Formerly joined a forum dealing with dysautonmia. Response was that yes, my symptoms definitely suggested a possibility. (Exhausted frequently, had been diagnosed (RVH) with PLMS (111 day and 122 night) in 1993, together with slow and shallow breathing (HYPOPNEAS which imitate OAS) but later CPAP for 2 years made things worse as breathing OUT was restricted! Had been described as "a fainter" in adolescence. (Not Jewish.) Still unsteady when stand up if do not breathe consciously beforehand. Still get near to fainting when in pain and call 911. It was suggested I take salt and drink lots more water. Now heart Dr. says to reduce salt! Never thirsty. Always, even now at 86, low BP, low temperature. Bloods always A1. 2 year exercise program has helped automatic deep breathing when exercising. Used to get breathless half way up a SMALL hill. PLMS seems to be controlled with 500 calc + 500 magnesium. Dysautonomia as an orphan disease is unknown to my medical people. Fragmented sleep (stage 1 and 2 only and REM without atonia) is my main exhaustion problem. WHAT DO YOU THINK? IDM
Any help on how to treat POTUS?
I also have inappropriate sinus tachycardia. Fatigue. I wonder about adrenal dysfunction.