Does anyone else have MGUS?
I was diagnosed with MGUS last October and although I've done a lot of research, I feel there's still so much I don't know. Does anyone else have MGUS?
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Hi Amber,
That means the world to me; thanks so much for sharing it. It's a waiting game for us as we're still awaiting medical assessments, so it gives me some hope while we wait. I wish you the best on your health journey as well. Hope you get the best care in the world. I will update ours when I know more.