Hi all, had first appointment since diagnosis with neurologist yesterday, as lemtrada is currently not available for first treatments & I am hoping to have a child they have suggested copaxone & then after having a child going on something stronger. I have to have another MRI first to see what’s going on. I’m worrying because we have been trying since February last year, had initial checks done & all seems okay & doctors advise need to be trying for 2 years before being referred to fertility clinic. Has anyone ever been in this situation? I feel so lost & in such a rut with it all. I’m thinking of maybe going private & paying for checks as I’ve read that copaxone isn’t that effective so long term I don’t really want to be on it. I’m 32 and 33 at end of year so not getting any younger, if only I’d known I’d get MS I’d have tried a couple of years ago. Everything is just a battle at the moment.
Any advice would be much appreciated. Thanks for reading.