Podcasts about invisible disability

Are you feeling overwhelmed by upcoming family gatherings where your homeschooling or motherhood choices are criticized? I understand how hard it can be when extended family members question your decisions, especially during the holidays when you're simply trying to connect and enjoy your time together. In today's episode, I'm sharing how to set healthy, loving boundaries to navigate these tough conversations with grace. You'll walk away with practical tips for shielding your kids from unwanted pressure and keeping your family values front and center—all while maintaining peace in your relationships.I'm here to help you reclaim the joy of family gatherings by learning to respond with grace and confidence.XOXO, KatieREVIEW LINK

Zach sits down again with friend of the show Dr. Nikki Coleman to talk about the reality of invisible disabilities and how employers can support them at work. Learn more about Living Corporate's offerings and services. https://www.living-corporate.com/about Check out our merch! https://bit.ly/375rFbY

One of the most extraordinary manifestations of human potential is:Our ability to grow and strengthen ourselves in the face of pain, trauma, and those moments where life falls apart.Today's guest, Dr. Amrita Sen Mukherjee, has not only studied what contributes to this deeply human capacity for post-traumatic growth but has experienced it first-hand. In our conversation we'll dive deep into her story and insights she's gained about what fosters positive psychological change in response to trauma and adversity.The qualities and conditions that support us in finding the courage to rise again after we fall,And the potential we have to come back stronger.  In today's episode Amrita will share:Parts of her own story including facing illness after childbirth, and the many layers of adversity she experienced as both a mother, and a physician with invisible disability.Insights into Post-Traumatic Growth and her original research that explored the lived experiences of doctors with invisible disability.The conditions that contribute to other people being courageous in the face of significant obstacles.Practical skills for creating psychological safety, compassion, and empathy.The importance of mattering, and feeling at home in our own skin, and at home on the earth.  Practices that support showing ourselves and each other we are valued and that we matter.Reflections on the healing power of silence.Why humility, curiosity, and the willingness to not know can lead to people feeling seen.Did you find this episode inspiring? Here are other conversations we think you'll love:The Courageous Journey Toward Wholeness | Parker PalmerGentle Power - Shifting the Way We Define True Strength | Dr. Elisabet LahtiEnjoying the show? Please rate it wherever you listen to your podcasts!A quick note about the conversation today. There were some occasional minor sounds you'll hear in the background as it wasn't a perfectly quiet spot during recording which comes with the territory from time to time. We feel it didn't detract much from the conversation though and are still very excited to share it with you.More about Amrita:Dr. Amrita Sen Mukherjee, Co-Chair of the Disabled Doctors Network, challenges the frameworks and biases that society imposes. She invites us to consider the potential for change when we unmask the strengths and abilities of the marginalised and to discover how adversity can enable growth, strength and compassion.  She is a dedicated Wellbeing Expert, Positive Psychology Coach, and accomplished Portfolio GP. Specialising in Posttraumatic Growth and guiding high performing professionals through life transitions, Amrita fosters environments of psychological safety and individual curiosity for personal and team growth. Amrita, conducted groundbreaking research on Posttraumatic Growth in Doctors with Invisible Disability, which was published in the British Journal of Health Psychology. As Co-Chair of the Disabled Doctors Network and EDI Lead at The Joyful Doctor, she actively promotes equality and is a Disability Advocate. She also serves as a Trustee for the Thomas Wall Trust and is the ambassador for Doctors in Distress. A sought-after TEDx speaker, Amrita has shared her expertise on wellbeing and equality across platforms like BBC News, podcasts, webinars, and International Conferences. For more please visit: yourwellbeing.doctorThanks for listening!Support the Show.

What is an Invisible Disability? An Invisible disability is a disability or health condition that is not immediately obvious. It defies the stereotypes of what people might think a disabled person looks like. It is crucial to emphasize that just because a disability cannot be seen, it does not mean it does not exist. People with Invisible disabilities want to be treated with respect and as individuals—just like people with visible disabilities and the general population. Even though you cannot see evidence of a disability, the disability still exists. This podcast aims to raise awareness about Invisible disabilities and provide guidance on how to seek help. --- Send in a voice message: https://podcasters.spotify.com/pod/show/she-heals/message

Send us a Text Message.Episode #97: Invisible disabilities can turn into a source of shame and unknowingly get in the way of friendships. What is an invisible disability? It's any condition that is not obvious, perhaps even to the closest of friends. Some examples are depression, anxiety, other mental health diagnoses, as well as physical conditions such as chronic pain, fatigue, and too many other examples to list where symptoms are felt but not seen.This week's guest, Estelle Erasmus, shares her experience with genetic hearing loss that began in her 20s and stayed a secret long after she started wearing hearing aids. In her piece for Shondaland.com, "I'm Learning to Listen in New Ways" Estelle shares the stress of keeping that secret from friends and the deep relief of telling the truth. I'm grateful to share her perspective with Dear Nina listeners.  Meet Estelle:Estelle Erasmus, author of Writing That Gets Noticed: Find Your Voice, Become a Better Storyteller, Get Published (June 2023), is a professor of writing at NYU, the host of the Freelance Writing Direct podcast, and a contributing editor for Writer's Digest. She has appeared on Good Morning America and has had her articles discussed on The View. She received the 2023 NYU School of Professional Studies Teaching Excellence Award, a 2023 Zibby Award for Best Book for the Writer, is in Poets & Writers “Best Books for Writers”, and is an American Society of Journalists and Authors award winner. Learn more at www.EstelleSErasmus.com (and receive a free pitching guide). Also, follow Estelle on Instagram, TikTok, and X, and sign up for her Substack of craft advice, stories and opportunities at estelleserasmus.substack.com* All transcripts are available on the main Buzzsprout "Dear Nina" site. Click on any episode and find the transcript tab. Let's connect over all things friendship! My Substack newsletter about friendship & more Dear Nina website with show notes and a guide to pitching yourself as a guest Instagram , TikTok, Twitter, Youtube, Threads JOIN the Dear Nina Facebook group Ask an anonymous question

In this episode of Fearless Singer, join me (Mel Lathouras) in a conversation with Ella Doneman, a Singer, Educator, and Advocate for people, especially performers, living with a disability, including the less spoken about invisible ones.  Ella shares her firsthand experiences with cerebral palsy and epilepsy, shedding light on the challenges of navigating life and the stage as a performer. She also discusses her journey in creating a tribute show to celebrate and honour Blossom Dearie on her 100th birthday. Tune in for insights and wisdom from Ella's remarkable journey! Follow Ella: Facebook InstagramBook Your Tickets to Blossoming Ella Tribute to Blossom Dearie on Sunday 28 April 3 pm.  Follow Mel: FacebookInstagram  Website Enrol in the Fearless Singer Membership  

This week, we discuss the challenges of living with ADHD, going beyond the core symptoms of inattention, hyperactivity, and focus issues. We'll explore the unseen struggles that impact both the person with ADHD and those who love and support them. Follow us on Instagram, TikTok, and YouTube: @adhdandmepodcast Theme song by @ItsEvbo

Joeita speaks with Beth Beattie and Carole Dagher about their new book “The Right Not to Remain Silent: The Truth About Mental Health in the Legal Profession” which discusses mental health and well-being amongst legal professionals. HighlightsMental Health Within the Legal Profession – Opening Remarks (00:00)Introducing Beth Beattie & Carole Dagher (01:29)“The Right Not to Remain Silent: The Truth About Mental Health in the Legal Profession” (03:12)Importance of Mental Health Amongst Legal Professionals (04:23)Fear & Secrecy Surrounding Mental Health Struggles (06:02)Contributors to “The Right Not to Remain Silent” & Mental Health Summit (08:31)What Can We Learn from Personal Essays on Mental Health? (12:27)Intersections of Mental Health, Sexism, Homophobia & Racism (15:56)Deciding to Disclose One's Invisible Disability (19:31)Reducing Stigma & Changing the Culture Within the Legal Profession (22:24)Significance of Mental Health Awareness Amongst Legal Professionals (24:22)Closing Remarks (25:23)More Info: The Right Not to Remain Silent: The Truth About Mental Health in The Legal Profession is a groundbreaking book that sets the stage for revolutionizing how mental health is perceived in the legal profession and beyond. It contains a series of candid and courageous memoirs by members of the legal profession living with mental health and addiction issues. The authors are judges, lawyers, and law professors with wide-ranging legal practices in British Columbia, Alberta and Ontario including at Bay Street and small boutique firms.Young lawyers and senior members of the profession share their experiences of working while living with various types of challenges – depression, anxiety, bipolar disorder, obsessive compulsive disorder, eating disorders, addiction, grief, imposter syndrome, and perfectionism.The Right Not to Remain Silent: The Truth About Mental Health in The Legal Profession addresses the insidious nature of mental health stigma and isolation in the legal community. But it is fundamentally a book about hope. As the authors discuss their sometimes harrowing journeys, they also show routes back to meaningful engagement with colleagues and work.To read these personal accounts is to be moved, inspired, and hopefully galvanized into action at the individual, collegial, and organizational level. This book offers practical solutions to change the culture of legal practice and beyond so as to bust apart stigma and isolation, foster people getting the support they need, and cultivate more diverse workplaces.Book ContributorsDavid S. GoldbloomThe Honourable George R. StrathyThe Honourable Michele HollinsBeth BeattieCarole DagherThomas TelferKatherine CooliganOrlando Da SilvaMichael R. FergusonMichael HermanAidan JohnsonImran KamalRyan MiddletonYadesha SatheaswaranLeslie Anne St. AmourDan SteinCourtney WilsonLeena YousefiBrett D.M. JonesShayan ImranM. Ishrat Husain“Postpartum depression made me feel hopeless. Not Today.” article by Carole Dagher for the Centre for Addiction and Mental Health (CAMH) Guest Bio: Beth BeattieCalled to the Bar in 1994, Beth Beattie has a broad-based health law litigation practice.Since January 2018 Beth has been a Friend of the Bell Let's Talk campaign. Her story of working as a lawyer with bipolar disorder has been featured on television, radio, podcasts, print media and even billboards across the country. Television appearances include The Marilyn Denis Show, CTV News, CTV North News, CP24 and a CTV prime time special, “In Their Own Words”.In 2021, 2022 and 2023 Beth co-chaired with the former Treasurer of the Law Society of Ontario, Teresa Donnelly, Mental Health Summits for Legal Professionals. Each year the Summits were watched by nearly 6,000 registrants.Beth is a founding member of Voices for Mental Health which is a group of employees at the Ontario Ministry of the Attorney General who have lived mental health experience or who have cared for loved ones with lived experience. Voices provides programming within the Ministry of the Attorney General and beyond on topics relating to mental health.In 2022 Beth was awarded the Law Society Medal, the highest honour available to a lawyer in Ontario. The Medal was awarded for outstanding service within the profession in accordance with the highest ideals of the profession. She was also awarded the Ontario Psychiatric Association's Mental Health Advocate of the Year Award. About The PulseOn The Pulse, host Joeita Gupta brings us closer to issues impacting the disability community across Canada.Joeita Gupta has nurtured a life-long dream to work in radio! She's blind, moved to Toronto in 2004 and got her start in radio at CKLN, 88.1 FM in Toronto. A former co-host of AMI-audio's Live from Studio 5, Joeita also works full-time at a nonprofit in Toronto, specializing in housing/tenant rights. Find Joeita on X / Twitter: https://twitter.com/JoeitaGupta The Pulse airs weekly on AMI-audio. For more information, visit https://www.ami.ca/ThePulse/ About AMIAMI is a not-for-profit media company that entertains, informs and empowers Canadians who are blind or partially sighted. Operating three broadcast services, AMI-tv and AMI-audio in English and AMI-télé in French, AMI's vision is to establish and support a voice for Canadians with disabilities, representing their interests, concerns and values through inclusion, representation, accessible media, reflection, representation and portrayal. Learn more at AMI.caConnect on Twitter @AccessibleMediaOn Instagram @accessiblemediaincOn Facebook at @AccessibleMediaIncOn TikTok @accessiblemediaincEmail feedback@ami.ca

Disabilities are not always going to be obvious to others! The decision to share one's disability is also highly personal and it can be a difficult one as they may face skepticism, disbelief, or stigma from others who cannot understand the extent of their disability or needs.  In this insightful podcast/vodcast episode, we sit down with a remarkable young adult, entrepreneur, and self-advocate, who explains the reality of growing up with an invisible disability. Even at a young age, he is determined to have a voice, as he speaks up for himself and others with disabilities. Join us for a story of resilience, creativity, and living life to the fullest!

Welcome back to "Parenting the Intensity!"In today's episode, we are joined by Michelle Steiner, who bravely shares her experience living with invisible disabilities, including dyscalculia, limited hand dexterity, and visual perception issues. Michelle works as a paraeducator, advocating for people with disabilities and emphasizing the importance of connecting with others who share similar experiences. She discusses her childhood diagnosis, the invaluable support she received from her parents, and the profound impact of their advocacy. Join us as Michelle candidly unpacks the challenges she faces due to her disability and sheds light on the empowerment found in focusing on one's abilities rather than limitations. We'll also explore the importance of disability representation, the impact of societal views on learning disabilities, and the support resources that Michelle passionately advocates for. This is an episode you won't want to miss as we delve into the complexities of living with and parenting a child with invisible disabilities.3 Key Takeaways:1️⃣ Empowerment through Connection: Michelle emphasized the importance of connecting with others who share similar experiences. Finding a supportive community and focusing on abilities rather than limitations can be transformative for individuals with disabilities.2️⃣ The Power of Advocacy: Michelle's story highlighted the crucial role of parental advocacy in supporting a child with special needs. Her parents' unwavering support, reassurance about her intelligence, and proactive advocacy significantly impacted her journey.3️⃣ Embracing Adaptive Solutions: Michelle's experiences shed light on the impact of technology and adaptive solutions in education and daily life. Recognizing the value of personalized learning experiences and adaptive tools can make a profound difference for individuals with learning disabilities."My parents did a lot of advocacy for me when I was younger, and I can remember having my mom was great for explaining my disability to other people and they were accepting, and I thought to myself, oh, I wish I could do that."Connect with Michelle Steiner:Links: https://www.michellesmission.net/https://www.facebook.com/profile.php?id=100013356902200 https://www.instagram.com/steiner7250/References:Non- Verbal Learning Project: NVLD Home | The NVLD Project | Non-Verbal Learning DisabilityEye to Eye: Home - Eye to Eye (eyetoeyenational.org)All Abilities Media: All Abilities MediaMake sure to subscribe to our podcast for future episodes and leave a rating and review, that helps us get in front of more parents. Don't forget to check out the resources mentioned on our website at www.parentingtheintensity.caJoin the "Parenting the Intensity Community" to find the right things that works for YOUR child and adapt them to YOUR reality.To be able to enjoy your life and kids, not always being afraid of the next outburstTake a deep breath, keep going, we're all in this together!Music by Oleksii Kaplunskyi from Pixabay

Neurodiversity is a fairly new topic in the world of DEI but affects an estimated 1 in 7 people, with diagnosis rates on the rise. This is a topic we expect to see more of over the next year with its prevalence in many more organisations' agendas for 2024. Our CEO and Host, Stuart Elliott is joined today by an expert in this field Ritu Kiran, Founder and CEO of Aubilities.  Throughout the conversation, Stuart and Ritu discuss her career, how and why she founded Aubilities and neurodiversity in the workplace. They take a deeper dive into what neurodiversity is and why it's important, discussing the rise in cases and whether it is due to trends or general awareness around the subject. They also look into the recent high number of diagnoses within adults and what organisations can do to be more neuro-inclusive and how they can adapt the recruitment process to ensure they are getting the best out of people. Lastly, they discuss what Aubilities can offer and do to allow those with neurodiverse needs to thrive. Prior to founding Aubilities, Ritu had a corporate career for many years, starting her journey working for a major global Management Consultancy firm, specialising in HR consulting and HR projects across a multitude of clients. After this, she moved into the global learning and development space. In 2016 Ritu had her first child, who was diagnosed with autism in 2018, shortly after his diagnosis Ritu began researching autism to learn more about her son's needs and quickly identified a gap in the corporate market of utilising these talented and specialist thinkers to add value to businesses. Ritu is also a Trustee Board member for the UK national charity – Resources for Autism. She has recently been picked up by Jessica Kingsley Publishers and has an impending book launch in 2025 on parenting autistic children.  Key Timestamps:01:19 – Intro to Ritu & Aubilities 08:35 – Definition of Neurodiversity 11:13 – Neurodiversity at work15:40 – The rise in neurodivergent diagnoses18:53 – Tips to start supporting neurodiverse employees22:47 – Adapting the recruitment process 21:47 – The person-centric approach – does it work for everyone?36:30 – The 3 key pillars to start the conversationYou can listen to and download HR Insights from Apple Podcasts, Google Podcasts, Spotify and most popular podcast apps, subscribe so the latest episodes are directly available! You can also join our HR Community and follow us on LinkedIn and Instagram. Thank you so much for listening and please rate and review!

 Episode 152: January 2,2024Summary: Amy shares her top four things she wishes she could have done differently through her 31-year journey as a mom, particularly to her kids with invisible disabilities. Things like managing emergencies, acknowledging responsibility boundaries, and understanding the limitations of love are topics she touches on in this episode. Join the conversation and discover that you are a great mom as you walk your special needs journey!Key Moments:[2:45] Not everything is an emergency[4:45] Hurry is an inner condition that is fear based[7:50] Being present but not responsible[9:45] Loving my child in her wayResources:The Good and Beautiful God: James Bryant SmithIf you enjoyed the show:Have you purchased our new book, The Other Side of Special? Subscribe to our newsletter on the Take Heart WebsiteGet our free resource on finding Gratitude, Peace, and HopeReview and like us on Apple Podcasts Share us with others from wherever you listen to podcastsFollow us on Instagram @takeheartspecialmomsFind Amy at www.amyjbrown.com/  or on Instagram @amyjbrown_writerFind Carrie at www.carriemholt.com or on Instagram @carriemholtFind Sara at www.saraclime.com or on Instagram @saraclimeSupport the show

When Sophie discovered she was pregnant, she was filled with joy but also concern as she thought back to the nights that she had enjoyed a glass of wine before knowing she was expecting. Fourteen years later, her son was diagnosed with foetal alcohol spectrum disorder (FASD). This week, Sophie shares the struggles her son faces, how she and her husband have supported him and her passion to break down the stigmas surrounding FASD.  LINKS Check out NOFASD on Instagram https://www.instagram.com/nofasd.australia/For more information on FASD check out https://www.nofasd.org.au/For the FASD free helpline call 1-800-860-6113 Check out Every Moment Matters website https://everymomentmatters.org.au/ See omnystudio.com/listener for privacy information.

Episode 148:: November 7, 2023  How to Be Content When Your Life Isn't EasySummary: In this episode, Amy discusses the concept of contentment and how it can be challenging to achieve when life isn't easy. Amy explores the impact of unmet expectations, "if only" thinking, and comparison that contribute to our discontent. She shares personal stories and offers practical steps to help you shift your perspective, find gratitude, and embrace delight in your life.Key Moments:[3:10] Three traps that lead to discontent[5:11] Endless "if onlys" suggest we're never enough[9:08] Delight doesn't fix what's broken, gives us fuel to press on[10:36] Noticing the goodResources:Is this what you expected? Lisa Qualls On Delight and Why it Matters: Shauna Niequist If you enjoyed the show:Have you purchased our new book, The Other Side of Special? Subscribe to our newsletter on the Take Heart WebsiteGet our free resource on finding Gratitude, Peace, and HopeReview and like us on Apple Podcasts Share us with others from wherever you listen to podcastsFollow us on Instagram @takeheartspecialmomsFind Amy at www.amyjbrown.com/  or on Instagram @amyjbrown_writerFind Carrie at www.carriemholt.com or on Instagram @carriemholtFind Sara at www.saraclime.com or on Instagram @saraclimeSupport the show

I had a stroke nine years ago, which divided their life into pre and post-stroke. They used to work in marketing but can no longer do so due to the stroke. They now prioritize their family, friends, and community, considering everything else as a bonus. They find it strange how their perspective on life changed. Aphasia is a condition where a person is unable to communicate effectively through speaking, writing, reading, or understanding. This can be a scary and frustrating experience.  Marcia's book, "Stroke Forward, How to Become Your Own Healthcare Advocate One Step at a Time," can be found on Amazon. She emphasizes the importance of looking ahead and not dwelling on the past.  Listeners can visit her website http://strokeforward.com, where they can book appointments or email their questions. 

EPISODE 1803: In this KEEN ON show, Andrew talks to Andrea Dobynes Wagner, a contributor to GOING FOR BROKE, on life in America as a black woman with an invisible disabilityTwenty-six years ago, Andrea Dobynes Wagner didn't pass her preschool vision test. She was later diagnosed with retinitis pigmentosa, a group of genetic eye disorders that lead to peripheral vision loss and difficulty seeing at night. Growing up legally blind, doctors warned Andrea that she'd never lead a normal life. They recommended she work a clerical job after high school and live with her parents. Andrea rejected that destiny. She learned to navigate the world with her limited vision and enjoyed a childhood full of academic achievement, sports, dating and friends. In college, she lived independently and by age 24 she bought a house. Today, at 31, Andrea holds multiple advanced degrees and lives with her husband in Tuscaloosa, Alabama.Despite everything Andrea has overcome, one challenge persists: navigating the job market with an invisible disability. Even with laws prohibiting discrimination, people with disabilities face many obstacles to employment. In this piece, Andrea shines a light on the cracks in the system and why she's devoting her career to advocating for those pushed to the margins.Named as one of the "100 most connected men" by GQ magazine, Andrew Keen is amongst the world's best known broadcasters and commentators. In addition to presenting KEEN ON, he is the host of the long-running How To Fix Democracy show. He is also the author of four prescient books about digital technology: CULT OF THE AMATEUR, DIGITAL VERTIGO, THE INTERNET IS NOT THE ANSWER and HOW TO FIX THE FUTURE. Andrew lives in San Francisco, is married to Cassandra Knight, Google's VP of Litigation & Discovery, and has two grown children.

Living with an invisible disability is a highly individualized experience, shaped by the nature and severity of the specific condition. These disabilities encompass a wide range of health issues, from chronic pain and mental health disorders to autoimmune diseases and neurological conditions. What sets them apart is their hidden nature, making it challenging for others to grasp the daily struggles and limitations faced by those affected. Often, individuals with invisible disabilities cope with fluctuating symptoms, which can disrupt their routines and require flexible accommodations. They frequently encounter skepticism, misunderstanding, and even stigma from society, adding emotional strain to their already complex journey. Self-advocacy becomes a crucial skill, as they navigate the need for accommodations, educate others about their condition, and strive to strike a balance between managing their health and pursuing their goals. Invisible disabilities can take a toll on a person's mental and emotional well-being, contributing to feelings of isolation and frustration. Despite these challenges, many individuals with invisible disabilities demonstrate remarkable resilience and determination, finding ways to adapt, seek treatment, and build supportive networks. The support and understanding of friends, family, employers, and healthcare providers play a vital role in helping them live fulfilling lives. Ultimately, recognizing and acknowledging the unique struggles and triumphs of those with invisible disabilities is essential to fostering empathy, inclusion, and a more supportive society. If you'd like more information or to get involved in helping advocate for these women, head on over to https://invisiblewarriors.org.

Chloe Jessamy is the founder and Director of Supportal Business Services, a highly acclaimed virtual assistant agency known for its excellence in matching 5* Virtual assistants with busy professionals and SME's business support needs. Her mission is simple, to help clients do less and achieve more. With a multitude of awards under her belt, and features in esteemed media outlets such as the BBC, she continues to further solidify her reputation as a recognised figure in the industry. As a certified business foundations coach and mentor, Chloe extends her expertise to empower online service providers and VAs in strategically starting and scaling their ventures. Her remarkable journey spans over 16 years, during which she has refined her skills in organisation, systems, and marketing, earning a stellar reputation. Chloe also uses her digital creative skills to create a wealth of resources and templates to support business owners, particularly those navigating the DIY stage of their ventures. In this Episode Alicia and Chloe Discuss: What keeps Chloe constantly motivated despite health, life and circumstancial set backs  Alicia's experience using Supportal Services  How Chloe started Supportal and how it supports SME's The reason why being organised can make or break your business  How Chloe has made life adjustments to work around her disability  The experience of being physically disabled for a year of her life  How Chloe aquires long term retainers and high paying clients Learn more here about Supportal: https://timefreedomlab.supportalservices.com/  https://www.instagram.com/supportalservices/  https://www.supportalservices.com  Connect directly with Chloe here: https://www.instagram.com/chloejessamy/ https://www.linkedin.com/in/chloejessamy/

Today we're talking about Invisible Disabilities on CCnDoc Talk. Doc plays devil's advocate (to prove a point) during this meaningful and sometimes humorous discussion about what IS an Invisible Disability and what BIASES we have that impact our ability to be compassionate and understanding to others who have big things going on in their bodies that the outside world can't see. We also introduce a syndrome called LARS (lower anterior resection syndrome) in this episode. LARS is a common invisible disability for those who have had surgeries for colorectal cancer, ulcerative colitis and irritable bowel diseases.  If you love this podcast, please share it with a friend! If you're not already following us @CCnDoc on social media, we welcome you to join us!  And, CC has a NEW Cancer-themed Blog: ⁠⁠⁠Medium.com/MyBadASSLife⁠ Find all of our adventures at linktr.ee/ccndoc to get freebies, grab merch from our store, leave a tip, make a donation, or buy one of our books: Courageous Money: Your Adventure Through Money National Park, Coaching for Commitment Simplified or The Big Book of Southern Colorado Wildflowers for kids of all ages. (Contains affiliate links). --- Send in a voice message: https://podcasters.spotify.com/pod/show/ccndoc/message Support this podcast: https://podcasters.spotify.com/pod/show/ccndoc/support

Laura Hernandez and her husband, Tony, are raising their ten children in the Dallas area. Over less than five years, their family grew from six to twelve, adding three biological children and three adopted children. Struggling to maintain a peaceful home and learning to care for children living with invisible disabilities, Laura developed practices to turn her family into a peaceful team, relying on the Lord.Laura works as a coach, educating mothers in areas such as:The invisible disability of Fetal Alcohol Spectrum DisordersIdentifying and learning about disability as an adoptive parentPractical ways special needs parents can systematically bring calm to the chaos at homeLearn more from Laura KEY QUESTIONS:How can parents create a peaceful home amid challenges?What do adoptive parents need to know about identifying signs of disability and caring for children with special needs?How can churches support adoptive and special needs parents? KEY SCRIPTURES:“I am the vine; you are the branches. If you remain in me and I in you, you will bear much fruit; apart from me you can do nothing.” John 15:5“Carry each other's burdens, and in this way you will fulfill the law of Christ.” Galatians 6:2 ----Find more encouragement on Joni Eareckson Tada's Sharing Hope podcast and daily devotional.Follow Joni and Friends on TikTok, Instagram, Facebook, and YouTube.Your support makes this podcast possible!Joni and Friends envisions a world where every person with a disability finds hope, dignity, and their place in the body of Christ. Founded by Joni Eareckson Tada, we provide Christ-centered care through Joni's House, Wheels for the World, and Retreats and Getaways, and offer disability ministry training.

In this episode Of Pushing Forward with Alycia | A Disability Podcast, we wind down Disability Pride Month by featuring inspirational Joze Piranian - a global speaker, trainer, and coach, and personal friend of Alycia's. Joze champions inclusion and resilience, overcoming personal obstacles to become an acclaimed public speaker. With his captivating story and valuable insights on invisible disablity, Joze is truly shaping the world, one stutter at a time. Joze Piranian - A Journey of Transformation A five-time TEDx speaker, a Forbes-featured stand-up comedian, and the 2017 Inspirational Speaker of the Year, Joze Piranian has made a profound impact across continents and cultures. He has spoken to global giants like Boeing, Google, Tesla, Meta, and TikTok, inspiring millions with his talks on inclusion and resilience. However, his journey hasn't been an easy one, as Joze has had to overcome the invisible disability of stuttering. Episode Highlights Confronting Adversity: Joze shares his personal journey of transformation and his hard-earned insights about conquering fears and healing through laughter. His approach to adversity is not about the elimination of obstacles but changing our relationship with them. Growing Up Different: Joze talks about growing up in the Middle East and the challenges he faced due to a lack of awareness about ways people can be different. The Power of Silence and Avoidance: For a large part of his life, silence and avoidance were Joze's "heroes," protecting him from potentially hurtful reactions. This profoundly impacted his life and choices. Rumi and Freedom: Joze discusses the impact of the famous Rumi quote, "Why do you stay in prison when the door is so wide open?" and its relevance to his life. Changing The Relationship with Obstacles: He highlights the significance of understanding our internal obstacles and changing our relationship with them, using his own journey with stuttering as an example. Connect with Joze Piranian Joze is helping people who hold back turn fear into action so that they overcome their “inner stutter” and unlock their true potential in life. By empowering others to own their uniqueness and conquer their obstacles, Joze delivers transformational experiences allowing his keynote audience members and coaching clients to access the hidden powers of fear and become champions of inclusion. Visit Joze's website. Follow him on Instagram, LinkedIn, Facebook, and Twitter to keep up with his work and appearances. Connect with Alycia: Feedback | Instagram | LinkedIn Book Alycia for Speaking  Book Alycia to Train Your Employees in Disabling Ableism  Buy Alycia's DEI Micro Learning Video Series Full transcript

In this episode, we are joined by emergency medicine physician, and DIO, Dr. Anne Messman for a conversation about disability disclosure, seeking and receiving accommodations, and creating inclusive and welcoming spaces for trainees.   Bio:  Dr. Anne Messman is an emergency medicine physician in Detroit, Michigan. In addition to clinical work, Dr. Messman also serves as the Vice Chair of Education for the Wayne State University School of Medicine's (WSUSOM) Department of Emergency Medicine and the WSUSOM Associate Dean of Graduate Medical Education. She was diagnosed with multiple sclerosis in 1999 while a junior in high school. In her free time, she enjoys spending time with her husband, children, and dogs and reading.   Episode Transcript: https://docs.google.com/document/d/1JzScpxljua4i2clt2f8fI9osboDwsF2aSv9un2-hfHQ/edit    

For Disability Pride Month, we do a check-in on our personal experiences with disability and internalized ableism.See omnystudio.com/listener for privacy information.

In this episode, Ashanti Bentil-Dhue interviews Jes Osrow, a HR DEI and L&D practitioner who for over twelve years has helped mostly high growth startups who are based in the US and have an international presence.  “So really devising your team, even if it's just you, as a solo practitioner, bring someone else on temporarily for the project, or those opening conversations if you need to have a compliment. And yeah, that's where not having humility in those pieces and rather, having humility and ego in the work is really important. Because if you can't get your foot in the door, you can't go forward. And that's where you start meeting a lot of closed doors or doors that people say get slammed in your face.” Episode Highlights:  ● The importance of having a business development team ● The difference between growing a business and delivering expertise ● Nurturing your competency in this space About Jes Osrow:    Jes' goal is to create fundamental change in people operations. She is Co-Founder and DEIBA Specialist at The Rise Journey where she works with growing companies to operationalize DEIBA (diversity, equity, inclusion, belonging, and accessibility) strategies as part of building foundational and sustainable organisational cultures. Empowering inclusive, diverse, equitable, and accessible workplaces for all employees is the forefront of everything she does.    Jes coined the term DEIBA™ in 2019 after recognizing DEI alone was not enough. She officially trademarked the term in September 2021. She was named to Mogul's Top 100 Leaders in DEIB in 2021 and 2022. Jes is a strong advocate for Invisible Disability awareness and fair compensation for ERG leads.   Resources:  Download The Rise Journey's 2022 State of the ERG Report for the latest trends on ERG Lead Compensation and budgeting, structural best practices and more: https://www.therisejourney.com/blog/2022-erg-report Take advantage of Rise with OPHR, a self-service resource centre built with the one person Human Resources teams in mind. It offers over 200 HR and DEI resources, many can be accessed for free by signing up for OPHR Essentials. Listeners can use the code $100OFF2023! to receive a discount for OPHR Advanced membership. Learn more: https://www.risewithophr.com/   Follow Jes Osrow on LinkedIn: https://www.linkedin.com/in/jesosrow/ Learn more about The Rise Journey: https://www.therisejourney.com/ Follow The Rise Journey on LinkedIn: https://www.linkedin.com/company/therisejourney/ _ If you would like to apply to be a guest on the show email: operations@goodsoilleaders.com   If you would like to schedule a capability briefing call with our team, email: operations@goodsoilleaders.com    If you would like to apply for DEI PRO Coaching, email: operations@goodsoilleaders.com  Stay Connected with Ashanti:  LinkedIn: Ashanti Bentil-Dhue 

Listen to Dr. Tom Roselle, DC discuss why fibromyalgia is considered the "un-disease and invisible disability." Fibromyalgia (FM) is a complex, chronic, painful musculoskeletal syndrome that is characterized by extreme fatigue, disordered sleep, and other associated physical and cognitive problems. Because its etiology is unknown, and because no specific pathophysiological mechanisms have been found to underlie the syndrome, making a diagnosis is very difficult.  For this episode and more episodes, please visit: https://www.drtomroselle.com/ageless-health-podcast/

You can follow Leonard Cheshire on Twitter or Instagram @LeonardCheshire. Find out more at leonardcheshire.orgGet in touch by emailing disabilitydownload@leonardcheshire.org More information: Mili mentions DecodeME – a large scientific study of people with M.E. launched in September 2022. You can read media coverage from the launch. 

In this episode I chat with Michelle Steiner, from the blog Michelle's Mission, about her lived experience with a learning disability. Michelle talks about the impact her invisible disability had on her while growing up, and some of the adaptations she has made to accommodate her disability as an adult. We also discuss how Michelle's learning disability empowers her in her work as a paraeducator of learners with disabilities. Finally, we chat about Michelle's photography and the role it plays in her life. Find Michelle's Blog and photography at: Website: https://michellesmission.blog/ Facebook: https://www.facebook.com/profile.php?id=100013356902200 Instagram: https://www.instagram.com/steiner7250/ Contact Lois at Web: https://www.loisstrachan.com/ Facebook: https://www.facebook.com/loisstrachanspeaker This episode was edited by Craig Strachan using Hindenburg PRO – find out more on Hindenburg.com Credits and music by Charlie Dyasi of Naledi Media.

Katie checks in with playwright (Great Plains Theatre Conference Selection, Edward F. Albee Fellow, Rona Jaffe Foundation Graduate Fellow, upcoming: Brainsmash at 59E59) and writer (New York Magazine, The Virginia Quarterly), Sophie Weisskoff.

The 2023 vision at Silverdale is "A Year of Victory." In Episode 8 of Finding Victory Lori shares about finding God's grace in raising a child with an invisible disability.Hello and Welcome to Silverdale Baptist Church's Podcast! We hope this episode is helpful to you in your relationship with Jesus. We would love to connect with you! To contact Silverdale, click the link to our website below, then click Connect at the top right. ABOUT SILVERDALE BAPTIST CHURCH Silverdale exists to lead people into an authentic relationship with Christ so they will worship God, grow in their faith, and serve the Lord in our community and world. Silverdale's Lead Pastor is Tony Walliser. FIND US ONLINE Website http://silverdalebc.comYouTube: https://www.youtube.com/channel/silverdalebcInstagram https://www.instagram.com/silverdalebcFacebook: https://www.facebook.com/silverdalebc

Jill Griffin is an Executive Coach, Career Strategist, and an Invisible Disabilities Advocate with her own sticky floor story.Jill had an accident resulting in a traumatic brain injury that took years to diagnose.  Doctors couldn't figure out what was going on with her, or how to help her.Through research, mindset, and perseverance, Jill has learned how to not only live with her invisible disability but also how to THRIVE. Fear, forgiveness, and forging a new path are all a piece of her story.Jill's LinkedInThe Career Refresh Podcasthttps://jillgriffincoaching.com/FREE WEEKLY SUCCESS PLANNERJoin our Facebook Group! Find me on InstagramCheck out our PINS on PinterestAnd YES - I'm on TikTok!

Jill Griffin is an Executive Coach, Career Strategist, and an Invisible Disabilities Advocate with her own sticky floor story.Jill had an accident resulting in a traumatic brain injury that took years to diagnose.  Doctors couldn't figure out what was going on with her, or how to help her.Through research, mindset, and perseverance, Jill has learned how to not only live with her invisible disability but also how to THRIVE. Fear, forgiveness, and forging a new path are all a piece of her story.Jill's LinkedInThe Career Refresh Podcasthttps://jillgriffincoaching.com/FREE WEEKLY SUCCESS PLANNERJoin our Facebook Group! Find me on InstagramCheck out our PINS on PinterestAnd YES - I'm on TikTok!

Welcome to The Special Interest Podcast! We are Alex and Karly, two late-diagnosed autistic women, bringing our stories and special interests to you to help broaden the spectrum. In episode five, we discuss what it's like to have an invisible disability. Thank you for listening!

About This Episode: Mom Heather is a wonderful friend, a warm and kind-hearted mother, and struggles with her neurodivergent child. You will be absolutely nodding your head while you listen to the issues and stories she shares about her child with severe ADHD. Here are just some of the topics we discussed:-Hyperactivity in boys is dismissed as being "all boy"-When people think the "bad behavior" is because you can't control your child-When medical professionals miss the mark-High metabolizers-When your child is a "runner"You can email Heather at heatherm105@gmail.com.Please shower Heather with love and support by SHARING this episode with a mom who needs to hear her story!MORE:-Want to be a part of my support group community, Mothers Together? Head over to ontheharddays.com/motherstogether to sign up. New groups start 11/1!-Subscribe to On The Hard Days via Apple, Spotify, or however you get your podcasts.  *Please leave a review*  to spread the word to other moms around the world!

Welcome to Body Talk with Becks , brought to you by Becks Carlyle ! In this week's episode Dating with an Invisible Disability , we get to hear from my boyfriend Aaron about what it's like to date someone with an invisible disability. Thank you for listening! If you wish to come on the show as either an expert or to share your story, please use the contact page on https://body-talk-with-becks.captivate.fm (Body Talk with Becks website) .

Welcome back to the third season of the Take Heart Podcast. As we kick off this new season, we wanted to start by going back to the beginning of how Take Heart came to be, and share with you the reason we do this work, and the importance of our name Take Heart. In this episode, Amy J. Brown shares the scripture that the podcast name comes from and what this message holds for us special needs moms. Sep 6, 2022; Ep. #97Show Links:Scripture mentioned: Deut 31:6 MSGShow Takeaways: [1:07] Hear the importance behind the name of the podcast and the piece of scripture it is taken from. [3:03] Listen in as Amy shares a personal story about a time when she was afraid and taking heart was the last thing she felt like doing, but she did it anyway. [6:41] Discover how we can practically take heart and have courage in the midst of the things in this life that scare us.If you enjoyed our podcast, please...Subscribe to our newsletter on the Take Heart WebsiteGet our free resource on finding Gratitude, Peace, and HopeReview and like us on Apple Podcasts Share us with others from wherever you listen to podcastsFollow us on Instagram @takeheartspecialmomsFind Amy at www.amyjbrown.com/  or on Instagram @amyjbrown_writerFind Carrie at www.carriemholt.com or on Instagram @carriemholtFind Sara at www.saraclime.com or on Instagram @saraclime

In this episode, I sit down with Taylor Efford, whose life changed drastically after receiving a Type 1 Diabetes diagnosis.   As you'll hear in our conversation, coming to terms with her new reality and learning to live her life differently has brought many challenges and also many blessings to her life.   Taylor is an Actor and influencer on TikTok and Instagram, where she shares authentic and real content about skincare and makeup.    **TRIGGER WARNING** This episode covers sensitive subject matter and is not suitable for all listeners. If this topic could be a trigger for you, listen to this episode with a friend, a sibling, a loved one or a parent so you can talk about any emotions that come up for you. The contents of this episode are not intended to replace therapy and should not be taken as such. If you need immediate help, please call the crisis hotline listed below in our resources. Listen in as we talk about: [1:30] Life before Type 1 Diabetes [10:40] The difference between Type 1 and Type 2 Diabetes [12:00] How this diagnosis changed Taylor's life and the grieving that came with it [23:30] The insights Taylor has had about life since her diagnosis [28:25] The impact this has had on her family and friends [31:26] How Taylor processed her grief [46:40] What self love looks like for Taylor now   Resources mentioned in this episode: Rock On: Mining for Joy in the Deep River of Sibling Grief by Susan E. Casey   Grief Hotline:  https://www.griefresourcenetwork.com/crisis-center/hotlines/    Connect with Taylor here: https://www.tiktok.com/@taylorefford https://www.instagram.com/uraveragegirlytaylorefford  Connect with Susan Instagram Facebook YouTube http://susanecasey.com/  TikTok

Today we talk about Dynamic Disability and understanding your own journey better, which could lead to being able to communicate your needs for better support.  This is our final LIVE Q&A for Season 2. Our weekly interviews continue each Wednesday. Be sure to tune in next week if you'd like to hear more about menopause.   Watch the Invisible Disability short film here: https://youtu.be/CAOsa2PQyKs Request to join the online free support group for women living with prolapse. 

In this episode, I sit down with Phil Spade, who talks about the grief he experienced after partially losing his eyesight, and subsequently losing his father a few years later.   Phil currently heads up Growth and Strategy for Swell, a new voice-based social platform that launched at SXSW in 2021. Prior to Swell, Phil led Client Services at Skava who ran and powered ten of the top thirty retailers' mobile websites.   **TRIGGER WARNING** This episode covers sensitive subject matter and is not suitable for all listeners. If this topic could be a trigger for you, listen to this episode with a friend, a sibling, a loved one or a parent so you can talk about any emotions that come up for you. The contents of this episode are not intended to replace therapy and should not be taken as such. If you need immediate help, please call the crisis hotline listed below in our resources. Listen in as we talk about: [2:10] How Phil lost his eyesight  [5:35] Preparing mentally and spiritually for surgery [11:30] The gift in losing his eyesight  [13:05] How his life was impacted by losing his eyesight [15:30] Who Phil's dad was [18:20] The impact of losing his dad [28:10] Tips to cope with grief [38:00] What self love looks like for Phil now Phil is a graduate of Indiana University (BS Math) and the University of Minnesota's Carlson School of Business (MBA Finance/MIS). After graduating from the University of Minnesota, Phil led growth initiatives at BigCharts.com in the infancy of the internet age, licensing financial information to the world's biggest banks and brokerages.    Phil is always looking at ways of how technology can influence and change the way we look at the world and solve our problems. Phil also owns and runs a small horse racing operation and is a licensed professional boxing judge.   Resources mentioned in this episode: Rock On: Mining for Joy in the Deep River of Sibling Grief by Susan E. Casey   Grief Hotline:  https://www.griefresourcenetwork.com/crisis-center/hotlines/    Connect with Phil Spade here: https://www.instagram.com/Swell_talk www.twitter.com/Swell_talk  https://www.linkedin.com/in/phil-spade-067700/  https://www.facebook.com/swelltalk  https://www.swellcast.com/phil  https://www.swell.life/  Connect with Susan Instagram Facebook YouTube http://susanecasey.com/  TikTok

The planning and preparation for traveling via plane come with their challenges. These are only amplified when you're also dealing with an invisible disability. In this episode, Whitney Lauritsen opens up about how she's navigating her neurodivergence in the context of travel. Whitney will be flying out for the first time since 2019. With all the self-discovery and new things she's learned about herself since then, plus the new rules surrounding flights due to the pandemic, she will be letting us into her process and preparations. She shares things you can do to improve the experience, along with some tools and gadgets she uses. Plus, Whitney opens up about the prejudice regarding invisible disabilities like ADHD and ASD and why it's important to advocate for yourself.Love the show? Subscribe, rate, review, and share!Here's How »Join the This Might Get Uncomfortable community today:wellevatr.comWellevatr FacebookWellevatr TwitterWellevatr Instagram

Millions of people are dealing with invisible illness, possibly not even knowing it. Guest co-host and contributor Yves Jeffcoat discusses women with invisible illnesses in this classic episode. See omnystudio.com/listener for privacy information.

Today's guest is special needs ministry leader from Brentwood Baptist Church in Tennessee, Tiffany McCullough. She discusses the joys and challenges of special needs ministry, the importance of eduating, equipping, and allowing all friends to find community, serve, and be a visible part of the body of Christ.June 14, 2022; Ep. 90Timestamps & Key Topics:0:00-    Intro2:04-    About Tiffany McCullough5:47-    Get Out of God's Way10:31-  Caring Beyond The Individual17:20-  Educating & Equipping24:22-  Start With The Need30:56-  Closing Prayer33:30-  OutroEpisode Links & Resources:Brentwood Church Special Needs MinistryIf you enjoyed our podcast, please...Get our free resource 7 Advocacy Practices & PitfallsGet our free resource on finding Gratitude, Peace, and HopeSubscribe to our newsletter on the Take Heart WebsiteReview and like us on Apple Podcasts Share us with others from wherever you listen to podcastsFollow us on Instagram @takeheartspecialmomsFind Amy at www.amyjbrown.com/  or on Instagram @amyjbrown_writerFind Carrie at www.carriemholt.com or on Instagram @carriemholtFind Sara at www.saraclime.com or on Instagram @saraclime

Jillana is a foster, adoptive mom, and special needs mom. She shares how her life has been stretched by love and how she has learned to look for signs of hope in her life. June 7, 2022; Ep. 88Timestamps & Key Topics:0:00-    Intro1:19-    Meet Jillana Goble3:49-    Glimpse Into Fostercare9:55-    Misconceptions About Trauma17:35-  Sustainable21:09-  Vulnerability In Friendship31:43-  Hope37:53-  Acknowledging The Toll46:25-  OutroEpisode Links & Resources:Jillana Goble's Web-siteA Love-Stretched Life by Jillana GobleNo Sugar Coating: The Coffee Talk You Need About Foster CareJillana on InstagramIf you enjoyed our podcast, please...Get our free resource 7 Advocacy Practices & PitfallsGet our free resource on finding Gratitude, Peace, and HopeSubscribe to our newsletter on the Take Heart WebsiteReview and like us on Apple Podcasts Share us with others from wherever you listen to podcastsFollow us on Instagram @takeheartspecialmomsFind Amy at www.amyjbrown.com/  or on Instagram @amyjbrown_writerFind Carrie at www.carriemholt.com or on Instagram @carriemholtFind Sara at www.saraclime.com or on Instagram @saraclime

 Discouragement is a powerful tool the devil uses to block the light of hope from God. In today's collaborative, Sara, Amy, and Carrie talk about how the devil uses this sneaky tool in our lives, how to recognize it, the pitfalls, and some ways to turn toward encouragement.May 24, 2022; Ep. 87Timestamps & Key Topics:0:00-    Intro1:25-    Spiritual Warfare7:42-    Reoccuring Discouragement16:36-  Addressing Discouragement25:57-  Nourishing the Soul30:12-  Encouraging Others32:05-  Encouragement Challenge33:36-  Poem & ClosingEpisode Links & Resources:Scripture mentioned: John 8:12, Romans 8:28Disarm Discouragement! By Worthy DevotionsDon't Quit by Edgar A. GuestIf you enjoyed our podcast, please...Get our free resource 7 Advocacy Practices & PitfallsGet our free resource on finding Gratitude, Peace, and HopeSubscribe to our newsletter on the Take Heart WebsiteReview and like us on Apple Podcasts Share us with others from wherever you listen to podcastsFollow us on Instagram @takeheartspecialmomsFind Amy at www.amyjbrown.com/  or on Instagram @amyjbrown_writerFind Carrie at www.carriemholt.com or on Instagram @carriemholtFind Sara at www.saraclime.com or on Instagram @saraclime

When you feel discouraged, it's easy to believe that God doesn't care. In this episode, Sara encourages us to invite God into our spaces of discouragement, and how to adjust our posture to receive God's care. You don't have to look at the world as though your glass is half-full or half-empty because God restores our glasses when they shatter and refills them when they're empty.May 17, 2022; Ep. 86Timestamps & Key Topics:0:01-    Intro1:28-    God in the Spaces4:06-    Facing Discouragement8:30-    Turning Your Face11:47-  A Refillable Glass13:17-  OutroEpisode Links & Resources:No Wonder We Need by Deborah AnnIf you enjoyed our podcast, please...Get our free resource 7 Advocacy Practices & PitfallsGet our free resource on finding Gratitude, Peace, and HopeSubscribe to our newsletter on the Take Heart WebsiteReview and like us on Apple Podcasts Share us with others from wherever you listen to podcastsFollow us on Instagram @takeheartspecialmomsFind Amy at www.amyjbrown.com/  or on Instagram @amyjbrown_writerFind Carrie at www.carriemholt.com or on Instagram @carriemholtFind Sara at www.saraclime.com or on Instagram @saraclime

Sara Alepin was really passionate about being a teacher - and still is! But one day she was forced to quit her job teaching when she became permanently disabled from breaking up a fight at her school where a student stomped on a foot and crushed one of her nerves, making it difficult for her to walk, especially on the linoleum floors that usually line the floors of classrooms. Ever since then, she has only been able to be on her feet for 3-4 hours a day. What did the school do? Did it pay her medical bills and try to support her transition out of teaching? You guessed it: not it did not. Not only did they not do they, they actually hired a private investigator to follow her around to try to get out of paying the medical bills, who likely cost many times the amount they would have paid had they simply agreed to pay the medical bills. (The alternate title for this episode is Yet Again We Hear About Why the School System is Fucked.) On top of hearing Sara's story, we hear about why it can be so difficult having an invisible disability: for one thing, when you are not obviously disabled, you can get some really dirty looks when you go to park in the handicapped spot, or try to get a wheelchair in the airport. For her, some of the most difficult aspects of her disability have not actually been as much around how the world is not designed to accommodate her needs (in fact, as many jobs ave become even more sedentary during Covid, one could argue that many people's lifestyles have been changing to become more like hers!) as much as it has been around the judgements and assumptions of other people. Links: Sara's podcast, The Wedding Dish: https://www.theweddingdishpodcast.com/ Sara's other podcast, Laughing with Gingers: https://podcasts.apple.com/us/podcast/laughing-with-gingers/id1524216963 Laughing with Gingers Instagram: https://www.instagram.com/laughingwithgingers/?hl=en Sara's wedding photography business, Photos from the Harty: https://www.photosfromtheharty.com/ Sara's other business, District Bliss Events: https://www.instagram.com/districtblissevents/?hl=en --- Support this podcast: https://anchor.fm/im-the-villain/support

Daily Discouragement can make us feel like we are walking in the dark. In this episode, Amy shares four ways she is learning to walk towards the light of God's love and provision and how this moves us away from discouragement.May 3, 2022; Ep. 84Timestamps & Key Topics:0:00-    Intro1:25-    Blinding Discouragement4:03-    Holding On To The Rope6:47-    Step Into the Light of Home9:20-    Reach Out To Others10:04-  Look Up11:10-  Choose Joy13:30-  Questions to Consider14:31-  OutroEpisode Links & Resources:Scripture mentioned: 1 Kings 19:5-9 NIVEp. 29 Self Care with AmyEp. 30 Self Care with Carrie Ep. 31 Self Care with Sara Ep. 32 Self Care Collaborative- Part 1Ep. 32 Self Care Collaborative-Part 2 Ann Voskamp Instagram The Slow Way Podcast: Micha Boyett Ep. 16The Return of the Prodigal Son: A Story Of Homecoming by Henri NouwenIf you enjoyed our podcast, please...Get our free resource 7 Advocacy Practices & PitfallsGet our free resource on finding Gratitude, Peace, and HopeSubscribe to our newsletter on the Take Heart WebsiteReview and like us on Apple Podcasts Share us with others from wherever you listen to podcastsFollow us on Instagram @takeheartspecialmomsFind Amy at www.amyjbrown.com/  or on Instagram @amyjbrown_writerFind Carrie at www.carriemholt.com or on Instagram @carriemholtFind Sara at www.saraclime.com or on Instagram @saraclime

As special needs parents, we have a deep-seated fear that we are messing up our kids. It's important to remember to trust God to give us what we need., to nurture the soil of our children's hearts, and love each one in their own unique way. In this episode, Sara, Amy, and Carrie discuss how to help your children feel heard, things they might have changed in their parenting journey, and how to celebrate the uniqueness of your family. April 26, 2022; Ep. 83Timestamps & Key Topics:0:00-    Intro1:36-    Fear of Messing Up5:04-    Nurture the Soil10:02-  Life's Not Fair14:05-  What Would You Change26:30-  Younger Self34:33-  Closing PrayerEpisode Links & Resources:The Big Six by Adam Young (Scroll down to choose title; will need to put in e-mail)Episode 47: Interview With Sandra PeoplesSharing Love Abundantly in Special Needs Families: The Five Love Languages For Parents Raising Children with DisabilitiesIf you enjoyed our podcast, please...Get our free resource 7 Advocacy Practices & PitfallsGet our free resource on finding Gratitude, Peace, and HopeSubscribe to our newsletter on the Take Heart WebsiteReview and like us on Apple Podcasts Share us with others from wherever you listen to podcastsFollow us on Instagram @takeheartspecialmomsFind Amy at www.amyjbrown.com/  or on Instagram @amyjbrown_writerFind Carrie at www.carriemholt.com or on Instagram @carriemholtFind Sara at www.saraclime.com or on Instagram @saraclime

Special needs moms often worry that they are not doing enough. This is especially true when it comes to our other kids.  We make assumptions about how our other kids are doing. In this episode, Anna Brown shares her perspective of being a sibling to a child with RAD and FASD and the blessings and challenges that brings. April 5, 2022: Ep. #80Timestamps & Key Topics:0:00-    Intro1:22-    Meet Anna Brown4:41-    Biggest Challenge8:37-    Giving Siblings a Voice12:19-  Compassion18:01-  Advice23:23-  Closing ThoughtsIf you enjoyed our podcast, please...Get our free resource 7 Advocacy Practices & PitfallsGet our free resource on finding Gratitude, Peace, and HopeSubscribe to our newsletter on the Take Heart WebsiteReview and like us on Apple Podcasts Share us with others from wherever you listen to podcastsFollow us on Instagram @takeheartspecialmomsFind Amy at www.amyjbrown.com/  or on Instagram @amyjbrown_writerFind Carrie at www.carriemholt.com or on Instagram @carriemholtFind Sara at www.saraclime.com or on Instagram @saraclime

Special needs families have heard all types of fixes, remedies, and advice throughout their parenting journey. How do we react to these phrases with love and grace, and figure out the false beliefs behind these statements? Listen to today's collaborative episode to find out. March 29, 2022; Ep. #79Timestamps & Key Topics:0:00-    Intro1:26-    Things People Say2:48-    You're An Inspiration5:54-    Intentional Hospitality12:08-  Where Strength Originates15:18-  Deserve An Answer23:22-  Have You Tried?24:42-  With God's Strength28:35-  Fight Like A Mother31:50-  Comparative Suffering35:45-  Closing PrayerIf you enjoyed our podcast, please...Get our free resource 7 Advocacy Practices & PitfallsGet our free resource on finding Gratitude, Peace, and HopeSubscribe to our newsletter on the Take Heart WebsiteReview and like us on Apple Podcasts Share us with others from wherever you listen to podcastsFollow us on Instagram @takeheartspecialmomsFind Amy at www.amyjbrown.com/  or on Instagram @amyjbrown_writerFind Carrie at www.carriemholt.com or on Instagram @carriemholtFind Sara at www.saraclime.com or on Instagram @saraclime

All moms struggle with believing lies about their motherhood: who they should and shouldn't be, what they should or shouldn't feel or do. In this episode, Amy, Carrie and Sara dive into some of the lies special needs moms believe, ways to recognize them, and how to replace them with the truth.March 22, 2022; Ep. 78Timestamps & Key Topics:0:00-    Intro1:24-    The “Perfect” Mom6:25-    Good Moms Wouldn't…11:03-  Connection Lies16:05-  Self-Care Lies23:08-  Self-Sufficiency Lies30:01-  Recognizing Lies35:18-  Closing PrayerEpisode Links & Resources:Episodes 38-41 on GuiltScripture mentioned: Psalm 25:4-5The Great Dance by Baxter, Kruger If you enjoyed our podcast, please...Get our free resource 7 Advocacy Practices & PitfallsGet our free resource on finding Gratitude, Peace, and HopeSubscribe to our newsletter on the Take Heart WebsiteReview and like us on Apple Podcasts Share us with others from wherever you listen to podcastsFollow us on Instagram @takeheartspecialmomsFind Amy at www.amyjbrown.com/  or on Instagram @amyjbrown_writerFind Carrie at www.carriemholt.com or on Instagram @carriemholtFind Sara at www.saraclime.com or on Instagram @saraclime