I was stage 3. I am very careful about nutrition and hydration and a set sleep schedule. I am still using Revlimid and getting Velcade weekly. So with that context, I kept exercising (walking, lifting light weights and yoga) during treatment. During my stem cell transplant admission to the hospital I had some tough days but I kept moving. So I had fatigue but it has lessened dramatically over time. I still occasionally take a 20 minute nap, but I am active for most days. I think easy movement a pushing a little bit (but reasonably) every week has helped tremendously.

I'm 17 years free of MM but am fatigued everyday side effect of the treatment.
SCT. So tired of being tired ALL the time.
I know. I am greatful that I had a positive outcome. That I don't take and meds.
I just feel like my life has been stolen.
Sorry. I'm having a bad day and just had to vent to some people that might just really understand.
And the neuropathy is not just in my feet anymore its gone up my legs to my thighs. ARGG.

DM my husband agrees with you👋

Don't know if it's worse but it doesn't seem to go away after 6 years. Even little tasks like cooking tire me out....