that's how dr's are when they aren't familiar with ANS problems - look on those links I gave you and see if you can find a dr near you that may be able to help; if not make a post and see if anyone can recommend someone in your area
it may take some work & searching, but once you find the right dr hopefully they'll be able to help with the right treatment
I still have a ton of unanswered questions about my TTT & testing since none of the things they've had me do or meds have helped in the past 14 months or so
Hi,yea i guess i will request a full copy of all the test i have done.Thats wat i have been told too by others who suffered the same thing that,sometimes even the specialist,cardiologist could not see this as POTS or so,most of the time they would have a listen to ur heart,run an ECG and if its normal sinus rhythm or sinus tachy,they would just said its anxiety.
I am also tired of going from one doctors to another,ENTs to Endo to neurologist and cardiologist,most of the time felt like being pass to another specialist,sigh.Sometimes i actually dont know wat to tell them when i met the doctors,as they keep saying ecg is fine,so is blood and ur just anxious.And also because my tilt table test dint not show BP drops through out the test,the cardiologist was quick to say its anxiety even though heart rate 90s suddenly race to 130s.
I would get a copy of all of my tests regardless if you go to another doctor, it's always good to have them.
Just reading over what you said - could be POTS 90-130 can be a definition of it but it could be other ANS related stuff also. You have symptoms of POTS patients, have you went to the dysautonomia forum and read there? Alot of us have mixed disorders and seem to cross over into other disorders/diseases.
I was told my problems were stress/anxiety related for years and that wasn't the case - that's the "I don't know" catchall cop out dr's use when they don't have a clue.
I would take my test results and a symptom log and try to find a doctor who deals in or has knowledge about autonomic dysfunction - in the DYS forum there's a list as well as on Dinet. org (D I N E T . O R G) which can take many years for some to get a proper diagnosis - for me I fainted since age 9 but it took a dr until age 42 to take my fainting seriously.