Interesting Query. Trouble is, there are so many possible variants that one really can not say certainly and totally that MM is in no way genetic.To say that MM is at least rarely, if ever, genetic, would be a fair statement. But I, and four or more of my family, all have it now. Also, Four have had it at death. oldkarl

Definitely, at least see a hemotologist for testing. Bring your X-rays and any recent labs.

I would definitely seek another Dr. They found my MM by accident. They were looking at my spine for a spot and they did a biopsy and it turned out to be MM. My Dr called me 3 times to make sure I understood what was going on. I have stage 3 MM. been on Infusion since February.
Please see another Dr.

Thank you for your reply. Still trying to wrap my head around things. I just found out about my mom yesterday. Before that i thought my granfathers cancer was just a qiurk, maybe from being in the navy in WW2.

I see a big malpractice lawsuit in the making. As soon as X-rays show lesions you should have gotten MRI, CAT scan, PET scan. I got an X-ray and within minutes the doc said “this doesn’t look good.” Then MRI the PET. Then bone marrow biopsy. Then he said “is surgery on Monday ok?” In any case I would get a reputable law firm and let them recommend new team of doctors. We have a law firm here in Cherry Hill, NJ with 5 lawyers that are all doctors! Consultation is free and, of course, if they take your case you don’t pay a dime. WITH A FAMILY HISTORY OF MYELOMA YOUR PRIMARY SHOULD HAVE BEEN ON TOP OF THIS. For example, my Dad and his mom had Crohn’s disease and colon cancer so I got a regular colonoscopy to check. In any event it sounds like you need immediate diagnosis and treatment. Please keep us posted which may help others on this platform.