How do we find a doc to help us find te CAUSE of pOTS symptoms...I feel like I've been playing whack a mole of symptoms for 7 years! I control most with salt and fluids. I now have neuropathy (pins and needles) in legs and feet..... And still times of painful slow gastric emptying. One doc thought this was caused by low cortisol and rec. Cortef (hydrocortisone)...before I knew I had POTS and my symptoms took a downward spiral straight into a year of ****......ER visits, Dysautonomia clinic in AL, MAYO and tons more neurologists etc. question: if I had low grade pots (dizziness, dehydration and slow gastric emptying) and the CORTEF ruined me....any idea why? Thank you for your time.