Down and worried ...

[MABS]

Just really need to moan to you all - sorry. My 21 month ds has to go for lung function tests, blood tests to check immunity , chest xray and ,possibly - get this - a test for cystic fibrosis, all tomorrow morning. I've known about it for a few weeks but have managed to put it to the back of my mind. Now, sitting here by myself (dh at work tonight) its finally hit me that its 9.20 tomorrow morning.

It's really not fair - he's already got mild cerebral palsy - he doesn't need all this.

Bye for now (sorry for herself) MABS

mabs, have a good evening out. Hope your ds has a good long sleep tonight and all his other test results come back fine.

Best wishes, MABS x.

Glad it wasn't so bad after all. Hope you get the results you want with the tests. P.S. Wouldv'e posted before but been away for w/e.

so glad it wasn't Cf Mabs. Hopefully the bloods will show up something simple and easy to treat. Waiting is hard but hopefully you'll get positive news soon. For what its worth one of my ds has numerous unrelated medical conditions and has been through hell but at the moment he's really well (sunshine helps) and has dropped from 14 medicines 5 times a day to a mere 1 at night!!! took time and traumas but every year he's got stronger. Oh and if it helps I have an aunt and a bil with CP... the latter is a v successful architect,would you believe...
good luck to you, I've been thinking of you lots..

MABS, just caught up with this thread, glad it's not cf, and I really hope the other tests come back OK. Thinking of you.

Just wanted to add my best wishes to you too

hows it going Mabs? thinking of you