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We are off the oxygen mask! Her pneumothorax has reduced enough in size that blowing bubbles and walking around or using a treadmill should be sufficient. Some bakers came today and dropped off a gingerbread house for Morgan to decorate (and mommy to eat anything …

Yeah, haven’t been on in a while, and I know that many of you have been waiting for updates on Morgan’s fight.  Cause that’s what we are doing…fighting.  The experimental chemo is kicking ass, but kicking hers as well.  Morgan’s hair is pretty much out …

So last night was pretty quiet..which is a good thing. We are on the same program as last time with the road map of where we need to be on this second times the charm journey. We are working toward getting Morgan to remission within …

We’re back, and sooo excited.  Today Morgan climbed on the bus to go to her first day back to school, and the start of 4th grade.  Not gonna lie, hope that the home schooling has prepared her for 4th grade, but I know she will …

Received a call this morning from the the Gift of Life, bone marrow donor program.  Morgan is going to have the opportunity to meet her donor and HIS family in New York at a Mets game, then dinner!  The organization is going to send us …

We’re here…and exhausted!  Morgan was a trooper on the flight over with very little drama.  The Mayfair Hotel is so quaint, and Morgan has already taken two very luxurious baths!!  She uses her two mastered words of Bonjour and Merci everyday! We are sweating our …

So, we were back at the pool this year for Morgan’s actual birthday!  Such a great sunny day.  We followed up the day with a movie and sleepover for some of the girls…who stayed up till 2am this morning!!!!  What a difference a year makes.  …

I do! I upload pictures all the time with Morgan, so I forget to update the blog because I update Facebook! So enough of my ranting. Morgan is doing GREAT! She still has some of her gut GVHD, but not as often. As the weather …