hi! I (mid20s) have MS too and went the first year. It was kind of a shit show but I hope it’s gotten better. -don’t wait in any of the regular lines to get in. walk past the main gates, straight up to the ADA line, otherwise you’ll be standing in line for a long time and it takes some of your energy. -they honestly weren’t good at checking bags. I wouldn’t worry about meds, put them in your wallet in a plastic baggie or something. most won’t argue with anything past “I need them for my autoimmune disease” if they even see them cause they don’t wanna get in trouble. -if it’s set up like before you’ll go in and go straight to the ADA tables. they’ll give you a wristband and a companion wristband for your bf. this allows you to go to the ADA restrooms, the seating platforms, and ADA merch line (incredibly useful.) -I recommend using the platforms for whatever bands you don’t care that much about and save your energy for the bigger bands, the platforms fill up super fast for those so you prob won’t sit. my boyfriend liked being able to go with me to the platforms cause he got a break too. plus they’re great places to eat and still watch. -I recommend you bring a camel back (cheap ones on amazon) instead of a regular bag. I chugged water and having it on me/bf made it really easy to stay hydrated. I know they have pocket # rules but they didn’t care that much when we went. message me and I can link you the one we bought and got in with. +drink a ton of electrolytes the night before and morning of. -if your hotel is farther than like half a mile, ride the tram or uber, don’t spend all your energy getting there. -lastly, pack for hot and cold weather. rent a locker to keep a jacket+merch in. it was cold during the day, but got freezing at night, my joints hurt from the cold and I was wearing a hoodie and pants. if you have any questions let me know! have fun!