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

Wednesday, July 1, 2009. Astra is finally moving forward with her recovery. For awhile it seemed like she was hitting one stumbling block after another. She was having anxiety attacks coupled with coughing attacks that would last hours at a time. While throwign up her feeding tube came out so they thought they would let her try eating real food before putting it back in.

Monday, February 6, 2012. New Year, New Heavier Ben. The day of surgery he weighed 30. He is packing on the pounds and that makes for a happy Mom and Dad. He did well after surgery and was back to his spitfire self very quickly! We only had to spent one night in the hospital. Mott is very nice and it was great to have our own room. In December, we flew to Hawaii, to see my brother graduate from U of H. Ben had a great time and he did well on the long flight there and back! The speec.

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.

The Revolution Will be Televised. Sunday, November 15, 2009. Dad, sit down before you read this one. I went to church today. They used the Bible and everything. They even sang one song I knew from childhood. They bowed in prayer several times, they took an offering, the whole nine.

Thursday, October 16, 2014. And I was right again. There should be a better word for it.

Little Tad Pole, Big Pond. A little froggy trying to make it through life in the pond. Monday, May 13, 2013. In a weird way it fe.

Love To Breathe Pendants by Lissabird. Love to Breathe was established in 2001 so I could give hope and positive energy to the Cystic Fibrosis community, especially to the families with newly diagnosed children. I believe it is important. 8203;I try to live each day to the fullest by keeping my hopes high, and dreams big! .