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Re: Lou and K

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Lou and K, I have been on O2 for 3 years and am currently

on 3L sleeping 4 to 5L with activity.

I was diagnosed in June,2004. This hateful disease will be quite for

a while then you realize you need a little

more O2. And the increase in O2 gets you more comfortable. Don't be

afraid of it. Your body needs it.

Please don't let this disease scare you out of living. We gotta do

what we gotta do. I was on prednisone for

almost a year gained an huge amount of weight. 70 lbs in 8 weeks. I

lost about 40 pounds of it and all of a sudden

I needed to make a transplant decision and just can't do it so I have

just baked and cooked and gone sweet

crazy.. I am trying to quit. Lordy it is hard not to go in there and

bake a pie...NO NO NO I'm gonna behave myself.

LOL

Joyce D has been fighting this monster for 10 years. She is THE TROOPER.

ANY questions you have ASK. We have been just where you are and

nothing is a

crazy question..or off limits.

Just remember You are a child of the King and He will give you

strength to endure.

Take Care of You.

Love and Prayers, Peggy

ipf 6/04 Florida

" Worry looks around,

Sorry looks back,

Faith looks up. "

Hi Lou,

I am like you. I want to know what to expect. I was diagnosed just five

weeks ago and I'm not on oxygen yet. There are a lot of members on here

but we only hear from a dozen or so. I want to know who's been dealing

with this for eight or ten years? How many years have some been on

oxygen?

Kay

> I do have one BIG question. If I am on oxygen (level 2) 24/7

> forever, does that mean I am in the end stage??????? truth now,

> guys!!! I have had PF for 5 years, non-progressive up until this

> past Feb. now it is moving. Love, Lou

>

>

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