← Return to Waldenstrom macroglobulinemia (WM) 3 years: Might I be in remission?

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It's good to know I'm not alone in this IgM MGUS journey. I have so many questions. My impression is my Oncologist/Hematologist is just using the HMO playbook. Fortunately, she is willing to play along with my requests for tests like LDH & MRI. My IgG levels are low, Free light chains seem normal. I don't know if my IgM is Kappa or Lambda and I don't know if it makes a difference anyway.
The first time we talked, she seemed to promote a BMB, but I declined at the time mainly because at that time I was still hoping this whole situation would progress very slowly. Unfortunately, my IgM levels have been rising exponentially. In a few months, I'll get all the testing done again including the BMB and then put the results into the Dana Farber calculator and know which Risk Group I'm in.
Depending how those tests go, I may then ask for FISH (MYD88 L265P), maybe Flow Cytometry to identify clonal markers (CD19, CD20, CD5, CD10, CD38, CD138, etc.) on abnormal B-cells/plasma cells.
I don't think she will be happy about doing more tests. The MRI I talked her into, didn't find any lesions but did find an unrelated AVN condition affecting my hips and that resulted being assigned to an orthopedic surgeon. Who knows what these tests will find.
I'll let you know how my testing goes. Let me know if you have any questions and how your journey progresses.

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Replies to "It's good to know I'm not alone in this IgM MGUS journey. I have so many..."

I’m on Brukinsa a half dose and it is bring my IGM down pretty notably.

I’m not sure you need all these tests. The MDY88 is over 90 % positive for WM with Congo Red by histology. I later asked for the CXCR testing as the outcomes aren’t as good. I take IVIGG infusions for the low IGG levels to boost the immune system. You may want to ask for the Fat Pad test which further confirms WM.