Well, it certainly sounds like a plan is set in place. It's so much better to have something to do instead of all the waiting and listening to doctors cogitate and ruminate. I've never heard of a power port but I hope it works twice as well as the regular types. Hugs
I for one will NEVER give up on YOU!!
Love,
Sharon
Hooray! I am so glad there is a plan in place and that you have a doctor who cares about you as a person and is an advocate for what is best for you. Keeping you in my prayers!
I have returned from my Peoria onc appointment feeling much better than I felt after leaving Chicago. My onc had not yet heard from the U of Chicago onc, but had a plan of action of her own ready. She was thinking that since I have had so much time since chemo without detectable signs of recurrence that I am platinum sensitive to some degree. She wanted to try Carboplatin and Taxotere. I told her the other onc wants to try the oxiliplatin 5fu combo and was sending my slides and discs to the tumor board next Wednesday. My doc wants to get the recommendations from the full tumor board before deciding which to use. She may or may not go with their advice. Since she seems more confident in helping me than the other one I told her I would go with what she chooses. She also said that surgery will be part of my treatment. That I agreed with 100%. Why leave anything in if it can be cut out?? She will do some chemo first, check the results, remove what is left then finish chemo. Sounded like the way to go to me. When I told her the other doc was so negative she assured me that I will be ready to give up long before she will be ready to give up on me. That really made me feel better. I go next Friday to have a power-port put in. Then on 3/2 I start chemo with whatever agents she decides to try. That is the plan. Sorry to go on and on, but if you could see how hyper I am right now it would make more sense. Thank you everyone for all of your help. Love, Marie
Dear Marie...never give up hope. I am so, SO sorry that the doctor in Chicago left you feeling a little hopeless. You are a fighter. I say stick to your ONC and don't go back to the Chicago one. Who needs that???
Love you,
L
You have such a positive attitude and you're a fighter, and obviously well educated in this damn disease! I know you won't just sit back!
I agree with Flicka, she gave me a smile too, "poop" on that Chicago Dr., their politics are a mess there also.
We'll be waiting to hear what your oncologist and you decide is the next best step for you.
Jane