Does anyone else get anxious prior to important appointments with your rheumatologist? I feel my appointments are like my Mt. Everest. I am always wishing I could explain every symptom and pain to my doctor as it happens in real time so I try to remember and when I finally get to my appointment, I have so many things to say and so many different areas of concern that I end of feeling like I never quite get my point across like I had intended. I feel like there are so many things to cover and so many different flares and symptoms that can occur over a 6 month period that I always leave and get home and say, “Man, I forgot to mention that one thing.” My anxiety starts to build the week of my appointment up until I actually get there and my blood pressure is through the roof with worry and anticipation. I want to be able to really explain how I feel and am so used to no one understanding that I hardly ever speak my truth regarding my pain so it’s almost foreign to be totally open and honest about how bad you truly hurt. I just realize I am putting a lot of pressure on each appointment because I’m so desperate for relief but without the proper communication with my doctor, I leave and always feel I am not quite being heard (mostly because I struggle to remember to mention every single symptom I’ve experienced over the past 6 months because there are so many). Any advice on communicating with your rheumatologist? How to feel heard and how to really explain the depths of the pain? And how to not build up so much anticipation that it always feels like a make it or break it situation? I’m sure others have experienced the same doubts and questions regarding doctors visits and would love to hear some feedback/advice/suggestions. Wishing everyone in this community a happy pain free day and appreciate all the knowledge and support I always find here.