Guest guest Posted December 15, 2007 Report Share Posted December 15, 2007 Lou, I have even gotten the Helios filled, opened the garage and then drove down my driveway ( it is very steep- 150 ft long) to get the mail!!!! I can walk down...gravity helps.It's the walking back up that is impossible! Z fibriotic NSIP/05 Z fibriotic NSIP/o5/PA And “mild” PH/10/07 and Reynaud’s too!! Potter, reader,carousel lover and MomMom to Darah “I’m gonna be iron like a lion in Zion” Bob Marley Gwynne Keyland wrote: (((((((((((((((((((((( Lou and Sandie))))))))))))))))))))))) Sandie, We have to set boundaries and keep 'em in taking care of ourselves. Don't you feel guilty for one minute. I've been through the ringer when it comes to worrying about a daughter, and at some point you have to "let life happen to them". You've done all you can already. It's time for you to put yourself first now - it's critical to your health and the best example you could set. You are loved. Lou, I can relate to having to drive across the street. ugh. I hate this disease. You've had so many hard things in your life. I'm glad that your meds keep you from puddling up in a corner somewhere. Sometimes that's what we're all inclined to do, even though it's never helpful. You're important to us. Hang in there. Bruce and , I refuse to think cancer. Positive thoughts are drenching you both. Now that I know what ROFLMAO is, PMPLMAO is even funnier! Sadder, truer... but funnier. Very clever, . , I agree that certain situations seem to demand more colorful language, although I try to keep it to a minimum. I think context is important. I have a cousin that curses for attention or shock effect - that's very unappealing. I certainly don't want to have to pay for my indiscretions - egads - although the PFF is a worthy cause. :-) I often get a charge out of the descriptive words you use. I think we're "spout off" friendly here. Joyce, I'll be anxious to hear what you decide about the new med. I hate your decline and hearing that the CellCept is likely not benefitting you. I'm still on it. Is your flow still 8L continuous with exertion (basically, moving)? Beth, I'm glad you'll get to see next week! Bet you'll get plenty of those wonderful hugs that sons give their mamas. I can't wait for mine next week, too. Jane, Please don't ignore yourself or your limitations, no matter what the season or circumstance. You're the only one who can control your reaction to the grumpies around you. I hate to think of the possible health consequences of you pushing too hard or being anxious and angry. I want you to be good to you even when no one else is (easier said than done). God loves you lots, and we do too. Hugs and blessings, Gwynne IPF 7/04 listed for transplant 3/07 Texas No virus found in this incoming message. Checked by AVG Free Edition. Version: 7.5.503 / Virus Database: 269.17.2/1185 - Release Date: 12/15/2007 12:00 PM Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 17, 2007 Report Share Posted December 17, 2007 Hi Gwynne I actually have a poem that Sher gave me it sits on my frigerator its the one " To let Go is to Fear Less and to love more " its a good poem and it is so true! But unfortunately they still dont get it. Its a slow process I suppose. Sandie > > (((((((((((((((((((((( Lou and Sandie))))))))))))))))))))))) > Sandie, > We have to set boundaries and keep 'em in taking care of > ourselves. Don't you feel guilty for one minute. I've been > through the ringer when it comes to worrying about a > daughter, and at some point you have to " let life happen > to them " . You've done all you can already. It's time for > you to put yourself first now - it's critical to your health > and the best example you could set. You are loved. > > Lou, > I can relate to having to drive across the street. ugh. I hate > this disease. You've had so many hard things in your life. > I'm glad that your meds keep you from puddling up in a > corner somewhere. Sometimes that's what we're all > inclined to do, even though it's never helpful. You're > important to us. Hang in there. > > Bruce and , > I refuse to think cancer. Positive thoughts are drenching > you both. > > Now that I know what ROFLMAO is, PMPLMAO is even funnier! > Sadder, truer... but funnier. Very clever, . > > , > I agree that certain situations seem to demand more > colorful language, although I try to keep it to a minimum. > I think context is important. I have a cousin that curses for > attention or shock effect - that's very unappealing. I certainly > don't want to have to pay for my indiscretions - egads - > although the PFF is a worthy cause. :-) I often get a charge out > of the descriptive words you use. I think we're " spout off " > friendly here. > > Joyce, > I'll be anxious to hear what you decide about the new med. > I hate your decline and hearing that the CellCept is likely > not benefitting you. I'm still on it. Is your flow still 8L > continuous with exertion (basically, moving)? > > Beth, > I'm glad you'll get to see next week! Bet you'll get > plenty of those wonderful hugs that sons give their mamas. > I can't wait for mine next week, too. > > Jane, > Please don't ignore yourself or your limitations, no matter > what the season or circumstance. You're the only one who > can control your reaction to the grumpies around you. I > hate to think of the possible health consequences of you > pushing too hard or being anxious and angry. I want you > to be good to you even when no one else is (easier said > than done). God loves you lots, and we do too. > > Hugs and blessings, > Gwynne IPF 7/04 listed for transplant 3/07 Texas > Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.