Brain Friends
Brain Friends: The Podcast is a survivor-led show about stroke, brain health, aphasia, recovery, and health equity.
Hosted by Angie Cauthorn, a two-time stroke survivor and aphasia advocate, Brain Friends takes complicated medical and research topics and turns them into everyday clarity. The show is for survivors, care partners, families, clinicians, researchers, and anyone trying to understand what life after stroke can really look like.
Brain Friends began with me and my friend and co-host, Dr. D. Seles Gadson, a neuroscientist, speech-language pathologist, and champion for equity in aphasia care. Dr. Seles’s work focused on health disparities, representation, and making science useful for real communities. Her voice still opens and closes every episode, and her legacy remains part of the show’s foundation.
Since launching in June 2022, Brain Friends has reached listeners in more than 100 countries, with conversations that center stroke recovery, aphasia, cognition, communication, prevention, brain health, and the real-life “now what?” after a neurological event.
Regular segments include:
The Breakdown: Clear explanations of stroke, aphasia, brain health, research, and recovery topics.
Smart Cookie: The thoughtful question Angie asks guests about brain health, recovery, equity, or what they wish more people understood.
OTC with the Commish: “On The Clock” style recovery talk, where Angie uses football draft energy to break down the moves, tools, and first-round picks that matter.
The Check-In: Short, honest reflections on life after stroke, recovery, advocacy, and what comes next.
Brain Friends is not here to give medical advice or empty inspiration. It is here to make the science clearer, the recovery road less lonely, and the next step easier to see.
Welcome to Brain Friends.
Brain Friends
Five Ways to Advance Health Equity for Black People With Aphasia
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Black stroke survivors with aphasia face compounding barriers to care, and the research is clear on what needs to change. This episode breaks down five concrete actions clinicians, researchers, and care partners can take right now: implicit bias training, workforce diversity, representation in research, health literacy support, and patient-reported outcomes. Hosted by Angie of Brain Friends: The Podcast. Resources included for caregivers seeking compensation and for speech-language pathologists committed to closing the equity gap in aphasia care. For SLPs, researchers, care partners, and anyone working toward more equitable outcomes for Black people with aphasia.
In this episode of Brain Friends, we discuss 5 ways everyone can contribute to health equity for Black people with aphasia. We give resources for caregivers to get compensated and encourage speech-language pathologists (SLPs) to support health literacy in clients.
1. Implicit Bias Training- to help practitioners recognize stereotypical beliefs that contribute to health inequities.
2. Workforce Diversity- may help clients with communication and participation in research by having practitioners who look like them.
3. Representation in Research- helps ensure generalization of findings and that all voices are included. http://www.aphasiaresource.org/ Also, how are researchers sharing clinical findings? How many researchers have collected data from participants, published the findings, and gone back to the participants to share their study results?
4. Health Literacy- helps individuals understand medical information to make an informed decision. It is important to encourage care partners and provide disability resources that compensate the caregiver https://www.usa.gov/disability-caregiver
5. Patient Reported Outcomes- helps give people with aphasia a voice in therapy by sharing goals that are important to the individual. Patient-reported outcomes can be challenging to read and should be diversified with large print, pictures, audio versions, or available on assistive devices.
https://aphasiaadvocates.com/ for Brain Friends Merch
https://aphasia.org/event/ask-the-expert-february-2026/
https://www.cognitiverecoverylab.com/seles
https://aphasia.org/stories/announcing-the-davetrina-seles-gadson-health-equity-grant-program/
Our beloved colleague, Dr. Davetrina Seles Gadson, passed away January 11, 2025. Dr. Gadson was an extraordinary speech-language pathologist and neuroscience researcher who devoted her energy to studying health disparities in aphasia recovery. She was a fierce advocate for improving services for individuals with aphasia, particularly Black Americans. Her research transformed our understanding of these health disparities and shed light on how we can address them. We were privileged to have Dr. Gadson as a cherished member of our lab community for four years, first as a postdoctoral fellow and then as an Instructor of Rehabilitation Medicine. She was still a close collaborator and friend to many of us at the time of her passing. Dr. Gadson was an incredible person—compassionate, inspiring, and full of life. Her dedication to advancing equity in aphasia recovery and her profound impact on our community will never be forgotten. ...
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