Finally got to discuss Micah with the hematologist that heads the vascular malformation clinic. Her recommendation
is 7-10 days of i.v. vancomycin. She has seen a handful of LM/vascular
children who don't respond to anything but vanc. His ENT doesn't want
to do that yet. He wants to see what happens come early next week (his
10 days of current meds ends Thursday, but we should be seeing results
now/soon). There's a chance we can go home or ronald mcdonald house w/ a picc line after a few
days. So, we'll see. (again)...
The saga continues.
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