Good morning,
is anyone able to give any wise advice please?
DD was recently diagnosed with a rare genetic condition that causes global delay and some mobility issues. She is in mainstream nursery and likely to go to mainstream school. She’s due to start school in September 2026.
We have an action for inclusion meeting coming up and I am not sure what to expect/the process. She’s a very sweet girl and has struggled with communication and physical development, she’s almost 4 and learnt to run recently and her communication is coming on a lot but she needs some time to process information. I see people ask her back to back questions which is too much and also speak over her when she doesn’t answer quickly enough. She’s not bothered at this stage but I’m worried it’s going to be a barrier to school education and really want to get this pathway we are on right.
Does anyone have any positive stories of the school transition please? Any advice for the EHCP pathway?