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1,827 total results
Comments (1,727)
I had IgA kappa MGUS for 8 years, diagnosed this summer with SMM. They tested me...
https://connect.mayoclinic.org/comment/1158835/
I had IgA kappa MGUS for 8 years, diagnosed
@treinbold Welcome to Mayo Clinic Connect! I am attaching several articles here that speak to your...
https://connect.mayoclinic.org/comment/914636/
Many of us are diagnosed first with MGUS
@michelle151 Welcome to Mayo Clinic Connect. It is always an interesting journey when we have health...
https://connect.mayoclinic.org/comment/788973/
have proven, getting a diagnosis of MGUS
Hi teresa, thank you for your reply...yes I see an endo, and she has taken bloodwork....
https://connect.mayoclinic.org/comment/90589/
I have mgus, which may be a contributor
@dazlin My MGUS advanced into smoldering multiple myeloma officially in Nov 2019, so I am on...
https://connect.mayoclinic.org/comment/292603/
@dazlin My MGUS advanced into smoldering
Sometimes I think we miss the forest for the trees. Everyone's case seems to be different....
https://connect.mayoclinic.org/comment/1048525/
Non-ankylosing spondylo-arthropathy, and MGUS
I just had some test because I started getting numb tingling feet and now lower legs...
https://connect.mayoclinic.org/comment/1074303/
I read about MGUS and it seems related
Nancy, It's mg/dL. Other conditions: peripheral neuropathy (neurologist said all sensory nerves in legs were "shot")'...
https://connect.mayoclinic.org/comment/994549/
osteoporosis (before I was diagnosed with MGUS
I had my second liver transplant in 2017, my first was in 2000. Since 2018 I...
https://connect.mayoclinic.org/comment/1086669/
I read this is MGUS and an indicator
Thank you kayabbot - I’m also from a medical background and found those studies you cited...
https://connect.mayoclinic.org/comment/1035072/
now being explained as possibly not MGUS
Actually I'm talking all of them... I'm 86 with osteoporosis per DEXA. I've been prescribed both...
https://connect.mayoclinic.org/comment/1167486/
Drake) that MGUS, which I have, has
Sorry to hear what you’re going through - your situation seems really similar to mine (however...
https://connect.mayoclinic.org/comment/938993/
Once they found MGUS, they stopped proactive ... searching for treatments and said MGUS ... they’re even questioning if I have MGUS ... and IgA, it’s feasible that due to MGUS ... but that doesn’t mean I don’t have MGUS
@whitepine66 Talk about adding unwanted anxiety into your life, right? As @colleenyoung mentioned, the waiting game...
https://connect.mayoclinic.org/comment/721458/
The biggest majority of MGUS patients
Does anyone take Actonel? I'm wondering if anyone has experienced side effects? I'm back on it...
https://connect.mayoclinic.org/comment/74557/
My endo told me mgus may be a contributor
@pmm Hi patty, Thank you for such kind words of wisdom. I am just over one...
https://connect.mayoclinic.org/comment/869520/
t yet have a definite diagnosis of MGUS
Hi, I was diagnosed with MGUS 18 months ago. The neuropathy in my feet, I was...
https://connect.mayoclinic.org/comment/887490/
Hi, I was diagnosed with MGUS 18 months
I have had peripheral polyneuropathy for 12+ years. No pain ever, but increasing numbness/weakness/leg fatigure/balance issues,...
https://connect.mayoclinic.org/comment/1022903/
specialist MD diagnosed me with lgM MGUS
Dear mgusPixi25, I have heard a little bit about your health care system over there. Ours...
https://connect.mayoclinic.org/comment/884013/
you cant’t change the fact you have MGUS
Thanks, but they are mostly controlled by synthroid, not eating gluten or NSAIDs, and escaping stress...
https://connect.mayoclinic.org/comment/943424/
has been dormant for 30+ years and MGUS
I understand. I have suffered from eczema on-and-off for about 30 years, mostly "on" in the...
https://connect.mayoclinic.org/comment/1036847/
, I've not been diagnosed with MGUS
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