inahaze3

Hey I just wanted to add to Katies comment. I to have the same problem, i had a lot of smae symptoms...they pain i would get after eatting was unreal..it hurt so much that i grew to dislike food bc i knew it would make me sick or have the worse pain ever...doctors would ask me if its all in my head..or making it up for attention which would get me soso mad...

Hi..I have been diagnosed with SMAS 4 months ago and my symptoms aren't getting any better...I'm not myself anymore and I fell bad being a burden to my family a friends when I have an episode and can't do anything..my uncle who is a doctor wants me to go to another doc. and see what he says...I want to pin point my problem but those 4 months of test and operations...