← Return to MGUS diet: Any tips on food to enjoy or prevent progression?

Discussion
Comment receiving replies
@pmm

@bobweller
It’s estimated that 3% of people under 70 and 5% of those over 70 (if I remember correctly) have the M Paraprotein. I suspect the incidence is much higher because unless there are symptoms, the M paraprotein is usually discovered because they’re looking for something else. There are three diagnoses (and some subtypes) for those of us with this pesky M paraprotein. MGUS is not cancer. It’s a “precursor” condition, but that’s not even really accurate because many people who have MGUS will not progress to cancer. Smoldering myeloma and multiple myeloma are blood cancers. Not everybody who has MGUS will get smoldering or multiple myeloma, but everybody who has smoldering multiple myeloma or multiple myeloma had MGU first. At least that is my lay person’s understanding. The risk of progression is very small for MGUS patients. 1% to 2% a year.
https://www.mayoclinic.org/diseases-conditions/mgus/symptoms-causes/syc-20352362
So if you don’t mind sharing, will there be follow up on your false positive blood test?

Jump to this post


Replies to "@bobweller It’s estimated that 3% of people under 70 and 5% of those over 70 (if..."

I am a 69 year old Caucasian male. I am not sure who to followup with for further blood tests. I saw my Neurologist a few months ago for followup of pheriferial neuropathy in my feet and moving to my ankles and calfs. Since the M Protein is negitive it sounds like I should be OK according to all I've read so far.

Since the alpha and lambda lightcell tests were done once, should I get it done again with the M protein tests?