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breath to blog: one breath at a time

James has cystic fibrosis and is on a quest for a second double-lung transplant following the development of bronchiolitis obliterans.

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breath to blog: one breath at a time | breathtoblog.blogspot.com Reviews
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James has cystic fibrosis and is on a quest for a second double-lung transplant following the development of bronchiolitis obliterans.
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breath to blog: one breath at a time | breathtoblog.blogspot.com Reviews

https://breathtoblog.blogspot.com

James has cystic fibrosis and is on a quest for a second double-lung transplant following the development of bronchiolitis obliterans.

INTERNAL PAGES

breathtoblog.blogspot.com breathtoblog.blogspot.com
1

breath to blog: one breath at a time: Cystic Fibrosis

http://breathtoblog.blogspot.com/p/cystic-fibrosis.html

Breath to blog: one breath at a time. James is the love of my life. He has cystic fibrosis and rapidly declined into active lung failure within days of our wedding. James got his second double lung transplant on May 29, 2013! We are documenting our moments and memories together as we search for hope in the dark and hold each other close for comfort and strength. James' Quest For Lungs. According to Cystic Fibrosis Canada, 1 person dies from CF in Canada every week. Go to Cystic Fibrosis Canada. Organ Don...

2

breath to blog: one breath at a time: April 2015

http://breathtoblog.blogspot.com/2015_04_01_archive.html

Breath to blog: one breath at a time. James is the love of my life. He has cystic fibrosis and rapidly declined into active lung failure within days of our wedding. James got his second double lung transplant on May 29, 2013! We are documenting our moments and memories together as we search for hope in the dark and hold each other close for comfort and strength. James' Quest For Lungs. Friday, April 24, 2015. Great Strides and NOTDAW. Team Awesome it back! We love being healthy enough to give back! James...

3

breath to blog: one breath at a time: photo dump!

http://breathtoblog.blogspot.com/2014/03/photo-dump.html

Breath to blog: one breath at a time. James is the love of my life. He has cystic fibrosis and rapidly declined into active lung failure within days of our wedding. James got his second double lung transplant on May 29, 2013! We are documenting our moments and memories together as we search for hope in the dark and hold each other close for comfort and strength. James' Quest For Lungs. Tuesday, March 18, 2014. A couple of months in a couple of photos (in no particular order):. March 19, 2014 at 11:38 AM.

4

breath to blog: one breath at a time: June 2015

http://breathtoblog.blogspot.com/2015_06_01_archive.html

Breath to blog: one breath at a time. James is the love of my life. He has cystic fibrosis and rapidly declined into active lung failure within days of our wedding. James got his second double lung transplant on May 29, 2013! We are documenting our moments and memories together as we search for hope in the dark and hold each other close for comfort and strength. James' Quest For Lungs. Monday, June 29, 2015. We feel pure and complete joy with each day closer and closer to our daughter's arrival! Subscrib...

5

breath to blog: one breath at a time: October 2014

http://breathtoblog.blogspot.com/2014_10_01_archive.html

Breath to blog: one breath at a time. James is the love of my life. He has cystic fibrosis and rapidly declined into active lung failure within days of our wedding. James got his second double lung transplant on May 29, 2013! We are documenting our moments and memories together as we search for hope in the dark and hold each other close for comfort and strength. James' Quest For Lungs. Thursday, October 30, 2014. My pride for James is endless. (I am less inclined to be in photographs):. We are well. ...

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pj-sharedjourney.blogspot.com pj-sharedjourney.blogspot.com

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.

pj-sharedjourney.blogspot.com pj-sharedjourney.blogspot.com

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...

pj-sharedjourney.blogspot.com pj-sharedjourney.blogspot.com

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).

pj-sharedjourney.blogspot.com pj-sharedjourney.blogspot.com

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...

pj-sharedjourney.blogspot.com pj-sharedjourney.blogspot.com

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...

pj-sharedjourney.blogspot.com pj-sharedjourney.blogspot.com

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...

pj-sharedjourney.blogspot.com pj-sharedjourney.blogspot.com

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 ...

pj-sharedjourney.blogspot.com pj-sharedjourney.blogspot.com

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).

pj-sharedjourney.blogspot.com pj-sharedjourney.blogspot.com

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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Breath to blog: one breath at a time. James is the love of my life. He has cystic fibrosis and rapidly declined into active lung failure within days of our wedding. James got his second double lung transplant on May 29, 2013! We are documenting our moments and memories together as we search for hope in the dark and hold each other close for comfort and strength. James' Quest For Lungs. Monday, June 29, 2015. We feel pure and complete joy with each day closer and closer to our daughter's arrival! Great St...

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