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1,826 total results
Comments (1,726)
I feel better reading these post from people that are in the same situation with this...
https://connect.mayoclinic.org/comment/723056/
many medical people don’t know what MGUS ... in August, Doctor didn’t know what MGUS ... if there is a reason to worry about MGUS ... Clinic, don’t know how they rate with MGUS
@gmichelle There is no clearcut evidence that it is always linked, but some people do experience...
https://connect.mayoclinic.org/comment/796157/
experience low iron and anemia with MGUS ... I advanced from MGUS to Smoldering Myeloma ... My kidney disease is not related to MGUS ... what John Hopkins has to say about MGUS
Yes I have MGUS and recurring mouth sores. Not as often now. A month ago was...
https://connect.mayoclinic.org/comment/1144140/
Yes I have MGUS and recurring mouth ... cancer oncologist/ hematologist for my MGUS
Welcome to Connect @lisa54. I see that you connected with @dawn_giacabazi and @johnwburns on another discussion...
https://connect.mayoclinic.org/comment/106648/
introduce you to @briansr who also has MGUS ... momofthree1 who were talking about MGUS ... you've received information about MGUS ... www.mayoclinic.org/diseases-conditions/mgus
I have MGUS and am on Forteo. I have questioned this and my Dr has said...
https://connect.mayoclinic.org/comment/951626/
I have MGUS and am on Forteo. ... One of my MGUS levels has increased
Hi @suzye and welcome to Connect. I wanted to introduce you to fellow Connect members @gingerw...
https://connect.mayoclinic.org/comment/264592/
anniemaggie as they have experience with MGUS ... treated for osteoporosis while having MGUS
I'm 69 and was diagnosed with IgA light chain kappa MGUS 8 years ago. My kappa/lambda...
https://connect.mayoclinic.org/comment/1038722/
diagnosed with IgA light chain kappa MGUS ... Risk of MGUS morphing to SM or MM is ... I don't have any symptoms from MGUS ... Here are some papers on MGUS: https ... one on covid vaccines not impacting MGUS
Angie, I'm 66, diagnosed with IgA Kappa MGUS 2/15/23, husband died of Multiple Myeloma 7/24/22. Mine...
https://connect.mayoclinic.org/comment/1053450/
#39;m 66, diagnosed with IgA Kappa MGUS ... extremities, I'm going to test you for MGUS ... rash at one point during his supposed MGUS ... because "MGUS has no symptoms.& ... MGUS definitely has symptoms.
Yes, I am past that half century mark as well, and try to stay active, but...
https://connect.mayoclinic.org/comment/991022/
stay active, but one Dr., tells me MGUS ... here some of the people going through MGUS ... says neuropathy isn't caused by MGUS
Welcome, Patty. I love that you put your pending retirement date in your bio. Working until...
https://connect.mayoclinic.org/comment/658722/
you were hoping for retirement with MGUS ... changes suggested for people with MGUS ... and can even be beneficial should MGUS ... Patty, how did you discover you have MGUS
I've had MGUS for 8 years so far. MGUS represents precancerous plasma cells, but only a...
https://connect.mayoclinic.org/comment/1112564/
I've had MGUS for 8 years so far ... MGUS represents precancerous plasma ... have a lot of peer-reviewed papers on MGUS ... A lot of us on this site have had MGUS
What is MM? I was diagnosed by my neurologist with peripheral neuropathy about 2 years ago...
https://connect.mayoclinic.org/comment/1062297/
which led to a further diagnosis of MGUS ... I am re-tested for MGUS every 6 months ... I really know very little about MGUS ... anything about other symptoms related to MGUS ... up in knowledge about either PN or MGUS
how do I get on the MGUS support group board???
https://connect.mayoclinic.org/comment/73352/
how do I get on the MGUS support group
Recently diagnosed with MGUS and need advice.....physicians, nutrition, etc.
https://connect.mayoclinic.org/comment/74533/
Recently diagnosed with MGUS and need
My MGUS was 8 years ago. I'm not immunocompromised because the deranged plasma cells (I prefer...
https://connect.mayoclinic.org/comment/1036361/
My MGUS was 8 years ago. ... there is any relationship between MGUS ... someone is immunocompromised from MGUS
I'm sorry you are experiencing this @quarksunite. I too have MGUS and numbness, which my hematologist...
https://connect.mayoclinic.org/comment/851801/
I too have MGUS and numbness, which ... told me was probably not caused by my MGUS
Hello @billh, It has been awhile since you have posted. I just wanted to know how...
https://connect.mayoclinic.org/comment/74559/
know how you were doing with your MGUS ... experience with your journey with MGUS
Or even a third or fourth I have MGUS with many symptoms. Some doctors say it's...
https://connect.mayoclinic.org/comment/864580/
Or even a third or fourth I have MGUS ... Some doctors say it's not the MGUS
@gingerw, Can I ask you how long you had MGUS before it progressed to MM? Did...
https://connect.mayoclinic.org/comment/739027/
,
Can I ask you how long you had MGUS ... Did you ever have any symptoms with MGUS
I’ve had MGUS since 2015: long before covid. Subsequently I had two Modernas, then three Moderna...
https://connect.mayoclinic.org/comment/780087/
I’ve had MGUS since 2015: long before ... They did not seem to alter my MGUS status ... However MGUS seems to have interfered
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