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Hi all, I was recently diagnosed with EDS. I think I might be once again experiencing gastroparesis. Everything I eat slowly regurgitates back up I cannot keep much of anything at all down. I'm super bloated, constipated and in a lot of pain. My GI specialists aren't listening to my concerns and i'm having a hard time getting a hold of my rheumatologist. I'm just curious what you guys do when you have gastroparesis or is ita worth going to the ER at all? I feel like the ER isn't going to do anything to help, but im in a lot of pain and can't eat. TIA
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