u/sounds-of-silence11

Question for all of you.

When I was first diagnosed with High Risk Smoldering Multiple Myeloma my skin felt very sticky, especially when I sweat.

I was assuming it was because of the plasma cells.

I did two years of chemotherapy and that problem cleared up.

I just started treatment again with Darzalex Faspro in January 2026 and I am
getting that sticky feeling on my skin again.

Has anybody had this problem?
Do you think this has anything to do with the Multiple Myeloma?

Someone I care about ( Adult male) has scheurrmans disease and scoliosis. Looking for a medical provider, physical therapist trained in Schroth method for severe chronic pain in Orange County, CA.