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Tuesday, July 13, 2010

Surgery is set.

Next tuesday is nolans surgery day, for his fundo repair and g tube placement.We are feeling very nervous as it's so soon in such little notice, but we pray and hope for the best, we know nolan will be a much happier little boy without a tube going down his nose.I will update next week after its all done, please pray that his recovery goes smoothly.

2 comments:

May said...

hi amanda,

yes life will be so much better without the ng tube. fingers crossed all goes smoothly for his extubation.

Nan P. said...

Hello Amanda, I came across your blog by chance and have been touched by your story and by beautiful little Nolan. Yourself and Nathan are very brave – I am sorry if this sounds corny, most parents are brave and will do anything for their children; but some are not as brave as others. You definitely belong to the latter group.

I am the grandmother of a 2 year old boy with Trisomy 21 (Down Syndrome). Cathal was born with 3 severe heart defects and had his 1st heart surgery at 5 weeks old, and his 2nd one (a long open-heart surgery) on the eve of his 1st birthday. I know how hard it is to have such a young child going for surgery, and can barely try to imagine how difficult this time is for you both. I will think of you both and of Nolan in the days to come, and watch out for news on your blog.

I wish you all the best.


Oh, and Lexi is such a little cuttie! :-)