Update for my family and friends~~
OHSU has been great, and my Docs are great...
I am just going with the flow ~
don't know what to expect ~
am enjoying every day like I never have before ~
it's strangely calming for me in this situation~
I don't know why~
except that it is all going to be OK~
Of that I am SURE.
The tests and appointments up to this date:
July 17, My Doc, Astoria
Aug 14, Columbia Memorial, Astoria, Mammogram and Ultrasound
Oct 1, OHSU, Core Needle Biopsy
Oct 9, OHSU, Fine Needle Biopsy
Oct 14, OHSU, PET/CT Scan
Oct 27, OHSU, Meeting for Surgical Biopsy to be done Nov 11, 2008
The only definite answer I have had so far was given to me over the phone on October 6th, 2008 and it was when OHSU called to tell me that I did indeed have cancer. They said it was Invasive Ductal Carcinoma. ( A type of Breast Cancer)
The Core Biopsy of Oct 1 and the Surgical Biopsy to be done on Nov 11 have this in common:
Both of them provide tissue that the pathologist tests: then you get the answers. The pathologists seem to be the final word, everything else seems to be educated guesses....
I told my Docs at OHSU that I was not in any huge rush... and that I was patient.
They told me that they have found that if you are patient, you will most likely have a better outcome.
(I hope that makes sense: Patient patients and all that...)
I can assure you that my type of cancer is slow growing, and the more truth they extract with their tests, the better it is for me and for those who follow after me who have cancers like mine.
Usually you hear of the Surgery (mastectomy or lumpectomy) being done ASAP after finding a cancerous lump.
My Docs and I think it is SMART to do the Chemo first, because that way we can find the right chemo drugs and/or combinations of drugs which hopefully will make the tumor melt down....
That way we can have the actual physical demonstration of the right drugs while the tumor is being assaulted by chemo while situated in your body------ INSTEAD of guessing about the right chemo drugs AFTER the tumor is cut out and studied in a lab or whatever they do.....and then wondering if all the little 'starts' might form-up new cancers because they were not wiped out properly at the beginning.....
Makes perfect sense to me!
No matter if the tumor shrinks or not, I WILL have something like a mastectomy, some time after the Chemo.
The Chemo will have to wait until after this newest surgical biopsy of Nov 11, 2008 and after a few weeks of recovery time. Timeframe: first part of December???
The Chemo is planned at this time to consist of 8 treatments, given every 2 weeks, to last a total of 16 weeks.
Maybe that would be: something like December, January, February and March for Chemo and then the mastectomy surgery.
OK?
Hope that helps everyone ---
In the meantime, I am determined to get out and exercise as much as I can.... I know that will help me more than any other thing besides having a positive attitude.
Thanks so much for telling me I am in your prayers.
I am returning the favor, and praying for all of you!
I am getting a lot of comfort reading the Bible lately and enjoying Nature....
Heaps and Heaps of Love to All,
Love,
Cynthia
Note: I have been at the Docs in the Day today, and I have written two posts, the first of which I did delete, because even though I thought it was funny, Dave thought it was too black-humorish.
I think he was correct, and I hope this post is a lot better.
But I want to say, that because I had to rewrite, I have now arrived at the Day October 28 --which is the day that my Mother died at Emanuel Hospital in Portland Oregon. Her name was Ruth Elaine Frances Johnson DeWitt, and she was buried at St Paul's Lutheran Church in Sherwood Oregon on November 1, 1985. It was 23 years ago today that we witnessed our Mother dying -- all of us were there. It was the most intense spiritual experience EVER, and since that time, I have not had a fear of death. Thank you to my Mother for showing us courage and fortitude, you will not be forgotten.