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228 total results
Comments (211)
I'm sorry to hear of your diagnosis. Though I'm still watching and waiting, I find the...
and educating everyone affected by WM ... 's Weekly is a free service to WM ... community members to share WM related
Since I am very new to this, I was hesitant to or not sure what I...
or not sure what I felt applied to WM ... I did not associate this with WM,as ... thinking it would be connected to WM
Thank you for reaching out for support. WM is a very rare blood cancer. While it...
WM is a very rare blood cancer. ... and was immediately referred to a WM ... new member packet with invaluable WM
Since everyone responds differently, I highly recommend joining the IWMF (International Waldenstrom’s Macroglobulinemia Foundation) - either...
Also, the IWMF has a list of WM specialists ... Personally, my local hem/onc coordinates my WM ... We are all here to support you with WM
Posted: May 25, 2024
Mike - my story is similar to yours. I was diagnosed with WM over a year...
I was diagnosed with WM over a year ... oncologist didn't think it was from WM ... So, I think it was my WM that caused ... latest Bone marrow biopsy shows the WM
Posted: Aug 14, 2023
I am assuming you had a bone marrow biopsy to be diagnosed with WM. Depending on...
marrow biopsy to be diagnosed with WM ... The mutations and data help our WM specialists
Posted: Apr 20, 2023
I, too, was diagnosed with WM in 2015. I am stable so there are no treatments....
I, too, was diagnosed with WM in 2015 ... I've been told that some people with WM ... says she has one other patient with WM ... girl not far from me with the same WM
Posted: Apr 8, 2017
Thank you for reaching out for help. No doubt you are overwhelmed right now. Mayo Clinic...
Mayo Clinic has several WM specialists ... WM is rare and most doctors are not ... davidyoung.com.au He can connect you with WM
Posted: Mar 19, 2023