It is good that Jeremy will now let us push his medicines down his nasogastric tube at a very fast rate. For many weeks post-transplant we had to do it ever so slowly, otherwise his gut could not handle it and everything would come straight back up ... and we would have to give his medicines all over again!
Some days he seems to be eating as much as Stephanie, so hopefully he won't need his nasogastric tube much longer. But then again, on other days he goes back to his old habits and only picks at his food.
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