We are waiting for the targeted molecular therapy, pemigatinib, to arrive so mom can begin to take it.  It can have many side effects similar to chemo, but shouldn’t drop her counts. It is two weeks of oral pills, and then a week off, with a CT scan after two cycles:  We are hoping inhibits the cancer’s growth  and  spread  for a while. She will still get weekly labs during treatment and dose may need to be adjusted down depending on side effects and labs. We are grateful for every day that she feels good!