I just read the research article about CHIP and am thinking I need a discussion with my oncologist. Three years after my SMM dx, I was found to have CHIP with the DNMT3A mutation. The article sounds as if this was a good thing, however, I was treated with cyclosporine because the leukemia specialist believed it was the cause of infections and neutropenia (unrelated to SMM). The neutropenia is now resolved but I am wondering if the mutation persists?