We keep seeing the term ‘side effects’ to the toxins in all chemical drugs for cancer treatment, including for multiple myeloma, thus, the effects of chemo on the body, the horrible ‘side effects’ of these toxic drugs are Direct Effects, bec we have been programmed and fear mongerered by big pharma and the medical monopoly, aka, the toxic oncologist, aka, big pharma drug dealers, that if you don’t take their drugs you will die and they discard and devalue any alternative treatments, from plant based options and key myeloma supplements to repurposed medications, that have been proven to work to treat cancer and MM, myself included. There are other treatment options IF we take the time to do our research and have the courage to say no to big pharma and their toxic drugs that wreak havoc on our bodies. They are not side effects, they are direct effects bec they effect you directly.

Thank you for your input Bamaboan. My husband is 68. He was diagnosed in 2023. He just started the Ninlaro. I do see him being more tired and sleeping more on the day he takes it and the following day. I think the dex he takes with it might cause some too. Hope all keeps going well with you.

Always low. Ben low for 9 years.

W is ur RBC count ?

Peggy, I have been on Ninlaro for 9 years now. I couldn't take the other drug, allergic to it. My Drs say I am doing very well on it. Still in remission. They also told me not everyone has done as well as I have. Do your research on it. Hey Peggy I'm 76 years old and still kicking it for 9 years, so keep praying that works the most. As for the side effects. Mine are mild, I do feel all of those side effects but not too terrible on any one of them. My low blood cell count is pretty bad but I keep having faith in it. DON"T GIVE UP!!!! Hope this helps a little.