Podcasts about disabled child

We are all connected to folks with disabilities, whether they're part of our inner circle, or members of our broader community. Unfortunately, there's a great deal of stigmatization, misunderstanding, and judgement that crops up around disabled folks and their families. Parents of disabled children are traveling on a different path than other parents, and often need more support, but the people around them don't always know how to provide it. Therapist Amanda Griffith-Atkins joins Dr. Alexandra on this episode to offer guidance to those parents, as well as the people around them. When Amanda's son Asher was born, she discovered her life's purpose: to help parents of children with disabilities find their stride. She has become a leading expert in helping parents of kids with special needs navigate their emotions, relationships, and parenting, and her book, How to Handle More Than You Can Handle: Caring for Yourself While Raising a Disabled Child, is out in the world today. Amanda and Dr. Alexandra discuss parenting as well as the experience of partners who are raising a disabled child together and what this journey can bring up for couples. There's so much goodness in this conversation for everyone, whether this is a new topic for you or one that's near and dear to your heart."Your Anxiety Toolkit" on MasterClass: www.masterclass.com/youranxietytoolkitHow to Handle More Than You Can Handle: Caring for Yourself While Raising a Disabled Child by Amanda Griffith-AtkinsOrder Dr. Alexandra's book, Love Every DaySubscribe to Dr. Alexandra's NewsletterSubmit a Listener Question

Hello Brave Friends! Welcome to today's expert episode, #217. These are conversations with experts in fields relevant to caregiving parents. Today, Brave Together founder, Jessica Patay and author Kelley Coleman interview Tom Chiodo. Tom Chiodo is the Executive Producer Special Projects, National Productions at WETA, flagship PBS station in Washington D.C., developing primetime documentary films and original digital content, accompanied by national impact and engagement campaigns, for 330+ PBS stations. Tom joins us to discuss the upcoming PBS documentary on caregiving, called Caregiving, highlighting the joys and challenges faced by caregivers. He shares personal experiences and emphasizes the importance of community support and resources for caregivers. The discussion also touches on mental health, self-care, and the need to change the narrative around caregiving to foster understanding and support. Tom advocates for breaking routines to find joy and suggests innovative resources to assist caregivers in their journey.Caregiving, the documentary created with executive producer Bradley Cooper highlighting the challenges and triumphs of caregiving in America, will premiere Tuesday, June 24, 2025 at 9 p.m. ET on PBS (check local listings), and on the PBS YouTube Channel. Caregiving will be available to stream on PBS.org and the PBS App beginning Tuesday, May 27, 2025.Check out the Caregiving trailer at wellbeings.org here.Check out Kelley Coleman's book, Everything No One Tells You About Parenting a Disabled Child here.Find our first book from We Are Brave Together here.Find full episodes from Season 7 and clips from Season 8 on Youtube here.Brave Together Parenting is the podcast for We are Brave Together, a not-for-profit organization based in the USA. The heart of We Are Brave Together is to strengthen, encourage, inspire and validate all moms of children with disabilities and other needs in their unique journeys. JOIN the international community of We Are Brave Together here. Donate to our Retreats and Respite Scholarships here. Donate to keep this podcast going here. Can't get enough of the Brave Together Podcast? Follow us on Instagram or on Facebook. Feel free to contact Jessica Patay via email: jpatay@wearebravetogether.org If you have any topic requests or if you would like to share a story, leave us a message here. Please leave a review and rating today! We thank you in advance! Disclaimer

Hello Brave Friends! Welcome to today's expert episode, #211. These are conversations with experts in fields relevant to caregiving parents. Our guest today is LMFT Amanda Griffith-Atkins, who is another Brave PWS mom as well as an author with a book coming out in June! Hooray! Her book is called How to Handle More Than You Can Handle: Caregiving for Yourself While Raising a Disabled Child.We've had Amanda on before too, so if you want to hear more from her we'll link to that episode, #144, and, of course, we encourage you to pre-order her book, using the link above. On this episode, we will be focusing on those understandable times when we catch ourselves wishing our child had a different diagnosis and comparing our caregiving challenges to other parent's challenges. It's so common, so understandable and as you'll hear, we ALL find ourselves there from time to time, so it's nothing to feel shame about. Our discussion highlights how navigating these feelings can ultimately lead to a deeper understanding of oneself and one's parenting journey.Find Amanda on IG here and here.Find our first book from We Are Brave Together here.Find full episodes from Season 7 and clips from Season 8 on Youtube here.This episode was sponsored by Rise Educational Advocacy. Brave Together Parenting is the podcast for We are Brave Together, a not-for-profit organization based in the USA. The heart of We Are Brave Together is to strengthen, encourage, inspire and validate all moms of children with disabilities and other needs in their unique journeys. JOIN the international community of We Are Brave Together here. Donate to our Retreats and Respite Scholarships here. Donate to keep this podcast going here. Can't get enough of the Brave Together Podcast? Follow us on Instagram or on Facebook. Feel free to contact Jessica Patay via email: jpatay@wearebravetogether.org If you have any topic requests or if you would like to share a story, leave us a message here. Please leave a review and rating today! We thank you in advance! Disclaimer

Send us a textIn episode 158, Noisy Disabled Child, Lovdev discusses his solo show, delves into a dilemma involving a disabled child, and muses on whether leap years are simply made up. Today's weird news spotlights a peculiar tictac object.Support the show

Join Sarah Marie Bilger in this inspiring episode of the Entering Motherhood podcast as she sits down with Kelley Coleman, a passionate mom and advocate. Kelley shares her personal journey as a mother of two, navigating life with a son who has multiple undiagnosed disabilities. In this episode, Kelley talks about the importance of community and finding support while advocating for her child's needs. She emphasizes trusting parental intuition and the role of self-care and creativity in sustaining her caregiving journey. Listeners will gain insights into the challenges and rewards of raising a child with disabilities and discover the importance of sharing experiences and knowledge to help empower others. Kelley offers hope and encouragement to all mothers facing similar paths. Click here for full show notes

About the Guest(s):Kelley Coleman is an influential advocate and author specializing in parenting children with disabilities. Over a decade into her journey of raising a child with multiple disabilities, Kelley has become a voice of insight and support for many parents navigating similar paths. She recently authored the book, "Everything No One Tells You About Parenting a Disabled Child," where she imparts practical advice on various aspects of managing disabilities, both in daily family life and navigating the education system. Kelley is a champion for inclusivity, grounded in her personal experiences and extensive engagement with parents, educators, and the disabled community.Episode Summary:In this captivating episode of "Think Inclusive," host Tim Villegas interviews Kelley Coleman, offering a heartfelt discussion about parenting a disabled child and striving for inclusive education. Kelley shares insights from her book, "Everything No One Tells You About Parenting a Disabled Child," drawing from her decade-long journey of raising a child with multiple disabilities. Her perspective challenges listeners to rethink societal perceptions of disability and underscores the importance of fostering strong, collaborative relationships between parents and educators.Kelley discusses the power of vision statements in IEP meetings to streamline educational goals for children with disabilities. The episode presents a balanced view, recognizing both the struggles and triumphs associated with advocating for the best educational outcomes for disabled children. The conversation expands to discussing inclusivity in schools, the undercurrent of fear surrounding disability, and strategies for educators to better support inclusive practices. The insights shared in the conversation are aligned with current themes in education and disability advocacy, offering a roadmap for both parents and educators to foster a more inclusive environment.Transcript: https://otter.ai/u/e5WjDGn5-klsWtmOr0C48R8LL6QKey Takeaways:Creating a vision statement for a child with disabilities is crucial for setting clear, achievable educational goals and establishing a unified direction for their learning journey.Establishing ongoing communication between parents and teachers is essential for building trust and fostering a collaborative approach to education and inclusion.Normalizing disability in society reduces fear and stigma, which can lead to more meaningful and supportive interactions between disabled and non-disabled individuals.Teachers require sufficient training and resources to implement effective inclusive practices, which simultaneously benefit students with and without disabilities.The Paralympics exemplifies a successful platform for showcasing the excellence of disabled athletes without resorting to inspiration porn.Resources:Kelley's Website: https://www.kelleycoleman.com/MCIE: https://www.mcie.org/Thanks to our sponsor, IXL: https://ixl.com/inclusiveDonate to MCIE: https://bit.ly/MCIE-Donate Hosted on Acast. See acast.com/privacy for more information.

UPDATE for 2025: First, we want to say how much this podcast community means to us. Over the past seven years, we've released 290 episodes, reaching millions of listeners worldwide. You've been with us through laughter, tears, challenges, growth, and friendships. This podcast exists because of you, and we're deeply grateful for your support. To keep The Lucky Few Podcast thriving, we'll be making some changes early this year. While we focus on restructuring and exploring new ideas, we invite you to revisit past episodes or relisten to your favorites. Stay up-to-date by following us on social media @theluckyfewpod. We're excited for what's ahead! Until then, know we're cheering you on and love you so much. ... Throwback: Everything No One Tells You About Parenting A Disabled Child (w/Kelley Coleman) We're so excited to welcome feature film executive turned author and disability advocate, Kelley Coleman to the show! Her book Everything No One Tells You About Parenting a Disabled Child: Your Guide to the Essential Systems, Services, and Support releases TODAY!! Friends, this book is like gold, it provides the kind of support and confidence we all need to navigate and understand the complex systems, services, and supports no matter what diagnosis our kids have. It's a resource we'll be looking to for years to come, providing us with helpful questions, checklists, and ways to access services based on your child's individual needs. We celebrate finding friendship and community throughout the disability community, and Kelley shares how the Down syndrome community has embraced her and her son. She even shares how disability rights activist Judy Heumann shared her enthusiasm for a resource like Kelley's book and emphasized the importance of sharing stories as self-advocates and nondisabled advocates in the disability space. This is a book and conversation we're so grateful for, this is an episode you don't want to miss! --- SHOW NOTES Order Kelley's new book⁠ Everything No One Tells You About Parenting a Disabled Child: Your Guide to the Essential Systems, Services, and Support⁠ To learn more, visit⁠ https://www.kelleycoleman.com/⁠  Follow Kelley on⁠ Instagram⁠ and⁠ Facebook⁠ ⁠Learn more about Judy Heumann's legacy⁠ THANK YOU TO OUR SPONSOR: Thank you,⁠ Enable SNP⁠ for sponsoring this episode! ⁠47. Planning for the Future w/Phillip Clark from Enable SNP⁠ ⁠191. Future Planning for the WHOLE Family - ft. Phillip Clark, Enable SNP⁠ HELP US SHIFT THE NARRATIVE Interested in partnering with The Lucky Few Podcast as a sponsor? Email hello@theluckyfewpodcast.com for more information! LET'S CHAT Email hello@theluckyfewpodcast.com with your questions and Good News for future episodes.

Veda Austin is a water researcher, public speaker, mother, artist and author. She has dedicated the last 10 years observing and photographing the life of water. She believes that water is fluid intelligence, observing itself through every living organism on the planet and in the Universe. Her primary area of focus is photographing water in its ‘state of creation', the space between liquid and ice. It is through her remarkable crystallographic photos that water reveals its awareness of not only Creation, but thought and intention through imagery. Veda brings a message of hope and joy from the very source of life itself, she says “Water is transparent, it knows no colour, creed or religion. Water does not judge, nor does it label, it will enter the body of an ant as easily as it will enter the body of a king, or a homeless person or a tree or a dragonfly. ___________________ PODCAST CHAPTERS 0:00 - Introduction & Prayer with Water 1:50 - Veda Austin on Current Excitements 3:38 - Impact of Water on People's Lives 7:11 - Is Water an Extraterrestrial Life Form? 12:14 - Veda's Conversations with Water 19:21 - Origins of Veda's Journey with Water 32:43 - Water as a Mirror of Emotions 49:10 - Future Discoveries in Water States 59:51 - The Spiritual Aspect of Water 1:09:21 - Water's Sense of Humor 1:16:59 - Visual Journey Through Water Imagery 1:22:47 - Water as the Root of Language 1:25:19 - Facial Recognition in Water Crystallography 1:28:09 - Water Reading Future Events 1:30:52 - Symbolism and Hydro Glyphs in Water 1:34:49 - Water Responds to the Name Yeshua 1:41:13 - Understanding Hydroglyphs and Their Meanings 1:45:26 - Water's Communication with a Disabled Child 1:48:42 - Healing Power of Liquid Crystal Medicine 1:54:41 - The Mystery of Thought Materialization 2:00:38 - Homeopathy and Water's Memory 2:05:55 - Water's Self-Healing Through 5G Exposure 2:12:00 - How Water Sees Humanity 2:18:48 - Healing by Proximity: The Power of Free-Range Eggs 2:20:08 - Closing Reflections on Water and Humanity ___________________ Guest: Veda Austin | Water Researcher Website | https://www.vedaaustin.com/ Veda's Freezing Techniques | https://www.vedaaustin.com/shop Veda's UK/EU Tour | https://www.vedaaustin.com/event-list Instagram | https://www.instagram.com/vedaaustin_water/ The Living Language of Water Book | https://www.vedaaustin.com/vedas-book Host: Emilio Ortiz Instagram | https://www.instagram.com/iamemilioortiz/ Subscribe to YouTube Channel | ​⁠​https://www.youtube.com/@EmilioOrtiz Watch Emilio's latest series on 4biddenknowledge TV l https://bit.ly/AwakenThe6thSense ___________________ Special Offerings to Support the Show: ✦ Make a One-Time or Recurring Donation on PayPal

Joakim Valsinger is an Award-Winning Fitness Instructor and 2nd Generation Pilates Teacher who opened Bälans Pilates Studio in Perth, Scotland in 2005.A Swedish-born Australian, Joakim came to the UK in 1998. He is a former Australian Army Reserve SF Commando, Bondi Beach Surf Life Saver, and Territorial Army Physical Training Instructor. Joakim's son has a rare genetic condition called Prader Willi Syndrome which brings with it several challenges. Pilates has helped Albie improve his physical capacity, and the creativity required to keep Albie engaged and improving has taught Joakim a lot. This unique experience has honed Joakim's skills to achieve tangible results for clients through thoughtful applications of Pilates techniques. Joakim believes Pilates should be accessible, achievable, and assessable. Joakim has presented at Pilates conferences across the UK, Germany, Switzerland, Spain, Brazil, and the USA, as well as several online Conferences with international audiences. Joakim is an Educator for Lolita's Legacy, the Comprehensive Pilates Teacher Training program developed by his mentor. Students travel from around Scotland, the UK, Europe, and even Japan to attend his courses. He is also a regular presenter at Pilates Industry Conferences here and abroad. Before the birth of his son, Joakim was the expert on Pilates for the Military. Since learning to cope with Albie's disabilities, he now teaches other Pilates professionals Pilates for the Disabled Child. In 2023, Joakim was invited to work as a Subject Matter Expert with the US-based National Pilates Certification Program (NPCP) to help create their Certification Exam for Matwork Pilates Teachers.In this episode, we discover the following:What attributes make the best teachers and students?How Pilates has a positive impact on the mind-body connection.The main benefits of Pilates and how they can help someone with a disability.The value of listening with your eyes.With podcast host: Mark SephtonHope you'll enjoy the episode! Hosted on Acast. See acast.com/privacy for more information.

Lackey introduces bill to classify rape of disabled child as violent felony   Please Subscribe + Rate & Review KMJ's Afternoon Drive with Philip Teresi & E. Curtis Johnson wherever you listen!  ---     KMJ's Afternoon Drive with Philip Teresi & E. Curtis Johnson is available on the KMJNOW app, Apple Podcasts, Spotify, Amazon Music or wherever else you listen.  ---   Philip Teresi & E. Curtis Johnson – KMJ's Afternoon Drive  Weekdays 2-6 PM Pacific on News/Talk 580 & 105.9 KMJ  DriveKMJ.com | Podcast | Facebook | X | Instagram  ---   Everything KMJ: kmjnow.com | Streaming | Podcasts | Facebook | X | Instagram    See omnystudio.com/listener for privacy information.

Lackey introduces bill to classify rape of disabled child as violent felony   Please Subscribe + Rate & Review KMJ's Afternoon Drive with Philip Teresi & E. Curtis Johnson wherever you listen!  ---     KMJ's Afternoon Drive with Philip Teresi & E. Curtis Johnson is available on the KMJNOW app, Apple Podcasts, Spotify, Amazon Music or wherever else you listen.  ---   Philip Teresi & E. Curtis Johnson – KMJ's Afternoon Drive  Weekdays 2-6 PM Pacific on News/Talk 580 & 105.9 KMJ  DriveKMJ.com | Podcast | Facebook | X | Instagram  ---   Everything KMJ: kmjnow.com | Streaming | Podcasts | Facebook | X | Instagram    See omnystudio.com/listener for privacy information.

Parents of disabled children are responsible for navigating a number of complex systems, from educational services and accommodation to medical care. Author Kelley Coleman, whose son has an undiagnosed genetic syndrome, says that parenting a disabled child can be hard–but hard is not bad. That's the central framework of her book, Everything No One Tells You About Parenting a Disabled Child, which came out earlier this year. In today's episode, Coleman speaks with Here & Now's Deepa Fernandes about their joyful and difficult parenting moments, how to access the support needed for kids to thrive, and teaching self-advocacy.To listen to Book of the Day sponsor-free and support NPR's book coverage, sign up for Book of the Day+ at plus.npr.org/bookofthedayLearn more about sponsor message choices: podcastchoices.com/adchoicesNPR Privacy Policy

 Parenting A Disabled Child.  (Let's not be awkward.) The challenges of parenting a disabled child are unique to each family, but these families are not alone! The Impactful Parent wants to help! Introducing Kelley Coleman! Kelley is a mom of 2 boys, one of which with both physical and mental disabilities. Kelley is welcomed onto the Impactful Parent stage to share her story, her struggles, her insights, and her knowledge about raising a child with disabilitie. In this episode, learn about Kelley's unique story,

In this episode, I sit down with Kelley Coleman, a former feature film development executive turned author and advocate for parent caregivers and individuals with disabilities. Kelley opens up about her personal journey of over a decade raising a child with multiple disabilities, and how it led her to write her book, Everything No One Tells You About Parenting a Disabled Child: Your Guide to the Essential Systems, Services, and Support.With a heart full of passion, Kelley emphasizes the need for understanding, not pity, and challenges the idea that everyone's opinion is necessary. We dive into the realities of navigating life as a parent of a child with disabilities, the crucial resources that many parents don't know about, and how she's helping new mamas find their way with confidence and support. Statistically, 1 in 33 babies are born with birth defects, 1 in 6 children are diagnosed with developmental disabilities, and 1 in 4 adults has a disability. Kelley's mission to equip families with the information they need is both practical and deeply inspiring. This conversation is full of wisdom, heart, and real talk about the journey of parenting through challenges.CONNECT WITH GUEST:WEBSITE: http://www.kelleycoleman.comINSTAGRAM HANDLE: @hellokelleycolemanCONNECT WITH HOST:Website: www.mamayouredoinggreat.comIG: @kendahlyanezWant to get connected with other mamas like you?Join the CommunityText the word WELCOME to 855.486.5757 or sign-up HERE to get a weekly encouragement text delivered straight to your phone!

Hello Brave Friends! This is an Ask Us Anything episode in which YOU, the listener, get to write or call in and, you guessed it, ASK US ANYTHING! In this Ask Us Anything episode, #189, we are responding to the question, Do you have any tips for navigating life with a disabled child after a divorce?This is a VERY relevant topic for our community because the added stress of caregiving for disabled children is not known to help marriages last longer. Also two of our three hosts have been through divorce and continue to co-parent with their disabled children's fathers. So we have A LOT of first hand experience and advice for this caller. In this episode we offer: important things to consider in the divorce process, ways to break the news to our kids and the realities of what co-parenting with your ex-partner can look like as the primary caregiver. Keep the vulnerable questions coming. We're here to support you! We see you and we love you!Whether you have questions as a parent to a child with complex medical or mental health needs or you're someone looking to support a care-giving parent, we would LOVE to hear from you. If you have any topic requests or if you would like to ask a question, leave us a message here.Find more information about Licensed Psychotherapist, Dr. Zoe Shaw here. Find more information about Life Coach, Susanna Peace Lovell here.Find Susanna's book, Your True Self is Enough here.Find our first book from We Are Brave Together here.Thank you to our BIG, beautiful 5k sponsors!! Our TOP sponsors that we want to acknowledge and appreciate are: RISE Advocacy, GHJ Foundation, Torrance Memorial Medical Center, CMS Creative Management, Inc., the Patay Family and MRM Education. We are so grateful to these generous sponsors and so excited about our 5K, which will be accessible and truly a family friendly event! Learn more about our 5K here.Brave Together is the podcast for We are Brave Together, a not-for-profit organization based in the USA. The heart of We Are Brave Together is to strengthen, encourage, inspire and validate all moms of children with disabilities and other needs in their unique journeys. JOIN the international community of We Are Brave Together here.Donate to our Retreats and Respite Scholarships here.Donate to keep this podcast going here.Follow our Instagram Page @wearebravetogether or on Facebook.Feel free to contact Jessica Patay via email: jpatay@wearebravetogether.orgPlease leave a review and rating today! We thank you in advance!Disclaimer

In this episode of Parenting in the First Three Years, Kelly Coleman, a feature film executive turned author and disability advocate. Kelly shares her personal parenting journey raising a child with disabilities, offering invaluable insights and practical advice for parents who are navigating similar experiences. Ann and Kelley discuss everything from the emotional challenges of receiving a diagnosis, finding community support, and managing the day-to-day responsibilities of caregiving. Kelley also provides helpful strategies, including how to prepare for travel with a disabled child and ways to educate others about disabilities. Tune in to hear Kelley's inspiring story and her hopeful message for parents of disabled children: you are exactly the parent your child needs. --- Support this podcast: https://podcasters.spotify.com/pod/show/ann-mckitrick/support

Kelley Coleman is a feature film development executive turned author, who is active in the disability advocacy community. She serves on committees for Children's Hospital Los Angeles, the Los Angeles Unified School District, and Canine Companions. Her book Everything No One Tells You About Parenting a Disabled Child: Your Guide to the Essential Systems, Services, and Supports stems from her own parenting experience, giving parents the tools to spend less time navigating the stuff and more time just loving their kids exactly as they are. Her book is available for sale on Amazon. She lives in Los Angeles with her husband, two children, and her son's service dog. To learn more, please visit:Kelley's Website Connect with Kelley on:Instagram Facebook Looking to save money on quality, bulk foods? Shop Azure StandardWatch on YouTubeVisit The Motherhood Experience WebsiteFollow us on Instagram

Show notes: https://www.tamihackbarth.com/blog/episode-241 Happy back to school aka new year! While I love the fresh start energy of a new school year, it also brings a deep feeling of anxiety. Will the teacher like my kid? Will the teacher be fair? Will the other kids include mine and be kind to her? The second day of kindergarten was the first time I got a behavior call from school and I have spent every beginning of the school year since educating teachers and administrators about disabilities and disability rights within the public school system. We have had to learn about special education laws and disability rights all while raising our little firecracker. Sometimes I feel like the universe had this kid in mind for me because what else would explain my past work as a lobbyist, a public school teacher AND a coach? These jobs gave me the skills to go to bat on her behalf.  But not all families have the time, money, expertise or experience to help their students.  This is lonely work for parents of kids who don't fall into the school system because of learning and thinking differences. A lot of times we parents share similar  struggles as our kids. Between me and my husband we have 36 years of direct classroom experience. AND THIS IS STILL A MYSTERY. The education system needs help and no place is that more apparent than in special education. If your student needs an IEP or a 504, uses a wheelchair or other medical equipment or has ADHD you have to know a whole lot more stuff than parents who never deal with special education. The craziest part of this is so much of special education is settled law. It should be this hard to access services legally required for students under settled law, right? Individuals with Disabilities Education Act (IDEA) guarantees students with disabilities free and appropriate education was passed in 1975 and updated in 2004. The Americans with Disabilities Act (ADA)  was enacted in 1990 - 34 years ago. Why is this still such a struggle? I recently asked my friends, neighbors and former teacher colleagues what they wished everyone knew about special education. They came through… everyone feels like every single part of the system is set up to fail. I just discovered our school district has been under scrutiny since 2017 about their failure in special education. They have been involved in lawsuits and are just now trying to get it sorted. Needless to say I will be throwing in my two cents because this has been a shitshow. People who aren't directly involved have no idea how much extra work we are all putting in trying to sort out a complicated and confusing process. It is a privilege to not have to advocate for your student. People who live this every day are exhausted and anxious because we all want the same thing for our kids: a quality education that will help them be lifelong learners.  This isn't the last you'll be hearing from me about systemic changes in education, but I did want to share a resource I found. Of course I immediately checked this out from the library, devoured the contents and then reached out to the author to be a guest on the podcast. Meet Kelley Colman. Kelley Coleman is a feature film development executive turned author and advocate for parent caregivers and individuals with disabilities.  Her book Everything No One Tells You About Parenting a Disabled Child: Your Guide to the Essential Systems, Services, and Supports draws upon over a decade of experience, including her own experience parenting a child with multiple disabilities.  Kelley lives in Los Angeles with her husband, two boys, and her son's trusty service dog. Who can you share this episode with? Does anyone you know know a student with thinking and learning differences like ADHD, autism, dyslexia or other learning difficulties? Do you know a family that has visible disabilities? Do you know a teacher, principal or school board member? Please pass it on.

Lost and in the dark about your child's disability? Not anymore! Kelley Coleman, author of Everything No One Tells You About Parenting a Disabled Child: Your Guide to the Systems, Services, and Supports, sits down with Biz to talk about educational resources, the beauty of an amazing index, and the major of Trader Joe's.Get your copy of Kelley's book, Everything No One Tells You About Parenting a Disabled Child: Your Guide to the Systems, Services, and Supports, at the bookshop of your choice. Learn more about Kelley Coleman by visiting her website, www.KelleyColeman.com.Go to MaximumFun.org/join to support One Bad Mother in its final year!Share a personal or commercial message on the show! Details at MaximumFun.org/Jumbotron.Visit our Linktree for our website, merch, and more! https://linktr.ee/onebadmotherYou can suggest a topic or a guest for an upcoming show by sending an email to onebadmother@maximumfun.org.Show MusicSummon the Rawk, Kevin MacLeod (www.incompetech.com)Ones and Zeros, Awesome, Beehive SessionsMom Song, Adira Amram, Hot Jams For TeensTelephone, Awesome, Beehive SessionsMama Blues, Cornbread Ted and the ButterbeansMental Health Resources:Therapy for Black Girls – Therapyforblackgirls.comDr. Jessica Clemmens – https://www.askdrjess.comBLH Foundation – borislhensonfoundation.orgThe Postpartum Support International Warmline – 1-800-944-4773 (1-800-944-4PPD)The Substance Abuse and Mental Health Services Administration (SAMHSA) Helpline – 1-800-662-4357 (1-800-662-HELP)Suicide Prevention Hotline: Call or chat. They are here to help anyone in crisis. Dial 988 for https://suicidepreventionlifeline.org and there is a chat option on the website.Crisis Text Line: Text from anywhere in the USA (also Canada and the UK) to text with a trained counselor. A real human being.USA text 741741Canada text 686868UK text 85258Website: https://www.crisistextline.orgNational Sexual Assault: Call 800.656.HOPE (4673) to be connected with a trained staff member from a sexual assault service provider in your area.https://www.rainn.orgNational Domestic Violence Hotline:https://www.thehotline.org/help/Our advocates are available 24/7 at 1-800-799-SAFE (7233) in more than 200 languages. All calls are free and confidential.They suggest that if you are a victim and cannot seek help, ask a friend or family member to call for you.Teletherapy Search: https://www.psychologytoday.com/us/therapists/online-counseling

The journey of caregiving is a delicate dance of emotions and responsibilities, especially for parents of disabled children who face societal pressures. Home and community care services provide essential support and respite, allowing families to maintain a safe environment and caregivers to recharge. Self-care, such as meditation or exercise, is critical for caregivers to sustain their well-being and continue their responsibilities.   In this episode, host Annette Hines sits with Kelley Coleman as she shares her journey of parenting a disabled child, revealing how it led her to write "No One Tells You About Parenting a Disabled Child: Your Guide to the Essential Systems, Services, and Supports." Kelley expresses the importance of accessing accurate information and insights directly from individuals with disabilities to combat stigma and misconceptions. Her book serves as a practical guide for caregivers, filled with invaluable checklists, personal stories, and strategies for self-care, effective communication, and advocacy. Kelley and Annette bond over their shared love for practical tools, discussing the significance of job training in caregiving and urging caregivers to establish boundaries and prioritize their well-being. They reflect on their own experiences, the emotional toll of caregiving, and the power of a supportive community.   In this episode, you will hear: Why it is important to seek insights from individuals with disabilities Addressing the challenges faced by parents of disabled children How caregivers can prioritize self-care and establish boundaries Why it is important to advocate for home and community-based care services What resources are available for caregivers of children with disabilities Resources from this Episode: Kelley Coleman: www.kelleycoleman.com  Facebook:  @kelley.coleman.56 Instagram: @hellokelleycoleman    Engage with us: Join our community: Circle of Care Visit:  https://annettehines.com Read Butterflies and Second Chances LinkedIn: @annette-hines-snc  Instagram: @parentingimpossible Facebook: @SpecialNeedsCompanies Twitter: @SpecialNeedsCo   Follow and Review: We'd love for you to follow us if you haven't yet. Click that purple '+' in the top right corner of your Apple Podcasts app. We'd love it even more if you could drop a review or 5-star rating over on Apple Podcasts. Simply select “Ratings and Reviews” and “Write a Review” then a quick line with your favorite part of the episode. It only takes a second and it helps spread the word about the podcast.  

We're happy to bring you some of our listener favorites during the next few weeks. These episodes are sure to pique your interest by featuring topics important to each of us Enjoy!We are pivoting from our normal education-centric topics today to take a broader view of the financial side of raising a child with a disability. We want to make sure that families, and people working with these families, have all the resources and tools for a well-rounded toolkit for supporting their kids. We welcome James Lange to the podcast to share his practical insights and expertise.James Lange is a CPA, a state attorney in Pennsylvania, and the author of nine best-selling financial books. He is a nationally recognized IRA, 401(k), and retirement plan distribution expert. As a result of his daughter's disability, James developed a passion for helping parents who need to provide sufficient care for a disabled child even beyond their own lifetime. He explains how he and his wife are providing for their daughter's future and what parents of a disabled child should do right now to ensure the financial future of their child. Show Highlights:James' plan to provide for his daughter for the rest of her lifeJames' mission to help parents of children with disabilities optimize their financial assetsThree steps to take right now for your disabled child: Get your child qualified for government benefits in the SSI or SSDI. (James explains the #1 mistake most parents make in applying for these benefits.)Get your estate planning done appropriately with the proper trust or conservatorship option. (Don't rely on “Joe Schmo Attorney” for this!)Get the Roth IRA conversion strategy done right by a financial professional. (The difference in doing this correctly and incorrectly can amount to a huge difference in available funds for your child.) Best resources for parents to use in their education and planning:Get James' FREE book, Retire Secure for Parents of a Child with a Disability. Click here!Sign up for Expert Advice for Parents of Children with Disabilities: A Virtual Summit, June 18-20, 2024. Click here for more information about this FREE event!Links/Resources:Connect with James Lange: Disabled Child Planning, Pay Taxes Later, and LInkedInContact us on social media or through our website for more information on the IEP Learning Center: www.inclusiveeducationproject.org Thank you for listening! Don't forget to SUBSCRIBE to the show to receive every new episode delivered straight to your podcast player every Tuesday.If you enjoyed this episode and believe in our message, then please help us get the word out about this podcast. Rate and Review this show on Apple Podcasts, Stitcher Radio, or Google Play. It helps other listeners find this show.Be...

On this episode of The Brainy Moms podcast, Dr. Amy and Sandy are joined by Kelley Coleman, a feature film development executive turned author and advocate for parents and caregivers of individuals with disabilities. Kelley is here to talk about the concepts and information in her book, “Everything No One Tells You About Parenting a Disabled Child: Your Guide to the Essential Systems, Services, and Supports.” Kelley is the mother of two boys, one of whom has multiple disabilities and a service dog, and she shares her own experiences about learning to navigate the world in a new way to best support the journey for her entire family. You'll hear her advice for other parents who are parenting a disabled child, including where to find support, tips for advocating for your child, and how the process of getting a service dog works. Whether you're new to the caregiving journey or are just looking for inspiration, don't miss this jam-packed episode!ABOUT US: The Brainy Moms is a parenting podcast hosted by cognitive psychologist Dr. Amy Moore. Dr. Amy and her rotating co-hosts bring listeners conversations with experts on topics in parenting, child development, education, psychology, mental health, and neuroscience. Listeners leave with tips and helpful advice for helping moms and kids thrive in life, learning, and relationships. This episode is co-hosted by Sandy Zamalis.  CONNECT WITH US: Website: www.TheBrainyMoms.com Email: info@TheBrainyMoms.com Social Media: @TheBrainyMoms Dr. Amy's website: www.AmyMoorePhD.comSponsor's website: www.LearningRx.com

Each week, I share a new episode and guest, but I realized that it's been a long time since I've shared much of me, Madeline, with you. So today, I'm peeling back the curtain today and sharing all sorts of fun (and maybe a few not so fun) facts about me, my life, and my family. I'm sharing what motherhood looks like these days, traits that I do and don't love about myself, and lots of other lower stakes facts. I'm so grateful for this opportunity to be vulnerable with all of you, and I am so excited to share this episode. Also, huge thank you to our sponsor Functional Formularies! They make incredible, nutritious food for our tube-fed kids that's easy to access and use. Honestly, if our kids are eating Functional Formularies formula, they're probably eating better than us! Links: Visit the Functional Formularies website and get easy, nutritious, tube-friendly meals for your child! Listen to Ep 127 on traveling with our disabled children. Read our list of Top 5 Travel Carriers! Read the original "10 Must-Haves for Traveling with a Disabled Child” blog post. Follow us on Instagram @the_rare_life! Donate to the podcast or Contact me about sponsoring an episode. Fill out our contact form to get a reminder about upcoming discussion meetings and the Skype link to join! Follow the Facebook page. Join the Facebook group Parents of Children with Rare Conditions. Access the transcript on the website here. And if you love this podcast, please leave us a rating or review in your favorite podcast app!

Our guest this week is Kelley Coleman of Los Angeles, CA a feature film maker turned author, disability advocate, wife and mother of two including a son with an undiagnosed rare disease and many disabilities.Kelley and her husband, Eric, have been married for 16 years and are the proud parents of two boys: Sean (12) and Aaron (10) who has multiple disabilities, including: An Undiagnosed Genetic DisorderCortical Visual ImpairmentFailure to ThriveAutismEpilepsyCerebral PalsyMicrocephaly, andA Feeding TubeKelley is also the author of Everything No One Tells You About Parenting a Disabled Child, available on Amazon.Kelley has lots to say about a host of supporting organizations, including the Undiagnosed Disease Network, Canine Companions, and Painted Turtle Camp to name a few.   That's all on this episode of the SFN Dad to Dad Podcast.  Show LinksEmail - kelleyellek@gmail.comWebsite – https://www.kelleycoleman.com/Facebook - https://www.facebook.com/kelley.coleman.56Instagram - https://www.instagram.com/hellokelleycoleman/Undiagnosed Diseases Network - https://undiagnosed.hms.harvard.edu/Canine Companions - https://canine.org/Painted Turtle local camp - https://www.thepaintedturtle.org/ SNAP Special Needs Aquatic Program with Stepping Stones https://snapaquatics.org The book -Everything No One Tells You About Parenting A Disabled Child. Your Guide to the Essential Systems, Services, and Supports - https://tinyurl.com/5casy743Special Fathers Network - SFN is a dad to dad mentoring program for fathers raising children with special needs. Many of the 700+ SFN Mentor Fathers, who are raising kids with special needs, have said: "I wish there was something like this when we first received our child's diagnosis. I felt so isolated.  There was no one within my family, at work, at church or within my friend group who understood or could relate to what I was going through."SFN Mentor Fathers share their experiences with younger dads closer to the beginning of their journey raising a child with the same or similar special needs. The SFN Mentor Fathers do NOT offer legal or medical advice, that is what lawyers and doctors do. They simply share their experiences and how they have made the most of challenging situations.Check out the 21CD YouTube Channel with dozens of videos on topics relevant to dads raising children with special needs - https://www.youtube.com/channel/UCzDFCvQimWNEb158ll6Q4cA/videosPlease support the SFN. Click here to donate: https://21stcenturydads.org/donate/Special Fathers Network: https://21stcenturydads.org/

Episode 22 of Trailer Tales! Is Dave neglecting his disabled child?! Tammy's Trampoline accident. Tea or Coffee? Karaoke got a little wild last night... Tammy, Dave, and Crystal will remain friends no matter what! #ChelcieLynn #JeremiahWatkins #Podcast #LibbieHiggins GET YOUR NEW TRAILER TALES MERCH HERE!: https://thecomedyoutlet.com/collections/trailer-tales New episodes every Friday on this channel. Subscribe! New Trailer Tales merch is here!: https://thecomedyoutlet.com/collections/trailer-tales Jeremiah's Patreon is LIVE: https://www.patreon.com/jeremiahwatkins NEW MERCH IS HERE!: https://www.jeremiahwatkins.com FOLLOW us on Instagram: https://www.instagram.com/trailertalespod See Tammy LIVE on tour: https://www.eatmytrash.com  @ChelcieLynn See Jeremiah LIVE on tour: https://www.jeremiahwatkins.com  @jeremiahwatkins Support Crystal: https://www.libbiehiggins.com  @LibbieHiggins   Want to send some mail into the show?  P.O. BOX JEREMIAH WATKINS/TT P.O. BOX # 78375 LOS ANGELES, CA 90016  Sponsored by: Factor Meals Support the show & get 50% off your 1st Factor box, plus 20% off your next month while your subscription is active. Head to https://www.factormeals.com/TRAILER50 and use code TRAILER50 Sponsored by: Joymode Support the show and get 20% off Joymode and free shipping. Head to https://www.usejoymode.com and use code TRAILER Edited by Jeremiah Watkins  Assistant Editor Jackie Lang Intro Music: Produced by https://www.instagram.com/professorcmusic  Intro Vocals: Jeremiah Watkins

Text us your financial questions! Chief Investment Officer Troy Harmon, CFA, CVA, along with Senior Associate Logan Daniel, CFP®, CRPC®, and Tax Manager Jessie Thomas, CPA, from Henssler CPAs & Advisers, offer valuable tax advice for a couple with a disabled child. They share insights on what may qualify as a medical expense deduction.  Read the Article: https://www.henssler.com/essential-tax-tips-for-families-with-disabled-or-special-needs-children 

Text us your financial questions!Henssler Money Talks — June 8, 2024Season 38, Episode 23This week on “Money Talks,” Chief Investment Officer Troy Harmon, CFA, CVA, is joined by Senior Associate Logan Daniel, CFP®, CRPC®, and Tax Manager Jessie Thomas, CPA, with Henssler CPAs & Advisers to cover economic news including the Manufacturing and Nonmanufacturing indices, personal income and interest rates. In our case study, Jessie provides some tax advice for a couple with a disabled child, sharing tips on what may count as a medical expense deduction. The experts round out the show with listeners' questions on market timing and portfolio positioning.Timestamps and Chapters00:00 Market Roundup: June 3 – June 7, 202423:25 Case Study:  Tax Benefits for Parents of Disabled Children34:28 Q&A Time: Market timing and portfolio positioningFollow Henssler:  Facebook: https://www.facebook.com/HensslerFinancial/ YouTube:  https://www.youtube.com/c/HensslerFinancial LinkedIn: https://www.linkedin.com/company/henssler-financial/ Instagram: https://www.instagram.com/hensslerfinancial/ TikTok: https://www.tiktok.com/@hensslerfinancial?lang=en X: https://www.x.com/hensslergroup  “Money Talks” is brought to you by Henssler Financial. Sign up for the Money Talks Newsletter: https://www.henssler.com/newsletters/ 

Navigating Parenting a Disabled Child: Insights from Kelley ColemanIn this episode of the Docs2Dads podcast, Dr. Scott Grant sits down with Kelly Coleman, author of 'Everything No One Tells You About Parenting a Disabled Child.' Together, they discuss Kelley's personal journey of raising a disabled child, the unexpected challenges and rewards, and her motivations behind writing the book. Kelley shares practical advice for parents, emphasizes the importance of community and partnership with medical professionals, and touches on balancing the needs of siblings and maintaining strong familial relationships. Kelley's insights aim to empower parents, clinicians, and caregivers to navigate the complexities of parenting a disabled child with confidence and compassion.00:00 Introduction and Guest Welcome04:40 Kelley Coleman's Background and Book Overview09:38 Navigating Diagnostic Uncertainty18:47 Building a Supportive Community24:15 Fatherhood and Partnership Dynamics38:06 Balancing Attention Between Siblings43:55 Finding the Right Medical Partners58:22 Conclusion and Where to Find the BookHave a question about this or other topics? Connect with Dr. Scott at the Social links below: Linkedin: https://www.linkedin.com/in/drscottpeds Instagram: https://www.instagram.com/docs2dadspod Email: docs2dadspod@gmail.com Facebook: https://www.facebook.com/docs2dadspod

Kelley Coleman is a mom to two amazing boys, one of whom has multiple disabilities (including a yet-undiagnosed genetic syndrome, cerebral palsy, autism, CVI, epilepsy, and more).  Presented with empathy and humor, Everything No One Tells You About Parenting a Disabled Child gives parents the tools to conquer the stuff, so that they can spend less time filling out forms, and more time loving their children exactly as they are.  Kelley's message resonates with everyone, even parents whose children are not disabled. We all know someone in this camp (whether it's a kid with ADHD or a rare disease). Kelley's tools and resources change lives for families who have a child with disabilities and all of those who interact with them. https://www.kelleycoleman.com/ https://www.instagram.com/hellokelleycoleman/ Get her Book: https://www.amazon.com/dp/0306831708/ref=cm_sw_r_as_gl_api_gl_i_DF8V5JNJ5HVZHY13K8HP?linkCode=ml2&tag=elizabethsand-20 Connect with Liz https://www.instagram.com/esandoz/?hl=en https://www.Elizabethjoy.co Get the First Trimester Survival Guide https://elizabethjoy.co/freebie Join the Waitlist https://elizabethjoy.co/join-waitlist

0:00 Intro 0:05 Line in the sand 4:58 Not the mother 8:30 Elsewhere Learn more about your ad choices. Visit megaphone.fm/adchoices

When you have a medically complex child, you probably have some realization that the experience you have with your child isn't “typical.” But sometimes, it's hard to understand just how different from the “norm” it was, until another child comes along – particularly one without disabilities or medical complexities. In this episode, Brianna, a mom of disabled son who went on to have another nondisabled child, joins me to discuss how vastly the experience has been from one child to another. We also play audio clips from listeners as they share their own grief, joy, and insights that came up for them after having a nondisabled child after their disabled child. And we end the episode by reiterating the honor and privilege it is to be able to raise our nondisabled and disabled children alongside each other, while still the conflicting emotions that come up for us. This episode is so poignant and full of so many thoughtful reflections. Don't miss it! Links: Fill out our contact form to get a reminder about upcoming discussion meetings and the Skype link to join! Listen to Brianna's story in Ep 105 and Ep 106. Listen to Ep 99 on Family Planning. Follow Brianna on Instagram @brianna.alcox! Follow us on Instagram @the_rare_life! Donate to the podcast or Contact me about sponsoring an episode. Follow the Facebook page. Join the Facebook group Parents of Children with Rare Conditions. Access the transcript on the website here. And if you love this podcast, please leave us a rating or review in your favorite podcast app!

We are pivoting from our normal education-centric topics today to take a broader view of the financial side of raising a child with a disability. We want to make sure that families, and people working with these families, have all the resources and tools for a well-rounded toolkit for supporting their kids. We welcome James Lange to the podcast to share his practical insights and expertise.James Lange is a CPA, a state attorney in Pennsylvania, and the author of nine best-selling financial books. He is a nationally recognized IRA, 401(k), and retirement plan distribution expert. As a result of his daughter's disability, James developed a passion for helping parents who need to provide sufficient care for a disabled child even beyond their own lifetime. He explains how he and his wife are providing for their daughter's future and what parents of a disabled child should do right now to ensure the financial future of their child. Show Highlights:James' plan to provide for his daughter for the rest of her lifeJames' mission to help parents of children with disabilities optimize their financial assetsThree steps to take right now for your disabled child: Get your child qualified for government benefits in the SSI or SSDI. (James explains the #1 mistake most parents make in applying for these benefits.)Get your estate planning done appropriately with the proper trust or conservatorship option. (Don't rely on “Joe Schmo Attorney” for this!)Get the Roth IRA conversion strategy done right by a financial professional. (The difference in doing this correctly and incorrectly can amount to a huge difference in available funds for your child.) Best resources for parents to use in their education and planning:Get James' FREE book, Retire Secure for Parents of a Child with a Disability. Click here!Sign up for Expert Advice for Parents of Children with Disabilities: A Virtual Summit, June 18-20, 2024. Click here for more information about this FREE event!Links/Resources:Connect with James Lange: Disabled Child Planning, Pay Taxes Later, and LInkedInContact us on social media or through our website for more information on the IEP Learning Center: www.inclusiveeducationproject.org Thank you for listening! Don't forget to SUBSCRIBE to the show to receive every new episode delivered straight to your podcast player every Tuesday.If you enjoyed this episode and believe in our message, then please help us get the word out about this podcast. Rate and Review this show on Apple Podcasts, Stitcher Radio, or Google Play. It helps other listeners find this show.Be sure to connect with us and reach out with any questions/concerns:Facebook

Having grown up with a sibling (my twin brother, to be exact) who has autism was one of the biggest things that ever happened to my family. In the 80's and 90's, there weren't that many resources available for parents who had kids with disabilities. My parents did the best that they could in raising us, but there were a lot of struggles. Now that I'm a mother myself, I can only imagine all of the days and nights they worried about my brother and his future as they looked for therapies and support. My brother has been a major blessing in our lives, and I believe he has taught us more than we have taught him. Thankfully, our world has progressed and is doing a lot more for disabled people and their families. Today's guest even wrote a book about parenting a disabled child and what parents need to know. I'm excited for you to listen to this episode. In my opinion, it's not just for parents who have disabled children. This episode is something everyone should listen to. Who is Kelley Coleman? Kelley Coleman is a feature film development executive turned author who is active in the disability advocacy community. She serves on committees for Children's Hospital Los Angeles, the Los Angeles Unified School District, and Canine Companions. Her book Everything No One Tells You About Parenting a Disabled Child: Your Guide to the Essential Systems, Services, and Supports stems from her own parenting experience, giving parents the tools to spend less time navigating the stuff and more time loving their kids exactly as they are. Kelley is a mom to two amazing boys, one of whom has multiple disabilities (including a yet-undiagnosed genetic syndrome, cerebral palsy, autism, CVI, epilepsy, and more). She lives in Los Angeles with her husband, two boys, and her son's service dog. What Did We Discuss? In this episode, we're chatting with Kelley Coleman about everything you need to know about parenting a disabled child. As I mentioned, having a twin brother with autism, this topic is very near and dear to my heart, and it was a great conversation. To see some of the questions that we covered in this episode, go to our show notes! Kelley's Resources Website: KelleyColeman.com Kelley's book: Everything No One Tells You About Parenting a Disabled Child: Your Guide to the Essential Systems, Services, and Supports Facebook: @kelley.coleman.56 Instagram: @hellokelleycoleman Thank you for listening to this episode! Follow us on our podcast Instagram page @thebabychickchat, and let us know what you think and if there are any other topics you'd like us to cover. Cheers to navigating your unique parenting journey! Learn more about your ad choices. Visit megaphone.fm/adchoices

Hey Friends~  Do you know anyone doing EXTREME CAREGIVING?  Is it YOU?  This means, not only are you dealing with the speech or language delays we talk about on this podcast, but you ADD to that… other complex care.  When your parenting has been altered by severe disability. Your life changes dramatically.  Today's guest, Jessica Patay, author of “Becoming Brave Together,” is a caregiver advocate and community builder. She uses storytelling to shout the worth of caregivers and caregiving.  Even if you are not an extreme caregiver, this is a wonderful episode that will change you and your perspective.   This amazing episode is worth your listening time!  Join the FREE Interactive Webinar!  "Beyond Obedience: Unveiling the Power of Listening in Kids,"  https://dinalynnr.systeme.io/workshop-free-2ddd5182   Always cheering you on!  Dinalynn CONTACT the Host, Dinalynn:  hello@thelanguageofplay.com   ABOUT THE GUEST:   Founder/Exec Director of We Are Brave Together; author of Becoming Brave Together and host of the Brave Together Podcast.  Jessica Patay is a caregiver advocate and community builder. She uses storytelling to shout the worth of caregivers and caregiving.  CONTACT THE GUEST:   jpatay@wearebravetogether.org Website: https://www.wearebravetogether.org/ IG: https://www.instagram.com/wearebravetogether/ Facebook Page: https://www.facebook.com/wearebravetogether Book: https://www.wearebravetogether.org/book Brave Together Podcast:  iTunes: https://podcasts.apple.com/us/podcast/brave-together/id1511571105 Spotify:https://open.spotify.com/show/1y7WAuQtwwM2UbghMbevHN?si=ClH1ElXHTaSNh4TE17RvNw   RESOURCES from The Language Of Play: Join the FREE Interactive Webinar!  "Beyond Obedience: Unveiling the Power of Listening in Kids,"  https://dinalynnr.systeme.io/workshop-free-2ddd5182 Sign up for my newsletter!   Newsletter Opt-In Sign up for FREE 21 Days of Encouragement in your inbox!  21 Daily Thoughts of Encouragement Join my Facebook Page:  Facebook Page Sign up for a 15 min "Let's Meet Session" on zoom!  Schedule a 15 minute Zoom! For Speaking Engagements or For 1:1 or Group Parent Coaching (virtual or live), contact me at hello@thelanguageofplay.com   If You Liked This Episode, You Will Want To Listen To These Episodes:  20 SUCCESS STORY: Kathryn Johnson Grew Up With Disabilities. Her Tips For Facing Obstacles 125 Kelley Coleman: Everything No One Tells You About Parenting a Disabled Child  

‌Today's conversation answers so many questions you're likely too afraid to ask.My guest today immediately makes uncomfortable topics comfortable, sensitive subjects approachable and speaks from so much experience, get ready to pull up a chair.Kelley Coleman is a feature film development executive turned author and advocate for parent caregivers and individuals with disabilities. Her book Everything No One Tells You About Parenting a Disabled Child: Your Guide to the Essential Systems, Services, and Supports  combines the wisdom of 40 experts and all sorts of cheat codes to save time in all the logistics of raising a disabled child,  including her own experience parenting a child with multiple disabilities.Disability remains such a taboo topic, and there is so much to learn from Kelley. She shares what parents of disabled children wish we knew, as well as speaking hope and validation directly to parents of disabled children.IN THIS EPISODE, WE COVERED...The most respectful terminology to useHow to handle when your child is curious and you don't know the first thing to sayAll the emotions that are normal to have when your child gets diagnosedDON'T MISS-Kelley pouring her heart out with ways to make your caregiver role sustainable while sharing validation and hope// CONNECT WITH KELLEY //Link to order the book: Everything No One Tells You About Parenting a Disabled Child: Your Guide to the Essential Systems, Services, and SupportsWebsite: www.kelleycoleman.comInstagram: @hellokelleycoleman// MENTIONED IN THE EPISODE //Emily Ladau: https://emilyladau.comTiffany Hammond, aka Fidgets and Fries: https://www.fidgetsandfries.coElspeth, aka Neurodivergent Parenting: Think Outside the Box: Neurodivergent Parenting: Think Outside The BoxI believe in you + I'm cheering you on.Come say hi!  I'm @parent_wholeheartedly on Insta.Apply to work together: parentingwholeheartedly.com/ApplySend us Fan Mail over Text.Failing Motherhood is turning 4 years old!Rate the podcast with 5 Stars on Spotify and/or Leave a Review for Failing Motherhood in Apple Podcasts, screenshot it before hitting SUBMIT, and send it to Danielle for a chance to win a $50 Amazon gift card!DM: @‌parent_wholeheartedlySupport the Show.*FREE* MASTERCLASS: Learn how to CONFIDENTLY parent your strong-willed child WITHOUT threats, bribes or giving in altogether so you can BREAK FREE of power struggles + guilt www.parentingwholeheartedly.com/unapologeticwww.parentingwholeheartedly.com

Welcome back to Voices of Your Village! I got to hang out with Kelley Coleman. She is the author of Everything No One Tells You About Parenting a Disabled Child. Kelley is a feature film development executive turned author and a passionate advocate for parents and caregivers and individuals with disabilities. She is the parent of two amazing boys, one of whom has multiple disabilities, and her book, Everything No One Tells You About Parenting a Disabled Child draws upon over a decade of advocacy with candor, humor, and relatability earned in her prior career of writing and developing talking animal movies. She was recently named best mom ever by her two discerning children and received a congratulatory mug. I had a blast hanging out and chatting with Kelley. There are a lot of nuances in the conversation and think that this is really key for all humans. Whether you are parenting a disabled child or not, there's so much learning for us all to do as a community about systems and support and the worth of every human on the planet. All right, folks, let's dive in.  Connect with Kelley: Instagram: @hellokelleycoleman Website: https://www.kelleycoleman.com/ Order the book: Everything No One Tells You About Parenting a Disabled Child: Your Guide to the Essential Systems, Services, and Supports  Connect with us: Instagram: @seed.and.sew  Podcast page: Voices of Your Village Seed and Sew's Regulation Quiz: Take the Quiz Order Tiny Humans, Big Emotions now!  Website: seedandsew.org Music by: Ruby Adams and Bensound This show is brought to you by BetterHelp. Learn more about your ad choices. Visit megaphone.fm/adchoices

Have you ever felt paralyzed by all the “stuff” involved in charting a path and advocating for your child? I'm sure I'm not the only one who's put off calling the insurance company or establishing a relationship with a new health care provider because at the time it felt too overwhelming and daunting. But what if there was a resource that provided everything parents and caregivers need to know about navigating all the complex, but critical, aspects of raising a neurodivergent child? How great would that be? I've got some good news for you! Today's guest, Kelley Coleman, has created that resource — it's her brand new book called Everything No One Tells You About Parenting a Disabled Child: Your Guide to the Essential Systems, Services, and Supports. Kelley's book draws upon over a decade of experience, including her own experience parenting a child with multiple disabilities. It's an honest, relatable, actionable roadmap to the practicalities of parenting a disabled child, featuring personal stories, expert interviews, and the foundational information parents need to know about topics including diagnosis, school, doctors, insurance, financial planning, disability rights, and what life looks like as a parent caregiver. In this conversation, Kelley, a feature film development executive turned author and advocate for parent caregivers and individuals with disabilities, shares so many insights from her book, including the difference between being a parent and being a caregiver, strategies for navigating Insurance, working with medical teams, and other daunting systems, future care planning, and so much more. Seriously, Kelley has created SUCH an incredible resource in this book, because she's researched, and mapped, and made simple and doable the key things and tools parents need to stop wasting unnecessary time, money, and stress as they navigate this journey. Enjoy the episode, and please share it with others who would benefit from Kelley's insight and positive approach so that they can spend less time filling out forms, and more time loving their children exactly as they are.   About Kelley Coleman Kelley Coleman is a feature film development executive turned author and advocate for parent caregivers and individuals with disabilities. Her book Everything No One Tells You About Parenting a Disabled Child: Your Guide to the Essential Systems, Services, and Supports draws upon over a decade of experience, including her own experience parenting a child with multiple disabilities. Kelley lives in Los Angeles with her husband, two boys, and her son's trusty service dog.   Things you'll learn from this episode What the difference is between parenting and caregiving and why it's an important distinction to make What some of the most common challenge nondisabled parents face embracing disability in their children Why it's critical that parents and caregivers have access to practical information (and why it's so hard to find) Strategies for navigating Insurance, working with medical teams, and other daunting systems Why financial planning is so important and how to get started The benefits of connecting with experts and disabled leaders in the disability community   Resources mentioned for Everything No One Tells You About Parenting a Disabled Child Kelley Coleman's website Everything No One Tells You About Parenting a Disabled Child: Your Guide to the Essential Systems, Services, and Supports by Kelley Coleman Kelley Coleman on Instagram Kelley Coleman on Facebook Emily Ladau's website Demystifying Disability: What to Know, What to Say, and How to be an Ally by Emily Ladau Activist Emily Ladau on Demystifying Disability (Tilt Parenting Podcast) Judy Heumann (disability rights activist) Rebecca Cokley (disability rights activist) After Revealing He Couldn't Read, Former Convict Is Inspiring Others on TikTok — Here's How (People Magazine article about Oliver James) Learn more about your ad choices. Visit megaphone.fm/adchoices

Kelley Coleman is a feature film development executive turned author and advocate for parent caregivers and individuals with disabilities. Her book Everything No One Tells You About Parenting a Disabled Child: Your Guide to the Essential Systems, Services, and Supports draws upon over a decade of experience, including her own experience parenting a child with multiple disabilities. Kelley lives in Los Angeles with her husband, two boys, and her son's trusty service dog.

In this episode, I have a candid interview with Kelley Coleman, author of Everything No One Tells You About Parenting a Disabled Child: Your Guide to the Essential Systems, Services, and Supports, which was released earlier this month. In this book, Kelley provides parents with a very precious resource - time back - by presenting templates, advice, and wisdom from her own experience and those of dozens of experts. In our conversation, Kelley shares candidly about her experience, with a sense of humor and ease, including the mental health impacts of parenting a child with disabilities and the importance of taking time for ones own well-being. You can learn more about Kelley and this resource on her website: https://www.kelleycoleman.com/books To learn more about me and my reproductive & integrative psychiatry clinic helping patients across California, please visit - AnnaGlezerMD.comTo sign up for the Fellowship in Reproductive & Integrative Psychiatry, please visit: PsychiatryFellowship.com

How can we get our disabled children the support to which they are entitled? How do we find the confidence that we're adequate enough to provide what they need? Kelley Coleman, parent of a disabled child and author of the new book EVERYTHING NO ONE TELLS YOU ABOUT PARENTING A DISABLED CHILD, provides practical advice and templates for navigating systems and accessing services. Kelley and Amy discuss: Kelley's personal story of parenting her disabled son and the challenges she's faced the frustrating experience of "reinventing the wheel" for each parent of a disabled child why the language of disability matters—and why it was the first thing Kelley had to learn why the best place to get real, practical information is often from other parents—until we become the informed parents Here's where you can find Kelley: https://www.kelleycoleman.com @hellokelleycoleman on IG Buy EVERYTHING NO ONE TELLS YOU ABOUT PARENTING A DISABLED CHILD: https://bookshop.org/a/12099/9780306831706 We love the sponsors that make this show possible! You can always find all the special deals and codes for all our current sponsors on our website: https://www.whatfreshhellpodcast.com/p/promo-codes/ mom friends, funny moms, parenting advice, parenting experts, parenting tips, mothers, families, parenting skills, parenting strategies, parenting styles, teenager, tween, child development, parent child relationship, default parent, child with disability, disabled child, parenting disabled child, parenting disability, special needs, disability protections, Learn more about your ad choices. Visit megaphone.fm/adchoices

Thanks for joining me today:) In this episode, Kelley Coleman and I are chatting about her new book - Everything No One Tells You About Parenting a Disabled Child. We are covering SO much goodness. Some of the topics we are covering are -  Parenting versus caregiving Resources Inclusivity Ableism Visible and non-visible disabilities Acceptance Finances Judgement Safe people and spaces Accommodations Supports and more! ❤️ Holly- The Mom/Psychologist Who Gets It CLICK HERE for Holly's ONE STOP RESOURCE - Social Success Guide, Behavior Guide, and MORE! Learn more about Holly's private practice in North Carolina Learn more about Holly's speaking services and courses Learn more about Kelley Get Kelley's book! ⭐️Join the Facebook Groups ➡️ Parents, Come on over and join the Autism ADHD Facebook Group for Parents ➡️ Professionals, Join the Facebook Group for Therapists and Educators

We're so excited to welcome feature film executive turned author and disability advocate, Kelley Coleman to the show! Her book Everything No One Tells You About Parenting a Disabled Child: Your Guide to the Essential Systems, Services, and Support releases TODAY!! Friends, this book is like gold, it provides the kind of support and confidence we all need to navigate and understand the complex systems, services, and supports no matter what diagnosis our kids have. It's a resource we'll be looking to for years to come, providing us with helpful questions, checklists, and ways to access services based on your child's individual needs. We celebrate finding friendship and community throughout the disability community, and Kelley shares how the Down syndrome community has embraced her and her son. She even shares how disability rights activist Judy Heumann shared her enthusiasm for a resource like Kelley's book and emphasized the importance of sharing stories as self-advocates and nondisabled advocates in the disability space. This is a book and conversation we're so grateful for, this is an episode you don't want to miss! --- SHOW NOTES Order Kelley's new book Everything No One Tells You About Parenting a Disabled Child: Your Guide to the Essential Systems, Services, and Support To learn more, visit https://www.kelleycoleman.com/  Follow Kelley on Instagram and Facebook Learn more about Judy Heumann's legacy JOIN THE MOVEMENT Join us in celebrating and supporting The Lucky Few Podcast! For just $0.99, $4.99, or $9.99 a month, you can help us continue shouting worth and shifting narratives for people with Down syndrome. Your support makes a difference in our ability to create meaningful content, enable us to cover production costs, and explore additional opportunities to expand our resources. Become an essential part of The Lucky Few movement today!  THANK YOU TO OUR SPONSOR: Thank you, Enable SNP for sponsoring this episode! 47. Planning for the Future w/Phillip Clark from Enable SNP 191. Future Planning for the WHOLE Family - ft. Phillip Clark, Enable SNP DISCOUNT CODE Friends, grab your narrative shifting gear over on The Lucky Few Merch Shop and use code PODCAST for 10% off! HELP US SHIFT THE NARRATIVE Interested in partnering with The Lucky Few Podcast as a sponsor? Email hello@theluckyfewpodcast.com for more information! LET'S CHAT Email hello@theluckyfewpodcast.com with your questions and Good News for future episodes. --- Send in a voice message: https://podcasters.spotify.com/pod/show/theluckyfewpod/message Support this podcast: https://podcasters.spotify.com/pod/show/theluckyfewpod/support

Hey Friends~  If you have a child with a disability, you no doubt have questions about how to navigate the systems & services so that you have the support you need! It can be overwhelming!   Today's guest has walked this journey with her son.  And.. She  wrote a book on the topic so YOU won't have to struggle as she did.   Kelley Coleman has walked this journey and is here to help!     Always cheering you on!  Dinalynn   CONTACT the Host, Dinalynn:  hello@thelanguageofplay.com ABOUT THE GUEST-  Kelley Coleman is a feature film development executive turned author and advocate for parent caregivers and individuals with disabilities. Her book Everything No One Tells You About Parenting a Disabled Child: Your Guide to the Essential Systems, Services, and Supports draws upon over a decade of experience, including her own experience parenting a child with multiple disabilities. Kelley lives in Los Angeles with her husband, two boys, and her son's trusty service dog.  CONTACT THE GUEST -  www.kelleycoleman.com IG: @hellokelleycoleman Preorder the book on Amazon: https://www.amazon.com/Everything-Tells-About-Parenting-Disabled/dp/0306831708/   RESOURCES from The Language Of Play Sign up for my newsletter! Newsletter Opt-in Sign up for FREE 21 Days of Encouragement in your inbox! Encouragement Sign-up Join my new FREE Facebook Community HERE! Sign up for a 15 min "Let's Meet Session" on zoom!  Let's Meet Session For Speaking Engagements or For 1:1 or Group Parent Coaching (virtual or live), contact me at hello@thelanguageofplay.com   If You Liked This Episode, You Will Want To Listen To These Episodes:  51 LaDawn Hickman: Successfully Teaching Communication in the Messy with Autism 55 Sarah Brumley on Simultaneously Navigating Reactive Attachment Disorder and Autism Spectrum Disorder with her adopted children 87 Lynn Greenberg:  Is Dyslexia Your Superpower?  Find Out How! 89 Kimberly Gawne: Alternative Education is an Option. How Do You Know The Best Educational Model For Your Child? 117 April Rehrig: On Being The Best Advocate For Your Child In The Special Education Process. What You Need To Know!  

This week, Rachel interviews Kelley Coleman, speaker, author, and advocate! Kelley talks about her family's AAC journey and her role as the mother of Aaron, a complex communicator in the 4th grade who uses AAC to communicate. She shares about her new book, Everything No One Tells You About Parenting a Disabled Child, as well as some of the high- and lowlights of her family's AAC journey, including when Aaron's school SLP suggested he go from high-tech AAC to a picture flip book!   Before the interview, Rachel shares about turning a client's questions about her microphone into a naturally occurring communication opportunity about podcasting - that also supported his independence!   Key ideas this week:  

Raising a child with a disability can be challenging. So, we invited Kelley Coleman for an eye-opening conversation on the challenges of parenting kids with disabilities and practical ways to support these families. Ditch the pity party and be empowered to create a fulfilling life for children with special needs by tapping in!     Key takeaways to listen for: A major fear in parenting children with disabilities Why breaking isolation for kids with special needs matters Powerful ways to balance the needs of your children Common challenges in raising a child with a disability Actionable steps to support parents of children with special needs     Resources  Everything No One Tells You About Parenting a Disabled Child by Kelley Coleman | Kindle and Paperback   Do you want to create a legendary family life like Jim and Jamie? Go to www.JJPlaybook.com to schedule a call with a sales counselor and download your own copy of their book, Passive Income Playbook, so you never have to choose between work and family ever again!   It's time to rediscover and deepen your connection with your loved ones! Spend time with Jim and Jamie's family while strengthening the connection with yours in the Blue Zone paradise of Nosara, Costa Rica, on June 20-22, 2024. Reserve your retreat spot at 18summers.com/retreat to join us in enjoying good food, sun-kissed beaches, and precious family moments that will last for a lifetime!     About Kelley Coleman Kelley is a feature film development executive turned author and advocate for parents, caregivers, and individuals with disabilities. Her writing and advocacy draw upon over a decade of experience accessing the necessary support for children with disabilities to succeed, including her own child. She lives in Los Angeles with her husband, two boys, and her son's trusty service dog.     Connect with Kelley Website: Kelley Coleman Facebook: Kelley Coleman  Instagram: @hellokelleycoleman     Connect with Us To learn more about us, visit our website at www.18summers.com or email us at info@18summers.com. To get a copy of our book “The Family Board Meeting”, click here.   Subscribe to 18 Summers Podcast and leave a rating and written review!     Social Media Channels Facebook Group: 18 Summers LinkedIn: Jimmy Sheils Instagram: @18summerstribe

We can't wait to dive in with our guest today, Kelley Coleman, author of “Everything No One Tells You About Parenting a Disabled Child”. No joke, this is one of the best books on autism and parenting disabled kids we've ever read! We talk about the book and venture into other topics including:  The “Go Home, Google, and Cry” method isn't the only option anymore Invisible vs. NOT visible vs. visible disabilities. Say that three times fast. The cost of “Cognitive Labor”, this is a big one “Parent” and “Caregiver” are two different jobs. You didn't know you were doubly employed, did you? Best takeaway: Find a place for a victory, no matter how small. It makes a difference! Buy Kelley's book: Everything No One Tells You About Parenting a Disabled Child It's going to be available as an audiobook too, read by Kelley! Kelley's Instagram Kelley's Website

Hello Brave Friends! On this story episode, #166, we are stepping into the shoes of a brand new care-giving parent, who, like so many of us, left the hospital and was immediately faced with piles of paperwork, prescriptions to administer, insurance issues, medical supplies to order and the endless phone calls, transfers and holds that become our JOB to navigate.Kelley Coleman had a new baby with multiple disabilities, a toddler, and was getting no calls back from the Regional Center. So, on one particularly rainy day, she took matters into her own hands and started her journey towards figuring it out, for all of us! Welcome to today's story episode: Crying on the Steps of the Regional CenterAuthor and advocate Kelley Coleman is the parent of two amazing boys, one of whom has multiple disabilities. Her book Everything No One Tells You About Parenting a Disabled Child draws upon over a decade of advocacy, with the candor, humor, and relatability earned in her prior career of writing and developing talking animal movies. She was recently named Best Mom Ever by her two discerning children and received a congratulatory mug.Find Kelley Coleman's Website here.Find Kelley Coleman's Book here.Brave Together is the podcast for We are Brave Together, a not-for-profit organization based in the USA. The heart of We Are Brave Together is to strengthen, encourage, inspire and validate all moms of children with disabilities and other needs in their unique journeys. JOIN the international community of We Are Brave Together here.Donate to our Retreats and Respite Scholarships here.Donate to keep this podcast going here.Can't get enough of the Brave Together Podcast?Follow our Instagram Page @wearebravetogether or on Facebook.Feel free to contact Jessica Patay via email: jpatay@wearebravetogether.orgIf you have any topic requests or if you would like to share a story, leave us a message here.Please leave a review and rating today! We thank you in advance!Disclaimer

On this new episode Dr. Dan and guest Kelley Coleman discuss disability and her must-read book Everything No One Tells You About Parenting a Disabled Child: Your Guide to the Essential Systems, Services, and Supports. According to the CDC, “Every 4 ½ minutes a baby is born with a birth defect in the United States.” That's 1 in 33. Dr. Dan and Kelley talk about how to navigate the practicalities of parenting a disabled child including diagnosis, school, doctors, insurance, financial planning, disability rights, and what life looks like as a parent caregiver. With over a decade of experience navigating these systems for her own child, author Kelley Coleman helps parents of disabled children feel less overwhelmed. Kelley Coleman is a feature film development executive turned author and disability advocate. Her book stems from her own parenting experience – giving parents the tools to spend less time navigating the challenging stuff and more time just loving their kids exactly as they are. Kelley lives in Los Angeles with her husband, two children, and her son's trusty service dog. For more information visit www.kelleycoleman.com. Email your parenting questions to Dr. Dan podcast@drdanpeters.com (we might answer on a future episode). Follow us @parentfootprintpodcast (Instagram, Facebook) and @drdanpeters (X). Please listen, follow, rate, and review on Apple Podcasts, Spotify, or wherever you listen to podcasts. For more information: www.exactlyrightmedia.com www.drdanpeters.com Learn more about your ad choices. Visit megaphone.fm/adchoices

Gypsy Rose Why Were Men 'Attracted' To What Appeared to Be A Disabled Child In a recent episode of the "Hidden Killers" podcast, hosts Tony Brueski and retired FBI Special Agent Robin Dreeke delve into the complex and controversial life of Gypsy Rose Blanchard. Blanchard, who has recently been released from prison and is the subject of a new Lifetime docu-series, has become a focal point of public attention. Her story, marked by severe child abuse and a high-profile legal case, raises profound questions about the nature of victimhood, love, and the search for normalcy under extraordinary circumstances.    Brueski expresses his unease about Blanchard's situation, particularly her decision to marry while in prison. "There's just so many points on this that just hit the creepy ick factor with me," he says, reflecting a sentiment shared by many who have followed Blanchard's journey. Dreeke, with his background in behavioral analysis, offers insights into the psychological aspects of such relationships, noting the unusual nature of Blanchard's husband's attraction to her, given her portrayal as a special needs child.    The podcast explores the complexities of Blanchard's psychological state, her husband's motivations, and the broader societal implications of their relationship. "I'm glad the school fired him," Brueski remarks, referring to Blanchard's husband, a former special education teacher who lost his job due to his involvement with her. Dreeke agrees, highlighting the deviation from standard normal behavior in this case.    The conversation also touches on the broader theme of seeking redemption and healing through relationships. "Recognize unhealthy behaviors. You know what to avoid," Dreeke advises, emphasizing the importance of cautious optimism in such situations. The hosts discuss the role of Blanchard's family, who were not supportive of the marriage, and the influence of external factors like media attention on her decisions.    Brueski and Dreeke draw parallels between Blanchard's case and other high-profile cases, noting the potential for manipulation and exploitation by the media. "How much of it was producers sitting there going, 'You deserve love, Gypsy,'" Brueski wonders, questioning the authenticity of the narrative being presented to the public.    The hosts express hope that Blanchard's family will provide the necessary support and guidance as she navigates her new life outside prison. "Hopefully, they're close enough in their relationship to set guardrails around her," Dreeke says, highlighting the importance of maintaining open communication and trust.    As the episode concludes, the hosts leave the audience with a lingering question: Can Gypsy Rose Blanchard find true healing and stability in her life, or is her search for love and normalcy a prelude to more tragedy? Blanchard's story continues to challenge our perceptions of love, justice, and redemption, compelling us to ponder the complexities of the human heart and the paths it chooses to follow. Want to listen to ALL of our podcasts AD-FREE? Subscribe through APPLE PODCASTS, and try it for three days free: https://tinyurl.com/ycw626tj Follow Our Other Cases: https://www.truecrimetodaypod.com The latest on Catching the Long Island Serial Killer, Awaiting Admission: BTK's Unconfessed Crimes, Delphi Murders: Inside the Crime, Chad & Lori Daybell, The Murder of Ana Walshe, Alex Murdaugh, Bryan Kohberger, Lucy Letby, Kouri Richins, Malevolent Mormon Mommys, Justice for Harmony Montgomery, The Murder of Stephen Smith, The Murder of Madeline Kingsbury, and much more! Listen at https://www.truecrimetodaypod.com

Gypsy Rose Why Were Men 'Attracted' To What Appeared to Be A Disabled Child In a recent episode of the "Hidden Killers" podcast, hosts Tony Brueski and retired FBI Special Agent Robin Dreeke delve into the complex and controversial life of Gypsy Rose Blanchard. Blanchard, who has recently been released from prison and is the subject of a new Lifetime docu-series, has become a focal point of public attention. Her story, marked by severe child abuse and a high-profile legal case, raises profound questions about the nature of victimhood, love, and the search for normalcy under extraordinary circumstances.    Brueski expresses his unease about Blanchard's situation, particularly her decision to marry while in prison. "There's just so many points on this that just hit the creepy ick factor with me," he says, reflecting a sentiment shared by many who have followed Blanchard's journey. Dreeke, with his background in behavioral analysis, offers insights into the psychological aspects of such relationships, noting the unusual nature of Blanchard's husband's attraction to her, given her portrayal as a special needs child.    The podcast explores the complexities of Blanchard's psychological state, her husband's motivations, and the broader societal implications of their relationship. "I'm glad the school fired him," Brueski remarks, referring to Blanchard's husband, a former special education teacher who lost his job due to his involvement with her. Dreeke agrees, highlighting the deviation from standard normal behavior in this case.    The conversation also touches on the broader theme of seeking redemption and healing through relationships. "Recognize unhealthy behaviors. You know what to avoid," Dreeke advises, emphasizing the importance of cautious optimism in such situations. The hosts discuss the role of Blanchard's family, who were not supportive of the marriage, and the influence of external factors like media attention on her decisions.    Brueski and Dreeke draw parallels between Blanchard's case and other high-profile cases, noting the potential for manipulation and exploitation by the media. "How much of it was producers sitting there going, 'You deserve love, Gypsy,'" Brueski wonders, questioning the authenticity of the narrative being presented to the public.    The hosts express hope that Blanchard's family will provide the necessary support and guidance as she navigates her new life outside prison. "Hopefully, they're close enough in their relationship to set guardrails around her," Dreeke says, highlighting the importance of maintaining open communication and trust.    As the episode concludes, the hosts leave the audience with a lingering question: Can Gypsy Rose Blanchard find true healing and stability in her life, or is her search for love and normalcy a prelude to more tragedy? Blanchard's story continues to challenge our perceptions of love, justice, and redemption, compelling us to ponder the complexities of the human heart and the paths it chooses to follow. Want to listen to ALL of our podcasts AD-FREE? Subscribe through APPLE PODCASTS, and try it for three days free: https://tinyurl.com/ycw626tj Follow Our Other Cases: https://www.truecrimetodaypod.com The latest on Catching the Long Island Serial Killer, Awaiting Admission: BTK's Unconfessed Crimes, Delphi Murders: Inside the Crime, Chad & Lori Daybell, The Murder of Ana Walshe, Alex Murdaugh, Bryan Kohberger, Lucy Letby, Kouri Richins, Malevolent Mormon Mommys, Justice for Harmony Montgomery, The Murder of Stephen Smith, The Murder of Madeline Kingsbury, and much more! Listen at https://www.truecrimetodaypod.com