HI everyone, I found this wonderful website through an internet search. I've been reading a lot here and decided it was time to post. I was just recently diagnosed with POTS. I had laproscopic surgery for endometriosis at the end of June and my symptoms started in early July. Thankfully I was sent to a great cardiologist who suspected right away it was POTS, so I was diagnosed only about two weeks after symptoms started. I'm really struggling with this illness, as it is all new to me. I have dizziness, nausea, tachy, sleep problems, blurry vision, tingly sensations, brain fog, and extreme fatigue. I am on a high salt diet, lots of liquids, compression stockings, Midodrine and swimming for exercise (when possible). I know there are some folks here who are far worse off than I am, but I am still struggling. I feel like my life has changed overnight and things that I used to take for granted are now far out of reach. I am grasping for any straw of hope, to help me get through this. My cardio said that 80% of folks who have sudden development of POTS get better within a year. I have read differently in some posts here, so I know that is no guarantee. I don't know if I need to hope that it will go away or just focus on getting through each day. I just feel lonely, scared and discouraged. Every day is so long and such a struggle to get through. I have to continue working to maintain health benefits, which is tough. I know I need to find and maintain a positive attitude and I just don't know how to get there from here. Anyone have any suggestions? They would be much appreciated!