Rich, you need to delegate a bit more - couldn’t Scott help you out?
Great news on the results, that’s a big positive and a weight off your minds, but more tough stuff is still to follow.
You were so right in one of your earlier posts about men often looking for practical solutions, coming up with the answers, getting on and doing things in the best engineering spirit, and I can see how that can be a potential cause for disagreement and lots of feelings of powerlessness for you. But your description of how you are with each other sounds deep and strong. Waiting is SUCH a hard thing to do, but sometimes there are times when sitting back and letting “the powers that be” get on with it is actually the quickest way to get to the end point. (Until they put the brakes on of course, in which case a bit of assertive communication keeps them on track!)
As treatment progresses you may find your lovely wife needs a bit more support to do “stuff”, so if you can, step back and let her keep control of things until she needs you to take over, and be ready to relinquish control again when she’s up to taking back what she sees as her role.
Nice things like unexpected treats might be welcome (the odd bunch of flowers won’t do any harm, I’m sure, or could you ask her if you can cook a romantic dinner, candles, table cloth, chocolate dessert of some kind, if you’re ok in the kitchen? I don’t know a woman who doesn’t like being treated like a princess every now and again - still have to persuade my OH of the idea!)
I think it might be because we feel so much as if control has been taken away from our lives by the disease, we don’t want any more of it to be taken away from us.
Oh, I’m sure you’ve got a much better picture of what works for the two of you, so just ignore any of that if it doesn’t fit. As for support for me, the lovely people on here are FANTASTIC! and it’s that kind of emotional support that I think I value as much as people offering me lifts to places. (Though of course people saying they’ll have the kids overnight while I’m having surgery is always a good thing, and very valued.) And after my first surgery (WLE and SNB) my lovely man let me stay at his house, and he just left me to sleep, occasionally interrupted by questions of whether I needed any food, drink or painkillers. Just what I needed.
Keep smiling if you can,
CM
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