Hello All, Wondering if anyone has taken Dararumamab after relapsing and if so, what type of side effects did you experience and were you able to work? I’m 60 and was diagnosed in August 2017 with renal failure, anemia, and numerous lytic lesions. Achieved remission fairly quickly 🙏 after an agressive CyBorD regimen for 4 months, continued with Velcade and Ninlaro for another 15 months. I’ve been medication free since then. I continued with blood work every three months and for the past 20 months the Kappa Light Chains have slowly and steadily climbed upward and are now at 428. My hematologist/Myeloma specialist and I met yesterday and agreed to continue to monitor once a month and set parameters on the numbers he is most concerned with so that if/when the numbers reach or exceed the parameters, we will have a conversation about Daratumamab treatment. I am feeling good now without any symptoms besides a little fatigue.Thanks in advance!