letmefly-jamie.blogspot.com
Let Me FlyMy thoughts and feelings on different life experience's and being a Mom living with Cystic Fibrosis.
http://letmefly-jamie.blogspot.com/
My thoughts and feelings on different life experience's and being a Mom living with Cystic Fibrosis.
http://letmefly-jamie.blogspot.com/
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My thoughts and feelings on different life experience's and being a Mom living with Cystic Fibrosis.
letmefly-jamie.blogspot.com
Let Me Fly: Knowing when it's time to head to the hospital.
http://letmefly-jamie.blogspot.com/2013/05/knowing-when-its-time-to-head-to.html
My thoughts and feelings on different life experience's and being a Mom living with Cystic Fibrosis. Sunday, May 12, 2013. Knowing when it's time to head to the hospital. You get where I'm going with this don't you? My Great Strides for CF walk is Sunday May 19th! Would it go on and be as successful without me there? Yes I'm sure it would, but i just can't stand the thought of missing it, it's my baby! Either way it will be fine and life will go on, but as always I have to do what's best for my health.
Let Me Fly: My opinion on Sarah Murnaghan.
http://letmefly-jamie.blogspot.com/2013/06/my-opinion-on-sarah-murnaghan.html
My thoughts and feelings on different life experience's and being a Mom living with Cystic Fibrosis. Monday, June 10, 2013. My opinion on Sarah Murnaghan. And other peoples experiences with it. Opinions are always going to vary and especially on hot topic issues like organ donations. In fact my Mom and I disagree on this case. Putting this into words has been a challenge for me over the last couple days, so bare with me if my thoughts seem jumbled or not put together. It's not fair, CF never seems to be,...
Let Me Fly: July 2012
http://letmefly-jamie.blogspot.com/2012_07_01_archive.html
My thoughts and feelings on different life experience's and being a Mom living with Cystic Fibrosis. Sunday, July 15, 2012. But I don't want too.(insert 5 year old whiny voice here). No Do I feel great? No Do I always let myself slowly feel worse until I realize I need it? That's more time Colton is home, when I am his primary care giver it makes it hard to be away, not to mention I miss him (although I will admit the first couple days away are not to bad! Well sue me then because that's how I feel!
Let Me Fly: Transplant Evaluation
http://letmefly-jamie.blogspot.com/2013/07/transplant-evaluation.html
My thoughts and feelings on different life experience's and being a Mom living with Cystic Fibrosis. Tuesday, July 16, 2013. As much as they suck and hate me and I hate them I'd still like to keep them as long as possible. July 16, 2013 at 7:07 PM. Personally if this is the route you choose, I know youll do great! Youre a motivated person and take your meds, not here or there, or whenever you feel like it, but everyday. Two keys of living with a successful transplant. July 17, 2013 at 4:56 AM. We all lov...
Let Me Fly: November 2012
http://letmefly-jamie.blogspot.com/2012_11_01_archive.html
My thoughts and feelings on different life experience's and being a Mom living with Cystic Fibrosis. Wednesday, November 14, 2012. Doubtfully Optimistic for a cure. In a previous blog I spoke of CF Advances and my thoughts on it. In that post I stated that I didn't believe there would be a cure found in my lifetime. I still believe this and stated I would explain at another time, I think I'm ready to try and explain. Please visit www.cff.org. And look through some of the info they have, you can read all ...
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Let Me Fly
My thoughts and feelings on different life experience's and being a Mom living with Cystic Fibrosis. Saturday, September 27, 2014. Q&A about my Lung Transplant and CF. Through my transplant journey page and my personal page I have received questions over the last 20 days since transplant. I would like to answer to the best of my ability, but some answers are not cut and dry because transplants vary person to person. I will give the best answer I possibly can. Let's begin! Will cf hurt these lungs as well?
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