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.
Friday, March 7, 2014
Hopefully soon
The cath lab just called and they said they should be ready for Magnus within an hour! Next big obstacle will be seeing how he tolerates the anesthesia gas mask. This has been bad in the past.
Fingers crossed.
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