The reason I started this blog site was to not only document my story of living with multiple myeloma, but also hopefully create a set of resources for others who become diagnosed with multiple myeloma – letting them know they’re not alone, that others are experiencing the same (or at least similar) situations, and hopefully providing some insights into how to approach and deal with all that might be forthcoming (or even informing them of stuff they don’t know might be forthcoming). To that end, today, I want to talk about chemotherapy and a very common side effect, nausea. During my six months of induction treatment after being diagnosed with…