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Re: Re: [bronchfriends] a treasure

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Hi Lee,

You are truly one of the treasure I’ve met on these groups !!! Yeah, I know the feeling....gawd wot DID I do in ...how many, past lives???!!! It musta been orrrfull!

we’ve been having rambling, rumbling thunderstorms.....seems like they’re miles away then FLASH-CRASH- BANG (doors slamming) !! So I turn the ‘puter off and pull the plug out the wall – better than any surge protector. No, hopefully no infx currently !

A cpap is a mystery to me, so maybe I was talking out of turn – wouldn’t be the first!! - I can’t sleep w/ fans on high, or noisy air-cons, so god knows what something strapped to your face, blowing in it....... !!!!!! I tried the nosivent thing, just hurt way too much, so will manage, at least if do a nasal rinse daily I’m breathing better than most of my life !

But, I’d still say it would be worthwhile to look online about Psa – with bronch we’re vulnerable, but only in hospital environments really. Sounds like health care may be affected by being regional and depend on which state you live in....here is different to living in Bris, same as diff if you lived in Melbourne. Funny, no members in either group from Sydney??? Maybe they get well looked after?

Tis late, so am off to bed

Cheers,

joy

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LOL Hi Joy

I sure have been called many things but never a treasure hee hee thanks for that.

Was wondering if you are on facebook at all?

Any ideas about pain, I have a referral for a bone scan but have to go to Ballarat to get it done so will need to book for after christmas. Something is going on with my body. both arms cant even lift my coffee cup without pain and my back, shoulders eeeek it goes on.

Hope you are feeling heaps better. stay well ok

let me know if you are on facebook

cheers Lee

To: "bronchiectasis " <bronchiectasis >Sent: Thursday, 11 December, 2008 1:50:20 AMSubject: Re: Re: [bronchfriends] a treasure

Hi Lee,You are truly one of the treasure I’ve met on these groups !!! Yeah, I know the feeling....gawd wot DID I do in ...how many, past lives???!!! It musta been orrrfull!we’ve been having rambling, rumbling thunderstorms. ....seems like they’re miles away then FLASH-CRASH- BANG (doors slamming) !! So I turn the ‘puter off and pull the plug out the wall – better than any surge protector. No, hopefully no infx currently !A cpap is a mystery to me, so maybe I was talking out of turn – wouldn’t be the first!! - I can’t sleep w/ fans on high, or noisy air-cons, so god knows what something strapped to your face, blowing in it....... !!!!!! I tried the nosivent thing, just hurt way too much, so will manage, at least if do a nasal rinse daily I’m breathing better than most of my life

!But, I’d still say it would be worthwhile to look online about Psa – with bronch we’re vulnerable, but only in hospital environments really. Sounds like health care may be affected by being regional and depend on which state you live in....here is different to living in Bris, same as diff if you lived in Melbourne. Funny, no members in either group from Sydney??? Maybe they get well looked after? Tis late, so am off to bedCheers,joy

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