Chronic Fatigue Syndrome / Myalgic Encephalomyelitis

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The original was posted on /r/cfs by /u/crunch1227 on 2024-08-08 12:19:45+00:00.

Since being officially diagnosed ~3 years ago, I get less and less excited about plans. When I was initially dx’d I still tried to push myself to enjoy life and defy my diagnosis because I’d coped for long enough already.

I now actually panic about having plans and definitely don’t look forward to them because I know how tired I’ll be afterwards, even if I have a nice time.

It’s frustrating because people are inviting me to be part of important events in their life but I just feel like this.