I know my fatigue is not as awful as many of my MS family, but I really hate the mind-numbing effect is has on my brain. Seriously. I have to take usually one day a month to stay home and do NOTHING all day. And I mean NOTHING. Getting out of my recliner to pee or eat is a chore. I don't even watch anything enlightening on TV, just daytime crap. Although, a paternity results show on Maury can be entertaining in a demented way.
Here's the other thing I hate about the fatigue. People who don't have MS don't get it. They will say something like, "Oh yeah, I get so tired, too!" The only non-MS person who doesn't piss me off with those statements is my friend who has nine kids and has a business out of her home. Just thinking about trying to live a day of her life makes me tired!
Do others have a difficult time describing their fatigue to people, especially their partner?
2 hours ago