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
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Through my transplant journey page and my personal page I have received questions over the last 20 days since transplant. I would like to...
1 comment:
Friday, March 21, 2014
I'm only Human...
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For those who are friends with me on facebook know I was listed for transplant on January 20th. I had been in the evaluation process since J...
1 comment:
Tuesday, December 17, 2013
CF Hurts...
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CF hurts. That is the one thing I wish people knew or could understand. It hurts physically, emotionally, and spiritually. Let me start wi...
Tuesday, July 16, 2013
Transplant Evaluation
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As I wrote about in a blog back in September I have been seeing the transplant doctor at my hospital in Grand Rapids, Spectrum health. They ...
2 comments:
Monday, June 10, 2013
My opinion on Sarah Murnaghan.
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I don't know if you've seen or are following the story of Sarah Murnaghan, 10 year old cystic fibrosis sufferer who is dying from CF...
1 comment:
Sunday, May 12, 2013
Knowing when it's time to head to the hospital.
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I have talked in other blog post about certain signs to me that I may need to go in for a clean out. Being tired more, not being able to kee...
2 comments:
Saturday, May 11, 2013
Mothers Day
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Mom and I on the night of a lifetime! At P!NK's Truth About Love Tour concert. One of thee best nights of my life! Tomorrow is Moth...
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