Aphasia Blog

Medical research has had a huge impact on our lives, from the discovery of antibiotics to new cures for cancer and treatments for heart disease. Similarly, research efforts are leading to steady progress in the diagnosis and treatment of aphasia. Below are some major advances in aphasia research in recent decades, and how you can help support these efforts to improve the lives of people with aphasia.

Research plays a critical role in improving the lives of people with aphasia — and everyone should be able to participate in that progress. We’re proud to announce the launch of two upgraded features on our website, designed with both researchers and research participants in mind. They reflect our commitment to making research more accessible, inclusive, and impactful—and to supporting the professionals who help move aphasia science forward.

The NAA is proud to announce the recipients of the 2025–2026 Research Grants. This year’s cohort reflects the continued growth of our organization and our commitment to supporting innovative, person-centered research in aphasia.

Each year, the NAA bestows our aphasia advocacy award in honor of our founder, Dr. Martha Taylor Sarno. Today, we celebrate our 2025 recipient, Thomas Broussard. Read on to learn about Dr. Broussard and the advocacy award.

There’s a new project being led by the NAA with funding support from PCORI. This project puts the voices of people with aphasia at the center of the conversation. It’s called a CORE Impact project, and the goal is to identify the most important impacts and challenges of living with aphasia.

On October 3rd and 4th, the NAA’s Speaking Out 2025 gathered hundreds of people with aphasia, caregivers, and professionals for two days of stories, strategies, and shared strength. During the sessions, participants filled the chat with ideas, tools, and community recommendations. Read on to learn more and for links to the recording.

June was Aphasia Awareness Month around the country and around the world! Aphasia Awareness Month is an opportunity for the NAA to educate the general public about aphasia… what it is, and what it is not.  We are also able to share all of the amazing programs serving people with aphasia and their families in communities across the nation.

Living with aphasia can be frustrating and stressful. Communication difficulties often impact communication with friends and family, basic life activities, and can lead to major life changes. The related stresses may continue even with adjustments to life with aphasia. Learn about symptoms of depression and what supports and strategies are available.

June is National Aphasia Awareness Month, and the NAA is excited to announce our initiatives for this year! From puzzle-themed projects  to community/library showcases , there’s something for everyone – and it all starts with you.

The one-hour International PPA Awareness Day webinar allowed people with PPA to share their experience through photos, art, poetry and more! The webinar included information from leading clinician-researchers including Drs Maya Henry, Sharon Antonucci, Stephanie Grasso, and Jeanne Gallée. Watch the webinar recording and find additional PPA resources!