I have written this before but my computer crashed, the thing is that due to medical neglect I'm going to start consuming fludrocortisone (brand name florinef) to treat my ME/CFS related POTS (diagnosed unequivocally by a ppositivetilt table test), since no doctor knows or is willing to treat me. I got good results using pseudoefedrine on my own, which is a vasoconstrictor, so I spect that the most commonly prescribed drug for POTS which is also a vasoconstrictor, will help me even more. I can't stand this no more, I´m control of my treatment. I've already bought the fludrocortisone pills, and I´m completely determinate to take them, but I´m afraid of the risks. Is anybody familiarized with this drug or has any advice on how to minimize it risks? Thank you!!