I have been on hydroxyurea for 3 months and was diagnosed with PV in March. My white blood count is almost 17 and my allele burden is 91.3%. My hematocrit is 46. I went to see a new hematologist in Seattle and asked her if she would consider changing me to Besremi considering the recent research indicating higher risk of blood clots for people over 60 and allele burden over 50% and high white blood count, and it can also lead to faster disease progression. She agreed to go ahead after I get a bone marrow biopsy. If I can't get help with financing it, Pegasus might be OK.
It would be a weekly instead of biweekly injection.