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Charlotte Wyatt - looks like the end may be in sight

34 replies

wannaBe1974 · 24/02/2006 18:01

very sad

OP posts:
Kelly1978 · 24/02/2006 19:57

I really sympathise with her parents. I'd like to say that I would have let her go, but I don't think I would. Part of me thinks that action should have been taken sooner to allow her to die, but then you look at the small improvements that Charlotte did make, which must have been amazing to her parents and you can't blame them for fighting. When you have a child with special needs the smallest thing can mean so much. Charlotte has pulled through it all before and I personally won't be surprised if she does again although I'm not sure if that will be a good thing or not.

Milge · 24/02/2006 20:17

Whilst biglips' description of Charlotte was vivid, blunt and emotive, it gets across the level of mental impairment the poor girl has. the latest news report I heard said that although her body has developed, her mind is still at the 3 month development stage.

chonky · 24/02/2006 20:38

Why not just say she has the cognitive ability of a 3 month old then? Far more appropriate.

crazydazy · 24/02/2006 20:56

Some people just don't know how to say things correctly, I don't think biglips meant it to sound offensive.

Kelly1978 · 24/02/2006 21:06

Cabbage may be rather distasteful and cruel but I suppose it isn't that insulting really. I wouldn't be that quick to judge. My ds has SN and I call him a lemon on occasion. He thinks it is funny and has used it himself!

WestCountryLass · 24/02/2006 22:19

I am not sure Charlottes parents expected her to recover or improve but that she had a right to live.

I jsut hope that Charlotte does not suffer, whether she lives or dies.

biglips · 25/02/2006 09:19

i didnt mean it in a insulting way by using that word - SORRY everyone!

giddy1 · 25/02/2006 10:04

Message deleted

stephanie21 · 25/02/2006 10:59

my dd has cf,and although you wouldnt think to look at her,she has a serious illness that will shorten her life.when we got told she was only 6 weeks old.i remember thinking 'why us?' and when the doctors explained it all to us,they said that some children are really poorly with it and die very young,others lives to be around 30.knowing that my dd will die young has been something very hard to come to terms with.and if i could take it away fom her i obviously would.but i think these things are sent to test us and make us stronger.im not a religious person,and often think that if there was a god he wouldnt let children get ill and die.but i do think that having a child with a serious illness has made me a stronger person,and i would never wish that i hadnt had her.im sure many parents with poorly children think 'i wish they didnt have that' but not many would wish they hadnt had them.im extremely grateful that ive got my dd,and no matter how long she is with us for,i cherish every moment with her.she is my little angel!

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