I’ve been dealing with Lupus like symptoms for just over two years with my most recent flare kicking off in September. I’ve seen doctors and I still don’t have an answer. My GP ordered an ANA and since that came up negative she refuses to investigate lupus any further. Has anyone had any experience with an early negative ANA? Did you end up being diagnosed with Lupus? I have many of the symptoms of lupus including visible signs such as butterfly rash and scleritis. I also get pain in my legs and arms, muscle twitches and spasms, low grade fever, frequent urination, hair loss, pericardial effusion, jaundice, iron deficiency that needed infusion. But worst of all is the unending and unbearable fatigue and brain fog.