Our son Magnus was born November 19, 2009 with a serious congenital heart defect, HLHS. I set up this blog to keep our family and friends updated on his condition, and to connect with other families dealing with HLHS.
Thursday, May 21, 2015
Cath day again
After twice rescheduling due to illness, we are now in pre-op waiting to go back to the cath lab. You never know when you'll actually get to go back when you're second case, but so far things seem to be on schedule (KNOCK ON WOOD). Will update throughout the day!