In this episode, we sit down with Vanessa Abraham, a certified Speech-Language Pathologist whose life took an unexpected turn when she became the patient. After a sudden illness left her paralyzed and unable to speak, Vanessa faced the daunting task of reclaiming her voice and identity.
Vanessa shares her harrowing experience of battling Post-Intensive Care Syndrome (PICS), the emotional toll of being unable to communicate, and her path to recovery. Her story is not just one of survival but of transformation, leading her to become an advocate for ICU survivors and author of the memoir Speechless: How a Speech Therapist Lost Her Ability to Speak and Her Silent Struggle to Reclaim Her Voice and Life.
In this episode, we discuss:
- The sudden onset of her illness and ICU experience
- The psychological impact of PICS
- Her journey from patient back to practitioner
- Insights from her memoir, Speechless
- Her mission to educate others about the unseen challenges ICU survivors face
Vanessa’s resilience and dedication to helping others navigate similar challenges are truly inspiring. Whether you’re a healthcare professional, a survivor, or someone interested in stories of human strength, this episode offers valuable insights.
🔗 Learn more about Vanessa’s work: Aneu Healing – https://aneuhealing.com/
📘 Check out her memoir: Speechless on Amazon – https://www.amazon.com/Speechless-Therapist-Ability-Struggle-Reclaim/dp/B0DS96R6XT
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Civil rights advocate Marc Fishman joins host Mike Bolland to shed light on a critical but overlooked issue: the routine denial of disability accommodations in America’s family courts. After a devastating car accident left him with long-term disabilities and communication challenges, Marc entered a 49-month legal battle—not just for his parental rights, but for his basic ADA protections. He details how New York courts repeatedly refused accommodations like real-time transcription, the federal ADA victories he secured, and how Tennessee v. Lane shaped his fight for access. Marc also reveals the retaliation he faced from judges and public officials and discusses his successful advocacy during COVID helping disabled tenants obtain rent grants. With recent legislative wins offering hope, Marc emphasizes the urgent need for accountability and reform to protect disabled parents nationwide.
Today, I’m honored to sit down once again with Brooke Brown — an “ink weaver of life, faith, and fiction,” an honors graduate of ASU’s Walter Cronkite School of Journalism, Ms. Wheelchair Arizona 2022, and founder of Brooke’s Butterfly Touch, a ministry that helps individuals discover the power and purpose of their own stories. Brooke is also the author of Rolling in Grace: Volume 1 — A Foundation of Faith and Imagination, now available in audio format. Having read it myself, I can promise you: it’s full of relatable, uplifting, and beautifully practical stories. Living with cerebral palsy and using an augmentative communication app, Brooke demonstrates that every voice — every single one — can inspire hope, healing, and opportunity. This is her second appearance on the show, so after watching, don’t forget to visit WereNotStumped.com to catch her first episode.
In this inspiring episode of We’re Not Stumped, host Mike Bolland sits down with Caitlin Conner, founder of Be More Adaptive, to explore how she’s building a global hub for disability resources designed to empower people with disabilities to live fulfilling, confident, and sustainable lives. Caitlin shares her powerful journey — from surviving a life-changing motorcycle accident while pregnant to becoming a Paralympic-level athlete, model, and outspoken disability advocate. She talks candidly about adapting to life as an amputee, the importance of self-advocacy, and how adaptive sports helped her rebuild her identity, purpose, and strength.
