Open foot insert mouth

The online support group has turned out to be actually an amazing source of information. Some people have lost children to asplenia, polysplenia, heterotaxy, etc and others are battling it every day...these people have more information than any of the doctors....and they are amazingly supportive. I was just being impatient as usualy.

Just wanted to let anyone who is reading know that I had a very bright and happy day today (anything to do with the venti iced latte this morning?) And that I miss the little beetle bug but am feeling happy.......