← Return to Does anyone else have MGUS?

Discussion

Does anyone else have MGUS?

Blood Cancers & Disorders | Last Active: Sep 19 12:31pm | Replies (818)

Comment receiving replies
@gingerw

@pmm Patty, I had the same experience. When I needed to get a specialist, I had my memory kick in. There was a hematologist oncologist who had been an expert witness in a trial I worked. I contacted her office and was able to become her patient. While we did quarterly testing, she graduated me to six months. In hindsight, she felt really bad, because my numbers rose significantly. And I was moving 800 miles away. So, we did comprehensive testing, I had already connected with my current specialist and all records were sent. Two weeks after moving here I was in the new-to-me cancer center, with my current doctor. He has been a godsend in managing my condition.

MGUS does not need to be considered a death sentence, nor a hindrance to living our lives. It gives us the chance to have complete bloodwork more often, and feel comfortable that we are indeed being followed for things. Moderate exercise, good diet, stress-free living all go a long way to making the wheels turn smoothly. And being here on Mayo Clinic Connect to share with others. Nothing better than support from peers!
Ginger

Jump to this post


Replies to "@pmm Patty, I had the same experience. When I needed to get a specialist, I had..."

Ginger! That would be awful to start over with a new team. I guess I could do it because I’ve moved around in my adult life but yuck! I’m glad you have someone in whom you have so much confidence.
Yes, resounding yes, here! MGUS is not a death sentence at all. If anything, it has squared my shoulders in the face of my own mortality, and I have embraced life fully. I pay more attention to friends, family, and even those beautiful spiderwebs crafted skillfully by the orb spiders in the fall. Life is good. We shouldn’t miss it.
Hugs.