Does anyone else have MGUS?
I was diagnosed with MGUS last October and although I've done a lot of research, I feel there's still so much I don't know. Does anyone else have MGUS?
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Thank you; this is helpful. I also have translocations but a quite low plasma level of 1.6 (are we comparing on the same scale?). Trying to get all my climbing done sooner rather than later, just in case! Adams and Rainer this summer, anyone? 😉
MGUS can have all sorts of associated translocations and mutations. I also have gains on chromosomes 5, 7, and 9, but those supposedly buffer the 1q21 gain. Most of my non-MGUS bloodwork, including plasma level are OK. A bit low on red blood cells but that might be celiac associated. Life is best lived sooner than later. Before I got covid 2 years ago, I biked ~6000 mi/year. After long covid I still get in ~3000 mi/year plus cross training. BTW, peripheral nephropathy was why I was tested for MGUS (associated with that and celiac). It hasn't worsened over the years, but my hobbies keep my extremities working. I do take about 3 gm/day of bioavailable curcumin; works on lab rats to decrease TNF (tumor necrosis factor) so who knows. Regular turmeric and curcumin are poorly absorbed by the GI tract and low concentration. Adding peperine (from black pepper) and lipids (fats) increases absorption.
@buckett Welcome to Mayo Clinic Connect. It's quite the journey, as you say, to get the correct diagnosis.
Please come back and let us know how the biopsies and scan go, will you please?
Ginger
I have a positive mgus diagnosis
This is the first time I have seen anything about 1q21. Now you know your 1q21 issue, how does that information change anything you're doing?
I'm also taking 3 gm/day of the curcumin (C3 formulation). My hope is that the C3 somehow makes it more likely bioavailable than the run of the mill, garden variety curcumin and black pepper. I have no way to actually verify that.
I became interested in curcumin after seeing this study.... https://clinicaltrials.gov/study/NCT04731844?cond=MGUS&page=3&rank=26&tab=table
I met their requirement to participate and tried to get more info, but only found out that to be part of the study would require too much travel. My PET scan from 18 months ago didn't show bone lesions, but MRI results I just got, does mention a lesion and another bone issue called AVN. That was a complete surprise and don't believe the AVN is related to MGUS. So I guess I'm not a qualified participant anyway.
This trial is using 8g/day curcumin. Right now, I'm thinking of staying at 3 until I get my next 6 month blood work results. If my M protein is still doubling or if the trial results are promising, I may then bump it up to 8g/day.
The 1q21 gain is just more info that I try to compartmentalize and not stress over. It would be nice if the curcumin was chocolate flavored. I am still asymptomatic although my kidneys might be getting slapped around a bit by the kappa proteins (GFR is decreasing a bit). Not at any stage where I could be in clinical trials yet. I mostly try to have fun, work out, do hobbies, and not stress over what might be lurking over the horizon. Having been an avid cyclist I already am familiar with lurking things coming at me. The 3.1 mg/day curcumin (lipid and peperine) aren't causing GI or other problems and I'll see with next week's bloodwork if it is having any effect on kappa or other results.
@dave7 Welcome to Mayo Clinic Connect! How long ago was your diagnosis, and what has your medical team advised for "watch and wait"?
Ginger
Hello kayabbot! I have been diagnosed for over 3 years with mgus, initially biclonal (IgM lambda, IgG kappa, but also once IgG lambda). Now my latest tests show no identifiable monoclonal protein but I do have elevated Lambda (5.36 g/dl I think is the units).
I was given a BMB at that time and while it showed small percentage (1-4%) the FISH studies showed a Tp53 mutation and a gain of 1q which was terrifying. I went to 3 MM specialists who said those mutations were not significant because they were around 10% of the cells. I have been told repeatedly that it is doubtful that this will ever progress and I don't need to worry about it. I haven't had any other bmb but did have a full work up of complete pet/ct scan, mris and skeletal surveys.
I have finally let go of the extreme anxiety, yay! I wish I had never had the testing done as I continue to have no symptoms. I agree we should put it out of our minds and live as healthy as we can. I am 66 and hoping to live a lot longer.