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Hi Jojo!
Thanks for asking about Carole. The truth is I haven't wanted to post because it's rather depressing and the last thing I want to do is scare anyone on this website. I'd have to begin by stressing how, in many ways, unique her case has been. Her cancer has been VERY agressive and it's only been 2 years since her original diagnosis. She has never been NED, nor has she ever been even close to being in remission. When she received her original breast cancer diagnosis, she already had extensive liver and bone mets. When she received her original brain mets diagnosis, there were too many mets to count..her doctor ONLY gave her an MRI when she was having significant symptoms.
She is off her trial in Boston still because of low liver function. Although she will receive a last blood test on Wed., it is highly unlikely that her liver function will be high enough to resume the study drug.
She is currently at home. They delivered a hospital bed for her and she is receiving some care from a nurse 4 days per week. She requires care most of the time and my parents, her husband and children are with her constantly. It's, obviously,a very sad time for us and we are all having much difficulty understanding and accepting that there is nothing left to do. But we continue to pray and we will always hope for a miracle. She is in no pain, still eating quite well, but she sleeps a great deal and has more frequent periods of confusion. She is quite weak and though she can walk from room to room, she requires help standing up.
It is so nice to read about everyone on this site enjoying their lifes and in some small way, their good fortunes...because there are many. The drugs and drug combinations today are bigger and better than ever, and I know that everyone will continue to do well, taking each challenge has it comes and forging ahead knowing a cure or something so very close to it is around the corner.
Happy healing to everyone,
Celina
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