Well, I am finally going to introduce myself to the forum. My name is Sarah and I am 26 and live in a very rural area of West Virginia. I was diagnosed with POTS in November 2004 followed by an agreed diagnoses from an EP in Feb 2005. Along with POTS, I was also diagnosed with SVT, Arrythmia/Disrrythmias and ARVD. In March of 2005 I was discharged from the military and subsequently lost all of the current treatments because I had to move back to WV. Since then, I have had some trouble finding any doctors who are familiar with POTS. I was recently hospitalized because of a 2nd heart attack and had another Echo done, this echo came with the diagnoses of Cardiomyopathy and Paroxysmal Tachy, as well as an EKG which told us that I have silent Ischemia. I have been getting treatment at our local VAMC, which has been fair, but I haven't seen a cardio since last year, and can't get in to see one until next month. So I am pretty much just sitting around waiting, and it is frustrating. I am on 100mg of Atenolol (50mg 2x a day), but since the heart attack 3 weeks ago, my BP was so low that now I have to check it 2x a day before I can take my heart meds. I was prescribes propanolol for the Arrythmia, but I didn't care much for the Cardio at the hosp who prescribed it. He met with me for about 10 minutes, completely seemed to dismiss the idea of POTS and just didn't seem to care, so I am waiting to see my doctor before starting any new medications. Well, I hope that I haven't rambled too much, and if anyone has any opinions or advice, please feel free to tell me. I need all the help I can get from people who know what this disorder does. Things just seem to have gotten worse over the past 6 months and, as all of you know, it is hard to function some days. So I hope everyone is doing well.