Guest guest Posted June 15, 2009 Report Share Posted June 15, 2009 Bruce: I would applaud that story, if there was a way to do that online. Good for you! B Barbara McD IPF, Sept 08 Beautiful Western NC Let us not become weary in doing good, for at the proper time we will reap a harvest if we do not give up. Galatians 6:9 To: Breathe-Support Sent: Monday, June 15, 2009 11:29:16 AMSubject: Wonderful Weekend all on Oxygen Just want to share the great weekend I had and remind all too that itwas all on oxygen and as far as I can tell it in no way impacted myenjoyment of the weekend at all. Did use many refills of my Marathonthough.Thursday around noon my friend was due at the DFW airport fromMinneapolis. We hadn't seen each other in 28 years but were inseparablein our much younger days. Well, about the time she was suppose to landas I was waiting at the airport, she texted me from the Tarmac in OkCity. They ran out of gas circling in Dallas due to the weather. At anyrate she arrived around 3 and then I drove her to her hotel to check in.We then went in search of food. The first restaurant we went to waswithout power, so we continued. Ate and talked at Pappas Brothers SteakHouse and then went back to the hotel lounge and talked for hours.Friday I picked her up at 11 and we had seafood at Papadeaux. I alsowent a bit crazy and had the best chocolate cake. Then we headed toFossil Rim, which is a wildlife reserve beyond compare. It was about anhour and 45 minute drive. At Fossil Rim we got a bag of animal food andset out to drive through the reserve. In all we spent about 3 hoursthere and fed all the animals at our car windows with them eating out ofour hands. We fed six varieties of Antelope (didn't see the seventh,Wilderbeast) , Aoudad (Barbary Sheep), four varieties of birds includingEmu and Ostrich, five different varieties of deer, Giraffes, threevarieties of Oryx, Gazelles and three varieties of Zebras. We thenheaded back to town and had dinner at the Cheesecake Factory and thentalked more in the hotel lounge. Of course the entire day was talking.Saturday, I picked her up a bit before 11 and drove her around to showher more the area I live in. Drove by some ranches not far away and outaround South Fork. Then to my home where she met and the three ofus went to Mimi's for lunch. After lunch, she and I headed to the DallasWorld Aquarium and spent a couple of hours there. Then to the hotel formore talking before a light dinner at 's Deli.Yesterday, I met her for breakfast at the hotel and then drove her tothe airport.Things were as if we'd never been apart. The fact I am on oxygen wasirrelevant. So was the fact I have a terminal disease and may not havelong to live. We've been honest and open about that but we have way toomuch to enjoy to dwell on it. Life after diagnosis and with the diseaseand with oxygen can be wonderful. It involves sharing time with thoseyou care most about. It involves living each day to the fullest you can.For those who don't know I have UIP/IPF diagnosed summer of 2007. I'vebeen on oxygen since diagnosis and am on 2 lpm for sleep, 2 lpm sitting(sometimes require none sitting) and 3-5 lpm for activity. I have manyother conditions too including most that are common among the group andsome that aren't. I'm taking several medications but none other thanoxygen for my disease. I was put on oxygen at the time of diagnosis.Now I plan some more one or two day outings with (ex-wife, bestfriend, closest family, housemate) and a couple of lunches and outingswith some board members and some trips for the fall including the one toChattanooga. Even if you can't go there, get together with some othermembers from your area. You'll find it so nice. I've now met a total ofat least 15 members and when you throw in families probably 35-40 peoplefrom the boards. And thats without counting the entire town of Snyder,TX which is apparently all family to Wally.Death happens when life ends, but every moment until then is life to beused and nurtured in the best way possible. I enjoy mine and intend tocontinue to do so even when I reach the end and am sitting at home doinglittle and taking morphine. Now, I will not be responsible for what Imight say or type at that point. But for those new to the disease, Ihaven't had two better years in my life than the last two. Now, today,I'm relaxing and resting. But my mind is at work making future plans.Have a good day all, every day you can. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 15, 2009 Report Share Posted June 15, 2009 What a wonderful weekend you had, Bruce! And, yes you are so right you can't stop living! I emailed a couple of friends in CA and told them of my new car and how I was itching to take a journey and they have encouraged me as soon as I fully recover from the VATs to take my 5 dogs and head out their way and I will do it! My new Honda hybrid has been getting 57 mpg in stop and go traffic! I'm itching to get on the road. I just have to figure out the logistics of getting oxygen. Thanks for the delightful story! I hope you have many, many more weekends and days like that one. Joyce Wonderful Weekend all on Oxygen Just want to share the great weekend I had and remind all too that itwas all on oxygen and as far as I can tell it in no way impacted myenjoyment of the weekend at all. Did use many refills of my Marathonthough.Thursday around noon my friend was due at the DFW airport fromMinneapolis. We hadn't seen each other in 28 years but were inseparablein our much younger days. Well, about the time she was suppose to landas I was waiting at the airport, she texted me from the Tarmac in OkCity. They ran out of gas circling in Dallas due to the weather. At anyrate she arrived around 3 and then I drove her to her hotel to check in.We then went in search of food. The first restaurant we went to waswithout power, so we continued. Ate and talked at Pappas Brothers SteakHouse and then went back to the hotel lounge and talked for hours.Friday I picked her up at 11 and we had seafood at Papadeaux. I alsowent a bit crazy and had the best chocolate cake. Then we headed toFossil Rim, which is a wildlife reserve beyond compare. It was about anhour and 45 minute drive. At Fossil Rim we got a bag of animal food andset out to drive through the reserve. In all we spent about 3 hoursthere and fed all the animals at our car windows with them eating out ofour hands. We fed six varieties of Antelope (didn't see the seventh,Wilderbeast), Aoudad (Barbary Sheep), four varieties of birds includingEmu and Ostrich, five different varieties of deer, Giraffes, threevarieties of Oryx, Gazelles and three varieties of Zebras. We thenheaded back to town and had dinner at the Cheesecake Factory and thentalked more in the hotel lounge. Of course the entire day was talking.Saturday, I picked her up a bit before 11 and drove her around to showher more the area I live in. Drove by some ranches not far away and outaround South Fork. Then to my home where she met and the three ofus went to Mimi's for lunch. After lunch, she and I headed to the DallasWorld Aquarium and spent a couple of hours there. Then to the hotel formore talking before a light dinner at 's Deli.Yesterday, I met her for breakfast at the hotel and then drove her tothe airport.Things were as if we'd never been apart. The fact I am on oxygen wasirrelevant. So was the fact I have a terminal disease and may not havelong to live. We've been honest and open about that but we have way toomuch to enjoy to dwell on it. Life after diagnosis and with the diseaseand with oxygen can be wonderful. It involves sharing time with thoseyou care most about. It involves living each day to the fullest you can.For those who don't know I have UIP/IPF diagnosed summer of 2007. I'vebeen on oxygen since diagnosis and am on 2 lpm for sleep, 2 lpm sitting(sometimes require none sitting) and 3-5 lpm for activity. I have manyother conditions too including most that are common among the group andsome that aren't. I'm taking several medications but none other thanoxygen for my disease. I was put on oxygen at the time of diagnosis.Now I plan some more one or two day outings with (ex-wife, bestfriend, closest family, housemate) and a couple of lunches and outingswith some board members and some trips for the fall including the one toChattanooga. Even if you can't go there, get together with some othermembers from your area. You'll find it so nice. I've now met a total ofat least 15 members and when you throw in families probably 35-40 peoplefrom the boards. And thats without counting the entire town of Snyder,TX which is apparently all family to Wally.Death happens when life ends, but every moment until then is life to beused and nurtured in the best way possible. I enjoy mine and intend tocontinue to do so even when I reach the end and am sitting at home doinglittle and taking morphine. Now, I will not be responsible for what Imight say or type at that point. But for those new to the disease, Ihaven't had two better years in my life than the last two. Now, today,I'm relaxing and resting. But my mind is at work making future plans.Have a good day all, every day you can. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 15, 2009 Report Share Posted June 15, 2009 Bruce....what a terrific weekend to tuck away in your memories! I think it is so special to re-connect with those we love, loved, whatever. .....and a good time was had by both... Thanks for sharing. MamaSher; 70, IPF 3-06, OR. NasturtiumsDon't fret about tomorrow, God is already there! Wonderful Weekend all on Oxygen Just want to share the great weekend I had and remind all too that itwas all on oxygen and as far as I can tell it in no way impacted myenjoyment of the weekend at all. Did use many refills of my Marathonthough.Thursday around noon my friend was due at the DFW airport fromMinneapolis. We hadn't seen each other in 28 years but were inseparablein our much younger days. Well, about the time she was suppose to landas I was waiting at the airport, she texted me from the Tarmac in OkCity. They ran out of gas circling in Dallas due to the weather. At anyrate she arrived around 3 and then I drove her to her hotel to check in.We then went in search of food. The first restaurant we went to waswithout power, so we continued. Ate and talked at Pappas Brothers SteakHouse and then went back to the hotel lounge and talked for hours.Friday I picked her up at 11 and we had seafood at Papadeaux. I alsowent a bit crazy and had the best chocolate cake. Then we headed toFossil Rim, which is a wildlife reserve beyond compare. It was about anhour and 45 minute drive. At Fossil Rim we got a bag of animal food andset out to drive through the reserve. In all we spent about 3 hoursthere and fed all the animals at our car windows with them eating out ofour hands. We fed six varieties of Antelope (didn't see the seventh,Wilderbeast), Aoudad (Barbary Sheep), four varieties of birds includingEmu and Ostrich, five different varieties of deer, Giraffes, threevarieties of Oryx, Gazelles and three varieties of Zebras. We thenheaded back to town and had dinner at the Cheesecake Factory and thentalked more in the hotel lounge. Of course the entire day was talking.Saturday, I picked her up a bit before 11 and drove her around to showher more the area I live in. Drove by some ranches not far away and outaround South Fork. Then to my home where she met and the three ofus went to Mimi's for lunch. After lunch, she and I headed to the DallasWorld Aquarium and spent a couple of hours there. Then to the hotel formore talking before a light dinner at 's Deli.Yesterday, I met her for breakfast at the hotel and then drove her tothe airport.Things were as if we'd never been apart. The fact I am on oxygen wasirrelevant. So was the fact I have a terminal disease and may not havelong to live. We've been honest and open about that but we have way toomuch to enjoy to dwell on it. Life after diagnosis and with the diseaseand with oxygen can be wonderful. It involves sharing time with thoseyou care most about. It involves living each day to the fullest you can.For those who don't know I have UIP/IPF diagnosed summer of 2007. I'vebeen on oxygen since diagnosis and am on 2 lpm for sleep, 2 lpm sitting(sometimes require none sitting) and 3-5 lpm for activity. I have manyother conditions too including most that are common among the group andsome that aren't. I'm taking several medications but none other thanoxygen for my disease. I was put on oxygen at the time of diagnosis.Now I plan some more one or two day outings with (ex-wife, bestfriend, closest family, housemate) and a couple of lunches and outingswith some board members and some trips for the fall including the one toChattanooga. Even if you can't go there, get together with some othermembers from your area. You'll find it so nice. I've now met a total ofat least 15 members and when you throw in families probably 35-40 peoplefrom the boards. And thats without counting the entire town of Snyder,TX which is apparently all family to Wally.Death happens when life ends, but every moment until then is life to beused and nurtured in the best way possible. I enjoy mine and intend tocontinue to do so even when I reach the end and am sitting at home doinglittle and taking morphine. Now, I will not be responsible for what Imight say or type at that point. But for those new to the disease, Ihaven't had two better years in my life than the last two. Now, today,I'm relaxing and resting. But my mind is at work making future plans.Have a good day all, every day you can. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 15, 2009 Report Share Posted June 15, 2009 Bruce, It sounds wonderfully busy and fun! I'm so glad you had this time with your friend and made the most of it. It just sounds like you both had so much fun!! Beth Moderator Fibrotic NSIP 06/06 Dermatomyositis 11/08 To: Breathe-Support Sent: Monday, June 15, 2009 11:29:16 AMSubject: Wonderful Weekend all on Oxygen Just want to share the great weekend I had and remind all too that itwas all on oxygen and as far as I can tell it in no way impacted myenjoyment of the weekend at all. Did use many refills of my Marathonthough.Thursday around noon my friend was due at the DFW airport fromMinneapolis. We hadn't seen each other in 28 years but were inseparablein our much younger days. Well, about the time she was suppose to landas I was waiting at the airport, she texted me from the Tarmac in OkCity. They ran out of gas circling in Dallas due to the weather. At anyrate she arrived around 3 and then I drove her to her hotel to check in.We then went in search of food. The first restaurant we went to waswithout power, so we continued. Ate and talked at Pappas Brothers SteakHouse and then went back to the hotel lounge and talked for hours.Friday I picked her up at 11 and we had seafood at Papadeaux. I alsowent a bit crazy and had the best chocolate cake. Then we headed toFossil Rim, which is a wildlife reserve beyond compare. It was about anhour and 45 minute drive. At Fossil Rim we got a bag of animal food andset out to drive through the reserve. In all we spent about 3 hoursthere and fed all the animals at our car windows with them eating out ofour hands. We fed six varieties of Antelope (didn't see the seventh,Wilderbeast) , Aoudad (Barbary Sheep), four varieties of birds includingEmu and Ostrich, five different varieties of deer, Giraffes, threevarieties of Oryx, Gazelles and three varieties of Zebras. We thenheaded back to town and had dinner at the Cheesecake Factory and thentalked more in the hotel lounge. Of course the entire day was talking.Saturday, I picked her up a bit before 11 and drove her around to showher more the area I live in. Drove by some ranches not far away and outaround South Fork. Then to my home where she met and the three ofus went to Mimi's for lunch. After lunch, she and I headed to the DallasWorld Aquarium and spent a couple of hours there. Then to the hotel formore talking before a light dinner at 's Deli.Yesterday, I met her for breakfast at the hotel and then drove her tothe airport.Things were as if we'd never been apart. The fact I am on oxygen wasirrelevant. So was the fact I have a terminal disease and may not havelong to live. We've been honest and open about that but we have way toomuch to enjoy to dwell on it. Life after diagnosis and with the diseaseand with oxygen can be wonderful. It involves sharing time with thoseyou care most about. It involves living each day to the fullest you can.For those who don't know I have UIP/IPF diagnosed summer of 2007. I'vebeen on oxygen since diagnosis and am on 2 lpm for sleep, 2 lpm sitting(sometimes require none sitting) and 3-5 lpm for activity. I have manyother conditions too including most that are common among the group andsome that aren't. I'm taking several medications but none other thanoxygen for my disease. I was put on oxygen at the time of diagnosis.Now I plan some more one or two day outings with (ex-wife, bestfriend, closest family, housemate) and a couple of lunches and outingswith some board members and some trips for the fall including the one toChattanooga. Even if you can't go there, get together with some othermembers from your area. You'll find it so nice. I've now met a total ofat least 15 members and when you throw in families probably 35-40 peoplefrom the boards. And thats without counting the entire town of Snyder,TX which is apparently all family to Wally.Death happens when life ends, but every moment until then is life to beused and nurtured in the best way possible. I enjoy mine and intend tocontinue to do so even when I reach the end and am sitting at home doinglittle and taking morphine. Now, I will not be responsible for what Imight say or type at that point. But for those new to the disease, Ihaven't had two better years in my life than the last two. Now, today,I'm relaxing and resting. But my mind is at work making future plans.Have a good day all, every day you can. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 15, 2009 Report Share Posted June 15, 2009 Hi Bruce,I loved your post. I have eaten in all those restaurants in Denver - it's almost a crime that so many are chains but it made me feel a part of your post. You seem like my father. He had COPD (smoker for 40 years - 4 packs a day so what did he expect, right) but never let it interfere with him having a fun life. He had to limit his activities and even his talking (that was probably the worst for him) a bit but he continued to make people laugh around him right until he slipped into a coma and died at age 83. I think the hardest thing for me has been the awakening that I probably am not going to be living into my 80's or even 90's as much of my family has. I had always thought that I'd probably be the last one in our family to check out and with this diagnosis I might be the first. On the other hand, maybe hanging out to help them all through it isn't such a great idea anyway! LOLYou are right though - it is important to absolutely enjoy the days as they come. We could get killed tonight by a drunk driver too so living each day as it might be your last is a great way to look at it and live it. Do you suppose they'd accept that if I just quit paying bills? I hate that job!LOL - Peggy E.Subject: Wonderful Weekend all on OxygenTo: Breathe-Support Date: Monday, June 15, 2009, 8:29 AM Just want to share the great weekend I had and remind all too that it was all on oxygen and as far as I can tell it in no way impacted my enjoyment of the weekend at all. Did use many refills of my Marathon though. Thursday around noon my friend was due at the DFW airport from Minneapolis. We hadn't seen each other in 28 years but were inseparable in our much younger days. Well, about the time she was suppose to land as I was waiting at the airport, she texted me from the Tarmac in Ok City. They ran out of gas circling in Dallas due to the weather. At any rate she arrived around 3 and then I drove her to her hotel to check in. We then went in search of food. The first restaurant we went to was without power, so we continued. Ate and talked at Pappas Brothers Steak House and then went back to the hotel lounge and talked for hours. Friday I picked her up at 11 and we had seafood at Papadeaux. I also went a bit crazy and had the best chocolate cake. Then we headed to Fossil Rim, which is a wildlife reserve beyond compare. It was about an hour and 45 minute drive. At Fossil Rim we got a bag of animal food and set out to drive through the reserve. In all we spent about 3 hours there and fed all the animals at our car windows with them eating out of our hands. We fed six varieties of Antelope (didn't see the seventh, Wilderbeast) , Aoudad (Barbary Sheep), four varieties of birds including Emu and Ostrich, five different varieties of deer, Giraffes, three varieties of Oryx, Gazelles and three varieties of Zebras. We then headed back to town and had dinner at the Cheesecake Factory and then talked more in the hotel lounge. Of course the entire day was talking. Saturday, I picked her up a bit before 11 and drove her around to show her more the area I live in. Drove by some ranches not far away and out around South Fork. Then to my home where she met and the three of us went to Mimi's for lunch. After lunch, she and I headed to the Dallas World Aquarium and spent a couple of hours there. Then to the hotel for more talking before a light dinner at 's Deli. Yesterday, I met her for breakfast at the hotel and then drove her to the airport. Things were as if we'd never been apart. The fact I am on oxygen was irrelevant. So was the fact I have a terminal disease and may not have long to live. We've been honest and open about that but we have way too much to enjoy to dwell on it. Life after diagnosis and with the disease and with oxygen can be wonderful. It involves sharing time with those you care most about. It involves living each day to the fullest you can. For those who don't know I have UIP/IPF diagnosed summer of 2007. I've been on oxygen since diagnosis and am on 2 lpm for sleep, 2 lpm sitting (sometimes require none sitting) and 3-5 lpm for activity. I have many other conditions too including most that are common among the group and some that aren't. I'm taking several medications but none other than oxygen for my disease. I was put on oxygen at the time of diagnosis. Now I plan some more one or two day outings with (ex-wife, best friend, closest family, housemate) and a couple of lunches and outings with some board members and some trips for the fall including the one to Chattanooga. Even if you can't go there, get together with some other members from your area. You'll find it so nice. I've now met a total of at least 15 members and when you throw in families probably 35-40 people from the boards. And thats without counting the entire town of Snyder, TX which is apparently all family to Wally. Death happens when life ends, but every moment until then is life to be used and nurtured in the best way possible. I enjoy mine and intend to continue to do so even when I reach the end and am sitting at home doing little and taking morphine. Now, I will not be responsible for what I might say or type at that point. But for those new to the disease, I haven't had two better years in my life than the last two. Now, today, I'm relaxing and resting. But my mind is at work making future plans. Have a good day all, every day you can. Quote Link to comment Share on other sites More sharing options...
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