The sunglasses are going on…

By | July 16, 2012

D got diagnosed 3.5 years ago – its been a very long 3.5 years but a productive time.

She’s been statemented, been in her SN school for just over 2 years, learn to read (albeit by memory as opposed to phonics) and learnt to write her name *proud grin*

She’s able to walk to the school hall in her SN school and sit there (sometimes unwillingly) for assemblies and generally “move about school” – in mainstream she was often too anxious to enter the classroom, way too much noise & sensory overload.

We are due to go to CAMHS in the summer holidays for the first time, as meltdowns and anxieties for D have increased since Christmas. I was sent questionnaires that both ourselves (as parents) and school had to fill in.

I received school’s completed questionnaire today. It’s very hard reading that “certainly true” is ticked for:
Often unhappy, downhearted or tearful
Picked on or bullied by other children
Gets on better with adults
Many fears, easily scared
And overall “severe difficulties”.

I knew all this from previous knowledge, intuition and little things that D is able to tell me, so why has it hit me so hard seeing it written down?

Putting a positive spin on it, the fact that school have been so honest will hopefully mean that the meeting will enable D to receive the help (and us the guidance) that she needs.

Until then and certainly for the majority of today, the sunglasses are on irrespective of whether the rain stops or not.

20120716-102023.jpg

Thanks for reading Jx 😘

Facebook Comments

2 Comments

Deb on 16th July 2012 at 4:12 pm.

Oh Jeanette, I understand how you’re feeling. As you know, reading my daughter’s recent educational psych assessment has saddened both me and my husband. Its reading it in black and white that hurts. We know how wonderful our children are and we adjust to their difficulties and love them for who they are but sometimes a report can be a shock as we are reminded of their difficulties. As hard as it is to read these reports, I tell myself that they are there to help us and hopefully CAMHS will be able to help your daughter soon.

Hope you soon feel a bit better.

Deb xx

PS your daughter is beautiful; love her smile.

Reply

AutismMumma on 16th July 2012 at 7:46 pm.

Thanks Deb, she is a little bundle of fun at times! Like you say, it’s seeing it written down in black and white. I hope CAMHS can offer advice etc x

Reply

Leave Your Comment

Your email will not be published or shared. Required fields are marked *

You may use these HTML tags and attributes: <a href="" title=""> <abbr title=""> <acronym title=""> <b> <blockquote cite=""> <cite> <code> <del datetime=""> <em> <i> <q cite=""> <s> <strike> <strong>

CommentLuv badge