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Comments (2,297)
@sallylynn I had very slight neuropathy, no other symptoms. My primary care provider said, I'm going...
https://connect.mayoclinic.org/comment/948532/
@suzykaye I’ve read studies suggesting MGUS and SMM can cause these problems due to “thickening” of...
https://connect.mayoclinic.org/comment/1585171/
@joyelizabeth Have you been formally diagnosed with MGUS? What tests were done, and by whom? If...
https://connect.mayoclinic.org/comment/1018739/
PS Despite being diagnosed with MGUS in 2002, I still am categorized as MGUS. Each joint...
https://connect.mayoclinic.org/comment/1290887/
Thank you for your information and it is helpful to know you have been able to...
https://connect.mayoclinic.org/comment/1174311/
@lgb55 Sorry, I have no specific studies to cite. I think everyone is different and alot...
https://connect.mayoclinic.org/comment/1569547/
I think being very healthy and this hitting your makes it harder to deal with. I've...
https://connect.mayoclinic.org/comment/1184774/
I don't really have anything to treat (yet anyway). MGUS is considered a risk for MM,...
https://connect.mayoclinic.org/comment/1209159/
mgus rarely!! goes to MM!!! Forget about it and just live your life !!!
https://connect.mayoclinic.org/comment/870150/
Most people with MGUS also have a form of anemia. I am IDA
https://connect.mayoclinic.org/comment/1310652/
Hi Colleen, thank you - I will check on that. Thanks for adding others with MGUS.
https://connect.mayoclinic.org/comment/632387/
I should have said that you hope to achieve MGUS like state.
https://connect.mayoclinic.org/comment/1148897/
Thank you for responding to me. Have you had MGUS a long time?
https://connect.mayoclinic.org/comment/1142207/
I’ve read everyone’s comments. Thanks for the info. Something I read in association with MGUS was...
https://connect.mayoclinic.org/comment/1417044/
I have MGUS too, stable these 5 years. But I would get a second opinion I...
https://connect.mayoclinic.org/comment/1608955/
Hi I also have been diagnosed with MGUS I have so many other symptoms and issues...
https://connect.mayoclinic.org/comment/1234404/
What are you doing for the itching? I have the same t-cell lymphoma and MGUS.
https://connect.mayoclinic.org/comment/886704/
I have BIg kappa light chain too but said I had mgus??!!
https://connect.mayoclinic.org/comment/81214/
@hsminc Thank you for sharing your experiences on this strange and convoluted journey called MGUS!!!
https://connect.mayoclinic.org/comment/1424148/
@barbarian1 Hello! Somehow I found this post of yours from last year, so glad I did!...
https://connect.mayoclinic.org/comment/1609086/
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