Does anyone else also have R-CPD (Retrograde Cricopharyngeus Dysfunction) and feel like it makes their GP worse? The bloat and pain is so bad all the time with the gas having nowhere to go. I have to drink tea and blast my heating pad to get gas out the other end for any bit of relief.
Does anyone else get their vagus nerve triggered when pooping? Not all the time, but occasionally when I go, I’ll start to get a little woozy, nauseous, a little faint or flush and sweaty. It usually happens if I haven’t gone in a while which is all the time, but it’s usually a 50/50 chance I get triggered by it.
I don’t really get much pain from gastroparesis, mostly unbearable nausea on and off all day. I do get some pain with bloating and stomach dissension, but at the moment I do have a stitch in my side kind of pain, specifically my left side. Does anyone get this?
So I was finally diagnosed last week. I was able to eat for the most part, though a bit limited too due to also having gastritis. I’d get really sick a few times a week, no vomiting, but severe nausea. That’s not new to me. Anyways, I got diagnosed and since then, I just can’t really eat at all. I don’t know if I’m in a flare up or if it’s my anxiety and I somehow mentally shocked my system or what, but I’m pretty much living on apple sauce, baby food pouches, liquids like water and Gatorade and the occasional crackers here and there. Even when I am “eating”, it’s making me feel sick. I haven’t been taking the diagnosis well. I really didn’t think I would have this so I wasn’t expecting to go into my check up with my GI and being told I had a decent amount of delay in my gastric emptying study. I don’t know maybe I’m just stressing my body out. It’s hard to talk to my family about it when I’ve never been one to get all down with my feelings to them. I’m just having a hard time.