Today is my fourth day of this journey we all are sharing. I am very optimistic and thankful to be diagnosed with a condition that has had such success in treatment possibilities. I have read everything I could find on the internet but am so new that I’m not familiar with a lot of the terms and abbreviations.
This forum is most appealing to me and I look forward to following everyone’s situations. I decided from the initial diagnosis that I would rather not hear war stories from neighbors and friends as many are not CML and there are so many types of leukemias. Knowing that we are all going through the same experience is assuring that the information is accurate.
My first question is: How soon do side effects begin?