CorinaH's Journal

Well this has proved to be a very motivational site for me as my goal was to convince myself that I am not the only young person dealing with this disease. I have such a wonderful support group at home, with my family, boyfriend, and friends. They would do anything for me but they still can not understand what this feels like first hand. I am sick of talking about CML but at the same time it seems to be the only thing that runs through my mind. I am really sick of being tired and my muscles cramping! Although I am extremely grateful for Gleevec it has made me feel worse even though I am getting better????