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Hi Marie,
Thanks for checking in with mostly good news - seems the mets are shrinking, except for the one"angry" one, which I hope will be gone as well ASAP.
Unfortunately, I have sometimes come across rude arrogant doctors in my time - I'm glad you put that SOB in his place - I doubt he would talk like that if it had been his father/brother/uncle/child in the bed instead of the Mighty Oak -
3 years ago when my DH was being misdiagnosed by every doctor and specialist around (he had a brain aneurysm, but was missing the most usual symptom - worst headache of your life), his GP was major arrogant with us - he said that "in no way was Allan's condition neurological", and that I (his wife) had "no business getting all these tests ordered "- CT scan, MRIs etc. Yeah well when DH finally got diagnosed by the most caring brilliant neuroradiologist around - I phoned that a**hole up and left a nasty message on his answering machine - We have to advocate and fight for ourselves and our loved ones wherever we are -
I wish you and Ed a very happy holiday Marie - you certainly deserve it.
all the best
caya
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ER90%+/PR 50%+/HER 2+
1.7 cm and 1.0 cm.
Stage 1, grade 2, Node Negative (16 nodes tested)
MRM Dec.18/06
3 x FEC, 3 x Taxotere
Herceptin - every 3 weeks for a year, finished May 8/08
Tamoxifen - 2 1/2 years
Femara - Jan. 1, 2010 - July 18, 2012
BRCA1/BRCA2 Negative
Dignosed 10/16/06, age 48 , premenopausal
Mild lymphedema diagnosed June 2009 - breast surgeon and lymph. therapist think it's completely reversible - hope so.
Reclast infusion January 2012
Oopherectomy October 2013
15 Years NED!!
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