Caused by systemic lupus erythematosus, lupus nephritis is a serious, and relatively common, kidney disorder.
In September, Selena Gomez shared with her fans via Instagram that she had received a kidney transplant due to complications of lupus. The two kidneys are the primary members of the renal system in the body and are crucial in ensuring that:
- waste and toxic substances are removed;
- hormones controlling blood pressure and volume are regulated; and
- the proper levels of fluids exist throughout the body
Lupus nephritis is a common condition, impacting nearly 40% of people with lupus, according to the Lupus Foundation of America. However, the symptoms of kidney disorders are are often subtle and easy to miss. Because of this, it is important to know the symptoms of lupus nephritis and to speak with your lupus treatment team if you are experiencing any symptoms.
Know the symptoms of lupus nephritis? Learn More
24 thoughts on “Lupus Nephritis: 6 Classes of Kidney Disease”
I’m currently hospitalized for renal and pulmonary complications high ANA labs two years straight, inconclusive diagnosis on specific condition with active symptoms need direction
Sorry to hear it! Here is a LupusCorner article on some of the pulmonary conditions that have been linked to lupus or are common complications. The diagnosis process for lupus and other autoimmune conditions is unfortunately quite difficult. Best wishes!
Has anyone with SLE nephritis tried cbd to control symptoms.
Yes/ 10yr Lupus/ I just started using Natural treatments/ Marujaua(any form)cbd for sure/ sea moss (keep it simple w/capsules / B12/CBD oil/ waaaaay better results / nnnnnoooo more pharm meds 4me/ VitC/ ALL pain doesn’t clear but definitely treating EACH symptom one@a time/ STEROIDS ARE KNOWN FOR DEMENTIA GUYS/// don’t be afraid to switch up BUT according to what’s BEST 4YOU…. CAN’T DIE TRYING diff things/ depression TOUGH TOO BUT HEY remembering RIGHT AWAY that YOU THINK YOU’RE DEPRESSED BUT YOU’RE REALLY NOT…. 😧🥺😬😁😁😁😊
I was diagnosed with arthritis in the ER because of positive ANA when I was 16. I’m 23 now and I’m falling apart. I have to urinate every 5 minutes and everyone keeps saying it’s diabetes. I just got an mri back which was specifically for my spine but more than that popped up kidney cysts popped up. Do I have lupus, how do I get my doctor to listen?
You need to go to a Rheumatologist and have ANA test again. Your doctor can take these test also, so you might just ask him to run A good Rheumy, which sometimes takes a while to find, will test your blood in many different ways. Peeing that often is dangerous. Please keep hydrated and get to a doctor. Is anyone watching you glucose and checking you for diabetes. Do you have a regular doctor? If not, you need to find one. Or do you KNOW you do have Diabetes?
You may want to go to a nephrologist and confirm that you do not have PKD, Polycystic Kidney Disease. It can be very serious, depending on how quickly the cysts grow and type one has. It is a directly heritable disease. My mom just had a kidney transplant as a result of the disease. I have SLE, but did not inherit PKD, though both my sister and my niece did. Whenever I hear about cysts instead of lesions or scarring, I think of PKD not lupus.
hi i had surgery on 29th of november 2019, why am i still having complication , like it feel like water movement .. i was given antibiotics for phnemonia and inflammation on my kidneys but it still feels funny but my pain did stop.. it just feels like in my kidney area some fluid is moving..
Was diagnosed over 15 years ago, 4 years ago was hospitalized for 2months with bacterial meningitis in January 2020 had heart surgery, but with all of this and more, I think I’ll kick lupus butt. Once I realized I’ll be In some sort of discomfort for the rest of my life only made it easier.
I am 27 years old and I was taken to the hospital for my rapid spreading vasculitis and dark deep leg ulcers. I have had ANA profiles done which confirmed that I have class 4 lupus. Treatment is to be on prednisone and celcept for up to 2-4 months. I was explained the complications that come with taking both drugs such as osteoporosis, weight gain and eye sight issues. I was also warned against getting pregnant as that could severely affect me and my baby. What can I do while taking the drugs to not affect my possibility of getting pregnant in the future?
I have been on hydroxychloroquin for 4 years now. I carried my baby just fine. I had to do 2 blood thinner shots a day for 7 months and a lot of extra ultrasounds and appointments. I would discuss this possibility with your doctor.
I was on Hydrochloroquin for 18 years. I developed crystals in my eyes. I can no longer use it for my joint pains. I’m hurting so bad now. Make sure you have regular eyes check ups. It’s not reversible.
I was diagnosed with Lupus two years ago. Since then I have this pain ony right kidney that feels like I’m passing a kidney stone , but no stone. The pain comes in waves, like contractions. It is very painful and nothing helps. I don’t have this all the time. Often I will go for weeks, even months without this pain. Then all of a sudden it will start up again, and last for several days. I have had numerous blood test, urine tests and CT Scans. Nothing ever shows up. Any one else ever have this? Any ideas on what it could be? Thanks for your response.
I am experiencing the same issue 😢.
Same exact thing – just happened today! My urologist is no help. Need to speak to my Rhemotologist. Has anyone had an answer to this?i know it’s kidney bc I’ve had stoned and a big surgery 20 years ago on the other side
Look up diverticulitis
I have SLE, was diagnosed at 17, again at 25, I’m now 49. I have right flank pain, I get cysts, they are very painful, I had one burst once, it was like a hot poker shoved in my upper back. Have a doctor check protien and creatinine levels in your blood. If urine is foamy or cloudy with side pain it could be the reason. They can also do an ultrasound for cysts.
I’m experiencing the same thing- Between right hip, and right shoulder blade on my back … it’s driving me insane
Experiencing the same. I can also feel the inflammation in the kidney when this happens. I also have random proteinuria episodes.
I am experiencing the same pain on my right kidney I’ve had blood work X-ray taken CT scans they see crystals there’s blood in the urine my pain gets so intense that I walk holding my ribs . My lower back is so painful but my doctors Or RA dr says there’s just flare ups how can I get my DR to listen to me I’m in so much pain my legs get so swollen my back of the knees feel so heavy or stiff when I walk they think I might of passed a stone but this pain on my kidney is so painful it’s hard to even sleep on the right side how can u get my RA to listen to me that I’m in a lot of pain ? Should I request a new RA dr?
I am in bad pain every day
Hi, I have been struggling with hives and facial edema or angioedema going on 2 years now. My labs come back extremely low on C3 and C4 complements and a low C1Q. The tests have come back a couple of times in the same manner, from my research I have seen that this points to SLE with Acquired angioedema. I am going to see a rheumatologist on the 15th but I have been retaining water at a rapid rate and am quite concerned about this. I can’t seem to stop it. Water pills seem to have slowed it but I am still gaining. Any advice?