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Gastroparesis stories
I was diagnosed with GP in 2011 but was not helped for 4 months and it landed me in the hospital for 3 months until finally I was put on TPN and Got a feeding tube. I am now on TPN through a port. Which gives me so much more energy. I have severe Gas...
Views: 1185 by Bailey
I have gastroparesis, pelvic floor dysmotility, and chronic intestinal pseudo obstruction disorders. I have an ostomy, a g tube for decompression, and a j tube for nutrition. I love fashion, ballet, yoga, and running! I also love my family, hot tea, ...
in a nutshell, I've had GP for three years. I've lost heaps of weight. Been tube fed now over 2.5 years with various nj, j and pegs. Many problems with all of them and my first J nearly killed me perforating the bowel and turning me septic. Suffer fr...
I was diagnosed with Gastroparesis 2 years ago after having a year of pain and test after test. They decided my gallbladder wasn't working they removed it and things got worse. I am no appetite. I could go days without eating anything or maybe a few ...
Views: 924 Dec 18, 2015, 2:11 PM by Annette Sirmans
Nicola, Aged 6yo. Had since birth. Jejunostomy tube feed.
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