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228 total results
Comments (211)
Recently diagnosed with WM. Also have CLL.
https://connect.mayoclinic.org/comment/845215/
Recently diagnosed with WM.
I'm sorry to hear of your diagnosis. Though I'm still watching and waiting, I find the...
https://connect.mayoclinic.org/comment/787689/
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...
https://connect.mayoclinic.org/comment/813277/
or not sure what I felt applied to WM ... I did not associate this with WM,as ... thinking it would be connected to WM
WM is Waldenström macroglobulinemia, a type of cancer affecting two types of B cells: lymphoplasmacytic cells...
https://connect.mayoclinic.org/comment/1166512/
WM is Waldenström macroglobulinemia, ... WM is characterized by high levels of
Just diagnosed with WM. I have minimal symptoms. No treatment yet.
https://connect.mayoclinic.org/comment/989827/
Just diagnosed with WM.
Thank you for reaching out for support. WM is a very rare blood cancer. While it...
https://connect.mayoclinic.org/comment/812866/
WM is a very rare blood cancer. ... and was immediately referred to a WM ... new member packet with invaluable WM
The following link is an IWMF physician directory for WM specialists. Please note that there are...
https://connect.mayoclinic.org/comment/692109/
is an IWMF physician directory for WM ... see if I can also find you a young WM
I am so sorry about your daughter’s rare WM diagnosis. May I ask if she gad...
https://connect.mayoclinic.org/comment/855382/
so sorry about your daughter’s rare WM ... After a BMB, I was diagnosed with WM
Hi @kjberend12. Losing 75 pounds without trying is a substantial number. Was that your first symptom...
https://connect.mayoclinic.org/comment/1313934/
Was that your first symptom of WM?
Since everyone responds differently, I highly recommend joining the IWMF (International Waldenstrom’s Macroglobulinemia Foundation) - either...
https://connect.mayoclinic.org/comment/1074361/
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
Mike - my story is similar to yours. I was diagnosed with WM over a year...
https://connect.mayoclinic.org/comment/912773/
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
I am assuming you had a bone marrow biopsy to be diagnosed with WM. Depending on...
https://connect.mayoclinic.org/comment/846322/
marrow biopsy to be diagnosed with WM ... The mutations and data help our WM specialists
I, too, was diagnosed with WM in 2015. I am stable so there are no treatments....
https://connect.mayoclinic.org/comment/113918/
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
Seek eval from pulmonologist and/or WM specialist. I am established at Bings Center at Dana Farber.
https://connect.mayoclinic.org/comment/907109/
Seek eval from pulmonologist and/or WM
My hemotologisr/ oncologist said no live vaccines and not be be near anyone newly vaccinated. He...
https://connect.mayoclinic.org/comment/1294087/
He is an expert in WM….
My husband has been diagnosed. There are only a few mentions of WM on this site....
https://connect.mayoclinic.org/comment/623023/
There are only a few mentions of WM
I was diagnosed with WM in Dec 23' had a lymph node biospy in Nov came...
https://connect.mayoclinic.org/comment/996169/
I was diagnosed with WM in Dec 23' ... came back low-grade B cell lymphoma/WM
Are you a WM specialist AND Pulmonolgist? If so, how can I find out more about...
https://connect.mayoclinic.org/comment/907126/
Are you a WM specialist AND Pulmonolgist
Thank you for reaching out for help. No doubt you are overwhelmed right now. Mayo Clinic...
https://connect.mayoclinic.org/comment/828678/
Mayo Clinic has several WM specialists ... WM is rare and most doctors are not ... davidyoung.com.au
He can connect you with WM
get a test for anti- mag titers I forget the exact test (chemo-brain) but it's rare...
https://connect.mayoclinic.org/comment/1311526/
chemo-brain) but it's rare but 4% of WM
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