the title of my blog isn't to be funny but i feel like im "it" because im the first one in my family to get lupus. usually this illness is passed down by someone.
I'm so tired of dealing with Eeyoore Days. I want to be able to live again. Just when things start to go right again something goes wrong. It's so totally not fair.
I was just thinking that my mood swings are getting worse. I probably need my hormones adjusted again. I need to get hyper so I can do. Of course it's not going to happen the endo wouldn't allow it. Nice thought though. I just need to push through the pain and start doing. I've been letting my body shit down and
was recently diagnosed with discoid lupus. can anyone give me a website that discusses discoid lupus in detail? all the web pages that I have found discuss SLE in detail....I am just wanting to know what I am in for Other than loss of hair, constant blood work, scarring and fatigue. Any help or suggestions are greatful
Yea its the same old worn out saying among people with lupus, but I just wish I wasn't so tired all the time. I want my life back!! I was 13 when diagnosed so 7 years later at 20 i'm stuck in a limbo of sorts because i'm not feeling well but i'm not in a relapse. Even though I have complained my doctor just keeps writing it off as me being crazy. It's been over a year since I had to drop out of college because I just got too sick too keep up, I miss it and I don't know what to do anymore when
Hi My name is Tabatha. I have recently turned 41. I was diagnosed in 2002. Since that time, I have gone thru a series of doctors. My concern is I have been diagnosed as having Lupus by positive ANA and other tests. I have some symptoms, such a chronic fatigue, swelling of joints, legs, hands and feet. Chronic pain and deep depression. I have no signs of organ failure, including heart and kidneys, I only get a very light rash on my cheeks from time to time. But, I do have the headaches, dizziness,