Today is my fifth day of the first AC session of the total four. Not bad but feeling very tired. As you all, we just want to go through this journey with all ups and downs like all the amazing women in this network. I hope too that the paclitaxel will be easier on my body. What really helps me is the rest, eating small meals frequently and drinking water. I also do not want my family to worry, so I am really trying to listen to my body and try to recover for the next chemo infusion. Just wondering if any of you are on Pegfilgrastim PEG) injection, and if so , did you have any side effects? I have not although I was told to expect chills and joint pain.