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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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.
Jeanette Jones returns to the We’re Not Stumped podcast with host Mike Bolland for a powerful conversation that goes beyond music. She shares a shocking and emotional story about the accessibility barriers she and her partner Frank encountered at a Def Leppard concert at the Bethel Woods Center for the Arts. From steep hills to discriminatory treatment by staff, their experience sheds light on how accessibility still falls short—even in 2025. But that’s just the beginning. Jeanette also opens up about her own journey—surviving childhood cancer, transitioning from prosthetics to a wheelchair, and the incredible resilience of her partner Frank after his life-changing accident. This episode is about more than one bad night—it’s a call to action for accessibility, empathy, and real change.
