Life with the oldest sister who loves theater and fashion, a boy who has Hypoplastic Left heart Syndrome, now Heart transplant and partial Liver from Aspergillius, but thinks fishing and electronics rule. The most amazing middle-child-sister-aspiring artist. Also, a girl and her Tethered Spinal Cord Syndrome, Neuro Endocrine Cell Hypoplasia, Lumbar Hemangioma, asymmetrical gluteal cleft, Pectus Carinatum who loves littlest pet shops, American girl dolls, playdates. And one yummy baby brother who has a coarctation and bicuspid valve and thinks super heroes are the best.

Monday, October 8, 2007

Couldn't wait

I couldn't wait to hear how Ian and the rest were doing.... So I called and left a message... It just happened to be the exact time that they were taking Ian off the ecmo ..... A HUGE step... I just wanted all to know that he is doing as well as can be expected for the tiny steps he is taking, it has been a long and hard weekend for the Pearson's and I know Jenn will write when she feels she can take a few minutes away from her little man. Just know that the prayers and fasting are going in a great direction and being answered in our families behalf. We feel them each day. This Sunday being fast Sunday please remember the little heart babies... Thanks so much everyone


Anonymous said...

Thanks Brynn. You do such a good job at all of this. You are a great friend and I appreciate you so much. We are going to get through this, aren't we?!? Thanks for giving us strength,and hope and love. Your family is great. Love you guys!

Anonymous said...

We're are thinking of Ian and Alex and hoping for the best. Even the smallest little steps are still steps to be thankful for (which I'm postitive you are very thankful)! These babies are such beautiful little babies! We pray for you daily!