Riding the Roller Coaster
Let me just say that I am realizing that Ehlers Danlos and POTS are such weird disorders. There is so much inconsistency with how they affect me day to day. Last week was such a better week for me. I didn’t need my cervical collar as much, it felt like my meds were really doing a good job controlling the POTS, and I was able to rehab with much more stamina. Then Sunday and Monday came and POTS and EDS decided to hit me like a ton of bricks. My joints felt so loose and I had to use my wheelchair again. Sigh.
I keep saying I just don’t understand these disorders. I have kept journal after journal trying to pinpoint patterns so I can try and predict good days and not so good days. So far these are a few of the patterns I have been able to find…