New to aphasia? Start here!
Education and Training, Interactive Virtual ProgramsAn introduction to aphasia and the National Aphasia Association (NAA). If you are new to aphasia - start here!
View DetailsAn introduction to aphasia and the National Aphasia Association (NAA). If you are new to aphasia - start here!
View DetailsJoin us for an evening support group for care partners and communication parters of people with primary progressive aphasia (PPA) and primary progressive apraxia of speech (PPAOS). This is a space for care partners, family, and friends of people with PPA/PPAOS to share resources and strategies, learn about and increase awareness of PPA/PPAOS, and find community with one another.
View DetailsA support group is for individuals who were diagnosed with primary progressive aphasia (PPA) or primary progressive apraxia of speech (PPAOS) under the age of 65.
View DetailsAn opportunity for people living with bvFTD and their care partners to connect and support one another.
View DetailsAphasia does not only impact the person who has it. This monthly program welcomes care partners of people who have aphasia due to stroke or brain injury.
View DetailsThis inclusive, aphasia-friendly group addresses a wide range of topics, including sharing tips and some of the challenges faced living while Black and struck by an invisible, severely underknown disability called aphasia. We welcome all who acknowledge the existence of the unique challenges each quality poses and support the mission of creating an emotional refuge for Black people living with aphasia.
View DetailsThis program offers in-depth, practical education specifically focused on Primary Progressive Aphasia (PPA) and Primary Progressive Apraxia of Speech (PPAOS). It is designed for people living with PPA or PPAOS, their care partners and loved ones, and healthcare professionals seeking disease-specific information.
View DetailsParticipants learn about using and advocating for technology such as apps, augmentative and alternative communication (AAC) devices, smartphones, AI, and more. We discuss how to use and personalize the many options that are out there so you can become more independent in your environment.
View DetailsJoin us to support well-being in your daily life. This may include movement, mindfulness, social connection, nutrition, or music and art. Participants share ideas and learn to approaches to living well with aphasia. This group is advised by Katherine Noyes and Sharon Mosley.
View DetailsThis inclusive, aphasia-friendly group addresses a wide range of topics, including sharing tips and some of the challenges faced living while Black and struck by an invisible, severely underknown disability called aphasia. We welcome all who acknowledge the existence of the unique challenges each quality poses and support the mission of creating an emotional refuge for Black people living with aphasia.
View DetailsJoin us for an evening support group for care partners and communication parters of people with primary progressive aphasia (PPA) and primary progressive apraxia of speech (PPAOS). This is a space for care partners, family, and friends of people with PPA/PPAOS to share resources and strategies, learn about and increase awareness of PPA/PPAOS, and find community with one another.
View DetailsYoung adults with aphasia have a unique experience in the aphasia community. Join us to learn, share strategies, and advocate for relationships, work, school, health care and insurance, therapy, and more. This program is advised by Kitti Tong and Katie Breece, both of whom are young adults with aphasia.
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Clinical trials test the safety and effectiveness of new treatments. Also known as intervention studies, clinical trials test whether a new type of treatment, compared to a control or “usual” treatment, may be beneficial for people with aphasia.
Qualitative studies, including interviews and focus groups
Qualitative studies can provide deeper insight into what it means to live with aphasia.