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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In this episode of We’re Not Stumped, Mike Bolland sits down with Meegan Winters, CEO and founder of AbleVu, the innovative accessibility search platform making the world easier to navigate for everyone. Meegan shares her inspiring journey—from special education teacher to tech entrepreneur—and how her friendship with Jessica, a power wheelchair user, sparked her mission to improve accessibility for all. Mike and Meegan explore AbleVu’s evolution from virtual tours to a “TripAdvisor for accessibility,” the business model that empowers contributors, and why accessible information benefits both consumers and businesses. Along the way, Meegan opens up about leaving a stable career, overcoming the challenges of building a startup, and the fulfillment that comes from creating real-world impact. Discover how technology and empathy intersect to make the world more inclusive.
Podcast host Mike Bolland is looking to connect with individuals willing to share their experiences with prosthetists and prosthetic care. If you’ve ever faced challenges with a prosthetist, received a prosthetic that didn’t meet your needs, or discovered a provider who went above and beyond, your story can make a difference. On his show, We’re Not Stumped, Mike engages in open, honest conversations about life with limb loss, prosthetics, and advocacy. His mission is to give a voice to the limb loss community, spotlight real experiences — both the good and the bad — and work toward improving the system for everyone. Mike invites you to be part of this important dialogue, knowing that your insights could help others navigate their own prosthetic journeys with greater confidence and support. 📩 Interested in being a guest? Visit: https://werenotstumped.com/were-not-stumped-limb-loss-podcast-guest-guide/
In this heartfelt and uplifting episode of We’re Not Stumped, host Mike Bolland welcomes Katie Thomas for a conversation filled with honesty, humor, and hard-earned wisdom. Born without her right arm below the elbow, Katie began receiving care at Shriners Hospital in Tampa at age 3 and experimented with various prosthetics throughout her childhood. Over time, she discovered that prosthetics were a helpful tool—but not essential for her to live a full, capable life. Now a devoted parent, Katie opens up about raising her son, who has Witteveen Colk syndrome, a rare genetic disorder. She shares her journey through early intervention services, advocating for genetic testing, and ensuring her child receives the support he needs. Her advice to parents? Trust your instincts, push for answers, and never hesitate to speak up for your child.
