Hi guys! I'm Kayla, I'm 22. I just joined the site a couple of days ago, but I was diagnosed with dysautonomia (nothing more specific, but I'm fairly certain it is a combination of NCS, CFS, IBS, and possibly fibromyalgia) back in May. I had symptoms for a while before seeking treatment, but things didn't get really bad until September-October. Anyway, at the moment my symptoms are largely uncontrolled. I take atenolol to control my heart rate, midodrine to help control my hypotension, and I just started IV saline infusions last week. At the moment I'm on 1L of normal saline infused over the course of 1 hour, Once per week, as needed. So, my question is this: Do any of you guys have any experience with saline? I've been researching a lot, and from what I've read it sounds like it's most beneficial for patients to have nightly infusions, generally over the course of about 8 hours (although I'm not certain how many liters that is). My long term goal is (if it helps) to get set up with daily infusions, at home, through a cathport so I can do them myself. So, how often have any of you gotten it? How much? And what type of saline? I've also read about the "Dysautonomia Cocktail"? Any experience with that? And most of all, was it worth it? I felt pretty good after my one infusion, so I'm hopeful I can get back to semi-functioning.