← Return to Starting MGUS journey: It feels like the "in limbo" disease

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@orla. Hello, I am also new here! I just got diagnosed with MGUS. How has your journey gone so far? Do you have any more answers?

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Replies to "@orla. Hello, I am also new here! I just got diagnosed with MGUS. How has your..."

Hi, apparently it is your light chain ratio that is important. We could live with this and never become anything. Just don’t overthink it. Live your life like normal. It’s non symptomatic. Keep ur blood appointments and get your results. My protein is always increasing but still within normal limits. I was told if it increases again I will need to get a bone marrow test. I’m feeling good and I’m thinking of it as nothing being honest. It could be nothing and if I worry I have wasted precious time unnecessarily. How are you doing what has your journey been like??