So if anyone wonders, yes, this is what it is like for me, though, I suspect I usually start out the day with a few extra spoons than most living with lupus and fibromyalgia, and today, I am borrowing against tomorrow's spoons already.
So if anyone wonders, yes, this is what it is like for me, though, I suspect I usually start out the day with a few extra spoons than most living with lupus and fibromyalgia, and today, I am borrowing against tomorrow's spoons already.
.
From:
no subject
I'm sorry to hear it.
From:
no subject
I've had about 11 years now to learn how to manage it, but I'd still say the hardest part is dealing with friends who get upset with you because you can't always go out at a moment's notice.
From:
no subject
From:
no subject
From:
no subject
edit... I suppose that the type of spoons may be different for "physical" and "mental" chronic illnesses but the outcome is the same.
From:
no subject
From:
no subject
Hope life throws in a few extra spoons for you. :)