Hello @doriprovince,

I combined your discussion with an existing discussion titled:

"Diagnosed: MGUS"
- https://connect.mayoclinic.org/discussion/diagnosed-mgus/

I wanted you to meet @sandramgus, @smiles1951, @oneonly and @positivethinking who shared their experiences with getting diagnosed with MGUS.

@doriprovince, if you are comfortable sharing, were you recently diagnosed? If so, how are you doing?

@doriprovince yes I was diagnosed in 2019 I've recently been having very serious health complications and my cortisol level is virtually nonexistent so I have addisons disease now and im a nurse so I've been researching alot and it says when mgus is progressing it will cause low cortisol levels. Im going to my new oncologist in a couple of weeks and im asking them to do another bone marrow biopsy as I believe im progressing into multiple myeloma