Well, gals and guys, I know what you mean. It seems that because I have hair, eyebrows, and eyelashes that now I am to be FINE. "You beat it!" is what they say. I do not bother to explain that my future is not a certain thing, not that it ever was, but that it is perhaps less certain. Did that make sense?
I stopped wearing my wig and my hair is manishly short. It serves as a reminder to everyone that I just went through chemo, so for now I suppose I am allowed to speak of my cancer experience, but not for too long, too much, or too often. People in my office were surprised to hear I am having surgery on Monday (I am getting my expanders exchanged for big balls of silicone! Yeah!). Well, why does she need more surgery?
Ah well, I can only hope none of my friends and co-workers experience the BC blues. May they always remain ignorant of our deep suffering, loss, and fears.
I do think this is something that will ease with time as we move onward in our lives. Here's to hopin' anyway!
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Smile On!
Laurel
Dx'd w/multifocal DCIS/IDS 3/08
7mm invasive component
Partial mast. 5/08
Stage 1b, ER 80%, PR 90%, HER-2 6.9 on FISH
0/5 nodes
4 AC, 4 TH finished 9/08
Herceptin every 3 weeks. Finished 7/09
Tamoxifen 10/08. Switched to Femara 8/09
Bilat SPM w/reconstruction 10/08
Clinical Trial w/Clondronate 12/08
Stopped Clondronate--too hard on my gizzard!
Switched back to Tamoxifen due to tendon pain from Femara
15 Years NED
I think I just might hang around awhile....
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