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Hi everyone, I joined the group awhile ago.

Just been reading and not shearing much.

I am almost 71, married and we are both on oxygen.

Hubby has COPD.He had a lung collapse in 1991.

He has been almost completely disable sense.

I try to take care of the both of us.

I was diagnosed with IPF. in 1992

caused from work related chemicals,from old history.

I did public work until about 5 years ago.

I started using my oxygen to sleep with after a sleep study was done

in 2006.During the study my oxygen went down so low they woke me up

to see if I was breathing.Said I could have a heart attack from it

being so low.

My breathing just got real bad the end of 2007 now I am on it all the

time set on 3. I started using the liquid the first of this year.

Always complaining it does not work right.

It only comes out on one side of the nose tube.They tell me this is

right.

Question is who is right? They are coming out again tomorrow and I

hope get it right.When I do go out I feel like I can't hardly breath

at all. I stay home now seldom get out. just don't have the energy to

do much any more. I also have a lot of other health problems.

I would appreciate any advise on the Helios Plus.

thanks for taking the time to read this .

Ruth

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