I was diagnosed with CMML last year and started receiving treatment with Luspatercept injections in September. I got my last injection of Luspatercept last Thursday….to date there have been no positive results….I go for bloodwork again tomorrow. I have been getting blood transfusions every 2-3 weeks. The doctor is suggesting a next step of a low dose oral chemo called Inqovi…..I would like to hear from anyone who has been on or is currently taking Inqovi to understand the ramifications and side effects. With Luspatercept I have experienced a great deal of fatigue and irritability…..for a very active and otherwise healthy person….I am not on ANY drug medications for anything else….the fatigue and irritability is a lot to handle.