Postby midlifemom » Fri Jun 13, 2014 9:10 pm
Making progress. Did #9out of 12 folfox today. Told onc of the new side effect of muscle fatigue, he did extra blood work but all in normal ranges. He suggested rehab for cancer related fatigue. Has anyone else done this? Did it help? Any issues getting it paid by insurance?
Happy fathers day to all you dads out there.
Stage 3 cc - dx Jan '14 age 53, cea 2.9
t2n2m0, KRAS mutant, MSS
Folfox Feb - Aug '14
Nov '14 cea 27.7 -2 liver masses
Dec '14 left lobectomy and HAI
Jan '15 FUDR and FOLFIRI
Aug '15 fudr done, liver clear, add avastin for lungs. Cea 4.3
Feb '16 CEA rising
May '16 2 wk break then drop Iri for 6 weeks.
Jul '16 cancer grew, constricted main bile duct. Stent inserted. On break till jaundice clears. CEA climbing. Doing reduced Folfox. Allergic to Oxali.
Sep'16 chemo failed. Trial or hospice?