Stupid Google. I need to hear your brain mets success stories
Hi Ladies,
As I reported last week, my 3 month scans continue to show worsening of the disease. From the neck scan, a spot was found on the lower brain. I am scheduled for an MRI Friday (Feb 6). I am scheduled to see the radiation doctor on the 10th. I am terrified.
Now like I know I shouldn't have done, I just googled the brains mets. etc. I have made myself beyond being terrified again. I need to hear your success stories, Please!
I don't know why I googled. I always know it's a stupid thing for me to do.
Did any of you have vomiting prior to your diagnosis? I am not having any neurological symptoms, from which I understand is very good. I am just 2 weeks past a 3 cycle irinotecan, which does cause nausea.
Please ladies, just anything to help me calm down!
Thanks,
Carla
Comments
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Hi Carla
Check out the post from Leesa ("Leesag") from November 11, 2014. She was diagnosed with brain mets in 2011 and reported that she is doing just fine! Her message: don't ever give up hope!
You've been so much already and you know you are a strong woman. You can get through this too! And we are here to support you.
http://csn.cancer.org/node/289331
Sending lots of calming prayers your way!
Hugs,
Kelly
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Thinking of you Carla
I can imaging how terrifying this is. How was your MRI?
I am sure you already know how rare of a symptom it is and how much the outcome depends on the number and location of brain tumors. A few months ago after sudden-onset vertigo, I looked into ovca mets to the brain. I counted 12 users on CSN Ovarian board who at different times claimed that they or their loved ones had brain mets. Most of them were one-time posters. Lisa is the only one I know who is consistently coming back. I saw that you already found the recent "brain mets" thread on Inspire.
Best wishes to you,
Alexandra
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