Was dxed 2002, think I had stuff I now recognize in 1994. In a chair 24/7 since 2009. Mostly have physical problems (no walking) but other than a little MCI (Minor Cognitive Impairment - Is it age or MS?) doing OK. Pain level not great (Neuropthy) but everyone is so different from another on this terrible Journey.
Part of thanks goodness I'm 55, no problems when raising my kids, Thanks goodness it's me and nothing for them but this ride isn't over yet. I hope little else will happen but won't be surprised if it does. My Neuro (Without words really) sees theres nothing he can do for me - no meds, etc. He no longer asks me to get MRIs, we both know I have PPMS and I hate them and so why bother with them? He answers my e-mails within 24 hours and will do most things I ask for if something comes uWas dxed 2002, think I had stuff I now recognize in 1994. In a chair 24/7 since 2009. Mostly have physical problems (no walking) but other than a little MCI (Minor Cognitive Impairment - Is it age or MS?) doing OK. Pain level not great (Neuropthy) but everyone is so different from another on this terrible Journey.
Part of thanks goodness I'm 55, no problems when raising my kids, Thanks goodness it's me and nothing for them but this ride isn't over yet. I hope little else will happen but won't be surprised if it does. My Neuro (Without words really) sees theres nothing he can do for me - no meds, etc. He no longer asks me to get MRIs, we both know I have PPMS and I hate them and so why bother with them? He answers my e-mails within 24 hours and will do most things I ask for if something comes up. I think this thread gets fairly unactive cause there's not much to say.
I think your husband is correct in not thinking and analyzing his journey. No one knows what will happen next. Doctors and others can guess but who knows?