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Structure - boy isn't that the truth! I feel like a baby on a schedule. I eat breakfast and take my am Xeloda between 7-8 am. I am on a trial for hand/foot syndrome and need to put the cream on my palms and soles so I do that after I bathe in the morning. At noon, I take the B6 for the trial, my clonidine for hot flashes and a calcium. I eat my evening meal so that I can take my evening Xeloda around 7-7:30, the take my Tykerb between 9-9:30 and do the cream thing to my palms and soles again. So far this routine is working pretty well for me. I am more fatiqued on this than any of the other chemos I have taken. I have had 3 times I needed the imodium, but then things stabilize after that. The last couple of days I have had a few zits on my chin. Tomorrow I start the week off of the Xeloda, so I am curious to see how I feel then.
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Andi
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Stage IIIC, 17 of 20 Nodes +, E+, Her2+++
Diagnosed 6/30/05
Lumpectomy 7/13/05
Dose Dense A/C x 4
Weekly Taxol + Herceptin x 12
Remainder of year Herceptin Every 3 weeks (completes 9/13/06)
Radiation completed 2/28/06
Currently on Tamoxifen
Dec 06 - Pleural effusion treated with pleurodesis
Now er/pr-, her2++
1/07 started weekly Navelbine plus Herceptin
Discontinued Tamoxifen
4/27/07 CTshowed progression
5/01/07 Began Tykerb/Xeloda + Zometa
5/22/07 Stopped treatment due to great progression
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