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A friendship became a movement when a survivor searching for culturally competent therapy met a clinician who refused to treat equity like an optional add-on. What started as a phone call turned into Brain Friends—a space where lived experience and rigorous science work side by side to make aphasia, stroke recovery, and neuroplasticity feel human, practical, and possible.

We walk through the real story: how instant respect turned into a partnership, how roles formed—one voice translating from the trenches, the other anchoring with research—and how that rhythm made complex ideas usable for families, caregivers, clinicians, and researchers. Then the pivot no one wanted: sudden loss. Grief shows up as silence, stalled projects, and episodes too tender to edit. Naming that pain opens a path forward. “Progress over perfection” becomes more than a motto; it’s a care strategy for speech attempts, therapy homework, and the messy edits that stay in the final cut to normalize real recovery.

Legacy grounds the work. We highlight the scholarship honoring Dr.Seles Gadson, designed to fund equity-centered clinicians and researchers who center patient-reported outcomes and culturally responsive care. Scholarships don’t run on vibes, and support here turns memory into infrastructure—training, mentorship, and research that actually changes lives. Along the way, we talk about trust in healthcare, the realities Black women face in brain health systems, and why clear, simple language outperforms jargon when the brain is tired and the heart is full.

We close with gratitude for a new advocacy award that carries responsibility, an audio message that still lights the room, and a promise to keep showing up for survivors, caregivers, and the professionals who serve them. If this resonates, share it with someone who needs hope they can use, and help sustain the scholarship that keeps this legacy working. Subscribe, leave a review, and tell us how you’re choosing progress over perfection today.

www.aphasiaadvocates.com for Brain Friends Merch

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. We are committed to honoring her memory by continuing to push our field forward and fight for equitable services for all people with aphasia.

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Words don’t just disappear; sometimes the path to them does. We explore what aphasia really is—evidence of brain injury—and why that framing changes everything for survivors, caregivers, and clinicians. Instead of waiting at a broken bridge, we focus on building new routes: consent-based support, yes/no prompts, two-choice options, functional descriptions, and shared signals that turn help into partnership. The result is less pressure, more access, and conversations that actually include the person who’s fighting to be heard.

We also dig into the messy truth of inconsistency. On one day, automatic phrases might show up on cue; on another, a simple sentence can stall. That doesn’t mean the thought is gone. Capacity rises and falls with fatigue, stress, speed, and noise. The wardrobe analogy makes it clear: the clothes are there, the drawers are jammed. So we shift the goal from perfect words to being understood—reframing success as clear meaning, not flawless speech. Along the way, we talk about when “take your time” helps and when it hurts, and how a quick reset like “let me say it another way” can unlock progress.

Caregivers and clinicians will find pragmatic guidance for protecting dignity while improving outcomes: pace the exchange, reduce choices, offer help with consent, and respect “never mind” as triage, not attitude. We name the emotional weight too—grief and depression that often travel with aphasia—and offer a way forward grounded in partnership. If you suspect aphasia after a stroke or head injury, seek an evaluation and bring these tools to your team. Subscribe, share this with someone who needs it, and leave a review to help more people find the conversation. Your support keeps this work moving and makes the path to language a little smoother for everyone.

www.aphasiaadvocates.com for Brain Friends Merch

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. We are committed to honoring her memory by continuing to push our field forward and fight for equitable services for all people with aphasia.

Send us a text

A face that slips, a word that won’t come, an arm that won’t lift—tiny moments that point to massive truths about how the brain works, heals, and sometimes declines. I invited Dr. Roy Hamilton, neurologist, neuroplasticity researcher, and one of the clearest teachers in our field, to help us untangle aphasia, dementia, and stroke with practical language and unforgettable analogies.

We start by separating terms people often blend. Dementia isn’t just memory loss; it’s a progressive decline across thinking skills that eventually limits independence. Aphasia is a language disorder: after stroke it strikes suddenly and often improves over time, while in primary progressive aphasia it creeps in gradually and can ultimately meet criteria for dementia. Along the way, we explore why prior stroke raises future risk, how small vessel disease can silently chip away at cognition, and what high blood pressure, cholesterol, diabetes, and smoking do to the brain’s “sprinkler system.”

Then we get tactical. Dr. Hamilton breaks down ischemic versus hemorrhagic stroke, how atrial fibrillation forms clots that travel to the brain, and why time is brain when speech slips or a face droops. Don’t sleep it off—modern teams can give clot‑busting drugs, thread catheters to dissolve or remove clots, and save language if you act fast. We spotlight neuroplasticity as the engine of recovery and show why practice is the original brain‑changing tool. We also share how non‑invasive brain stimulation—magnetic and electrical—aims to boost language networks in subacute stroke and help people with primary progressive aphasia hold on to communication longer.

If you or someone you love is navigating aphasia—whether after a recent stroke or as language slowly changes—this conversation blends clarity, science, and hope. Share it with your circle, watch for FAST warning signs, and ask your care team about therapy intensity, prevention, and research options. If this helped you see the brain more clearly, follow the show, leave a rating or review, and pass it on to someone who needs it.

www.aphasiaadvocates.com for Brain Friends Merch

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. We are committed to honoring her memory by continuing to push our field forward and fight for equitable services for all people with aphasia.