I'm interested in knowing if anyone here has MS and uses an injection? I don't have MS but my sister does (relapsing remitting - on pain meds only now, but the vile chemo tablets are pending). She is considering (and YES we will ask the doc too and take advice!) but wanted to hear anecdotal experiences, if anyone would be up for sharing.
I have read some potentially positive reports about GLP-1 meds and the progression of MS.