Hi everyone – have been on CDT for 4 months and was due to end the treatmnt but now am not suitable for SCT (have to wait for my heart to improve) so the CDT treatment is to continue for a while longer. I would really appreciate some advice / tips on dealing with the nausea associated with CDT (whether its from the steroids or the chemo). I take both the steroids and chemo on a Tuesday and am in a dreadful way on wednesdays, thursdays and fridays. It starts to improve over the weekend. Thought I could cope while there was an end in sight but now my treating team aren't giving an "end date" for the CDT. Have tried ginger and various medication….Any advice would be so much appreciated
Cinzia