I’ll preface with the disclosure that I am not someone who stutters but who does have a disability. Normally I’d stay out of these conversations, but I hope it’s okay for me to bring this up… I’m curious seeing all this discourse lately that no one (that I’ve seen anyway) seems to be talking about disability justice and ableism/anti-ableism and the medical vs social models of disability and how this all relates to stuttering. Are these conversations happening in the stuttering community? Is there any involvement with the broader disability community?