Hi everyone I’ve been on Copaxone for over 4months now & the lumps which i get under the skin where I inject seem to be hanging around longer making it harder to find an area to inject into. I’ve also noticed that when I inject on my stomach I get a slight swelling not very nice considering I’m going on holiday soon. I’m taking antihistamine tablets which has helped with itching but don’t seem to be able to get rid of the lumps. I’ve coped well with MS so far but getting a little fed up of injecting daily. A lot of people said you get used to it & becomes part of your daily routine. I shouldn’t moan I know as a lot of people suffer more than me & I understand that avoiding relapses is the priority but can’t help but feel down when I see the marks. Has anyone else gone through this? Charlotte xx