Honestly, the EHCP process can make you feel like you need a law degree just to advocate for your child.
I've spent so much time confused, why does the plan feel unclear? Why is something as simple as "speech therapy" so open to interpretation?
My DS's EHCP says "regular access to speech and language therapy" and "support as needed" but when I ask the school what that actually means in practice, I get different answers depending on who I speak to.
Does anyone else feel like their child's plan is full of vague phrases that could mean anything? How do you pin down what support your DC is actually entitled to?
I'm not trying to be difficult, I just want to know what my child should be getting!