PPA Chat is for people with PPA / PPAOS and their communication partners to learn, share strategies, and connect with others. We start as a group, sometimes with a short presentation. Then, we split into breakout rooms based on PPA type or symptoms, including a room for care partners.
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 DetailsIn this monthly interactive educational session, we will have an opportunity to learn more about the topic shared in this month’s “Ask the Expert” webinar and have more questions answered. All are welcome; bring your questions, feedback, and ideas!
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 DetailsThis monthly interactive, educational program is an opportunity to learn from experts and each other. The topic varies each month, but features practical information, research updates, communication strategies, and other resources. All are welcome.
View DetailsThis townhall discussion is an extension of the NAA/PCORI Aphasia Patient Centered Core Impacts project. Discuss the impacts of living with aphasia that are most important to you.
View DetailsPPA Chat is for people with PPA / PPAOS and their communication partners to learn, share strategies, and connect with others. We start as a group, sometimes with a short presentation. Then, we split into breakout rooms based on PPA type or symptoms, including a room for care partners.
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. This group is advised by Brooke Lang and Bryn Bowles
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.
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