Wednesday, 3 June 2015

Left hand/Right hand confusion part 2

So following a productive meet up between the SENCO plus myself and M on Monday, a few plans were made.

The SENCO agreed that J should not be writing down his homework and said she would email all teachers to remind then of this.

Today....J has come out of school telling me he has a lunchtime detention tomorrow for not doing his IT homework. Oh really, what IT homework would that be then? Something they evidently have not written down.

Secondly on checking J's homework book I found he had yet again been left to write in his French homework.  I have now asked three times for an adult to record the homework
 J has hypermobility in his joints, this means that writing is difficult for him. Asking him to write down homework in the rush that is the end of each lesson means barely legible scrawl.  Add to this his
impaired executive function issues and you have a problem. Not only can I not read J's writing. ..nor can J!

Got home, phoned the school and left a terse message for the SENCO and the IT teacher pointing out that J's Statement was not bring adhered to and that I wanted a call back from ons or both of them before midday tomorrow . In fact scratch that as tomorrow morning I am going in there. ....again.

Monday, 1 June 2015

Oh dear, the left hand and the right hand are not talking!

Today I went into J's school to discuss the letter I recieved at the beginning of half term.

I spoke with the SENCO, the conversation regarding the letter went like this.....

Me: "Were you aware this letter was being sent out"?

SENCO: "No I wasn't".


So the school has my child with a Statement of SEN, the teachers are experiencing problems with J and are expressing concern about effort and level of progress.  Wouldn't you think the obvious thing to do would be to the SENCO about the concerns?

Instead they sent out a blanket letter with no real plan beyond signing a report card each day which reports on how he has been in class with regards to his work. I have no issue with this per se as J has just had an increase in medication. Monitoring how he is responding is a good thing and will allow me to see how effective the increased dose is.  I am not happy for it to be used as a punitive sanction though, especially when there has been no discussion with the SEN department.

I then had the joy of a discussion with J's caseworker at the LEA, I wanted to know if his case had been to Panel yet for possibke admission to a local special school which offers a mainstream curriculum.  The caseworker's response was "actually no. I didn't think we were going ahead with that'."
"Ummm.....yes we are, in fact J's Dad is especially keen for this to be looked I explained to you at the Annual Review."

I despair, I really do.