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Re: update - what to do?
Pam, the mouth sores are totally the pitts. I remember standing out on the point by my condo looking at the water and just crying giant tears, my mouth hurt so much. Then I'd get mad, eat ice, and go some more. I think when you get some relief from the mouth sores and other crumby stuff, your mind will get peaceful about which decision to make.
If you do decide on the trip, isn't there an organization that pays for your room if you have to stay over for treatment. My brain won't recall the name of the org., but I remember visiting with a patient in the radiation waiting room who was riding the bus and the bus and room were paid for by some org. Wish I could remember more. Maybe someone will know who to call.
Much love to ya, ma
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MA in TX.
Grateful for each and every day....
Diag. 12/05 at age 60
Stage II, Grade 3, 4.5 cm primary tumor
ER/PR- Her2 +3 strongly positive
Her2 by FISH 7.7 amplified
vascular invasion
Ki67 20% borderline
Jan - March '06 Taxotere/Adriamycin X 3 to try to shrink tumor - it grew
April '06 Rt Modified Radical Mas, 7 of 9 nodes positive
April - Aug. '06 Herceptin/Taxol/Carboplatin X 8 (dose dense)
Sept - Dec. '06 Navelbine/Herceptin x 8 (dose dense)
Radiation & Herceptin Jan. 22 - March 1, 2007
Finished Herceptin Dec. 10 '08! One extra year.
Port removed August, 2012.
8 1/2 years since diagnosis! 5 1/2 Years NED!
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