Building Community Through Advocacy with Matt Pashby | Dont Call On Me, The Dyslexia Podcast Ep. 31
Dont Call On Me, The Dyslexia Podcast
Release Date: 09/02/2025
A Family's Journey with Dyslexia and Dysgraphia | Dont Call On Me, The Dyslexia Podcast Ep. 39
Dont Call On Me, The Dyslexia Podcast
In this powerful episode of the Don't Call On Me Podcast, hosts Megan and Eryn sit down with Lucia and her remarkable daughter, Ansley, to share a family's journey through years of misdiagnoses, academic struggles, and ultimately, triumph. Ansley, along with her twin brother Dawson, both have dyslexia and dysgraphia, yet each faced unique hurdles to get the right support. Misdiagnosed with anxiety in first grade, Ansley endured frustration and even reached a breaking point before finally receiving an Independent Educational Evaluation (IEE) and finding a school where she could learn in a way...
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A Parent’s Advocacy: The Lisa Jensen DeLaet Story | Dont Call On Me, The Dyslexia Podcast Ep. 38
Dont Call On Me, The Dyslexia Podcast
In this powerful episode of the Don't Call on Me Podcast, Megan and Eryn welcome Lisa Jensen DeLaet, a mother of two children with dyslexia, who has become a fierce advocate for early intervention and the science of reading. She shares her journey of discovering her 9-year-old son’s dyslexia in kindergarten and the uphill battle she waged to secure evaluations, accommodations, and an IEP—all while learning how to navigate a system that often overlooks early signs of learning differences. Lisa also shares the story of her 16-year-old daughter, a straight-A student whose dyslexia went...
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Raine Anderson’s Dyslexia Story: Thriving Through the Journey: | Dont Call On Me, The Dyslexia Podcast Ep. 37
Dont Call On Me, The Dyslexia Podcast
In this heartfelt episode of Don't Call on Me, Megan and Eryn sit down with Raine Anderson and her family to share their inspiring journey through dyslexia. From the early signs at age four to thriving as an incoming high school freshman, Raine’s story is a testament to resilience and the power of a supportive community. Hear how Raine’s family navigated a maze of IEPs, ARDs, private schools, homeschooling, and an incredible team of teachers and administrators to ensure her success. With Megan playing a key role in their early journey, this conversation highlights the determination it...
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Homeschooling & Dyslexia: The Power of Consistency and Proper Intervention| Dont Call On Me, The Dyslexia Podcast Ep. 36
Dont Call On Me, The Dyslexia Podcast
In this episode, Megan and Eryn sit down with Jen Milton, a homeschooling mother of four who has been educating her children at home from the very beginning. Jen shares her unique journey as a parent of two children with dyslexia. Her first child was diagnosed in 2021, and since then, her family’s approach to education has evolved. Jen talks candidly about the transformative power of consistent dyslexia therapy, the impact of a structured curriculum taught with fidelity, and how her family found the courage to connect with others facing similar challenges. Whether you’re a homeschooling...
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From Undiagnosed to Unstoppable: The Ameer Baraka Story| Dont Call On Me, The Dyslexia Podcast Ep. 35
Dont Call On Me, The Dyslexia Podcast
Ameer Baraka, Emmy-nominated actor, author, and advocate, turned years of struggle with undiagnosed dyslexia into a life of purpose. From academic frustration and hardship to self-discovery and advocacy, his journey shows the power of resilience, the impact of literacy, and the courage it takes to rewrite your own story. to discuss CALT therapy. to discuss advocacy services.
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Made for More: Janae Harris on Dyslexia, Confidence, and Advocacy | Dont Call On Me, The Dyslexia Podcast Ep. 34
Dont Call On Me, The Dyslexia Podcast
Miss Nebraska’s Teen 2024, Janae Harris, was diagnosed with dyslexia and ADHD in third grade after struggling to read despite a high IQ. Now a passionate advocate, Janae shares how she turned her challenges into strengths, and why she believes every learner deserves to thrive. Join Megan and Eryn for a powerful conversation about confidence, neurodiversity, and embracing your story. to discuss CALT therapy. to discuss advocacy services.
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Transforming Dyslexia Support Through Technology with Amir Bar| Dont Call On Me, The Dyslexia Podcast Ep. 33
Dont Call On Me, The Dyslexia Podcast
In this episode of Don't Call on Me, The Dyslexia Podcast, hosts Megan and Eryn sit down with Amir Bar, CEO and co-founder of UCNLearn. A passionate advocate and innovator, Amir draws on his own experiences with dyslexia to design technology that makes reading intervention more accessible and effective. With a degree from the Harvard Graduate School of Education, contributions to the Texas Dyslexia Handbook, and presentations at national literacy conferences, Amir has spent his career at the intersection of education and technology. Join us as he shares his personal journey, his vision for the...
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Literacy as a Civil Right: Kareem Weaver’s Fight for Every Child to Read | Dont Call On Me, The Dyslexia Podcast Ep. 32
Dont Call On Me, The Dyslexia Podcast
In this episode of Don’t Call on Me – The Dyslexia Podcast, Megan and Eryn sit down with Kareem Weaver, Co-Founder and Executive Director of FULCRUM and one of today’s most powerful voices for literacy justice. Featured in the 2023 documentary The Right to Read, Kareem brings a lifetime of experience as an educator, administrator, and community leader to the urgent conversation about why so many children are still not learning to read. From his own educational journey to his classroom teaching and leadership roles across the country, Kareem has seen firsthand how access to evidence-based...
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Building Community Through Advocacy with Matt Pashby | Dont Call On Me, The Dyslexia Podcast Ep. 31
Dont Call On Me, The Dyslexia Podcast
In this episode of Don’t Call on Me - The Dyslexia Podcast, Megan and Eryn talk with Matt Pashby about how a late diagnosis of a learning disability in high school changed the course of his life. Matt shares openly about the challenges he faced before diagnosis, the relief of finding people who understood, and the ways that community continues to shape his life today. His story highlights the power of belonging, self-acceptance, and the transformative impact of advocacy. From struggling student to dedicated advocate, Matt’s journey reminds us how vital it is for neurodiverse...
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Parent Power: Brett Tingley and the Fight for Reading Justice | Dont Call On Me, The Dyslexia Podcast Ep. 29
Dont Call On Me, The Dyslexia Podcast
In this episode of Don't Call on Me, The Dyslexia Podcast, Megan and Eryn are joined by Brett Tingley, a leading force in the national movement for effective literacy instruction. As Founder and President of Parents for Reading Justice and producer of the widely viewed documentary Our Dyslexic Children, Brett has mobilized thousands of parents to demand systemic change in how schools identify and support students with dyslexia. Brett shares how her personal journey led to public advocacy and how grassroots parent efforts can shift state laws, influence districts, and hold institutions...
info_outlineIn this episode of Don’t Call on Me - The Dyslexia Podcast, Megan and Eryn talk with Matt Pashby about how a late diagnosis of a learning disability in high school changed the course of his life.
Matt shares openly about the challenges he faced before diagnosis, the relief of finding people who understood, and the ways that community continues to shape his life today. His story highlights the power of belonging, self-acceptance, and the transformative impact of advocacy.
From struggling student to dedicated advocate, Matt’s journey reminds us how vital it is for neurodiverse individuals to feel seen, supported, and connected.
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Book a consultation with Megan to discuss CALT therapy.
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Book a consultation with Eryn to discuss advocacy services.