Embrace the Blessing

ETB 58: What if the future of your loved one with a disability could be bright, secure, and filled with choices and alternatives? Envision a world where guardianship isn't the only path, where supported decision-making reigns supreme, and personal rights are preserved. This episode offers a detailed dissection of guardianship and its alternatives, shedding light on the game-changing Right to Make Choices supported-decision making toolkit - a Texas-based initiative.We take you on a journey through the pivotal Jenny Hatch case and the subsequent reform of the Texas guardianship system in 2015, highlighting the importance of considering alternatives to guardianship such as medical power of attorney, durable power of attorney, and more. Hear the ins and outs of these alternatives, and how they can shape a brighter future for your loved ones. So, tune in, soak up the knowledge, and empower yourself to make informed decisions that truly make a difference.Supported Decision-Making Toolkit:https://disabilityrightstx.org/wp-content/uploads/2018/08/The-Right-to-Make-Choices-SDM-toolkit-jan-2018-1.pdfSupported Decision Making Agreement - see page 89-90 in the link below:https://disabilityrightstx.org/wp-content/uploads/2018/08/The-Right-to-Make-Choices-SDM-toolkit-jan-2018-1.pdfGuardianship in Texashttps://www.hhs.texas.gov/regulations/legal-information/guardianshipConnect with Sandy:IG: https://www.instagram.com/sandydeppischEmbrace the Blessing Facebook Group: http://bit.ly/ETB4MEWebsite: http://www.embracetheblessing.com/

ETB 57: When your child is hospitalized, what means of comfort do you find? As a mother who's been down this road with my son Josiah, I will share how the power of pen helped me through those dark times. Transcribing our story and drawing strength from those lines, I found a way to navigate the painfully frequent hospitalizations. The silver lining we discovered in this storm cloud was the round-the-clock care provided by CNAs. Their gift of caregiving brought the serenity our family needed, and they turned into our lifeline.This episode isn't just about our journey, but also celebrates the CNAs who make a significant difference. Being a parent to a child with medical needs is exhausting, both physically and emotionally. I'll take you through a personal anecdote, where the support of a CNA allowed me a much-needed respite. It's a story that could resonate with many of you out there. Remember, support and help are always available. So, join me and let's walk this path together, find inspiration, share a few laughs, shed a few tears, and above all, help each other through.Connect with Sandy:IG: https://www.instagram.com/sandydeppischEmbrace the Blessing Facebook Group: http://bit.ly/ETB4MEWebsite: http://www.embracetheblessing.com/

ETB 56: Ready to journey into the heartwarming world of Carlee Ragains, a creative spirit, mother, wife, and mimi?  Carlee's story weaves a rich tapestry of love, courage, and perseverance, as she shares the joys, challenges, and unimaginable fulfillment that come from parenting her 16-year-old daughter, Ellen, who was born with Down syndrome. Carlee paints a vibrant portrait of Ellen, a high functioning, verbal, independent, sensitive, and personality-packed young woman - an inspiring beacon of hope and testament to the beauty of embracing uniqueness.Carlee's creativity doesn't stop at parenting; she has harnessed her experiences and channeled them into the creation of a beautiful children's book. Would you believe the ideas for this book started flowing in the shower? This book aims to promote self-advocacy, create connections, and foster understanding about disabilities. Carlee talks about her journey from an initial rejection by a publisher to eventually seeing her labor of love come to life. Carlee dreams big. She envisions a series of books that illuminate different diagnoses and disabilities, engaging readers in an inviting and non-threatening way. This woman's relentless optimism and her dreams for her daughter to thrive are as beautiful as her project. So, if you're ready to be inspired, uplifted and enlightened, this is an episode you don't want to miss. Come, join us on this journey of celebrating uniqueness and potential in all children, regardless of their abilities.Connect with CarleeNewsletter: https://mailchi.mp/498c1a387cc6/bqr1oq075oIG: @carleeragainswritesBlog: https://carleeragains.wordpress.comEleanor's eXtraordinary Dreams Illustrator:Megan WebberMegan's IG:  @megan_webber_artEleanor's eXtraordinary Dreams Publisher:https://unitedhousepublishing.com/Connect with Sandy:IG: https://www.instagram.com/sandydeppischEmbrace the Blessing Facebook Group: http://bit.ly/ETB4MEWebsite: http://www.embracetheblessing.com/

ETB 55: Prepare to be deeply moved by the remarkable journey of Josephine Sullivan, founder and CEO of the Christina Sullivan Foundation. This episode offers a powerful narrative of love, faith, and unwavering commitment as Josephine shares the story of her daughter Christina, a vibrant soul who was born with severe brain injury, cerebral palsy, and a seizure disorder. Listen as she chronicles how her unconditional love for Christina spurred the creation of a foundation that has since then sparked hope and positivity to over 247 athletes of varying abilities.As we steer the conversation towards inclusive sports for children and adults with differing abilities, we uncover the deep ties Josephine formed with medical professionals. These resulting collaborations have been instrumental in the growth  of the Christina Sullivan Foundation's comprehensive adaptive and inclusive activities and sports programs. The Christina Sullivan Foundation is not just about sports, it's about creating a nurturing and inclusive environment. From adaptive tennis, bowling and bocce ball to choirs and eSports, the foundation aims to offer a wide range of activities that cater to every individual's unique talents and interests. And, there's more to come with the upcoming music and art camp pilot program and a chess club.As we gear up for the upcoming event at Moody Gardens, a collaboration with the Christina Sullivan Foundation, we discuss the exciting array of activities and the celebration of hope and inclusion it promises. This free event is a testament to the foundation's dedication to fostering a sense of belonging and inclusion for people of all abilities and their families. We wrap up our conversation by focusing on adaptive exercises for children with intellectual and physical disabilities, discussing the importance of community support for such initiatives, and uncovering Josephine's latest creative venture – a café at the foundation. Tune in for a heartening discussion and learn how you can contribute to this noble cause.Connect with the Christina Sullivan Foundation:The Christina Sullivan Foundation is dedicated to helping medically dependent children and adults with intellectual and physical challenges and their families. Our intake specialists can help guide your search for necessary resources involving medical, educational, legal, and social networks to assist in caring for your loved one's health, safety, and well-being. Contact us and let us know how we can help!https://www.christinasullivanfoundation.org/http://info@christinasullivanfoundation.orgGriefSharehttps://www.griefshare.org/Connect with Sandy:IG: https://www.instagram.com/sandydeppischEmbrace the Blessing Facebook Group: http://bit.ly/ETB4MEWebsite: http://www.embracetheblessing.com/

ETB 54: What does it really mean to be a parent of a child with autism? How do you navigate the challenges and celebrate the milestones? Join us on a deeply personal journey with Heather, a resilient mother who opens her heart about her experiences raising her son, Chase, who was diagnosed with autism at a tender age of 2.5 years. Currently a stay-at-home mom who transitioned to homeschooling Chase after working as a para in schools, Heather offers unique insights into the world of children with special needs. She speaks about the bond she shares with her son, and how she has juggled through the challenges of his adolescence, including medication struggles and the tricky terrain of puberty. As our conversation unfolds, Heather candidly discusses the aggressive behaviors Chase displays and the strategies she has employed to manage these situations. She underlines the importance of consistency, external intervention and support, a key aspect often overlooked. . This episode is a testament to Heather's resilient spirit and unconditional love for her son, delivering a message of hope, insight, and valuable experiences for parents facing similar challenges. This is a conversation you won't want to miss. Join us to understand the realities, the hardships, and the triumphs of parenting a child with autism – a story told by a mother who has walked the path.Connect with Heather:Chase_sam@live.comTraining that Emphasizes Safety, Consistency, and Restraints as a Last Resorthttps://www.crisisprevention.com/Blog/physical-restraints-as-a-last-resortChristina Sullivan Foundationhttps://www.christinasullivanfoundation.org/Connect with Sandy:IG: https://www.instagram.com/sandydeppischEmbrace the Blessing Facebook Group: http://bit.ly/ETB4MEWebsite: http://www.embracetheblessing.com/

ETB 53: What if you could turn the toughest moments of parenting a child with a disability into a source of strength and inspiration? Join me, Sandy Deppisch, as I take you on a roller coaster ride of emotions in the hospital stays that have become an all too frequent part of our lives. You'll learn how to communicate your needs effectively to your support network, and understand the importance of asking for specific help, whether it's a warm blanket or home-cooked meal. Staying awake through the hospital nights, changing pull-ups, feeding, comforting, and dealing with beeping machines - sound familiar? Let's embark on this journey of shared experiences, struggles and strength, as I read a touching blog post, "Going Home," that vividly portrays our fears, tears, and triumphs. Find out how we can all make a difference by reaching out to each other, and remember that there's always a community ready to lend a hand and a heart. Because parents like us, we're not alone on this road less traveled, and together, we create a realm of understanding and support.Connect with Sandy:IG: https://www.instagram.com/sandydeppischEmbrace the Blessing Facebook Group: http://bit.ly/ETB4MEWebsite: http://www.embracetheblessing.com/

ETB 52:  Have you ever wondered what it takes to raise a child with Down syndrome? Embark on an intimate journey with Susan Aguilar, a mother who shares the honest truth about the joys and challenges she's encountered while raising her son, Adrian. From the ease of his younger years to the hurdles of his adulthood, she paints a vivid picture of their undying resilience.We unravel the secrets of her success in homeschooling a child with Down Syndrome, with Susan sharing her experiences of crafting and tweaking curriculums for Adrian. Experience the flexibility of homeschooling firsthand, and appreciate how it has allowed Adrian to hone essential skills.  We then shed light on a darker side of their journey, as Susan recounts their struggles with Adrian's anxiety, which ebbs and flows with  the weekdays and weekends. Our discussion about the impact behavioral therapist, Josie Avila brought, reveals the coping strategies that have been instrumental in managing Adrian's anxiety.Lastly, we look towards the horizon as we envision Adrian's future. As Susan shares her dreams for Adrian's independence, we talk about the importance of a robust personal support network. Ending on an uplifting note, we introduce you to Adrian's Tasty Treats, a testament to Adrian's entrepreneurial spirit. This endeavor not only helps Adrian manage his anxiety but also enhances his social skills. We invite you to join us as we celebrate love, resilience, and hope in this unparalleled journey of parenting.Adrian's Tasty Treatshttps://www.facebook.com/profile.php?id=100088650903014The Jet Pac https://www.thejetpac.com/Swallowing and Speech Serviceshttps://www.swallowingandspeechservices.com/Psychologisthttps://www.drmgarcia.com/https://www.psychologytoday.com/us/therapists/michelle-garcia-the-woodlands-tx/77407A Good Life Bookhttps://www.amazon.com/Good-Life-Your-Relative-Disability/dp/B000W5TBH6/ref=sr_1_1?crid=28PO1Q01XYIOA&keywords=a+good+life+by+Al+Etmanski&qid=1693769736&sprefix=a+good+life+by+al+etmanski%2Caps%2C113&sr=8-1Connect with Sandy:IG: https://www.instagram.com/sandydeppischEmbrace the Blessing Facebook Group: http://bit.ly/ETB4MEWebsite: http://www.embracetheblessing.com/

ETB 51: Have you ever pondered over the therapeutic power of writing in dealing with overpowering emotions? Join me, Sandy Deppish, on this personal journey as I revisit an old blog post titled 'It's Not About Me.' You'll discover how documenting the highs and lows of raising a child with a disability has helped me process my feelings and paved the path for resilience and hope.This episode is also a heartfelt tribute to my son Josiah, and all children living with disabilities - the true heroes of our stories. Their courage, strength, perseverance, and infectious joy in the face of daily struggles are awe-inspiring. I hope my recount of their journey brings you the same inspiration and admiration they bring me every day. Let's embrace the blessings our amazing kids bring to our lives, together!Connect with Sandy:IG: https://www.instagram.com/sandydeppischEmbrace the Blessing Facebook Group: http://bit.ly/ETB4MEWebsite: http://www.embracetheblessing.com/

ETB 50: Ever tried to trim a child's toenails? Now imagine that child has sensory issues that make the task as perilous and nerve-wracking as a high-wire act. Join me, Sandy Deppisch in this candid discussion on Embrace the Blessing podcast, where we navigate the choppy waters of personal grooming for children with disabilities, specifically, trimming toenails. We share my personal struggle with my son Josiah's toenail trimming, a task that ended with exhaustion and frustration, yet also highlighted the resilience and strength of such special children.In this heartfelt narrative, we unravel the remarkable spirit of children like Josiah who, despite their daily challenges, possess an amazing capacity for joy and happiness. This episode is also a sincere appeal to listeners who might have figured out the remedy for this seemingly mundane but complex task. It's a peek into a day in the life of a parent of a child with disabilities, an opportunity to glean insights on handling similar challenges, and an invitation to marvel at and draw inspiration from the strength and resilience of these special children. Join us as we traverse the joys, the struggles, the victories, and the constant quest for solutions on this extraordinary path less traveled.Connect with Sandy:IG: https://www.instagram.com/sandydeppischEmbrace the Blessing Facebook Group: http://bit.ly/ETB4MEWebsite: http://www.embracetheblessing.com/

ETB 49: I'm thrilled to introduce you to Darcy, a devoted parent and former teacher who's turned her personal journey into a mission to unlock the potential in children with Down syndrome. Imagine the heartache of knowing your child has thoughts, ideas, dreams locked away in their mind - simply because they struggle to communicate. Darcy, all too familiar with this struggle, has dedicated her life to tearing down these barriers using the unique and highly effective Speller's Method.Darcy's son, Brady, is a loving 20-year-old with Down syndrome and apraxia. Darcy shares the trials, triumphs and transformative power of communication in Brady's world. Overcoming common misconceptions and trauma often associated with Down syndrome, she paints a powerful picture of Brady's journey. You'll be inspired hearing how he has learned to express himself by spelling, sharing his dreams, and even using mathematical equations to make sense of his world. Communication is more than just words. It's a lifeline for individuals like Brady who face unique challenges due to Down syndrome and apraxia. Listen in as we delve into the importance of repetition, coaching, and purposeful motor skills in helping these children unlock their full potential. With Darcy's insights, we hope to inspire parents, educators, and anyone touched by special needs, offering hope and strategies to foster communication and inclusivity. Lets celebrate Brady's story - it's a testament to the power of patience, love, and the right strategies. It's proof that where there is a will, there is way - a way to unlock potential and give voice to beautiful minds.Connect with Darcy:https://brandnewday.life/Email:darcy@brandnewday.lifeBrady, Darcy's son is part of The Army of Spellers that is giving hope to new SPELLERS.  https://spellers.com/an-army-of-spellers/brady-mohrUNDERESTIMATED https://a.co/d/ioga9Xg Spellers Moviehttps://spellersthemovie.com/Website for SPELLERS https://spellers.com/about-spellers-methodFB:  Darcy Day  (you can find me with a picture of my son on a 26 letter board)  https://www.facebook.com/darcy.mohr.12Connect with Sandy:IG: https://www.instagram.com/sandydeppischEmbrace the Blessing Facebook Group: http://bit.ly/ETB4MEWebsite: http://www.embracetheblessing.com/

ETB 48: Have you heard about the positive impact of creating a personal network to support you as you care for your loved one with a disability?  Our guest, Jennifer Vincent, brings her experience as a parent and network facilitator to help answer this crucial question. Jennifer shares the importance of personal networks in empowering families and individuals with disabilities. She introduces us to the book, A Good Life for You and Your Relative with a Disability by Al Etmanski, a practical guide to establishing such networks that promote strategic planning, decision-making, and provide vital sustainability resources.Navigating the journey with Jennifer, you'll learn firsthand the intricate process of inviting members, defining roles, and fostering qualities essential for a thriving network. The lively discussions are peppered with enlightening insights on the significance of guest speakers, educational components, and the creation of a care notebook. She underlines the importance of the individual's comfort and active participation as the team members work together to provide support.We also get an intimate look into Jennifer's personal journey of crafting a support network for her daughter, Alexandra.  The conversation touches on the role of a facilitator, and the importance of varying support types. Jennifer shares creative solutions to building a support network, like including family members, thinking out of the box to include other members and using Zoom for out-of-state connections.  This conversation is a goldmine for anyone looking to learn more about support networks for the special needs community, so tune in and join the discussion.Jennifer is a licensed Vocational Nurse, president of GHFEDS: Galveston-Houston Families Exploring Down Syndrome, State Medicaid Managed Care Advisory Council Member,  Partner in Policy Making 2018 graduate and a Texas Networks Connection Personal Network Facilitator.Connect with JenniferEmail address: Jennifervincent71@comTexas Parent 2 Parent Website: https://www.txp2p.org/Texas Parent 2 Parent Care Notebook:https://www.txp2p.org/services/family-to-family-health-info/care-notebookTexas Network Connections:https://www.txp2p.org/services/texas-network-connectionsA Good Life for You and Your Relative with a Disability:https://www.amazon.com/Good-Life-Your-Relative-Disability/dp/B000W5TBH6Connect with Sandy:IG: https://www.instagram.com/sandydeppischEmbrace the Blessing Facebook Group: http://bit.ly/ETB4MEWebsite: http://www.embracetheblessing.com/

ETB 47: Ever thought of how daunting the prospect of going on a vacation with special needs children might be? Imagine being a single parent to two wonderful boys on the autism spectrum and deciding to embark on a solo trip. That's exactly what my guest, Mary Ann Hughes, courageously did. Mary Ann's incredible journey of managing a cruise vacation with her sons is filled with insightful experiences and practical advice. We talk about the pre-journey preparations, making dining and accommodation comfortable, and special tips and tricks for sensory-sensitive children. Mary Ann's accounts are filled with realism and honesty, making it relatable for every parent or guardian navigating through similar paths. One of the highlights of our conversation is Mary Ann's well-thought-out use of social stories to prepare her boys for the trip. We delve into the details of how she ensured a smoother journey via cruise, considering the comfort of consistency that it offers for her sons and many other families. We also share the importance of headphones and locating quiet spots, making the experience enjoyable for sensory-sensitive children.Mary Ann talks about her business, Special Family Transitions which was birthed from her personal experience of navigating through the challenges of special needs divorce.  As a certified divorce coach she is able to provide guidance and support to others who find themselves in a similar situation.Lastly, we shed light on the wealth of resources that are available for families with special needs children in the process of transitioning from school to life after school.. From private to public and church-based programs, we navigate through the sea of options and offer guidance on how to make the most of these resources.  It's a heartening conversation filled with useful advice, personal anecdotes, and hope for those in the special needs community. Join us for an episode that promises to inspire, educate, and offer a fresh perspective.Connect with Mary Ann:Email address: Maryann@specialfamilytransitions.comWebsite: https://www.specialfamilytransitions.comSpecial Family Transitions Facebook Page:https://www.facebook.com/specialfamilytransitionsSpecial Family Transitions on Instagram:https://www.instagram.com/specialfamilytransitions/Special Family Transitions YouTube channel:https://youtube.com/@specialfamilytransitionsAnd here is a low-priced 1-hour course Mary Ann developed for moms of children with disabilities to learn how to plan for success in a special needs divorce:https://maryannhughes.mastermind.com/masterminds/37115Connect with Sandy:IG: https://www.instagram.com/sandydeppischEmbrace the Blessing Facebook Group: http://bit.ly/ETB4MEWebsite: http://www.embracetheblessing.com/

ETB 45: This is Part 2 of a 2 part interview. In this episode I talk with Victoria De La Garza and her mother Jennifer Gongora about their business, VK Girl Creations.  Victoria started in her High School Life Skills class learning to knit beanie hats on a round knitting loom.  She held her first pop up market at age 18, selling beanies to her fellow classmates.  Now, at age 24, Victoria's hobby has blossomed into a growing business. She currently sells handcrafted beanies, bracelets and T-shirts online and at local vendor markets. The motto that Victoria and Jennifer live by is, "If you believe it, you can achieve it!". Be sure to catch the Part 1 of this inspiring interview, ETB 44.VK Girl Creations:https://www.vkgirlcreations.com/Victoria's Photography Portfoliohttps://intro2photographyg4.wixsite.com/victoria-de-la-garzaJ.J. Watt Dream Big, Work Hard Award Winner - Victoria De La Garzahttp://jjwfoundation.org/dbwh-winners/Connect with Victoria and Jennifer:IG:  https://www.instagram.com/vkgirl_creations/Facebook:  https://www.facebook.com/VKGirlCreationsConnect with Sandy:IG: https://www.instagram.com/sandydeppischEmbrace the Blessing Facebook Group: http://bit.ly/ETB4MEWebsite: http://www.embracetheblessing.com/

ETB 44:  In this episode I talk with Victoria De La Garza and her mother Jennifer Gongora about their business, VK Girl Creations.  Victoria started in her High School Life Skills class learning to knit beanie hats on a round knitting loom.  She held her first pop up market at age 18, selling beanies to her fellow classmates.  Now, at age 24, Victoria's hobby has blossomed into a growing business. She currently sells handcrafted beanies, bracelets and T-shirts online and at local vendor markets. The motto that Victoria and Jennifer live by is, "If you believe it, you can achieve it!".  Be sure to catch the 2nd part of this inspiring interview next Wednesday, September 21, 2022.VK Girl Creations:https://www.vkgirlcreations.com/Victoria's Photography Portfoliohttps://intro2photographyg4.wixsite.com/victoria-de-la-garzaJ.J. Watt Dream Big, Work Hard Award Winner - Victoria De La Garzahttp://jjwfoundation.org/dbwh-winners/Connect with Victoria and Jennifer:IG:  https://www.instagram.com/vkgirl_creations/Facebook:  https://www.facebook.com/VKGirlCreationsConnect with Sandy:IG: https://www.instagram.com/sandydeppischEmbrace the Blessing Facebook Group: http://bit.ly/ETB4MEWebsite: http://www.embracetheblessing.com/

ETB 43:  If you have a child with a disability who likes to disrobe at night, I have just the thing for you!  For years we would wake in the wee hours of the morning to find our son undressed and sometimes enjoying finger paining fun with the contents of his full pull up!  When we discovered THIS product, it was a game changer!  I have 8 of these in larger sizes looking for a good home.  Reach out to me if they would make a difference in your life too and they are yours! Little Keeper Sleeperhttps://littlekeepersleeper.com/Connect with SandyIG: https://www.instagram.com/sandydeppischEmbrace the Blessing Facebook Group: http://bit.ly/ETB4MEWebsite: http://www.embracetheblessing.com/

ETB 42:  In this episode I talk with Kathryn Kane-Neilson about her 19 year old son, Clark who has Down syndrome.   She talks about her experiences raising Clark, through life in NYC, through divorce, through medical misadventures and fresh beginnings in Texas.Kathryn shared,  " At 22 years old, I was aware of the fact that I was carrying a child with Down syndrome and it absolutely changed my paradigm.  it changed my brain.  Clark is the joy of my life.  He gave me purpose."GHFEDS - Greater Houston Families Exploring Down Syndromehttp://ghfeds.org/Connect with Heather - frequently mentioned on this podcast!Medicaid Resources Website:  http://texasmedicaidwaivers.comConnect with SandyIG: https://www.instagram.com/sandydeppischEmbrace the Blessing Facebook Group: http://bit.ly/ETB4MEWebsite: http://www.embracetheblessing.com/

ETB 41- In this episode I talk with Beverly Parrish about her daughter Hannah, age 28, who has Down syndrome.   Beverly and her husband Chris learned that Hannah had Down syndrome in utero.   Feeling a bit overwhelmed at their lack of knowledge about Trisomy 21 they began to research, trusting that God had his perfect plan in place.Beverly is a mother of 7 with 9 grandchildren and has been married for 40 years.  She homeschooled the kids for 30 years and currently works with dyslexic children and adults as a facilitator in the Davis Dyslexia program.  Beverly also tutors struggling readers.  In her free time, she published a book, Beyond the Diploma - Homeschooling with the End in Mind.  See link below. As the only girl, sandwiched between 6 brothers, Hannah is a cheerful, engaging young lady who brings joy and seems unaffected by circumstances that impact many of us.   Beverly believes in embracing the uncertainty.  Instead of having your expectations dashed or unmet all the time,  she recommends just embracing the idea that you don't know.  It's not a race and it's not a competition.  Embrace the uncertainty and don't compare your situation.Davis Dyslexia Program https://https://learnyourway.biz/Beyond the Diploma - Homeschooling with the End in Mind by Beverly Parrishhttps://www.amazon.com/Beyond-Diploma-Homeschooling-End-Mind/dp/1946629456The Gift of Dyslexiahttps://www.amazon.com/Gift-Dyslexia-Smartest-Revised-Expanded/dp/0399535667Welcome to Hollandhttps://www.dsasc.ca/uploads/8/5/3/9/8539131/welcome_to_holland.pdfConnect with Beverlybeverlyparrish.comwww.beverlyparrish.com  www.learnyourway.biz   281-638-0297Connect with SandyIG: https://www.instagram.com/sandydeppischEmbrace the Blessing Facebook Group: http://bit.ly/ETB4MEWebsite: http://www.embracetheblessing.com/

ETB 40 - In this episode I talk with Gerrie Bourque, mother of 3 whose 26 year old son Tyler has a dual diagnosis of Down syndrome and autism, is medically complex and has rare disorders.  Gerrie shares the various caregiving options they have explored over the years.  Tyler has a Texas Medicaid Waiver which provides services for him including a support staff to care for him as needed.  Initially, Gerrie's husband/Tyler's dad was the first paid caregiver.  They have also hired staff from Care.com,  enrolled Tyler in Day hab a couple days a week and had a  family member as his primary caregiver. Each waiver offers varied options for care with the ability to try different ones to find which works best for each individual.   Families are able to alter the caregiving situation as circumstances and support needs change.  Currently, Tyler is attending Day hab  5 days a week and thriving! No matter which avenue you take to find support for your child, remember often times your child is the best barometer for who is a good fit.Tyler's story: Recovering from intestinal malrotation:https://www.texaschildrens.org/blog/tylers-story-recovering-intestinal-malrotation Verne Cox Adaptive Recreation Centerhttps://www.pasadenatx.gov/189/Adaptive-Recreation Next Step Transition Centerhttps://www.nextsteptransitioncenter.org/Care.comhttps://www.care.com/Connect with Gerriegerriebeauticontrol@yahoo.comConnect with SandyIG: https://www.instagram.com/sandydeppischEmbrace the Blessing Facebook Group: http://bit.ly/ETB4MEWebsite: http://www.embracetheblessing.com/

ETB 39 -  In this episode I talk with Mary Ann Hughes, mother of 2 young adults with Autism about finding quality care for loved ones with special needs.  As a single mother managing her company, Special Family Transitions, Mary Ann has had to stretch her comfort zone most recently when she sent both of her boys for the very first time to a week long summer camp. Mary Ann believes as special needs moms and parents we don't spend enough time taking care of ourselves.  She notes there is so much stress involved with having special. needs children it can take a toll on the family and sometimes the marriage.  Mary Ann encourages you to take time for yourself so you can be the best parent you can be for your kids.   To help you find quality caregivers you can trust,  Mary Ann shares an abundance of possibilities for securing respite care, some of which you may not have ever considered.   Connect with Mary Ann:Email address: Maryann@specialfamilytransitions.comWebsite: https://www.specialfamilytransitions.com/ Special Family Transitions YouTube channel (please subscribe ) https://youtube.com/channel/UChI4BaUMGf50O2yPE_YnjFASpecial Family Transitions Facebook Page:https://m.facebook.com/specialfamilytransitionsPrivate Facebook group:Divorce Journey Support for Moms of Children with Autism & Special Needs:https://www.facebook.com/groups/309739357366936/Special Family Transitions on Instagram:https://www.instagram.com/specialfamilytransitions/Respite Resources:Take Time Texas https://apps.hhs.texas.gov/taketimetexas/search.cfmTexas State Information on Respite Providers or Programshttps://archrespite.org/respite-locator-service-state-information/176-texas-infoConnect with SandyIG: https://www.instagram.com/sandydeppischEmbrace the Blessing Facebook Group: http://bit.ly/ETB4MEWebsite: http://www.embracetheblessing.com/

ETB 38: In this episode I share a few stories about Josiah from the past few years when he was walking through a very long, very difficult season.  With so many challenges including aggression, destruction and self-injurious behaviors it was easy at times to lose sight of hope. As a mom desperately trying to figure out how to best help my child,  it was heartbreaking to watch him struggle so much.  There is nothing like watching someone you love suffer and feel powerless to alleviate it.  Even after all the interventions, it was discouraging to see little to no improvement. But I'm here to tell you, things drastically improved.  Despite the daunting forecast from a psychiatrist who told us Josiah would spend the rest of his life in a long-term psychiatric facility because he was too combative and self-injurious to live at home,  Josiah has become a different person.  He has made remarkable progress and continues to amaze me with his growth and abilities.Don't give up on your kids!  If you are in a difficult season and can't imagine how things could ever get better, hang in there!  Pray without ceasing, reach out to others, seek support from those who has been where you are,  get respite if you need it but don't ever give up hope! Respite Care:https://www.navigatelifetexas.org/en/family-support/respite-care-for-children-with-disabilities Support Groups for Parents of Children with Special Needs:https://blog.bayada.com/be-healthy/eight-support-groups-for-parents-raising-children-with-special-needsGHFEDS - Galveston Houston Families Exploring Down Syndrome http://ghfeds.org/Connect with SandyIG: https://www.instagram.com/sandydeppischEmbrace the Blessing Facebook Group: http://bit.ly/ETB4MEWebsite: http://www.embracetheblessing.com/

ETB 37 - In this episode I talk with Fredia Bassham, grandmother of Heather Jo, age 26.  Freida and her husband Joe have been caring for their granddaughter who has cerebral palsy, a seizure disorder and is non-verbal, for 22 years.  Heather Jo recently won Texas Miss Amazing, the Miss Division.  The Texas Miss Amazing pageant celebrates the abilities of girls and women across TEXAS with disabilities.  providing opportunities for them  to build self-esteem.  The Miss Amazing pageant creators believe options to girls with disabilities should reflect their boundless potential.  At the end of July, Heather Jo  will be going to Nationals. Freida shares an option  for finding special needs caregivers some may not have considered.  The Nextdoor app has been a successful avenue for locating ideal candidates to step in and provide quality care.   Not only was Freida able to find a great caregiver who lives just one street over, but she also was able to help a neighbor find care for her son who has autism.Miss Amazinghttps://missamazing.org/Nextdoor https://nextdoor.com/Connect with SandyIG: https://www.instagram.com/sandydeppischEmbrace the Blessing Facebook Group: http://bit.ly/ETB4MEWebsite: http://www.embracetheblessing.com/

ETB 36 - In this episode I talk with Mike Lutey, owner of Special Strong - South East Houston. Special Strong provides science-based adaptive and inclusive fitness programs for children, adolescents, and adults with mental, physical and cognitive challenges.Mike believes giving up his corporate job to become the very first franchise in Special Strong's history, is his calling.  The franchise was founded in 2016 by Daniel and Trinity Stein. Daniel Stein was diagnosed with a learning disability, mood disorder and autoimmune issues at an early age and used specialized exercises to overcome his challenges.Mike noticed with his sister Melissa, who has Down syndrome that after high school there were no real outlets for activity, fitness or even social outlets.  That's one reason he puts a big emphasis on group classes.  Melissa was a big inspiration for Mike making his career move.  He saw so much growth when she was just part of a group.  Along with the group classes, Mike also offers one-on-one classes for anyone who needs that extra attention or maybe just needs to build up a trust factor before joining group activities.Currently,  his class offerings include Boot Camp, Kickboxing, Bounce Camp, Adaptive Aquatic Fitness and Adaptive Dance.  Special Strong - South East Houston offers  a 7 day free trial.  Mike invites people to come in for a week and try all the classes. He says, "Come and try them out.  See what you like, what works, what doesn't work.  We also have a free session for our one-on-ones.  Come and try it all.  We welcome that. "Special Strong has a non-profit scholarship for services for anyone who may need it.  See the link below.Connect with Mike: Email:  Mike.Lutey@specialstrong.comFacebook:  https://www.facebook.com/specialstronghoustontxCell:  832-338-4861Special Strong Champions Foundation Sponsorship Applicationhttps://form.jotform.com/specialstrong/sschampions-scholarship-applicationConnect with SandyIG: https://www.instagram.com/sandydeppischEmbrace the Blessing Facebook Group: http://bit.ly/ETB4MEWebsite: http://www.embracetheblessing.com/

ETB 35 - In this episode I talk with Timothy Glover, corporate trainer by day and real life superhero, Dash Gordon by night.   Initially created to raise some extra money for a vacation, Tim started having fun with the whole Dash idea and began texting people that he was Dash Gordon.  Eventually he decided to add a costume before heading out to do deliveries and the rest is history.Dash has a heart for the special needs community, for people who are living through difficult times and for people going through serious medical issues.  He makes a difference by showing up, putting a smile on their faces and helping out anyway he can.  Dash believes his calling is to work in the community with anyone that needs help.  His total goal is just to put smiles and laughter in people's life.   He gets to meet incredible people, find out what they need and how he can team up with them to do greater things.  He brings joy to everyone he meets and has made an incredible difference for some well deserving individuals and families around town.Dash is a community superhero created by the community.   Since April, when Tim first stepped out in costume as his alter ego, he's been getting lots of media attention first appearing in a League City news story, then on ABC/Channel 13  and KHOU/Channel 11 in Houston.  Next,  Dash will be featured on 104.1 KRBE radio.   He is working with Saved by Faith Productions on a 10 part series called the Dash Gordon Chronicles.  Dash is also focused on working with Angela Bishop and Brewed Blessings to help bring her dream of a special needs coffee shop in League City to fruition.  Be sure to connect with Dash Gordon on social media for more exciting adventures.Connect with Dash:YouTube:  https://www.youtube.com/channel/UCu6xVo_Ds3_-MbtBdCbQiVQFacebook:  https://www.facebook.com/profile.php?id=100079491165658TikTok:  https://www.tiktok.com/@dashgordon2022IG: http://www.instagram.com/dash_gordon2022Dash Gordon in the Media:https://www.leaguecitytx.gov/4270/Timothy-Gloverhttps://abc13.com/dash-gordon-door-delivery-driver-timothy-glover-league-city-texas/11776281/https://www.khou.com/video/news/local/dash-gordon-delivery-driver-spices-up-gig-by-wearing-superhero-costume/285-ed8e1e2d-a71f-4f38-ac2d-d68916ea8475Brewed Blessings:  https://www.brewedblessings.com/Connect with SandyIG: https://www.instagram.com/sandydeppischEmbrace the Blessing Facebook Group: http://bit.ly/ETB4MEWebsite: http://www.embracetheblessing.com/

ETB 34:  In this episode I talk with Beth Haas, teacher and mother of 3 beautiful daughters about her oldest daughter, Annalee who has Down syndrome.   During the 18th week of Beth's first pregnancy, she and her husband John were told their unborn baby had hypoplastic left heart syndrome and was probably not going to be compatible with life.  Hypoplastic left heart syndrome (HLHS) is a birth defect that affects normal blood flow through the heart. As the baby develops during pregnancy, the left side of the heart does not form correctly.  Without surgery, hypoplastic left heart syndrome is deadly, usually within the first few days or weeks of life.  With treatment, many babies survive, although most will have complications later in lifeWhen they learned at birth that Annalee's diagnosis was Down syndrome, not hypoplastic left heart syndrome, it was a miracle. Annalee was in the NICU for a while and had open heart surgery at 23 months.  She also was unable to have thin liquids without aspirating them into her lungs, so initially she had an NG tube.  All of her liquids needed to be thickened for years, but with therapy and training and the right kinds of straws, Annalee eventually learned not to aspirate. Now at age 17, Annalee is included in general education classes, participates in student council and was also invited to be a part of the Groundbreaker's Leadership team at her high school.She takes classes at the Kennedy Dance Studio, has choreographed her own dances, going all the way to the national level in the PTA Reflections Annual Art Contest under the category of Dance Choreography and brought home a bronze medal this year.  She has her own Youtube channel where you can see her perform some of her dances.Annalee will be in the TET (Teacher Education Training) Class at high school this year,  teaching classes in the same elementary school where her mom teaches.  TET provides high school students with teaching experiences to determine whether or not they would like to pursue a career in public education.  The goal is for Annalee to get a certification to become a teacher's assistant. Teaching Your Child with Special Needs To Ride A Bicycle in 4 Easy Stepshttps://twominuteparenting.com/how-to-teach-your-child-with-special-needs-to-bike-in-4-easy-steps/Kennedy Dance Theatre:https://www.kennedydance.com/PTA Reflectionshttps://www.pta.org/home/programs/reflectionsConnect with Annaleehttps://www.youtube.com/channel/UCQrw1d2I2ShE0tcecHJBQbAConnect with SandyIG: https://www.instagram.com/sandydeppischEmbrace the Blessing Facebook Group: http://bit.ly/ETB4MEWebsite: http://www.embracetheblessing.com/

ETB 33:  In this episode I announce a brief break as we quarantine, then head out on a family vacation.I will see you on July 6th with another amazing parent to inspire and encourage you.  Until then, here are some things to keep you entertained:Play Wordlehttps://www.nytimes.com/games/wordle/index.htmlBecome a Lego Sculptor (and leave your Law Degree behind)https://youtu.be/8CP9hzSm60YLearn to Frost a Cake - A Beginner's Guidehttps://youtu.be/OxcWDrPAeWMPlay the Harmonicahttps://youtu.be/ddM5RlWSJ4EStart Your Own Podcasthttps://youtu.be/Q8pfZna6H6QConnect with Sandy:IG: https://www.instagram.com/sandydeppischEmbrace the Blessing Facebook Group: http://bit.ly/ETB4MEWebsite: http://www.embracetheblessing.com/

ETB 32:  In this episode I share a story about a time when Josiah at 9 years old, left our home unescorted and none of us were aware that he was even gone.   Sadly, this was not the first time it happened and it most definitely was not the last.  We had some pretty frightening experiences with Josiah eloping.   Despite our best efforts to keep him safely INSIDE our home, he was clever and oh so fast at figuring out how to slip away unattended.  He had no sense of danger or the ability to protect himself.  Fortunately, we either found him pretty quickly each time or he was returned to us by a kind stranger.   I'm so grateful Josiah's eloping days are over.  It was a terrifying time for us.  Statistics suggest nearly half of children with autism wander or bolt from safe places.  If you have a child who wanders, my heart goes out to you.  Elopement is a very difficult behavior to work through. Here are some resources and products that may help:What to Do When Your Child Elopeshttps://www.marcus.org/autism-resources/autism-tips-and-resources/what-to-do-when-your-child-elopesWandering Off (Elopement) Autism Tool Kithttps://pediatrust.com/Autism-Wandering-Off-ElopementThe Autism Project - Elopement Prevention Communityhttps://theautismproject.org/training-education/elopement-prevention/elopement-prevention-general-resourcesAngelSense Tracking Devicehttps://www.angelsense.com/gps-for-autism-wandering/Autism Elopement and Wandering Kit for Familieshttps://parentingchaos.com/autism-elopement-wandering-kit-for-families/Pathfinders for Autism - Tracking Deviceshttps://pathfindersforautism.org/resources/safety/tracking-devices/The Best Kids GPS Trackers and Wearables of 2022 https://www.safewise.com/resources/wearable-gps-tracking-devices-for-kids-guide/Connect with Sandy:IG: https://www.instagram.com/sandydeppischEmbrace the Blessing Facebook Group: http://bit.ly/ETB4MEWebsite: http://www.embracetheblessing.com/

ETB 31:  In this 2nd half of a 2 part episode I continue to talk with former guests Jean and Brianna TenBrink, a dynamic mother/daughter duo about Project LEAH (Leaders Ending Abuse & Harm) a community coalition against educator abuse and mistreatment of children with disabilities in Texas public schools.Jean,  an advocacy coordinator and mother of 3 daughters, 2 of whom are on different ends of the autistic spectrum  talks about the abuse her youngest daughter Leah was subject to in her self-contained classroom by teachers Jean knew well and trusted.  The abuse was misrepresented and school officials lied about the mistreatment.  It wasn't until Jean watched video footage of the abuse herself, that she was made fully aware of all that her daughter endured at the hands of those they believed had Leah's best interest at heart.Brianna, Jean's oldest daughter is the Director of Marketing and Sales for Neural Divergence, LLC.  As a Partner in the Texas Partners and Policymaking Program and a very recent MBA graduate, Brianna has been a tireless advocate for individuals with disabilities for the past 13 years, winning the Sibling Scholarship from Knapps and Roberts law firm, the Rose Award from disAbility Connections, Inc., and Advocate of the Year award from the Arc of the Gulf Coast which granted her the opportunity to speak on the experiences of being a sibling at district-wide conferences.Together Jean and Brianna have co-founded Project LEAH (Leaders Ending Abuse & Harm), an organization that armors parents, families and allies of loved ones of students in the Texas Public School System who have endured restraint, assault or seclusion with educational, legislative advocacy training to foster macro-level change. Project LEAH is affiliated with The Arc of Texas, Disability Rights Texas, Alliance Against Seclusion and Restraint, and Texas Partners in Policymaking.This is part 2 of a 2 part series.   If you haven't heard the first half of the Project LEAH interview,  be sure to listen to it in its entirety.  Jean and Brianna share their hearts and vision for ending abuse and harm in schools.Project LEAH TXhttps://linktr.ee/projectleahtxEnd #restraint #assault & #seclusionProject LEAH Private Facebook Group: https://www.facebook.com/groups/4127855043987645/Arc of Texashttps://www.thearcoftexas.org/Disability Rights Texashttps://www.disabilityrightstx.org/en/home/Alliance Against Seclusion and Restrainthttps://endseclusion.org/Texas Partners in Policymakinghttps://txpartners.org/Connect with Brianna:Instagram: https://www.instagram.com/thebriannashley/Facebook: https://www.facebook.com/briashtenConnect with Jean:Instagram: https://www.instagram.com/superautismmom/Facebook: https://www.facebook.com/jean.tenbrinkConnect with Sandy:IG: https://www.instagram.com/sandydeppischEmbrace the Blessing Facebook Group: http://bit.ly/ETB4MEWebsite: http://www.embracetheblessing.com/

ETB 30:  In this episode, I talk with former guests Jean and Brianna TenBrink, a dynamic mother/daughter duo about Project LEAH (Leaders Ending Abuse & Harm) a community coalition against educator abuse and mistreatment of children with disabilities in Texas public schools.Jean,  mother of 3 daughters, 2 of whom are on different ends of the autistic spectrum is an advocacy coordinator who helps build bridges between home and school for families that have a child with a disability.  She talks about the abuse her youngest daughter Leah was subject to in her self-contained classroom by teachers Jean knew well and trusted.  The abuse was misrepresented and school officials lied about the mistreatment.  It wasn't until Jean watched video footage of the abuse herself, that she was made fully aware of all that her daughter endured at the hands of those they believed had Leah's best interest at heart.Brianna, Jean's oldest daughter is the Director of Marketing and Sales for Neural Divergence, LLC.  As a Partner in the Texas Partners and Policymaking Program and a very recent MBA graduate, Brianna has been a tireless advocate for individuals with disabilities for the past 13 years, winning the Sibling Scholarship from Knapps and Roberts law firm, the Rose Award from disAbility Connections, Inc., and Advocate of the Year award from the Arc of the Gulf Coast which granted her the opportunity to speak on the experiences of being a sibling at district-wide conferences.Together Jean and Brianna have co-founded Project LEAH (Leaders Ending Abuse & Harm), an organization that armors parents, families and allies of loved ones of students in the Texas Public School System who have endured restraint, assault or seclusion with educational, legislative advocacy training to foster macro-level change.  Project LEAH is affiliated with The Arc of Texas, Disability Rights Texas, Alliance Against Seclusion and Restraint, and Texas Partners in PolicymakingProject LEAH TX https://linktr.ee/projectleahtxEnd #restraint #assault & #seclusionProject LEAH Private Facebook Group: https://www.facebook.com/groups/4127855043987645/Arc of Texashttps://www.thearcoftexas.org/Disability Rights Texashttps://www.disabilityrightstx.org/en/home/Alliance Against Seclusion and Restrainthttps://endseclusion.org/Texas Partners in Policymakinghttps://txpartners.org/Connect with Brianna:Instagram: https://www.instagram.com/thebriannashley/Facebook: https://www.facebook.com/briashtenConnect with Jean:Instagram: https://www.instagram.com/superautismmom/Facebook: https://www.facebook.com/jean.tenbrinkConnect with Sandy:IG: https://www.instagram.com/sandydeppischEmbrace the Blessing Facebook Group: http://bit.ly/ETB4MEWebsite: http://www.embracetheblessing.com/

ETB 29:  In this 2nd half of a 2 part episode I talk with Ricky Broussard, Self-Advocate, Peer Support Leader and all around great guy, who at the age of 10 had to move out of his family's home and into a large facility for people with disabilities.  Ricky lived in 4 different facilities over the next 29 years.  He went from  having most of his decisions made for him, to surrounding himself with people he knew and trusted to support him as he began to speak up for himself and advocate for changes in his life.Today, Ricky lives in his own place, has an accessible van, hires his own support staff,  manages his schedule and  works full time at a job he loves.  As a Peer Support Leader, Ricky works for Imagine Enterprises, training others on self-advocacy and self-determination.  He's traveled all over Texas, sharing his story and teaching others the importance of learning to advocate for themselves.Ricky sits on various boards, speaks at state conferences, has won numerous awards and  has presented his testimony at legislative sessions in Austin.  He meets monthly with a group of self-advocates and is also a member of Toast Masters.In 2013, the Ricky Broussard Act was signed into law. The law provides that improved and consistent transition services be available to high schoolers regardless of their school district, thus increasing the likelihood of graduates obtaining post-secondary education and employment opportunities.Ricky believes anyone who wants to work, should be given every opportunity to do so.   He encourages others with a disability to pursue meaningful employment and says, "All we need is support, an opportunity and a chance!"This is part 2 of a 2 part series.   If you haven't heard the first half of Ricky's  interview,  be sure to listen to it in its entirety.  You won't want to miss any of his incredible story. My Life With a Disabilityhttps://www.youtube.com/channel/UC6ewlo1-mDOOlqUmYj3GAigArc of Texashttps://www.thearcoftexas.org/Arc of the Gulf Coasthttps://thearc.org/chapter/the-arc-of-the-gulf-coast/Imagine Enterpriseshttps://www.imagine-enterprises.org/Gulf-Coast Self-Advocateshttps://www.facebook.com/gulfcoastselfadvocates/What is Self-Advocacy/Texas Advocateshttp://www.texadvocates.org/our-history/Texas Council for Development Disabilitieshttps://tcdd.texas.gov/The Ricky Broussard Act:https://cdn.ymaws.com/www.tcase.org/resource/resmgr/Bill_Summaries/HB_617_Bill_Summary.pdfThe Arc of Texas 2021 Virginia Eernisse Legacy Award Winner - Ricky Broussard:https://www.thearcoftexas.org/get-informed/newsroom/the-arc-of-texas-2021-virginia-eernisse-legacy-award-recipient-announced/Connect with Ricky:ricky.broussard@imagine-enterprises.orgConnect with Sandy:IG: https://www.instagram.com/sandydeppischEmbrace the Blessing Facebook Group: http://bit.ly/ETB4MEWebsite: http://www.embracetheblessing.com/

ETB 28:  In this episode I talk with Ricky Broussard, Self-Advocate, Peer Support Leader and all around great guy, who at the age of 10 had to move out of his family's home and into a large facility for people with disabilities.  Ricky lived in 4 different facilities over the next 29 years.  He went from  having most of his decisions made for him, to surrounding himself with people he knew and trusted to support him as he began to speak up for himself and advocate for changes in his life.Today, Ricky lives in his own place, has an accessible van, hires his own support staff,  manages his schedule and  works full time at a job he loves.  As a Peer Support Leader, Ricky works for Imagine Enterprises, training others on self-advocacy and self-determination.  He's traveled all over Texas, sharing his story and teaching others the importance of learning to advocate for themselves.Ricky sits on various boards, speaks at state conferences, has won numerous awards and  has presented his testimony at legislative sessions in Austin.  He meets monthly with a group of self-advocates and is also a member of Toast Masters. In 2013, the Ricky Broussard Act was signed into law. The law provides that improved and consistent transition services be available to high schoolers regardless of their school district, thus increasing the likelihood of graduates obtaining post-secondary education and employment opportunities.Ricky believes anyone who wants to work, should be given every opportunity to do so.   He encourages others with a disability to pursue meaningful employment and says, "All we need is support, an opportunity and a chance!"This is part 1 of a 2 part series.  Tune in next week for the second half of Ricky's interview.My Life With a Disabilityhttps://www.youtube.com/channel/UC6ewlo1-mDOOlqUmYj3GAigArc of Texashttps://www.thearcoftexas.org/Arc of the Gulf Coast https://thearc.org/chapter/the-arc-of-the-gulf-coast/Imagine Enterpriseshttps://www.imagine-enterprises.org/Gulf-Coast Self-Advocateshttps://www.facebook.com/gulfcoastselfadvocates/What is Self-Advocacy/Texas Advocateshttp://www.texadvocates.org/our-history/ Texas Council for Development Disabilitieshttps://tcdd.texas.gov/The Ricky Broussard Act:https://cdn.ymaws.com/www.tcase.org/resource/resmgr/Bill_Summaries/HB_617_Bill_Summary.pdfThe Arc of Texas 2021 Virginia Eernisse Legacy Award Winner - Ricky Broussard:https://www.thearcoftexas.org/get-informed/newsroom/the-arc-of-texas-2021-virginia-eernisse-legacy-award-recipient-announced/Connect with Ricky:ricky.broussard@imagine-enterprises.orgConnect with Sandy:IG: https://www.instagram.com/sandydeppischEmbrace the Blessing Facebook Group: http://bit.ly/ETB4MEWebsite: http://www.embracetheblessing.com/

ETB 27:  In this episode I talk with Vivecca Hartman, mother of 2 and new grandmother, about life with her 24 year old son Christopher, born with a rare genetic mutation, Leber Congenital Amaurosis. Physically healthy in every other way, his vision and hearing was all that was affected at birth.  Very curious, physically fit and funny, Christopher likes to stay active and keep busy.  He communicates with tactile sign language.  As long as he feels safe, Christopher is a very happy person, very independent within his home. Vivecca is cofounder of Touch Base: Center for the Deafblind, a nonprofit organization that benefits deafblind people after they graduate from school. Currently, Touch Base is located in Houston, Texas. It is a small organization with a board consisting of parents of deafblind children, experienced staff from the Texas School for the Blind and Visually Impaired, and other dedicated professionals.  The purpose of Touch Base is to provide deafblind men and women with a day habilitation facility where they can participate in organized, meaningful, and purposeful activities. Vivecca is also a long standing board member for the Lighthouse for the Blind, having served 10+ years.  The Lighthouse of Houston serves 5,000 individuals annually through health and community programs, independent living centers and assisted living facilities.  Of those they employ, nearly 40% are blind or visually impaired. Employees are trained to work in their service or products division.  Their programs and services provide individuals with the ability to live independently and to reach their full emotional, social and educational potential. Deaf-Blind with Multiple Disabilities (DMBD) Medicaid Waiver https://www.hhs.texas.gov/providers/long-term-care-providers/deaf-blind-multiple-disabilities-dbmdDeaf-Blind Multihandicapped Association of Texas (DBMAT)   https://dbmat-tx.org/Community Living Assistance and Support Services (CLASS)https://www.hhs.texas.gov/providers/long-term-care-providers/community-living-assistance-support-services-class. Texas Medicaid Waiver Programs for Children with Disabilitieshttps://www.navigatelifetexas.org/en/insurance-financial-help/texas-medicaid-waiver-programs-for-children-with-disabilitiesPhone Number: 1-877-438-5658 Lighthouse for the Blind https://www.houstonlighthouse.org/PPCDhttps://www.navigatelifetexas.org/en/education-schools/what-is-ppcdTouch Base Center for the Deafblind https://www.touchbasecenter.org/about-touch-baseTouch Base: Center for the Deafblind Facebook Pagehttps://www.facebook.com/TouchBaseCenterConnect with Vivecca Hartman hartmanfam28@sbcglobal.net1-713- 231-7508 Connect with SandyIG: https://www.instagram.com/sandydeppischEmbrace the Blessing Facebook Group: http://bit.ly/ETB4MEWebsite: http://www.embracetheblessing.com/

ETB 26:  In this episode I talk with Rick Deppisch. the first dad to be featured on the podcast who also just happens to be my husband and the father of our 5 children.  Rick shares his perspective on the challenges our family has endured and overcome over the years as we've navigated life with Josiah, our 20 year old son who has Down syndrome and non-verbal Autism. Rick believes faith is what sustained him through the darkest days when Josiah, only 8 years old at the time, spent 10 months living away from home in a residential Behavior Treatment and Training Center.  He advocates the need for community and encourages parents who have a child with a disability to reach out to others to find a group of people to plug into for encouragement, resources and support. Acknowledging that men handle their emotional responses differently than women and often times struggle to support other men who may be going through difficult times, Rick feels there should be more opportunities for dads to gather to be heard, strengthened and encouraged. He also believes that if someone has helped you in your struggles, it's your responsibility to reach back to offer a helping hand to others in need.Meyer Center for Developmental Pediatricshttps://www.texaschildrens.org/location/meyer-center-developmental-pediatricsDr. Kathryn Ostermaierhttps://www.texaschildrens.org/find-a-doctor/kathryn-katy-klish-ostermaier-mdSleep Safe Bedhttps://sleepsafebed.com/products/bed-models/Connect with Rickrdeppisch@gmail.comConnect with SandyIG: https://www.instagram.com/sandydeppischEmbrace the Blessing Facebook Group: http://bit.ly/ETB4MEWebsite: http://www.embracetheblessing.com/

ETB 25:  In this episode I talk with Teresa Trent,  author of  3 different mystery series, whose 29 year old son Andrew has a dual diagnosis of Down syndrome and Autism.   He's  also non verbal, has a seizure disorder and from that he's developed a need for a  Peg tube.   Andrew is a sweetheart, greatly loved and never in a bad mood.  It's no mystery that accepting your child's diagnosis can be challenging.  When Andrew was born, it was very difficult for Teresa.  She had a hard time accepting it and did not have the best reaction.  It took her about 2 years to just truly accept it and be at peace with it. Though she loved her precious baby all the way through, something  just didn't click for her initially.If that rings true in your case, Teresa encourages you to reset your mind and focus on going day to day, milestone to milestone, living in the present and just enjoying your child.Teresa started writing at age 49.  She believes you are never too old or too young to begin writing.  Her Pecan Bayou series includes a character with Down syndrome named Danny.You can find Teresa's website and all her books at the links below.Connect with Teresa TrentFacebook:   https://www.facebook.com/teresatrentmysterywriter Twitter:   https://twitter.com/ttrent_cozymys Blog:   https://teresatrent.blog/     (Books to the Ceiling) Website:   http://teresatrent.com Goodreads:  https://www.goodreads.com/author/show/5219581.Teresa_Trent Instagram:   https://www.instagram.com/teresatrent_cozymys/ Bookbub:      https://www.bookbub.com/profile/teresa-trent Teresa's Amazon Author Page - https://www.amazon.com/Teresa-Trent/e/B005O7FIE2/Connect with SandyIG: https://www.instagram.com/sandydeppischEmbrace the Blessing Facebook Group: http://bit.ly/ETB4MEWebsite: http://www.embracetheblessing.com/

ETB 24: In this episode I talk with Heather Burdeaux, a former guest from episode ETB 4 Paying Attention to Behavior Changes, Expectation Management & Maintaining Friendships.As a  case manager Heather shares about Community First Choice (CFC), a program in Texas that provides certain services and supports to individuals living in the community who are enrolled in the Medicaid program and meet CFC eligibility requirements. Services and supports may include:activities of daily living (eating, toileting, and grooming), activities related to living independently in the community, and health-related tasks (personal assistance services);acquisition, maintenance, and enhancement of skills necessary for the individuals to care for themselves and to live independently in the community (habilitation);providing a backup system or ways to ensure continuity of services and supports (emergency response services); andtraining people how to select, manage and dismiss their own attendants (support management).Medicaid Buy In for Children: https://texasmedicaidwaivers.com/medicaid/medicaid-buy-in-programs/medicaid-buy-in-for-children/Community First Choice: https://texasmedicaidwaivers.com/medicaid/benefits-of-medicaid/community-first-choice/CLASS Form 3596 PAS/Habilitation Plan: https://www.hhs.texas.gov/handbooks/community-living-assistance-support-services-provider-manual/formsHCS Form 8510 HCS/TxHmL CFC PAS/HAB Assessment: https://www.hhs.texas.gov/handbooks/home-community-based-services-handbook/formsPaths to Medicaid: https://texasmedicaidwaivers.com/medicaid/Disability Rights Texas: https://www.disabilityrightstx.org/en/home/Connect with HeatherHeather Burdeaux: heatherburdeaux@gmail.comConnect with Sandy:IG: https://www.instagram.com/sandydeppischEmbrace the Blessing Facebook Group: http://bit.ly/ETB4MEWebsite: http://www.embracetheblessing.com/

EBT 23:  In this 2nd half of a 2 part episode I continue to talk with Cynthia Rodriguez, amazing mom, grandma, and special needs advocate who loves to reach out and help others.  If you have a child with a disability and happen to  cross Cynthia's path somewhere out in the world,  more than likely she will strike up a conversation to check in with you to see how things are going.  She'll offer suggestions and resources and may even accompany you to the right agency to get you the help you may need.   That's just who she is.Yet, 24 years ago when her son Victor was born with Down syndrome, Cynthia didn't even want to hold him for the first few days.   Life took an abrupt turn at that point and it took Cynthia a little while to accept all the changes.  From initial reluctancy to totally embracing her new journey, Cynthia is a source of love and laughter, drawing others in with her joy and making a positive difference for so many. In addition, Cynthia does Court monitoring visits for people who have guardianships to make sure they are being treated properly and have everything they need.If you haven't heard the first half of Cynthia's interview,  be sure to listen to it in its entirety.  You won't want to miss any of her inspiring perspective.GHFEDShttp://ghfeds.org/HCS - Home and Community Based Serviceshttps://www.hhs.texas.gov/providers/long-term-care-providers/home-community-based-services-hcsHealth Insurance Premium Payment (HIPP) Programhttps://www.hhs.texas.gov/services/financial/health-insurance-premium-payment-hipp-programSide by Side Parent Support Team: League Cityhttps://www.facebook.com/groups/155613631266509STAP - Specialized Telecommunications Assistance Program (STAP)https://www.hhs.texas.gov/services/disability/deaf-hard-hearing/stap-servicesSwallowing and Speech Serviceshttps://www.swallowingandspeechservices.com/Texas Medicaid Waivershttps://texasmedicaidwaivers.com/Connect with SandyIG: https://www.instagram.com/sandydeppischEmbrace the Blessing Facebook Group: http://bit.ly/ETB4MEWebsite: http://www.embracetheblessing.com/

EBT 22:  In this episode I talk with Cynthia Rodriguez, amazing mom, grandma, and special needs advocate who loves to reach out and help others.  If you have a child with a disability and happen to  cross Cynthia's path somewhere out in the world,  more than likely she will strike up a conversation to check in with you to see how things are going.  She'll offer suggestions and resources and may even accompany you to the right agency to get you the help you may need.   That's just who she is.Yet, 24 years ago when her son Victor was born with Down syndrome, Cynthia didn't even want to hold him for the first few days.   Life took an abrupt turn at that point and it took Cynthia a little while to accept all the changes.  From initial reluctancy to totally embracing her new journey, Cynthia is a source of love and laughter, drawing others in with her joy and making a positive difference for so many.  In addition, Cynthia does Court monitoring visits for people who have guardianships to make sure they are being treated properly and have everything they need. GHFEDShttp://ghfeds.org/HCS - Home and Community Based Serviceshttps://www.hhs.texas.gov/providers/long-term-care-providers/home-community-based-services-hcs Health Insurance Premium Payment (HIPP) Program https://www.hhs.texas.gov/services/financial/health-insurance-premium-payment-hipp-programSide by Side Parent Support Team: League Cityhttps://www.facebook.com/groups/155613631266509STAP - Specialized Telecommunications Assistance Program (STAP)https://www.hhs.texas.gov/services/disability/deaf-hard-hearing/stap-servicesSwallowing and Speech Serviceshttps://www.swallowingandspeechservices.com/Texas Medicaid Waivershttps://texasmedicaidwaivers.com/Connect with SandyIG: https://www.instagram.com/sandydeppischEmbrace the Blessing Facebook Group: http://bit.ly/ETB4MEWebsite: http://www.embracetheblessing.com/

In this episode I talk with Jennifer Fetter-Matthys about Ecologist School - Houston, an  engaging outdoor learning community that encourages children and families to get out in nature. Students learn about Science, Technology, Engineering, Art, Math, Outdoor Skills, Volunteerism and Leadership through hands-on, immersive lessons focused on nature.With a bachelor's degree in psychology, multiple years teaching K-5, and experience working with exceptionalities, Jennifer's  great at modifying and differentiating activities to meet individual needs .  She has experience with autism and ABA and welcomes children with special needs. In addition to  part time and full time outdoor events for students in K through 5th grade, Jennifer also offers an after school program, special events, camps, workshops and birthday parties.  Ecologist School-Houston workshops can be tailored for scouts, youth, family groups, service projects and any other organization. Connect with Jennifer Fetter-MatthysEmail: ecologistschoolhouston@gmail.com Instagram: https://www.instagram.com/ecologistschoolhouston/ Facebook: https://www.facebook.com/ecologistschool Recent Article About Ecologist  School - Houston: https://leaguecity.macaronikid.com/articles/62190bb8be5c2c2bdf149db9/the-ecologist-school---houston%3A-taking-education-outdoorsConnect with SandyIG: https://www.instagram.com/sandydeppischEmbrace the Blessing Facebook Group: http://bit.ly/ETB4MEWebsite: http://www.embracetheblessing.com/

In this episode I talk with Shae Spears, a Special Education teacher who has personally walked the journey of life with a disability.  With Dyslexia, an auditory processing disorder and ADHD,  Shae struggled all through school, never really learning to read or even comprehend what she was supposed to be reading.Shae was part of the first group of students to receive services under IDEA (The Individuals with Disabilities Education Act) of 1975.  IDEA is a law that makes available a free appropriate public education to eligible children with disabilities throughout the nation and ensures special education and related services to those children.She was in special education with an IEP until 8th grade.  Despite her learning challenges, Shae went on to earn an undergraduate degree in Early Childhood Education, a Masters degree in Special Education and a Master Certificate as an IEP coach.She has been teaching Special Education for 26 years, keeping her disabilities silent most of her professional life.   Shae is also a Special Ed Consultant and Master IEP Coach, supporting the neurodiverse community.Shae helps parents and students navigate special education and the IEP process or anything else they may be struggling with.  As a life coach she supports teens and young adults with disabilities to feel accepted, empowered and encouraged.Though she resides in Texas, Shae is available to help no matter where you live in whatever way you may need her support.Connect with Shae Spearshttps://ww.shaespears.comEmail: Shaespears4u@gmail.com Instagram: https://www.instagram.com/shae_spears4u/Facebook: https://www.facebook.com/shae4uConnect with SandyIG: https://www.instagram.com/sandydeppischEmbrace the Blessing Facebook Group: http://bit.ly/ETB4MEWebsite: http://www.embracetheblessing.com/

In this episode I talk with Angela Bishop, owner of Brewed Blessings, a community coffee shop where special needs adults can gain meaningful employment and education in a fun and relaxed atmosphere.  Angela sees everybody as an individual.  Since God loves us all she believes we should love each other for who we are no matter what our differences are.Five years ago, Angela had a dream of opening a coffee shop that employs individuals with special needs.   She knows God definitely called her to this.  No matter how many times she tried to ignore it, the dreams kept coming back.  It wasn't until she had the same dream multiple times that Angela decided it was time to act on it.   With encouragement and support from her husband Jim, Angela moved forward, filing the necessary paperwork for a non profit business.   God is working out all the details and sending the right people to help Angela make Brewed Blessings a reality.  Angela knows that anyone who works at, volunteers at, or visits Brewed Blessings will walk out blessed and walk away knowing they are making a difference in someone's life.Brewed Blessingshttps://www.brewedblessings.com/Facebook: https://www.facebook.com/profile.php?id=100070764337143IG: https://www.instagram.com/brewedblessings/Connect with Angela BishopEmail: angela@brewedblessings.com Dr. Grilli ~ Pediatric and Family Dentistryhttps://www.dcadentist.com/Connect with SandyIG: https://www.instagram.com/sandydeppischEmbrace the Blessing Facebook Group: http://bit.ly/ETB4MEWebsite: http://www.embracetheblessing.com/

In this 2nd half of a 2 part episode I continue to talk with Ashley Bennett, boy mom of 3 and amazing Special Education teacher.  Her oldest son, Ashton was born when Ashley was  just 19 years old.  He  was diagnosed with Autism at age 1.  As a teen mom,  taking college classes in addition to working, Ashley had to come to terms with the unexpected discovery that her baby boy had developmental delays.  When Autism was mentioned, Ashley didn't even fully comprehend what that meant for Ashton or for the future.Ashley talks about the early years when much of her time and attention was devoted to educating herself and helping her young son get all the interventions and therapies he needed.  She believes her son's diagnosis prompted a calling for her life's work.  Ashley persevered through the challenges to achieve not 1, but 3 college degrees.   She currently motivates and inspires her High School Life Skills students every day, making a positive difference for them and for their families.If you haven't heard the first half of Ashley's interview,  be sure to listen to it in its entirety.  You won't want to miss any of this amazing episode.Center for Autism and Developmental Disabilitieshttps://www.uhcl.edu/autism-center/Early Childhood Intervention Serviceshttps://www.hhs.texas.gov/services/disability/early-childhood-intervention-servicesConnect with Sandy:IG: https://www.instagram.com/sandydeppischEmbrace the Blessing Facebook Group: http://bit.ly/ETB4MEWebsite: http://www.embracetheblessing.com/

In this episode I talk with Ashley Bennett, boy mom of 3 and amazing Special Education teacher.  Her oldest son, Ashton was born when Ashley was  just 19 years old.  He  was diagnosed with Autism at age 1.  As a teen mom,  taking college classes in addition to working, Ashley had to come to terms with the unexpected discovery that her baby boy had developmental delays.  When Autism was mentioned, Ashley didn't even fully comprehend what that meant for Ashton or for the future.Ashley talks about the early years when much of her time and attention was devoted to educating herself and helping her young son get all the interventions and therapies he needed.  She believes her son's diagnosis prompted a calling for her life's work.  Ashley persevered through the challenges to achieve not 1, but 3 college degrees.   She currently motivates and inspires her High School Life Skills students every day, making a positive difference for them and for their families.This is part 1 of a 2 part episode.   Tune in next week for the second half of Ashley's adventures.Center for Autism and Developmental Disabilities https://www.uhcl.edu/autism-center/Early Childhood Intervention Serviceshttps://www.hhs.texas.gov/services/disability/early-childhood-intervention-servicesConnect with Sandy:IG: https://www.instagram.com/sandydeppischEmbrace the Blessing Facebook Group: http://bit.ly/ETB4MEWebsite: http://www.embracetheblessing.com/

In this 2nd half of a 2 part episode I continue to talk with Sandra Weber, special needs preschool teacher and mother of 8.  Though life has come at her full force, Sandra's outlook in the midst of numerous difficult circumstances is truly remarkable.  She faces challenges with a positive perspective and staunch determination; enduring overwhelming hardship.  She is most definitely a pillar of strength for her family and an inspiration to others. Sandra discusses the unique situations her family has faced, including the birth of triplets born at 32 weeks; 2 of whom have Down syndrome, while a 7 year old sibling was battling brain cancer and their 20 month old sibling passed away from an accidental drowning.If you haven't heard the first half of Sandra's interview,  be sure to listen to it in its entirety.  You won't want to miss any of this incredible conversation.Connect with GHFEDS ~ Greater Houston Families Exploring Down SyndromeWebsite:  http://ghfeds.org/Connect with Special Olympics:https://www.specialolympics.org/Teslong Digital Otoscope:https://www.amazon.com/Otoscope-Teslong-Microscope-Inspection-Adjustable/dp/B07PHLG4C2/ref=sr_1_3?crid=273P8VKK659J&keywords=teslong+digital+otoscope+with+ear+wax+remover&qid=1644004963&sprefix=teslong+digit%2Caps%2C110&sr=8-3Connect with Sandra:sandraw1121@gmail.comhttps://www.facebook.com/sandradwConnect with Sandy:IG: https://www.instagram.com/sandydeppischEmbrace the Blessing Facebook Group: http://bit.ly/ETB4MEWebsite: http://www.embracetheblessing.com/

In this episode I talk with Sandra Weber, special needs preschool teacher and mother with 8 children of her own.  Though life has come at her full force, Sandra's outlook in the midst of numerous difficult circumstances is truly remarkable.  She faces challenges with a positive perspective and staunch determination; enduring overwhelming hardship.  She is most definitely a pillar of strength for her family and an inspiration to others.  Sandra discusses the unique situations her family has faced, including the birth of triplets born at 32 weeks; 2 of whom have Down syndrome, while a 7 year old sibling was battling brain cancer and their 20 month old sibling passed away from an accidental drowning.  This is part 1 of a 2 part episode.  Tune in next week for the second half of the story.Ronald McDonald House:https://www.rmhc.org/Connect with Sandy:IG: https://www.instagram.com/sandydeppischEmbrace the Blessing Facebook Group: http://bit.ly/ETB4MEWebsite: http://www.embracetheblessing.com/

In this 2nd half of a 2 part episode I continue to talk with Brianna TenBrink, an eloquent, wise and compassionate 23 year old big sister to 16 year old Myah and 15 year old Leah, her younger siblings who are on opposite ends of the Autism spectrum.  Brianna shares her perspective on how her experiences as the only neurotypical  child in the family shaped the person she is today.   From a young age Brianna took it upon herself to become the 'glue' that helped hold the family together.   Her sisters made her a better person and influenced and directed Brianna's purpose and passion in life.  Service and Teaching are at the heart of who she is and Brianna has aspirations to make lasting positive changes for all people with disabilities.Brianna is the eldest sibling to two younger sisters with Autism on vastly different sides of the spectrumFor the past 13 years, Brianna has been a tireless advocate for individuals, much like her siblings, winning the Sibling Scholarship from Knapps and Roberts law firm, the Rose Award from disAbility Connections, Inc., and Advocate of the Year award from the Arc of the Gulf Coast which granted her the opportunity to speak on the experiences of being a sibling at district-wide conferences.Brianna is a Partner in the Texas Partners in Policymaking Program, a Marketing Advisor & Sensitivity Panelist for Disability Book Week, and the Director of Marketing and Sales for Neural Divergence, LLC.Brianna is the co-founder of Project LEAH (Leaders Ending Abuse and Harm), which is an organization that armors parents, families, and allies of loved ones of students in the Texas Public School System who have endured abuse with educational, legislative advocacy training to foster macro-level change. If you haven't heard the first half of Brianna's interview,  be sure to listen to it in its entirety.  You won't want to miss any of this awe-inspiring conversation.Connect with Brianna:Instagram: https://www.instagram.com/thebriannashley/Facebook: https://www.facebook.com/briashtenProject LEAH Facebook Group: https://www.facebook.com/groups/4127855043987645/Connect with Sandy:IG: https://www.instagram.com/sandydeppischEmbrace the Blessing Facebook Group: http://bit.ly/ETB4MEWebsite: http://www.embracetheblessing.com/

In this episode I talk with Brianna TenBrink, an eloquent, wise and compassionate 23 year old big sister to 16 year old Myah and 15 year old Leah, her younger siblings who are on opposite ends of the Autism spectrum.  Brianna shares her perspective on how her experiences as the only neurotypical  child in the family shaped the person she is today.   From a young age Brianna took it upon herself to become the 'glue' that helped hold the family together.   Her sisters made her a better person and influenced and directed Brianna's purpose and passion in life.  Service and Teaching are at the heart of who she is and Brianna has aspirations to make lasting positive changes for all people with disabilities. Brianna is the eldest sibling to two younger sisters with Autism on vastly different sides of the spectrumFor the past 13 years, Brianna has been a tireless advocate for individuals, much like her siblings, winning the Sibling Scholarship from Knapps and Roberts law firm, the Rose Award from disAbility Connections, Inc., and Advocate of the Year award from the Arc of the Gulf Coast which granted her the opportunity to speak on the experiences of being a sibling at district-wide conferences.Brianna is a Partner in the Texas Partners in Policymaking Program, a Marketing Advisor & Sensitivity Panelist for Disability Book Week, and the Director of Marketing and Sales for Neural Divergence, LLC.Brianna is the co-founder of Project LEAH (Leaders Ending Abuse and Harm), which is an organization that armors parents, families, and allies of loved ones of students in the Texas Public School System who have endured abuse with educational, legislative advocacy training to foster macro-level change.  This is part one of a 2 part series.  Tune in January 26th for the second half of this awe-inspiring conversation.Connect with Brianna:Instagram: https://www.instagram.com/thebriannashley/Facebook: https://www.facebook.com/briashtenProject LEAH Facebook Group: https://www.facebook.com/groups/4127855043987645/Connect with Sandy:IG: https://www.instagram.com/sandydeppischEmbrace the Blessing Facebook Group: http://bit.ly/ETB4MEWebsite: http://www.embracetheblessing.com/

In this episode I talk with Laura Tayerle, the very first special needs mom I met many years ago when her daughter Morgan was just 5 years old.   Laura inspired me in so many ways long before my own special needs child was ever born.  She was the mom who modeled how to be a voice for your child,  how to treat them just like anyone else and how to juggle it all with strength and determination. Laura discusses Morgan's early years and what life was like for a young mom in a new town navigating the complexities of an unexpected diagnosis.  She walks us through the joys and challenges of raising Morgan, who is now 32 years old, along with her 2 younger sisters and discusses the successful transition Morgan has made in living away from home with a support staff to assist her.Perinatal Stroke - Child Neurology Foundation:https://www.childneurologyfoundation.org/disorder/perinatal-stroke/GI Symptoms Linked to Behavioral Problems in Children, Especially Those with Autismhttps://health.ucdavis.edu/newsroom/news/headlines/gi-symptoms-linked-to-behavioral-problems-in-children-especially-those-with-autism/2020/08Autism & GI Problems:  How to Helphttps://www.elemy.com/studio/mood-disorders/autism-and-gi-issues/Bristol Stool Scalehttps://www.webmd.com/digestive-disorders/poop-chart-bristol-stool-scaleBaby Sense Alarmhttps://www.amazon.com/Babysense-Temperature-Infrared-Lullabies-V24R/dp/B083KMZD58/ref=pd_lpo_1?pd_rd_i=B083KMZD58&psc=1Sleep Safe Bed:  https://sleepsafebed.com/Sleep Safe Bed GiveAway - One Free Bed is Given Away  Each Quarter:https://sleepsafebed.com/giveaway/Connect with Sandy:IG: https://www.instagram.com/sandydeppischEmbrace the Blessing Facebook Group: http://bit.ly/ETB4MEWebsite: http://www.embracetheblessing.com/

In this episode I talk with Mary Ann Hughes, mother of 2 young adults with Autism  as she shares her special needs divorce story.   Mary Ann went from being completely blindsided and overwhelmed, unsure of what next steps were needed, to assembling a support team  of professionals who helped her successfully navigate a lengthly 2 year divorce process which culminated in a trial.Some have estimated the divorce rate among families with children with autism or other disabilities to be as high as 70-80%. Mary Ann used the wisdom she gained through her own experience in addition to ongoing work in the field to make a difference for others.  She created a company, Special Family Transitions, to guide special needs families through divorce with the best possible outcome and as little stress, time, and expense as possible.Connect with Mary Ann:Email address: Maryann@specialfamilytransitions.comWebsite: https://www.specialfamilytransitions.com/ Special Family Transitions YouTube channel (would love for people to subscribe )  https://youtube.com/channel/UChI4BaUMGf50O2yPE_YnjFASpecial Family Transitions Facebook Page: https://m.facebook.com/specialfamilytransitionsPrivate Facebook group: Divorce Journey Support for Moms of Children with Autism & Special Needs:https://www.facebook.com/groups/309739357366936/Special Family Transitions on Instagram: https://www.instagram.com/specialfamilytransitions/For Information on LoneStar LEND, or  to apply for the program:https://med.uth.edu/pediatrics/neurology/pediatric-neurology-fellowship-programs/lonestar-lend-fellowship/Connect with Sandy:IG: https://www.instagram.com/sandydeppischEmbrace the Blessing Facebook Group: http://bit.ly/ETB4MEWebsite: http://www.embracetheblessing.com/

In this episode I talk with Kileen McDonald as she shares her struggles with infertility, her subsequent adoption of a beautiful baby boy with Down syndrome and her greatest joy in being a mom to her now 13 year old son, Ches.   Kileen also discusses the death of her spouse, Pam and talks about lovingly helping Ches process everything during those difficult days.  Kileen believes in educating yourself about your child's diagnosis but encourages parents to make sure to get your education from the right sources.   NDSS - National Down Syndrome Society and NDSC - National Down Syndrome Congress are two great places to begin if you have a child with Down syndrome.Connect with NDSS - National Down Syndrome Societyhttps://www.ndss.org/Connect with NDSC - National Down Syndrome Congresshttps://www.ndsccenter.org/Connect with GHFEDS ~ Greater Houston Families Exploring Down SyndromeWebsite:  http://ghfeds.org/Connect with Sandy:IG: https://www.instagram.com/sandydeppischEmbrace the Blessing Facebook Group: http://bit.ly/ETB4MEWebsite: http://www.embracetheblessing.com/

In this episode I talk with Mary Jane Williams, Executive Director of Family to Family Network.   Family to Family Network helps individuals with disabilities and their family members define and achieve success for themselves and their loved ones. As a mother of 2 young adults with disabilities, Mary Jane discusses first hand the positive impact connecting with other families had made for family.  She encourages parents to learn everything possible about their child's diagnosis by attending training events offered through school districts and local organizations.   Mary Jane firmly believes it is important for families to see possibilities in their kids with disabilities.  ALL children should be included and supported in our schools and community in order to ensure the future success of children with disabilities.  Connect with Family to Family Network:https://f2fn.org/Email Address:  info@familytofamilynetwork.orgPhone Number: 713-466-6304Texas Partners in Policy Making :https://txpartners.org/Partners in Policy Making Online Courses:https://partnersonlinecourses.com/Connect with Sandy:IG: https://www.instagram.com/sandydeppischEmbrace the Blessing Facebook Group: http://bit.ly/ETB4MEWebsite: http://www.embracetheblessing.com/https://uniquelyhuman.com/

In this episode I talk with Kim Lindquist about life with Cowboy,  her 23 year old son who has Autism.  Kim shares how her faith helped her through early dark days of behavior challenges, anxiety and discouragement.  She encourages parents to seek help if they begin to notice signs of anxiety or depression.  Kim recommends Biomedical intervention and proposes it can work in conjunction with traditional medicine to bring about positive outcomes.  She believes that taking care of ourselves better equips us to care for others. Kim is a gifted writer, who injects humor into her stories of life with Autism.  Her desire is to help others have joy and most of all hope.Connect with Kim:https://www.kimlindquistauthor.com/Autism Support: autismsocietytxgulfcoast@gmail.comConnect with a Bible Study for Caregivers:https://www.sagemontchurch.org/women/#/Connect with Imagine Enterprises:https://www.imagine-enterprises.org/Medicaid Waivers Website:  http://texasmedicaidwaivers.comHIPP - Texas Medicaid program that helps families pay for employer-sponsored health insurance premiums:https://www.hhs.texas.gov/services/financial/health-insurance-premium-payment-hipp-programConnect with Sandy:IG: https://www.instagram.com/sandydeppischEmbrace the Blessing Facebook Group: http://bit.ly/ETB4MEWebsite: http://www.embracetheblessing.com/