Hi all, I'm just a month into my MM journey, and have started on infusion therapy a few weeks ago. I was glad to see the 55 and under group. I'm wondering if anyone here has gone through talking to middle-school aged children about your diagnosis. I have 2 boys - ages 10 and 12, and thus far I have been pretty vague about what I'm going through and just said I have a "blood disorder I'm getting medicine for." I will have an autologous stem cell transplant this summer, so I clearly need to have more of a conversation with them before then. Wondering if this group has anything to share. Thanks!

As I have diabetes and excess weight in addition to MM, I'm curious about the weight loss drugs. Has any here with MM tried them? What have been the impacts?

Hi! This is my first time asking a question, do I appreciate any response. I was diagnosed with Smoldering myeloma December 2022. My question is have anyone heard of Hypogammaglobulinemia and nephrotic syndrome. This was indicated on my serum protein results.