Im on a different therapy called nivolumab im not sure the spelling is correct I had my 1st scan after 3 months and they gave me the best news considering I was given 6 months without treatment they said there was no new lesions and the ones that were there had slightly reduced in size so all ive done is hit the reset button and said ok its another 6 months I have.... I know I've been told its not curable but I just want to make it to my daughters wedding in March apparently I get scanned every 3 months so I'm due another in September so just have to see how it goes expect the worse but hope for the best I just keep getting more tired as the weeks go on my next therapy session is tomorrow I get it every 2 weeks im not sure what else to say how does anyone cope I'm not sure to take it as well we are all going to die at some stage and we have been given the opportunity to plan for it where as some don't I have meltdowns every other week or maybe sometimes more but I prefer to have them on my own does anyone else feel like this ...is it normal?
