[Darice]

I kind of keep holding my breath wondering what's going to happen next . . . and we've had plenty of problems . . . but my hubby's blood counts seem to be holding their own pretty well (he'll never be normal, of course) with just a Neulasta injection every two weeks. I can't quite get comfortable with this because I know that the treatment-related MDS is harder to treat, has a poorer prognosis, and that the chromosome 7 involvement makes things more difficult . . . it's like I'm waiting for the next shoe to fall, but I'm sure not going to look a gift horse in the mouth. I just don't know whether I can relax. Is there something I should be watching for or doing differently? I know that statistics are always behind the times, but we aren't benefitting from any new-fangled treatment . . . just good old-fashioned Neulasta. Guess I should just be thankful it's working.