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Meg

Welcome to the family, I work as the Weekend Manager at a drug and alcohol treatment center of women, and women with children under the age of six. It really wipes me out. If my job was any harder on my body I would have to quit. Most of the time all I have do do is think, listen, talk, and keep what every child that running down the hall from her/his mother form escaping. I get a lot of support from my partner, and the people on this list. Hope you find what I have here.

JoyGet your FREE download of MSN Explorer at http://explorer.msn.com

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  • 4 years later...

Oh sorry , OZ, is just what a lot of people in the US say and I suppose

we use it to identify Australians, just slang.

I live in Queensland, Australia.

Hervey Bay to be precise.

Hugs

Sandy

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Thanks, Barb, Sandy and All --

I did get the directions and video for the flutter valve. (Haven't

had time to watch the video yet, partly because I need my kids to

show me how to play it on the complex hook-up of TV/DVD/VCR/sub-

woofer/who knows what else). I just didn't want to knock myself out

only to find you need a therapist to tell you if you're doing it

right. Also I have no point of comparison yet to tell if I am

coughing up enough to make it worthwhile. It is definitely

inspiring to hear that you've been infection and mucus-free for so

long, Sandy.

More questions: What is a Pari Pep? What is the role of high

protein, calcium and magnesium? Is it possible to do all the

maintenance required AND work full-time AND raise teenagers AND keep

a house going? I can't even handle all of that WITHOUT a serious

chronic disease! I'm getting within reach of retirement -- maybe

I'd better seriously consider it despite the fact that we have two

boys heading to college in the next three years. Yikes!

Thanks to whoever shared the " Anagrams " -- I hadn't seen that one

before. I have a funny one about " useful Latin phrases " if anyone

is interested. Is it better to include something in a message, or

can you send attachments to these posts? (Example: " Catapultam

habeo. Nisi pecuniam omnem mihi dabris, ad caput tuum saxum immane

mittam. " " I have a catapult. Give me all of your money, or I will

fling an enormous rock at your head. " )

Take care,

Vicki

-- In bronchiectasis , " sandy taylor "

<sillysandy82@h...> wrote:

> Vicki and Barb, isn,t it great to be able to swap ideas, and

information, I

> just think so many people miss out on learning so much from each

other. lots

> of good money wasted in some cases.

> We are all on some kind of benefit, ot have our jobs part time

etc,

> sometimes because of our ill health.

> And there are so many products, devises etc, that work and some

that don,t.

> Just as some work okay for some and not for others, the trial and

error with

> devises can be so costly.

> This is a wonderful site to find out more about anything you may

be

> contemplating purchasing, then have the time and the info to weigh

up the

> pros and cons.

> This cannot be done with meds etc, but it often can be a guide,

and

> something to ask your doctors about too.

> What a great arena/ forum for sharing and again caring.

> Love to all

> Sandy from OZ

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Vicki,

The instructions really are easy to

follow. You’ll actually be

able to feel your lungs vibrate if you’re using it correctly. It’s most effective for me when I

have an active infection. It really

helps to get the garbage out. I

haven’t had much luck with it preventing infections though, but we’re

all different. It’s my

opinion that anything you cough out of your lungs is worthwhile, so give it a

good try.

When I was diagnosed nearly eight years

ago, all five of my kids lived at home and I worked (and still do) full-time. We’ll be moving our youngest son

up to college at the end of the week. That means two in college for at least

the next few years, so I can’t even think about a life of leisure. I’ve found that I just can’t

do it all. If the housework doesn’t

get done, then it just doesn’t get done. And if I’m too tired to cook when

I get home, take-out pizza fills everyone up. So, my advice is do what you can but don’t

feel guilty about what you can’t do.

And, save a little energy to enjoy your kids while they’re still

home. If your kids don’t

already do their own laundry, teach them how to work the washer (and pretend

that you don’t notice when they do a load that’s only a shirt and a

pair of socks).

You and your doctor will figure out what

your maintenance routine will be.

Sometimes it take a while to get it all working—and just when you

think that you’ve got it down, it’ll have to be changed for one

reason or another. Don’t get

discouraged when that happens, just go with the flow. The only things that you can count on

with this disease are that you’ll be tired and infections happen.

Re: new

member

Thanks, Barb, Sandy and All --

I did get the directions and video for the flutter

valve. (Haven't

had time to watch the video yet, partly because I

need my kids to

show me how to play it on the complex hook-up of

TV/DVD/VCR/sub-

woofer/who knows what else). I just didn't

want to knock myself out

only to find you need a therapist to tell you if

you're doing it

right. Also I have no point of comparison

yet to tell if I am

coughing up enough to make it worthwhile. It

is definitely

inspiring to hear that you've been infection and

mucus-free for so

long, Sandy.

More questions: What is a Pari Pep?

What is the role of high

protein, calcium and magnesium? Is it

possible to do all the

maintenance required AND work full-time AND raise

teenagers AND keep

a house going? I can't even handle all of

that WITHOUT a serious

chronic disease! I'm getting within reach of

retirement -- maybe

I'd better seriously consider it despite the fact

that we have two

boys heading to college in the next three

years. Yikes!

Thanks to whoever shared the " Anagrams "

-- I hadn't seen that one

before. I have a funny one about

" useful Latin phrases " if anyone

is interested. Is it better to include

something in a message, or

can you send attachments to these posts?

(Example: " Catapultam

habeo. Nisi pecuniam omnem mihi dabris, ad caput

tuum saxum immane

mittam. " " I have a catapult. Give me all

of your money, or I will

fling an enormous rock at your head. " )

Take care,

Vicki

-- In bronchiectasis , " sandy

taylor "

<sillysandy82@h...> wrote:

> Vicki and Barb, isn,t it great to be

able to swap ideas, and

information, I

> just think so many people miss out on

learning so much from each

other. lots

> of good money wasted in some cases.

> We are all on some kind of benefit, ot have

our jobs part time

etc,

> sometimes because of our ill health.

> And there are so many products, devises etc,

that work and some

that don,t.

> Just as some work okay for some and not for

others, the trial and

error with

> devises can be so costly.

> This is a wonderful site to find out more

about anything you may

be

> contemplating purchasing, then have the time

and the info to weigh

up the

> pros and cons.

> This cannot be done with meds etc, but it

often can be a guide,

and

> something to ask your doctors about too.

> What a great arena/ forum for sharing and

again caring.

> Love to all

> Sandy from OZ

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LOL, , well over the rain bow, is cold today where I live, and my group

is expanding.

We are having chicken cor don bleau, with mushroom and broccoli in white

wine sauce, served with pasta, with roasted garlic and bacon .

They are really becoming good cooks and using a variety of foods.

Must go, as I am being picked up soon, and I have the old gent to shower and

give his porridge.

Bye for now, Sandy

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  • 7 months later...
Guest guest

Hi everyone and thanks for letting me join. I was dx Chiari Malformation

in Dec 'o1 and had my decompression, laminectomy,duraplasty and a few

other things done in Dec '02 in Toronto Ontarion. I live in Saskatchewan

Canada.

I have not improved and its been a long three and a half years. I

finally took matters into my own hands and went to The Chiari Institute

in New York last week. Wow ! What a positive experience that was !!

Dr B dx me with tethered cord. I'm new to it so am learning all I can

and welcome comments ok. Are there any Canadians on this site ?

Regardless what Country you live in, I'm interested in hearing from you

and how you've delt with the lower back & leg pain. I'm not handling it

well and am wanting relief - if you have tips, I'm all ears !!

I look forward to hearing from you and hearing your stories. Thanks,

Mojo

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