I posted last week about meeting with my GP. I showed him the pictures and notes I had made with my symptoms. I said I have an open mind but I know something is wrong with my body.
He said it can't be Lupus - I am too young (my sister was my age when she was diagnosed)
Convinced my headaches are migraines ( because that's what neurology decided via a questionnaire nothing else) but they aren't reacting to painkillers and my old headaches used too.
He said my joint pain is probably down to my Psoriasis ( well I would have PA if that's what he is thinking)
My ANA blood test was neg in 2013 so won't do another test.
He started asking about work and if I was stressed ( I have suffered low mood and anxiety in the past) but I am actually great at work and I love it. ( they are fab when I have bad days so they are incredibly understanding as I already suffer from Endometriosis)
I am weak most of the time, constant lightheadness and dizzy. Artificial lighting is killing me at the moment. The joint pain is so bad at the moment but it's just shrugged off. I keep getting a spasm and pain in my leg too. Mouth ulcers/cold sores all the time etc etc. I know something is wrong
I have watched my mum sister and aunty suffer RA. sister Lupus and my aunty with MS - i know the horrible things autoimmune diseases do. I AM NOT IMAGINING THIS.