184 Episodo

  1. 83. The Self Determination Learning Circle at Club 21 with Kelly Kulzer-Reyes

    Publicado: 17/12/2021
  2. 82. John’s Crazy Socks - Spreading Happiness with John & Mark Cronin

    Publicado: 10/12/2021
  3. 81. USA Skateboarding’s “Skateboarding For All” Initiative with Miki Vuckovich

    Publicado: 3/12/2021
  4. 80. Bertie’s Heart Surgery: Talking About The Scary Stuff with Melissa Kynoch

    Publicado: 25/11/2021
  5. 79. Reaching Our Advocation Milestones As Parents - with Julie Picot

    Publicado: 19/11/2021
  6. 78. A Son’s Advocacy: Another Conversation with Sader Issa

    Publicado: 12/11/2021
  7. 77. Practicing Gratitude Without Expectations: An Interview with Karen Maezen Miller

    Publicado: 5/11/2021
  8. 76. Catching Up with Melissa Kynoch: A Year and a Half Later

    Publicado: 29/10/2021
  9. 75. A Loving Kindness Meditation Gift from Paul Denniston

    Publicado: 15/10/2021
  10. 74. Creating An Inclusive Superhero Universe: A Conversation with Jack and Caitie Clonan

    Publicado: 7/10/2021
  11. 73. Down Syndrome Awareness Month: Acknowledging Those Who Came Before Us

    Publicado: 1/10/2021
  12. 72. Gifts of the Journey: A Sibling Conversation with Amy Hyde

    Publicado: 24/9/2021
  13. 71. Fasten Your Seatbelts: A Crash Course on Down Syndrome for Brothers and Sisters

    Publicado: 17/9/2021
  14. 70. Insights of a Teenage Sibling: with Sophia Saux

    Publicado: 10/9/2021
  15. 69. Uncertainties About the Return to School? You’re Not Alone.

    Publicado: 2/9/2021
  16. 68. The Importance of Special Needs Trusts and a Conservatorship: with Enrique Perez

    Publicado: 27/8/2021
  17. 67. The Beginner’s Mind: An Interview with Karen Maezen Miller

    Publicado: 20/8/2021
  18. 66. A Conversation About Alzheimer’s with Dr. Brian Skotko

    Publicado: 13/8/2021
  19. 65. The Down Syndrome Resource Foundation, Part 2 with Liv Meriano and Danielle McKinney

    Publicado: 6/8/2021
  20. 64. Changing Our Mind and Approach to Education: Down Syndrome Resource Foundation

    Publicado: 30/7/2021

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We are Stephen and Lori Saux and welcome to the If We Knew Then Podcast. We are parents of two children and one of them has Down Syndrome, Liam. When Liam was born we didn’t know very much about Down Syndrome and most of the information we did have didn’t seem very hopeful and positive. Well this podcast aims to share honest and useful conversations about supports, therapies, education and society as it pertains to Down Syndrome advocacy and parenting.

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