It is time for my annual blood test and I usually do a search on MGUS because it is on my mind. I found this website and read the posts of people who are newly diagnosed. I wanted to give comfort.
I was diagnosed with MGUS at the age of 37. Within a two year time span, I had blood tests every 3 months and two bone marrow biopsies. The diagnosis remained MGUS thank goodness. I can completely relate to everyone who is trying to deal with the initial shock.
It is now ten years later. As I mentioned above, I go in every year for a blood test. It is only at this time that I experience a bit of anxiety.
My prayers are with you.