https://lupuscorner.com/monoclonal-antibodies-the-immune-system-and-lupus/ Health Info on Lupus Symptoms, Treatments & Research Mon, 15 Jan 2024 22:55:22 +0000 hourly 1 https://wordpress.org/?v=6.2.4 https://lupuscorner.com/monoclonal-antibodies-the-immune-system-and-lupus/#comment-314903 Mon, 15 Jan 2024 22:55:22 +0000 https://lupuscorner.com/?p=5570#comment-314903 I have been diagnosed with an autoimune disease but i have a lot of symptoms related to lupus. They keep doing blood work but it isn’t showing up. Yet they diagnose me with. so many other things such as gout, fibromyalgia, Pshoriatric arthritis, RA. I’ve tried to get a second opinion but I am left more confused because they say there is nothing wrong. I feel horrible and the flares are dibilitating.

]]> https://lupuscorner.com/monoclonal-antibodies-the-immune-system-and-lupus/#comment-314181 Fri, 12 Jan 2024 14:10:18 +0000 https://lupuscorner.com/?p=5570#comment-314181 I have progressive peripheral neuropathy for past two years. Diagnosed as auto immune. I have mild lupus with only symptom; inflammation of the hands. Seeking treatment. Has anyone tried IViG?

]]> https://lupuscorner.com/monoclonal-antibodies-the-immune-system-and-lupus/#comment-314182 Fri, 12 Jan 2024 14:10:18 +0000 https://lupuscorner.com/?p=5570#comment-314182 I have progressive peripheral neuropathy for past two years. Diagnosed as auto immune. I have mild lupus with only symptom; inflammation of the hands. Seeking treatment. Has anyone tried IViG?

]]> https://lupuscorner.com/monoclonal-antibodies-the-immune-system-and-lupus/#comment-314184 Fri, 12 Jan 2024 14:10:18 +0000 https://lupuscorner.com/?p=5570#comment-314184 I have progressive peripheral neuropathy for past two years. Diagnosed as auto immune. I have mild lupus with only symptom; inflammation of the hands. Seeking treatment. Has anyone tried IViG?

]]> https://lupuscorner.com/monoclonal-antibodies-the-immune-system-and-lupus/#comment-63033 Fri, 04 Jun 2021 02:35:38 +0000 https://lupuscorner.com/?p=5570#comment-63033 I have been diagnosed for 35yrs. I was allergic to the drug of choice which was Plaquenil, so steroids and anti inflammatories were used, I now take Rituxin, mycophenolate,Gabapentin,and others that are more to deal with the effects from lupus not to control it.

]]> https://lupuscorner.com/monoclonal-antibodies-the-immune-system-and-lupus/#comment-54851 Wed, 21 Apr 2021 05:53:13 +0000 https://lupuscorner.com/?p=5570#comment-54851 My Wife is getting treated with Plasmoquinine and side effects are terrible. nausea, dizziness, muscular pain. What can you suggest

]]> https://lupuscorner.com/monoclonal-antibodies-the-immune-system-and-lupus/#comment-54480 Sun, 18 Apr 2021 19:30:22 +0000 https://lupuscorner.com/?p=5570#comment-54480 I have every single symtom for Lupas but having a very hard time getting diagnosed. Are there any studies that involve diagnosing and monoclonal antibody treatment?

]]> https://lupuscorner.com/monoclonal-antibodies-the-immune-system-and-lupus/#comment-54009 Sat, 17 Apr 2021 05:10:01 +0000 https://lupuscorner.com/?p=5570#comment-54009 Is the side effect. The same as haveing lupus? Or worse? Have studies been done?

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