Friendship & Support for Kids Who Stutter
Our virtual kids’ group is a welcoming space where children who stutter can feel safe and supported, have fun, build confidence, and make friends who share their experiences. Each session is led by a caring adult facilitator, often someone who also stutters, and it’s completely free to attend. We meet every month, giving kids a regular opportunity for friendship and fun.
Who it's for
Kids ages 6–11 who stutter. If your child is 12 or older, check out our Virtual Teen Group
When we meet
Every second Saturday of the month at 11:00 AM Eastern
Next sessions: February 14, 2026 and March 14, 2026
If you have any questions
Please don’t hesitate to reach out to us at friends@friendswhostutter.org
Free, fun, and every month
Join us on one of these upcoming dates! First-timers and returning Friends are all welcome.
SAT
14
FEB
SAT
14
MAR
Follow the button below for our quick sign-up form. You will receive a Zoom link in your confirmation email.
To SLPs and Graduate Students: A Quick Note!
Thanks for taking an interest in stuttering support groups. Groups play an important role in normalizing stuttering and fostering acceptance, growth, and resilience. We are grateful to so many therapists for spreading the word about our no-cost virtual groups.
If you are looking to attend a group, please note that we do not offer opportunities to observe or participate in these peer support groups.
For SLP educational and training opportunities, please see our one-day events and annual convention. We also recommend visiting our YouTube channel to watch panels of young people who stutter, parents, adults who stutter, and presentations by fellow SLPs.
Join our mailing list below to get the latest updates about upcoming CEU and training opportunities.
Here’s what the group talked about recently:
We started with optional intros, reducing threat by having names on our “boxes.” Friends could share where they are from and something cool they got during the recent holiday season, something they are having a hard time with about transitioning back to school after winter break, or something they like about being back in school. Some exciting geographic connections were made (two kids from Columbus, OH who didn’t know one another), and also shared hobbies were discovered.
Video games, legos, and Pokemon cards became big topics of shared interest. About 20 minutes in, I introduced the idea that I would step back from the role of “teacher,” since I had been calling on kids as they raised their hands and it felt (to me) very school-like and prohibited free flowing conversation. Since “jumping into” conversations is often a skill that many of us PWS don’t give ourselves a lot of practice doing, I thought this was a good chance to practice that skill. So I tossed it to the kids and said just try jumping in and sharing rather than waiting for me to call on you. A kid named Will piped in, very insightfully, “that’s like building with legos or in Minecraft, building conversation step by step, and like it builds on itself.” Ok king…
That mostly worked really well actually, and they continued to talk about shared interests, ie Roblox and Minecraft. I would pipe in occasionally to help clear the floor for quieter ones in the group, and gently cut off some of our more loquacious friends. A couple of friends shared successes in giving presentations about stuttering to their classmates. As the discussion continually reverted to gaming, I threw out an observation that going through life, especially with a stutter, can be like gaming. It’s challenging, and there can be real setbacks, but rewarding to grow in confidence and get to the next level. I think my king Will was the only one who vibed with my analogy :-))))
The chat was active too–although it never overshadowed actual talking, which was voluminous. In the chat at one point someone posed the question: “McDonalds or Del Taco?” This was toward the end, so I piped in and asked if any of them ever ordered for themselves at drive through windows or even at the counter at restaurants. One or two said yes sometimes. I shared that as an AWS, I have found that choosing to stutter can be really helpful, rather than the default way of going around the world where I used to brace myself and try to avoid. I tossed it out there that it could be a really useful experiment for anyone who wanted to actually volunteer to order for their family sometime. By choosing to talk and stutter it can feel really different than being forced into it.
— Jenny McGuire on facilitating the Friends Kids Group in January
Meet the facilitation team
Arin Sheeler I am the proud parent of a young boy who stutters. Our family found Friends through The Ohio State University One-Day Event in 2018, and we attended our first annual convention in Chicago in 2019. My husband and 3 children and I live in Columbus, Ohio, and both my husband and I work for The Ohio State University. I am a speech language pathologist specializing in adults with acquired neurogenic communication disorders. I work part time as a Clinical Supervisor in the Department of Speech and Hearing Sciences and at The Ohio State University Wexner Medical Center in the Rehabilitation Hospital. We fell in love with Friends because of the fantastic people that we have met and the welcoming community. Our son especially has felt a real sense of belonging in the Friends family, and I am excited to be a part of helping Friends continue to flourish! Email Arin
Kristel Kubart, M.S., CCC-SLP, is a speech-language pathologist and a passionate person who stutters. She has been volunteering with Friends for 14 years. She believes that it is important to ‘show up’ for members of the stuttering community and to live the message that, “It’s ok to stutter.” She works as a speech therapist at an elementary school in Brooklyn, NY where she also supervises NYU graduate students. Additionally, she is a speech therapist at the American Institute for Stuttering, where she works exclusively with children, teens, and adults who stutter, both in-person and virtually. She received her B.A. in Psychology from the College of the Holy Cross and her M.S. in Speech and Language Pathology from Purdue University. At Purdue she worked as part of a team of researchers to help understand how stuttering develops in young children. She is happily married and lives with her husband Jason and their cat Winnie in Brooklyn, NY. Email Kristel
Sophie Tabrizi is a person who stutters and has been a part of the Friends community for 13 years. She is currently in graduate school at the University of Colorado, Boulder studying Speech-Language Pathology. Sophie will be graduating next summer and hopes to specialize in fluency disorders down the line. Friends gave Sophie a lifelong community at the age of 10. She looks forward to meeting others who stutter through the Friends virtual groups! Email Sophie

