184 Epizód

  1. 183. The Adolescent Brain with Christina Aries

    Közzétéve: 2025. 04. 03.

  2. 182. World Down Syndrome Day - March 21, 2025

    Közzétéve: 2025. 03. 21.

  3. 181. Olivier and Hilda Bernier and Their IEP Experience

    Közzétéve: 2025. 03. 03.

  4. 180. Liam Turns 15: What Have We Learned In This Journey?

    Közzétéve: 2025. 02. 25.

  5. 179. Forget Me Not: Inclusion in the Classroom Documentary - Hilda & Olivier Bernier

    Közzétéve: 2025. 02. 10.

  6. 178. The 2025 DSDN Rockin' Dad Retreat with Ben Hughes

    Közzétéve: 2025. 02. 03.

  7. 177. Showing Up For The Challenges - Karen Maezen Miller

    Közzétéve: 2025. 01. 27.

  8. 176. Revisiting 10,000 Maniacs Founding Member Steven Gustafson

    Közzétéve: 2024. 07. 20.

  9. 175. Communicating Our Stories with Sid and Vaish Sarathy

    Közzétéve: 2024. 06. 17.

  10. 174. Advocating For Speech Therapy - Julie Picot

    Közzétéve: 2024. 06. 10.

  11. 173. The Endless Possibilities of People with Down Syndrome: Revisiting Jake Pratt

    Közzétéve: 2024. 05. 27.

  12. 172. Happy Mothers Day: We Celebrate You

    Közzétéve: 2024. 05. 12.

  13. 171. Alzheimer’s Disease In People with Down Syndrome - Dr. Elizabeth Head

    Közzétéve: 2024. 04. 29.

  14. 170. Celebrating The Life of Carl Erskine with Ted Green

    Közzétéve: 2024. 04. 21.

  15. 169. The Annual DSDN Retreats with Ben Hughes

    Közzétéve: 2024. 04. 15.

  16. 168. Liam's 14th Birthday: Sharing Some Insight

    Közzétéve: 2024. 03. 08.

  17. 167. A Discussion About Using The R-Word with Lynette Louise

    Közzétéve: 2024. 02. 26.

  18. 166. Finding The Right Supports Without Shame - Julie Picot

    Közzétéve: 2024. 02. 19.

  19. 165. Picking The Right Pediatrician with Dr. Ilona Kleiner

    Közzétéve: 2024. 01. 29.

  20. 164. Charlotte and Riley: Not Taking No For An Answer

    Közzétéve: 2024. 01. 22.

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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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