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Autistic Ang's avatar

Thanks for sharing this, it really gave me a glimpse into the daily grind of living with ME/CFS. I can’t even imagine how exhausting and frustrating it must be to constantly push through, only to feel like you’re getting nowhere. The part about how lockdown didn’t change much for you made sense. Most people just don’t get what it’s like to live with those kinds of limits all the time. It’s tough to keep going when your body is working against you, but your resilience really shines through, even on the rough days.

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