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DiscussionMGUS diet: Any tips on food to enjoy or prevent progression?
Blood Cancers & Disorders | Last Active: Sep 3 4:57pm | Replies (137)Comment receiving replies
Replies to "Has anyone had MGUS discovered after taking the COVID vaccine?"
Hello Deryl,
Given that MGUS is usually present for many years before it is discovered, it is unlikely the vaccine contributed in any way to a recently diagnosed case. I found the following article helpful.
"Incidence of Monoclonal Gammopathy of Undetermined Significance and Estimation of Duration Before First Clinical Recognition", Terry M. Themeau, et al. https://pubmed.ncbi.nlm.nih.gov/22883742/
There are MGUS patients that report an increase in their M spike post vaccine. I think your scenario for MGUS post vaccine could be possible - but also impossible to determine without doing MGUS screening pre and post vaccine - so no way to confirm the theory.
Can only say that my PCP informed that after 2 Moderna Innoculations + 2 M boosters, I do not have covid immunity.
Possibly this is due to IgM kappa MGUS dx 7 years ago. Now suggested to take extremely new med: Evusheld. Anyone have any experience with it? Thank you! @rae
Me…I’m wondering if that’s what did it.
Hi Deryl, welcome to Mayo Clinic Connect. You'll notice that I moved your question to the Blood Cancers & Disorders group. I did this because you'll find members talking about MGUS in this group and can connect with people like @gingerw @auntieoakley @anniemaggie @susangs @momofthree1 @gmajudy @cctoo @dazlin
Here are a couple of other discussions that may interest you.
- Always run down with MGUS: https://connect.mayoclinic.org/discussion/always-run-down-with-mgus/
- MGUS https://connect.mayoclinic.org/discussion/mgus-2d464e/
I see that you are looking for a cause for your recent MGUS diagnosis and ask about the vaccine or a-fib meds being the potential culprit. The precise cause of MGUS isn't known. Genetic changes and environmental triggers appear to play a role. It may be a frustrating pursuit to seek the cause. By connecting with others here, I hope that you can turn your focus and energies to coping with the diagnosis and staying healthy.
What questions do you have? Has your doctor set up a follow-up schedule? How frequent?