When I first got severe myalgic encephalomyelitis (ME), I absolutely hated all the time I had to spend in bed. It’s been two years now, and I still have to spend a large percentage of time in bed.
But I’ve found some ways to make it less tedious, and thought I’d share them with anyone in the same position, whether through ME or another condition.
Some of the suggestions might be beyond your capabilities, and I know how depressing that can be. Personally, I find it very hard reading about people with mild ME and their tips that are beyond my reach.
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