Save the Date · July 22 – 24, 2027
30th Annual Convention · Dallas, TXEmbassy Suites by Hilton Grapevine DFW Airport North
That’s a wrap on Chicago · Thank you, Friends community!
With gratitude to all who attended on July 23–25, 2026
To everyone who joined us in Chicago, thank you. Your energy, openness, and support are what make Friends more than just a convention. You made this space come alive, and we’re so grateful to have shared it with you.
We welcomed 280 people from across the country: kids, teens, and young adults who stutter, their families and friends, and all of the allies and professionals who support them.
Keep the momentum going by joining a virtual group in August and stay tuned for our upcoming one-day events.
Our 2027 convention will be held at the Embassy Suites by Hilton Grapevine DFW Airport North
You can book your hotel room today! Our discounted group reservation link is now available. Simply follow this button:
Never been to Friends?
Whether you’re a young person who stutters searching for community, a parent seeking support, or a speech-language pathologist looking to grow your understanding, this short video gives you a glimpse of what Friends is all about, and why our annual convention might be just what you need.
What is Friends all about?
Our mission is to provide support and education to young people who stutter, their families, and clinicians. Instilling a sense of empowerment, providing an environment where feelings of isolation disappear and growing confidence and self-esteem continues to be the foundation of our vision. We want our young people who stutter to know they are strong, they have support, they are not alone, and they have Friends who will listen to them. Learn more here »
If you haven’t already, join our mailing list below to hear the latest updates about the convention. If you have any questions, please email us at friends@friendswhostutter.org.
What to expect
You can expect to meet young people who stutter, parents and relatives, siblings, significant others, and SLPs all hoping for the same support, growth, and unforgettable time as you. When you leave on Sunday, we are positive you will tell your new Friends how happy you are that you decided to come to a Friends convention, followed by a ‘See you next year!’
The magic of a Friends convention is made up of:
- Individualized workshops for all attendees: Kids, teens, and adults who stutter, their families and loved ones, and professionals take part in sessions tailored to their needs.
- A supportive foundation to learn about stuttering: From start to finish, you are surrounded by people who get it. You’ll find community wisdom, professional insights, and connection all in one place.
- Led by experts in stuttering: You’ll learn from world-renowned stuttering researchers and clinicians, and people who stutter who bring deep lived experience.
- Chances to normalize stuttering: Throughout the convention, stuttering is talked about openly and met with understanding. Panels, keynotes, open mics, and informal conversations make space to share stories, be heard, and feel less alone.
- Immersion in our stuttering community: For three days, people who stutter aren’t the 1%… we’re the majority! As attendees have shared time and again, the convention is a treasured time where stuttering doesn’t need explaining. From the moment you walk in, you’re understood.
- Moments to connect and recharge: Beyond workshops, the convention is full of community. Shared meals, family activities, and welcoming spaces create countless opportunities to connect and head home feeling renewed.
Kids, Teens, & Adults
Increase your confidence
communicating
Meet others who stutter
Find role models who stutter
Have fun talking!
Learn about stuttering
Parents & Caregivers
Meet other parents & share experiences
Hear tips and support from fellow parents & young people who stutter
Join in roundtable discussions
Find out what you can do to support your child
SLPs & Teachers
Receive invaluable education from experts and researchers
Gain more confidence in working with people who stutter & their families
Learn more about stuttering, effective social/clinical strategies, & support services
Support someone’s chance to attend
Friends touches many lives every year, but not everyone who wants to attend our annual convention can afford to. Our scholarships are often the difference between them joining us and them staying home.
Will you help an individual or family get to Friends? 100% of your donation will go towards scholarships. Give to our scholarship fund here »
Snippets
Hear from a teen who stutters, adult who stutters, parent, and speech-language pathologist on what it’s like to attend a Friends conference.
Research Corner
Why attend a Friends Convention? We partnered with researchers at the University of Iowa to understand the positive impact our conventions have on young people who stutter. They found the following five results:
- Children and teenagers built strong relationships and a sense of community in a safe environment.
- Collaborative learning facilitated personal growth.
- Communicative and cognitive changes persisted beyond the convention.
- Hearing and sharing personal stories increased self-acceptance and acceptance of others.
- Living with stuttering can be hard, but the convention helped normalize stuttering.
SPEECH PATHOLOGISTS & STUDENTS
Our annual convention is a fantastic place for speech-language pathologists and students to learn more about stuttering, current treatments and the support available to people who stutter, while earning 1.2 ASHA CEUs.
Read Financial and Non-Financial Disclosures
Rick Arenas, Ph.D. is a salaried employee of the University of New Mexico and a compensated board member of Friends: The National Association of Young People Who Stutter. He has no non-financial disclosures.
Nicholas Brow, M.A., CCC-SLP is a salaried employee of George Washington University and an independent contractor at the Sisskin Stuttering Center and Friends: The National Association of Young People Who Stutter. He has no non-financial disclosures.
Julie Gasway MA, CCC-SLP, BCS-SCF owns Speech Therapy Associates LLC, a private practice. She has no non-finacial disclosures to report.
Heather Grossman, Ph.D., CCC-SLP is a salaried employee of the American Institute for Stuttering. She has no non-financial disclosures.
Caryn Herring, M.S., CCC-SLP is a salaried employee of Friends. She has no non-financial disclosures.
Eric Jackson, Ph.D., CCC-SLP is a salaried employee of New York University. Non-financial disclosures include: board member of Friends: The National Association of Young People Who Stutter.
Kristel Kubart, M.S., CCC-SLP is a salaried employee of the American Institute for Stuttering and New York City public schools. She has no non-financial disclosures.
Hallie Mintz, M.S., CCC-SLP owns Philly Speech Services and receives an honorarium from Friends as the Social Media Coordinator. She has no non-financial disclosures.
Mark O’Malia, M.S., CCC-SLP is a salaried employee of the American Institute for Stuttering. Non-financial disclosures: board member of Friends: The National Association of Young People Who Stutter.
Naomi Hertsberg Rodgers, Ph.D., CCC-SLP receives a salary from the University of Iowa. She has no non-financial disclosures to report.
Mandy Rodstrom, MA, CCC-SLP has no relevant financial or non-financial disclosures at this time.
Arin Sheeler, M.A., CCC-SLP is a salaried employee of Ohio State University. Non-financial disclosures include: board member of Friends: The National Association of Young People Who Stutter.
Patricia Zebrowski, Ph.D., CCC-SLP, BCS-SCF has no financial disclosures. Non-financial disclosures include: board member of Friends: The National Association of Young People Who Stutter.
CONFERENCE OBJECTIVES for CEUs
At the completion of the conference, participants are able to:
- Explain the relationship between effective intervention, support services, and self-esteem in children and adolescents who stutter;
- Identify social and clinical strategies for supporting children who stutter and their families;
- Apply problem-solving skills to address common treatment obstacles.
Friends Accommodation Statement
Friends is committed to providing accessible programming in accordance with ASHA standards and our values of inclusion and equity. Accommodation requests will be reviewed individually, and we will make every effort to meet those needs based on available resources.
To request accommodations or ask questions, please contact us at friends@friendswhostutter.org at least 5 days in advance.