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Re: Digest Number 2514

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Hello everyone at CF parents!

Haven't posted for ages, but I've been reading and thinking about everyone.

Hey (and anyone else in this drought stricken land down under) who's

going to the Conference in Melbourne in August? I'm thinking about it, and

if I'll get to meet some of my list friends, that'll probably push me over

to go!

Torsten, that baby girl of yours can't be old enough for school yet, surely!

How's Silke going? And the bump?

As soon as I heard about the tornado, I started worrying about the CF

family. Isn't it strange, how we have all these friends all over the world,

who we wouldn't know about, but for two little genes......

Sian is her usual self ie running amok, probably starting to block up

again...(I mean, it's been over two weeks since she got flushed out, of

course it's starting to build up again. That's why we're in the process of

sorting out a barium enema.) On that note, what do people think. Should I

get the enema done here in Canberra, at the local hospital where there is no

CF gastro. ped. specialist, or should I travel to Sydney for a few days and

have it done at the Children's Hospital with her gastro.ped. in the room?

Much love to all,

-

Mum to Cate 10yrs wocf and Sian 6yrs wcf, asthma, GERD and ADD

Canberra Australia-

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