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.
I watched it . It was interesting and seemed to work at first but I’m not sure how long it would last. The man seemed quite grumpy I felt a bit sorry for his wife, maybe his ms made him grumpy . His cognitive functions were very good . I suppose it effects everyone differently. Michelle and Frazer x
Medically it showed me that once MS takes hold. It doesn’t just destroy a persons health. The frustration is a normal reaction. Fare do’s to getting on as best as he could in a social media enviroment. Writing text on the internet is getting bad enough. Voicing an oppinion, when the real goal is to improve a health situation & keeping the future motivation. Knowing it’s just going to get more difficult as time passes. It’s all a MESS. Too many people in the kitchen & chaos will persist. Deep breaths & a fresh menu is on the cards. Seeing how people cope is an inspiration. Especially if they are trying to improve things. Hydration, a good diet & self pushing physically, seems to get results. Keeping the mind on a better outcome is paramount.
Not seen it I will try over the weekend, I didnt get up till after 3 today Heather got e up showered and dressed. I was asleep all morning and only got up then to go to the bathroom.