Thread: brain mets
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Old 03-04-2011, 02:19 PM   #17
kiwigirl
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Join Date: Jan 2010
Location: Matakana which is one hour north of Auckland, New Zealand.
Posts: 89
Re: brain mets

We will survive it just means a little bit of hard work. I'm on the same page as you but I've already started. So far I've had 6 wbr at a lower dose with a further treatment of VMAT at a very high dose. Spent one night in hospital (vomiting) .

I'm on decadron I've just lowered this dose seems to take two days to kick in on a lowered dose.

I've got 20 rads in total and plan on being like Christine as I'm sure you are to. And we will get there.

Please be strong you have been through alot and your not alone I'm there with you every step of the way.

As i go through this i know i have others with me to give me strength.

Rest is good look after yourself. oooxxx
__________________
Oct 2009 Masectomy 6 cm Tumor . Sentinal node biopsy , Node Positive . Her2 + er/pr -.
Nov 2009 X3 Taxane and Herceptin, X3 FEC
March 2010 25 Rads
March 2010 continued on Herception untill 16 Dec 2010
May 2010 Ultra Sound .... ALL CLEAR... NED
August 2010 started vaccine trial University of Washington
7th Dec 2010 finished vaccine trial
20th Dec 2010 Port removed
3rd Feb no longer ned brain mets
23r Feb start VMAT radiation
August 2011 two new mets to brain and others starting to grow again !!!!
August start tykerb and xeloda
Dec 1 MRI all small brain mets gone. Largest shrunk by 50% only three small ones to go 17mm,8mm,6mm. Mets on there way out. Yeah
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