Taylor's MRI didn't come back as we had hoped it would Mom. Her tumor is showing some enhancement and a little growth. We had planned on starting a new drug, but with these results we decided to wait on the new drug and go back to the temodar/vincristine. Her dose is a little stronger this time, hopefully after 3 months of a little aggressive treatment we will see some improvement on the MRI. Maybe if that happens we'll substitute the interferon with the new drug. I don't know Mom...you always believed that things happen for a reason, maybe these results were a sign that we weren't suppose to start the new drug. I know you are watching over Little Taylor...I feel your presense often. She's strong and I know she'll do well on her chemo. We go back on Friday for counts and vincristine. I just gave her the first dose of temodar a couple hours ago. She'll get it for 5 days then 3 weeks off. She goes to the ENT on Tuesday for the second part of her tube placement. Her ear is starting to get infected again, so Dr C gave her an antibiotic. I LOVE AND MISS YOU MOM!!!!!! ((((((HUGS))))) *****KISSES*******