← Return to Waldenstrom macroglobulinemia (WM): Deciding treatment options

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Profile picture for charlotte44 @charlotte44

I do not have this, but I have looked into it a lot. I have so many symptoms. Can you tell more about yours?

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@charlotte44 hello, I was diagnosed with WM in April of 2025 and hav found that the WIMF has a lot of information on WM. My symptoms are only weakness and bone pain so I'm not in any treatment yet. I'm hoping that my treatment won't start for years from now so it's still wait and watch. What has helped you with weakness?