Cathya
05-10-2018, 01:25 PM
Hi all;
I am now being treated for her2- MBC with a new 3 week on, 1 week off Palbociclib pill (iBrance) plus Letrozole every day. As this is new to me I have been lurking and reading past posts on an ibrance link on community.breastcancer.org. It's been very helpful to me and I have noticed how many other women have had their various tumours mutate over time. It's a stage 4 site (unfortunately this is my new reality) and so I'm hearing about all sorts of new treatments which are becoming quickly available. This has gotten me thinking.
I loved,loved my bc oncologist and totally credit him with saving my life first time around. He was very well respected by the hospital I attend and is missed by the younger oncologists. I would no doubt be seeing him now if he hadn't retired. Now I'm seeing a young (young to me, he's in his early 40's) man who is very energetic, upbeat and totally into all of these new drugs. He is convinced that I will be living a longer life than I might otherwise have expected. He is the lead investigator for the OCTANE program at our hospital and is having my ovarian and lung tumour genetically tested as well as my own blood. I am receiving a drug that has been available for only two months in Ontario.
So, I've been kicking around the idea that having someone totally new at this point in my treatment, someone who has worked recently in the US and is up to date on all of the newest treatments and is open minded to all the in's and out's my cancer might offer isn't this the very best thing that could have happened. How comfortable I was with my oncologist and him with me. I wouldn't have changed but if he hadn't retired, should I have? Just a thought.
my best wishes to all,
Cathy
I am now being treated for her2- MBC with a new 3 week on, 1 week off Palbociclib pill (iBrance) plus Letrozole every day. As this is new to me I have been lurking and reading past posts on an ibrance link on community.breastcancer.org. It's been very helpful to me and I have noticed how many other women have had their various tumours mutate over time. It's a stage 4 site (unfortunately this is my new reality) and so I'm hearing about all sorts of new treatments which are becoming quickly available. This has gotten me thinking.
I loved,loved my bc oncologist and totally credit him with saving my life first time around. He was very well respected by the hospital I attend and is missed by the younger oncologists. I would no doubt be seeing him now if he hadn't retired. Now I'm seeing a young (young to me, he's in his early 40's) man who is very energetic, upbeat and totally into all of these new drugs. He is convinced that I will be living a longer life than I might otherwise have expected. He is the lead investigator for the OCTANE program at our hospital and is having my ovarian and lung tumour genetically tested as well as my own blood. I am receiving a drug that has been available for only two months in Ontario.
So, I've been kicking around the idea that having someone totally new at this point in my treatment, someone who has worked recently in the US and is up to date on all of the newest treatments and is open minded to all the in's and out's my cancer might offer isn't this the very best thing that could have happened. How comfortable I was with my oncologist and him with me. I wouldn't have changed but if he hadn't retired, should I have? Just a thought.
my best wishes to all,
Cathy