commentr/StutterOctober 23, 2025

Content

There is a lot of information provided by the US National Stuttering Association, Friends Who Stutter or UK's STAMMA, I'd recommend consulting those resources as they are created by experts for parents of stuttering children. The also provide consultation opportunities, self-help groups, outreach programmes for parents and children :). Similar organizations exist in many countries, see Stamily's list for national associations :). [https://www.stamily.org/links](https://www.stamily.org/links) [https://www.westutter.org/families/parents](https://www.westutter.org/families/parents) [https://friendswhostutter.org/virtual-parent-groups/](https://friendswhostutter.org/virtual-parent-groups/) [https://stamma.org/get-help/parents](https://stamma.org/get-help/parents) You're not alone in this, but I'd be careful of some of the advices given on Reddit, some people have scientifically disproven beliefs or "solutions" to stuttering.

Themes

Community & SupportParent & Caregiver

Subthemes

Research & ResourcesEarly Concern & OnsetTreatment DecisionsSchool/Clinical Advocacy