@Elephantino Well, then I hope work does exactly what you need it to do. And that stuck feeling, at least in my experience, is so normal. The world will slowly pick up speed again, with you in it. OH! And here's that BBC article on the medieval sleep pattern: www.bbc.com/future/article/20220107-the-lost-medieval-habit-of-biphasic-sleep
@bloodywhitecat Oh no. I can't tell you how sorry I am to hear that. I don't blame you for being terrified. Cancer is a right bastard, always. I really do realize how lucky I am to have the time I have left, even if my symptoms are progressing, especially when I know there are people like your husband facing situations like you're facing right now. I'm sure the thought of waking up tomorrow is scary, not knowing what it will bring, and fearing more bad news. You already faced the cancer. Then the stroke. Then the news that the stroke has ruined the chances of treatment. I don't know if this will help you, but my therapist tell me to take 5-10 minutes in the morning and take either a journal or just do it in your mind if you want, and let yourself give in to it. Let out all the worry and anger and everything. Think of all the worst possible case scenarios. Get mad or sad. And then, I think it's most useful to write them, because then, you close the book and put it in a drawer. It doesn't mean that you won't think of them at all during the day, but know that you (have tried to) put them away for the day so that you can live and enjoy the day with your husband as much as possible, with the time you have left. And I'm not pretending even that will be easy, with how scary it all is, but it might just be something worth trying. You don't need to buy anything new - you can even just right on spare paper, and keep a stack of it in the drawer.
@LovelyYellowLabrador Maybe get a piece of paper and start making a plan? I'm all for thinking, especially at this time of night, but there's also a lot to be said, for having a list of the direction you want to take when the sun rises. If there's a million ways to change it, could you do one in the next week? Five? Ten? Or are they all big changes? Regardless, I wish you the very best luck, and hope they're all good changes.
@weegiemum I know exactly what CIDP is actually! My grandmother had a different form of polyneuropathy and she ALSO had IVIg. Small, small world. That's an incredibly tough disease, and I'm so sorry to hear that you're living through it. I hope you find ways to find special bits and humor in your days, still, even with the pain. I'm also so sorry to hear about the shortage, especially when you need it. I haven't experienced it, maybe because I do it subcutaneously, because if I do it through IV, I get aseptic meningitis (have had it three times now, because they tried: original try, tried more slowly, tried a different brand). But I have to administer it to myself once a week (not much fun sticking four needles in my legs). Good luck, and I hope sleep finds you soon.