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SN children

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

Riven how are you today

30 replies

2shoes · 02/02/2010 17:32

??

OP posts:
sarah293 · 04/02/2010 16:33

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Phoenix4725 · 04/02/2010 20:11

offers pegs all round

hey im a cheapskate have spent dla on the chocalate.

Can you squeeze up please my arse is on he large size

CardyMow · 04/02/2010 21:58

So's mine atm, after all the chelsea buns...I checked my Body Mass Index earlier...NOT a good move, as it was 19.5 exactly a year ago...and is now 29.8 ...nearly had a blimmin heart attack!!
If only I could find the willpower to diet/only eat one chelsea bun when they come in a 4 pack....

cloelia · 04/02/2010 22:11

Riven this may be an absolutely useless idea but children with CF can use a nebuliser type thing, hand held,battery or mains powered, and drugs can be put in the bowl to breathe in. It is called an E-Flow. You can put saline nebules in it to loosen the mucus, DD uses every three hours to help suction. Would it be any use at all for your dd?

Lauree · 05/02/2010 19:08

sorry, Riven for being insensitive earlier, I think I must've missed something,
really sorry to hear you're having such a tough time... hope the vaporiser helps ... x

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