From ongoing virtual programs to aphasia education and training opportunities, our programs are created with accessibility, inclusion, and education at their core.
The NAA also helps people with aphasia and their families find in-person and virtual groups across the country. Whether you’re looking for a regional meet-up or a specialized group, we’re here to help connect you. Visit our provider directory or email us at answers@aphasia.org for assistance.
The National Aphasia Association hosts a select number of virtual programs that align with our mission of education, connection, support, and empowerment for persons with aphasia and their care partners. Most programs meet once or twice per month and are listed on our events calendar. Please review each program for a description and to see if a program may be a good fit for your specific needs.
The NAA offers education and training to help people better understand aphasia and how to support communication. These programs are for people with aphasia, families, healthcare providers, and the public. We offer monthly online sessions with different topics and tracks. Some sessions are designed for people who are new to aphasia, while others are for those who want to learn more. You’ll find practical tips, real stories, and helpful tools.
All upcoming sessions are listed on our events calendar. If you’re not sure which session is right for you, or if you have questions, email us at answers@aphasia.org, and we’ll help you find the best fit.
The National Aphasia Association hosts special events throughout the year to celebrate, educate, and bring the aphasia community together. These events highlight creativity, connection, and shared experiences.
Our special events include things like the Night of Aphasia Arts, unique workshops, our Speaking Out conference, annual awards, and more. Some events are virtual, others are in person, and all are designed to honor the voices and talents of people with aphasia and their families.
Upcoming events are listed on our calendar. We hope you’ll join us! For questions or more information, email answers@aphasia.org.