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amatteroflifeandbreath.blogspot.com
A Matter of Life and Breath: May 2012
http://amatteroflifeandbreath.blogspot.com/2012_05_01_archive.html
A Matter of Life and Breath. Life, Lung transplant, and Cystic Fibrosis. And Everything In Between. I am a 33-year-old wife, sister, daughter, friend, law school graduate, CFer, lifelong student of public service, blog writer, patient, Sagittarius, reader, Top chef fan, double-lung transplant recipient (twice! View my complete profile. Want to Contact Me? Please email me suggestions, thoughts, comments, or criticism. Seriously, I love hearing from you guys! Send all emails to:. A Breath of Fresh Air.
amatteroflifeandbreath.blogspot.com
A Matter of Life and Breath: February 2013
http://amatteroflifeandbreath.blogspot.com/2013_02_01_archive.html
A Matter of Life and Breath. Life, Lung transplant, and Cystic Fibrosis. And Everything In Between. I am a 33-year-old wife, sister, daughter, friend, law school graduate, CFer, lifelong student of public service, blog writer, patient, Sagittarius, reader, Top chef fan, double-lung transplant recipient (twice! View my complete profile. Want to Contact Me? Please email me suggestions, thoughts, comments, or criticism. Seriously, I love hearing from you guys! Send all emails to:. Transplant: The Fairy Tale.
amatteroflifeandbreath.blogspot.com
A Matter of Life and Breath: January 2014
http://amatteroflifeandbreath.blogspot.com/2014_01_01_archive.html
A Matter of Life and Breath. Life, Lung transplant, and Cystic Fibrosis. And Everything In Between. I am a 33-year-old wife, sister, daughter, friend, law school graduate, CFer, lifelong student of public service, blog writer, patient, Sagittarius, reader, Top chef fan, double-lung transplant recipient (twice! View my complete profile. Want to Contact Me? Please email me suggestions, thoughts, comments, or criticism. Seriously, I love hearing from you guys! Send all emails to:. A Breath of Fresh Air.
mycfjourney.blogspot.com
Mastering the Art of Breathing, One Stitch at a Time: Surgery is a MUST
http://mycfjourney.blogspot.com/2014/03/surgery-is-must.html
Mastering the Art of Breathing, One Stitch at a Time. This 30-something's journey with Cystic Fibrosis, Lynch Syndrome, CFRD and the Lung Transplant process. Thursday, March 13, 2014. Surgery is a MUST. I was told I HAVE to have the cyst removed. No but's about it. So I see the surgeon in May and we will decide on a date then. Subscribe to: Post Comments (Atom). My Blog List / Friends. To love and be loved. It's All Good In Joshland. Terrible Twos All Over Again. Less than 24 hours. Where has time gone?
mycfjourney.blogspot.com
Mastering the Art of Breathing, One Stitch at a Time: First Appointment at MGH
http://mycfjourney.blogspot.com/2015/06/first-appointment-at-mgh.html
Mastering the Art of Breathing, One Stitch at a Time. This 30-something's journey with Cystic Fibrosis, Lynch Syndrome, CFRD and the Lung Transplant process. Tuesday, June 2, 2015. First Appointment at MGH. Today was a very long day. But it was worth it. I really like the clinic at MGH and I am going to stay there. I got a little panicky in the booth when they blocked the air for the test. But I only had to stop once. The woman was very nice and didn't get annoyed thankfully! My Blog List / Friends.
mycfjourney.blogspot.com
Mastering the Art of Breathing, One Stitch at a Time: CF Awareness Post Question Day 26
http://mycfjourney.blogspot.com/2015/05/cf-awareness-post-question-day-26.html
Mastering the Art of Breathing, One Stitch at a Time. This 30-something's journey with Cystic Fibrosis, Lynch Syndrome, CFRD and the Lung Transplant process. Tuesday, May 26, 2015. CF Awareness Post Question Day 26. I took a break from CF awareness this weekend to celebrate Memorial Day and remember why we celebrate. God bless the fallen service men and their families. I know you like the winter months the most. Having CF is there any seasons that are better for you. Or months. My Blog List / Friends.
mycfjourney.blogspot.com
Mastering the Art of Breathing, One Stitch at a Time: Colon Cancer Gene Results
http://mycfjourney.blogspot.com/2009/07/well-i-got-results-of-cancer-screening.html
Mastering the Art of Breathing, One Stitch at a Time. This 30-something's journey with Cystic Fibrosis, Lynch Syndrome, CFRD and the Lung Transplant process. Monday, July 13, 2009. Colon Cancer Gene Results. Well I got the results of the cancer screening test back and I am positive for the hMLH1 gene. If you are not sure what I am talking about read this post. And stay up to date will ya? And Steve podcasts but it wasn’t helping. I couldn’t seem to concentrate on my work that desperately ...Well, Im of c...
mycfjourney.blogspot.com
Mastering the Art of Breathing, One Stitch at a Time: Some amazing news!
http://mycfjourney.blogspot.com/2009/02/some-amazing-news.html
Mastering the Art of Breathing, One Stitch at a Time. This 30-something's journey with Cystic Fibrosis, Lynch Syndrome, CFRD and the Lung Transplant process. Sunday, February 1, 2009. Well I am going to blog about some interesting information I discovered last night. . I went to dinner with my dad and step-mom. . I was able to fill in all the information needed about my family’s colon cancer history. . I was floored at it! So here is my list, just first name initials. . The x2 means they had it twice!
mycfjourney.blogspot.com
Mastering the Art of Breathing, One Stitch at a Time: Home from the Hospital
http://mycfjourney.blogspot.com/2013/12/home-from-hospital.html
Mastering the Art of Breathing, One Stitch at a Time. This 30-something's journey with Cystic Fibrosis, Lynch Syndrome, CFRD and the Lung Transplant process. Friday, December 13, 2013. Home from the Hospital. I am home from the hospital. I actually got out on Monday but I have been so busy finishing up my paper, that I turned in Wednesday, and appointments, that I haven't been able to update. Subscribe to: Post Comments (Atom). My Blog List / Friends. To love and be loved. It's All Good In Joshland.
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