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Waldenstrom macroglobulinemia: What to expect during watch & wait?

Blood Cancers & Disorders | Last Active: Nov 14, 2023 | Replies (90)
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@ejrquast

Thank you for reaching out for support. WM is a very rare blood cancer. While it can be an overwhelming diagnosis, there are treatment options and hope. I was diagnosed with Waldenstrom’s Macroglobulinemia in 2014 and was immediately referred to a WM specialist at Mayo to coordinate my care with my Mayo Rochester specialist.
I contacted the International Waldenstrom’s Macroglobulinemia Foundation, I.W.M.F., for support and amazing educational resources. If you go to the following website: https://iwmf.com/join-the-iwmf/#
you can then click on the JOIN button. You will receive a new member packet with invaluable WM information.

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Replies to "Thank you for reaching out for support. WM is a very rare blood cancer. While it..."
mxx | @mxx | Feb 17, 2023

Thank you so much for sharing your experience. I have joined the I.W.M.F and look forward to educating myself .
Appreciate your prompt response!
.

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catalinae | @catalinae | Feb 18, 2023

Thank you for the information,I will pursue.
Thank you,thank you! Please excuse any errors in responding, trying to figure out the system.

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