r/Apraxia

▲ 2 r/Apraxia+1 crossposts

Non verbal 2yr4m old?!

My son is 2y4m and has essentially no spoken words. He seems to understand around 90% of what we say and communicates really well through pointing, eye contact, gestures, signs and noises. He has good joint attention, affection, pretend play and social interaction, but has always babbled very little and rarely attempts to copy speech sounds.

He also seems to get overstimulated quite easily. When excited/overwhelmed he can run around a lot, and he can have meltdowns or “shutdowns” where he cries, goes floppy and doesn’t want interaction. He has some strong interests/preferences (hats, particular TV programmes) but isn’t particularly rigid about routines or change, doesn’t have much repetitive play and generally copes well with noises/textures.

His fine motor/problem-solving skills seem good, although his gross motor development has been slightly slower (walked at 18 months and isn’t quite properly running/jumping yet).

Has anyone had a child with a really similar overall profile? Did it eventually turn out to be a speech/motor-speech issue, autism, sensory/regulation differences, general developmental delay or something else? And how are they doing now?
oh and yes he had had hearing checked and is in regular speech therapy

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u/Designer-Wheel9317 — 10 days ago
▲ 12 r/Apraxia

24M med student in Philly with CAS, looking to connect with others who grew up with it

Hi all,

I'm a 24-year-old med student in the Philadelphia area, and I grew up with childhood apraxia of speech (CAS). I've come a long way with it, but I never really had anyone to talk to who'd been through the same thing. Growing up, it was mostly speech therapists, teachers, and family who were supportive but didn't really get it.

Now that I'm in a new city and starting a new chapter, I'd love to meet others with CAS, whether you're still working through it or it's mostly in the past. I'm hoping to swap experiences: what it was like growing up, how it shows up now (or doesn't), dealing with school and work, that kind of thing.

I'm open to grabbing coffee, a casual meetup, or just messaging if that's more comfortable. Parents of kids with CAS are welcome to reach out too, but I'm mainly hoping to find other adults who've lived it.

Feel free to comment or DM me. Thanks for reading!

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u/Tricky_Cover_5408 — 11 days ago