Re: Re: Chatt and other stuff

[Guest guest]

Dyane, I have probably already ask this but OD rules my life right now.. LOLsend me your Skype name and I'll add you on as soon as I get it. promise. Anyone else that wants to Skype while we'er there just send me your Skype name.. Love & Prayers, Peggy Florida, IPF/UIP 2004"I believe that friends are quiet angels who lift us to our feet, when our wings have trouble remembering how to fly." Peggy,Know that the jazzy will help, when I am moving around and walking I too am on 8 liters and I still drop, but If I can use my chair I can turn the o2 to 3 liters and stay above 90 and feel better. Know that we all love you and are sending waves of love and comfort to you. I hope You make the trip, I would love to have you all skype me too so I can see all your wonderful faces. God bless you.Dyane phoenix ipf 02>> So group here is the thing.. my saturation is dropping with every > movement.. so I am now on 9 to 9 1/2 L to go to the bathroom and it > goes to around 85 -86.. How crazy is that..> has called to get me a jazzy or some other chair thing.. (he > just trusts me WAYYYY to much) I will be glad to be able to move without> needing to sit every ten feet.. this is just such so humbling to be > dependent to this degree. I do thank God I have my wonderful > husband. ( who is fixing me sharp cheese, crackers and an apple > right now)> > After our trip we are going to have the hospice people come talk to > us so we will better understand their process. For the life of me I > don't know why some need morphine. I guess it helps relax your chest > mussels to make breathing easier. Odd I have not ask my Dr. about > that.... I will.> > I think I am just going to keep myself in the electric lounger as > much as I can. should get me ready to go.. I would leave now but we > would be> all alone.. we'll wait 7 more days yeahhhhhhhhhhhhh.> > Please keep us in your prayers. is struggling almost as I am.> > > Love & Prayers, Peggy> Florida, IPF/UIP 2004> > "I believe that friends are quiet angels who lift us to our feet,> when our wings have trouble remembering how to fly."> > > >

[Guest guest]



Peggy...you of course already have mine. You must be offline most of the time. I can't reach you by Skype...

The Chatt trip will be such fun for me too. I can "see" what's going on.

MamaSher; 71, IPF 3-2006, OR.Don't fret about tomorrow, God is already there!

Re: Re: Chatt and other stuff

Dyane, I have probably already ask this but OD rules my life right now.. LOL

send me your Skype name and I'll add you on as soon as I get it. promise.

Anyone else that wants to Skype while we'er there just send me your Skype name..

Love & Prayers, Peggy

Florida, IPF/UIP 2004

"I believe that friends are quiet angels who lift us to our feet,

when our wings have trouble remembering how to fly."

Peggy,Know that the jazzy will help, when I am moving around and walking I too am on 8 liters and I still drop, but If I can use my chair I can turn the o2 to 3 liters and stay above 90 and feel better. Know that we all love you and are sending waves of love and comfort to you. I hope You make the trip, I would love to have you all skype me too so I can see all your wonderful faces. God bless you.Dyane phoenix ipf 02>> So group here is the thing.. my saturation is dropping with every > movement.. so I am now on 9 to 9 1/2 L to go to the bathroom and it > goes to around 85 -86.. How crazy is that..> has called to get me a jazzy or some other chair thing.. (he > just trusts me WAYYYY to much) I will be glad to be able to move without> needing to sit every ten feet.. this is just such so humbling to be > dependent to this degree. I do thank God I have my wonderful > husband. ( who is fixing me sharp cheese, crackers and an apple > right now)> > After our trip we are going to have the hospice people come talk to > us so we will better understand their process. For the life of me I > don't know why some need morphine. I guess it helps relax your chest > mussels to make breathing easier. Odd I have not ask my Dr. about > that.... I will.> > I think I am just going to keep myself in the electric lounger as > much as I can. should get me ready to go.. I would leave now but we > would be> all alone.. we'll wait 7 more days yeahhhhhhhhhhhhh.> > Please keep us in your prayers. is struggling almost as I am.> > > Love & Prayers, Peggy> Florida, IPF/UIP 2004> > "I believe that friends are quiet angels who lift us to our feet,> when our wings have trouble remembering how to fly."> > > >

[Guest guest]

Sher, I have spent the past day or so in bed. When I get up I get myself into a pickle at times. Yes I do have yours and will post from there to let everyone know when we will be skyping.. Gonna be so much fun.. Love & Prayers, Peggy Florida, IPF/UIP 2004"I believe that friends are quiet angels who lift us to our feet, when our wings have trouble remembering how to fly."  Peggy...you of course already have mine. You must be offline most of the time. I can't reach you by Skype... The Chatt trip will be such fun for me too. I can "see" what's going on. MamaSher; 71, IPF 3-2006, OR.Don't fret about tomorrow, God is already there! Re: Re: Chatt and other stuff Dyane, I have probably already ask this but OD rules my life right now.. LOL send me your Skype name and I'll add you on as soon as I get it. promise. Anyone else that wants to Skype while we'er there just send me your Skype name.. Love & Prayers, Peggy Florida, IPF/UIP 2004 "I believe that friends are quiet angels who lift us to our feet, when our wings have trouble remembering how to fly." Peggy,Know that the jazzy will help, when I am moving around and walking I too am on 8 liters and I still drop, but If I can use my chair I can turn the o2 to 3 liters and stay above 90 and feel better. Know that we all love you and are sending waves of love and comfort to you. I hope You make the trip, I would love to have you all skype me too so I can see all your wonderful faces. God bless you.Dyane phoenix ipf 02>> So group here is the thing.. my saturation is dropping with every > movement.. so I am now on 9 to 9 1/2 L to go to the bathroom and it > goes to around 85 -86.. How crazy is that..> has called to get me a jazzy or some other chair thing.. (he > just trusts me WAYYYY to much) I will be glad to be able to move without> needing to sit every ten feet.. this is just such so humbling to be > dependent to this degree. I do thank God I have my wonderful > husband. ( who is fixing me sharp cheese, crackers and an apple > right now)> > After our trip we are going to have the hospice people come talk to > us so we will better understand their process. For the life of me I > don't know why some need morphine. I guess it helps relax your chest > mussels to make breathing easier. Odd I have not ask my Dr. about > that.... I will.> > I think I am just going to keep myself in the electric lounger as > much as I can. should get me ready to go.. I would leave now but we > would be> all alone.. we'll wait 7 more days yeahhhhhhhhhhhhh.> > Please keep us in your prayers. is struggling almost as I am.> > > Love & Prayers, Peggy> Florida, IPF/UIP 2004> > "I believe that friends are quiet angels who lift us to our feet,> when our wings have trouble remembering how to fly."> > > >

[Guest guest]

Ellen...my heart is so sad for what you and Peggy face now. God Bless you both.

Hugs.

MamaSher; 71, IPF 3-2006, OR.Don't fret about tomorrow, God is already there!

Re: Chatt and other stuff

Peggy,Sorry to hear you are struggling so. I am on 10 L and I understand what you mean by being this dependent just to get to the bathroom. my saturation gets down to 70 sometimes and I think, ", this is the big one!!" But I keep on trucking......I have to drag a tank with me (along with my tubing)using both so I can recoup. I did ask my Dr. what to expect from here on out and he answered so elequently. He works with hospice and they sound so wonderful. I am taking chemo so hospice can't get involved until I am finished with that. Please let me know how it goes with your motor chair, we are thinking I need one of those for use in the house. ellen>> So group here is the thing.. my saturation is dropping with every > movement.. so I am now on 9 to 9 1/2 L to go to the bathroom and it > goes to around 85 -86.. How crazy is that..> has called to get me a jazzy or some other chair thing.. (he > just trusts me WAYYYY to much) I will be glad to be able to move without> needing to sit every ten feet.. this is just such so humbling to be > dependent to this degree. I do thank God I have my wonderful > husband. ( who is fixing me sharp cheese, crackers and an apple > right now)> > After our trip we are going to have the hospice people come talk to > us so we will better understand their process. For the life of me I > don't know why some need morphine. I guess it helps relax your chest > mussels to make breathing easier. Odd I have not ask my Dr. about > that.... I will.> > I think I am just going to keep myself in the electric lounger as > much as I can. should get me ready to go.. I would leave now but we > would be> all alone.. we'll wait 7 more days yeahhhhhhhhhhhhh.> > Please keep us in your prayers. is struggling almost as I am.> > > Love & Prayers, Peggy> Florida, IPF/UIP 2004> > "I believe that friends are quiet angels who lift us to our feet,> when our wings have trouble remembering how to fly."> > > >