After many more doctor consultations we (I) have made a decision to have surgery on December 2nd.
I am taking one step at a time. I understand that there are 4 parts to the treatment of this cancer. I may need all 4 or I may need only 2 - but none if that is known until surgery is complete.
Part 1 is Surgery itself.
Part 2 is Chemotherapy
Part 3 is Radiation
Part 4 is Hormone Replacement Therapy or ovary removal
We are going to MN for the Thanksgiving Holiday. Greg is going a week ahead of us to hunt with brother-in-law Rob. He got the bug last year and I'm afraid we may be spending all Thanksgivings in MN from now on!!! Thanks Rob - for that!
Jess is driving up from the Rosebud Indian Reservation to have Thanksgiving with the Johnson Family. Ally, her boyfriend Kyle and myself will be back to Oregon on the 30th.
I will have my pre-op stuff done on Tuesday, December 1st and then surgery on Wednesday, December 2nd.
There will be a pathologist in surgery with Dr. Mary - so we will have an answer on any lymph node involvement right away. The second test will come back in a couple of days and the final pathology report will take about 2 weeks. From that report - we will know what the next step is.
I will be meeting with the medical oncologist before my trip.
My big work event on November 5th (Greg's birthday) is keeping me very focused and is a good distraction right now. After that - it will be one day at a time to not freak out or obsess about what is ahead of me.
Please keep the prayers coming - for all of us....Greg and the girls too!
Much love,
June
Wednesday, October 28, 2009
Tuesday, October 20, 2009
All Doctor's-- All Week
Monday afternoon we met with a plastic surgeon for 2 hours.
Tuesday the cancer counseloor
Wednesday morning with the Radiologist/Oncologist
Thursday back to Dr. Mary for more questions
I was informed yesterday that the "clinical study-radiation therapy" is not an option for me. the Dr.'s are not happy with the results they have seen and decided to take it off the table for me!
So - more appointments - more questions - then decision making time.
Whatever surgery is chosen - it will happen the first week of December.
Tuesday the cancer counseloor
Wednesday morning with the Radiologist/Oncologist
Thursday back to Dr. Mary for more questions
I was informed yesterday that the "clinical study-radiation therapy" is not an option for me. the Dr.'s are not happy with the results they have seen and decided to take it off the table for me!
So - more appointments - more questions - then decision making time.
Whatever surgery is chosen - it will happen the first week of December.
Thursday, October 15, 2009
My Gratitude List
Ok - I feel myself starting to sink into that "why me" place and thought maybe if I spent some time on my gratitude it would help.
I am grateful for:
My Faith - I know I "can" and I "will" walk through this to a healthier me!
My Family - Greg is very supportive and encouraging - the girls are my cheerleaders!
My Friends - You all know who you are - I love you!
My Work Family/Firends: The great people that I work with and those that I work for.
My Job/career - I love my job and know I am right where I am meant to be - it feels good!
My Pets - Nikki and Bella - who doesn't love a big wet, hairy dog panting and slamming its tail against your bed waking you up every morning and a small yippy dog to sleep with you at night!
My Doctor: Mary Barnhart is the best - and I feel surrounded by care, concern and comfort.
I feel better already!
I am grateful for:
My Faith - I know I "can" and I "will" walk through this to a healthier me!
My Family - Greg is very supportive and encouraging - the girls are my cheerleaders!
My Friends - You all know who you are - I love you!
My Work Family/Firends: The great people that I work with and those that I work for.
My Job/career - I love my job and know I am right where I am meant to be - it feels good!
My Pets - Nikki and Bella - who doesn't love a big wet, hairy dog panting and slamming its tail against your bed waking you up every morning and a small yippy dog to sleep with you at night!
My Doctor: Mary Barnhart is the best - and I feel surrounded by care, concern and comfort.
I feel better already!
Tuesday, October 13, 2009
It's Tuesday!
Well - the waiting is over and now time to digest all of the information. Greg and I met with Dr. Mary for almost 3 hours today! She was patient and did a great job of explaining, educating, informing and anwering questions. Pathology reports were read by 4 separate doctors - all reports confirmed the same results.
Invasive Ductal Cancer!
Now we decide on surgery options/treatment. The good news is that I have "time" to make a good educated decision. Dr. Mary is coordinating a few consultations for me: If I am a candidate for "clinical study" of a new type of radiation - I will meet with a Radiologist/Oncologist from one of the 3 Portland Hospitals that are offering/performing this procedure. I will also meet with a Radiologist/Oncologist from a local hospital to discuss the benefits/risk factors of radiation. The third meeting is with a plastic surgeon who does reconstruction surgery. Once we have talked with these Dr.'s and met with Dr. Mary again - I will make a final decision on how to proceed.
More to come - thank you for your continued prayers!
Invasive Ductal Cancer!
Now we decide on surgery options/treatment. The good news is that I have "time" to make a good educated decision. Dr. Mary is coordinating a few consultations for me: If I am a candidate for "clinical study" of a new type of radiation - I will meet with a Radiologist/Oncologist from one of the 3 Portland Hospitals that are offering/performing this procedure. I will also meet with a Radiologist/Oncologist from a local hospital to discuss the benefits/risk factors of radiation. The third meeting is with a plastic surgeon who does reconstruction surgery. Once we have talked with these Dr.'s and met with Dr. Mary again - I will make a final decision on how to proceed.
More to come - thank you for your continued prayers!
Saturday, October 10, 2009
gregs deep thoughts
kancer is STOOPID. good friends and family r the BEST. I will send this to cyberspace n see where it goes. If u r a nigerian royalty member who needs my help, a ukranian girl who wants a "friend" or sumone from indonesia who wants to improve my love life by enlarging parts of my body..thanks but no thanks..PS if you have a cure for cancer you can respond to this..or ask your God if he has one to hand out..that'd help. In lieu of that prayers are the only request that we have.thanks
Thursday, October 8, 2009
Tuesday is the "BIG REVEAL"
Dr.'s office called and we are meeting with her on Tuesday morning. She said to be prepared for 2-1/2 hours. Tuesday seems like along time from now---but at that point they will have all results and a plan, schedule and direction in place for me and Greg.
Wednesday, October 7, 2009
Today is a new day!
Just got back from the hospital having had the PET Scan.
I'm sure I must be glowing because they said they got "great" pictures of me!
Now I wait! I wait to hear from the Dr. - I wait to hear about the stage of cancer - I wait to hear about how we fight this!
I'm sure I must be glowing because they said they got "great" pictures of me!
Now I wait! I wait to hear from the Dr. - I wait to hear about the stage of cancer - I wait to hear about how we fight this!
Tuesday, October 6, 2009
Another Speed Bump In My Life
While I love giving of myself to help others, and feel very fortunate to have the "career" that I am meant to have, I am destined to learn to "receive with grace".
Once again, I am faced with a life sitution that I would prefer to keep private. However, I also know that my faith along with the love and support of friends and family are what carried me through the darkest part of our family tragedy. Because I consider you all a part of my extended family - there is news that must be shared, no matter how personal the news.
On Monday, September 21st, I had my annual mammogram. I was feeling pretty good that everything has gone digital and I was done when the procedure was done - no more waiting. the technician said that I would hear from the Dr. if anything looked bad - otherwise everything is sent to my Dr. At noon that day, I received a call from my primary care physician explaining that the mamogram reports were not good and I needed to return for a biopsy of 3 small areas in my left breast. I scheduled the procedure for Monday the 28th. I left for the TIP Annual meeting on Wednesday the 23rd - determined to enjoy my very first visit to Disneyland - you know the happiest place on earth!
On Monday, September 28th, I had a core biopsy.
On Tuesday, September 29th, I received word from my doctor that I definately have malignant core cancer.
On Thursday October 1st, I had a Breast MRI. I did not tolerate this procedure well. I became quite ill and caused quite an emergency in the MRI area. The good news is I do not have aspiration induced pnemonia as they thought. The bad news is that they really did a number on my throat and vocal chords.
So where are things now:
Yesterday (10/5) I had a bone density test and chest x-ray. This morning I had blood work done. Tomorrow I have a PET scan.
Once my doctor get results from these tests, Greg and I will meet with her while she explains the best plan of attack.
In trying to find "balance" (keeping work at work and health at home so I have a choice on when to deal with it) I have created this blog to keep my situation updated and not wear me out with trying to keep everyone in the loop. This website will be updated regulary.
If you subscribe to it, you will automatically receive all updates. I can appologize now for any sense of humor you receive from my husbands postings or my friend Dawn!
You all know I have already faced and survived the most horrific tragedy one can endure, and I had no choice but to live it out publicly. This cannot be any worse than what myself and my family have already experienced. I ask your help in prayer and support.
I do have a great support group with a large family (even though they are 2,000 miles away) and close friends. Please feel free to send me emails and questions via this website.
The best thing you can do to help me, is to keep our mission of "Citizens Helping Citzens in Crisis" going.
With much love,
June
Once again, I am faced with a life sitution that I would prefer to keep private. However, I also know that my faith along with the love and support of friends and family are what carried me through the darkest part of our family tragedy. Because I consider you all a part of my extended family - there is news that must be shared, no matter how personal the news.
On Monday, September 21st, I had my annual mammogram. I was feeling pretty good that everything has gone digital and I was done when the procedure was done - no more waiting. the technician said that I would hear from the Dr. if anything looked bad - otherwise everything is sent to my Dr. At noon that day, I received a call from my primary care physician explaining that the mamogram reports were not good and I needed to return for a biopsy of 3 small areas in my left breast. I scheduled the procedure for Monday the 28th. I left for the TIP Annual meeting on Wednesday the 23rd - determined to enjoy my very first visit to Disneyland - you know the happiest place on earth!
On Monday, September 28th, I had a core biopsy.
On Tuesday, September 29th, I received word from my doctor that I definately have malignant core cancer.
On Thursday October 1st, I had a Breast MRI. I did not tolerate this procedure well. I became quite ill and caused quite an emergency in the MRI area. The good news is I do not have aspiration induced pnemonia as they thought. The bad news is that they really did a number on my throat and vocal chords.
So where are things now:
Yesterday (10/5) I had a bone density test and chest x-ray. This morning I had blood work done. Tomorrow I have a PET scan.
Once my doctor get results from these tests, Greg and I will meet with her while she explains the best plan of attack.
In trying to find "balance" (keeping work at work and health at home so I have a choice on when to deal with it) I have created this blog to keep my situation updated and not wear me out with trying to keep everyone in the loop. This website will be updated regulary.
If you subscribe to it, you will automatically receive all updates. I can appologize now for any sense of humor you receive from my husbands postings or my friend Dawn!
You all know I have already faced and survived the most horrific tragedy one can endure, and I had no choice but to live it out publicly. This cannot be any worse than what myself and my family have already experienced. I ask your help in prayer and support.
I do have a great support group with a large family (even though they are 2,000 miles away) and close friends. Please feel free to send me emails and questions via this website.
The best thing you can do to help me, is to keep our mission of "Citizens Helping Citzens in Crisis" going.
With much love,
June
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