I am diagnosed with SLE. I took Cellcept from June 2025 through September 2025, and auto injected myself with Benlysta from September through April 2026. , It did not work because I found out I have a lesion in one of lungs. I received two Rituxan infusions which is really for cancer and not approved for Lupus, however in trials it worked for some patients. None of these treatments has worked to help with swollen joints and the pain.
Learn more about the drug treatment mentioned above.It's genuinely frustrating to have your blood work looking relatively normal while your joints are still swollen and painful. Normal complement and anti-dsDNA levels are encouraging signs, but they don't always tell the full story — lupus joint pain can persist even when those markers are stable.
Here's why joint symptoms Show Full Answer
I just had a full list of blood work done, I haven't had ANA done in 3 years. I had some issues from March labs so I talked to my doctor for more blood work, ANA, Thyroid and others. I have a never ending flair for a month so I have mu results. Lupus antibodies are up parathyroid dropped more in 10 days, calcium is up. Now I'm waiting to see a endocrinologist, But I'm still dealing with joint pain,stiffness and the flair could be aggravating my osteoarthritis and I have severe osteoporosis. Steroids are not a option for me because of the other health issues I have, I had steroid shots years avo for SI joint pain. It didn't work except I put on 35lbs and that made things worse.Praying everyday to get through each day and trying to keep positive. God Bless