Explore Over 11,000+ Conditions, Medications, and Symptoms.
Get a personalized feed by signing up for free.
All Conditions
Systemic Lupus Erythematosus (SLE)
by Alike Medical Team ∙ Updated on June 13, 2023
This group contains additional names: - Lupus nephritis
Systemic lupus erythematosus (SLE) is an autoimmune disease in which the immune system attacks its own tissues, causing widespread inflammation and tissue damage in the affected organs. It can affect the joints, skin, brain, heart, lungs, kidneys, and blood vessels. There is no cure for lupus, but patients that get proper medical care, preventive care, and education can significantly improve function and quality of life.
1278 people with Systemic Lupus Erythematosus (SLE)
People with SLE may experience a variety of symptoms that include fevers, fatigue, skin rashes, sun sensitivity, oral ulcers, hair loss and pain or swelling in the joints (arthritis). Internal organs may also be affected by SLE, and cause lung problems, heart problems, kidney problems, seizures, psychosis, and blood cell and immunological abnormalities. Symptoms of SLE tend to appear as flares, followed by a period of remission (lasting from weeks to years).
Lupus can be hard to diagnose because it has many symptoms that are often mistaken for symptoms of other diseases. Diagnostic tests may include: - Medical history and family history - Complete physical exam. Your doctor will look for rashes and other signs of SLE. - Blood tests, including complete blood count, blood chemistry and typical SLE antibodies. - urine tests - Skin or kidney biopsy. A biopsy is a minor surgery to remove a sample of tissue. Skin and kidney tissue can show signs of an autoimmune disease.
Treating SLE often requires a team approach because of the number of organs that can be affected. Several different types of medicines are used to treat SLE. Commonly uses medicines are Nonsteroidal anti-inflammatory drugs (NSAIDs), Corticosteroids, Antimalarial drugs (Hydroxychloroquine) and immunosuppressive drugs that inhibit activity of the immune system.
☝ We provide information on prescription and over-the-counter medicines, diagnosis, procedures and lab tests. This material is provided for educational purposes only and is not medical advice, diagnosis or treatment.
National Institutes of Health ∙ World Health Organization ∙ MedlinePluse ∙ Centers for Disease Control and Prevention
☝ All information has been reviewed by certified physicians from Alike
Instantly get answers to medical questions with our AI, built from the collective wisdom of our community facing similar experiences
Several people in the discussion have shared their experiences with frequent low-grade fevers or feeling feverish without an actual increase in body temperature. Some individuals mentioned that they have conditions like IBS, SIBO, **Lupus**, and fibromyalgia, which might be related to their symptoms. However, none of them specifically mentioned having a fever of unknown origin (FUO).
It took me a while to figure it out I've been having joint issues for going on for 12+ years. I was told i had fluid behind my knee caps then runners knee. Then finally earlier this year I had the opportunity to get a bunch of blood work done that ruled out, RA,**lupus**, etc. The NP I was seeing wanted me back so we looked at a few more things before she officially diagnosed me.
"Yes, **lupus** got easier for me, but it took some time. When you’ll know which medication works the best for you, and what you should and shouldn’t eat, things will start going the right way." Another person shared, "Physically for me, it did. When I first was diagnosed I couldn’t walk, constantly cold and hot at the same time, lost my appetite completely, my lowest weight was 84 lbs, hair was shading off, skin was damaged. But now it’s been a year and now I can say with the help of some of my medicine, my hair grew back but it’s still fragile, my skin got a bit better but there seems to be permanent discoloration, I can walk and I even have a physical job now, and I’ve gained my natural body weight back."
Dealing with a New Lupus Diagnosis: Will the Pain Ever Improve?
Struggling with Chronic Pain Flare Up
Newly Diagnosed with Lupus, Seeking Advice on Seizures
Alike is a transformative platform that goes beyond just bringing together patients; it meticulously connects individuals based on multiple critical factors, such as age, gender, comorbidities, medications, diet, and more, fostering a community of knowledge, support and empathy.
© 2020-2024 Alike, Inc