The Apraxia Foundation Podcast

Join us as we chat with the phenomenal Cari Ebert M.S. CCC-SLP discussing neurodiversity affirming care in speech therapy. Cari has extensive knowledge in childhood apraxia of speech as a clinician, speaker, and mom to a child with CAS. In addition, she is a passionate advocate for the neurodivergent community! Come take a listen!

In this episode of The Apraxia Foundation Podcast, join host Mikayla Treynor, founder of Sandy Speaks Therapy (Instagram: @sandyspeakstherapy), as she delves into the crucial advocacy efforts aimed at addressing childhood apraxia of speech (CAS) in the state of Michigan.

Mikayla sits down with representatives from The Apraxia Foundation to explore the challenges faced by children with CAS in Michigan and the strides being made in advocating for their rights to access comprehensive communication support, including Augmentative and Alternative Communication (AAC) methods.

Listeners will gain insight into the initiatives undertaken by The Apraxia Foundation to raise awareness, educate policymakers, and enact change in policies and services to better serve children with CAS and their families across Michigan. From legislative advocacy to community outreach, discover the multifaceted approach employed to ensure that every child has the opportunity to communicate effectively and thrive.

Tune in to this enlightening conversation and learn how you can contribute to the ongoing efforts to support individuals with CAS and promote inclusive communication practices in Michigan and beyond. Don't miss this empowering episode of The Apraxia Foundation Podcast.

Laura Smith and Jordan LeVan from The Apraxia Foundation speak with Dr. Julie Case, Dr. Jenya Iuzzini-Siegel, and Nancy Tarshis to debunk the myths about DTTC therapy for childhood apraxia of speech. They discuss current findings about DTTC, the true definition of play-based therapy, and the importance of building feelings of safety with our loved ones with childhood apraxia.

Join us on "Voices of Change," brought to you by The Apraxia Foundation, as we dive deep into the intricacies of the public school system and the challenges Speech-Language Pathologists (SLPs) face within it. In this episode, we welcome special guest StraightupSLP, who shares her firsthand experiences navigating the public school district and transitioning to running a successful private practice. Discover the obstacles SLPs encounter, the systemic issues at play, and potential solutions to create a more supportive environment for both professionals and students. Tune in for an enlightening conversation that aims to advocate for change and improve the landscape of speech-language pathology in public education.

In this episode of The Apraxia Foundation Podcast, we tackle one of the most frequently asked questions in our community: "Will my child ever talk?" Join Laura Smith, our professional advisory board member, and Jordan LeVan, Founder & President of The Apraxia Foundation, as they provide insights, share personal experiences, and discuss the latest research on childhood apraxia of speech. Together, they offer hope, practical advice, and a deeper understanding of the journey toward communication for children with apraxia.