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Does anyone else have MGUS?

Blood Cancers & Disorders | Last Active: 14 hours ago | Replies (854)

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@gingerw

@crazbound Welcome to Mayo Clinic Connect! So many of us can definitely relate to having a lot of questions when we first get a surprise diagnosis.

I'm glad to hear you are going to have more testing done to narrow down exactly what is going on. In the meantime, here is some information you can read up on:
From Mayo Clinic's website related to MGUS: https://www.mayoclinic.org/diseases-conditions/mgus/symptoms-causes/syc-20352362
And from the Internaltional Myeloma foundation website: https://www.myeloma.org/what-are-mgus-smm-mm

And, as my oncologist always tells me, please don't spend a lot of time "Dr. Googling"! It is so easy to get wrapped up in many unrelated topics, scaring yourself, and thinking the worst. Be gentle on yourself. Wait to see what test results come back, and discuss them with your doctors. MGUS can stick around for a long time and never progress beyond that. It's important to remember that, okay?

Let me know if you have questions! We're here to help.
Ginger

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Replies to "@crazbound Welcome to Mayo Clinic Connect! So many of us can definitely relate to having a..."

Thank you