Cyclophosphamide started yesterday, I guess this is some really strong chemo. She has to get up to pee every two hours and they are testing the pee every two hours too.
Threw up a lot yesterday, but now they have her on alternating anti nausea and it seems to be keeping her stomach calm (so far). I think this has been the hardest chemo treatment that she’s been on so far (and we’ve been through a lot). But she is being a very strong young woman, I’m very proud of her!
Mom & Dad on the other hand are trying to stay strong, really hard when you know your baby is hurting & fighting for her life.
The paper change link to counting down the peeing every two hours
PS- what does the “Day -2” mean, days to bone marrow transplant (so her new birthday will be 1-5-2017)
She is my “super hero”! Honestly, she is amazing all she has been through on round 1, now round 2 has been even stronger chemo. Sending healing love to keep her strong and well while the new Bone Marrow heals her body.
BTW would you have Danielle make me one of those paper chain links for all the time I get up in the middle of the night to pee;-)