Living with POTS and EDS is hard, don’t let anyone tell you otherwise. But when I find myself getting angry at my body I try remember all the things it can do for me and not focus on all the things it can’t, for example;
My lungs - despite all the strenuous activity I insist on doing, they keep breathing in and out.
My muscles - sure, they’re way more stretchy than they should be, but hey! I can get from place to place and that’s a good start.
My bones - they don’t break 24/7 and I really really appreciate that.
My joints - they definitely don’t always work but you know what? They’re trying their best, A+ for effort.
And to my heart, you keep on beating no matter what (albeit somewhat irregularly) but hey, an irregular heartbeat is still a heartbeat.
So yeah, this life is hard. But I do my very best to try not to get too angry with my body, of course I still have bad days but it’s not my body’s fault, it’s no one’s fault and all I can do now is try make the best out of a bad situation. So I’m going to try take care of my body the way it tries to take care of me