mycfjourney blogspot.com

Mastering the Art of Breathing, One Stitch at a Time

This 30-something39;s journey with Cystic Fibrosis, Lynch Syndrome, CFRD and the Lung Transplant process

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LINKS TO WEB SITE

a breath of fresh air.

one breath at a time. Monday, June 18, 2012. When patient info becomes gossip on the tennis court. It was recently brought to my attention that a CF doctor revealed to a mutual family friend that he had seen me before.

A Matter of Life and Breath

A Matter of Life and Breath. Life, Lung transplant, and Cystic Fibrosis. Want to Contact Me? Please email me suggestions, thoughts, comments, or criticism. A Breath of Fresh Air.

Breath Sentence

The celebrations, exclamations, observations and ruminations of a twenty-something on a quest to figure out this adulthood thing, make her life matter and have some fun along the way. and do it all with Cystic Fibrosis. Friday, May 11, 2012. Awareness is pretty sweet, too.

Courtney Lynn Hill The disclosure of our sister the CFer.

Valid December 17th - 18th. We all miss Court SOOOO much, but with her passing has given us many blessings. She has changed our lives forever. Betting on a Cure! We think this event will be a lot of fun, and I hope we have a great turn out.

La Vie Cystique dune Femme Mystique

They say, oh! Wednesday, February 26, 2014. The dedication of this blog. I used to write so openly about dying and fearing death and coming to grips with my self and my disease. I think I did a pretty good job of it all actua.

Life and living it

Thank you for visiting my blog. Wednesday, May 12, 2010. That is how long the RX company says it will take which I find ludicrous. I have been lucky to make it a week, now I have to wait another? Hugs and well wishes to all,. Wednesday, April 21, 2010. could it be infection? Anything pretty much is suspect at this point. I follow him down the .

Living life breathlessly

Sunday, April 1, 2018. Coastal Roadtrip Part 1 - Gonubie. On Saturday the 17th we started our coastal road-trip. It consisted of 3 nights in Gonubie with my cousin Elette and her hubby Gareth. Then on to Port Elizabeth, my hometown, for 4 nights, and finally 6 nights at Storms River Mouth. My favourite place, out honeymoon destination and the place we always go back to. Saturday, March 31, 2018.

My Journey Through Life My Kitchen!

My Journey Through Life and My Kitchen! My name is Jen, I am a 30 year old who has Cystic Fibrosis. I originally started this blog to keep track of my time on the double lung transplant list. Well after 2 LONG years and a lot of bumps in the road I finally received my transplant on December 2nd, 2010. Now I write about life post-tx and all that goes along with it! View my complete profile. Since May 30, 2008. Monday, May 20, 2013. Cover with lid and co.

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Mastering the Art of Breathing, One Stitch at a Time

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This 30-something39;s journey with Cystic Fibrosis, Lynch Syndrome, CFRD and the Lung Transplant process

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This web page mycfjourney.blogspot.com states the following, "Mastering the Art of Breathing, One Stitch at a Time." We saw that the webpage said " This 30-somethings journey with Cystic Fibrosis, Lynch Syndrome, CFRD and the Lung Transplant process." It also said " Tuesday, January 26, 2016. Rest in Peace Aunt Marybeth. Monday my Aunt passed away. She had pancreatic and liver cancer. The past two months she has been hospitalized and this was expected, but not expected. She leaves behind 2 beautiful daughters in high school. I remember going to the baby shower for her first baby, my cousin. I had my 3 month cli."

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