29th Annual Convention · July 23 – 25, 2026

Embassy Suites by Hilton O'Hare Rosemont · Chicago, IL
Register TodayBook Your Hotel Room

Your Friends Await in Chicago · Registration now open!

Your Friends Await in Chicago

Registration opens February 2026

Spend three unforgettable days with our vibrant, supportive stuttering community

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 »

How to join us & where to stay

Join us as we celebrate 29 years of providing support and community for young people who stutter and their families.

Thursday, July 23th at 1:00 PM to Saturday, July 25th at 11:00 PM

Registration is now open. Join us for all three days (the most popular choice), or pick a single day that works best for you.

Embassy Suites by Hilton
Chicago O’Hare Rosemont

5500 North River Road, Rosemont, IL 60018
Hotel phone number: (847) 678-4000
Click here to view on Google Maps

We encourage you to reserve a room at our convention venue. Staying on-site means deeper connection, more spontaneity, and being fully immersed in everything that makes Friends unforgettable.

If you haven’t already, join our mailing list below to hear the latest updates about the convention, including information about registration, speakers, panels, and a detailed schedule. 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:

  1. Children and teenagers built strong relationships and a sense of community in a safe environment.
  2. Collaborative learning facilitated personal growth.
  3. Communicative and cognitive changes persisted beyond the convention.
  4. Hearing and sharing personal stories increased self-acceptance and acceptance of others.
  5. Living with stuttering can be hard, but the convention helped normalize stuttering.

FOR SPEECH PATHOLOGISTS AND 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.