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Re: My Idea for a Game Show
I have not seriously discussed my dealings with chemo brain with anyone other than family, and even then, it is only my husband who really knows how much it has affected me. As more evidence of chemo brain's reality comes to the front, I intend to let the rest of my family know more about it.
I have joked and made reference to "chemo brain" with friends, but for the most part they really don't know how serious the remark is. Maybe we need to have "a talk." I empathize, though that I am not looking for sympathy, but I would like to be understood, if that makes sense.
In the meantime, I often think of our Chemo Brain Jeopardy when I have a chemo brain moment. Still makes me laugh! Those of us who are playing the game certainly understand the catagories!
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Blessings and Peace,
Barbara
DX Oct 02 @ age 52 Stage 2B Grade 3 Mastectomy
"at least" 4.5 cm IDC 1+node ER+61% /PR-
Assiciated Intraductual component with Comedo Necrosis
Her2+ FISH8.6 IHC 2+
5 1/2 CEF Arimidex
Celebrex 400mg daily for 13 months
Prophylactic mastectomy
Estradiol #: 13
PTEN positive, "late" Herceptin (26 months after chemo)
Oct 05: Actonel for osteopenia from Arimidex.
May 08: Replaced Actonel with Zometa . Taking every 6
months.
Accepting the gift of life, I give thanks for it and live it in fullness.
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