Not sure what to expect. Hailing HSCT as a miracle cure for MS.
Suffering myself with PPMS & living alone, seeing how others cope with SPMS. Which isn’t great! Doesn’t fill me with much hope. Especially after some of the TV dramatizations of what MS is apparently like.
I tell folks & they say I’m acting. I must be good.
Personally, I think they are the ones, full of crap. Maybe they want an Oscar. I want to give them a black eye or two, instead.
Fakers make me sick to death & need one of my boots, stuck up their back side.