Dealing with EDS in College: Advice Needed

Thanks for all the feedback everyone! Sorry I havnt been responding much. To elaborate further on the stomach issues, my abdomen is tender to the touch. It's been a month of doctors appointments. I just had my preop appt. Today as they will be doing an EGD in hopes of finding the source of the pain

The majority of us have stomach motility issues. Some of us including myself have compression syndromes of the GI because of EDS such as SMAS, MALS and nutcracker. These symptoms are more disabling than motility. But Gastroparesis is the most common, rapid gastric emptying is a secondary motility disorder often overlooked.

2) I don’t have gastroparesis, but I have it’s opposite twin. I have enhanced gut motility, which is hell in its own way

1.) I will be starting college this fall as well but ive been diagnosed for years. You 100% should look into and disability services your college has to offer. 2.) Absolutely also check out gastroparesis

1. Get a mobility aid. I was SO TIRED from walking to and from class I couldn't even focus on my school work. 2. 10000% yes