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Does anyone else have MGUS?

Blood Cancers & Disorders | Last Active: 6 hours ago | Replies (866)

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@loribmt

Hi @kitkat1070 Welcome to Mayo Clinic Connect where you’ll find you’re not alone in this new diagnosis of MGUS.
I just wanted to make sure you see this very informative and comforting reply by @pmm who is sharing her experience with MGUS here: https://connect.mayoclinic.org/comment/812816/

How was your diagnosis discovered? Was this through a routine physical or were you having symptoms?

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Replies to "Hi @kitkat1070 Welcome to Mayo Clinic Connect where you’ll find you’re not alone in this new..."

I suddenly developed Trigeminal Neuralgia (most painful thing I have ever had). Neurologist requested some lab work and the M factor appeared. As you say, I am currently seeing a Hematologist in 3 month intervals with lab work. As I have said at 92 and all the other life medical problems, this just seems like one more blip on the horizon. I have buried almost all of my family including my daughter, and have only my son to worry about now, so I am happy to have one more day and the blessings of God. I have two knee replacements, two hip replacements, a shoulder replacement, and a double Mastectomy (one a Radical) and I am still living pretty much on my own. I am probably one of the luckiest woman alive. Thank you for your kind words, they certainly help make it one more day.