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Re: brain mets have arrived
Oh, Jackie, I am so bummed to hear your news! This just sucks!!!!!!!! That said, you know as well as I do there are many on this site who have kept their brain mets at bay with treatment, some with extended remissions. All is not lost, and there is much reason to remain very hopeful! Sending prayers heavenward for your healing.
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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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