Thank you cat1952. I started this whole process with a "neuropathy" in my feet, but the neurologist said I didn't have neuropathy per the electrical studies he did. (forgot what the tests are called). He is the one who discovered the MGUS and referred me to my oncologist/hematologist. From there I had a bone marrow biopsy that confirmed MGUS but was in the moderate range. Six months later had dramatic spike in Lambda and 2nd biopsy my plasma jumped from 7 to 27. So we will see what happens next in couple weeks. My fuzzy feet/leathery soles are no better but no worse through the treatments so far. Thanks again. Many blessings over you and your continued journey too!