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“He is like a tree, planted by streams of water, which yields its fruit in season, and whose leaf does not wither.” --Psalms 1:3

Location: BlogsThe cure4treebeard Blog    
Posted by: Daddy 12/6/2007 10:00 PM
December 6, the Feast of St. Nicholas, JT’s one-year anniversary. Thank you, Jesus.

I don’t know why JT has done so well through transplant while other children haven’t. I don’t know why he continues to struggle with awful skin issues and an inability to eat. I don’t know why he will have to walk a difficult path for the rest of his life. Here’s what I do know: we’ve had a glimpse of kingdom healing this year. We’ve heard, faintly, a few bars of music from the place where “everything sad will come untrue.” And we’re left with a weighty gratitude:  for God’s mercy, for kindness, and for the promise that in the end, all tears will be wiped away.

One thousand six hundred and sixty-three years ago the Church celebrated the first St. Nicholas Day to honor the patron saint of children. Three hundred and sixty-five days ago our own child was saved by an incredible gift from an anonymous donor: a bone marrow transplant giving him a new immune system and a second chance at life. Each and every day since has been a miracle.

So my only prayer request for tonight is for thanksgiving, and lots of it.

Tomorrow evening my parents and sister and Jodi’s Dad are joining us as we keep the Feast: to honor St. Nicholas and Jacob Treebeard and his donor, to celebrate gift-givers and children and miracles everywhere. I wish you could all be here.
Copyright ©2007 Brian Brown
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Raise money for the National Foundation for Ectodermal Dysplasias simply by clicking your mouseGoodSearch.com (powered by yahoo.com) is donating money to charities for use of their search engine.  To use it, install the GoodSearch toolbar to the top of your browser screen and then type in the charity (National Foundation for Ectodermal Dysplasias) and then search as you would on Google.com or Yahoo.com.  The NFED gets a monetary donation for every search!  The more folks that know about this, the greater the donation to NFED, and hence the more money there is to fund research on Jacob's condition and others like his.  Thank you!

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