Not a day goes by that I don't check on you and your beautiful son. So happy to hear of his progress...looks like all those prayers are being answered...
Mr. McKay is a miracle. He was diagnosed with a soup of congenital heart defects while still in utero including: double inlet left ventricle (DILV), Transposition of the Great Arteries (TGA), a large ASD which has now been modified to create a single atrium, pulmonary atresia, and dextrocardia. He has undergone a series of three open heart surgeries to reroute his plumbing into a flow more likely to meet his growing body's demand for oxygen. He is post BT Shunt (August 22, 2008) and post-Glenn (November 25, 2008), and most recently traveled cross country to have the Fontan procedure at the Children's Hospital of Philadelphia (July 9, 2010). Today, McKay is a growing near-three-year old challenged with developmental hurdles we are anxiously trying to help him overcome. McKay offers heart baby hope of the most robust proportions. This blog chronicles our adventures.
"Life is not about waiting for the storm to pass. It's about learning to dance in the rain."
PEACE
"It does not mean to be in a place where there is no noise, trouble or hard work. It means to be in the midst of those things and still be calm in your heart."
8 comments:
Great news! Praying for continued improvement for McKay! :)
HOORAY!!
Thank-you God...
Have a good day little one.
Thanks Mindi..your update made me
feel better..
I headed over here from Owen's blog and wanted to let you know that you have one more prayer warrier! Good news this morning McKay!!!
Baby steps:) Love it! Still praying!
Wonderful news! Any progress is still progress!! Keep moving forward McKay! Praying for all of you!!
So glad :)
Still Praying!!
Not a day goes by that I don't check on you and your beautiful son. So happy to hear of his progress...looks like all those prayers are being answered...
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