Morning all! I hope you are all okay during lockdown.
I have had joint pain for almost the entirety of the time I was diagnosed. My joints are usually quite puffy. The drs gave me an ultrasound and found no or hardly any inflammation so they don’t think the lupus is attacking my joint so more immunosuppression will work (they did put me on more immunosuppressants but it ended up oversupressing my immune system.
I was put on amitriptyline for PHN and was told that it can also help with joint pain. I just went on 50mg yesterday, I wanted to know has anyone had any experience with this drug for joint pain? And did your joint appear swollen but no marked inflammation?