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Every Breath I TakeMy Battle With Idiopathic Pulmonary Fibrosis And My Subsequent Journey To Receiving And Living With My New Lungs
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My Battle With Idiopathic Pulmonary Fibrosis And My Subsequent Journey To Receiving And Living With My New Lungs
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My Battle With Idiopathic Pulmonary Fibrosis And My Subsequent Journey To Receiving And Living With My New Lungs
Every Breath I Take
http://breathitake.blogspot.com/2014/02/where-oh-where-did-my-energy-go-ok-so.html
Every Breath I Take. My Battle With Idiopathic Pulmonary Fibrosis And My Subsequent Journey To Receiving And Living With My New Lungs. Wednesday, 5 February 2014. Where Oh Where Did My Energy Go? Ok, so another quick update. I’m not used to having to test my blood sugars so often since I am not normally diabetic and I don’t mind saying it’s a pain in the arse. Just a tad grumpy tonight I guess. Also I started on Prograf, my new anti-rejection med today, which may also be contributing to my irritability.
Every Breath I Take: 2014-02-02
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Every Breath I Take. My Battle With Idiopathic Pulmonary Fibrosis And My Subsequent Journey To Receiving And Living With My New Lungs. Wednesday, 5 February 2014. Where Oh Where Did My Energy Go? Ok, so another quick update. I’m not used to having to test my blood sugars so often since I am not normally diabetic and I don’t mind saying it’s a pain in the arse. Just a tad grumpy tonight I guess. Also I started on Prograf, my new anti-rejection med today, which may also be contributing to my irritability.
Every Breath I Take: 2014-01-19
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Every Breath I Take. My Battle With Idiopathic Pulmonary Fibrosis And My Subsequent Journey To Receiving And Living With My New Lungs. Thursday, 23 January 2014. Time flies and it’s been a long time since I’ve updated my blog. I decided the service I used before was just too much money so I decided to change blogger providers (hmm … is that even an actual term? It took me a long time to decide on one and then copy everything from the previous blog site to this one. A lot has happened since I last wrote.
Every Breath I Take: 2014-01-26
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Every Breath I Take. My Battle With Idiopathic Pulmonary Fibrosis And My Subsequent Journey To Receiving And Living With My New Lungs. Saturday, 1 February 2014. NINE MONTH CHECKUP COMPLETED. I finished my nine month checkup this past week. I would like to say all is well but unfortunately there was a complication. I heard the one word no transplant recipient ever likes to hear. It’s a scary word with lots of negative implications,. But still, not something to panic over. I take comfort in the knowledge.
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Our Post-transplant Journey: First Week Home - Part 2
http://pj-sharedjourney.blogspot.com/2013/04/first-week-home-part-2.html
Friday, 5 April 2013. First Week Home - Part 2. Thurs - Physio Finale for Jess. Left - Dad, me, Paula and Carman and Mom on the right. Today is a bittersweet day in The Treadmill Room - the last physio session in which the Squat Squad will be together. Yes, Jessica is in the preparatory stages of heading home to Nova Scotia and today marks her last day to work out with the Squad and Carman’s third day of being a Green Card holder! Jessica, Mark and Carman - peddling so fast -. Fri - Muscle Study Follow-up.
Our Post-transplant Journey: August 2012
http://pj-sharedjourney.blogspot.com/2012_08_01_archive.html
Tuesday, 28 August 2012. A Visit, A Victory and A Video. Carman, Arlene, Madi. Monday - Madi and Arlene came for a visit today. They were in town from London, visiting family and were able to squeeze in a quick lunch with us before we headed to the Treadmill Room. Service and food at The Blake was great as usual and we were left to concentrate on our visit. Thanks for treating us to lunch and for taking time to visit with us Madi and Arlene! Big hugs to Bealal and Ahmed! Big fist Pumps all around! The sh...
Our Post-transplant Journey: The Test Leave
http://pj-sharedjourney.blogspot.com/2013/06/the-test-leave.html
Friday, 28 June 2013. I have spent the past week packing, purging, wiping and vacuuming (the carpet and the storage bags - they're like Spanx for your bedding, clothes and towels - squishing huge piles into skinny packages for loading in the car). Today we are leaving our condo - the place we have called home for the past 390 days. A place of. Temporary residence, but home nonetheless. Meeting new neighbours (thanks for everything Karin, Gord and George). Meeting new friends (thank you Treadmill Room).
Our Post-transplant Journey: Recalling July & August
http://pj-sharedjourney.blogspot.com/2013/11/recalling-july-august.html
Tuesday, 5 November 2013. Recalling July and August. Adam, Shilpa, Hélène,. Hi - it's been awhile! These people know how to do the town in style! Canada Day itself, brought us a Potluck BBQ on the deck with many Capital friends. Carman and "all the girls. We both got in a couple of rounds of golf, and the ladies I played with at Greenhills organized a potluck evening (thanks for hosting Peggy! Our days were filled with coffee date, lunches and dinners with family and friends - memories to treasure! Carma...
Our Post-transplant Journey: March 2013
http://pj-sharedjourney.blogspot.com/2013_03_01_archive.html
Saturday, 16 March 2013. Today is a clinic day. What that means is that we leave home by 7:30am to arrive at the hospital before 8am and get a jump on the queue at the Blood Clinic. When we arrive, Carman is given number 98 and they are serving number 93. Not bad! This is the transplant community - two out of three get out their meds, so the obvious question to the third person is “hey, what about you! 8221; Don assures us that he has taken his already, but thanks everyone for their concern. Forced vital...
Our Post-transplant Journey: Clinic Day
http://pj-sharedjourney.blogspot.com/2013/03/clinic-day.html
Saturday, 16 March 2013. Today is a clinic day. What that means is that we leave home by 7:30am to arrive at the hospital before 8am and get a jump on the queue at the Blood Clinic. When we arrive, Carman is given number 98 and they are serving number 93. Not bad! This is the transplant community - two out of three get out their meds, so the obvious question to the third person is “hey, what about you! 8221; Don assures us that he has taken his already, but thanks everyone for their concern. Forced vital...
Our Post-transplant Journey: The Official Boot!
http://pj-sharedjourney.blogspot.com/2013/06/the-official-boot.html
Friday, 14 June 2013. Carman had his follow-up. Clinic and battery of tests on Wednesday this week - he flew solo for this and all is good. At the end of a very long day - 7:30 blood work, followed by Xray, PFTs, Support Group meeting, Dr. appt and clinic (2-5pm) he was officially bid a fond farewell along with a “and don’t come back till we call you for your 6 month assessment! Between the 6 and 9 month mark, they experienced a noticeable improvement over that feeling by the end of the first year after ...
Our Post-transplant Journey: June 2013
http://pj-sharedjourney.blogspot.com/2013_06_01_archive.html
Friday, 28 June 2013. I have spent the past week packing, purging, wiping and vacuuming (the carpet and the storage bags - they're like Spanx for your bedding, clothes and towels - squishing huge piles into skinny packages for loading in the car). Today we are leaving our condo - the place we have called home for the past 390 days. A place of. Temporary residence, but home nonetheless. Meeting new neighbours (thanks for everything Karin, Gord and George). Meeting new friends (thank you Treadmill Room).
Our Post-transplant Journey: October 2012
http://pj-sharedjourney.blogspot.com/2012_10_01_archive.html
Tuesday, 30 October 2012. Treadmill Training for Joyce. Wednesday - Carman’s sister, Joyce, came to visit today. She has suggested that she’d like to help out with Physio so has come today to be trained in what needs to be done to keep Carman on track. Phyllis was after Carman to do her stairs for her and at one point asked him to “Toss me that 10 lb weight when you’re done with it will you.” Oh Phyllis - living on the edge Girl! He really would likely toss it to you without too much encouragement! As I ...
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Mark J. Lindquist. Mark J. Lindquist in Concert - Saturday, November 21st , 2015 Fargo Theatre! Click to purchase tickets! Mark has worked with some amazing organizations - He would love to work with yours! LOST - Hawaii Five O - Universal Studios - CNN.com - The Washington Post - NATO - The White House - C-Span. The Minnesota Vikings - Minnesota Twins. Los Angeles Dodgers - New York Giants - Washington Redskins. The Home Depot - Department of Homeland Security - Brooks and Dunn - WE Fest -. Mark speaks ...
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Every Breath I Take
Every Breath I Take. My Battle With Idiopathic Pulmonary Fibrosis And My Subsequent Journey To Receiving And Living With My New Lungs. Wednesday, 5 February 2014. Where Oh Where Did My Energy Go? Ok, so another quick update. I’m not used to having to test my blood sugars so often since I am not normally diabetic and I don’t mind saying it’s a pain in the arse. Just a tad grumpy tonight I guess. Also I started on Prograf, my new anti-rejection med today, which may also be contributing to my irritability.
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