ME/CFS
Outcome unclear
ME/CFS, sleeping about 12 hours a day to function
- Condition
- ME/CFS
- At worst
- Not stated
- Ill for
- Not stated
- Last post
- Jan 2023
Read from 1 of their posts and comments; links to the one this page draws on
Summary
Horizon 42411 posted in r/cfs in January 2023 asking whether sleeping about 12 hours a day was acceptable with CFS. They said that getting about 12 hours of sleep was the only way they could at all function during the day. They gave no account of when or how their illness began, no other symptoms, no treatments and no change in their condition over time.
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Symptoms mentioned
Their words about their symptoms
- Sleep problems
The only way I’m able to at all function during the day is if I get about 12 hours of sleep.
In context ↗