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2,355 total results
Comments (2,228)
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
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
@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
@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
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
The update on hubby's appointment with the hematologist yesterday: Because of a 1.3 M spike, she...
https://connect.mayoclinic.org/comment/1132611/
have been caused by the underlying 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
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
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
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
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
@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
@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
Hello, I was just diagnosed with MGUS. I am 42 yr old white woman. Weight loss...
https://connect.mayoclinic.org/comment/937408/
Hello,
I was just diagnosed with MGUS
My husband has MGUS and amyloidosis and received treatments and then a stem cell transplant in...
https://connect.mayoclinic.org/comment/847175/
My husband has MGUS and amyloidosis
I was diagnosed with MGUS 2012 and only use haematologists for blood tests, MR scans and...
https://connect.mayoclinic.org/comment/781489/
I was diagnosed with MGUS 2012 and only
@pmm You took the words right out of my mouth! Absolutely right, a small percentage of...
https://connect.mayoclinic.org/comment/732393/
people go for years with a simple MGUS
Agree there is no link established (yet) with any known cause for MGUS, but human nature...
https://connect.mayoclinic.org/comment/1195952/
established (yet) with any known cause for MGUS
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