Hello
I’m just writting this post as lately I have been loosing a lot of weight as my swallow has started to pack up on me and they think I have gi dysmotility and gastroparesis. I was wondering if any one else has a peg or pej tube and if it has helped x
Thanks in advance x
Hi Carrie, I know a lot of folks who use a peg or pej tube, but I’d love to see you avoid that if possible. Did you check out the treatment trial I’ll be starting for our gastroparesis/chronic constipation/delayed gastric emptying? I’d love, love, love to see you respond to this medication! 😉 I also wanted to mention that if you are having swallowing issues, some of us develop eosinophilic esophagitis. Did your docs check for that, perhaps? So sorry you’re going through this. 🙁 It sucks. Been there! Gastroparesis was one of my first symptoms, in fact. It is no fun, FOR SURE. Hang in, Hon… 🙂