Update. CT showed new disease in serosal around liver, 3 lymph nodes around my heart, and lymph-nodes in my pelvic area. After our June holiday in Scotland I started chemotherapy again, same drugs. I was very ill after the first chemo and ended up in hospital on the Sunday night on a rehydrating drip for 6 hours. They did another CT which showed another new area of disease around my colon. The oncologist said he would reduce the chemo by 20% for the rest of the treatment. Second chemo was better but the nausea was dreadful, took 10 days before it went. This time I have also had really bad indigestion. I have not been someone who suffers indigestion and I couldn’t believe how painful it was! I asked for stronger anti sickness tablets which I did get for the 2 days following chemo and this reduced the nausea to one week. Following third and fourth chemos I just felt wiped out and it took me over a week to feel anything like normal. Also sessions 3 and 4 were both postponed a week because of low neutrophils. After the 4th I was given an injection to administer at home to try and stop the white blood cells from dropping too much. My 5th chemo is due next week so we will see if the injection has worked. I am on the same drugs and again using a cool cap but just can’t believe how badly my body has reacted this time around, First time I had very few side effects and those I had were not too bad but this time everything has been so much worse,I will be glad when the 6th chemo session is over.After chemo I am going to be taking cancer targeted tablets but don’t know which yet. I am hoping the side effects of these will not be so bad but will have to wait and see. I just can’t wait until the tinal chemo session is over!