Podcasts about disability advocates

Public transportation advocates in Michigan are especially excited about components in the Fiscal Year 2026 budget that provide additional funding to transit agencies across the state.State Rep. Jason Morgan, D-Ann Arbor, a co-chairman of the Legislature's transit caucus, touted it as an unprecedented investment."This is the largest increase in public transit funding in Michigan's history, as far as I'm aware," Morgan said. "This is a truly transformational investment."On this week's Talking Michigan Transportation podcast, David Bulkowski, executive director of Disability Advocates of Kent County and a long-time supporter of efforts to improve funding for transit services, explains why transportation is paramount for providing access for all.

October 8, 2025- In an excerpt from Dispatches from Planet Albany, we explore how advocates for New Yorkers with disabilities are hoping to wield more clout at the Capitol. Our guest is Mike Schweinsburg, president of the 504 Democratic club, which endorsed Lt. Gov. Antonio Delgado's bid for governor.

On today's episode of The Steve Gruber Show, Steve talks with Andrew Beardslee, Vice President of Government Affairs at Michigan Retailers. The focus: a rumored Senate delivery tax that has advocates for the disabled speaking out in strong opposition. Beardslee explains why this proposed tax would disproportionately hurt vulnerable communities, especially individuals who rely on delivery services for essential goods. Together, they break down the hidden costs of such policies, the burden on Michigan families and small businesses, and why lawmakers should think twice before pushing another tax on consumers already stretched thin.

In Dinner for Shoes podcast episode 74, host Sarah Wasilak chats with fashion-forward disability advocate and para surfer Cienna Ditri to celebrate Disability Pride Month. Cienna's bio on Instagram, where she goes by @chronicallypersevering, sums up her online presence: “My conditions are chronic, but my style is iconic.” Her aesthetic blends coastal ease with confident self-expression.Sarah and Cienna discuss the growing movement for disability visibility in fashion and beauty, the rise of disabled influencers on TikTok and Instagram, and how personal style can be a powerful tool for advocacy and inclusion. Sarah also spotlights a curated list of stylish disability advocates whose feeds deserve your follow.Inspired by Cienna's favorite meal, Sarah samples pasta with tomato and vodka sauces from Rosticeria Da Gigi in Hoboken — a nod to the sweet spot where fashion and food meet on Dinner for Shoes.In the episode, Sarah wears the popular Heidi Merrick Ginger dress of Meghan Markle fame. Dinner for Shoes viewers can enjoy 15% off at Heidi Merrick with code DFS15.✨ Need outfit advice? Dealing with a fashion emergency? Call or text the Shoe Therapy Hotline at 917-336-2057 or tag #ShoeTherapy on TikTok or Instagram — and you might be featured on an upcoming episode.THIS DINNERPasta with tomato sauce and penne pasta alla vodka from Rosticeria Da Gigi in Hoboken, NJTHESE SHOESNina Peggy Ballet FlatsTHIS OUTFITShop my look    Heidi Merrick dressVintage BaubleBar earringsMarrow Fine ringVintage ringTHESE CHAPTERS0:00 - INTRO3:40 - THE OUTFIT BEHIND THE SHOES8:13 - CIENNA DITRI INTERVIEW44:18 - DISABILITY FASHION CREATORS52:07 - PASTA WITH RED SAUCE X2THIS PRODUCTIONis created, written, hosted, and produced by Sarah Wasilak.is creative directed and executive produced by Megan Kai.is tech supervised by Nick.includes photos and videos in chronological order by Cienna Ditri, Sarah Wasilak, Heidi Merrick, Jillian Mercado, Rockahontaz, Clara Holmes, April Lockhart, Belle Bakst, Arianna Rose Phillips, Stephanie Thomas, Jessica Kellgren-Fozard, and Ashton McGrady.is made with love.Dinner for Shoes is a fashion podcast for people who love food, hosted by editor Sarah Wasilak. With appearances by her cats, Trish and Kit, and agendas that almost always go to shit, we aim to dive into a discussion about fashion and style and break some bread in each episode. Dinner for Shoes podcast episodes are released weekly on YouTube, Spotify, and Apple. You can follow along for updates, teasers, and more on TikTok, Instagram, and Facebook. If there are any fashion topics you've been pondering or good eats you think Sarah should try, don't hesitate to send a DM or an email.Dinner for Shoes is an original by The Kai Productions.Follow Dinner for Shoes: @dinnerforshoes on Instagram, TikTok, Facebook, and YouTube Follow host Sarah Wasilak: @slwasz on Instagram Follow producer Megan Kai: @megankaii on Instagram Get in touch: dinnerforshoes@gmail.comTo make this video more accessible, check out YouDescribe, a web-based platform that offers a free audio description tool for viewers who are blind or visually impaired.

In this episode, Rick shares his interview with Kelly Berger and Avery Roberts, community engagement leaders and fierce disability advocates at Cure CMD, a nonprofit advancing research and awareness for congenital muscular dystrophies.Kelly and Avery open up about their deeply personal journeys through misdiagnosis, medical adversity, and social exclusion—and how they transformed these challenges into platforms for empowerment, education, and visibility. Their story of connection, purpose, and advocacy is a powerful reminder that authentic representation and inclusion start with sharing your voice.Together, they've reshaped what it means to live boldly with disability, sparked systemic change on Capitol Hill, and inspired others to discover their own strength—one conversation, one webinar, one small act of kindness at a time.This episode is a MUST-LISTEN!

We're joined by Jeff Light, from Inclusive Futures, a resource focused on supporting families through the challenges of planning for loved ones with disabilities and aging family members.

We're joined by Dalia Torres, as she shares her experiences with disability and experiencing higher education.

Australians have been recognised for their outstanding service and achievements in the 2025 King's Birthday Honours List. People from areas as broad as policing, the arts and disability policy; reflecting the diversity and strength of Australian society today and the efforts of those who are working to make it a better place. - Сотни австралийцев отмечены наградами за выдающиеся заслуги и достижения в День рождения короля. Среди них представители самых разных областей, таких как полиция, искусство и политика в отношении людей с инвалидностью.

Australians have been recognised for their outstanding service and achievements in the 2025 King's Birthday Honours List. People from areas as broad as policing, the arts and disability policy; reflecting the diversity and strength of Australian society today and the efforts of those who are working to make it a better place. - ชาวออสเตรเลียจากหลากหลายสาขาได้รับรางวัลในวันเฉลิมพระชนมพรรษาสมเด็จพระเจ้าชาลส์ที่ 3 แห่งสหราชอาณาจักร ประจำปี 2025 โดยผู้ได้รับรางวัลจะพิจารณาจากผลงานและการอุทิศตนเพื่อสังคม

Australians have been recognised for their outstanding service and achievements in the 2025 King's Birthday Honours List. People from areas as broad as policing, the arts and disability policy; reflecting the diversity and strength of Australian society today and the efforts of those who are working to make it a better place.

 Episode 7 is here! We're joined by Jackson Botsford, DAKC's accessibility specialist, to talk about the ADA, inclusive design, and what it really takes to make spaces accessible for everyone.

One in five Americans have a disability. That’s according to the United States Census Bureau. The Trump administration has released statements promising to protect programs like medicaid, medicare and Social security - programs that people with disabilities rely on everyday. But in his recommendation for funding for fiscal year 2026, President Trump proposed cuts to housing for persons with disabilities and cuts to the National Institute of Disability. Today, we hear about the future of disability services from people living with disabilities. GUESTS: Tom Cosker: Disability Advocate at Disability Rights Connecticut Corey Pheez Lee: More Than Walking Peer Mentor Coordinator, Hip-hop artist and host "Super Adaptables" Podcast with More Than Walking Colin Killick: Executive Director of the Autism Self-Advocacy Network Support the show: http://wnpr.org/donateSee omnystudio.com/listener for privacy information.

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.

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

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.

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. 

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 |

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.