This is an event I am really going to need your help with. I want to collect a series of videos (which I’ve mentioned before in my groups) showing people what living with Gastroparesis (GP) is like. I thought it might help someone else who may be newly diagnosed, who might know how to tell their family and friends they have GP. Not only that, but I want people to see how different GP can be from one person to the next.
to Mar 11
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