continued. . .

I saved and then couldn't retrieve the blog entry I started, so here is the rest.

Our trip back was picture perfect, no construction, no traffic jams; we made it, without pushing, in 16 hours! 3 drivers helped.

We got home Monday eve at 9 pm, which was good because Gil had forgotten that he'd set up his next doc appt. on Tuesday morn. opps.

We spent most of Tuesday at UW Hospital and had his blood tests and bone marrow biopsy. This is the test done after 100 days which should show what myeloma activity is still there. It will be the confirmation (we hope)that he is indeed in remission. We've been acting "as if" ever since his good blood tests but this is the real deal test.

We should have the news in about a week.

Unfortunately, he's been having a good deal more peripheral neuropathy in his feet, ankles and lower legs in the lat month. Doctor Callandar says that that happens sometimes after a bone marrow transplant and that it should get better over time. It definitely cramped his style in NYC as he often took the bus when we walked. He's got pain meds but they bring there own side effects. All in all we have so much to be grateful for that some how the pain seems like a small price. And we hope it does, indeed, fade.

OK, my attempts to post some pictures of the most delectable baby in the world will commence. (don't hold your breath!)

It worked! Ah what a morsel she is! That sunny smile would greet me (almost) every time I got her up. Somehow seeing the turkeys just doesn't do it for me. But I am glad to be home in this spot of beauty surrounded by good friends. We are so fortunate.

More later, but all in all, we're doing well!