well hello everyone not been on here for a while but had to share what my husband and i thought was good news
since starting copaxone my ms seems to be on an even keel my neurologist said no one would know i had ms if they just looked at me. and no disrespect to the man that i trust we know that. sometimes that doesnt feel that way just been told to go to my doctor about pain i have with my back and with my feet because he doesnt beleive its the ms thats causing it even though i already done that and they put it down to my ms mm what to do now.
i must admit though for a moment there i really did beleive that all was good and id get better xxx
sorry if ive confused anyone i just write how i feel and that doesnt always make sense xx