Podcasts about down syndrome awareness

On this week's episode of The 1 Girl Revolution Podcast, we welcome Ellen Boyer — co-founder of The Brett Boyer Foundation, wife, mother, and advocate for individuals with Down Syndrome and congenital heart disease (CHD). Ellen and her husband Bo founded The Brett Boyer Foundation in memory of their beautiful daughter, Brett, who was born with Down Syndrome and a congenital heart defect. Though Brett's life was tragically short, her light continues to shine through the work of the foundation that bears her name. The Brett Boyer Foundation is dedicated to raising awareness for CHD—the most common birth defect in the world—and to celebrating the lives of individuals with Down Syndrome. In this powerful episode, Ellen shares her journey of grief, motherhood, and mission—and how she and Bo turned heartbreak into hope for others. Through education, advocacy, CHD grants, family support, and their joyful mission of love, The Brett Boyer Foundation is lighting up the world, one little legacy at a time. In this episode, you'll hear:

Happy International Down Syndrome Awareness Day (3/21/25). Join Robin, Abby and Angela as they talk about the 2025 campaign presented by CoorDown .No Decision Without Me- videoWorld Down Syndrome Day- websiteSecondary Transition Docs- DESE/MAPlease tell us how you found us by completing this surveyEmail us at ASTALPodcast@gmail.comFollow us on Instagram @astalpodcast

When it comes to making her voice heard - does Sheletta take a break? We chat it up with the queen herself, discuss some of the crimes in North Minneapolis, Down Syndrome Awareness, an amazing event she has going on Friday night and much more with Sheletta!

In this heartfelt and inspiring episode, Emma Foran takes us on her journey of self-discovery, career transformation, and personal growth. From her early aspirations to be an actor to navigating unfulfilling corporate roles, Emma shares how she found her true calling in social care and her current role as an Employment Officer at Down Syndrome Ireland.Emma reflects on the invaluable lessons she learned growing up alongside her aunt, who has Down Syndrome, and how it shaped her compassionate outlook on life. She discusses the challenges of leaving stable corporate jobs to pursue meaningful work and the joy she now finds in empowering adults with Down Syndrome to thrive in employment.Emma also opens up about the importance of living authentically, the struggles of societal expectations, and her evolving relationship with social media. With warmth and honesty, Emma reveals how embracing her passions has brought her a deep sense of purpose and fulfillment.If you've ever questioned your career path, struggled with conformity, or sought inspiration to make a meaningful change, this episode is for you.Let me know your thoughts on this eposideWebsiteInstagram TwitterFacebook

On this week's episode of Bakers Bantering, we have on our friend Jennifer to talk about her experience raising a child with Down Syndrome!Timestamps:0:00 - Intro4:15 - What is Riley like as a middle child?9:02 - Finding out Riley had Down Syndrome11:58 - Jennifer has family members with Down Syndrome19:09 - How to navigate mean language29:36 - How did Riley's diagnosis impact Jennifer's marriage?40:00 - When did Jennifer start posting to social media?

Peter Rosenberger hosts Truth Talk Live and talks with his friend Aron about his experiences and how we can have a better understanding of someone with Down syndrome.    If you would like to know more about Peter and being a caregiver, visit peterrosenberger.com

Send us a textWhat freedom could we offer one another as humans if we weren't so stuck on the treadmill of achievement and quantified learning? Pepper Stetler, PhD, is the author of A Measure of Intelligence: One Mother's Reckoning with the IQ Test. She joins Amy Julia Becker on the podcast to share her personal journey navigating the world of IQ testing with her daughter Louisa, who has Down syndrome. Amy Julia and Dr. Stetler explore: the historical roots of these intelligence assessmentsIQ testing's societal implicationsthe ethical dilemmas the tests present for parents and educatorshow IQ tests shape our understanding of intelligence and the pursuit of a fulfilling lifeways to challenge conventional notions of achievement and success_Noonday Lucky Few bracelet (in celebration of Down Syndrome Awareness month): https://noondaycollection.com/products/lucky-few-bracelet_On the Podcast:A Measure of Intelligence: One Mother's Reckoning with the IQ Test by Pepper Stetler Alfred BinetDSM (Diagnostic and Statistical Manual of Mental Disorders)Henry Goddard_Connect with Dr. Stetler on her website (pepperstetler.com) or X (@PepperStetler)._Watch this conversation on YouTube by clicking here. Read the full transcript and access detailed show notes by clicking here or visiting amyjuliabecker.com/podcast.Connect with me: Instagram Facebook YouTube Website Thanks for listening!

In this episode of T21Mom, Mary opens up about the significance of "Rocktober"-a special month for Down Syndrome Awareness.  She discusses her personal approach to celebrating this important month and candidly shares the struggles she faces, including feeling guilty for not being fully engaged in the festivities.  Despite her deep passion for advocacy, Mary talks about the exhaustion that sometimes comes with it, and how advocating can feel like a never-ending journey. Mary also highlights some of the amazing ways other Rockin' Moms are celebrating and advocating during Rocktober, offering inspiration and ideas for those looking to get involved.  Tune in to hear how you can make a difference this month, whether you're fully embracing Rocktober or finding your own unique way to contribute.  For more details, visit T21Mom.com

On this episode of Bakers Bantering Jenna catches us up on her trip to Orlando! We talk about:- Derek getting to wrestle!- Visiting the NHRA- Down Syndrome Awarenessand more!

Many of you have seen the ad #Assume I Can (and Maybe I Will)  created by the organization CoorDown.  Robin, Abby and Angela talk about the power of this campaign on the social inclusion movement. Check out some of the previous campaigns created by this organization (Esp. The Hiring Chain). Please tell us how you found us by completing this surveyEmail us at ASTALPodcast@gmail.comFollow us on Instagram @astalpodcast

In this week's episode, we have the incredible Chanene as our guest to share her inspiring journey. Chanene opens up about her experience of finding out during a growth scan, at 34 weeks pregnant that her little boy Jaxson has Down syndrome. Join us as she bravely shares the highs, lows, and beautiful moments of her unique parenting journey while spreading awareness on Down Syndrome, including pregnancy, her birth story & life as a mum of two. 

Dr Mark Wells, Dr Murugu Manickam, and Kari Jones visit the studio as we celebrate World Down Syndrome Day on March 21. This year's theme is “End the Stereotypes” and we will do that by answering questions and correcting misconceptions about this common genetic condition. We hope you can join us!

In this episode for Down Syndrome Awareness Week (18-24 March), Salise is joined by Geldards Paralegal Lacie Smith. They discuss Lacie's experience of growing up with a brother with Down Syndrome as well as her time working as a special education teacher in the United States. Website: www.geldards.com Production: Geldards LLP Music: Sunshine by lemonmusicstudio

I don't often see as much representation of Down Syndrome within the neurodivergent community, and since October is Down Syndrome Awareness month, I think that means now is the perfect time to expand our understanding.   So fellow curious minds, let's get started.  In this episode we will learn:The three types of Down SyndromeThe incidence of Down SyndromeCommon expressions of Down SyndromeThe medical conditions that have an increased risk of occurring in people with Down SyndromeThe episode concludes with a tribute to Daniel "Dan the Man" Wheat.  An extraordinary man who left us way too soon.  Thank you for being a friend Dan.❤️Sources for more information and/or support:The National Down Syndrome SocietyGreta Harrison and the Born Fabulous PodcastFollow Neuroversity on all our social platforms:Neuroversity WebsiteIGFacebookTwitterLinkedInPatreon

During pregnancy, parents usually imagine what their child will be like and everything they'll get to do together. You get excited about all the traditional milestones and look forward to experiencing this new reality.  But for parents who receive difficult news after the birth of their child, such as an unexpected Down Syndrome diagnosis, this reality is shattered in a matter of seconds. Even the most understanding of parents are faced with grieving and adjusting.  Amy Julia Becker (an award-winning writer and speaker on Disabilities and Family) experienced this first hand at the birth of her first child, Penny. Today, Amy Julia is sharing her family's journey: from grieving the child they “thought” they'd be receiving, to adjusting to their new normal, to eventually realizing all the beautiful things that come from embracing our humanity as is.  In honor of Down Syndrome Awareness Month, Amy Julia shares useful tips on things she wished she knew when her daughter was diagnosed, and on navigating the nuances of raising a child with different abilities.  This episode is perfect for any parent who is currently feeling overwhelmed, alone, or nervous about their child's disability and I hope you or someone you love and you get a ton of value from it. Key Takeaways with Amy Julia Becker The importance of Down Syndrome Awareness Month. Navigating a Down Syndrome diagnosis. Grieving and adjusting to the reality of parenting a child with disabilities. Finding community through shared parenting experiences. Dealing with pain, guilt, and shame as a parent of a child with a disability.  Validating the feelings of parents going through disability journeys.  Looking beyond the tragedy and negativity surrounding disabilities.  Hierarchy vs Mutuality: an inclusive approach to disabilities.  How to support your partner through a difficult diagnosis.  The growth opportunities in every challenge.  Accepting (and embracing) the uniqueness of every diagnosis.  Focusing on the present in order to find joy.  Show Notes: Get Full Access to the Show Notes by visiting: MatteasJoy.org/71. Rate & Review If you enjoyed today's episode of The Joy In The Journey, hit the subscribe button on Apple Podcasts, Spotify, Stitcher, or wherever you listen, so future episodes are automatically downloaded directly to your device. You can also help by providing an honest rating & review over on Apple Podcasts. Reviews go a long way in helping us build awareness so that we can impact even more people. THANK YOU!

Carmen got us started this morning with a great reminder of what walking by faith looks like from @ashley.morgan.jackson on Instagram.  After that, Dave told us about the not-so-surprising "health benefits" of coffee. While Bill told us about "beanless coffe"  Our good friend, Gregory, stopped by to say hi. He had a lot he wanted to talk about and his parents came along for the ride as we celebrate Down Syndrome Awareness this month.  For The Chosen...

Carmen got us started this morning with a great reminder of what walking by faith looks like from @ashley.morgan.jackson on Instagram.  After that, Dave told us about the not-so-surprising "health benefits" of coffee. While Bill told us about "beanless coffe"  Our good friend, Gregory, stopped by to say hi. He had a lot he wanted to talk about and his parents came along for the ride as we celebrate Down Syndrome Awareness this month.  For The Chosen...

Carmen got us started this morning with a great reminder of what walking by faith looks like from @ashley.morgan.jackson on Instagram.  After that, Dave told us about the not-so-surprising "health benefits" of coffee. While Bill told us about "beanless coffe"  Our good friend, Gregory, stopped by to say hi. He had a lot he wanted to talk about and his parents came along for the ride as we celebrate Down Syndrome Awareness this month.  For The Chosen...

Have you watched the new show on Netflix called Down for Love? It's a reality dating show for people with Down syndrome, and we're celebrating the start of Down Syndrome Awareness month with a conversation with the producer of Down for Love, Robyn Paterson. We talk about:How the show was createdThe diversity of the Down syndrome communityThe universal desire for love, relationships, and connectionBONUS CONTENT: At the end of the episode, I talk with Penny, our 17-year-old daughter who has Down syndrome, about her thoughts on Down for Love.___FREE DOWNLOAD: ​​5 THINGS I WISH I'D KNOWN WHEN OUR DAUGHTER WAS DIAGNOSED WITH DOWN SYNDROME___TIME ESSAY: Doctors Don't Know How to Talk About Down Syndrome___GUEST BIO:“Robyn Paterson is a New Zealand-based producer, director and writer known for Down for Love (2022), Grand Designs New Zealand (2015) and In the Zone (2018). She works across various roles within multiple formats, including television factual, documentary & entertainment series, documentary feature, web-series, comedy, and drama. She has a background as an actress and presenter, and is the current president of the Directors & Editors Guild of Aotearoa New Zealand.”___Connect Online:Website: https://www.robynpaterson.co.nz/Instagram: @_robynpaterson____On the Podcast:Down for LoveNew Zealand Down Syndrome Association ___TRANSCRIPT: amyjuliabecker.com/robyn-paterson/YouTube Channel: video with closed captions___Season 7 of the Love Is Stronger Than Fear podcast connects to themes in my latest book, To Be Made Well, which you can order here! Learn more about my writing and speaking at amyjuliabecker.com.Connect with me: Instagram Facebook Twitter Website Thanks for listening!

This week's episode of The 1 Girl Revolution Podcast features the two amazing founders of Extra Lucky Moms, Jess Quarello and Taryn Lagonigro. Extra Lucky Mom's is an organization that celebrates children with Down syndrome, autism, Jordan's Syndrome, trisomies, heart conditions, and many more through their blog, social media platforms, in-person events and brand and nonprofit partnerships.  Jess and Taryn, who both welcomed children with Down syndrome in 2020, found immediate support and connection from the Down syndrome community after welcoming their daughters, but kept encountering mothers of children with other disabilities who were missing that same level of community. Jess and Taryn connected through an online moms platform and quickly became friends and shortly after that, they decided to tap into their backgrounds in non-profit, marketing, and business, and they founded Extra Lucky Moms in May 2021.  Extra Lucky Moms is a community of love and support for mothers with children with Down syndrome and other differences and disabilities. And the mission of Extra Lucky Moms goes far  beyond providing community and support. Jess and Taryn and the Extra Lucky Moms community aim to challenge societal stereotypes and promote inclusivity by highlighting the abilities and achievements of individuals with Down syndrome and other differences and disabilities.  Jess and Taryn join The 1 Girl Revolution Podcast to share their inspiring stories and to talk about the incredible work of Extra Lucky Moms.  In this episode, you'll hear: Jess and Taryn's individual life stories; How they each found out that their daughter(s) had Down syndrome; Their individual reactions to the Down Syndrome diagnoses and how they and their friends and family responded; All about the little beacons of light, Rhea and Adeline; The story of how Jess and Taryn became friends and how they decided to start Extra Lucky Moms; About the Extra Lucky Moms community and the incredible work they're doing; And so much more. The 1 Girl Revolution Podcast is available on #ApplePodcasts, #Spotify, #Stitcher, #iHeartRadio, #YouTube, and everywhere you listen to podcasts.  For more information, please visit: www.1GirlRevolution.com/ExtraLuckyMoms

Host Sue Shilling speaks to parents of children with Down Syndrome for World Down Syndrome Awareness Day, which took place on March 21st.

    As March is a global awareness moth of down syndrome, Paediatric Specialist at Netcare Sunninghill Hospital Dr Lethabo Machaba joins Clement to talk about early signs of down syndrome in children and how parents can support their children who living with this medical condition.See omnystudio.com/listener for privacy information.

Author / photographer Sally Fetough is on the #ReadingWithYourKids #Podcast to celebrate Down Syndrome Awareness Day and her wonderful #ChildrensBook Jana's Brightly Coloured Socks. Sally tells us the book is inspired by her daughter who loves  to put her socks on all by herself and also happens to have Down syndrome. In Sally's book Jana  celebrates by collecting loads of brightly coloured socks as a gift from mum and dad. But what happens when Jana shows her favourite pair to everyone at school? This beautifully illustrated picture book celebrates diversity and inclusion and is sure to tickle your heart with joy as you join Jana on a full-filled adventure, learning about friendship and kindness. Click here to visit Sally's website - https://www.sallyfetouh.com/books  Click here to watch MELTDOWN! The Walls That Separate! - https://www.youtube.com/watch?v=sLwb5lW4YXY&t=236s  Click here to visit our website - www.readingwithyourkids.com 

Episode #141 Mark Tremonti is the guitarist and songwriter from Alter Bridge, Tremonti, and Creed. Mark sat down with Mistress Carrie and talked power washing, Frank Sinatra, fatherhood, charity work, Alter Bridge, touring, songwriting, Myles Kennedy, Las Vegas, Down Syndrome Awareness, Boston Marathon, guitars, Eddie Van Halen, Boston, and more.  Episode Notes Check out the custom playlist for Episode #141 here Support John Connolly's Marathon Run here! Find Mark Tremonti Online: Instagram Twitter Facebook Youtube Website Find Alter Bridge Online: Website Instagram Facebook Twitter Youtube Find Mistress Carrie online: Official Website The Mistress Carrie Backstage Pass on Patreon Twitter Facebook Instagram YouTube Cameo Pantheon Podcast Network Learn more about your ad choices. Visit megaphone.fm/adchoices

Ryan is joined on the Hope FM Breakfast Show by Erika from Shades of Different to talk about Down Syndrome Awareness Month 2022. Find out more at shadesofdifferent.com FIRST BROADCAST: 03/11/2022

This week, On The Sidelines, we're joined by someone I hold very near and dear to my heart: Teddy Kramer! You know him well...he's been capturing the hearts of thousands (if not millions) since he first stepped on the field at Great American Ballpark as the Honorary Batboy in 2013. So what's he up to now? Well, he's gearing up for a sold out event this Friday night with The Joe Nuxhall Foundation where they will be honoring him with the Nuxhall Humanitarian Award. To say I am proud would be an understatement. This episode also features the amazing Tyler Bradshaw, Executive Director of The Joe Nuxhall Miracle League Fields. On the Sidelines is presented by OrthoCincy Orthopaedics & Sports Medicine.

October is recognized as Down Syndrome Awareness Month across the world. In today's episode of Big Girl Panties Podcast, Alexis sits down with Eulannae Douglas to discuss Down Syndrome Awareness. Eulannae is a paraprofessional in the Bermuda public school system with a focus on working with students with Down syndrome. During this episode we will learn:How Eulannae chose to work with children with special needs as a professionWhat we should know about people with Down syndrome The challenges & successes that children with Down syndrome in her life experienceHow to create strong relationships with children with Down syndrome And more If you would like to get involved and support others with Down syndrome, and learn more information about Down syndrome Awareness, please visit:onespecialnightbda.comNdss.org ds-int.orgTo keep in touch with all things Big Girl Panties between episodes, please visit:Instagram - @bgplifeFacebook - @bgplifeblogWebsite - bgplife.com

To celebrate Down Syndrome Awareness Month, representatives from the Down Syndrome Association of Pittsburgh (DSAP) joined the podcast today to reflect on their experiences as parents as well as highlight the ongoing work of DSAP.  The highlight event of the year is the Buddy Walk which is coming up on October 23, 2022 at Schenley Plaza on the University of Pittsburgh campus.   Helpful websites related to the podcast discussion today: DSAP: https://www.dsapgh.org/ or call/text us 4125659936 Pittsburgh Buddy Walk: https://www.ds-stride.org/pghbuddywalk First Call Program: https://www.dsapgh.org/first-call or call/text us 4125524972 FB: https://www.facebook.com/dsapgh IG: https://www.instagram.com/dsapgh LinkedIn: https://www.linkedin.com/company/down-syndrome-association-of-pittsburgh Twitter: https://twitter.com/dsapittsburgh Shannons blog: https://www.thislifewegot.com If you would like to suggest a topic for us to cover on the podcast, please send an e-mail to DownSyndromeCenter@chp.edu. If you would like to partner with the Down Syndrome Center, including this podcast, please visit https://givetochildrens.org/downsyndromecenter. Thank you to “Caring for Kids” The Carrie Martin Fund for its support of the Down Syndrome Center Podcast.   

“You belong here, as you are, who you are. Come be in this place with us.” Down syndrome advocate and author Heather Avis joins Amy Julia to talk about the importance of people with Down syndrome, celebrating Down Syndrome Awareness Month, and creating spaces of belovedness and belonging.__Guest Bio:“Founder of The Lucky Few and The Lucky Few Foundation, Heather Avis is a New York Times bestselling author, podcaster, and Down syndrome advocate, working to create a more inclusive world where everyone belongs.”__Connect Online:heatheravis.comFoundation: theluckyfewfoundation.orgPodcast: theluckyfewpodcast.comInstagram: @theluckyfewfoundation; @theluckyfewofficialFacebook: @theluckyfewfoundation__On the Podcast:Heather's books: Everyone Belongs;  Different--A Great Thing to Be!; The Lucky Few: Finding God's Best in the Most Unlikely Places;  Scoot Over and Make Some Room: Creating a Space Where Everyone BelongsPodcast episode: 171. What does belonging actually mean? (Storytelling Tour Recap with Heather + Josh Avis!)Study: Disabilities in Newbery Books Newbery Award Winning Books 1975–2009: How Do They Portray Disabilities?Books: Wonder; Fish in a Tree; Counting by 7s; Out of My Mind; A Storm of StrawberriesCamp: Hope Heals CampVerse: Psalms 139:14For full show notes, transcript, and more, go to: amyjuliabecker.com/heather-avis/__BOOK GIVEAWAY:I'm joining Heather and other moms of kids with Down syndrome over on Instagram to give away our favorite picture books and memoirs in celebration of Down Syndrome Awareness month.You can find all the details on my October 5, 2022, Instagram post @amyjuliabecker.__Season 6 of the Love Is Stronger Than Fear podcast connects to themes in my latest book, To Be Made Well, which you can order here! Learn more about my writing and speaking at amyjuliabecker.com.__*A transcript of this episode will be available soon, as well as a video with closed captions on my YouTube Channel.

Karmel Garcia is on this episode sharing the story of her 3 year old, Zoe, who was born with Down Syndrome. She takes us from the beginning with a prenatal diagnosis, the birth and through her first three years of life. Karmel started to see a need for families to have therapuetic tools to work with their kids at home and has started Zoe's Tool Box. https://www.instagram.com/karmelita16/?hl=en https://www.instagram.com/zoes_toolbox/?hl=en Non Profit https://www.zoes-toolbox.com/ Every baby born with Down syndrome will have their own unique experiences and abilities. Some will have many medical procedures in their first year, and some will be born never spending a day in the hospital.  For any diagnosis the first year is the hardest to navigate, and we are here to be a box of sunshine to those families. Books to check out: You Are Enough Different - A Great Thing to Be What's Inside you, Is Inside Me Too Hannah's Down Syndrome Powers 47 Strings Connect with Liz https://www.instagram.com/esandoz/?hl=en https://miraculousmamas.com/    

Today is the first day of school for Uvalde CISD. Their start date was pushed back while campuses prepared new safety and security protocols following the shooting at Robb Elementary School in March. RJ Marquez and Erica Hernandez share viewers messages of hope as students and teachers returned to the classroom. Comfort dogs will also be on site for the next three weeks to ease the anxiety for students. Three iconic Alamo Plaza Businesses are shutting their doors for good to make way to the Alamo Master Plan. A local girl has been chosen as the ambassador for Down Syndrome Awareness month. Learn more about your ad choices. Visit megaphone.fm/adchoices

This is a milestone episode for two reasons. As you may have noticed, it's our 200th episode. Technically we had about 20 episodes prior to numbering them, but these are mini lessons and not really full episodes. These started when we were broadcasting live from WHUS 91.7 FM.The other milestone is that September 1st marks 10 years of DNA Today. We released our first episode in 2012. Back then our host and producer, Kira Dineen, was starting her senior year of high school, fast forward a decade and now she has her masters in genetics and has been practicing as a genetic counselor for 2 years! As a high schooler she dreamed of reaching people around the world, little did she think she would be producing DNA Today ten years later with two Podcast Awards, ranking in top 1% of podcasts globally with 40+ sponsors. This journey has been incredible. We have had countless guests on the podcast that have brought immense insight into the field of genetics, the life of living with a genetic condition or caring for someone who does, groundbreaking advancements in genetic technology, discussions exploring the ethics surrounding this technology, and so many more important conversations. During this episode we are looking back at the last 10 years and 200 episodes. We are featuring your voices. Voices of people that make this show possible. Listeners. Team members. Guests. And more. So you will hear these voice memos sharing people's favorite episodes, followed by clips from the episodes. We want to thank you so much. DNA Today would not be successful without you. It's your downloads, engagement, and support that keep this show going. We are so passionate about educating the world about genetics, it's you that keeps us going. I am humbled by your support and honored to be in this role. Shoutout to the following listeners, guests, and DNA Today team members for submitting voices memos featured in this celebratory episode: Corinne Merlino, Sophia Saladino, Ashlyn Enokian, Katie Lee, Amanda Andreoli, Daniel DeFabio, Faith McCarthy, Laura Markham, Paloma Boeck, Taila Stanford, Sanya Tinaikar, Kajal Patel, and Mahfuz Taofeeq. Episodes mentioned include…#67 Daniel DeFabio on Disorder: The Rare Disease Film Festival#87 Genetic Counseling Grad School Apps (Part 1)#97 Genetic Counseling Grad School Interviews, Ranking, Matching (Part 2)#101 Genetic Counseling Match Day#110 Gattaca, 22 Years Later#111: NSGC 2019 Recap#123 Infertility Series: Dr. Kara Goldman on Fertility Testing#128 DTC Series: Adam Rutherford on How To Argue With A Racist#131 DTC Series: Libby Copeland on Law Enforcement Use of Genetic Databases#135 NSGC 2020 Recap#164 Parkinson's Disease with the Parkinson's Foundation#166 Beta Thalassemia with Radhika Sawh#176 Glee's Lauren Potter on Down Syndrome Awareness#191 Overturning Roe v. Wade with Laura HercherStay tuned for the next new episode of DNA Today on Friday, September 9th where we will be discussing sickle cell disease in honor of the awareness month. Our host Kira Dineen is interviewed by Beverly Mills and Elaine Buck. If you want a sneak preview the episode has been released on their podcast, Lifting the Veil. New episodes are released on Fridays. In the meantime, you can binge all 200 episodes on Apple Podcasts, Spotify, streaming on the website, or any other podcast player by searching, “DNA Today”. Episodes since 2021 are also recorded with video which you can watch on our YouTube channel. DNA Today is hosted and produced by Kira Dineen. Our social media lead is Corinne Merlino. Our video lead is Amanda Andreoli. See what else we are up to on Twitter, Instagram, Facebook, YouTube and our website, DNApodcast.com. Questions/inquiries can be sent to info@DNApodcast.com. PerkinElmer Genomics is a global leader in genetic testing focusing on rare diseases, inherited disorders, newborn screening, and hereditary cancer. Testing services support the full continuum of care from preconception and prenatal to neonatal, pediatric, and adult. Testing options include sequencing for targeted genes, multiple genes, the whole exome or genome, and copy number variations. Using a simple saliva or blood sample, PerkinElmer Genomics answers complex genetic questions that can proactively inform patient care and end the diagnostic odyssey for families. Learn more at PerkinElmerGenomics.com. (SPONSORED)Support for DNA Today comes from the People for The Ethical Treatment of Animals (also known as PETA), whose scientists have developed the research modernization deal, a strategy to phase out ineffective experiments on animals with high-tech, state-of-the-art research. PETA has collected an abundance of evidence demonstrating that the use of animals in biomedical research hinders scientific progress and puts patients at risk. Learn more at PETA.org/NewDeal. (SPONSORED)

It's the most commonly diagnosed chromosomal condition in the U.S. On today's show, learn about Down Syndrome and hear from a mother who shares her family's experience with it. Plus, discover a project that's improving the quality of life for kids with cognitive and physical disabilities. We're learning and raising awareness about Down Syndrome, inside this edition of CTSI Discovery Radio!

This week, Michelle and Sasha chat with John and Mark, founders and owners of John's Crazy Socks. John is an entrepreneur, advocate, and sock tycoon living with down syndrome. His father Mark is his business partner.Connect with John and Mark:johnscrazysocks.comIG: @johnscrazysocksTwitter: @JohnsCrazySocksLinkedIn: John's Crazy SocksYouTube: John's Crazy SocksConnect with us:IG: @be.a.better.beingMichelle: @betterbeingsusSasha: @sasha.patriciaDon't forget to rate, review, and subscribe!

Hello and welcome back to ArtBeat Radio. My name is Renee and I am a student at Able ARTS Work San Diego.  In 2021, I was cast as the lead role of Audrey in "Little Shop of Horrors". In today's episode, I will be singing two of my favorite songs from the musical: "Suddenly Seymour" and "Somewhere That's Green". Not only did I sing, but I chose the instrumentation and tempo to make the songs my own! I hope you enjoy!  Suddenly Seymore Lyrics (Role of Audrey sang by Renee Evette Morneau, Role of Seymore sang by Kassidy King, MT-BC) Seymore (Kassidy:Lift up your head, wash off your mascara Here, take my Kleenex, wipe that lipstick away Show me your face clean as the mornin' I know things were bad but now they're okaySuddenly Seymour is standing beside you You don't need no makeup, Don't have to pretend Suddenly Seymour, is here to provide you With sweet understanding, Seymour's your friend Audrey (Renee)Nobody ever treated me kindlyDaddy left early, mamma was poor I'd meet a man and I'd follow him blindly He'd snap his fingers me I'd say, "Sure"Suddenly, Seymour is standing beside me He don't give me orders, he don't condescend Suddenly, Seymour is here to provide me Sweet understanding, Seymour's my friend Seymore (Kassidy)Tell me this feeling lasts 'til forever Tell me the bad times are clean washed away Audrey (Renee)Please understand that it's still strange and frightening Both losers like I've been it's so hard to saySuddenly, Seymour (Suddenly, Seymour) Is standing beside  He don't give me orders He don't condescend Suddenly, Seymour He's here to provide me  Seymore (Kassidy) With sweet understandingAudrey (Renee)(With sweet understanding) Seymore (Kassidy)With sweet understanding Audrey (Renee)With sweet understanding) Seymore (Kassidy)With sweet understanding Audrey (Renee)Seymour is your man Somewhere That's Green Lyrics (role of Audrey sang by Renee Evette Morneau) I know Seymour's the greatest  But I'm dating a semi-sadist  So I've got a black eye  And my arm's in a cast.  Still, that Seymour's a cutie  Well, if not, he's got inner beauty  And I dream of a place  Where we could be together at last  A small house of our own  A fence of real chain link,  A grill out on the patio  Disposal in the sink  A washer and a dryer and small plasma TV  In a tract house that we share  Somewhere that's green.  He rakes and trims the grass  He takes me to the park   I cook like Martha Stewart    And I look like Emelia Clark   There's plastic on the furniture  To keep it neat and clean  In the Pine-Sol scented air  Somewhere that's green  Between our frozen dinner  And our bedtime, nine-fifteen  We snuggle watchin' Lucy  On our big, enormous TV screen  I'm his December Bride  He's Father, he Knows Best  Our kids watching Newsies  As the sun sets in the west  A picture out of Better Homes and Gardens magazine  Far from Skid Row  I dream we'll go  Somewhere that's green.

Officer Daniels joins the show to talk about the Hawaiian shirt company he works for (21 Pineapples), Down Syndrome Awareness and how badly the government screws over people with Down Syndrome, and why he doesn't miss being a cop.     Buy Drinkin Bros' new HardAF Seltzer Here!   Get your Drinkin' Bros Merch here!    Go to ghostbed.com/drinkinbros and use code DRINKINBROS for 30% off EVERYTHING (Mattresses, Adjustable Base, and more) -- plus a 101 Night Sleep Trial and Mattresses Made in the USA!   When you go to DietSmoke.com and use promo code: DRINKINBROS, you'll get 20% off all of their delta-8 THC gummies.

Erika Petrie from Shades of Different joins Ryan on The Hope FM Breakfast Show to talk about Down Syndrome Awareness Week 2022. FIRST BROADCAST: 25/03/2022

Today we have the privilege of introducing you to Oklahoma Family Network's newest staff member and sharing a small portion of her experience and perspective learning her daughter has Down Syndrome. This is a real and honest conversation that will touch your heart. We Saved You A Seat, sat down with Jamese Siranga on March 21 (World Down Syndrome Day) and discussed the impact Down Syndrome has on their beautiful family.  You will walk away from today's podcast with a full heart after hearing from Jamese and want to hear more from her, as she shares her family and daughter, Selah, with us. Resources Mentioned: SoonerStart is Oklahoma's early intervention program designed to meet the needs of families with infants or toddlers (ages birth to 3 years old) with developmental delays and/or disabilities in accordance with the Individuals with Disabilities Education Act (IDEA). The program builds upon and provides supports and resources to assist family members to enhance infants or toddler's learning and development through everyday learning opportunities. For more information:  https://oklahoma.gov/health/family-health/sooner-start.html Song by India.Arie: I Am Not My Hair https://g.co/kgs/rqMSL2   #WorldDownSyndromeDay #DownSyndrome #Trisomy21 #TrisomyAwareness #SoonerStart #OklahomaDownSyndromeAssociation #IndiaArie  

Jason and Mikey sat down with John Cronin of John's Crazy Sock and his father Mark Cronin on the Knockin' Doorz Down podcast. They discussed Down Syndrome awareness, World Down Syndrome Day which is March 21st each year. During the conversation, Mark Cronin shares that mental health and addiction issues have affected their family. Mark's wife has struggled with mental health issues that led her to make some decisions that affected her law practice and family. As well one of John's brothers, Mark's sons struggled with addiction issues that were become rampant in the area where they lived. With financial hardship in the Cronin household along with members of the family struggling with these mental health and addiction issues. John was getting the age of wanting to find a career path was struggling to do so due to the lack of acceptance of those with special abilities of which John has Down Syndrome. As John and Mark had many ideas of what John could do to make a living and have his own independence they decided to build on John's passion for crazy socks. They built a website and gained local traction, including Jonh personally delivering orders to customers. One thing John always does is includes a personal thank you note and candy in each delivery. John's Crazy Socks was born. John's Crazy Socks is a father-son venture inspired by co-founder John Lee Cronin, a young man with Down syndrome. John's affinity for crazy socks paired with his love of making people smile made our mission clear: we want to spread happiness. They have a social mission and a retail mission, and they are indivisible. They want to show what is possible when you give someone a chance. Every day, they demonstrate what people with intellectual disabilities can do. And they believe in giving back: they donate 5 percent of our earnings to the Special Olympics as they've played a vital role in John's development. They continue to expand our charity partners by offering and creating socks with specific “awareness” themes, such as our Autism Awareness Socks and Down Syndrome Awareness Socks. They match their social mission with a commitment to being a great sock store. They have socks you can love with the widest array of fun, unique, and beautifully designed socks that let you express your passion and personality. And they deliver those socks with fast, personal service. They also provide same-day shipping and every package includes a hand-written thank you note from John and some candy. They love what we do. They hope you love your socks and that your experience with John's Crazy Socks brings you happiness. This is John Lee Cronin and Mark X. Cronin in their own words, on Knockin' Doorz Down. For more on John's Crazy Sock https://johnscrazysocks.com/ To subscribe to the Knockin' Doorz Down podcast wherever you listen for more celebrities, everyday folks, and experts on conversations to end the stigma around addiction and mental health issue conversations https://linktr.ee/knockindoorzdown © 2021 by KDD Media Company. All rights reserved.

This is a replay of an episode I did with my friend David Marmon. David has a daughter Maddox who has Down Syndrome and this little girl is an absolute world changer! Find out more about Down Syndrome and how you can be an ally and friend to these amazing individuals. Please support my sponsors! I know them all personally and can vouch for their integrity and quality. -Apparel Lab for all your shirts, hats, mugs hoodies, or WHATEVER you want to put your logo or ideas on! Go check out their brand new website at https://apparellab.ink/ -Go refinance that house with Dominic Garver! Call 256.714.1429 -Use Patnaik Realty for ANY real estate needs you have. I mean anything! Residential, commercial, property management, investments, acquisitions. He does it all. Call Teek at 256-694-0117 or e-mail him at Teek@PatnaikCo.com -Get your child caught up on their school math with Mathnasium of Madison. Their website is http://www.mathnasium.com/madisonal -Go check out my Amazon Best Selling Book "Relentless Positivity"- https://cutt.ly/Nj7jqNN --- Send in a voice message: https://anchor.fm/relentlesspositivity/message

Hey guys! Thanks for tuning in to another episode of Chris Behind The Mic! •On this weeks episode, I chat with Maria and Lucy two moms with a child living with Down syndrome they both share there stories and how they started using social media as an outlet to talk all things Down syndrome! They both have great stories and I'm so happy they were able to chat with me! • Follow them on Social Media: Maria: @oceanic.mama Lucy: @alittleextrachesterFollow along with both of them and learn about what they are all about! • Stay connected with me through Social Media!@chrisbehindthemic on all platforms! See you next episode! • Video used at the start of the show was by “Down Syndrome International” on YouTube! Watch the video here: https://youtu.be/Y6L7SgvFPgQ

We are ecstatic to introduce this week's guest, Lauren Potter! You might know Lauren as Becky Jackson from the TV show Glee. She was in all six seasons playing a character who, like her, has Down Syndrome! After graduating high school and attending college in California, Lauren began acting, starring in her first film at the age of 16. In 2012 she was nominated for a SAG award in the Ensemble in a Comedy Series category for her work in Glee, and she also received the SAG/AFTRA Harold Russell Award at the 2012 Media Access AwardsOn top of being a fabulous and successful actress, Lauren is also a fierce advocate. President Obama appointed her to the President's Committee for People with Intellectual Disabilities. She has advocated with AbilityPath, Best Buddies International, the National Down Syndrome Society, The American Association of People with Disabilities, and Special Olympics. We are honored to have Lauren on the show, and the timing couldn't be more perfect with World Down Syndrome Awareness Day coming up on March 21st! This day was chosen because people with Down Syndrome have three copies of chromosome 21, so the 21st day of the 3rd month.On This Episode We Discuss:What it is like growing up with Down SyndromeLauren's experience auditioning for the role of Becky on GleeWhat Lauren wants people to know about how the R word can affect peopleLauren's advocacy work with Best Buddies and the President's Committee for people with Intellectual Disabilities“A Guest Room” a short film where Lauren was the lead actress and executive producerInspirational advice for people with Down SyndromeAdvice for parents who may have just found out their baby has Down SyndromeBe sure to follow Lauren on Twitter, Facebook, and Instagram to stay up to date on her advocacy work and latest acting roles!Stay tuned for the next new episode of DNA Today on March 25, 2022 where we'll be discussing whole genome sequencing with world-renowned geneticist Dr. Madhuri Hegde, Senior Vice President and Chief Scientific Officer of Global Lab Services at PerkinElmer Genomics. New episodes are released on Fridays. In the meantime, you can binge over 175 other episodes on Apple Podcasts, Spotify, streaming on the website, or any other podcast player by searching, “DNA Today”. Episodes since 2021 are also recorded with video which you can watch on our YouTube channel. DNA Today is hosted and produced by Kira Dineen. Our social media lead is Corinne Merlino. Our video lead is Amanda Andreoli. See what else we are up to on Twitter, Instagram, Facebook, YouTube and our website, DNApodcast.com. Questions/inquiries can be sent to info@DNApodcast.com. Every pregnancy has a chance to have a genetic abnormality or complication. Mitera empowers you to make the most informed reproductive decisions through their at-home genetic tests, without needing your doctor's order. These tests include non-invasive prenatal screening (Mitera's Peaches&Me) and carrier screening (Mitera's 23pears). Request your own kit at miteragenetics.com and use code “DNATODAY” for 10% off. Mitera. Predict. Prevent. Prepare. (SPONSORED)Vizgen is dedicated to pioneering the next generation of genomics, providing tools that demonstrate the possibilities of in situ single cell spatial genomics. These tools are enabling researchers to gain insight into the biological systems that govern human health and disease. Stay tuned for our full episode with Vizgen where we explore single-cell spatial genomics. Get a sneak peak by visiting their website at vizgen.com. Vizgen, leaders in spatially resolved, single-cell transcriptomics. (SPONSORED)PerkinElmer Genomics is a global leader in genetic testing focusing on rare diseases, inherited disorders, newborn screening, and hereditary cancer. Testing services support the full continuum of care from preconception and prenatal to neonatal, pediatric, and adult. Testing options include sequencing for targeted genes, multiple genes, the whole exome or genome, and copy number variations. Using a simple saliva or blood sample, PerkinElmer Genomics answers complex genetic questions that can proactively inform patient care and end the diagnostic odyssey for families. Learn more at PerkinElmerGenomics.com. (SPONSORED)Did you know there is a genetic counselor that specializes in offering care to those in the adoptee community? Brianne Kirkpatrick co-wrote “The DNA Guide for Adoptees” to provide a resource for those in the adoptee community who are utilizing DNA testing to find biological relatives or to seek out medical information. She also started Watershed DNA to offer personalized genetic counseling to directly support people in the aftermath of a surprise DNA discovery. You can hear Brianne share her insight from her book in Episode 103 of DNA Today! Learn more atWatershedDNA.com where you can also book your consult today with Brianne. (SPONSORED)

Hey Girl Designs and going from Down Syndrome Awareness to Becoming a Business and Therapy That Lets Creativity Shine Deanna and Ashley Warren Founders of Hey Girl Designs with Hannah Burt Wilson _ Alabama Care is partially supported by http://www.ACDD.org The views expressed are not necessarily the views of these organizations.

Leissa Miller is a wife, mother of an 11-year old son with Down Syndrome, and advocate for people with disabilities. She has been making the world better for him and other parents of children with Down Syndrome.Bob and Leissa are taking the principles of leadership beyond The Back Room and into our communities. Leissa discusses her son's diagnosis, the medical staff that made a difference, and the programs, like Gigi's Playhouse, paraprofessionals, teachers  & Individuals with Disabilities Education Act (IDEA)  that have supported her family throughout their journey.  In this episode, we celebrate children with Down Syndrome and the various programs and initiatives that are making a difference.[00:01:24] Get to know Leissa's story [00:13:20]The different levels of Down Syndrome.[00:16:39] The benefits of sign language for nonverbal children[00:19:11] How leaders can get involved and Down Syndrome Initiatives[00:31:32] The one thing Leissa wants to share with new parents who have a child with Down Syndrome [00:33:42] Misconceptions about children with disabilitiesTakeaways:Resources are available on the federal, state, and local levels, but what can organizations do to support the Down Syndrome Community? In this episode, Bob and Leissa share a few resources.Leissa shows how you can take on a leadership role in your community by advocating for individuals with disabilities.  Last week we discussed mindfulness and its benefits in the workplace but did you know that studies show that mindfulness practice is equally beneficial for individuals with disabilities and their support network. --------------------------------------------------------Resources Mentioned In This Episode:  GiGi's PlayhouseDown Syndrome CreedU.S. Dept of Education The Individuals with Disabilities Education Act (IDEA) National Down Syndrome Society-----------------------------------------------------Get to Know the Host:Bob Howard has over 30 years of sales and management experience and has spent the last 16 years leading a subsidiary of a Fortune 1,000 technology solutions company. He currently resides in New Hampshire. Want to connect further?LinkedInFacebookGroup:http://www.inthebackroompodcast.comIf you have any ideas or suggestions on who would be an excellent guest to interview, or if you would like to appear on the show, don't hesitate to reach out!Send me an email: Bob@inthebackroompodcast.com

Griffin Claw Brewing Company, located in Birmingham and Rochester Hills, Michigan, was founded in 2013. Focusing on all things craft, including beer, spirits, ciders, and food, they are also well aware that these are just the beginning. This is their story of a worldwide open-ended beer collaboration created to raise awareness for individuals with Down syndrome. A craft beer recipe, so to say, on how to affect change.Meet Pat Craddock“In 2015, my wife and I were blessed with our second son, Ian, who was born with Down syndrome, and our world was flipped upside-down.”Meet Pat Craddock, the genius behind the TRI-21 Project. While he officially holds the title of CFO at Griffin Claw, like many others in the industry, Pat wears many hats. So it wasn't a surprise to anyone when he came up with the idea to create a recipe and brew a beer to bring about awareness, acceptance, and funds to those with Down syndrome.What is Down Syndrome and the TRI-21 Project?There are three types of Down syndrome with the most common being Trisomy 21 (TRI-21). This is caused by an error in cell division resulting in an embryo with three copies of chromosome 21 instead of two. (National Down Syndrome Society)Inspired by Sierra Nevada's Resilience project, getting critical funds to those impacted by California's Camp Fire, Pat recently launched the TRI-21 Project in time for World Down Syndrome month in October with plans to continue up until World Down Syndrome Day on March 21, 2022.How Does the TRI-21 Project Work?The TRI-21 Project is simple. Any brewery can participate. Sign up. Download the recipe. Contact the vendors for discounts. Have a brew day. Download and print the artwork. Host a party to celebrate. Donate the funds. Finding support at GiGi's Playhouse when his son was born, Pat realized they would be an excellent source to receive funds raised from this project. Founded in the Midwest by a parent who needed support, Nancy Gianni created that support for herself and others, emphasizing global acceptance of Down syndrome. GiGi's is now located in over 50 locations across the U.S. and one in Mexico, offering a multitude of resources to anyone impacted by Down syndrome.Where's the Beer?Griffin Claw Brewing Project currently has their TRI-21 Double New England Hazy IPA available in both taprooms. For the status on availability at other breweries, click here, and check back often.If you know of other breweries that may be interested in participating in this project, send them to tri21project.com or tag them on Instagram using #tri21project.Sign up to Brew for the TRI-21 ProjectBrewer or drinker, for all the information, including recipe, artwork, all the breweries participating, and more click here.To sign up now, click here.Tag your favorite brewery to let them know about this project using #tri21project or send them to tri21project.comCommunity and SustainabilityThe TRI-21 Project was born out of a desire to help a child, but it will endure out of a continued desire to build community.And Griffin Claw doesn't stop there. With great respect for the environment, as well as the community, their efforts also expand into sustainability. We were honored to get to talk to Pat about Ian and the rest of his family, the TRI-21 Project, their sustainability practices, and so much more. We hope you enjoy this conversation as much as we did.For complete show notes click here.Connect With Us:The Craft Beer Travel & Adventure Podcast is hosted by Living a Stout Life, where we share stories, community, and resources for all your craft beer travel and adventure lifestyle needs.We would absolutely love it if you subscribe to the podcast and leave us a review. As my nephew once said, "We say please and thank you!"Subscribe to Living a Stout Life:NewsletterYouTubeFacebookInstagramBuy Us a Beer:Like our podcast? Help keep it going with a donation for a beer. We'll even zoom ya for a happy hour, if you'd like. Click here.Shout Outs:A huge shout out to Nicole Henzel from Malteurop Malting Company for connecting us with Pat and the TRI-21 Project. Your dedication to much needed projects is phenomenal, and your love of community always shines through. To Pat for countless hours of dedication to a project that is needed throughout the world. Your dedication to your family and to others both in and outside of the craft beer industry will not go unnoticed. We appreciate your time, your effort, and your love for community.Support this podcast at — https://redcircle.com/craft-beer-travel-and-adventure/donations

October is really special because it is Down Syndrome Awareness month! For this Voices of Motherhood episode, I sat down with my dear friend and mama to a daughter with Down syndrome, Caewyn Barnett.  This conversation was such a gift to me because it was a precious opportunity to dive into the things Caewyn and her husband had to consider, process, and learn as they prepared to be parents to Ella. Discover how their journey - though not always smooth - has empowered them to embrace and enjoy every moment with their daughter.  This is a special two-hour-long episode because there were so many treasures in the course of our conversation. If you know someone who has a child with Down syndrome or maybe you just received the news of a diagnosis, you'll absolutely be encouraged. Check out the full show notes here: https://www.nourishedmotherhood.com/podcast/episode7 (www.nourishedmotherhood.com/podcast/episode7) Links & Resources Mentioned Email Caewyn at hello@nourishedmotherhood.com and we'll forward it on! https://nourishedmotherhood.com/newsletter-sign-up (Sign Up For Monthly Newsletter) The Lucky Few Podcast https://www.dsdiagnosisnetwork.org (Down Syndrome Diagnosis Network:) https://rubysrainbow.org (Ruby's Rainbow) - Scholarships for Adult Students with Down Syndrome Seattle Resources: Down Syndrome Community of Puget Sound

October is Down Syndrome Awareness Month! In today's podcast I chat with Blair Stayzer, co-founder of "G-Mc's Homies with Extra Chromies", a not for profit organization for people living with Down Syndrome. The group promotes social health and wellness, educational opportunities and a positive public awareness for Down Syndrome. Today Blair touches on; - how and why he started the foundation - what working with people with Down Syndrome has brought to his life - why it is important for EVERYONE to have the opportunity to belong to a group and enjoy the pride in that Check out G-Mc's Instagram account or reach out to Blair at: https://www.instagram.com/gmcshomiesextrachromies/ Reach out on Instagram at: https://www.instagram.com/amberpachla/ or email me at amberpachla@yahoo.ca Work with me! Lose weight and develop life changing health and wellness habits for long term success - book your free 45 minute consultation today! Email or DM me to book. Interested in Essential Oils? Check out my site and work with me!: my.doterra.com/amberpachla

In this episode Em and Chels highlight Down Syndrome Awareness month. Kicking off a month full of awareness with a topic near and dear to Em's heart. Join us as we explore the ups and downs of Downs Syndrome. --- Support this podcast: https://anchor.fm/chelsea-smithson/support

One of my favorite things about this podcast is meeting and talking to other experts in the field of pediatrics. There is no better expert than a mom. I started this series: "A mother's message" to invite mothers to share their stories. Our stories can help others and I am so excited to welcome @abbyrosegreen in honor of World Down syndrome Day. We discuss her family's journey when they found out their son has Down syndrome, the misconceptions out there regarding Down syndrome, and some of the invisible struggles that others may not realize. Abby's message is so important for the world to hear and I'm so honored she joined me today for this very important epiosde.Abby co-hosts her own podcast, called HERself sharing stories and motivation for every woman.Make sure to follow her on Instagram @abbyrosegreen and subscribe to her podcast to be inspired! https://podcasts.apple.com/us/podcast/herself/id1489878793 Learn more about your ad choices. Visit megaphone.fm/adchoices

Michelle Sullivan is the advocate behind Littlest Warrior, a platform inspired by her son, Eli. Before Michelle gave birth to her son Eli, she didn't know much about the amazing Down Syndrome community. Now, after giving birth to a child with Down Syndrome, she has been welcomed into this warm and friendly community, and has enjoyed learning everything she can about it. October is Down Syndrome Awareness Month, which made it perfect to have Michelle on the podcast. Kelly and Michelle discussed Eli's incredible story, how she has worked to create an impact in the Down Syndrome community, and how to get involved in spreading awareness. Michelle shared some of her favorite organizations to check out if you are interested in being more involved in the initiative. She suggests the Down Syndrome Diagnosis Network, Ruby's Rainbow, Global Down Syndrome Foundation, and Letter Case. It was great to hear about resources from a trusted source, and you can view the links to these organizations below. Thank you so much for being on the show, Michelle! I loved hearing about your mission and passion. Enjoy the episode, everyone!We've got swag! Buy Old Towne Orange merchandise, mugs, hats, clothes and more!https://shop.iheartoldtowneorange.com/BECOME A PATRON!Do you love A Circle in a Square podcast? Then I would love for you to become a more involved participant in this little community I have created. I put together a plan on Patreon with a few levels of involvement (that all involve a super cute custom-made sticker)! Take a look at our Patreon to see how to get the inside scoop that we don't give anyone else.https://www.patreon.com/iheartFind Michelle's blog, Littlest Warrior + more!Website: https://www.littlestwarrior.com/Facebook: https://www.facebook.com/littlestwarrior/Instagram: https://www.instagram.com/littlest_warrior/Personal Instagram: https://www.instagram.com/meeshellsullivan/Michelle's Podcast, Advocate Like A Mother: https://www.advocatelikeamother.org/Apparel: https://www.littlestwarrior.com/collections/allChildren's Book: https://amzn.to/35eG3fzSee how Eli inspired an entire clothing brand in this YouTube video:https://www.youtube.com/watch?v=LLJG-U1cZAoMore Resources:DSDN: https://www.dsdiagnosisnetwork.org/Ruby's Rainbow: https://rubysrainbow.org/Global Down Syndrome Foundation: https://www.globaldownsyndrome.org/Letter Case: https://www.lettercase.org/Follow US On Social Media!Website (Sign Up for our Newsletter): http://iheartoldtowneorange.com/Facebook: https://www.facebook.com/IHeartOldTowneOrange/Instagram: https://www.instagram.com/iheartoldtowneorange/Twitter: https://twitter.com/iheartotorangeThank you, everyone, Support the show (https://www.patreon.com/iheart)