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2,336 total results
Comments (2,209)
My lumbar MRIs just showed normal wear and tear. My Hematologist/Oncologist isn't concerned about it nor...
https://connect.mayoclinic.org/comment/1210948/
The noted lesion is not MGUS related
@projfan I do have pain which may be attributable to MGUS but when one has coexisting...
https://connect.mayoclinic.org/comment/1258449/
pain which may be attributable to MGUS
Yes, I was told the same thing nothing can be done about it. I'm what they...
https://connect.mayoclinic.org/comment/1158000/
#39;t believe it will help out the MGUS ... see what everyone is doing with the MGUS ... all the time but the Dr says its not MGUS
@j2c , @kayabbott , @like2dance2 , others 😂 I'm also dealing with MGUS and neuropathy. I...
https://connect.mayoclinic.org/comment/991043/
x1f602;
I'm also dealing with MGUS ... subsequent bone marrow biopsy confirmed MGUS ... Anyway, I found a study program for MGUS
The mind-body connection is so important. Anxiety can really throw your whole body chemistry for a...
https://connect.mayoclinic.org/comment/869269/
When I was first diagnosed with MGUS ... Now, trust me, I don’t want my MGUS ... I am thankful that my fellow MGUS patients
Welcome to the MGUS club. It does seem a bit maddening to rely on the wait...
https://connect.mayoclinic.org/comment/793954/
Welcome to the MGUS club. ... While it’s true, that sometimes MGUS ... As a result of my MGUS workup, I know
I was diagnosed 6 years ago but wonder if the Oncologist diagnosed correctly?? because I have...
https://connect.mayoclinic.org/comment/74591/
I do not feel MGUS is a timebomb. ... I wish anyone with a MGUS Dx. well as ... For me MGUS has muddied the waters.
Since the MGUS labs and the rheumatology labs are both twice a year, it would be...
https://connect.mayoclinic.org/comment/1132883/
Since the MGUS labs and the rheumatology
"Blood Thinners" In response to @kayabbott, These are usually anticoagulants. There is also a supplement risk...
https://connect.mayoclinic.org/comment/1128228/
at least slowing the progress of my MGUS
Is your grantulomus sarcoidosis? I’ve been diagnosed with MGUS (1/22) and pulmonary sarcoidosis (5/22) and looking...
https://connect.mayoclinic.org/comment/820551/
I’ve been diagnosed with MGUS (1/22)
In regard to treatments, I'm hoping I won't need an MGUS treatment strategy for a long...
https://connect.mayoclinic.org/comment/1258497/
I'm hoping I won't need an MGUS
A Neurologist diagnosed my neuropathy as polyneuropathy and he requested a light chains blood test for...
https://connect.mayoclinic.org/comment/858171/
ratio was high so that's how my MGUS
I was diagnosed in 2012 with MGUS. At that time I did have any treatments but...
https://connect.mayoclinic.org/comment/264709/
I was diagnosed in 2012 with MGUS.
Welcome back to Connect @momofthree1. @lisa54 recently joined Mayo Clinic Connect and is looking to connect...
https://connect.mayoclinic.org/comment/74543/
other people who have experience with MGUS
I was anemic and that is when they found it. My dr set me to an...
https://connect.mayoclinic.org/comment/1338932/
test and said it looks like you have MGUS
Your entry was most interesting to me. I have IgG lambda MGUS. My free light chains...
https://connect.mayoclinic.org/comment/1198517/
I have IgG lambda MGUS.
Smoldering Myeloma is not necessarily described by symptoms but a stage of the progression to multiple...
https://connect.mayoclinic.org/comment/1189359/
www.myeloma.org/resource-library/understanding-mgus-smoldering-myeloma
I would think if it’s pretty persistent then I’d worry. Sounds like yours is fleeting -...
https://connect.mayoclinic.org/comment/1033050/
I was diagnosed with MGUS but it’s been
My daughter was first diagnosed with MGUS and now WM. Had several chemo treatments, which seems...
https://connect.mayoclinic.org/comment/899545/
daughter was first diagnosed with MGUS
@gingererw @dianegrant I was diagnosed with MGUS last August 2022. I was a regular blood donor...
https://connect.mayoclinic.org/comment/852121/
dianegrant
I was diagnosed with MGUS
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