HER2 Support Group Forums - View Single Post

Carolyns · 08-03-2009, 04:59 PM

Hi Pam,
I am sorry to hear about your news… but I am with Chrisy and I would call it information. Sometimes the news is just the news. I don’t know if it helps but when I was diagnosed with Stage IV they said that I had the spray paint effect… meaning that I had mets on every bone that looked like spray paint. That was 3.5 years ago and I have been on Zometa (and a bunch of other things) ever since. My doctor always tells me that bones are so hard to read…
I am glad to hear that your treatment went well and that you have done some retail therapy. I have my fingers crossed that this will be your magic mix.
Love, Hope, Peace, Carolyn

08-03-2009, 04:59 PM	#32
Carolyns Senior Member Join Date: Jun 2006 Location: South Florida Posts: 477	Re: bone mets "too many spots to list" Hi Pam, I am sorry to hear about your news… but I am with Chrisy and I would call it information. Sometimes the news is just the news. I don’t know if it helps but when I was diagnosed with Stage IV they said that I had the spray paint effect… meaning that I had mets on every bone that looked like spray paint. That was 3.5 years ago and I have been on Zometa (and a bunch of other things) ever since. My doctor always tells me that bones are so hard to read… I am glad to hear that your treatment went well and that you have done some retail therapy. I have my fingers crossed that this will be your magic mix. Love, Hope, Peace, Carolyn