I've done one Zometa treatment and one cycle of Revlimid, Velcade, and dexamethasone (RVD). Blood tests done before my second cycle show my M-protein (M-spike) is down from 3.2 to 1.2 g/dL (32 to 12 g/L). Seems like a nice improvement and the oncologist is very pleased.
My IgA is down from 60 to 30. Normal range is 70 - 400. Does anyone know the significance of this?
Platelet count is down from 240 to 164, but it is still in the normal range. Beta 2 and light chains have not been reported this time.
Side effects have been relatively minor from the RVD so far. The most interesting is that my blood pressure has dropped from 140/90 to 110/70. I'm thinking it is the daily aspirin they put me on to stop blood clots, along with the lisinopril they already had me on for high blood pressure. Anyway, the drop in blood pressure resulted in a dizzy spell every time I stood up, and a complete black-out one time when going from lying down to standing up. My regular doc took me off the lisinopril for now, with a check up in two weeks. Dizzy spells are now gone.
Other side effects include: Unsettled stomach, easily dealt with by prochlorperazine (Compazine). Puffiness around my eyes when taking the dex (4 days in 3 week cycle). Ringing in the ears. Slight numbness in the hands. Burning feeling in the hands and arms in the off-week, when not taking any drugs. Constipation, taken care of with Miralax (polyethylene glycol 3350).
Severe back pain was my only noticeable symptom of multiple myeloma when I was diagnosed in April 2017 and for that I was taking 4 Norco (acetaminophen / paracetamol & hyrdrocodone) per day, plus muscle relaxants, plus chiropractic care 3 times a week. Now, I have improved so much that the back pain is controlled by Tylenol and maybe 1/2 a Norco, no muscle relaxants, and chiropractor on an as-needed basis.
Overall, I'm feeling as good as I did 6 months ago, before the transition from MGUS to multiple myeloma.

That's about it for now. I'll keep you posted.
Tony