25 episodes

This podcast serves as a platform for parents of children with special needs in order to gain insight, educate, and build community.

A Tour of Holland April Hammon

    • Kids & Family
    • 5.0 • 2 Ratings

This podcast serves as a platform for parents of children with special needs in order to gain insight, educate, and build community.

    Episode 26: An interview with Oksana Sergeyovich

    Episode 26: An interview with Oksana Sergeyovich

    In this episode Oksana shares her experience raising her 5 year old son Arthur, who has a diagnosis of autism and GDD (Global Developmental Delays)
    Connect with Oksana on IG @xeniathestranger

    • 50 min
    Episode 25: An Interview with Allison Harvey-Griffin

    Episode 25: An Interview with Allison Harvey-Griffin

    In this episode Allison shares her experience raising her 6 year old son Jackson who has a diagnosis of Diastrophic dysplasia, a rare form of dwarfism.

    Connect with Allison on:
    Instagram @allie0126 and @jackharveyg
    Email: harv79@gmail.com

    • 59 min
    Episode 24: An interview with Gina Evans D'Angelo

    Episode 24: An interview with Gina Evans D'Angelo

    In this episode Gina Evans D’Angelo shares her experience raising her daughter Jackie who has a diagnosis of Achondroplasia, a form of dwarfism. Gina lives with her two children in Farmington, Connecticut.

    Resources mentioned in this episode include:


    Parents of Little People support group
    Little People of America

    Connect with Gina on Facebook. The book she wrote for is also available online:

    Special Delivery From Pregnancy to Toddlerhood https://www.amazon.com/dp/B09JV97Z97/ref=cm_sw_r_cp_api_glt_i_PATN17BGJDMZJ2S8PM9Z

    • 57 min
    Episode 23: An Interview with Jill Pratt

    Episode 23: An Interview with Jill Pratt

    In this episode I have the pleasure of interviewing Jill Pratt, mother of Jiselle and co-founder of the Jisellle Lauren Foundation.  Jill is a mother of 3 young children and her oldest, Jiselle, has a diagnosis of Rett's syndrome a rare neurological condition.     Resources mentioned in this episode include:
    Katie Beckett program
    www.rettsyndrome.org
    www.jisellelaurenfoundation.org
    Rett University

    Connect with Jill on IG: @pratt_partyof5

    Follow the Jiselle Lauren Foundation on IG: @thejisellelaurenfoundation


    Watch the interview here: https://youtu.be/gVwYeNKVTG4

    • 40 min
    Episode 22: An interview with Effie Parks

    Episode 22: An interview with Effie Parks

    In this episode Effie Parks shares her experience raising her son Ford who has CTNNB1, a rare neurological syndrome.  Effie lives in Seattle, Washington with her husband and two children. She is the host of the award winning podcast: Once Upon A Gene.
    Resources mentioned in this episode include:
    Every Life Foundation
    Podcasts:
    The Two Disabled Dudes
    Global Genes
    Once Upon A Gene
    The Courageous Parents network
    The Disordered Channel
    Connect with Effie here: https://effieparks.com/

    • 47 min
    Episode 21: An Interview with Jeanine Lynn Arlene Blair

    Episode 21: An Interview with Jeanine Lynn Arlene Blair

    In this episode, Jeanine shares her experience raising her daughter Ami ("Aim-mee") who has a diagnosis of arthrogryposis as well as hearing impairment due to bacterial meningitis at the age of 6 months old.  Ami has 3 siblings and lives in Calgary Canada. 

    Get in touch with Jeannine or follow her accounts at 
    Facebook:  Jeannine Lynn Arlene Blair 
    Instagram: @jeanninelynnarleneblair
    TikTok: @jeannineblair2 
    Resources mentioned in this episode include: 
    Children's Hospital of Calgary 
    Duet Bike 

    • 40 min

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