Hi Linda --
Yes, I do remember reading this message some time ago, but I didn't respond because I really didn't know what to say.
He was give through a central line cistplatin,cytoxan,etoposide and doxrubicin. Orally he was given thal/dex.
I don't recognise any of these drugs and do not know why they would have chosen these to give to him when he reached stage 4. Obviously they worked in the initial stages, but because he was so far gone, they couldn't maintain him. I sometimes worry about what will happen to me when I reach the 'end' stage of this disease, but I do use pain medication and try to maintain as normal a lifestyle as possible. I know that the Revlimid will only work for a set period of time and that I have already gone further on it than most people ever do, but I am hopeful that it will continue working for me for a long time to come. If not, then I don't now where I'll turn at that point, but like you, I am grateful for this site and keep my ear to the ground for any new and novel drugs and treatments that are found. I will certainly ask my doctor - when the time comes - about your 'cocktail', but I'm not into adding new things into my regieme just because they 'might' be useful. I have been blessed so far, and am sharing what I have learned with anyone who wants to know. I only tell people what has worked for me. Thank you for sharing what you learned with Mike. This field is still in its infancy and there is much to learn for us all, patients, carers, and medical staff included! I hope life becomes easier for you as time goes by and that the happy memories that you have become the ones that are most often in your mind. Take good care -- kind regards, Cath