Learned about this group at an LLS program today. I’ve got 4.5 years since diagnosis. I was on Imatinib for 3 years. It worked well at first but I developed a mutation and my numbers started to edge up every three months. So I got in with a CML specialist at UC Irvine and am now on Tasigna. Last two tests have been “undetectable.”
So glad there are these support groups around.
