Copaxone injections
Hi everyone I’ve been using Copaxone now for nearly 10 years with really good results, but I’m running out of skin to inject because of scar tissue and lose of fat around my stomach. I’ve been diagnosed as secondary progressive now so my MS nurse says I’m not eligible for Oral DMD’S has anyone else had this problem thanks
Hi Niles, I think I can totally get where you’re coming from - been on Beta Interferon, Copaxone, Extavia until I couldn’t inject anymore like you ran out of spaces and lost padding! I was put on Tecfidera during Lockdown but now been taken off it as White blood cell count too low among other things. Before the latest blood results, I was told I could stay on Tec even though I am more or less spms now because of still getting the odd flare up. I have no idea what I will be offered (if anything) but got an actual ftf appointment with Neuro in a couple of weeks, who has only seen me via Video appointments since 2019. I hope you get some answers soon about what you can try next. Tecfidera has been fantastic for me and I’m really disappointed to have to come off it. Fingers crossed for you :-)