I wasn't diagnosed last Rare Diseases Day, so I really wanted to grasp the chance to talk about my Takayasu's Arteritis with you on my blog. I've mentioned bits and pieces here and there like on Instagram or my Youtube Channel, but here I'm going to go into what Takayasu's is and what that means for my daily life. I also have a selection of other Diagnoses which affect my treatment and flares, so I may talk about that a bit as well. I don't want to go through my story again of how I was diagnosed as it was pretty intense, I did film a video explaining it all before I was officially diagnosed that you can watch, My Doctor Didn't Believe Me. I will also be making a video specifically about the scans I had to diagnose Takayasu's if you are interested, subscribe to my channel.
This is officially my 100th post on here (though I have privated a few older posts recently, but it counts) and I don't know what to do with it. I thought maybe a general life and health update, I haven't done one of those in a while and things are pretty different. A lot has been happening.