I went back to this picture to remind everyone who we are.  This picture brings happy tears to my eyes every time I look at it.  It was the day before I heard "the best news ever" and we're smiling anyway.

So I haven't posted in a while but I haven't had much to share.  Meaghan's treatments haven't changed, she is working very hard to stay on track.  She continues to eat well (mostly) and her weight makes me very happy.  Enough that we went together to buy a new 3-in-one booster seat.  The new seat has a wild pink pattern on it and Meaghan is sooooo happy.  What an accomplishment!

Ok, one thing I (maybe) should mention.  Meaghan was invited to a formal photo shoot for the Cystic Fibrosis Foundation at the end of this month.  About a year ago she was photographed by a CFF team and I hear that those pictures have been used in several places.  I have a copy of one publication where Meaghan shares the cover with another beautiful CFer I know.  Our favorite doc came with it to Meaghan's room when she was inpatient and had her autograph it for him.  Who knows where the new pictures will end up but every little girl dreams of the star treatment, why shouldn't Meaghan.