth Grobe: Secretary, Citizens Coalition for Equal Access Jonathan Sigworth: Consumer Spokesperson, Connecticut Wheelchair Task Force; Member, CT Wheelchair Reform Coalition; Member, State Independent Living Council; Co-Founder, CEO and President, More Than Walking Carly Malesky: Student, UConn Medical School; Member, Disability Interest Group Support the show: http://wnpr.org/donateSee omnystudio.com/listener for privacy information.

Kelly talks to disabilities advocate David Lepofsky.

Jess Quarello and Taryn Lagonigro join the podcast to talk about their organization ELM, formerly known as Extra Lucky Moms. Jess and Taryn catch us up on what they've been up to and the wonderful things ELM has done in the disability community. These two incredible women are extra lucky in many ways. They are parents to beautiful children, entrepreneurs and advocates. At the start of 2024 I launched my own media company; Sprouting Productions, which focuses on producing top-notch podcasts. I have always loved the work Jess and Taryn do for the world and knew I wanted to produce a podcast for them. I'm happy to announce that The Extra Lucky Podcast will be launching in the Spring of 2024. You can find out more below. The Extra Lucky Podcast website Sprouting Productions website

Xander Van der Poll's life changed for the worse when he was a teenager.

Xander Van der Poll's life changed for the worse when he was a teenager.

Hey there, listeners! Welcome back to episode twenty of our podcast 'True Tales by Disability Advocates'. Ready for a deep dive into the theme of 'Smashing Ableism: Tales of Resilience'? Well, we've got two fantastic disability advocates with us - the brilliant Alina Arredondo and the charming Peter Richter. In this episode, they open up about their own life journeys filled with challenges, advocating for disability rights, supportive grandparents, and above all, demonstrating immense resilience. Alina pours her heart out about standing up for her rights and Peter shares golden nuggets on how gratitude supports his resilience. So, tie your seatbelts, folks! Tune in, and get ready for these genuinely enlightening narratives. Trust us; it's not just an episode, it's a vibe that will spark transformations!Guest 1Alina G.  Arredondo is a native El Pasoan who was diagnosed with Phocomelia. She does not allow her disability to be an excuse for why she cannot do certain things. Alina has a license Master in social work and currently works at the local independent living center where she empowers adults with disabilities to live as independently as possible. During her spare time, she enjoys spending time with family, dogs, and friends, panting, and singing. However, what she enjoys the most is helping out her community by volunteering with multiple agencies around the El Paso area.https://www.gograd.org/resources/students-with-disabilities/Guest 2 Peter Richter grew up in San Antonio and attended school and graduated from the Texas School for the Blind and Visually Impaired. He has two brothers and one sister and a dog he loves named Winnie. He lives with two roommates and enjoys working at his job at Whataburger. Peter has been involved with Art Spark and was an original actor with TILT Performance Group where he was in productions for 10 years.Hosts: Jennifer Howell and Joey GidsegClick here to listen with the full transcript.For more details about our programs go to Art Spark Texas, True Tales Podcast Page.

We spoke with Dave Bulkowski, Executive Director of Disability Advocates of Kent County, about serving people of West Michigan who live with disabilities, the history of Disability Advocates and more. Disability Advocates strives to eliminate systemic barriers and enhance programs so that people with disabilities can live the self-directed life they choose. They look to aid in community benefits by becoming more accessible, inclusive, and welcoming for all. They have become recognized locally and across the state, specifically for their transit advocacy, education, technical assistance on accessibility, and Universal Design through our Absolutely Accessible Kent program.  Online: Disability Advocates of Kent County

Patti and Kirk spoke with Nicki Vander Meulen and Martha Siravo. Nicki is an attorney, advocate for kids with special needs, and member of the Madison Metropolitan School District Board. Martha coordinates Madtown Mommas and Disability Advocates which supports parents and caregivers of students with disabilities.They helped us understand how why the voucher system has decimated the funds available for special education, and how the voucher system all-to-frequently hurts kids with special needs. Hosted on Acast. See acast.com/privacy for more information.

Listen to the top news from Australia and India in Hindi.

Garrett Brumfield has a dream, a dog and a high-tech mobility scooter. Cerebral palsy hasn't stopped him from living his life, it's just made him adapt and overcome. That's the encouraging message he delivers as a disability advocate. But it's not all positive messages and good vibes. Brumfield and others are on a mission to highlight accessibility gaps in rural Virginia. In this episode of Hometown Stories, we'll measure those gaps and learn how we might begin to bridge them. 

This week on the Talking Michigan Transportation podcast, conversations with two people committed to equity in transportation and access for all. First, Valerie Lefler, founder and executive director of Feonix - Mobility Rising (pronounced like "Phoenix"), talks about what inspires her work and this week's launch of the Mobility Wallet Pilot Program for veterans. Later, David Bulkowski, executive director of Disability Advocates of Kent County (DAKC), talks about his long career working on the same goals and DAKC's partnership in the program. Some references in this week's show: News release announcing the Mobility Wallet Pilot Programhttps://www.michigan.gov/mdot/news-outreach/pressreleases/2023/08/03/michigan-mobility-wallet-pilot-program-for-veterans-launches-on-purple-heart-dayDisability Advocates of Kent Countyhttps://www.dakc.us/Feonix - Mobility Risinghttps://feonix.org/team/ 

Step into the life of Albert 'Sparky' Metz, a relentless disability rights activist and country music fan who's been championing the rights of the disabled since his formative years. From his institutionalized childhood to his fiercely independent adulthood, Sparky's journey is as captivating as it is inspiring. Through it all, Sparky's spirit remained undeterred, fueling his passion for advocacy and his love for music.Join host  Joey Gidseg, who chats with Sparky and his attendant Pansy as they shed light on Sparky's experiences and challenges in his quest for independence and true love. Get familiar with the Speaking Advocates program, a virtual training initiative designed to teach people with Disabilities to use storytelling as a form of advocacy.  As we listen to Sparky's 2015 performance at the Vortex Theatre in Austin and hear his story through his personal AAC device, we realize the transformative power of stories in advocating for change, inclusivity, and disability rights. So, buckle up, lend us your ears, and support our mission of amplifying the voices of people with disabilities. Rate us on iTunes, share this episode, and join our movement towards a more inclusive world.Sparky is an actor and disability activist. He is a member of ADAPT of Texas and a big country music fan. He leads an active life and depending on the day you can find him at Morgan's Wonderland, going shopping, or attending Christian concerts. Sparky lives in Austin, Texas with his attendant and two cats, Smoke and Phoenix.Keep up with Sparky on Facebook:  https://www.facebook.com/albert.metz3To learn more about Adapt click this link.Joey Gidseg is an enthusiast of podcasts and disability policy who works to close the Justice Gap for disabled Texans through their organization Justice in Reach. A former multimedia producer, Joey is thrilled to collaborate with other disabled creators on the second season of Art Spark Texas' podcast,True Tales by Disability Advocates.You can connect or keep up with Joey on their Facebook, Twitter or Linkedin:https://www.facebook.com/joeygidsegfortexas/https://twitter.com/joeyinatxhttps://www.linkedin.com/in/joeygidseg/Learn more about closing the justice gap at https://www.justiceinreach.org/Click here to listen with the full transcript.For more details about our programs go to Art Spark Texas, True Tales Podcast Page.

Some disability advocates are voicing support for expanded robotaxis in San Francisco, a SF paper pits Uber against Waymo in a race, Cruise begins testing in Miami, Tesla begins production of DOJO supercomputer and talks to a major automaker about licensing Full Self Driving. That and more on episode 236 of Smart Driving Cars with Princeton's Alain Kornhauser and co-host Fred Fishkin. --- Support this podcast: https://podcasters.spotify.com/pod/show/smartdrivingcars/support

When it comes to the internet and technology access and eliminating tech bias, Olu Niyi Awosusi is a force to be reckoned with.See omnystudio.com/listener for privacy information.

Itto Outini is an international journalist, Fulbright scholar, human rights activist, accessibility advocate, and author of the forthcoming memoir Blindness is the Light of My Life. She holds an MA in journalism and strategic media from the University of Arkansas, Fayetteville, has practiced print and radio journalism in the US and Morocco, and has been invited to speak for organizations including Cal Tech University, Verizon Wireless, and North Seattle College.  Her work experience spans the for- and non-profit sectors and includes a stint with the United Nations Development Programme. In 2021, she founded Fulbrighters with Disabilities, a global, virtual chapter of the Fulbright Association dedicated to supporting students and scholars with disabilities around the world. In June of 2022, she made history by co-chairing a panel at the 15th Session of the Conference of State Parties to the UN Convention on the Rights of Persons with Disabilities. That same year, her life story was featured on BBC Outlook, and she and her husband, Mekiya Outini, co-founded The DateKeepers, an international media platform committed to publishing independent journalism, showcasing untold stories, and highlighting well-lived lives, especially those of people with disabilities, advocates, and allies worldwide.  Mekiya Outini is a writer and co-founder of the DateKeepers, an international media platform. He earned his MFA in fiction from the University of Arkansas, Fayetteville, and his short stories, essays, and poems have appeared in outlets such as Chautauqua Literary Journal, the Michigan Quarterly Review, and Willow Springs, respectively. His unpublished novel, Ashes, Ashes, has been selected as a finalist or semi-finalist in several contests, including the Chanticleer Somerset Awards, and its first two chapters were published in the West Trade Review. He lives with his partner in business and life, Itto Outini, in Kansas City, MO. Fulbright Scholar | Human Rights Activist | Founder of Fulbrighters with Disabilities | Co-Founder & Journalist at The DateKeepers | +1 (479) 502-3244 |

Host Jon Cauchi discusses an upcoming special event with Disability Advocates Board Member Marcus Fairfield. 

The Prime Minister reveals a crack down on rising costs for the NDIS will have an up-front bill of more than $700 million.

"The Next Generation Showcase," is a special bonus episode of True Tales by Disability Advocates,  the podcast where Advocates harness the power of storytelling to bring community to their peers and hope to develop empathy and others.The stories featured in this episode are written by fledgling storytellers from the Austin Independent School District Go-Project. The GO Project is a community-based transition program for students with disabilities who are 18-22 years of age. If you are a regular listener, you'll notice a change from our regular story slash interview format. For the first time, this episode includes more than two stories, just stories, no interviews. You'll get to hear seven short stories with topics ranging from Self-acceptance to Crunchy Barbecue Crickets, as well as Family Belonging, Speaking up, and Passions for Zombie Movies and Exercise.Stories and Storytellers"Speaking Up" by Adrian"The Start of Finding My Truth." By Maddison  "Travel With Family" by Miranda"Zombie Movies and Me." By Julio         "Belonging" by Chloe  "Musical Baking" by Abigair "To Eat, Jump Rope and Family Time." By Dezi We had so much fun working with these young folks and we are honored to share with you the work of these talented storytellers. Special thanks to the Go-Project staff - Laney, Sam, Mike, and Lori and our volunteers, Emily and Sulith, we couldn't have done this without y'all.Welcome you to the Next Generation Showcase. Music CreditsScandinavianz Sunbathers – 7385Feel the Sunshine - https://pixabay.com/users/oystudio-24430395/Feeling Good – Pixabay.comStages of Grief – Kevin MacLeod-funny-Jolly Boat – Pixabay.comHalloween-spooky-horror-scary-creepy - https://pixabay.com/users/soundgallerybydmitrytaras-11640913/Zombie - 315844__gneube__zombie-snarlComedy - https://pixabay.com/users/soundgallerybydmitrytaras-11640913/Cumbia Mexican Banda - https://pixabay.com/users/juliush-3921568/Summer Walkways - Pixabay.comClick here to listen with the full transcript.For more details about our programs go to Art Spark Texas, True Tales Podcast Page.

Local disability advocates are calling on the city of Detroit to better fund the Office of Disability Affairs. Plus, eligible Michigan residents can apply for a home heating credit, Back Alley Bikes is hosting their seasonal garage sale, and more. Do you have a community story we should tell? Let us know in an email at detroiteveningreport@wdet.org.

Heather and Jessica Tomko are sisters who both have a genetic, neuromuscular disease called Spinal Muscular Atrophy (SMA). SMA affects the motor neurons, which causes people with SMA to have weak muscles that atrophy over time. Heather and Jessica were both diagnosed as infants, and a life with SMA is all they have ever known. They strive to bring their full selves, disability and all, to a world that is often inaccessible and not accepting of disabilities.Watch full episode on YouTubeResources Mentioned:Heather's blog: https://theheatherreport.comHeather's Instagram: https://www.instagram.com/theheatherreportHeather's work: https://www.caregiving.pitt.eduJessica's Instagram: https://www.instagram.com/jessicatomkoArticle that Jessica wrote: https://triblive.com/opinion/jessica-tomko-disability-representation-in-the-entertainment-industryFilm Pittsburgh Reel Abilities Festival: https://filmpittsburgh.org/pages/reelabilitiesSupport the LYM Podcast:Subscribe to our YouTube channelLeave us a review on Apple Podcasts or SpotifyVisit our website Download our LYM mobile app (available on iOS and Android)Join our mailing listSend a gift to our host VinceWant to sponsor episodes of LYM? Reach out to us on our websiteSupport the show

Jonathan Cauchi is the Community Education Specialist for Disability Advocates and the host of its Flattening the Curb podcast. Located in Grand Rapids, Michigan, the organization, founded in 1981, works alongside persons with disabilities as they seek to lead self-directed lives and advocates for accessible and welcoming communities. Cauchi recently sat down with Randy Flood, [...]

In episode 123, host Kevin Schaefer talks with returning guests LaMondre Pough and Gabrielle Runyon, two Black Disabled advocates. In recognition of Black History Month, LaMondre and Gabrielle share their experiences growing up with SMA, the intersectionality of their identities, and the work they're doing now. ================================ To learn more about Evrysdi, please visit http://www.ApprovedForSMA.com ================================ To take part in our ongoing discussions regarding SMA, please visit http://www.smanewstoday.com/forums

Jan. 18, 2023 - New York Disability Advocates President Mike Alvaro discusses Gov. Kathy Hochul's State of the State address and outlines funding investments for industry staff, including money for an hourly wage increase and a cost-of-living adjustment.

Note: This episode is slightly longer than usual to honor the natural speech patterns of our guests.Welcome to the Mid-Winter Episode of True Tales by Disability Advocates, season two. Winter is the time of stillness and darkness when nature encourages us to look within and access what's ready to grow in the coming year. In this episode, “Practice Peace not Pity”, hosts Toby Al-Tarabulsi and Kristen Gooch talk to storytellers Kaye Love and Darla Murphy about the practices they use to find peace in their lives. We invite you to join them and take time to look within and discover new ways to find peace for yourself in the coming year.Part 1 “Pity Fatigue”Host Toby Al-Trabulsi and guest Kaye Love discuss her journey in life and the strategies she developed to protect herself from the toxic impact of ableism in her story “Pity Fatigue.”Bio Kaye Love - Kaye has over eight years of experience working with individuals with developmental and learning disabilities, including Intellectual Disability and Autism Spectrum Disorder, in Special Education and Vocational Rehabilitation. She has experience providing spiritually sensitive counseling to clients who identify with diverse belief systems, including Buddhism, Christianity, Ethical Humanism, Hinduism, Islam, Judaism, and Wicca.Click this link to listen to “Community Faith and Inclusion”ID:  Caucasian woman with light brown hair smiling. She is wearing a stole and a blue shirt and dark-rimmed glasses.Website: kayelove.comLinkedIn: J. Kaye Love, MSSW/MBA, LPC, Counseling on Thrive: Thriveworks Counseling - Janet Kaye Love  Acting: http://tiltperformance.org/Bio Toby Al-Trabulsi - Toby Al-Trabulsi is an actor, writer and creative access advocate for performers with disabilities based out of Austin, TX. Toby is a member of TILT Performance Group and ScriptWorks and is currently pursuing podcasting through the podcasting working group for Art Spark Texas, True Tales by Disability Advocates podcast. He is eager to see where this journey takes him. ID:  Toby Al-Trabulsi, a white male with brown hair. Toby is seated and holding a plate of food. He is wearing a red shirt with text “ZOO YORK”.Follow Toby on Twitter or InstagramTwitter: @Tobias_ZaneInstagram: @Tobias_Zanetext “ZOO YORK”. Part 2 “Peace Fountain”After Darla Murphy presents her story, “Peace Fountain,” host Kristen Gooch learns more about Darla's love of creative writing, storytelling, and the other things that bring her peace. Bio Kristen Gooch - Kristen Gooch is an Actress, Poet and Advocate from Austin, Tx with Cerebral Palsy and uses a wheelchair for mobility.  She hopes to broaden her horizons and branch out into film and television someday.  She currently facilitates a peer support group called Adapting Shero's for women with mobility disabilities through Imagineart.  She is a company member of TILT Performance Group and Paradox Player.ID: A caucasian young woman with shoulder-length auburn hair and pink lipstick smiling. She wears a pink short-sleeved dress with gray triangles, a blClick here to listen with the full transcript.For more details about our programs go to Art Spark Texas, True Tales Podcast Page.

Dec. 7, 2022 - Ruth Lowenkron, director of the Disability Justice Program for New York Lawyers for the Public Interest, respond to an aggressive new campaign from New York City Mayor Eric Adams to force more New Yorkers into temporary psychiatric evaluations.

Disability advocates are criticising a move by Auckland Transport to replace some trains with buses to allow for track maintenance. Work will begin early next year to rebuild foundations underneath three major railway lines, and will continue for two years. Auckland Transport says an alternative mobility taxi will likely be available, but they'll be recommending that customers book the service days in advance. Disabled Persons Assembly chief executive Prudence Walker spoke to Susie Ferguson.

Working-age people with disability are twice as likely to be unemployed as those without disabilities, and advocates say now is the time for the workforce to better reflect the Australian community. 

Quintin Jane speaks to Sean Prenter from the National Disabled Students Association. Tune into R1 News weekdays at 11am or catch up at https://www.r1.co.nz/news or https://instagram.com/r1newsnz

Western Australia is the only one of three states not adopting the national construction code to make homes more accessible for people with disabilities. Disability and housing advocates are calling for the standards to be made mandatory to join New South Wales and South Australia. 1 in 5 live with disability in WA.See omnystudio.com/listener for privacy information.

We end the first season of True Tales by Disability Advocates with "Positively Shining Bright". The stories in this episode highlight the power of choosing a positive mindset. Host Brittany Sessum introduces us to storytellers, Carlos Orellana, and Anne Marie Buckle. In their stories, "Listen to My World" and "Advocate Me," they share how in their own ways they practice having a positive mindset and how remembering to be grateful can help when they have a difficult day or have uncomfortable feelings.They remind us that focusing on positivity doesn't mean we won't have problems, but it will determine how we dance with them when they show up in our lives.When Brittany chats with Carlos and Anne Marie about their stories, their conversations offer us a sweet, sensitive insight into their lives living with Cerebral Palsy and Autism respectively. We titled this episode "Positively Shinning Bright" because [chuckles] that was our experience of both Carlos and Anne Marie during our recording sessions.We chose to launch this episode during August in the spirit of "Happiness Happens Month." I mean, we all wanna be happy, right? But happiness is an emotion and all emotions are fleeting, that is that they come and they go, they're not fixed, that's the nature of them. Every day we experience a range of feelings and emotions, no matter what's going on in our lives.  We can learn to practice choosing a positive outlook and focusing on the good in every situation, no matter what we are feeling. Guest Anne Marie BuckleMeet Anne Marie (Rie) Buckle. She is a vibrant young adult working every day to overcome autism, IDD and PANS. For Rie, adulthood brings new adventures like getting jobs in various sectors, exploring her passions, and becoming more independent. These things don't just happen overnight, however. With the ongoing support of her family, therapists, and mentors, Anne Marie has been able to accomplish many ofShe was crowned Texas Miss Amazing 2017.You can find her store at https://www.facebook.com/RiesMarketplace/And on Instagram at https://www.instagram.com/riesmarketplace Guest Carlos OrellanaA guy that's passionate about writing, U.S. History, Theater, and wrestling. Carlos is also a kid at heart even if he's 28 years old, that enjoys to laugh as well. He is extremely proud to be from Guatemala and loves his family too. He makes his friends happy and laughs when they have a hard day in their life. But, the most important thing to know about Carlos is that he has Cerebral Palsy. Even if his life is hard with Cerebral Palsy, it's also a happy one too.You can follow Carlos on Facebook at https://www.facebook.com/carlosrafael.orellana.7Photo ID: Carlos is an Hispanic male with black short and spiky hair wearing glasses. Carlos is smiling in the picture with an eagle pendant necklace, black long-sleeved shirt, and white sweats. Carlos is sitting in a black wheelchair with a grayish-blue door behind him. Host Brittany SessumBrittany Sessum is a Houston native and Army veteran that loves making connections with others. She has a passion to serve her family, the community, and her country by giving back in any capacity. She believes that her passions and actions live beyond herself. Brittany loves writing poetry, reading, traveling, and working as an entrepreneur.For more information about the Speaking Advocates Program, trainings and sign up for our newsletter go to Speaking Advocates - Art Spark Texas (artsparktx.org). 

This week I had some important conversations with my team about the future of our little company, where we're going, and what we have to do to get there. As a CEO and leader, I'm making big decisions and taking massive risks. It's scary but it's less scary when I admit how scary it is, and when my team shares their fears, too – and we all move forward anyway with humility and our shared sense of purpose.I was reminded this week that sometimes big risks don't pay off. Layoffs and hiring slowdowns have hit tech. What we're now seeing crystal clear is that there's a right way and a wrong way to reduce the workforce. Shopify laid off 1000 employees - and did so with humanity and compassion.In the letter to the team, CEO Tobi Lütke was transparent about the mistakes that were made that led to the staff reduction: Ultimately, placing this bet was my call to make and I got this wrong. Now, we have to adjust. As a consequence, we have to say goodbye to some of you today and I'm deeply sorry for that.Lütke also gave departing employees some generous perks beyond severance pay, including still paying for internet, money for new hardware, and organizing and distributing a list of employees looking for work.To those remaining employees, Lütke reiterated the company's purpose: Our customers are merchants, entrepreneurs, and small business owners - the bedrock of our economy and precisely those that are typically hit hardest during recessions. Most are already feeling it. We again have a clear objective in these challenging macro-economic times, and we will use everything we've got to help them succeed and come out stronger. That's our core mission.This matters because it shows humility. The CEO, in admitting his failures, also models a way to create psychological safety.Here are other good vibes I found this week:2.  VP Aims for Inclusivity: “I Am Kamala Harris. My Pronouns Are She and Her, and I Am a Woman Sitting at the Table Wearing a Blue Suit.”3. Disney Replaces ‘Fairy Godmothers' Title at Parks With Gender-Neutral ‘Apprentices'4. Pottery Barn Debuts 150+ Pieces of Furniture for People With Disabilities5. HSBC Offers Gender-Neutral Banking in Inclusivity BidTo learn more about Genesis Fisher, Esq. and her firm, visit: http://www.fisherlawpractice.nyc/ Join thousands of readers by subscribing to the 5 Things newsletter. Enjoy some good vibes in DEI every Saturday morning. https://5thingsdei.com/

Shrutilata Singh is a deaf-blind activist and advocate in the realm of disability and education. We share her story and accomplishments.   See omnystudio.com/listener for privacy information.

Women have long been leaders in the disability rights movement, and were the driving force in getting the Americans with Disabilities Act passed. We spotlight some of the notable women that made the ADA happen. See omnystudio.com/listener for privacy information.

Today we celebrate advocate for women and disability rights and environmental activist Neema Namadamu, her work, and how her mother inspired her. See omnystudio.com/listener for privacy information.

Full transcripts of all episodes available at https://truetalesbydisabilityadvocates.buzzsprout.comIn this episode, guests Laura Odom and Sheena Walter tell host John Beer about the “Awakenings” in their lives. Laura pushed through doubts brought on by years of narcolepsy to try her hand at a new adventure (“Finally Waking Up”), while Sheena flipped self-consciousness about her PICC line into a new and very public role of “Advocacy, Courage and Self-Compassion.” Both women took a stroke of boldness that ignited newfound lives of advocacy and pride in themselves! Listen in to learn about their victories. Toby Al-Trabulsi produces, Kristen Gooch and Ms. Boye mixing and editing, and Jennifer Howell and Joey Gidseg provide script and production.HOSTNo moss gathers on a rolling wheelchair, and throughout the state of Texas are sightings of John Beer and his travel trailer. With his wife's help, John spotlights the disability side of skydiving, fire evacuations and other topics for New Mobility magazine. You'll also find him on MS Connections at TheMighty.com – and he's wheelie excited being on the team creating Art Spark Texas' new podcast, True Tales by Disability Advocates. John was a member of our first Virtual Speaking Advocates Training and is one of the storytellers in Episode 2, “Life on Wheels”. Keep up with John Beer on his blog: Wheelieoutthere.blogspot.com Follow John on Instagram: https://www.instagram.com/wheelieoutthere/ GUESTLaura Odom is a Tyler, Texas-based advocate primarily for disability and rural causes. She is also the office manager for a locally owned textbook publisher. When she isn't working, she takes her Australian Shepherd/Border Collie-mix dog for car rides and loves to snuggle with her two black cats. She enjoys writing, playing guitar and cross-stitching. Laura was diagnosed with Narcolepsy Type 1 in January 2021 after pursuing a diagnosis for almost 20 years. She continues to raise awareness about Narcolepsy in hopes that more people won't have to wait that long to receive treatment.On social media, you can find her at: Instagram: @ordinarileighTikTok: ordinarileighTwitter: @lauradoestweetFacebook: Laura Ashleigh OdomGUESTSheena Walter is an artist at Imagine Art in Austin and also works for Art Spark Texas as a social media influencer. She wants to advocate for a change in how people with disabilities are viewed in our society and make sure we have not just a seat at the table, but a voice as well. Her sources of strength and inspiration are her faith, her friends, her family, her pets and walks in the outdoors.  Find Sheena and her art on Instagram @sheenawalter1 

In episode 107, host Kevin Schaefer talks about mental health with LGBTQ+ and disability advocates. Panelists include Ali Ramos (she/her), licensed social worker; Sherry Toh (she/they), columnist for SMA News Today; and Hugo Trevino (he/him), who works in academia. They all share their experiences managing their own mental health and offer advice for others in disability and LGBTQ+ spaces. ================================ Ali's Work Facebook page: https://www.facebook.com/aliramostherapy Sherry's column: https://smanewstoday.com/wandering-the-lines-sherry-toh/ Hugo's Instagram: https://www.instagram.com/htrevin2/ ================================ To learn more about Evrysdi, please visit http://www.ApprovedForSMA.com ================================ To take part in our ongoing discussions regarding SMA, please visit www.smanewstoday.com/forums ================================ For the most up-to-date information regarding SMA, please visit http://www.smanewstoday.com

In episode 106, host Kevin Schaefer talks with a group of rare disease and disability advocates about women's mental health. Panelists include Charlene Marshall, licensed mental health professional, and columnist for Pulmonary Fibrosis News; Brianna Albers, columnist for SMA News Today; Gabrielle Runyon, a college student with SMA at the University of Louisville; and Jessie Madrigal writer for endometriosis.net and mental health advocate. They all share their experiences managing their mental health and offer advice for others in disability spaces. ================================ Charlene's column: https://pulmonaryfibrosisnews.com/living-with-ipf-charlene-marshall/ Brianna's column: https://smanewstoday.com/the-wolf-finally-frees-itself-brianna-albers/ Gabrielle's Instagram: https://www.instagram.com/gab.davetta/ Jessie's Instagram: https://www.instagram.com/weemissjess ================================ To learn more about Evrysdi, please visit http://www.ApprovedForSMA.com ================================ To take part in our ongoing discussions regarding SMA, please visit www.smanewstoday.com/forums ================================ For the most up-to-date information regarding SMA, please visit www.smanewstoday.com

Dr George Taleporos speaks to a panel of disability advocates, where they examine the topics discussed in the previous episodes of the election series. They cover all things NDIS - funding cuts, operational issues, workforce, cost versus value and the damage of a ‘cost-first' mentality.

To listen with full transcript, go to https://truetalesbydisabilityadvocates.buzzsprout.com/In this episode, host Joey Gidseg talks to Jennifer Howell about her story, “From Ally to Self-Advocate.” Jennifer describes going from being the daughter of parents with disabilities to becoming someone with disabilities of her own, and the surprising things she learns along the way. Even for someone long familiar with disabilities, actually becoming a person with a disability of her own was for Jennifer a through-the-looking-glass kind of experience. Her story sparks an impassioned discussion between Jennifer and Joey, edited by Toby Al-Trabulsi and Ms. Boye, with script and production work by Kristen Gooch and John Beer.Jennifer HowellJennifer Howell's lifetime of personal experience with disability – as a caregiver, teacher and person with disabilities herself – has led to her work as an accessibility and creative placemaking consultant. She is a special education teacher, published author, award-winning artist and online instructor to students around the globe, ages 4 to 94. As an Accessible Yoga Ambassador, she has led classes for over a decade for seniors and persons with disabilities. Her other curricula include hand-lettering and cursive handwriting, and sustainable fashion. Jennifer is a member of IAMPETH (International Assoc. of Master Penmen, Engrossers & Teachers of Handwriting) and the Climate Reality Leadership Corps.Jennifer can be reached at https://www.linkedin.com/in/jennifer-howell-3179248/HostJoey Gidseg Joey Gidseg is an enthusiast of podcasts and disability policy who works to close the gaps in Access to Justice for disabled Texans. As chair of a statewide disability caucus and former multimedia producer, Joey is thrilled to collaborate with other disabled creators on Art Spark Texas' podcast, True Tales by Disability Advocates.You can connect or keep up with Joey on their Facebook, Twitter or Linkedin: https://www.facebook.com/joeygidsegfortexas/https://twitter.com/joeyinatxhttps://www.linkedin.com/in/joeygidseg/Learn more about closing the justice gap at https://www.justiceinreach.org/

In episode 105, host Kevin Schaefer talks with rare disease and disability advocates about men's mental health. Panelists include Paris Dancy, licensed mental health professional, and columnist for Cushing's Disease News; Matt Lafleur, columnist for Friedreich's Ataxia News; Michael Morale, multimedia specialist for SMA News Today; and Ty Dykema, artist and disability advocate. They all share their experiences managing their mental health and offer advice for others in disability spaces. ================================ Paris' column: https://cushingsdiseasenews.com/surviving-and-thriving-paris-dancy/ Matt's column: https://friedreichsataxianews.com/little-victories-matthew-lafleur/ Michael's videos: https://www.youtube.com/playlist?list=PLtRCVbeiSodlFLsjQBls3fM_EOnm4o6GV Ty's Instagram pages: https://www.instagram.com/breachthelevee/ https://www.instagram.com/tmd.art/ ================================ To learn more about Evrysdi, please visit http://www.ApprovedForSMA.com ================================ To take part in our ongoing discussions regarding SMA, please visit http://www.smanewstoday.com/forums ================================ For the most up-to-date information regarding SMA, please visit http://www.smanewstoday.com

Disability advocates are disappointed after a carer who left a disabled woman to die from horrific neglect was sentenced to six years' jail. Bumper box office for this year's Adelaide Festival and Fringe. Four more cases of Japanese encephalitis have been confirmed in South Australia. Former Adelaide coach Brenton Sanderson says his sister was so worried about the pressures of his job, she was relieved when he was sacked. For updates and breaking news throughout the day take out a subscription at advertiser.com.au See omnystudio.com/listener for privacy information.

Join Shannon & Christine as they chat about social wellness with our special guest Jennifer Howell a member of the True Tales by Disability Advocates podcast team. Shealo Glo - www.shealoglo.com  Now offering Subscriptions * Delivered on the 1st & 15th! Nominate your Shearo by emailing subject "My Shearo" to shealoglo@gmail.com Stillpoint - https://www.amazon.com/Stillpoint-Self-Care-Playbook-Caregivers-Breathe/dp/1732370400 Join us in community: https://women-connected-in-wisdom.mn.co/feed Listen to past episodes: https://womenconnectedinwisdompodcast.com/ Join Christine at an event: https://linktr.ee/christinegautreauxmsw Book a free coaching consult with Christine here: https://www.christinegautreaux.com Like & Subscribe to get notifications when we are live Instagram @womenconnectedinwisdompodcast - https://www.instagram.com/womenconnectedinwisdompodcast/ Facebook page Women Connected in Wisdom Podcast - https://www.facebook.com/womenconnectedinwisdompodcast NPR Life Kit show - https://www.npr.org/2022/02/18/1081713756/disability-disabled-people-offensive-better-word Demystifying Disability: What to Know, What to Say, and How to Be an Ally by Emily Ladau https://www.amazon.com/Demystifying-Disability-What-Know-Ally/dp/1984858971 Art Spark TX - https://www.artsparktx.org/ Reimagine: Grief, Growth, and Justice Schedule - https://letsreimagine.org/spring2022/schedule No Blame! No Shame! No Guilt! - https://letsreimagine.org/103965/no-shame-no-blame-no-guilt   Additional resources from NPR Life Kit: Books Being Heumann: An Unrepentant Memoir of a Disability Rights Activist by Judith Heumann and Kristen Joiner Disability Visibility: First-Person Stories from the Twenty-First Century edited by Alice Wong No Pity: People with Disabilities Forging a New Civil Rights Movement by Joseph P. Shapiro The Color of My Mind: Mental Health Narratives from People of Color by Dior Vargas We're Not Broken: Changing the Autism Conversation by Eric Garcia What Can a Body Do?: How We Meet the Built World by Sara Hendren Movies Crip Camp: A Disability Revolution (2020) Sins Invalid: An Unshamed Claim to Beauty (2013) Videos I Got 99 Problems. Palsy Is Just One. TED Talk by Maysoon Zayid I'm Not Your Inspiration, Thank You Very Much. TEDx Talk by Stella Young  

A team of disability advocates creates True Tales to give voice to the personal stories and lived experiences of disabled storytellers. We offer our unique, often underrepresented perspective, to the growing community of podcast listeners worldwide.This episode is being released in March, in honor of Women's History Month. We welcome back Kristen Gooch, the storyteller from episode 2, as host. She is joined by our two storytellers, producer, and sound engineer who are all powerful women with disabilities. According to the CDC, one in four Americans lives with some kind of disability. That's about 61 million adults with 61 million experiences and points of view about what it means to live with a disability.  Recognizing that everyone's life is enriched by the inclusion of multiple voices, Art Spark Texas, has been training Disability Advocates as storytellers for over 20 years.Click here to listen with a full transcript Host - Kristen GoochKristen Gooch is an actress, poet, and advocate from Austin, Texas with cerebral palsy and uses a wheelchair for mobility.  She hopes to broaden her horizons and branch out into film and television someday. She currently facilitates a peer support group through Imagineart called Adapting Sheros for women with mobility disabilities.  She is a company member of TILT Performance Group and Paradox Players.Jourdan HuertaJourdan is a performer who loves singing, dancing, and making unique greeting cards. Jourdan is also a huge advocate for mental health. She advocates for people with disabilities and for people that have non-epileptic seizures due to her personal experience with psychogenic non-epileptic seizures. Jourdan has such determination! She recently joined the TILT Performance Group and can't wait to start her next project and theater journey. Keep it up, Miss Huerta! Social media links: Instagram: https://www.instagram.com/greetingsbyj/?hl=en, https://www.instagram.com/jourdanthetheatregeek,Facebook: https://m.facebook.com/greetingsbyJ/, https://www.facebook.com/jourdansyeiraSharizod AboiiSharizod Aboii is a native Austinite who grew up in Pflugerville, Texas. She was born with arthrogryposis, a non-congenital condition that affects 1 in 3,000 live births. She is a graduate of Texas A&M University and is currently working on her MSW at Texas State University. Sharizod hopes to encourage and empower others through their journey in life with her shared experiences.Social Media Links:LinkedIn: https://www.linkedin.com/in/sharizod-aboii-0a0b7894/Email: sharizod@gmail.comWebsite: www.sharizods.com 

This episode, Judy chats with Leroy Moore and Keith Jones, the co-founders of Krip Hop Nation. Enjoy their discussion with Judy about the work they're doing, together and individually, as artists and activists. The transcript for this episode is available here. 2021 Emmy award winning Leroy F. Moore Jr. is the founder of Krip Hop Nation. Since the 1990s, Moore has been a key member of Poor Magazine, starting with the column "Illin-N-Chillin" and then as a founding member of the magazine's school, the Homefulness and Decolonize Academy. Moore is one of the founding members of National Black Disability Coalition and an activist around police brutality against people with disabilities. Leroy has started and helped start organizations including Disability Advocates of Minorities Organization, Sins Invalid, and Krip-Hop Nation. His cultural work includes the film documentary Where Is Hope, Police Brutality Against People with Disabilities, spoken-word CDs, poetry books and the children's book Black Disabled Art History 101 published by Xochitl Justice Press. His graphic novel Krip-Hop Graphic Novel Issue 1: Brown Disabled Young Woman Superhero Brings Disability Justice to Hip- Hop was published in 2019 and 2020 under Poor Press. Moore has traveled internationally networking with other disabled activists and artists. In fall of 2021, Leroy started his Ph.D. in Anthropology at UCLA. Moore has written, sang and collaborated to do music videos on Black disabled men. In July 2019 Leroy Moore under Krip-Hop Nation organized African Disabled Musicians San Francisco Bay Area Tour with disabled musicians from Uganda, Tanzania and The Democratic Republic of the Congo. In 2021 Leroy Moore published a book about Black disabled young men under SoulfulMediaWorks. Leroy has won many awards for his advocacy from the San Francisco Mayor's Disability Council under Willie L. Brown to the Local Hero Award in 2002 from Public Television Station, KQED in San Francisco and in 2014, San Francisco Bayview Newspaper named Leroy, Champion of Disabled People in the Media on Black Media Appreciation Night. Keith Jones is the President and CEO of SoulTouchin' Experiences. An organization aimed at bringing a perspective to the issues of access inclusion and empowerment, which affect him as well as others who are persons with a disability. Along with Mr. Leroy Moore the two men co-founded Krip Hop Nation an international collective of artist with disabilities. The tag line of Krip Hop Nation is, "Its more than music..." Mr. Jones is also extremely active in multi-cultural, cross-disability education and outreach efforts. Mr. Jones works to not only educate the disability community about enhanced community living, but also the community at large. Mr. Jones holds a strong desire to get the disability community more involved in the issues that concern their own lives and provides outreach support in relationship to the arts and independent living skills. Mr. Jones has been recognized for his emerging leadership by the state of Massachusetts and President's Commission for Employment for People with Disabilities. Over his years as and advocate Mr. Jones has been awarded New Leadership Development Award From The President's Committee on Employment of People with Disabilities. The Commonwealth Coalition's Progressive Leadership Award the 2006 Moro Fleming Consumer Involvement Award from the Massachusetts Rehabilitation Commission, with as well as, a recent graduate of the inaugural class of Initiative for Diversity in Civic Leadership. Also, in 2008 long shot 2008 U S Senatorial bid based on "Fulfilling America's Promise". Also, Mr. Jones was the Disability Law Center's 2011 Individual Leadership Award. While at the same time Mr. Jones continued his artistic endeavors. Krip Hop Nation Soul Touchin' Experiences LLC "Honoring" poem-song by Leroy Moore and Gabriel Wilson for Black History Month

Suzanne Stolz, Ed.D. serves as an Assistant Professor at the University of San Diego. A former high school English teacher, administrator, and leader of disability programs, she has expertise in online instruction, curriculum design, mentoring, school culture, Universal Design for Learning, and disability studies in education. Her research, related to conceptions of disability and disability pedagogy, often includes reflection about her experience as a disabled student. She has created disability curriculum for high school students, for out-of-school time programs, and for disability mentoring. She advises a student organization, Alliance of Disability Advocates, and also has served on the board of the Society for Disability Studies. Suzanne is especially passionate about working with preservice and inservice teachers to rethink their conceptions of disability and create inclusive school communities. Annually, she leads a fellowship program for general education teachers who want to become leaders of inclusion at their school sites. In this episode, Suzanne distinguishes between Disability Studies in Education and Special Education, and shares why it's important that we educate ourselves with a Disability Studies lens. Links Mentioned Johnson Fellows Program Teacher Leaders for Inclusion Teachers for Inclusion Learning about Disability Culture National Endowment for the Humanities Stay Connected with Diana Diana's Website Free Resource - 5 Keys to Going Beyond Awareness Beyond Awareness: Bringing Disability into Diversity in K-12 Schools & Communities - Diana's Book Ed Roberts: Champion of Disability Rights - Diana's Children's Book "Beyond Awareness" Digital Course Diana's TEDx Talk Beyond Awareness Facebook Page Diana on Instagram Credits and Image Description Intro and outro music courtesy of Emmanuel Castro. Podcast cover photo by Rachel Schlesinger Photography. Podcast cover image description: Black and white photograph of Diana, a Spanish-American woman with long, wavy, brown hair. She is wearing a flowy, white blouse and smiles at camera as she leans against wooden building. Photo is colorfully framed with gold and orange rays of seeming sunshine on top half, and with solid sage green color on bottom half. Text reads "Beyond Awareness: Disability Awareness That Matters, Diana Pastora Carson, M.Ed." Johnson Fellows Program https://www.sandiego.edu/soles/learning-and-teaching/johnson-education-fellows.php Teacher Leaders for Inclusion https://www.lead4inclusion.com/ Teachers for Inclusion Learning about Disability Culture https://www.facebook.com/groups/201578786622476

In this episode, host Toby Al-Trabulsi talks to John Beer and Kristen Gooch, who talk about ways they have developed resilience while pursuing their passions in life as wheelchair users and share their stories, “Is There a Doctor in The House?” and “I Was Meant to Shine.” John Beer takes us along his adventurous experience of trying to stay stocked up on staples during the covid era, and Kristen Gooch gives listeners insight into her experience as a disabled actress, following her dreams. The guests in this episode share their creativity, adaptability, and wisdom in their responses to the barriers that they encounter throughout their lives.   You can find this episode, and many more, by subscribing to the True Tales by Disability Advocates Podcast on iTunes, Google Podcasts, Spotify, Amazon Podcasts or your favorite platform.Click here to listen with a full transcript. Host: Toby Al-TrabulsiToby Al-Trabulsi is an actor, writer and creative access advocate for performers with disabilities based out of Austin, TX. Toby is a member of TILT performance group and ScriptWorks and is currently pursuing podcasting through the Art Spark podcasting workshop. True Tales by Disability Advocates. He is eager to see where this journey takes him. Follow Toby on Twitter or InstagramTwitter: @Tobias_ZaneInstagram: @Tobias_ZaneStorytellersJohn BeerJohn Beer profiles the people with disabilities and volunteers who enforce accessible parking for all in the upcoming issue of New Mobility magazine. You can also find him on TheMighty.com – and he's wheelie excited about being on the team creating Art Spark Texas' new podcast, True Tales by Disability Advocates.Keep up with John Beer on his blog:Wheelieoutthere.blogspot.com Follow John on Instagram:https://www.instagram.com/wheelieoutthere/ Kristen GoochKristen Gooch is an Actress, Poet, and Advocate from Austin, Tx with Cerebral Palsy and uses a wheelchair for mobility.  She hopes to broaden her horizons and branch out into film and television someday.  She currently facilitates a peer support group called Adapting Sheros for women with mobility disabilities through Imagineart.  She is a company member of the TILT performance group and Paradox Players.#Acting #Theatre #Auditions #Ableism #Discrimination #Job #Career #CP #CerebralPalsy #Wheelie #Wheelchair #Covid #Pacman #Barriers #Podcast #Disability #Disabilities #StructuralAbleism #Courage #Gutsy #Humor #Comedy #Adventure #Imagination #Actress #Texas #DisabilityAdvocate #DisabilityAdvocates #DisabilityTwitter #Disabled #Unstoppable #Creative #Artistic #RepresentationMatters #RoleModel #WindowIntoMyWorld #SliceOfLife #Pandemic #Shopping #NothingAboutUsWithoutUs #MobilityAide #AmbulatoryDisabilities 

Jonathan Cauchi discusses the past year of Disability Advocates with Executive Director Dave Bulkowski and Producer Joel Campbell. The three chat about what to expect in the new year, how to get involved, and what they're excited about!

Ali Ingersoll, Executive Board Member of Alliance of Disability Advocates of North Carolina (ADANC), joins the program to discuss her journey, which includes becoming a disability advocate after a shallow water diving accident left her in a wheelchair in her late 20's. Ali reveals why she decided to become a board member of Billion Strong, and some of the ways that she will be contributing to the global community. 

In this episode, host Brittany Sessum talks to storyteller Eric Clow, who talks about his journey with pride and bravery to live an authentic life and share his stories called "Coachella" and "Letter to My 10-Year-Old Self." You can find this episode, and many more, by subscribing to the True Tales by Disability Advocates on iTunes, Google Podcasts, Spotify, and Amazon Podcasts. If you don't use a podcast platform, you can listen to every episode with a full transcript by clicking here https://truetalesbydisabilityadvocates.buzzsprout.com/.Storyteller Eric ClowEric Clow is an Austin-based writer and musician. His dogs and birding hobby feature prominently in his poetry, as do his experiences living with a disability. His original music reflects his sincerity and twisted sense of humor. He works at Art Spark Texas, offering creative opportunities for artists with disabilities.Bandcamp: https://ericclow.bandcamp.com Instagram: https://www.instagram.com/disabsurdity/ Host Brittany Sessum Brittany Sessum is a Houston native and Army veteran that loves making connections with others. She has a passion to serve her family, the community, and her country by giving back in any capacity. She believes that her passions and actions live beyond herself. Brittany loves writing poetry, reading, traveling, and working as an entrepreneur.  #prideandbravery  #musculardystrophy  #liveitupFor more information about Art Spark Tx and the Speaking Advocates Program click this link: https://www.artsparktx.org/speaking-advocates/Intro and outro music - Sunbathers by Scandinavianz  Music by Scandinavianz https://soundcloud.com/scandinavianz 

Jonathan Cauchi discusses the Absolutely Accessible Kent program with Jackson Botsford and Patrick Parkes of Disability Advocates. The conversation about universal design and AAK's annual program continues with John Rizor of Progressive AE. To learn more about AAK, follow the program on Facebook or visit dakc.us/aak.

I really enjoyed this chat with Carly. I hope you do too! If you don't know who Carly is, she is a writer, speaker, disability advocate and arts worker. She has also been awarded The Order of Australia Medal. Learn more about Carly: Carly's website Carly's Twitter Carly's Instagram Carly's Books: Growing up disabled in Australia Say Hello You can ask Peta a question via: The website: www.icantstandpodcast.com Email: icantstandpodcast@gmail.com You can follow Peta on Instagram @petahooke Episode Transcript The documentary we mentioned: What does Australia think about... Disability The brand that Carly's top was from: Rattamatatt Get more information about: Job Access Melbourne Fringe YDAS The Disability Justice Network Mail HermansSee omnystudio.com/listener for privacy information.

Jonathan Cauchi sits down with staff members of Disability Advocates and Dirk Bakhuyzen, executive director of Beyond 26, to discuss issues around disabilities in the workplace.

September 21, 2021 - Center for Disability Rights President and CEO Bruce Darling makes the case for legislation approved unanimously by lawmakers this spring that would create an office of the advocate for people with disabilities and reflects on Gov. Andrew Cuomo's legacy on issues impacting New Yorkers with disabilities.

Jonathan Cauchi sits down with staff members of Disability Advocates and the Rapid to discuss transportation in west Michigan.

After almost 2 years of The Black Country Blokes and trying our best to raise awareness around mental health, we have decided to add to our challenges and stick up for the rights and raise awareness of disabled people and their carers.Who better to raise awareness than someone that has a disability and the carer of a disabled child.#disability #disabilityawareness #disabled #wheelchair #inclusion #wheelchairlife #autism #chronicillness #specialneeds #accessibility #spoonie #autismawareness #chronicpain #love #invisibleillness #disabilityadvocate #cerebralpalsy #disabilityrights #spinalcordinjury #mentalhealth #covid #disabilities #handicap #downsyndrome #anxiety #disabilitypride #wheelchairgirl #disabilityinclusion #abilitynotdisability #bhfypSupport this show http://supporter.acast.com/bcb. See acast.com/privacy for privacy and opt-out information.

Jonathan Cauchi sits down with staff members of Disability Advocates to discuss the American with Disabilities Act turning 31! He goes over its history, how it's used day to day, and our upcoming celebration on July 28!

Parents of children with special needs are being asked to reduce the hours their children attend school, or take an extended break to avoid being expelled altogether. Disability advocates say this form of informal exclusion is common and parents often comply because they fear being left with no options. For now, there is no disputes panel to oversee schools' decisions to expel children with special needs, but it's up to the school to place the student elsewhere. Amy Williams reports.

From the home of Mr. Rogers--Pittsburgh, PA--three disability advocates hold court on being helpful during COVID-19.

Disability Advocates and A Valid Podcast analysts Josie Badger, Alisa Grishman and Rachel Kallem-Whitman share what they're struggling with, and laughing at, during the stay-at-home orders. A Valid Podcast is co-produced by Unabridged Press and the Center for Media Innovation at Point Park University with support from The FISA Foundation.

We all love paying video games... Accessible gaming now being achieved by Xbox. Gaming companies can learn from Able Games and Xbox.The Satirically Challenged Show is presented by AMCPress&Co. We are the #1 disabled satirical news program in the world (65,000 and Counting) that provides uncensored news on numerous topics worldwide. You can find us wherever you listen to your podcasts. Subscribe to us through there.  Want to connect with us? Seek us out on Facebook under AMCPRESS&CO. You can find us at http://bit.ly/2fXFEFT.  * Some media (sound effects, news clips, and other sounds, etc) is protected by Fair Use and Transformative works this is has been AMCPress&Co Production. The main theme song is composed by Alison aka Pinkhood.  Disclaimer: Pinkhood.The end theme song is composed by Pinkhood.  This is an AMCPRESS&CO production. All Rights Reserved.  Cast Pinkhood & Johnnie  Sound Engineer: Pinkhood  Sound Design: Pinkhood  Board Op: Pinkhood  Tonight's episode is written by the Company of The Satirically Challenged Show  

Disney World is set to be the host for the Special Olympic games in 2022. This will be exciting for all those who are participating in the Special Olympics. Our final topic deals with how the FCC is stepping up with Robocalls.  The Satirically Challenged Show is presented by AMCPress&Co. We are the #1 disabled satirical news program in the world (65,000 and Counting) that provides uncensored news on numerous topics worldwide. You can find us wherever you listen to your podcasts. Subscribe to us through there.  Want to connect with us? Seek us out on Facebook under AMCPRESS&CO. You can find us at http://bit.ly/2fXFEFT.  * Some media (sound effects, news clips, and other sounds, etc) is protected by Fair Use and Transformative works this is has been AMCPress&Co Production. The main theme song is composed by Alison aka Pinkhood.  Disclaimer: Pinkhood.The end theme song is composed by Pinkhood.  This is an AMCPRESS&CO production. All Rights Reserved.  Cast Pinkhood & Johnnie  Sound Engineer: Pinkhood  Sound Design: Pinkhood  Board Op: Pinkhood  Tonight's episode is written by the Company of The Satirically Challenged Show  

Happy Veterans Day to all those who have served our country and continue to serve our country. Companies are honoring our veterans by giving veterans free meals and discounts today.  Our second topic of the night focuses on American Girl Catalog featuring a model with Down Syndrome.  Our last topic of the night focuses on the need for airlines need to carry EpiPens on all flights since this is a life-saving medication for those who have allergies. The Satirically Challenged Show is presented by AMCPress&Co. We are the #1 disabled satirical news program in the world (65,000 and Counting) that provides uncensored news on numerous topics worldwide. You can find us wherever you listen to your podcasts. Subscribe to us through there.  Want to connect with us? Seek us out on facebook under AMCPRESS&CO. You can find us at http://bit.ly/2fXFEFT.  * Some media (sound effects, news clips, and other sounds, etc) is protected by Fair Use and Transformative works this is has been AMCPress&Co Production. The main theme song is composed by Alison aka Pinkhood.  Disclaimer: Pinkhood.The end theme song is composed by Pinkhood.  This is an AMCPRESS&CO production. All Rights Reserved.  Cast Pinkhood & Johnnie  Sound Engineer: Pinkhood  Sound Design: Pinkhood  Board Op: Pinkhood  Tonight's episode is written by the Company of The Satirically Challenged Show Sources: http://bit.ly/2X6B0ua, https://yhoo.it/32BPSlw, http://bit.ly/34P1FhI

Ali Stroker made history at the 73rd annual Tony Awards as the “Oklahoma!” actress became the first wheelchair user to win a Tony - which was a huge moment for the disability community in regards to representation. In this episode we talk about paralysis, how people with disabilities are portrayed in movies and discuss the journey of Dr. Cohen's close friend that is an advocate and champion for disability rights. **GROSS ANATOMY PODCAST IS NOT INTENDED TO BE A SUBSTITUTE FOR PROFESSIONAL MEDICAL ADVICE, DIAGNOSIS, OR TREATMENT. ALWAYS SEEK THE ADVICE OF YOUR PHYSICIAN OR OTHER QUALIFIED HEALTH PROVIDER WITH ANY QUESTIONS YOU MAY HAVE REGARDING A MEDICAL CONDITION.

Technology is coming full circle to the point where there is now the potential for digital wallets. Will this be a success or a massive fail? A man with different abilities was allegedly denied supports because the person wasn't disabled enough. This is so dishearting. The Satirically Challenged Show is presented by AMCPress&Co. We are the #1 disabled satirical news program in the world (65,000 and Counting) that provides uncensored news on numerous topics worldwide. You can find us wherever you listen to your podcasts. Subscribe to us through there.  Want to connect with us? Seek us out on facebook under AMCPRESS&CO.You can find us at http://bit.ly/2fXFEFT. ReelAbilities Film Festival is starting April 2nd to the 9th. Learn more about the ReelAbilities Film Festival at http://bit.ly/2U050cX.  * Some media (sound effects, news clips and other sounds etc) is protected by Fair Use and Transformative works this is has been AMCPress&Co Production. The main theme song is composed by Redhood & Drizz.  Disclaimer: Ken Iselhart and Redhood.The end theme song is composed by Pinkhood.  This is an AMCPRESS&CO production. All Rights Reserved. Cast Pinkhood & Johnnie Sound Engineer: Pinkhood Sound Design: Pinkhood Board Op: Pinkhood Tonight's episode is written by the Company of The Satirically Challenged Show  

French youth are banned from using smartphones... Is it a good idea?  Here in the United States, the feds are wanting to track those who have different abilities social media accounts... Big brother is definitely going too far. The Satirically Challenged Show is presented by AMCPress&Co. We are the #1 disabled satirical news program in the world (65,000 and Counting) that provides uncensored news on numerous topics worldwide. You can find us wherever you listen to your podcasts. Subscribe to us through there.  Want to connect with us? Seek us out on facebook under AMCPRESS&CO.You can find us at http://bit.ly/2fXFEFT. ReelAbilities Film Festival is starting April 2nd to the 9th. Learn more about the ReelAbilities Film Festival at http://bit.ly/2U050cX.  * Some media (sound effects, news clips and other sounds etc) is protected by Fair Use and Transformative works this is has been AMCPress&Co Production. The main theme song is composed by Redhood & Drizz.  Disclaimer: Ken Iselhart and Redhood.The end theme song is composed by Pinkhood.  This is an AMCPRESS&CO production. All Rights Reserved. Cast Pinkhood & Johnnie Sound Engineer: Pinkhood Sound Design: Pinkhood Board Op: Pinkhood Tonight's episode is written by the Company of The Satirically Challenged Show  

How has it gone from Halloween to straight to Christmas? Our final topic of the night focuses on how tech companies are focusing on improving technology for those who have different abilities.  The Satirically Challenged Show is presented by AMCPress&Co. We are the #1 disabled satirical news program  in the world (65,000 and Counting) that provides uncensored news on numerous topics worldwide. You can find us wherever you listen to your podcasts. Subscribe to us through there.  Want to connect with us? Seek us out on facebook under AMCPRESS&CO. You can find us at http://bit.ly/2fXFEFT. * Some media (sound effects, news clips and other sounds etc) is protected by Fair Use and Transformative works this is has been AMCPress&Co Production. Main theme song is composed by Redhood & Drizz.  Disclaimer: Redhood and Ken Iselhart. End theme song is composed by Pinkhood. This is an AMCPRESS&CO production. All Rights Reserved. Cast: Pinkhood, Johnnie & Drizz Sound Engineer: Ken Iselhart Sound Design: Ken Iselhart & Andre Safodi-Guy Board Op: Ken Iselhart Tonight's episode is written by the Company of The Satirically Challenge Show  

Welcome to AMCPress&Co presents The Satirically Challenged Show. We are the #1 disabled satirical news program  in the world (65,000 and Counting) that provides uncensored news on numerous topics worldwide.  On Tonight's episode: We are ransacking how there is potental for traveling to London by a supersonic airline then we are discussing how disability groups renews call for abuse Royal Commission and our next topic we will be ransacking how a german company is trolling won't  stopping A Far-Right Politician. Our last topic of the night deals with researchers have claimed that playing video games will help depression. You can find us at www.amcpressandco.com.  * Some Media  (sound effects, news clips and other sounds. etc) is protected by Fair Use. Beginning theme song is composed by Redhood & Alison and is owned by AMCPress&Co Digital Entertainment. All rights Reserved.© No copyright infringement intended**   Disclaimer instrumental Credit: Blurr, Royal Philharmonic, Terry Jackson and Queen  

This episode you are going to get to hear, not one, not two, but THREE interviews with amazing disability advocates from the Lower Mainland with a diverse array of focuses. We kick things off with a past interview our producer Emily did With Monica Gartner (author of Overcoming the Impossible). Next, we listen our of Fundrive special interview with Nicholas Crier from Spikes and Bikes and producer Cherise. Lastly, we end things off with collective contributor Tasmia and president of the Wheelchair Dance Sport Association Canada (WDSACA) Olesya Kornienko.

We are the #1 disabled satirical news program  in the world (65,000 and Counting) that provides uncensored news on numerous topics worldwide.   AMCPress & Co is the brainchild of Redhood and Alison.  Johnnie is our resident Tech Wizard. Redhood is our resident international news satirist along with Alison who is the feeder of jokes and frank opinions.  Tonight's episode: we're discussing a new series on Netflix that is called Making of a Murderer and new information that has come out. We will be discussing two disablility news topics. Our last topic of the night relates to how someone got a sex toy due to posting poor feedback to a store on Amazon.  AMCPress & Co is also apart of the Uncensored Radio Network on Blog Talk Radio. You can find out more about Uncensored Radio at http://myuncensoredradio.com/.  Check out our new website at amcpressandco.com.   ** Some Media  (sound effects, news clips and other sounds. etc) is protected by Fair Use. Beginning theme song is composed by Redhood & Alison and is owned by AMCPress&Co Digital Entertainment. All rights Reserved.©  No copyright infringement intended**

We are the #1 disabled satirical news program  in the world (65,000 and Counting) that provides uncensored news on numerous topics worldwide.   AMCPress & Co is the brainchild of Redhood and Alison.  Johnnie is our resident Tech Wizard. Redhood is our resident international news satirist along with Alison who is the feeder of jokes and frank opinions.  Tonight's episode: we re-aired on of our favorite episodes which was episode #357. AMCPress & Co is also apart of the Uncensored Radio Network on Blog Talk Radio. You can find out more about Uncensored Radio at http://myuncensoredradio.com/.  Check out our new website at amcpressandco.com.   ** Some Media  (sound effects, news clips and other sounds. etc) is protected by Fair Use. Beginning theme song is composed by Redhood & Alison and is owned by AMCPress&Co Digital Entertainment. All rights Reserved.©  No copyright infringement intended**