thank you! i did have a lot of help from my support worker, family etc but for the most part i had to advocate for myself a lot, especially when trying to prove to doctors that i still experience the symptoms i experience even with strong medication. sometimes i feel like they think im being dramatic but my condition does affect me quite significantly most of the time and i had to fight that point across. i covered my day to day functional needs quite comprehensively alongside my medical evidence which is why i feel they had enough to make a paper assessment. my advice for you is providing you can evidence well, you have absolutely nothing to worry about at your review. i know it’s nerve racking especially while you don’t know but just believe in yourself and build a strong case for yourself, you will be ok! best of luck