My skin seems to be fitting a bit better today – I’ve been putting on the hand cream to stop them drying up which seems to have helped. I didn’t have much energy yesterday, the first day after stopping the dexamethazone is always a bad day. Today I have a bit more energy, but I keep getting sharp pins and needles in different parts of my face and arms. I will see how it is tomorrow and if it carries on, I will have to speak to the Myeloma team to get some advice. It is probably to do with the increase in the Thalidomide which effects the nerve endings.
