a year agoscabby4
I'm doing better the last few months than I have in the last 10 years, and I'm finding the last thing I want to do is pace. I have no idea how many good days I'm going to get and so I'm squeeze every last bit out if them. I know I should pace. I HAD to rest the last 2 days but if I think I can get up tomorrow and go. I will. Damned the consequences. I wanted to give up last winter. I wish I could give you some of my strength.
a year agomewithm.e.inhawaii
Love you Hollis!! ❤️ Thank you for using your limited energy for advocacy.
a year agokellysruta
The entire illness feels like a loss I have to re experience every day to a different degree.
a year agoeagleacupunctureidaho
Hang in there! As a recovered me/cfs sufferer as frustrating as pacing is, ultimately you can and will be able to do more things. 🙌 it is worth it to rest even when it feels endless
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