Podcasts about demystifying disability

From Sesame Street to the streets of advocacy, Emily Ladau has been using her voice to shift perspectives and spark change since the age of ten. Born with Larsen syndrome and never one to shy away from the spotlight, she's shown the world that disability is not a deficit—it's a story worth telling in full color and full volume. Whether through her editorial leadership, her bestselling book Demystifying Disability, or simply through conversations that crack open compassion, Emily leads with heart, humor, and honesty. In this conversation, we talk Big Bird, big myths, and even bigger truths—one question at a time.Featuring: Emily LadauInterviewed by: Allié McGuireMusic by: Alon PeretzProduced by: AwareNow MediaIn Partnership with: Change For Balance

Check out these links and extra resources Lauren mentioned during the show: https://emilyladau.com/ Emily Ladau's podcast https://www.theaccessiblestall.com/ ASSUME THAT I CAN https://www.youtube.com/watch?v=92ivgabfdPQ "Our negative assumptions about people with Down syndrome can lead us to treat them in such a way that these assumptions become reality. In sociology, this is called a 'self-fulfilling prophecy.' Why not reverse our perspectives? If we have positive assumptions about people with Down syndrome, they will have opportunities at school, at work, in relationships, and in other activities. And maybe these positive assumptions will become reality." “I'm Guilty”: People Check Their Own Biases Against Down Syndrome After Watching New Ad https://www.boredpanda.com/powerful-new-ad-challenges-stereotypes-about-down-syndrome/ From What If to What Next podcast Episode 63 - What if disability justice, deep inclusion and liberation were centred in healthcare, education and the arts? https://fromwhatiftowhatnext.libsyn.com/63-what-if-disability-justice-deep-inclusion-and-liberation-were-centred-in-healthcare-education-and-the-arts Episode 64 - What if the Black Fantastic reshaped the world? https://podcasts.apple.com/ca/podcast/64-what-if-the-black-fantastic-reshaped-the-world/id1538281063?i=1000586919985 Episode 97 - What if there was an alternative to capitalism, after all? https://podcasts.apple.com/ca/podcast/97-what-if-there-was-an-alternative-to-capitalism-after-all/id1538281063?i=1000648727593 Imperfect Resources, including a guide to 2SLGBTQ2AI++ inclusion, an inclusive language guide, ableist words and terms to avoid, and more https://www.theimperfect.network/resources --- Support this podcast: https://podcasters.spotify.com/pod/show/booksapplied/support

A theme we often touch upon on this show is how the discourse surrounding neurodivergence and the language used when referring to neurodivergence is ever-evolving. I've observed on social media and in other spaces how conversations about terminology can be confusing, divisive, alienating, and complicated to navigate. Disability is one of those terms that can be uncomfortable for some people, including parents of neurodivergent kids, to embrace, but my hope is that this conversation will help you have a deeper understanding of what it means to be disabled, how ableism shows up and hurts all members of the disability community, including our kids, and how we can be better allies in the disability To talk about this, I invited disability rights activist and writer Emily Ladau onto the show. Emily wrote a wonderful book called Demystifying Disability: What to Know, What to Say, and How to be an Ally, and in today's conversation, we explore some of the core ideas in her book. As always, we covered a lot of ground in this episode, including what it actually means to be disabled, why the euphemism “special needs” is problematic for many people, how ableism is normalized in our society, disability etiquette do's and dont's to keep in mind for future interactions, and so much more.   About Emily Ladau Emily Ladau is a passionate disability rights activist, writer, storyteller, and digital communications consultant whose career began at the age of 10, when she appeared on several episodes of Sesame Street to educate children about her life with a physical disability. Her writing has been published in outlets including The New York Times, CNN, Vice, and HuffPost and her first book, Demystifying Disability: What to Know, What to Say, and How to be an Ally, was published by Ten Speed Press, an imprint of Penguin Random House, in September 2021. Emily has spoken before numerous audiences, from the U.S. Department of Education to the United Nations. Central to all of Emily's work is harnessing the power of storytelling to engage people in learning about disability.   Things you'll learn from this episode The difference between models of disability, including the medical, social, and charity model Why it's critical that we recognize and address internalized ableism in order to promote inclusivity What intersectionality is and ways disability intersects with other marginalized identities What should be considered when looking at accommodations and accessibility when meeting the diverse needs of individuals Do's, don't's and best practices when it comes to disability etiquette   Resources mentioned for Demystifying Disability: What to Know, What to Say, and How to be an Ally Emily Ladau's website Demystifying Disability: What to Know, What to Say, and How to be an Ally by Emily Ladau The Accessible Stall (Emily's podcast) Words I Wheel By (Emily's Facebook page) Emily on Instagram Emily on LinkedIn Tyler Fedder (Illustrator) D'Arcee Neal The Platinum Rule   Learn more about your ad choices. Visit megaphone.fm/adchoices

For this week's episode of Off-Kilter, Rebecca sat back down with Emily Ladau. She's the editor of the Voices of Disability Economic Justice Project and the author of Demystifying Disability: What to Know, What to Say, and How to Be an Ally. She's someone who's done an immense amount throughout her career to shift narratives on disability in the United States and is a master storyteller whose many superpowers also include supporting other people in telling their stories. They had a far-ranging conversation about the Voices of Disability Economic Justice Project as it comes up on its one-year anniversary; why it's so important for people with disabilities to get to tell their own stories; why storytelling is critical to policy and culture change; how she ended up on Sesame Street; why she wrote her book Demystifying Disability; and lots more.  Links from this episode: Check out Emily's book Demystifying Disability: What to Know, What to Say, and How to Be an Ally Follow Emily on Twitter/X @emily_ladau  Learn more about the Voices project and how to write for it Here is the Off-Kilter episode feat. Emily with writer Alex Ashley Fox on the harms that come from autistic people being forced to mask at work, and here is Alex's Voices piece

About The Guest(s):Andy Arias: DEIA expert, national policy advisor, instructor at Georgetown University, actor, and producer.Diego Mariscal: Founder, CEO, and Chief Disabled Officer of 2Gether International, an accelerator that supports disabled entrepreneurs.Emily Ladau: Disability rights activist, author of "Demystifying Disability," and board member of Kids Included Together.Summary: In this episode, Torrie Dunlop hosts a panel discussion with Andy Arias, Diego Mariscal, and Emily Liddell to honor the legacy of Judy Heumann, a pioneer and advocate in the disability rights movement. The panelists discuss how Judy's work has inspired their own activism, the most important issues facing the disability community today, and the impact of intersectionality in disability rights. They also share personal stories and reflections on Judy as a person, highlighting her generosity, humor, and commitment to connecting people. The panelists discuss how they plan to continue Judy's legacy in their own work, emphasizing the importance of authentic representation and collaboration in the disability community.Transcript: https://otter.ai/u/_LOEalVNz27i_mdqvHaNnXHQVqQKey Takeaways:Judy Heumann's legacy is characterized by her commitment to collaboration, community building, and intersectionality in the disability rights movement.The most important issues facing the disability community today are interconnected and require a holistic approach to address barriers in healthcare, employment, education, transportation, and more.Judy's impact as a person extended beyond her advocacy work, as she was known for her humor, generosity, and genuine interest in connecting with others.To honor Judy's legacy, it is crucial to prioritize authentic representation and collaboration in all aspects of disability rights work, including storytelling, filmmaking, and entrepreneurship.Kids Included Together: https://www.kit.org/Andy Arias: https://www.instagram.com/andyswheelz/Diego Mariscal: https://www.linkedin.com/in/Diego-Mariscal/Emily Ladau: https://emilyladau.com/ Support Think Inclusive by becoming a patron! Hosted on Acast. See acast.com/privacy for more information.

For Disability Pride Month, Dr. Stephanie Van, a Johns Hopkins rehabilitation physician and founder of YouTube's @‌ThisAbilityClinic, talks with Lindsay Smith Rogers about her work as a pain management specialist and disability advocate. They discuss how she helps patients with newly acquired disabilities and what she's learned about the disability community in the process, as well as what needs to change from the individuals to industries to make the world a little more inclusive. This episode is also available as a video here: https://youtu.be/T2PUYFOBVYk  Learn more about disability and accessibility with the resources recommended in this episode by Dr. Van: Hashtags to follow on social media: #Disability, #Accessibility, #DisabilityVisibility Read or listen: Demystifying Disability by Emily Ladau

Like most other parents, my sense of identity forever changed with the arrival of my disabled child. And in many ways, it's helped me to embrace (at least on good days!) a lifestyle I used to resent. But I've noticed a pushback from the disability community in claiming our child's disabilities as part of our own identities. So, of course, we had to examine this controversial and intimate topic with the best of the best. In this conversation with famed disability activist, speaker, and author of Demystifying Disability, Emily Ladau and Amanda Griffith-Atkins guest from Ep. 81 and mom to a disabled teen, we tackle questions like: Is it ok for us as parents to find identity in our children's disabilities? If so, where is the line? IS there a line? How can I respect both my child's lived experience and my own? Can I share those experiences on social media? How can parents and disabled people soften towards each other and put down the proverbial weapons? *This is a rebroadcast of one of my favorite episodes of The Rare Life for you to listen to while we work on production for season 8, coming in August! If you'd like to discuss this episode with other members of The Rare Life community, we'll be holding three different meetings run by our amazing group facilitators every Tuesday at 8pm in PST/CST/EST. Fill out our contact form to get the Zoom link each week!* Links: Sign up to get an invitation for our community discussions every Tuesday during the off-season! Purchase Demystifying Disability by Emily Ladau via Penguin House or Amazon. Listen to The Accessible Stall podcast Follow Emily on Instagram. Follow Amanda on Instagram. Follow Madeline on Instagram. Listen to Ep. 81: Health Anxiety w/ Amanda Griffith-Atkins, LMFT Listen to Ep. 54: Disabled Adult Perspective w/ Erica Stearns Listen to Ep. 77: To Those Who Cannot Say, “I Wouldn't Have them Any Other Way” Join the Facebook group Parents of Children with Rare Conditions. Donate to the podcast via Buy Me a Coffee. Contact me about sponsoring the podcast. Follow the Facebook page. Access the transcript on the website here. And if you love this podcast, please leave us a rating or review in your favorite podcast app!

**This is the original version. A voiceover version is available on this platform. If you have hearing loss or auditory processing difficulties, or are listening in a noisy car, the voiceover version is here for you to access this awesome conversation! Have you ever given much thought to the terminology we use to describe our medically complex kids (and ourselves)? The words we use might seem inconsequential at first glance, but I'm talking with Kari Harbath (mom to a disabled daughter) and Hannah Setzer (disabled activist), to explain why the terms we use for our kids are really important and set the tone for how disabled children and adults can move about in the world. In this episode, Hannah describes her experience as a disabled child and now a disabled adult and why she prefers the term “disabled” instead of special needs. She and Kari also discuss how they've heard the term “special” used in society and why that just isn't an ideal description for our kids. And I want to add, this conversation isn't about calling out or shaming anyone! We're just here to give you another perspective and offer you an alternative to some very popular (but kind of infantilizing) terms often used in wider society. We're so grateful that you're here and willing to tackle topics like this with us.   Links: Watch this episode with subtitles ⁠on YouTube.⁠ Get a copy of Hannah's book “I'll Pray for You: and Other Outrageous Things Said to Disabled People.” Get a copy of Demystifying Disability by Emily Ladau. Listen to Ep 85 with Emily Ladau and Amanda Griffith-Atkins on the identity of parents related to their disabled children. Listen to Ep 121: When Strangers “Just Ask” with disabled author James Catchpole. Listen to Episode 10 and Episode 11 to hear Kari's first episodes on The Rare Life. Follow Hannah on Instagram! Follow Kari (and Sloan) on Instagram! Follow me on Instagram! Donate to the podcast via Buy Me a Coffee. Contact me about sponsoring the podcast. Follow the Facebook page. Join the Facebook group Parents of Children with Rare Conditions. Access the transcript on the website here. And if you love this podcast, please leave us a rating or review in your favorite podcast app!

**This is the voiceover version. There are two versions of this episode! One where you can hear directly from Hannah, and one where we used an AI voiceover. If you have hearing loss or auditory processing difficulties, or are listening in a noisy car, the voiceover version is here for you to access this awesome conversation! Have you ever given much thought to the terminology we use to describe our medically complex kids (and ourselves)? The words we use might seem inconsequential at first glance, but I'm talking with Kari Harbath (mom to a disabled daughter) and Hannah Setzer (disabled activist), to explain why the terms we use for our kids are really important and set the tone for how disabled children and adults can move about in the world. In this episode, Hannah describes her experience as a disabled child and now a disabled adult and why she prefers the term “disabled” instead of special needs. She and Kari also discuss how they've heard the term “special” used in society and why that just isn't an ideal description for our kids. And I want to add, this conversation isn't about calling out or shaming anyone! We're just here to give you another perspective and offer you an alternative to some very popular (but kind of infantilizing) terms often used in wider society. We're so grateful that you're here and willing to tackle topics like this with us. Links: Watch this episode with subtitles on YouTube. Get a copy of Hannah's book “I'll Pray for You: and Other Outrageous Things Said to Disabled People.” Get a copy of Demystifying Disability by Emily Ladau. Listen to Ep 85 with Emily Ladau and Amanda Griffith-Atkins on the identity of parents related to their disabled children. Listen to Ep 121: When Strangers “Just Ask” with disabled author James Catchpole. Listen to Episode 10 and Episode 11 to hear Kari's first episodes on The Rare Life. Follow Hannah on Instagram! Follow Kari (and Sloan) on Instagram! Follow me on Instagram! Donate to the podcast via Buy Me a Coffee. Contact me about sponsoring the podcast.

Author of Demystifying Disability, Emily Ladau, discusses her experiences with ableism and invasive questions on dating apps, and dealing with breakups. Erin and Lily join Emily in sharing their cringiest first dates and how to know when love is real.

Parenting a child with medical complexity or disability often means learning a ton of new skills—and new systems—often in a very short period. Making that process more difficult is the fact that many of the individuals working in those systems, like special education professionals and therapists, aren't actually parents of disabled children if they even have children at all. And because of this, communication between both sides can be... let's just say difficult at times. Here to help bridge the gap is a former Sp. Ed. professional and mom to a disabled son, Tiffany Goodchild.   In today's episode, Tiffany shares all the things she wishes she had known as a Sp. Ed. professional before she had her son. She shares difficult experiences that she's had navigating the Sp. Ed. system, even after having worked in it for years, and it's her goal to help educate other special education professionals to make the special education system better for both professionals and kids.  To this end, we've made digital and printable flyers that you can send to the Sp. Ed. Professionals in your life. We'd love for you to send this episode to anyone who works in special education so we can make the system work better for everyone. Get a copy of the flyers here.  Finally, an extra special thanks to Trexo for sponsoring this episode! Check out their website and Instagram to see their amazing robotic devices in action!  Links:  Visit Trexo's website to get more information about their assistive devices.  Follow Trexo on Instagram to see their products in action.  Send this flyer to your Sp. Ed. professionals! Printable version or digital.   Get a copy of No Such Thing as Normal by Megan DeJarnett.  Get a copy of Demystifying Disability by Emily Ladau.   Listen to Ep. 59 about IEPs with Catherine Whitcher, M. Ed.  Listen to Ep. 68: Dipping My Toes into Educational Advocacy.  Check out the Kourageous Karter Foundation.  Follow Tiffany on Instagram!  Follow me on Instagram!  Donate to the podcast via Buy Me a Coffee.   Contact me about sponsoring the podcast.  Follow the Facebook page.   Join the Facebook group Parents of Children with Rare Conditions.   Access the transcript on the website here.   And if you love this podcast, please leave us a rating or review in your favorite podcast app! 

Welcome to Awesome Etiquette, where we explore modern etiquette through the lens of consideration, respect and honesty. On today's show we take your questions on bringing a cocktail to the dinner table, passing by others at a theater, telling a stranger their shirt is inside out, and neighbors letting themselves in. For Awesome Etiquette Sustaining members our question is about calling people Miss, Mrs. or Mr. Plus your most excellent feedback, etiquette salute and a postscript with the second half of our interview with Emily Ladau author of Demystifying Disability, what to know, what to say and how to be an ally. Learn more about your ad choices. Visit megaphone.fm/adchoices

Welcome to Awesome Etiquette, where we explore modern etiquette through the lens of consideration, respect and honesty. On today's show we take your questions on hiring a makeup artist at a gay wedding, getting ready to go through security at the airport, getting a bonus you don't want, and enjoying what's on the rim of a cocktail. For Awesome Etiquette Sustaining members our question is about paying the bill when having dinner with your partner's mother for the first time. Plus your most excellent feedback, etiquette salute and a postscript on the first half of our interview with Emily Ladau Author of Demystifying Disability, what to know what to say and how to be an ally. Learn more about your ad choices. Visit megaphone.fm/adchoices

We welcome Em Williams, Supervisor for Media Accessibility at AMI. She recommends Demystifying Disability, by Emily Ladau, a welcoming read for anyone new to disability conversation.

Emily Ladau is a passionate disability rights activist, writer, storyteller, and digital communications consultant whose career began at the age of 10, when she appeared on several episodes of Sesame Street to educate children about her life with a physical disability. Her writing has been published in outlets including The New York Times, SELF, Salon, Vice, and HuffPost. Her first book, Demystifying Disability, was published by Ten Speed Press, an imprint of Penguin Random House, in September 2021. Emily has spoken before numerous audiences, from the U.S. Department of Education to the United Nations. Central to all of her work is a focus on and harnessing the power of storytelling as a tool for people to become engaged in disability and social justice issues. Timeline of the podcast: 00:10 - 01:24 Intro 01:25 - 03:00 Emily Ladau's background 03:05 - 05:02 Emily's definition of disability and concept of ableism 05:03 - 08:00 Language of Disability 08:01 - 10:17 Language of Disability 10:25 - 13:40 Intersectionality as it relates to disability discussion 13:45 - 15:12 Role of parents 15:15 - 16:30 What is infantilization? 16:35 -17:37 Current concerns in the community? 17:40 -18:35 Closing Remarks Emily's call to action: “Disability is not negative or shameful and allyship is action. This podcast was produced by Marsh Naidoo, Makendra Ezell, and Tanya Sierra. Melissa Mittelstaedt provided captioning and transcription at https://www.melissamitt.com/uaccess Link to transcript Related resources on the podcast and blog: https://www.raisingkellan.org/the-models-and-language-of-disability/ --- Send in a voice message: https://anchor.fm/marsh-naidoo/message

With the surge in popularity and need for hybrid and virtual events, Lou sits down with Intel's Director of Accessibility, Darryl Adams, to discuss how technology can make in-person and virtual conferences more accessible and inclusive to speakers and audience members with disabilities. He also speaks to how accessible conference design can be improved and fine-tuned for speakers with disabilities, and help those without disabilities feel more comfortable presenting. What kind of accessibility principles and design factors should conference hosts consider for audience members with disabilities and those without disabilities when setting up for in-person and virtual events? How does this technology increase engagement and diversity in attendance? Listen as Darryl and Lou touch on all these topics, and more. Darryl Adams recommends: Demystifying Disability by Emily Ladau Darryl Adams is the Director of Accessibility at Intel. Darryl leads a team that works at the intersection of technology and human experience helping discover new ways for people with disabilities to work, interact, and thrive. Darryl's mission is to connect his passion for technology innovation with Intel's disability inclusion efforts to help make computing and access to digital information more accessible for everyone and to make Intel an employer of choice for employees with disabilities. For the full transcript: https://rosenfeldmedia.com/announcements/podcast-making-conferences-more-accessible-with-darryl-adams-intels-director-of-accessibility/

On this month's episode we chat with Kendra Winchester of Book Riot and Read Appalachia. We talk about audiobooks and why they DO count as reading, Disability Pride Month, Appalachian writing and literature, podcasting, and more. About this month's guest: Kendra Winchester is a Contributing Editor for Book Riot where she writes about audiobooks and disability literature. She is also the Founder of Read Appalachia, which celebrates Appalachian literature and writing. Previously, Kendra co-founded and served as Executive Director for Reading Women, a podcast that gained an international following over its six-season run. In her off hours, you can find her writing on her Substack, Winchester Ave, and posting photos of her Corgis on Instagram and Twitter @kdwinchester. Use promo code: LIBROPODCAST when signing up for a Libro.fm memberhsip to get an extra free credit to use on any audiobook. Audiobooks mentioned in this episode: Demystifying Disability by Emily Ladau Disability Visibility by Alice Wong True Biz by Sara Novic Pachinko by Min Jin Lee Just by Looking at Him by Ryan O'Connell Left Behind: A Novel of the Earth's Last Days by Tim LaHaye & Jerry B. Jenkins

Have you ever had a moment when you just weren't sure what to say or do in relation to someone who has a disability? Perhaps you were nervous that you would say or do the wrong thing and offend someone?  There are lots of good people out there - you are probably one of them - who want to address ableism in themselves but are frankly too nervous to put themselves out there are risk messing up.  This week on the podcast I interviewed Emily Ladau. Emily is the author of Demystifying Disability.  Emily says, “the goal of demystifying disability was not to be the definitive encyclopedia or Bible on disability. It wasn't to speak for every single disabled person. It wasn't to say that I am the authority and the expert on disability because I'm none of those things, right? I'm only one person, but it was just my way of offering an overture, offering a way to bridge the gap for so many people who maybe don't know how to talk about disability, the language to use, maybe don't know about some of the history. Maybe they're not sure about media representation or etiquette. And I wanted to say, Hey, here's a safe place to start.” Emily's book might just be what you are looking for. If you don't need a primer on disability, I'm sure you know someone who does.  Not sure? Listen to the episode here. 

In the latest episode of Edelman Editions and our Powered by GWEN series, Ishtar Schneider, Director of Health at Edelman, caught up with Shani Dhanda, TedX speaker, award-winning disability specialist and advocate. In this episode, Shani shares her thoughts on the definition of disability and ‘ableism', provides tips on how to be a better ally to the disability community and aims to supports listeners to have confident conversations about disability within business and the wider community.

This month Avery read Demystifying Disability by Emily Ladau. She goes over the content, main themes, and tone of the book and shares what she learned, critiques, and her honest recommendation on whether to read or skip it.

Like most other parents, my sense of identity forever changed with the arrival of my disabled child. And in many ways, it's helped me to embrace (at least on good days!) a lifestyle I used to resent. But I've noticed a pushback from the disability community in claiming our child's disabilities as part of our own identities. So, of course, we had to examine this controversial and intimate topic with the best of the best. In this conversation with famed disability activist, speaker, and author of Demystifying Disability, Emily Ladau and Amanda Griffith-Atkins guest from Ep. 81 and mom to a disabled teen, we tackle questions like: Is it ok for us as parents to find identity in our children's disabilities? If so, where is the line? IS there a line? How can I respect both my child's lived experience and my own? Can I share those experiences on social media? How can parents and disabled people soften towards each other and put down the proverbial weapons? Links: Check out our sponsor WorthyBrands Eye and Port Patches. Purchase Demystifying Disability by Emily Ladau via Penguin House or Amazon. Listen to The Accessible Stall podcast Follow Emily on Instagram. Follow Amanda on Instagram. Follow Madeline on Instagram. Listen to Ep. 81: Health Anxiety w/ Amanda Griffith-Atkins, LMFT Listen to Ep. 54: Disabled Adult Perspective w/ Erica Stearns Listen to Ep. 77: To Those Who Cannot Say, “I Wouldn't Have them Any Other Way”

Guest Emily Ladau, disability rights activist joins to share her personal experiences, as well as insights from her book, Demystifying Disability: What to Know, What to Say, and How to Be an Ally. She discusses how we ought to redefine the term disability, the opportunity gaps for people with disabilities and how individuals, companies and lawmakers can help advance professional and financial opportunities for the community. Want more articles and videos by Farnoosh? Check out www.cnet.com/somoney. Subscribe to her weekly So Money newsletter for the latest updates and advice. Catch her weekly money videos on YouTube. Learn more about your ad choices. Visit megaphone.fm/adchoices

In this episode, I talk with Barb Zablotney, who sustained a spinal cord injury when she was just 21-years-old. She spent a decade in a very dark place. Her mother passed away and she lost her relationship with her fiance, but then she became Miss Wheelchair Pennsylvania. This wasn't a beauty pageant, although Barb is certainly beautiful. It was an honor bestowed on her for her ideas, ability to articulate those ideas and her dedication to advocacy for the community she finds herself a part of--the disability community. Barb is a model for Team Torrid, was featured in a commercial for the UPMC Health Plan, lobbied politicians in Harrisburg and D.C. and much more!  In this podcast, Barb reveals her goal of independence and how she wishes people would treat her. She also talked with me about what she wants abled-bodied people to know about the disabilities community. She has written an article on accessible parking http://digital.olivesoftware.com/olive/ODN/DailyAmerican/shared/ShowArticle.aspx?doc=SZDA%2F2020%2F09%2F25&entity=Ar02002&sk=5FBA4DE0&mode=text (here) and recommended the book, https://www.amazon.com/Demystifying-Disability-What-Know-Ally/dp/1984858971/ref=sr_1_1?crid=1PMJTRE681QAE&keywords=demystifying+disability&qid=1636340907&sprefix=demyst%2Caps%2C125&sr=8-1 (Demystifying Disability) by Emily Ladau for people interested in knowing more than we could possibly cover in a 30-minute podcast. If you would like to learn more from Barb, you can follow her on social media: https://www.facebook.com/barbzablotney (Facebook), https://www.instagram.com/therollingrainbow/ (Instagram) and https://www.youtube.com/c/RollingRainbowBarb (YouTube). 

At only 2.5 years old, Ivy has already faced discrimination based on her disability. In this episode, her mom Vanessa McLeod shares what that's been like for her to advocate to give her daughter everything she deserves in life. She talks about the ableism they've encountered, and her blazing confidence that Ivy will live a fulfilled life. She insists again and again that her daughter's disability is not sad at all—it's wonderful. Links: Follow Vanessa on Instagram @venessamcleod_ Follow Madeline on Instagram @the_rare_life Follow The Rare Life on Facebook. Check out our appointment day merch! Support the show and become a Patreon. Vanessa's Recommended Resources: Crimp Camp on Netflix (film) Demystifying Disability by Emily Ladau (book) Sitting Pretty by Rebekah Taussig (book) Instagram Accounts: @nina_tame @sitting_pretty @wheelchair_rapunzel @disabled_eliza @thislittlemiggy @emilyladau @theheumannperspective

In Episode 59, Emily Ladau, Disability Rights Activist, Author, and Communications Consultant at Words I Wheel By, introduces the topic of disability through an insightful discussion with Melinda on systemic ableism, disability history, representation, and rights. Emily explains why it's alright to use the term 'disabled', how accommodation and inclusion should be viewed upon, and how we can build allyship within the disability community.About EmilyEmily Ladau is a passionate disability rights activist, writer, storyteller, and digital communications consultant whose career began at the age of 10 when she appeared on several episodes of Sesame Street to educate children about her life with a physical disability. She serves as the Editor in Chief of the Rooted in Rights Blog, a platform dedicated to amplifying authentic narratives on the disability experience through an intersectional lens.Find Leading With Empathy & Allyship useful? Subscribe to our podcast and like this episode!For more about Change Catalyst, and to join us for our monthly live event, visit https://ally.cc. There, you'll also find educational resources and highlights from this episode.Connect On SocialYouTube: youtube.com/c/changecatalystTwitter: twitter.com/changecatalystsFacebook: facebook.com/changecatalystsInstagram: instagram.com/techinclusionLinkedIn: linkedin.com/company/changecatalystsProduction TeamCreator & Host: Melinda Briana EplerProject Manager: Emilie MaasFinance & Operations: Renzo SantosMarketing Communications Coordinator: Christina Swindlehurst ChanCreative Director @ Podcast Rocket: Rob Scheerbarth[Image description: Leading With Empathy & Allyship promo with the Change Catalyst logo and photos of Emily Ladau; a White woman who is wearing glasses and has curly brown hair pulled back halfway, with the rest framing her face. She is wearing a black dress dotted with red flowers and green leaves. She is sitting in a power wheelchair, facing the camera, and smiling. One of her hands is resting in her lap and the other hand is resting on the joystick of her wheelchair, turned so that a tattoo of a peacock feather is visible on her inner arm; and host Melinda Briana Epler; a White woman with red hair, glasses, and orange shirt holding a white mug behind a laptop.]Support the show (http://patreon.com/changecatalysts)

Disability Rights Activist Emily Ladau is discussing her new book “Demystifying Disability” and the importance of allyship for the disability community. --- This episode is sponsored by · Anchor: The easiest way to make a podcast. https://anchor.fm/app Support this podcast: https://anchor.fm/wid-org/support

Emily Ladau Here's a number for you, 1 billion. One billion people is the estimated number of disabled people in the world. One billion. One in 8 people on the planet. That means that each of us knows someone, likely many someones, with a disability whether visible or hidden. Yet disability is a subject that most of us give little or no thought to. Disability activist Emily Ladau joined me on the podcast to talk about Demystifying Disability, which is also the title of her new book. Emily and I talked about how to normalize disability as simply another part of the human experience. We spoke about the impact of intersecting marginalized identities and how diverse the disability community is. At the end of our talk I knew a lot more than I had before and increased my comfort level in how to talk about disability with members of both the disability and non disabled communities.  One billion people. Maybe we should be paying more attention to this than we typically do. For a written transcript of this conversation click here. About Emily: Emily Ladau is an author and disability rights activist whose career began at the age of 10, when she appeared on several episodes of Sesame Street to educate children about her life with a physical disability. Her writing has been published in outlets including The New York Times, SELF, Salon, Vice, and HuffPost and her first book, Demystifying Disability, was published by Ten Speed Press, an imprint of Penguin Random House, in September 2021. Emily's Action Items: 1) Listen to, learn from, and amplify the voices of the disabled 2) Know when to pass the mic 3) Take the time to get to know and understand the disability experience Resources: Demystifying Disability by Emily Ladau Connect with Emily: Website Facebook Twitter Instagram LinkedIn Credits: Harmonica music courtesy of a friend  

September 13, 2021 Discussion on the book "Demystifying Disability," Good Intentions by Dr. Farid Holakouee

S6 E63: In this episode, meet Editor-in-Chief of Highlights Magazine Christine French Cully, founder of PrepMatters Ned Johnson, and disability activist, podcast host, and public speaker Emily Ladau. Hear Christine French Cully reflect on the ways Highlights has brought joy and comfort to children (for 75 years and counting!), Ned Johnson on language parents can use to promote motivation and stress tolerance in teens, and Emily Ladau on making the disability experience accessible to everyone. Plus, learn what it was like for these authors to record their audiobooks. Dear Highlights by Christine French Cully: https://www.penguinrandomhouseaudio.com/book/704307/dear-highlights/ What Do You Say? by William Stixrud, PhD and Ned Johnson: https://www.penguinrandomhouseaudio.com/book/624704/what-do-you-say/ Demystifying Disability by Emily Ladau: https://www.penguinrandomhouseaudio.com/book/646508/demystifying-disability/

In this episode, I'm joined by Emily Ladau, disability rights activist & author of Demystifying Disability, to chat about her journey to becoming a disability rights activist, making the disability experience accessible to the world, and disability allyship. ---- Show notes & transcript: http://tiffanyyu.com/podcast/039 --- This episode is sponsored by · Anchor: The easiest way to make a podcast. https://anchor.fm/app --- Send in a voice message: https://anchor.fm/imtiffanyyu/message

Judy is chatting with Emily and Ellen Ladau, who are a mother-daughter duo that have the same physical disability. Emily and Ellen talk to Judy about their evolving relationship, working on Emily's upcoming book and their journey into activism. Transcript: PDF About Emily Ladau Emily is a passionate disability rights activist, writer, storyteller, and digital communications consultant whose career began at the age of 10, when I appeared on several episodes of Sesame Street to educate kids about life with a physical disability. I'm the Editor in Chief of the Rooted in Rights Blog, co-host of The Accessible Stall Podcast, and author of Demystifying Disability: What to Know, What to Say, and How to be an Ally.

Emily Ladau (https://twitter.com/emily_ladau) joins Good