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248 total results
Comments (230)
Because WM is a rare blood cancer, some oncologists have no experience with WM. I would...
Because WM is a rare blood cancer, some ... oncologists have no experience with WM ... strongly recommend consulting with a WM ... The IWMF website has a list of WM specialists
Posted: Mar 22, 2022
Being a WM patient and knowing other WM and Amyloidosis patients, I concur with Colleen that...
Being a WM patient and knowing other ... WM and Amyloidosis patients, I concur ... specialist who specializes in both WM ... , Mayo Clinic, specializes in both WM
Hello @janemichele. Here is some additional information: From a Mayo Clinic Hematologist, "A provider could apply...
Ann Arbor Staging for lymphoma) to WM ... However, in particular for WM, the Ann ... staging system is not helpful as all WM ... , which is designed for WM and actually ... Here is a link to the original IPSS-WM
Posted: Jan 9, 2020
@pices - I too have WM with wild type MYD88. Did you find treatment options to...
@pices - I too have WM with wild type ... find treatment options to manage your WM ... Did you find a WM physician for our
Posted: Jan 30, 2023
Hi Mr. Perezy, There is a very active support group for people with WM on Facebook....
active support group for people with WM ... WM is a very rare disease - it represents ... doctors may not be up-to-date with WM ... directory take a special interest in WM ... and are involved the latest WM clinical
Welcome to Mayo Connect. I was diagnosed with WM in 2014. I am an IWMF (International...
I was diagnosed with WM in 2014. ... Since WM is so rare, most hematologist ... possibly understand everything about WM ... With WM, there are two mutations, found ... specialists in determining the best WM
Posted: Aug 8, 2021
I am sorry to read of your PN symptoms. Being an I.W.M.F, MN/WI support group co-leader,...
have not already consulted one of the WM ... There are fewer than 1500 WM patients ... oncologists/hematologists have few WM ... The worldwide WM specialists not only ... have multiple patients but have other WM
Posted: Sep 4, 2023
Welcome to Connect, @jessabell I see you’re newly diagnosed with WM. We have quite a few...
I see you’re newly diagnosed with WM ... quite a few members who also have WM ... There is a good discussion in the WM ... if you haven’t already seen it: ~WM ... of information and guidelines for WM
Welcome, @cpu. I moved your question about Waldenstrom macroglobulinemia (WM) to this existing discussion: - Waldenstrom...
about Waldenstrom macroglobulinemia (WM ... - Waldenstrom macroglobulinemia (WM ... /connect.mayoclinic.org/discussion/wm-treatment-options ... posts and connect easily with other WM
What does your oncologist suggest as far as getting the genetic testing done to confirm WM?...
the genetic testing done to confirm WM ... There is a good discussion in the WM ... WM, What to expect during watch and ... You’ll be able to connect with other WM ... of information and guidelines for WM
Posted: Jan 3, 2024
Our genetics can sure play a large part in our lives beyond hair and eye color....
the treatments he needs to keep the WM ... to pull up related discussions on WM ... ~WM search: https://connect.mayoclinic.org ... search=WM ~Waldenstrom macroglobulinemia
Discussion: Treatment for WM
Posted: 1 day ago
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