Podcasts about disability support

In this week's episode, John and Cynthia go over some of the latest headlines about family caregiving and budget cuts impacting IDD families throughout the nation. John explains the history of family caregiving and all that goes into it for families, self-advocates, and the IDD community.  This episode is for everyone, whether you're a family caregiver, a provider, a policy advocate, or simply someone who believes that people with disabilities deserve to live, work, and thrive in their communities. Because as John reminds us, the question of family caregiving affects all of us, and will shape the future of disability support for the next 20 to 30 years. Episode Transcript  To learn more about MyQuillo visit MyQuillo.com Episode Transcript Want to share stories with us? Email us at Quillopod@myquillo.com To learn more about Quillo Connect visit MyQuillo.com

Submissions close today for a new bill which would shift the responsibility of care for people with disabilities onto their families, rather than the government. People with disabilities, their caregivers and advocates are calling for drastic changes before it becomes law. Health correspondent Kate Green reports.

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Two male employees accused of assaulting residents at a disability support facility in Kushiro, Hokkaido were arrested, it has emerged that several other staff members have also been voluntarily questioned by police. Episode notes: ‘Two Hokkaido Disability Support Facility Workers Arrested; Three Other Staff Members Voluntarily Questioned': https://barrierfreejapan.com/2026/05/30/two-hokkaido-disability-support-facility-workers-arrested-three-other-staff-members-voluntarily-questioned/

People with autism and other disabilities are living in fear over huge reforms to the National Disability Insurance Scheme - so how does it feel to be the man wielding the axe? Today, our reporter Sarah Ison joins us with the latest from the minister in charge of slicing 190 million dollars and 165,000 people out of the NDIS. Read more about this story at theaustralian.com.au and see Sarah Ison’s full interview with Health Minister Mark Butler by subscribing to our YouTube channel. NDIS growth jumps to 11.3 per cent in year Family supports to be considered before NDIS funding granted Budget 2026: NDIS savings set to hit $185bn This episode of The Front is presented by Claire Harvey, produced by Kristen Amiet and edited by Lia Tsamoglou. Our team includes Tiffany Dimmack, Joshua Burton and Jasper Leak, who also composed our music..See omnystudio.com/listener for privacy information.

The dire budget situation in Maryland and seeming mismanagement at the agency has put the crosshairs on the state's Developmental Disabilities Administration, DDA, which supports about 20,000 Marylanders with everyday assistance like employment, at-home assistance to round the clock 1-on-1 help. Sunil Dasgupta spoke with Greg Snyder, vice-president of the Maryland Association of Community Services, about the cuts and their impact. Music by Seth Kibel.

Kitakyushu City said it will revoke the designation of a Type B continuous employment support facility for people with disabilities in Yahatanishi Ward after its operator, based in Nakama, Fukuoka Prefecture, was found to have fraudulently claimed public support funds. According to the city, the company falsely reported that a full-time instructor was employed to improve participants' wages in order to receive additional staffing payments between May and September last year, and also inflated attendance records for a user approved for services by another municipality, billing for more days than were actually attended. The revocation, under the Comprehensive Support for Persons with Disabilities Act, will take effect on March 31. Episode notes: ‘Kitakyushu to Revoke Designation of Disability Support Facility Over Fraudulent Benefit Claims': https://barrierfreejapan.com/2026/03/03/kitakyushu-to-revoke-designation-of-disability-support-facility-over-fraudulent-benefit-claims/

The Government has launched a public consultation on a new permanent disability support payment, aimed at addressing the extra, everyday costs faced by disabled people. It follows years of debate — from the 2021 Indecon report which estimated additional annual disability-related costs of up to €12,000, to the scrapping of the controversial Green Paper reforms in 2024 after widespread backlash. Social Protection Minister Dara Calleary says this consultation will ensure disabled people's voices are central to shaping the new payment, with submissions open until April 7th. But against a backdrop of rising living costs and fresh protests over recent payment cuts — with some households said to be €1,400 worse off — questions remain about what meaningful support will actually look like. Alan Morrissey was speaking about this with Michael Meere of Clare Leader Forum on Monday's Morning Focus. Photo (c) thodonal from Getty Images via Canva.com

Australia is failing more than 130,000 people with significant psychosocial disability – despite spending billions every year on the NDIS. This gap is fuelling a growing problem. People without adequate supports are more likely to experience homelessness, be hospitalized, or have their needs escalate, putting pressure on systems that are already under strain. In this podcast, Sam Bennett, Mia Jessurun, and Reilly Polaschek, discuss the latest Grattan report, Bridging the Gap: Meeting the needs of Australians with psychosocial disability. In the report, they outline a plan to build a fairer and more effective system of psychosocial supports. Read the report: https://grattan.edu.au/report/bridging-the-gap-meeting-the-needs-of-australians-with-psychosocial-disability/

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Send us a textIn this episode of 'The Quest for the Good Life,' Dr. Mike Strouse and Ivo Ivanov welcome Marcy Davis, CEO of Candeo, who shares her journey in transforming the lives of individuals with disabilities through the innovative workforce strategies developed by GoodLife. The conversation explores the successful implementation of new work schedules that have led to a significant increase in applications and a decrease in vacancies. Marcy emphasizes the importance of communication and collaboration in navigating workforce challenges, providing valuable insights for other agencies facing similar issues.Marcy Davis emphasizes the importance of human connection in her work.Candeo has grown from serving 14 individuals to a larger community.Natural disasters can have a profound impact on local communities.The transition to a new work schedule strategies developed by GoodLife and Dr. Strouse can lead to increased employee satisfaction.Effective communication is key to implementing change in organizations.Marcy's experience highlights the importance of not going it alone during transitions.The quality of support improves when full-time employees work weekends.A dedicated recruiter can streamline the hiring process significantly.The new work model has led to a dramatic decrease in vacancies.Marcy's leadership style focuses on collaboration and understanding employee needs.Visit Candeo Iowa here: https://www.candeoiowa.org/

This interview first aired on Thursday the 6th of November, 2025 on ONE FM 98.5 Shepparton. One FM breakfast announcer Plemo interviews Athena Papadatos who is an advocate for people with a disability and is looking to run a monthly self help group at the South Shepparton Community House. To find out more and to get involved head to https://southcom.org.au/ You can call - (03) 5821 6172. or email - info@southcom.org.au Listen to One FM Breakfast with Plemo: Monday - Friday, 6am - 9am. Contact the station on admin@fm985.com.au or (+613) 58313131 The ONE FM 98.5 Community Radio podcast page operates under the license of Goulburn Valley Community Radio Inc. (ONE FM) Number 1385226/1. PRA AMCOS (Australasian Performing Right Association Limited and Australasian Mechanical Copyright Owners Society) that covers Simulcasting and Online content including podcasts with musical content, that we pay every year. This licence number is 1385226/1

Canberran Rossel Buan Mariano bravely quit her primary employment as a disability worker to pursue a full-time career in the food truck business, which she co-founded with her husband in 2022. - Sa episode ng May PERAan, tinalikuran ni Rossel Buan Mariano na taga- Canberra ang kanyang trabaho para subukin at pagtagumpayan ang food truck business na sinimulan niya kasama ang asawa noong taong 2022.

Send us a textDr Astrid Birgden is a consultant Forensic/Clinical Psychologist and NDIS Behaviour Support Specialist who has years of experience working in corrections and disability settings. Astrid's career is quite extraordinary. She is a trailblazer in behaviour intervention support in Australia and worked overseas on international projects. She has even been an assistant sheriff/warden of a remand centre in New Orleans.We caught up with Astrid at the Complex Needs Conference in March 2025 where she was part of a panel discussion on Integrating mental health, disability, and human rights for comprehensive support.ermha365 provides mental health and disability support for people in Victoria and the Northern Territory. Find out more about our services at our website.Helplines (Australia):Lifeline 13 11 14QLIFE 1800 184 52713 YARN 13 92 76Suicide Callback Service 1300 659 467ermha365 acknowledges that our work in the community takes place on the Traditional Lands of many Aboriginal and Torres Strait Islander Peoples and therefore respectfully recognise their Elders, past and present, and the ongoing Custodianship of the Land and Water by all Members of these Communities.We recognise people with lived experience who contribute to GET REAL podcast, and those who love, support and care for them. We recognise their strength, courage and unique perspective as a vital contribution so that we can learn, grow and achieve better outcomes together.

In this conversation, Garry Ashton and Ben Toll discuss their experiences in the lawn care industry, focusing on their involvement with the NDIS and the employment of individuals with disabilities. They explore the importance of skills development, the challenges of scaling a business, and the significance of effective communication and flexibility in employee management. The discussion also touches on the logistics of equipment and operational efficiency, highlighting the innovative approaches taken to create a supportive work environment for their diverse team. In this conversation, Garry Ashton and Ben Toll discuss various aspects of running a landscaping business, focusing on equipment durability, team management, and the importance of inclusivity in the workplace. They share insights on adapting to weather challenges, maintaining equipment, and ensuring safety protocols. The discussion also touches on the significance of community impact, managing client relationships, and the role of technology in streamlining business processes. Overall, the conversation highlights the balance between operational efficiency and fostering a supportive work environment.

In this no-holds-barred episode of The Court of Public Opinion, Jeremy Cordeaux reflects on government inefficiencies, absurd spending in aged care and education, and what he calls the “$48 billion NDIS con.” From a passionate critique of racial politics in Victoria’s new treaty, to Australia’s misguided Pacific climate deals and bloated federal departments, Jeremy doesn’t pull punches. With trademark wit, he calls out “talk therapists” earning $194/hr and proposes an audacious solution—become one himself. It’s thought-provoking, funny, and furious. Topics covered; 1 in 4 Australian children lacking verbal communication skills Overcrowded hospitals and aged care patients misallocated to hospital beds Jeremy questions the purpose of the Federal Department of Health Roy Morgan’s “Most Trusted Brands” survey (Bunnings, ALDI, Apple, etc.) Victoria’s Aboriginal treaty and third chamber of parliament $500 million climate deal with Vanuatu and Solomon Islands Australia's 1% emissions vs China’s 30% – climate hypocrisy Jason Clare’s new “Teaching and Learning Commission” NDIS absurdities: $194/hr art, music and “talk therapy” Stripper clubs as “therapy” – paid by taxpayers Jeremy’s comedic proposal to become a talk therapist himself Sponsor shoutouts: The Rising Sun and Elder Fine Art Birthday shoutouts and historical “On This Day” notes See omnystudio.com/listener for privacy information.

In this powerful episode of Focus on Outcomes, we're joined by Sean Moore, Community Relations Manager at Open Door Columbus, an organization with deep roots in disability support and a bold vision for the future.What You'll Learn:How Open Door's innovative use of remote support technology is reshaping independence for adults with disabilitiesThe story behind their new sensory park, a first-of-its-kind, fully inclusive space in West ColumbusWhy immersive tech, virtual art programs, and AI-assisted communication tools are game changers in human servicesHow Sean's background in fine arts and advocacy fuels Open Door's creative approach to careWhat it means to truly support people in “inspiring their life journey,” not just care, but connection, empowerment, and choiceWhether you're in healthcare, human services, education, or tech, this conversation will open your mind to how technology, compassion, and community-building can (and should) work together.Plus: Learn how local businesses, donors, and volunteers can get involved in bringing the Open Door sensory park to life!

A controversial cost-saving policy for carers for the disabled is being abandoned as part of changes to the disability support system. From next April, the government will remove purchasing guidelines that limit what disabled people can spend their money on, giving them more control over their budget.

A disability support service is worried the government could be about to cut a travel subsidy that helps people with disabilities get where the need to be. The Total Mobility Scheme is jointly funded by Waka Kotahi the New Zealand Transport Agency, Councils and the government, while card holders pay 25% of a taxi fare. The service is currently under review and Transport Minister Chris Bishop says future funding of the scheme is yet to be decided. Chief executive of Aspire Canterbury, spoke to Lisa Owen.

Subith Dey, a Darwin based Chef turned Disability Support worker, bought four off-market deals in six months, all within 1-2 weeks of searching. I'm proud to say he's a client of the Property Investment Accelerator, and in this discussion we cover:

Did you know you could be receiving free disability care through the OPWDD in New York? Explore the many benefits that you and your family may qualify for, as explained by a local provider. Learn more at https://ameliahomecareny.com/pediatric-home-care/ Amelia Home Care City: Brooklyn Address: 3007 Ocean Parkway Website: https://www.ameliahomecareny.com/

In a prefectural facility for people with disabilities in Toki City, Gifu Prefecture, 14 care workers physically abused residents, including hitting them forcefully. In response, the prefecture has issued an administrative punishment, suspending the intake of new residents for three months. According to the prefectural government, 14 male and female care workers in their 20s to 70s committed 40 acts of abuse against 18 residents between July and October of last year. These acts included forcefully hitting residents on the face or head for spilling food and kicking them in the legs while administering medication. Episode notes: ‘14 Staff Members Abused Residents at Gifu Disability Support Facility, Intake Suspended for Three Months': https://barrierfreejapan.com/2025/07/24/14-staff-members-abused-residents-at-gifu-disability-support-facility-intake-suspended-for-three-months/

On July 2nd, Goshogawara city conducted a second investigation following the one in June, following suspicions that a disability support facility in Goshogawara City, Aomori Prefecture, had physically abused residents. The city conducted an investigation on June 26, including interviewing those involved with the facility, but was unable to identify the suspected abuser or the resident who was abused, so city officials visited the facility on the 2nd and conducted a re-investigation. The facility has 39 residents from within and outside the prefecture, and about 50 staff members. In response to an interview by Aomori Television on July 1st, the facility said it was "confirming the facts.” Episode notes: ‘Second Investigation Conducted Over Abuse at Disability Support Facility in Aomori Prefecture': https://barrierfreejapan.com/2025/07/03/second-investigation-conducted-over-abuse-at-disability-support-facility-in-aomori-prefecture/

In this episode, Jeremy Cordeaux discusses a variety of current events, including the birthday of King Charles, environmental issues, social protests, and the challenges surrounding electric vehicles. The conversation also touches on political commentary, national identity, and the growing concerns regarding disability support in Australia. The host emphasizes the importance of community contributions and conservation efforts, while also reflecting on cultural and historical insights.takeaways The King's birthday is acknowledged with honors for various individuals. Environmental conservation is a pressing issue, particularly regarding ocean pollution. The state budget reveals significant debt and health care challenges. Public protests arise from social issues, including the death of an Aboriginal man. Media representation plays a crucial role in shaping public perception. Electric vehicles face scrutiny over safety and environmental impact. Political figures are often involved in controversies that distract from pressing issues. National identity is a topic of debate, particularly regarding the Australian flag. Concerns about the NDIS and its growing enrollment among young children are raised. Cultural reflections highlight the importance of animal welfare and conservation efforts. See omnystudio.com/listener for privacy information.

In this episode of the Friends for Life Podcast, Tony Stuart dives into the importance of emotional intelligence in the field of developmental disabilities (DD) and beyond. He explores how self-awareness, empathy, and adaptability play a crucial role in supporting individuals with disabilities, emphasizing the need to truly listen, affirm feelings, and respond with kindness. Tony shares personal experiences and insights on how emotional intelligence impacts not only professional interactions but also personal relationships, parenting, and navigating the complexities of society. He breaks down key strategies for DSPs, SSAs, and administrators to cultivate emotional intelligence, ensuring they can connect with and support those they serve more effectively. Whether you're in the DD field or just looking to improve your emotional awareness, this episode is packed with valuable takeaways. Tune in and start building better connections today! #EmotionalIntelligence #DevelopmentalDisabilities #FriendsForLife #Podcast #Empathy #ListeningSkills

According to the Health Services Union (HSU), Australia is facing a shortfall of 100,000 disability industry staff, with one in four workers planning to leave the sector because of low pay, inadequate training, and lack of career pathways. The union is calling for a $5-an-hour pay rise. Listen to SBS Sinhala pocast for more information. - ඕස්ට්‍රේලියාවේ ආබාධිත පුද්ගලයින් සඳහා උපකාරක සේවා සපයන්නන්ගේ විශාල අඩුවක් පවතින බව ඕස්ට්‍රේලියාවේ සෞඛ්‍ය සේවා වෘතීය සමිති පවසා සිටිනවා. මේ සඳහා විවිද හේතු බලපෑ ඇති අතර මෙයට විසඳුමක් ලෙස වැටුප් වැඩි කිරීම් ඇතුළු විවිද යෝජනා ඔවුන් ඉදිරිපත් කර සිටිනවා.

On this episode of IDD Health Matters, Dr. Craig Escudé sits down with Johnathon Crumley, Chief Operations Officer of IntellectAbility, to discuss his unexpected journey into the field of intellectual and developmental disability (IDD) support. Originally planning a career as a military chaplain, Jonathan's path shifted when he discovered his passion for improving services and quality of life for individuals with IDD. In this insightful conversation, Johnathon shares how person-centered thinking, proactive healthcare approaches, and celebrating small wins can transform support systems. He also dives into the critical work IntellectAbility is doing to provide tools, training, and resources that enhance care for people with IDD. Tune in to learn how balancing health, safety, and personal choice leads to a more fulfilling life for individuals with disabilities. For more information on IntellectAbility's resources, visit ReplacingRisk.com.

On this episode of IDD Health Matters, Dr. Craig Escudé sits down with Johnathon Crumley, Chief Operations Officer of IntellectAbility, to discuss his unexpected journey into the field of intellectual and developmental disability (IDD) support. Originally planning a career as a military chaplain, Jonathan's path shifted when he discovered his passion for improving services and quality of life for individuals with IDD. In this insightful conversation, Johnathon shares how person-centered thinking, proactive healthcare approaches, and celebrating small wins can transform support systems. He also dives into the critical work IntellectAbility is doing to provide tools, training, and resources that enhance care for people with IDD. Tune in to learn how balancing health, safety, and personal choice leads to a more fulfilling life for individuals with disabilities. For more information on IntellectAbility's resources, visit ReplacingRisk.com.

What if the standard support systems for people with disabilities are just not enough? In this episode, we explore how AIM is challenging the status quo by offering innovative, personalized services for individuals with developmental and intellectual disabilities and traumatic brain injury. We also discover how AIM empowers those it serves by providing more opportunities, choices, and meaningful connections, helping them shape their futures. Because at AIM, simply getting by isn't the goal—we're always AIMing for more. AIM Services: https://www.aimservicesinc.org/ Find Heather and Jake's Help from Heaven: ❤️ Heather's Instagram: https://www.instagram.com/heathersstraughter/ ❤️ Jake's Help from Heaven: http://jakeshelpfromheaven.org/ ❤️ Jake's Help from Heaven IG: https://www.instagram.com/jakeshelp/ ❤️ Facebook: https://www.facebook.com/jakeshelpfromheaven ❤️ Our YouTube Channel: https://www.youtube.com/@APlaceofYesPodcast Learn more about your ad choices. Visit megaphone.fm/adchoices

Music has a way of connecting people, transcending language barriers, and healing the soul. The discipline and dedication required to master an instrument can translate into valuable life skills that go beyond the music classroom.  In this episode of Parenting Impossible, Annette Hines spoke with Annie Ray, the founder of the Crescendo Orchestra program, a music class tailored for students with significant disabilities, and Parent Orchestra, which invites parents to join their children in learning music, fostering a vibrant community, and encouraging parental involvement in their kids' musical journeys. Annie passionately advocates for music education as a core subject, emphasizing the need to meet students where they are and tailor instruction to their unique needs. Her approach showcases music's profound impact on students, transcending mere notes and rhythms. The Crescendo Orchestra program is a shining example of how music can transform the lives of young students, providing them with a sense of community, purpose, and hope for the future.   In this episode, you will hear: Why emphasizing a student-centered approach fosters a joyful space for musical exploration without fear of judgment. Ways the Parent Orchestra program has built a vibrant community of over 200 parents on a shared learning journey. How music education sharpens cognitive abilities and instills resilience, helping students navigate challenges and embrace imperfections. Ways fellow educators can launch inclusive music programs, advocating for equal access to the transformative power of music education. Resources from this Episode: Watch Annie's TEDx Talk: https://www.ted.com/talks/annie_ray_the_sound_of_sucess Learn More About Annie's Program and GRAMMY win - Annie Ray: Music Educator Learn More about the Parent Orchestra -

Join Dr. Brad Schlaggar, president and CEO of Kennedy Krieger Institute and Dr. Lisa Carey, the Assistant Director of the Center for Innovation and Leadership in Special Education as well as an education specialist for the Neuropsychology Department at Kennedy Krieger. Accommodations for college require self-advocacy. It is the student themselves who must request those accommodations at the school—not the parents. Services such as occupational therapy, speech therapy, reading support, and instructional assistants, which may have been a part of a student's IEP, are not a part of college accommodations. Additionally, since many students live on a college campus, there may be additional accommodations to consider for housing, dining, and recreation. Listen as they dive into the process of requesting accommodations and the importance of working with the college's Disability Support office. Families need to start preparing their child early for this change so that students have the self-advocacy skills to be successful in college.   Resources for students and families: Understood.org has great resources for understanding disability services in higher education Kennedy Krieger has a guide specifically for college students with a history of cancer. The US Department of Education Office for Civil Rights offers a guide of student rights and responsibilities in postsecondary education. Edutopia has a helpful blog post on this topic.See omnystudio.com/listener for privacy information.

Footnote incoming!! In the off week, we'll be going back and picking out the best bits of our episodes so far and maybe even adding in some bonus content here and there.We've returned to our episode on disability on campus with current students Grant and Jack. They share with us their experiences as students with disabilities, how you can be an ally on campus and how they've made the most of Disability Support.Guests: Grant Freeman and Jack McKenzieHosted by: Shannon PearceThis episode was produced by Grace Atta and Shannon Pearce.Full episode here: Disability on campusTo support the show, click ‘subscribe' on Apple Podcasts or ‘follow' on Spotify. For more Take Note and UoA goodness, check out our Instagram page @uoa.oncampus and drop us a DM to let us know what you think of the show.If you or another student you know needs some mental health or wellbeing support, head to UoA's Wellbeing Hub: Student Health and Wellbeing or check out Getting Support for a list of services. You can also check out Student Life for support across all areas of university life at UoA.Take Note is a UoA On Campus Production.Thanks for listening!

Welcome to the Friends for Life Podcast, where we delve into the nuanced world of providing support for individuals with developmental disabilities. In this episode, we discuss the complexities surrounding pet ownership among our clients. Pets can offer comfort and companionship, but they also bring challenges in care, training, and company liability. Join us as we share practical tips for Direct Support Professionals (DSPs), Service and Support Administrators (SSAs), and agency providers. We emphasize the importance of efficient team meetings, understanding the unique needs of both individuals and their pets, and navigating scenarios where allergies, past traumas, or cultural beliefs come into play. We also explore alternative pet options and stress the importance of safety for both caregivers and clients. Learn more about our mission to empower and improve the quality of life for individuals with disabilities through services like Adult Day Support and Home Health Care. We are dedicated to the motto "my ability is stronger than my disability" and invite passionate individuals to explore career opportunities with us. For more information and career opportunities, visit friendsforliferc.com.

In our Catholic faith, we recognize that every person is created in the image and likeness of God. This truth extends to individuals with disabilities, who bear within them a unique reflection of the divine. Join Jason Nunez as he speaks with Lauren Stadelman, Director for Human Dignity and Pastoral Care for the Archdiocese of San Antonio, and the inspiring mother-daughter duo Jean and Emma Olech. This program is a testament to the power of faith, resilience, and community. On today's journey, we will: Learn what a Disability Ministry is and its role in supporting disabled individuals in their spiritual journey. Explore ways to assist those with disabilities in their walk with God. Hear from guests about how living with a disability shapes their faith and resilience Continue Your Journey: Guest information, helpful resources, and watch the replay of the Disabilities Mass celebrated in San Antonio, TX on May 11, 2024. Jewel for the Journey: "For we walk by faith, not by sight." (2 Corinthians 5:7) Learn more at PilgrimCenterOfHope.org/Journeys Help us spread hope! PilgrimCenterOfHope.org/Donate Images courtesy of Veronica Markland at Today's Catholic Newspaper, and Jean Olech. All rights reserved. We are so grateful to this month's Journeys of Hope sponsors, Deanna & Owen Villarreal, for making this episode possible. We invite you to consider becoming a Missionary of Hope by sponsoring a week or month of Journeys of Hope 2024 Radio Broadcast & Podcast programming! Click here to get started.

Filipinos are known for their outstanding qualities such as being caring and hardworking, which is why they are renowned worldwide. What could be the story of Filipinos as disability support workers? - Kilala ang mga Pilipino sa natatanging katangian bilang maalaga at masipag magtrabaho kaya tanyag ito sa buong sa buong mundo. Ano naman kaya ang kwento ng mga Pinoy bilang disability support worker?

Advocates for New Zealanders with disabilities are welcoming Louise Upston taking over from Ms Simmonds as the new Minister for Disability Issues. Chief executive of the New Zealand Disability Support Network, Peter Reynolds speaks to Lisa Owen

Parents and disability advocates say families of autistic kids are falling through the cracks when it comes to provincial disability funding in Nova Scotia. CBC reporter Celina Aalders brings us this story.

The Labour party says it's a "massive vote of no confidence" in the Disability Issues Minister that Cabinet has now assumed responsibility for future decisions about disability funding. This comes after Whaikaha, the Ministry for Disabled People, and its minister, Penny Simmonds, blindsided the sector by announcing changes to purchasing rules for disabled people's equipment, services, and respite funding. The minister has subsequently admitted the communication was badly handled. Peter Reynolds, chief executive of the country's not-for-profit Disability Support Network, says there's plenty of blame to be shouldered by Labour as well for having set up the ministry with relatively scant funding. Reynolds spoke to Corin Dann.

Welcome back to Take Note! The podcast where we give you the best notes on everything you need to know from the day you start uni to the day you graduate. This episode falls on Neurodiversity Celebration Week. So, listen in to conversations with current students, Tessa, Grant and Jack, who share with us their experiences as students with disabilities. They'll chat about study tools for neurodiverse folk, how to access Disability Support and how you can be an ally on campus. Guests: Tessa Gloede, Grant Freeman and Jack McKenzie Hosted by: Shannon Pearce This episode was produced by Grace Atta and Shannon Pearce. To support the show, click ‘subscribe' on Apple Podcasts or ‘follow' on Spotify. For more Take Note and UoA goodness, check out our Instagram page @uoa.oncampus and drop us a DM to let us know what you think of the show. If you or another student you know needs some mental health or wellbeing support, head to UoA's Wellbeing Hub: Student Health and Wellbeing or check out Getting Support for a list of services. You can also check out Student Life for support across all areas of university life at UoA. Take Note is a UoA On Campus Production. Thanks for listening!

Danielle Neff is a Senior Direct Support Professional (DSP) at a provider organization in Long Island, New York. Danielle supports individuals with intellectual and developmental disabilities. She is passionate about helping these individuals achieve their goals and live independent lives. Danielle's career in the field of disability support started as just a job, but it quickly became her calling. She finds purpose and fulfillment in her work, and considers the individuals she supports as part of her extended family.In this episode of DSP Talk, host Gina Scarpa interviews Danielle Neff, a Senior Direct Support Professional (DSP) from Long Island, New York. Danielle shares her journey into the field of disability support and how it has become more than just a job for her. She discusses the importance of supporting individuals with intellectual and developmental disabilities in achieving their goals and living independent lives. Danielle emphasizes the strong relationships she has developed with the people she supports, considering them as part of her family. She also highlights the qualities that make a successful DSP and offers advice to those considering a career in this field.Key Takeaways:Supporting individuals with intellectual and developmental disabilities is more than just a job; it is a fulfilling career that gives purpose and meaning to DSPs.The individuals supported by DSPs are like family, and strong relationships are formed based on empathy, care, and mutual respect.Successful DSPs are empathetic, caring, observant, and hardworking individuals who genuinely care about the well-being and goals of the people they support.Taking a chance and entering the field of disability support can lead to a rewarding career that makes a difference in the lives of others.Notable Quotes:"I feel like I have my family that I have now and that I grew up with and everything, and then I have my work family. And the individuals we support are all a part of my family." - Danielle Neff"The people we support…each and every one of them are just so different and have these amazing personalities and abilities and talents. And that's really why the work matters, because it's really just all about them." - Danielle Neff"It's the one job that I actually didn't feel miserable in. I enjoyed doing it. I felt like it mattered, and I felt like it was making a difference." - Danielle NeffResources:East End Disability Associates, Inc. Regional Centers for Workforce Transformation Listen to the full episode of DSP Talk to gain valuable insights into the field of disability support and the rewarding career of a DSP. Discover how Danielle Neff found purpose and fulfillment in supporting individuals with intellectual and developmental disabilities, and learn about the qualities that make a successful DSP. Stay tuned for more inspiring conversations on DSP Talk. Hosted on Acast. See acast.com/privacy for more information.

We often hear about society's high achievers but there are others acting as role models of change. In this episode of Change Agents we meet Yasser Zaki, who runs a disability support service which has now branched out overseas and employs many people with disability.

Ever wondered how a career in constitutional law can ignite a passion for human rights advocacy? Nicole Smith, our esteemed guest, takes us through her inspiring transition into nonprofit work, where she's breaking new ground with digital campaigns that touch hearts and change minds. Her journey is a reminder that when we're armed with education and empathy, we can reshape the world—one freed prisoner, one enlightened influencer at a time. She brings to life the idea that our upbringing and the values we're taught can spark a lifelong commitment to justice and community service.We then turn to the triumphs and trials faced by children with disabilities and their families, stories that often go unheard. The tales we share aren't just about milestones and inclusion; they're about the power of support networks, both online and in our neighborhoods, that provide much-needed guidance and solace. Nicole's insights challenge us to reflect on the beauty of life's simple moments and the profound lessons we can learn from the resilience and joy of these extraordinary children.Our discussion culminates with Nicole's latest groundbreaking venture—a disability committee dedicated to filling the voids in support systems for those with disabilities. We examine the significance of comprehensive care that goes beyond the hospital walls, the importance of recognizing and valuing every individual, and how the concept of 'symptom industries' ties into our cultural perceptions. Walk away feeling energized to contribute to this collective mission of building communities that not only offer aid but celebrate the diversity of human dignity and strengths.Support the show

On this week's episode, Hilda Dunford shares her journey as a mother of a special needs child, focusing on the resilience and independence of her blind son. She delves into the challenges and triumphs of parenting a blind child, emphasizing the importance of community support and the beauty of the blindness community on social media. Hilda discusses the complexities of managing her child's medical condition, including septal optic dysplasia, and celebrates his growing independence in medication management. She also touches on the emotional aspects of raising a child with a disability, from handling grief to finding strength in their resilience.The conversation extends to the importance of balancing caregiving with self-care and the dynamics of attention among siblings in a family with a special needs child. Hilda highlights her children's empathy and the family's collective effort in supporting each other. She concludes with a powerful message on the importance of inclusivity and awareness, encouraging engagement with online communities for support and advocating for open conversations about disabilities. Her insights offer invaluable guidance for parents in similar situations and inspire a broader understanding of inclusivity and acceptance in society.Connect with Brianna!Instagram: @mombossinaustinLinkedIn: linkedin.com/in/briannademikeFollow the Podcast on Instagram: @badassbasicbitchLove the podcast? We would love if you would leave a review!Thank you to this week's sponsors! Shopify: Sign up for a $1/month trial period at shopify.com/bbbHelloFresh: Go to HelloFresh.com/bbbfree and use code bbbfree for FREE breakfast for life

Join us in this compelling episode of "Disability, Support, and Parenting," where host Sarah Davies welcomes John Ross Comes, a remarkable individual living with a disability. In a candid discussion, John Ross shares his experiences and insights, offering a unique perspective that is enlightening for parents, caregivers, and anyone interested in understanding the nuances of disability. This episode delves into various aspects of living with a disability, as John Ross Comes opens up about his life's journey. His experiences provide valuable lessons and viewpoints, particularly relevant to those involved in parenting and supporting individuals with disabilities. Key topics covered in this episode include: Life with a Disability: John Ross Comes talks about his personal experiences, challenges, and the common misconceptions about living with a disability. Support Systems and Empathy: The conversation explores the critical role of empathy and robust support systems in improving life quality for those with disabilities. Guidance for Parents: Although not a parent himself, John Ross provides thoughtful advice for parents raising children with disabilities, focusing on the importance of patience, understanding, and resilience. Inclusion and Community: Sarah and John Ross discuss the significance of community support in promoting inclusivity and how societal views on disability are changing. Overcoming Obstacles: John Ross reflects on his journey of personal growth, discussing how he has navigated and overcome various challenges. This episode is more than a discussion about the difficulties associated with disabilities; it's a testament to the strength, courage, and optimism that can flourish in challenging circumstances. Whether you're directly involved in the disability community, a parent, or simply someone seeking a deeper understanding of these experiences, this conversation with John Ross Comes is sure to be enlightening and inspiring.

In this heartfelt and insightful episode of "DSP: Disability, Support and Parenting," host Sarah Davies and guest Lisa Comes delve into the complexities and joys of parenting, with a special focus on raising children with disabilities. They share their personal experiences and the lessons they've learned along the way, offering a blend of humor, honesty, and wisdom. The discussion covers a range of topics, including the value of including children with disabilities in regular activities like karate or swim classes, emphasizing the benefits of socialization and seeing others face similar challenges. They also explore the role of schools in children's lives, advocating for the value of experiences outside the traditional educational system, such as family vacations and advocacy events. Lisa and Sarah share their parenting philosophies, highlighting the significance of listening to their children, validating their feelings, and fostering open communication. They challenge conventional views on parenting, discussing how to balance respecting children's opinions while guiding them as a parent. The conversation touches on building resilience in children, recognizing their individual strengths and weaknesses, and avoiding overemphasis on diagnoses or labels. The hosts offer practical advice on parenting, from using sticker charts for behavior management to understanding that as a parent, it's okay to change your mind based on new information. Lisa and Sarah conclude the episode with a reminder that parenting is a journey of progress, not perfection. They encourage parents to love their children the best they can, understanding that there's no one-size-fits-all approach to parenting. Listen to this episode if you're a parent seeking guidance, inspiration, or just a sense of camaraderie in the often challenging but rewarding journey of raising children, especially those with unique needs. Note: This description is based on the transcribed content of the YouTube video provided. The actual video should be referred to for complete details and context.

This week FemCity CEO, Violette de Ayala is joined by Michele Leahy, Founder at Leahy Life Plan. Join in the conversation as they dive into Services and Support You May Not Know You Need.  About Michelle Leahy  // Ms. Leahy is the founder and CEO of Leahy Life Plan, a firm dedicated to life planning for those with disabilities as well as their families. She understands disability challenges from both a professional and personal perspective. Her goal is to assist in developing strategies of funding special needs trusts and creating a roadmap to meaningful adult supports. She has her Certification in Work Incentive Planning through an approved Social Security Administration (SSA) program established through the SSA Ticket To Work Program. Ms. Leahy received her M.S. in Non-Profit Management from Eastern University and an B.A. in Communications, Division of Humanities, from Penn State. She has 15+ years of varied professional work experiences before she established her own company.  She was the first non-veteran Executive Board Member of the United Spinal Association, a national disability rights organization, where she served for over 8 years. In 2018, she spoke on disability issues at the Philadelphia Women's March on the steps of the Art Museum. She has been a key player in organizations such as AHEDD (a specialized human resource organization), the Epilepsy Foundation of Eastern PA, assisted in the establishment of the Bucks County Center for Independent Living and has served on many community advisory boards that advocate for individuals with disabilities. Ms. Leahy has spoken both nationally and locally on disability at PBI's Exceptional Children Conference, PaTTAN, Spina Bifida National Conference, VoiceAmerica and on the floor of the Pennsylvania Senate. Learn more at https://www.leahylifeplan.com/ About FemCity //  FemCity offers a Free 30-Day Trial Membership and Memberships start at only $15.99. You can also learn more about launching a FemCity Chapter in your community. FemCity has been seen in Gilt, Vogue, AP News, Entrepreneur, Forbes, and MarieClaire. Learn why FemCity is more than just a women's networking group at www.femcity.com and on all social platforms @FemCity. About Violette de Ayala // Violette is a Cuban-American serial and social Entrepreneur, Founder of FemCity®, and virtual mentor to over 20,000 women. Violette has been quoted in Success, Entrepreneur, CNBC, Yahoo Small Business, Business Insider News as a small business expert. You can connect with Violette on IG, FB, LinkedIn at Violette de Ayala. About Lynn Pelzer // Lynn is the COO of FemCity and has held a chair position on boards, currently part of a DEI board with FemCity, she has been awarded the Rising Star Award and Crystal Executive Award in her previous company. She has been a contributor on podcasts as well as blogs, and has been a speaker in women's groups on the topics of business. You can connect with Lynn on Facebook or Linkedin @lynnpelzer.

Are you ready to untangle the complexities of transition planning and become an effective advocate for your disabled person? Host Annette Hines, founder of Special Needs Law Group and Special Needs Family Services brings you an episode that can be a beacon to guide you through the maze of supports and resource systems. Whether you're a young disabled person stepping into adulthood, a caregiver stepping in for a sibling, or a professional wanting to offer the best for your clients, this episode promises to be a haven of insights.Let's begin by exploring person-centered planning. Identifying key questions, making sure the disabled person's voice is at the center of the life plan, and putting together an appropriate support team are all vital. But that's not all! We move forward into the unknown terrain of flexibility in planning and the pivotal role of evaluations and assessments in making transition as smooth as possible. There's also a discussion about how to navigate public benefits, housing, and state agencies, and even the legal decision-making process including understanding guardianship, supported decision-making agreements, power of attorney, and healthcare.Lastly, we invite you to check out and enroll in our exciting online transition planning course, the Special Needs Advocacy & Planning Masterclass (SNAP).  Designed for parents, caregivers, professionals, or disabled adults, this on-demand course offers the ability to design a personalized disability support and life plan through video modules, a course and workbook. With the optional group coaching sessions, participants receive an individualized support network and a platform to discuss and learn from others embarking on the same transition journey.   We look forward to welcoming you on this journey to become an empowered advocate! You can check out the course online and even get a free Disability Support Plan Worksheet: enroll.specialneedsfamilyservices.com/p/advocacy-planning-masterclass If you have questions about the course or coaching programs, we invite you to schedule a call with our team here: calendly.com/imartinez-31/specialneedsacademy Let us know what you think of this episode! Leave your comments or requests for new topics on our website: specialneedscompanies.com/podcasts

Welcome back lovely people, what a week it's been for the yayborhood!!! Nic aka Mr YAYvidson's return to the show last week for a hilarious Valentine's episode – thank you all so much for listening and for the cute littlee love notes… But even more excitingly, our first in real life event in over three years and it was EVEN MORE AMAZING THAN WE COULD HAVE IMAGINED.   I won't spend much time on it this week because we recorded some audio on the night and are putting it together for a proper debrief episode with Ang about the event next week, but I just wanted to quickly reiterate just how incredibly special it was and how grateful we are to everyone who came. There was so much laughter, beautiful tears, wonderful new friendships and memories for a lifetime. And we're doing it all again this week in Sydney for another sold out event, which still blows my mind! So we'll have the full reflection yays of our lives episode next week for you but for now we've got a fascinating guest who I can't wait to share.   I first heard of Ben Mcintosh when we joined my amazing management team at Day Management – should out to the Day family, we love you so much – and, along with nearly a million other people and counting, I very quickly wanted to know pretty much every detail about his life. He, like many others, has grown a loyal and engaged community and uses his platform to educate and positively impact others but unlike many others, it wasn't born out of business, reality TV or nepotism – it's through sharing his day-to-day life as a disability support worker.   In very Seize the Yay fashion, Ben spent most of his life unsure of what he wanted to do dabbling in AFL and even going to college in the US for American Football but not really knowing what his passion was. Turns out, he had been building the perfect skills for a career in disability support work as a big brother to Grace, who was born with Down's Syndrome.   Today you'll hear the story of how he stumbled into doing it for work and found that feeling of purpose we always talk about when you forget what time it is or don't feel like what you're doing is a job. His content is so endearing, empowering and educational helping demystify so much about disability – I mean I'm really only friends with him for Grace, but let's not tell him that. I found this one so fascinating and different, and hope you guys enjoy it too! I think it night have been his very first if not second podcast ever so make sure to tag him and share to encourage him to do it more!!! + Announcements on Insta at @spoonful_of_sarah + Join our Facebook community here + Subscribe to not miss out on the next instalment of YAY!

Social Security Disability Insurance helps support millions of Americans, but it's a slow-moving program that rejects most people who apply. This Jobs Friday: The 10 million working-age people who are neither working nor seeking a job — and they're living with a disability. For sponsor-free episodes of The Indicator from Planet Money, subscribe to Planet Money+ via Apple Podcasts or at plus.npr.org.