Podcasts about specialneedsmom

Receiving a special needs diagnosis for your child is a moment you will never forget. Jillian Benfield Down Syndrome mom and author of The Gift of the Unexpected joins me today for a really great conversation. We talk about Jillian's journey through grief and parenting, how ableism might affect your vision of a diagnosis, and finding hope despite life's expectations. 

Jill wraps up the podcast! I started in 2016 interviewing my kids and how they were affected by Tuberous Sclerosis Complex. It was absolutely divine inspiration from the start and branched out shortly after to interviewing community members and other professionals who worked with those affected. From there, I explored many different topics, providing information and resources in interview form, all with relevance to the individuas and/or parent/caregivers affected by a chronic illness like TSC. Pushing the boundaries of what was deemed "safe and effective" by our medical system, I continued to put info out there based on my own lived experience as a parent/caregiver living and dealing with what I'd come to discover is CPTSD if you want to use a label. It was my vision and still is that all "remedies" for improving the quality of life of all involved in the wheels of chronic illness, particularly one such as TSC which affects all the vital body organs, will be an option for all. Why should we hold back the river when there are so many speaking about how their lives have been impacted by sharing their truths, sharing what's worked for them and what potentially might help another ease the very real and almost daily traumas of attempting to live with an open heart and navigate our inverted systems of care.Many of these podcasts go against the grain of what people are comfortable hearing. There are always positive takeaways but there are some heavy heavy experiences that people are walking through and talking about and must be given voice. I think through honest conversation, and taking full responsibility for one's reactions to other's sharing from their most painful, heart-wrenching moments, we can begin to hear each other once again at least long enough to realize, we're all having vastly different experiences yet we all long to be here now, safe, loved, whole, home.Thanks for tuning in and being here there and everywhere. It's been the pleasure of a lifetime to have the opportunity to create and share this work. Love Jill

Jill wraps up the podcast! I started in 2016 interviewing my kids and how they were affected by Tuberous Sclerosis Complex. It was absolutely divine inspiration from the start and branched out shortly after to interviewing community members and other professionals who worked with those affected. From there, I explored many different topics, providing information and resources in interview form, all with relevance to the individuas and/or parent/caregivers affected by a chronic illness like TSC. Pushing the boundaries of what was deemed "safe and effective" by our medical system, I continued to put info out there based on my own lived experience as a parent/caregiver living and dealing with what I'd come to discover is CPTSD if you want to use a label. It was my vision and still is that all "remedies" for improving the quality of life of all involved in the wheels of chronic illness, particularly one such as TSC which affects all the vital body organs, will be an option for all. Why should we hold back the river when there are so many speaking about how their lives have been impacted by sharing their truths, sharing what's worked for them and what potentially might help another ease the very real and almost daily traumas of attempting to live with an open heart and navigate our inverted systems of care. Many of these podcasts go against the grain of what people are comfortable hearing. There are always positive takeaways but there are some heavy heavy experiences that people are walking through and talking about and must be given voice. I think through honest conversation, and taking full responsibility for one's reactions to other's sharing from their most painful, heart-wrenching moments, we can begin to hear each other once again at least long enough to realize, we're all having vastly different experiences yet we all long to be here now, safe, loved, whole, home. Thanks for tuning in and being here there and everywhere. It's been the pleasure of a lifetime to have the opportunity to create and share this work. Love Jill

I recently had the distinct pleasure of interviewing Lisa Smith recently on TSC Talks. I met Lisa through a mutual friend, as is explained in the podcast. I was thrilled to do a podcast with another special needs parent and local to Massachusetts. Lisa is a parent of 22 years old Nick, who experiences nonverbal autism, has adopted several children, and over the years has fostered 27. During our interview not only was Lisa able to draw from and articulate profound experiences and topics in such a way as to not only connect them to her lived experience, but she was also able to illustrate how she's taken the time to integrate and utilize all of it to further evolve as a soul but to also facilitate trust, healing, and connection for all her children, biological, adopted and fostered. Her words tell the story, her faith guides her. One of the most important points of our discussion was the realization that it is not these children that are “lucky to have her,” but it is she that is lucky to have them. As a special needs parent myself, this awareness was a true turning point in my understanding of this divine assignment where I became the student and realized my children are my teachers, one that Lisa feels and experiences every day. “It's biblical, she said at one point “And when I began to read the Bible, I had learned that some of my actual walks in life, were very biblical… There's a story that says, God got the 99 sheep, but there was one on the hill. He went back for that one. Most people in life. So God has designed me through my journey, not to forget the one.” “Presence, presence, and presence. And to me? Be present. People always say things like, oh, if I win the lottery, I will do that. And I always tell people all the time I won the lottery five times, five children and people say, oh, they're so lucky to have you, but really….How do I know that I'm going to take care of my disabled son someday? Right? How do I know they're not there to help me when I become disabled someday? We do not know, you know, so we, you know, and, and we don't do it for those selfish reasons. So, we don't do anything to get things, you know, and, and, you know, we do things because that's who we are and that's our heart.” I appreciated this podcast so much and hope you will too. I feel it was put in front of me by my higher self, as sound bite after sound bite so many of Lisa's words not only related to me personally but also inspired and challenged me. Her faith in God is huge and expansive but she shares honestly the hard truths she's faced personally to get to where she is now. Thanks, Lisa, for all the ways you are serving a higher calling and being willing to share your journey with me and this audience. An article about Lisa Smith: https://www.wickedlocal.com/story/archive/2012/04/27/taunton-mom-using-what-she/38199711007/ Time stamps to be added!

I recently had the distinct pleasure of interviewing Lisa Smith recently on TSC Talks. I met Lisa through a mutual friend, as is explained in the podcast. I was thrilled to do a podcast with another special needs parent and local to Massachusetts. Lisa is a parent of 22 years old Nick, who experiences nonverbal autism, has adopted several children, and over the years has fostered 27. During our interview not only was Lisa able to draw from and articulate profound experiences and topics in such a way as to not only connect them to her lived experience, but she was also able to illustrate how she's taken the time to integrate and utilize all of it to further evolve as a soul but to also facilitate trust, healing, and connection for all her children, biological, adopted and fostered. Her words tell the story, her faith guides her. One of the most important points of our discussion was the realization that it is not these children that are “lucky to have her,” but it is she that is lucky to have them. As a special needs parent myself, this awareness was a true turning point in my understanding of this divine assignment where I became the student and realized my children are my teachers, one that Lisa feels and experiences every day. “It's biblical, she said at one point “And when I began to read the Bible, I had learned that some of my actual walks in life, were very biblical… There's a story that says, God got the 99 sheep, but there was one on the hill. He went back for that one. Most people in life. So God has designed me through my journey, not to forget the one.”“Presence, presence, and presence. And to me? Be present. People always say things like, oh, if I win the lottery, I will do that. And I always tell people all the time I won the lottery five times, five children and people say, oh, they're so lucky to have you, but really….How do I know that I'm going to take care of my disabled son someday? Right? How do I know they're not there to help me when I become disabled someday? We do not know, you know, so we, you know, and, and we don't do it for those selfish reasons. So, we don't do anything to get things, you know, and, and, you know, we do things because that's who we are and that's our heart.”I appreciated this podcast so much and hope you will too. I feel it was put in front of me by my higher self, as sound bite after sound bite so many of Lisa's words not only related to me personally but also inspired and challenged me. Her faith in God is huge and expansive but she shares honestly the hard truths she's faced personally to get to where she is now. Thanks, Lisa, for all the ways you are serving a higher calling and being willing to share your journey with me and this audience.An article about Lisa Smith: https://www.wickedlocal.com/story/archive/2012/04/27/taunton-mom-using-what-she/38199711007/ Time stamps to be added!

Talking about ALL of the kids today. We discussed the ins and outs of parenting neuro-divergent and neuro-typical children within each of our families. Age gaps, sibling dynamics, and what we hope the future holds for each of our kids as they grow up and become more independent.  We hope you can relate to one or more of our stories today. All of our families are very different, which means sibling relationships can be very different. There is no right way to do this parenting thing, but hearing others' stories can hopefully spark some ideas to implement in your own home. Most importantly, we hope this episode gives you hope on how to discuss divergence within your own family and close friends.  *In what ways do you parent each of your children differently? What are their unique needs? *How can we talk about autism and our family dynamic in an open and honest way? With others outside our family? *Consider opening up to your children about your family concerns. How can your typical kids participate in including their special needs siblings? Where to find Moms Talk Autism Website  Email  Instagram  Where to find Jody Website  Email Instagram  Where to find Shannon Email  Instagram  Where to find Jean Email  Instagram  Where to find Tash Email  Instagram  Where to find Brittney Website Email Instagram

Today we talked about trusting others to care for our autistic children. Whether family members, teachers or therapists. We talked about how we can gain that trust and also how to let go of our fears and find confidence in others. We hope you'll gain better insight into why we are sometimes stuck in wanting to control situations involving our kids. We also want to shed light on how trusting others can alleviate some of the stress of needing to do everything for our kids. *What is the deeper cause of distrust with family members/ *What can we do to help and gain more trust and better communication with those who care for our kids? *What would be the benefit of letting go of control and trusting?   Check us out and say hello Where to find Moms Talk Autism Website  Email  Instagram  Where to find Jody Website  Email Instagram  Where to find Shannon Email  Instagram  Where to find Jean Email  Instagram  Where to find Tash Email  Instagram  Where to find Brittney Website Email Instagram

I'm sure you've said, "I wish I would've known.." many times. We have. That's why we decided to have a whole episode on it! We're sharing things that we wish we had known from the beginning. Talking about family & friends, services, diagnosis & more. When we start this journey of autism with our families, we are sorta thrust into a lifestyle that we have no clue how to navigate. There are so many things that we are focusing on. One foot in front of the other. Trying to manage everything, including our emotions, and navigate the world with our new reality. Amid all that, lessons we are learning that we wish we would have known BEFORE they hit. "I wish I'd known ______." That's what we'll be talking about today!   Check us out and say hello Where to find Moms Talk Autism Website  Email  Instagram  Where to find Jody Website  Email Instagram  Where to find Shannon Email  Instagram  Where to find Jean Email  Instagram  Where to find Tash Email  Instagram  Where to find Brittney Website Email Instagram  

Ever feel caregiver burnout? Ever feel like you are in a hamster wheel as a caregiver?   Listen to this convo.   Grief isn't linear; it's a wheel of adaptation.   Dr. Nancy Miller, psychologist and social worker, wrote Nobody's Perfect: Living + Growing with Children Who Have Special Needs. In this book, she worked with four moms over five years and distilled their experiences into one book.   The model is derived from communication with the moms, experience of the working families, the writings of parents and professionals. "Adaptation" kicks in when we feel robbed of our chance and our Child's chance for living an equal life.   There are four stages, and stick with us as we will dive into each. Think of them like four hemispheres, similar to a Venn diagram nature, constantly shape-shifting through your journey.   The 4 S's: Survival, Searching, Settling In, and Separating are very real and relevant to understanding what we may all be feeling, whether it's exclusively or simultaneously.   Advocacy is a muscle, and this is a journey about endurance.   Hot tips and takeaways from the conversation to ease the distress you as a parent would experience at any of the stages:   Make time for yourselves, understand your feelings + create a support system. Honor yourself as well as validate your feelings. Always remain hopeful even when it feels hopeless.   All easier said than done; that is why we are here to offer the support we all have been longing for.   Check us out and say hello Where to find Moms Talk Autism Website  Email  Instagram  Where to find Jody Website  Email Instagram  Where to find Shannon Email  Instagram  Where to find Jean Email  Instagram  Where to find Tash Email  Instagram  Where to find Brittney Website Email Instagram

If you have ever or currently been depressed, this is a great episode to listen to dial into different perspectives and times depression has hit other parents walking the autism parenting journey. Depression can be really sneaky sometimes. It can also be a very heavy topic. Here are some signs + symptoms how it may present or manifest: Persistent feelings of sadness + hopelessness Anxiety + Irritability Sleeping to much or too little Loss of interest in activities that were once enjoyable Difficulty concentrating, making decisions + remembering things Low energy + fatigue Thoughts or talk of Suicide Some others not so quickly correlated but to be considered: Temporary Mood Boosts Significant Weight gain or loss Increase appetite Heavy Feeling in arms + legs Body aches or headaches Insomnia or extended sleep Extreme negative response to perceived criticism or rejection It's important to recognize when you need to help. Know that medication is okay if it is prescribed + doesn't mean you are a terrible a parent. It means you are a great one, because you are willing to take whatever steps necessary to support your child. Depression is a real disorder, even in the absence of grief, some of us are easily predisposed to experiencing it more than others. When symptoms are lasting longer than a week, reflect and see what you might need to put in place or in play to take care of you. We love you + we want you to love yourselves just as much! Check us out and say hello Where to find Moms Talk Autism Website  Email  Instagram  Where to find Jody Website  Email Instagram  Where to find Shannon Email  Instagram  Where to find Jean Email  Instagram  Where to find Tash Email  Instagram  Where to find Brittney Website Email Instagram

Do you know what the bargaining stage of the grief process is?  Listen to this episode to find out. It isn't quite what most of us think   Check us out and say hello Where to find Moms Talk Autism Website  Email  Instagram  Where to find Jody Website  Email Instagram  Where to find Shannon Email  Instagram  Where to find Jean Email  Instagram  Where to find Tash Email  Instagram  Where to find Brittney Website Email Instagram

Anger, a stage in grief that sometimes feels unjustified! What happens when we get our kiddo's diagnosis, and then we feel consumed by anger? In this episode, we'll be chatting about this emotion, its relevance, and how we each worked through it. What did this stage of grief look like for you? Was this something you sat in for very long, and do you still go through stages where you get angry again about this diagnosis? Here's what I'll say...your anger is and was valid. This stage is normal and not linear; we can walk in and out of this stage from diagnosis until we take our last breath. This process and journey through the grief of what we thought our lives would look like are normal and very different for each of us, so please know that you are seen and heard in your feelings!   Check us out and say hello Where to find Moms Talk Autism Website  Email  Instagram  Where to find Jody Website  Email Instagram  Where to find Shannon Email  Instagram  Where to find Jean Email  Instagram  Where to find Tash Email  Instagram  Where to find Brittney Website Email Instagram

Could you ever imagine losing a child? What if that child's twin brother was then diagnosed with autism? Two very traumatic life events in a short period...would this have you questioning why me? What could I have possibly done to God to deserve this life?   In this episode, Natasha will share with you what felt like walking through fire only to come out the other side with nothing but love, acceptance and gratitude. She will also share with you how her and her husband decided that finding peace in their grief was easier than holding onto what they thought "should have been". And finding complete peace in the story they were making.   Check us out and say hello Where to find Moms Talk Autism Website  Email  Instagram  Where to find Jody Website  Email Instagram  Where to find Shannon Email  Instagram  Where to find Jean Email  Instagram  Where to find Tash Email  Instagram  Where to find Brittney Website Email Instagram

Brittney is a mom of four kids: two typical and two with autism. We talk about the beginning stages of diagnosis and what the future can hold for our kids. Can you know for sure what the future holds for your child? What does life as a teenager or an adult look like for our kids? How do I start building a new dream and life around my child now that they have a diagnosis? Every child and situation is different, but there are some universal things we can all do to find peace and happiness as we begin our autism journey. Check us out and say hello Where to find Moms Talk Autism Website  Email  Instagram  Where to find Jody Website  Email Instagram  Where to find Shannon Email  Instagram  Where to find Jean Email  Instagram  Where to find Tash Email  Instagram  Where to find Brittney Website Email Instagram

Shannon is a mom of two, and a wife to a first responder. We talk all things about going through the diagnosis. The struggle of processing things in your own way and what that looks like in a marriage. Shannon shares What the "new" picture may look like and how to best serve these exceptional babies that we have been given. Self-care any WHY we as mothers have to learn to take care of us. Check us out and say hello Where to find Moms Talk Autism Website  Email  Instagram  Where to find Jody Website  Email Instagram  Where to find Shannon Email  Instagram  Where to find Jean Email  Instagram  Where to find Tash Email  Instagram  Where to find Brittney Website Email Instagram

Welcome to the Moms Talk Autism Podcast! Jody, Shannon, Brittney, Jean & Tash are 5 moms raising children with autism, ADHD, epilepsy and a variety of other neurological differences. We're so happy you're here. And honored to walk this special needs journey with you. Don't forget to FOLLOW our podcast. You'll get each new episode right when it comes out. Today we're talking about who we are, why we decided to start a podcast and how we met. Check us out and say hello Where to find Moms Talk Autism Website  Email  Instagram  Where to find Jody Website  Email Instagram  Where to find Shannon Email  Instagram  Where to find Jean Email  Instagram  Where to find Tash Email  Instagram  Where to find Brittney Website Email Instagram

Enfócate en lo bueno y olvida lo malo, no te desgastes, sólo sé feliz, buenas vibras ante todo... Pueden ser ejemplos de ciertas frases que minimizan emociones naturales en momentos difíciles. Deben existir espacios para validarlas, como pueden ser por ejemplo, las etapas de duelo cuando llega un diagnóstico. Les contaré cómo el Positivismo Tóxico puede causarle a padres Neurodiversos muchas frustraciones, y al mismo tiempo, busco informar de este tema controversial, para que todos aprendamos y evitemos esa incomodidad social, que sin querer herir se logra lo que justamente se trata de evitar.

Autismo sin Miedo nace un poco de "Mis Miedos" que no logro superar y al mismo tiempo, he decido afrontar y compartir para que no me consuman. He encontrado que entre más abierta soy y más comparto, más ayuda y más empatía genero en mi entorno. Es importante NO sufrir en silencio y saber que con apoyo, uno tiene que afrontar los miedos de frente y aunque la incertidumbre del futuro siempre se encontrará presente, no nos queda de otra que ser familias Neurodiversas Valientes!

Today’s guest provides amazing insight into the life of a special needs mother. Darlene Rodrigo is the executive producer of the Ellen K show. Her 13 year old daughter Bella has Down syndrome and autism. This mother and daughter duo are on a mission to advocate and spread awareness. Michaela and Darlene talk about empath overwhelm, non verbal communication and how others reactions really do make a difference. Scott also shares an emotional story about someone giving him a chance, and how that then changed his entire life with Michaela Mystic Michaela Instagram Mystic Michaela Website Mystic Michaela Facebook Group Mystic Michaela Podcast Itunes Mystic Michaela Bonus Episode - Every Aura Color Explained Darlene Rodrigo Instagram Bella Rodrigo Instagram Download the Curtsy app and enter code “KYA” at checkout for 15% off! Curtsy - Thrifting, Delivered on the App Store (apple.com) Get a free 30 day trial at Dipsea! dipseastories.com/kya Get $25 your order at Brooklinen when you spend $100 or more with promo code “KYA”! brooklinen.com Get $20 off your test at Modern Fertility! modernfertility.com/kya Get 15% off your first month of Betterhelp! betterhelp.com/kya

 I'm hearing moms caring for kids with extra-ordinary needs telling me they want to live more intentionally. Their lives are hectic and chaotic - time seems to be slipping away and they have no idea where all the time has gone. When I ask people what they think of when they hear the word intentional they immediately go to accomplishments, tasks, and goals. To them living intentionally is making sure all the things they wanted to fit in, made it. I will have another podcast all about that! but for today let's stick with the IDEA of the intention. Go with me on this. Listen in and tell me if I've changed how you think of things. Facebook Instagram SurvivingTheWaitingRoom.co

We have come to the point of the year that either we've moved on from our shiny new year idea. Or we're putting things in place to make them happen. But sometimes if we're being honest, we need a little support to remind us of what's possible. I know last year, that is something that I did. Our secret thoughts keep us from moving forward and yet we often don't see them as big enough to get help with. Connect with me at: Facebook Instagram Mom, You Got This! Summit FocusedDirection.com And if you're interested in the course doors are open now until February 14! So Give yourself some lovin' and sign up!  

In my search to see if there were other moms of kids with medical needs drowning and needing help, I discovered we needed help in a lot of areas.  Creating the idea of a summit just for moms of kids with medical conditions. It's called the Mom, You Got This! Summit and is featuring 16 experts all there to help us in one place! Listen in and see if you recognize any of them!

Setting goals. It seems to be the thing to do when a new year starts. And indeed, they can be really helpful on what you want to focus your energy on. Is there a special skill you want to help your kid conquer? Is it something for yourself? It really can be anything: from developing a new skill to saving money for a treatment. But when setting the goal… 1. make sure they are your goals - your dreams. Not goals based on the expectations from the outer world. 2. Focus on the journey. 3. And while we’re at it: don’t forget to schedule in some fun!

In an effort to get to know why I’m the way I am, a few episodes will be dedicated to sharing some of my story. This week I’ve decided to share some of my Drew’s story. For full show notes head over to https://www.lesabeals.com. https://www.facebook.com/NotYourCollegeLife https://www.instagram.com/notyourcollegelife https://www.pinterest.com/bealslesa

Alma Ruth is originally from Monterrey, Mexico, a lover of people from different cultures and languages and a recent legal immigrant to the United States. Today she resides with her two special needs boys in McAllen, TX, working and serving among asylum seekers and international communities at the Mexico-Texas border.SHOW NOTESThe Lord began preparing Alma as a child. For the past ten years, her love of Jesus has guided her in her Love Mercy ministry by visiting refugee women in camps on the Texas/Mexico border, but not in an attempt to save them from their physical circumstances. Her focus is simple. It’s personal. She listens to their stories in order to know these women relationally, prays with and over them by name, and most importantly reminds them of their dignity as people and as children of God. Practicing compassion, empathy and mercy will change us all. To Alma, “That is the difference between charity and ministry.”Email alma@love-mercy.org for ways to help this growing ministry.For more Alma: Instagram @lovemercyblogFacebook Alma RuthTwitter @Alma_Ruthwww.love-mercy.org

Sasha is so amazing! She is a BCBA, M.A., is the founder and president of The Autism Helper, Inc. She is a board certified behavior analyst and former special education teacher. Sasha works full time as a consultant, writer, and behavior analyst. Sasha manages and writes The Autism Helper Blog, as a way to share easy to use and ready to implement strategies and ideas. Sasha also travels internationally as a speaker and consultant providing individualized training and feedback to parents, educators, therapists and administrators in the world of autism. She is currently an adjunct professor in the school of Applied Behavior Analysis at The Chicago School of Professional Psychology. Sasha received her undergraduate degree in Special Education from Miami University and has a Masters Degree in Applied Behavior Analysis from The Chicago School of Professional Psychology.    The Autism Helper has many resources for all ages and a lot for free! Check out her website here: https://theautismhelper.com/     Sasha has so many resources for homeschooling as well. We need these resources, especially right now with the stay at home order. Thank you Sasha for joining me on Autism Mastermind.       ___________________________ Inclusion@autismmastermind.co  autismmastermind.co  FB: @sautismmasterminds  IG: @autismmastermind Youtube: @AutismMastermind linktr.ee/autismmastermind        

  Wow, what a year. In April 2019, I decided to start a podcast. Then I talked Chad into joining me. We have both poured our hearts into episodes, interviewed amazing guests and met many friends along the way. We have also learned a ton and cannot wait for the future. Thank you all for joining us, subscribing, listening & reviewing our little podcast. We love our community.    I will share the podcasts I mentioned on our social media  ___________________________ Inclusion@autismmastermind.co  autismmastermind.co  FB: @sautismmasterminds  IG: @autismmastermind Youtube: @AutismMastermind linktr.ee/autismmastermind

Yay! Paige is 18!  Chad and I chat about Paige’s 18 social distancing party, how she is handling CoronaVirus Times, How we are coping as a quarantined family. It’s riveting …a must listen. Inclusion@autismmastermind.co  autismmastermind.co  FB: @sautismmasterminds  IG: @autismmastermind Youtube: @AutismMastermind linktr.ee/autismmastermind

This Episode is all about accepting what Life gives you and being able to move through the adversity to find your peace. AnGele is so inspiring, sharing everything she has been through and how she has created a life for herself and her family as well as reaching out and helping those less fortunate. She is the perfect example of someone who makes the world a better place! You'll be inspired to tackle your dreams after listening to our conversation! @angelecadethebrand www.angelecade.com www.s5blueprintconference.com https://execonthego.com https://www.eventbrite.com/e/empowering-the-business-of-you-finding-the-place-of-solution-for-life-business-tickets-60893079841?fbclid=IwAR3ALX824b4ATXgFWwWqbP9aV6FAf0Bw_V-VRtGBc9YGv2IAYub3NWuAZUk

Inspiring Conversation with Guest AnGele Cade CEO of Executive on the Go - she shares stories from her amazing life and how she’s overcome adversity to take care of her family, her son and back to others!

My guest, Chelsea Holman, is a TSC Mom from Nevada. Impacted personally by TSC, having a son, and various other family members affected with the diagnosis, Chelsea gives a raw look at receiving a diagnosis later in life, managing and reigning in chaos with medications, diet issues, depression, judgments from outsiders, amazing resolution of kidney issues, using CBD oil, angiofibromas, doctor run around, and more. This is part 1 of a 2 part episode. Throughout, Chelsea shares from her heart and soul with honesty, compassion, much inner fortitude, and love. (intro music: https://www.bensound.com

My guest, Chelsea Holman, is a TSC Mom from Nevada. Impacted personally by TSC, having a son, and various other family members affected with the diagnosis, Chelsea gives a raw look at receiving a diagnosis later in life, managing and reigning in chaos with medications, diet issues, depression, judgments from outsiders, amazing resolution of kidney issues, using CBD oil, angiofibromas, doctor run around, and more. This is part 1 of a 2 part episode. Throughout, Chelsea shares from her heart and soul with honesty, compassion, much inner fortitude, and love. (intro music: https://www.bensound.com

Jackie Woodside, certified (CPC, LICSW) and a best-selling author, TEDx speaker, radio and television personality and seminar leader who is passionate about expanding the edge of human potential, kindly granted TSC Talks this interview. She was willing to answer the more difficult questions about her past; overcoming much adversity to get to where she is today. Jackie also happens to be a special needs mom and shares her experience adopting a child with significant challenges and discusses in depth her experiences from initial days after adopting and integrating into her life to current day and the unique challenges this presented. (intro music credit: https://www.purple-planet.com/)

Jackie Woodside, certified (CPC, LICSW) and a best-selling author, TEDx speaker, radio and television personality and seminar leader who is passionate about expanding the edge of human potential, kindly granted TSC Talks this interview. She was willing to answer the more difficult questions about her past; overcoming much adversity to get to where she is today. Jackie also happens to be a special needs mom and shares her experience adopting a child with significant challenges and discusses in depth her experiences from initial days after adopting and integrating into her life to current day and the unique challenges this presented. (intro music credit: https://www.purple-planet.com/)

A discussion with Shannon Grandia, wife, mother, first-grade teacher, TS Alliance Volunteer, and Advocate! She shares her experience over the last 19 years with her children, Rylee, Jake and Luke, all affected by TSC as well as spouse Rob who is also affected. Shannon is an incredible human being and the love she has for her family truly permeates this discussion. We chat about diagnoses, manifestations, treatments, family impact and more. Shannon is able to truly understand the importance of acceptance and living in the present. Her choice to focus daily on the positive and cultivate joy in her family is truly inspirational and motivating. While acknowledging the extreme challenges and uncertainty involved in managing this disease she continually expresses gratitude for all the many ways the family has been fortunate, outlining how teamwork, organization, church and community support, TS Alliance involvement, have all contributed to this beautiful life that Shannon and her family live one day at a time.

A discussion with Shannon Grandia, wife, mother, first-grade teacher, TS Alliance Volunteer, and Advocate! She shares her experience over the last 19 years with her children, Rylee, Jake and Luke, all affected by TSC as well as spouse Rob who is also affected. Shannon is an incredible human being and the love she has for her family truly permeates this discussion. We chat about diagnoses, manifestations, treatments, family impact and more. Shannon is able to truly understand the importance of acceptance and living in the present. Her choice to focus daily on the positive and cultivate joy in her family is truly inspirational and motivating. While acknowledging the extreme challenges and uncertainty involved in managing this disease she continually expresses gratitude for all the many ways the family has been fortunate, outlining how teamwork, organization, church and community support, TS Alliance involvement, have all contributed to this beautiful life that Shannon and her family live one day at a time.