My POTS symptoms started getting worse again this week, especially in the mornings, so I decided to fork out the money for another IV to see if that once again helps. The woman who started my IV asked if there were any changes to my medical history and then felt the need to say that's good, she hoped they hadn't put me on any more meds because I'm unfortunately already on a lot. Why say something like that? I hate to think what her reaction would have been if I had chosen to start the corticosteroid the neurologist prescribed.

I'm extremely tired today so that hasn't been ideal. But, my mood is still pretty good.