• “A Life of Significance as Caregivers” with Marcus & Jen Jones
    2026/02/02
    Family. Series: “A Life of Significance as Caregivers” with Marcus & Jen Jones Thanks for joining us today as we begin our Family Series with Marcus and Jen Jones. We first met Marcus and Jen a few years ago when I saw an Instagram video of their family dancing and reached out knowing that we had mutual friends. Then last year we had the privilege of having them come and speak to our couples at Date Night. And now Ladies, I’m excited to share that Jen will be a speaker at our Moms Day Out conference this May 1-3. Marcus and Jen have been married for 25 years and have 4 children. Their oldest daughter has a diagnosis of Down Syndrome. They are authors, speakers, and entrepreneurs having founded, led and successfully grown both non-profit and for-profit organizations, with their latest endeavor being the co founding of the Significant Life Foundation in 2024 to advocate for adults with intellectual disabilities. Marcus is a pastor and leader with over 30 years of ministry experience and he is currently working as the Executive Director of the HIS EYES Foundation to combat homelessness. Jen is the founder and CEO of Jen Jones Direct LLC, and creative architect of the Significant Conference. She is also a certified health coach, having built a nationwide health and wellness business. Together Marcus and Jen know what it’s like to experience the unexpected and have to grow through life’s greatest challenges. This is an honest and beautiful conversation – one we know will resonate with you. So, Let’s Ilsten in to our conversation Marcus and Jen Jones. Bios: Marcus is a pastor, leader, creator and communicator with over 30 years of ministry experience. He is a long-time advocate for adults with intellectual disabilities and father of four, including her oldest daughter with Down Syndrome. He has written multiple books, including “The Five-Minute Marriage Mentor,” and “Holding Hands with Grace,” all about his journey of fatherhood with a child with intellectual disabilities. He founded “The Significant Life Foundation,” in 2024 to advance the cause of independent housing, employment and community for the intellectually disabled community. He serves on multiple non-profit boards and is the Executive Director of the HIS EYES Foundation to combat homelessness. Married over 25 years to his wife, Jen, Marcus enjoys traveling, Golfing and undiscovered cafes and cuisine. Jen Jones is the founder and CEO of Jen Jones Direct LLC, and creative architect of the Significant Conference. Through her books, courses, conferences, podcast and Significant Life groups, she equips and empowers women to create the life they love on the foundation of faith. Jen and her husband Marcus are living this great adventure with their four children in San Diego, California. Jen knows what it’s like to experience the unexpected and have to grow through life’s greatest challenges. She advocates for differently-abled kids and their parents because she is mom to a daughter with Down Syndrome. She helps families identify their core values and champions women to know and own their God-given worth to live a life of significance. She is a certified health coach, and has built a nationwide health and wellness business. She guides people on a path to help them take control of their health—mentally, physically and spiritually. She is in the personal transformation business. Jen has appeared as a speaker and coach in numerous conferences, retreats and podcasts, including ABC Family and the Live Out Loud Show. She is also the author of Thrive: Growing Through Life’s Greatest Challenges, Tribe: Building Your Family on What Matters Most, and The Five-Minute Marriage Mentor. https://significantlifefoundation.org/ jen@jenjonesdirect.com @jenjonesx4 https://jenandmarcusjones.com/marcus/ https://jenandmarcusjones.com/jen/ facebook.com/jonestribe For a family raising a child with special needs, life can be difficult. There are many storms to weather and struggles to address, and we often feel isolated and alone due to the nature of our circumstances. Families have a need to connect and find resources, a need to be encouraged, and a need for hope as we walk down what can be a very hard road at times. Hope on the Hard Road Special Needs Podcast was created for this purpose. Our vision is to grow a thriving community, where families with children of all ages with special needs can feel connected, be encouraged, and find hope for the road ahead. Connect with Us: If you enjoy this podcast please share us with others and be sure to follow us so won’t miss an episode. We’d love to hear from you so please leave us a comment or rating and connect with us on social media or on our website. Email us: info@hopeonthehardroad.org Website: https://hopeonthehardroad.org/ Instagram: https://www.instagram.com/hopeonthehardroad/ Facebook: https://www.facebook.com/hopeonthehardroad/ Facebook Group: https://...
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    46 分
  • "The Life of a Medical Caregiver" with Kara Ryska
    2026/01/19

    "The Life of a Medical Caregiver" with Kara Ryska

    Hey guys, Thanks for joining us today! We’re continuing on in our Medical Family Series with guest Kara Ryska, host of The Special Needs Mom Podcast. As a devoted mother of four, ranging from ages 7 to 17, Kara's life has been shaped by her role as a mother of a multiple brain tumor survivor and a child with diverse disabilities, encompassing physical, visual, behavioral, and medical challenges.

    Driven by her personal experiences, Kara has become an advocate for families facing similar hurdles, offering support through her role as a life coach. Kara’s resilience is inspiring and you’re absolutely gonna want to listen in or watch today’s episode.

    Bio

    Meet Kara Ryska, a compassionate and resilient force empowering families through her impactful journey as the host of The Special Needs Mom Podcast. As a devoted mother of four, ranging from ages 7 to 17, Kara's life has been shaped by her roles as a mother of a multiple brain tumor survivor and a child with diverse disabilities, encompassing physical, visual, behavioral, and medical challenges.

    Driven by her personal experiences, Kara has become an advocate for families facing similar hurdles, offering support through her role as a life coach. Her commitment extends beyond the microphone as the creator of "Pathway to Peace," a transformative group coaching community that has touched and changed countless lives. Kara's resilience and wisdom make her a sought-after speaker, sharing her insights on navigating the complexities of parenting children with special needs.

    Kara brings together strength and empathy, fostering a sense of unity among families navigating similar paths. Her dedication to creating a space of understanding and hope resonates in every episode of her podcast and within the transformative impact of her coaching programs. Kara Ryska is not just a podcast host; she is a beacon of inspiration, guiding others towards a life filled with purpose and peace.

    Contacts

    www.kararyska.com

    IG: https://www.instagram.com/thespecialneedsmompodcast/

    Podcast: https://podcasts.apple.com/us/podcast/the-special-needs-mom-podcast/id1523926612

    For a family raising a child with special needs, life can be difficult. There are many storms to weather and struggles to address, and we often feel isolated and alone due to the nature of our circumstances. Families have a need to connect and find resources, a need to be encouraged, and a need for hope as we walk down what can be a very hard road at times. Hope on the Hard Road Special Needs Podcast was created for this purpose. Our vision is to grow a thriving community, where families with children of all ages with special needs can feel connected, be encouraged, and find hope for the road ahead.

    Connect with Us:

    If you enjoy this podcast please share us with others and be sure to follow us so won’t miss an episode. We’d love to hear from you so please leave us a comment or rating and connect with us on social media or on our website.

    Email us: info@hopeonthehardroad.org

    Website: https://hopeonthehardroad.org/

    Instagram: https://www.instagram.com/hopeonthehardroad/

    Facebook: https://www.facebook.com/hopeonthehardroad/

    Facebook Group: https://www.facebook.com/groups/2621447987943459

    Free Youtube Resource Library: https://www.youtube.com/playlist?list=PLsSAfvTkSy87X-fEqtVR2qvo7w9UQBuxz

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    40 分
  • A Family’s Courageous Journey“ with Steve and Melissa Bundy
    2026/01/05

    Medical Family Series:

    “A Family’s Courageous Journey” with Steve and Melissa Bundy

    Intro:

    Today we begin our medical family series and you are about to be inspired by one family’s story.

    Steve and Melissa Bundy have been married for 33 years and have two adult sons. Their oldest son Caleb was born with a rare chromosome deletion and subsequent multiple medical diagnoses.

    Steve is the Senior vice president of International ministries at Joni and Friends International Disability Center and has been on staff for past 18 years. And Melissa is a part time wound care home health nurse. This incredible couple sat down with us to share their story. A courageous story where heartache is met with hope.

    Let’s listen into our conversation with Steve and Melissa.

    Bio:

    Steve and Melissa Bundy have been married for 33 years and have two incredible adults sons. Steve is the Senior vice president of International ministries at Joni and Friends International Disability Center and has been on staff for past 18 years. Melissa is a part time wound care home health nurse.

    Their 26 year old son Caleb was born with a rare chromosome deletion 2q37.1 partial terminal deletion. This missing piece of the chromosome means he has severe cognition delay, severe autism (unable to speak), apraxia of speech and body, and also a rare form of muscular dystrophy called Bethlem/Ulrich. They were given this diagnosis of the chromosome deletion at ages 10 months, autism at 2 years and muscular dystrophy when he was 12. Caleb has had a very difficult journey in life yet has had a family who has surrounded him with the love, support and advocacy he needed to be as functional and loved for who he is as much as possible.

    Caleb’s younger brother Jaron is 22 years old and has been such a huge supportive sibling even in the most challenging of times. Jaron graduated this past year from Belmont University in Nashville, TN with a degree in music production and now has his own business producing music and teaching students in guitar,piano and music production at jaronmicahmusic.com.

    Joniandfriends.org

    For a family raising a child with special needs, life can be difficult. There are many storms to weather and struggles to address, and we often feel isolated and alone due to the nature of our circumstances. Families have a need to connect and find resources, a need to be encouraged, and a need for hope as we walk down what can be a very hard road at times. Hope on the Hard Road Special Needs Podcast was created for this purpose. Our vision is to grow a thriving community, where families with children of all ages with special needs can feel connected, be encouraged, and find hope for the road ahead.

    Connect with Us:

    If you enjoy this podcast please share us with others and be sure to follow us so won’t miss an episode. We’d love to hear from you so please leave us a comment or rating and connect with us on social media or on our website.

    Email us: info@hopeonthehardroad.org

    Website: https://hopeonthehardroad.org/

    Instagram: https://www.instagram.com/hopeonthehardroad/

    Facebook: https://www.facebook.com/hopeonthehardroad/

    Facebook Group: https://www.facebook.com/groups/2621447987943459

    Free Youtube Resource Library: https://www.youtube.com/playlist?list=PLsSAfvTkSy87X-fEqtVR2qvo7w9UQBuxz

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    46 分
  • "Season Highlights & Happy Holidays" with Eric and Christen
    2025/12/15

    "Season Highlights & Happy Holidays" with Eric and Christen

    Hey everybody Merry Christmas and Happy Holidays!

    This season has had so many incredible episodes and there are so many more to come in the New Year!

    Lets take a moment and listen in to some of the highlights. And don’t forget you can always get caught up on the episodes you’ve missed over the holidays. Find us where ever you listen to your podcasts or watch us on our YouTube Channel at Hope on the Hard Road

    See you back here in the New Year!

    Amanda Owen www.piecesofme.org www.puzzle-pieces.org @piecesofmebyamanda

    Joel & Debbie Pearlman www.daniplan.com https://www.facebook.com/MyDaniPlan/ https://www.instagram.com/mydaniplan/

    Heather Avis @heatheravis @theluckyfewofficial heatheravis.com

    Kelly and Pamela Schlenz www.idyllwildpines.org autisticallyinclined.com @adventureswithnaiyagrace @Idyllwildpines

    J Brad and Paulette Britton @RealWordsWithSam www.realwordswithsam.com jbradbritton@gmail.com

    Dawnmarie Gaivin www.spellers.com www.spellersfreedomfoundation.org. dawnmarie@spellers.com www.underestimated.tv @spellers_freedomfoundation @spellers__ https://www.facebook.com/groups/spellerscommunity https://www.facebook.com/spellersfreedomfoundation https://www.facebook.com/spellersrev

    For a family raising a child with special needs, life can be difficult. There are many storms to weather and struggles to address, and we often feel isolated and alone due to the nature of our circumstances. Families have a need to connect and find resources, a need to be encouraged, and a need for hope as we walk down what can be a very hard road at times. Hope on the Hard Road Special Needs Podcast was created for this purpose. Our vision is to grow a thriving community, where families with children of all ages with special needs can feel connected, be encouraged, and find hope for the road ahead.

    Connect with Us: If you enjoy this podcast please share us with others and be sure to follow us so won’t miss an episode. We’d love to hear from you so please leave us a comment or rating and connect with us on social media or on our website.

    Email us: info@hopeonthehardroad.org Website: https://hopeonthehardroad.org/ Instagram: https://www.instagram.com/hopeonthehardroad/ Facebook: https://www.facebook.com/hopeonthehardroad/ Facebook Group: https://www.facebook.com/groups/2621447987943459 Free Youtube Resource Library: https://www.youtube.com/playlist?list=PLsSAfvTkSy87X-fEqtVR2qvo7w9UQBuxz

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    7 分
  • “The Spellers Method” with Dawnmarie Gaivin
    2025/12/01
    Spellers Series: “The Spellers Method” with Dawnmarie Gaivin Dawnmarie Gaivin, is the cofounder of Spellers MethodTM and the Executive Director of Spellers Freedom Foundation. A former trauma and transplant nurse who spent more than a decade working in prestigious teaching hospitals in Boston and San Francisco, when she became a mother in 2003, her life took an unexpected turn. By 2006, both of her children had been diagnosed with nonspeaking autism. Driven by an unwavering commitment to help her boys find their voices, Dawnmarie transformed her career. She became an assistive technology specialist and a DIR/Floortime® provider, ultimately founding Spellers Center - San Diego in 2017 and co-founding the revolutionary Spellers Method. Featured in the SPELLERS documentary, her impact has rippled far beyond her own family. Let’s listen in as Dawnmarie shares her story. Bio: Dawnmarie Gaivin, RN, AT-ACP, is a former trauma and transplant nurse who spent more than a decade working in prestigious teaching hospitals in Boston and San Francisco. When she became a mother in 2003, her life took an unexpected turn - by 2006, both of her children had been diagnosed with nonspeaking autism. Driven by an unwavering commitment to help her boys find their voices, Dawnmarie transformed her career. She became an assistive technology specialist and a DIR/Floortime® provider, ultimately founding Spellers Center - San Diego in 2017 and co-founding the revolutionary Spellers MethodTM. Her impact rippled far beyond her own family. In March 2021, speller Jamison Handley and his father JB chronicled their transformative journey with Dawnmarie in their book Underestimated, revealing how spelling opened entirely new pathways to communication. The movement continued to gain momentum. In 2023, the documentary SPELLERS was released, powerfully demonstrating how spelling and typing as AAC methodologies have liberated countless nonspeakers from lives of silence. This was followed in 2024 by Underestimated.tv, which illuminated more profound journeys of nonspeakers after they gained access to open communication. Today, as Executive Director of Spellers Freedom Foundation - a 501(c)(3) public charity - Dawnmarie has expanded her reach far beyond San Diego. The foundation empowers every speller to flourish through access to communication, community-building, and scholarships. She remains equally passionate about ensuring students with alternative communication needs receive age-appropriate curriculum throughout their lifespans, a commitment that has inspired her to pursue a master's degree in educational leadership. What drives her is a life mission that’s as clear as it is urgent: to dismantle the long-rooted paradigms that prevent nonspeakers from living their fullest, most inclusive lives possible - not just in one community, but everywhere. You can learn more about her work at www.spellers.com and www.spellersfreedomfoundation.org. dawnmarie@spellers.com www.spellersfreedomfoundation.org https://www.spellersfreedomfoundation.org/how-to-help www.spellers.com www.underestimated.tv Instagram: @spellers_freedomfoundation @spellers__ Facebook: https://www.facebook.com/groups/spellerscommunity/ https://www.facebook.com/spellersfreedomfoundation https://www.facebook.com/spellersrev The Spellers Guidebook on Amazon: https://a.co/d/2m3pcXf Underestimated on Amazon: https://a.co/d/iWOZQZg Spellers the Movie: https://www.spellersfreedomfoundation.org/spellers-the-movie For a family raising a child with special needs, life can be difficult. There are many storms to weather and struggles to address, and we often feel isolated and alone due to the nature of our circumstances. Families have a need to connect and find resources, a need to be encouraged, and a need for hope as we walk down what can be a very hard road at times. Hope on the Hard Road Special Needs Podcast was created for this purpose. Our vision is to grow a thriving community, where families with children of all ages with special needs can feel connected, be encouraged, and find hope for the road ahead. Connect with Us: If you enjoy this podcast please share us with others and be sure to follow us so won’t miss an episode. We’d love to hear from you so please leave us a comment or rating and connect with us on social media or on our website. Email us: info@hopeonthehardroad.org Website: https://hopeonthehardroad.org/ Instagram: https://www.instagram.com/hopeonthehardroad/ Facebook: https://www.facebook.com/hopeonthehardroad/ Facebook Group: https://www.facebook.com/groups/2621447987943459 Free Youtube Resource Library: https://www.youtube.com/playlist?list=PLsSAfvTkSy87X-fEqtVR2qvo7w9UQBuxz
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    39 分
  • “Finding Their Voice: A Family’s Journey with Spelling” with J Brad and Paulette Britton
    2025/11/17

    Spellers Series:

    “Finding Their Voice: A Family’s Journey with Spelling” with J Brad and Paulette Britton

    Today we continue our Spellers Series and are joined by Paulette and J Brad Britton. Paulette and J Brad have a 24-year-old autistic son with apraxia, named Sam. For years, his intelligence and humor were missed. That changed when he began using spelled communication to share his thoughts.

    Paulette has spent years connecting cutting-edge autism research with the families who need it. J Brad, a leadership mentor and business executive, brings a father’s honest reflection to the conversation. He talks openly about what it means to lead, learn, and show up when your child’s needs don’t follow the rulebook.

    Together, Paulette and J Brad have become thoughtful voices on “presuming competence”, advocating with compassion, and holding on to hope on the hard road.

    Their story is featured in the upcoming book Real Words with Sam, which includes Sam’s own writing—his ideas, his humor, his voice. Let’s Listen in as we hear Paulette and J Brad’s Story

    Bio:

    Paulette and J Brad Britton are the parents of Sam, a 24-year-old autistic man with apraxia. For years, his intelligence and humor were missed. That changed when he began using spelled communication to share his thoughts. Paulette has spent years connecting cutting-edge autism research with the families who need it. J Brad, a leadership mentor and business executive, brings a father’s honest reflection to the conversation. He talks openly about what it means to lead, learn, and show up when your child’s needs don’t follow the rulebook. Together, Paulette and J Brad have become thoughtful voices on presuming competence, advocating with compassion, and holding on to hope on the hard road. Their story is featured in the upcoming book Real Words with Sam, which includes Sam’s own writing—his ideas, his humor, his voice. The book invites readers to see through a different lens and reconsider communication, connection, and belief.

    Insta and Facebook: RealWordsWithSam www.realwordswithsam.com

    jbradbritton@gmail.com

    For a family raising a child with special needs, life can be difficult. There are many storms to weather and struggles to address, and we often feel isolated and alone due to the nature of our circumstances. Families have a need to connect and find resources, a need to be encouraged, and a need for hope as we walk down what can be a very hard road at times. Hope on the Hard Road Special Needs Podcast was created for this purpose. Our vision is to grow a thriving community, where families with children of all ages with special needs can feel connected, be encouraged, and find hope for the road ahead.

    Connect with Us:

    If you enjoy this podcast please share us with others and be sure to follow us so won’t miss an episode. We’d love to hear from you so please leave us a comment or rating and connect with us on social media or on our website.

    Email us: info@hopeonthehardroad.org

    Website: https://hopeonthehardroad.org/

    Instagram: https://www.instagram.com/hopeonthehardroad/

    Facebook: https://www.facebook.com/hopeonthehardroad/

    Facebook Group: https://www.facebook.com/groups/2621447987943459

    Free Youtube Resource Library: https://www.youtube.com/playlist?list=PLsSAfvTkSy87X-fEqtVR2qvo7w9UQBuxz

    Disclaimer: The views and opinions expressed by guests on this podcast are their own and do not necessarily reflect those of Hope on the Hard Road, Inc. This podcast is for informational purposes only and is not intended as professional, medical, or legal advice.

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    43 分
  • “Spelling Adventures and Advocacy” with Kelly and Pamela Schlenz
    2025/11/03

    Spellers Series:

    “Spelling Adventures and Advocacy” with Kelly and Pamela Schlenz

    Hey guys, we’re excited you’re joining us for this episode! Today we begin our Spellers Series, highlighting this incredible form of communication. You won’t want to miss this informative and heartwarming series this month!

    Kelly Schlenz is the Executive Director of Idyllwild Pines, a retreat and camp center nestled in the San Jacinto Mountains of Southern California. Along with his wife, Pamela, Kelly has dedicated his life to creating spaces where individuals and families can connect, grow, and find hope.

    Inspired by their daughter, Naiya, who communicates through spelling, the Schlenz family has become passionate advocates for the spelling community. At Idyllwild Pines, Kelly and Pamela host specialized camps for spellers and their families, offering opportunities for connection, inclusion, and empowerment in a beautiful, supportive environment. Their leadership reflects their deep faith, family values, and commitment to building a world where every voice can be heard and celebrated.

    Bio:

    Kelly serves as the Executive Director at Idyllwild Pines Camp and Conference Center, where he brings leadership, vision, and a heart for community. He sees camp ministry as a powerful way to share the hope of Christ, build meaningful relationships, and create space for spiritual growth in the lives of others. Pamela is a devoted homeschool mom of three, passionate about nurturing both faith and education at home. Inspired by their own journey with their 15-year-old minimally speaking daughter, Kelly and Pamela partnered with Autistically Inclined to create Spellers Family Camps—transformative retreats designed to support and empower families of nonspeaking, minimally speaking, and unreliably speaking individuals by providing connection, community, and practical support with multimodal communication. Their mission is rooted in faith, compassion, inclusion and lived experience. When they're not hosting camps or homeschooling, you can find them enjoying mountain life with their three kids, two dogs and tending to their flock of 17 chickens.

    www.idyllwildpines.org

    autisticallyinclined.com

    Instagram:

    @adventureswithnaiyagrace

    @Idyllwildpines

    For a family raising a child with special needs, life can be difficult. There are many storms to weather and struggles to address, and we often feel isolated and alone due to the nature of our circumstances. Families have a need to connect and find resources, a need to be encouraged, and a need for hope as we walk down what can be a very hard road at times. Hope on the Hard Road Special Needs Podcast was created for this purpose. Our vision is to grow a thriving community, where families with children of all ages with special needs can feel connected, be encouraged, and find hope for the road ahead.

    Connect with Us:

    If you enjoy this podcast please share us with others and be sure to follow us so won’t miss an episode. We’d love to hear from you so please leave us a comment or rating and connect with us on social media or on our website.

    Email us: info@hopeonthehardroad.org

    Website: https://hopeonthehardroad.org/

    Instagram: https://www.instagram.com/hopeonthehardroad/

    Facebook: https://www.facebook.com/hopeonthehardroad/

    Facebook Group: https://www.facebook.com/groups/2621447987943459

    Free Youtube Resource Library: https://www.youtube.com/playlist?list=PLsSAfvTkSy87X-fEqtVR2qvo7w9UQBuxz

    Disclaimer: The views and opinions expressed by guests on this podcast are their own and do not necessarily reflect those of Hope on the Hard Road, Inc. This podcast is for informational purposes only and is not intended as professional, medical, or legal advice.

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    38 分
  • “Happiness is Down Syndrome” with Misty Snyder
    2025/10/20

    Down Syndrome Awareness Month Series:

    “Happiness is Down Syndrome” with Misty Snyder

    Welcome back to the Down Syndrome Awareness Month Series! Today, we’re joined by a truly inspiring guest — Misty Coy Snyder. Misty is an actor, singer, writer, entrepreneur, and a powerful advocate for the Down syndrome community. After receiving a prenatal Down syndrome diagnosis for her second son, Misty created a global platform called Happiness is Down Syndrome, promoting inclusion, awareness, and the beauty of diversity.

    She currently serves as the Creative Director for Global Outreach and Advancement at RODS Heroes, and in 2023, she launched her own podcast, Bold Voices, Soft Hearts, sharing moving stories of those who’ve found passion through pain.

    Get ready for a heartfelt and hopeful conversation with Misty as we celebrate the voices that are changing the world — one story at a time.

    Bio:

    Misty Coy Snyder is an actor, singer, writer, entrepreneur, content creator and advocate for the Down syndrome community. She recently accepted the role of Creative Director for Global Outreach and Advancement for Down syndrome at RODS Heroes, which seeks to uncover the superpowers of individuals with Down syndrome. Upon receiving a prenatal Down syndrome diagnosis for her second son in 2020, she created a worldwide platform to promote inclusion and awareness called, Happiness is Down syndrome. She launched her own podcast in 2023 called, Bold Voices, Soft Hearts, which features stories of those who have discovered their passion through pain. She, along with her family hope to show the beauty of diversity on a global scale!

    Contacts:

    https://youtu.be/BYQuLinx_dA?si=9xW6pFLOQjtALp8g

    https://www.instagram.com/happinessisdownsyndrome?igsh=YjJ2dnlxaGNtazFq&utm_source=qr

    https://www.instagram.com/mistycoysnyder/profilecard/?igsh=NWg4OGJncDdkenoy

    For a family raising a child with special needs, life can be difficult. There are many storms to weather and struggles to address, and we often feel isolated and alone due to the nature of our circumstances. Families have a need to connect and find resources, a need to be encouraged, and a need for hope as we walk down what can be a very hard road at times. Hope on the Hard Road Special Needs Podcast was created for this purpose. Our vision is to grow a thriving community, where families with children of all ages with special needs can feel connected, be encouraged, and find hope for the road ahead.

    Connect with Us:

    If you enjoy this podcast please share us with others and be sure to follow us so won’t miss an episode. We’d love to hear from you so please leave us a comment or rating and connect with us on social media or on our website.

    Email us: info@hopeonthehardroad.org

    Website: https://hopeonthehardroad.org/

    Instagram: https://www.instagram.com/hopeonthehardroad/

    Facebook: https://www.facebook.com/hopeonthehardroad/

    Facebook Group: https://www.facebook.com/groups/2621447987943459

    Free Youtube Resource Library: https://www.youtube.com/playlist?list=PLsSAfvTkSy87X-fEqtVR2qvo7w9UQBuxz

    Disclaimer: The views and opinions expressed by guests on this podcast are their own and do not necessarily reflect those of Hope on the Hard Road, Inc. This podcast is for informational purposes only and is not intended as professional, medical, or legal advice.

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    42 分