Please or to access all these features

SN children

Here are some suggested organisations that offer expert advice on special needs.

Is it normal to be in denial?

10 replies

emkana · 19/09/2006 14:48

I still have moments where I'm thinking "Maybe ds is completely normal after all", when it's clear that that can't be right - his limbs are clearly short, he has ongoing health problems...

is it normal to be like that?

OP posts:
Twiglett · 19/09/2006 15:12

YES

bundle · 19/09/2006 15:13

I have no experience of SN, but I would imagine it is very normal, emkana

Bumblelion · 19/09/2006 15:15

Yes, totally. Even after my DD was diagnosed visually, it still hit me when I got the written confirmation. Now that she has started full time reception in a mainstream school (with a statement) I still think that may be she hasn't got Sotos as some other children that have the same condition don't walk, don't walk, don't socialise. She does all these things. I still sometimes think I am in denial but then on the other hand I totally embrace everything about her and her condition and think "yes, she has got Sotos but, luckily for us all, her included, I do believe quite mildly". Our next genetics appointment will be in January/February next year, just to see how she is getting on.

saggarmakersbottomknocker · 19/09/2006 15:30

Absobloodylutely normal Em.

Especially seen as you have no formal dx yet.

bundle · 19/09/2006 15:40

emkana, I forgot to say, arabica was asking how you were when I saw her on friday..she's not on here much these days, but seemed well and esja is lovely

PeachyClairHasBadHair · 19/09/2006 16:12

Oh gosh yes

I KNOW SD has huge issues on an intellectual level, yet do I completely believe it (as opposed to thinking it's my iamgination / fault / or as the H4ead Teacher syay, due to my non attendance of aprenting class )? Course not. It's an amazing ability of Sn aprents this, the ability to believe and yet NOT believe on two separate levels

Either that or I am barking LOL!

emkana · 19/09/2006 19:43

Thanks for letting me know, bundle

OP posts:
FioFio · 20/09/2006 19:46

This reply has been deleted

Message withdrawn

FioFio · 20/09/2006 19:46

This reply has been deleted

Message withdrawn

Piffle · 20/09/2006 19:58

YES
I can also tell you that for us the firat 3 years were the hardest - coming to terms with it, helping dd with her limitations - moslty physical and then accepting, and just getting on with everything at her pace
Now I get a bit surprised when people mention it, as I do ahve days even weeks where I forget she has Noonan Syndrome at all. She is 4 next month.

New posts on this thread. Refresh page