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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Hi Amber,
That means the world to me; thanks so much for sharing it. It's a waiting game for us as we're still awaiting medical assessments, so it gives me some hope while we wait. I wish you the best on your health journey as well. Hope you get the best care in the world. I will update ours when I know more.
Hi,
I am 50 years old, I recently did a blood test that showed I had Band 1 Monoclonal IgG with lambda light chains 2.3g/L. My GP believes it to be MGUS. I have my first haematology appointment on Thursday. I also have prediabetes, kidney stones and an inflammatory skin condition, hidradenitis supporativa of which I have been on Humira the past 2 years. What should I ask the Haematologist?
Can you please tell me about MGUS (IgG lambda) ?
Here is a website that can provide better answers than me:
https://www.mayoclinic.org/diseases-conditions/mgus/symptoms-causes/syc-20352362
I've got my first hematologist appointment next week, and I intend to ask whether the MGUS may have any impacts on any of the other medical issues I've got going on, or whether any of those issues or their actual/potential treatments might have ramifications for the MGUS.
At this point, I've got a multi-page table tracking my various medical issues: upcoming appointments, notes/questions for the appointments, past appointments, outcomes from past appointments, drugs, side effects of the drugs, actions I've taken to manage the side effects of the drugs, non-traditional stuff I've tried, etc. Really, it's a journal in table format. Because I've given up entirely on being able to hold it all in my head.
The medical community operates in silos -- not their fault, it's just how it is. But the human body/mind is not made up of silos -- it's an integrated whole. Expecting my excellent but overworked PCP to coordinate all that effectively is just absurd. So these days, when I see each physician (let's see -- at the moment, it's seven of them plus, of course, my pharmacist), I try to encourage them to think about the consequences of each diagnosis/treatment on all the other diagnoses/treatments.
I'm 72, I'm living a quite engaged life, and I am not my diagnoses. Since I want to hold onto that as long as possible, doing my best to help my medical providers operate as a team has become one of my priorities. Because it's really hard for them to do that if the patient isn't actively helping.
I recently asked my migraine neurologist to take a quick look at several possible insomnia drugs I planned to discuss with my PCP, and she flagged one that she routinely uses off-label with success as a migraine preventive. You never know what can pop when you try to be somewhat holistic about things.
I was diagnosed at 36. Depending on certain factors your H/O will decide your observation track. Ask to have a baseline though with your bloodwork and... 24hr Urine. . If your doctors office uses Labcorp then all your bloodwork get from there when going outside the office. Also, don’t Google doc yourself, typing in M-spike and other blood numbers kappa lambda, etc might shock you. Ask questions if your numbers only rise and never wave, plateau or decrease. CRAB is still looked at but other factors come into play. What type of MGUS?
Your hemonco will be the one to actually diagnose you with MGUS. Not that your pcp is not capable but there are autoimmune diseases and other factors that can have a high M-spike and KL numbers. Did your PCP also do a 24 urine Immunofixation (Bence-Jones Protein)?