Wow, what a year 2017 has been. It definitely had its high and low points, but the good thing is that it is ending on the up side.

To do a brief recap: the year started with our going to Green Valley, AZ in January followed by a two week trip to Cuba in February. That was when I discovered a lump in my armpit. The end of March I had it biopsied and it was diagnosed as a lobular carcinoma. Since we were scheduled to leave in two days for a two week photo expedition cruise around Baja, California, we were encouraged to go. It was a great distraction. (See photos under Photo Gallery menu above.)

We returned to Green Valley then home to Portland in mid April when the whirlwind started. An MRI showed that I had several tumors in the breast on the other side, which the 3-D Mammogram did not show. So, on May 10 I had a double mastectomy. My cancer type was Estrogen Responsive Positive (ER+) and the Oncotype DX test showed that I would benefit from Chemo. I started the four sessions of chemo on June 28 and the last session was on August 31. I managed the side effects, which you can read about in previous posts.

In October 13 I started radiation treatments. They were daily for 28 sessions, ending on November 20. (My November 4 Post tells the details of the sessions.) There were a couple of side effects. One was fatigue. Since I was already back to working out at Curves three days a week and walking three days, I found the fatigue minimal. The other effect was like a “sun burn.” I managed to keep that to a minimum by using two gels: Aloe Vera 99% and Calendula three times a day. After the last treatment I was given a prescription for 1% Silver Sulfadiazine Cream which is used on burns. I applied it thickly twice a day. Dr. Gannett, my radiation oncologist was always pleased with how well I was doing. I saw him on December 18, one month after my last treatment, and should not have to see him again.

Meanwhile, on November 29 I met again with Dr. Acheson, my medical oncologist. She was pleased with how well I am doing. We had a discussion about what comes next. My type of breast cancer is Estrogen Responsive Positive (ER+.) This means it feeds on estrogen. Believe it or not, our bodies continue to produce estrogen after menopause, so it is important to shut down all of it. Therefore, there are various medications that are recommended to reduce the risk of the cancer re-occurrence. Since I do not have a bone density problem, I qualify for the class of drugs called Aromatase Inhibitors (AI.) Dr Acheson is starting me with Letrozole. It is important to be able to take one of these for at least five years. If I tolerate this one, great, if not there are two other AI drugs to try. I started December 1, and so far so good.

Then there is my hair. It has now grown out to about an inch long. I can tell there will be some curl, at least for a while. It will be some weeks before I stop wearing something, hat, scarf or wig, because I’m cold otherwise.

Then there is my heart issue: totally unrelated to my cancer. I continued to have occasional AFib episodes. I had a 48 hour Holter Monitor test which showed no pauses over 2 seconds. I also had an echo stress test (with treadmill) which shows my heart muscle is healthy. All Good News!!! Since I’m on the blood thinner Eliquis I don’t have to worry about blood clots and strokes, so until my AFib episodes get to be too frequent or of concern, I don’t need to have anything done about them. It is good that I have two cardiologists looking after me.

About the time I started chemo I learned about the Breast Cancer Support Group sponsored by Providence St. Vincent, which meets twice a month. I have attended all but one session since then, and find them very helpful. I have been able to learn from others going through what I have, am or will go through. The women who run the sessions are also very helpful, and I plan to continue attending when I can.

So, this ends the year 2017, and I’m so thankful that I have made it through all of these annoyances and blips to my health. I’m looking forward to the new year and getting back to “normal.” We look forward to returning to Green Valley, AZ for the winter where I have twelve classes already scheduled for me to teach at the Camera Club.

I will post again in the future every once in a while to chronicle any changes, or to just let you know I’m doing fine. You can also check back periodically to see photos of our travels. That was the original purpose of my website, since travel and photography are my special interests.

Until then, thanks for reading about my breast cancer journey. I hope it has been informative.
May we all have a Happy New Year!

Grace

Dear Special Friends of Grace,
    Grace is my older sister.  We've been together for many years ;0)
She means the world to me. I would prefer to be the one to do all the things for her that I will mentioned. Since it was impossible for me to do all that, along came you folks, "Grace's Special Friends".
    "Thank you!" to each one of you for coming along side her, cheering, comforting, and doing whatever you did, to make her year bearable, enjoyable at times, and doable because you were there for her. I deeply appreciate what you have done and wanted you to know my observations as time went by and Grace's sense of well-being because you were there for her.
    This is Grace's last week-end before her last Radiation treatment, and then there is "recovery time."
    Some of you were with her from the beginning, making trips to the doctors, and taking notes which relieved her mind so she could focus on what was being said.  
    Some of you took on the "Care-Giver" role.
    Some of you periodically provided transportation.
    Some of you cooked special meals, and brought them over for Paul and Grace.
    Some of you sent her flowers, cards, and your prayers and love.
    Some chose to wait in the waiting room during her surgeries. I know that Paul appreciated your support, as well.
    Some called to see how she was doing; and, my guess is, some of you checked on Paul to see how he was doing.
    I'm sure I left out some of your acts of kindness toward Grace.
   Grace is a wonderful sister to me and a great example for me to follow on this road of recovery.  
   May each of you stay in good health for many years to come; and if not, may you be surrounded by the same kind of friends that you have been to Grace to help see you through.
    May God bless you as you have blessed others.

Very Sincerely,
Gayle

I see that my last update was dated September 20, which seems like a long time ago. It was three weeks after my last chemo infusion. Since then all of my side effects have disappeared with the exception of my fuzzy/numb feeling toes. My strength has slowly returned and a couple weeks ago I realized that I really was feeling very NORMAL. For three weeks now I have been back to doing full workouts at Curves, three days a week, and walking the other three days of the week. This is all very good since fatigue is a normal side effect of radiation and so far, I have not experienced any!

On October 3, I had the “mapping” for my radiation treatments. They made a mold of me in the right position so I can lay in it exactly the same each time. I started the 28 daily sessions on October 12. My regular appointment is 10:24 AM every day. I always go in early, just in case traffic is bad, and work on the group jigsaw puzzle they make available. The actual session only takes less than ten minutes, and the radiation from three angles is for 12, 10 and 19 seconds each. About day 12 my skin started to get a little pink. I have been faithfully using the recommended 99% Aloe Vera gel and Calendula gel three times a day. This is when it may be an advantage that much of the area is still numb from the surgery, so I’m not feeling many uncomfortable sensations.

Every week they take X-Rays of me in position to make sure everything is still being set up correctly. Once a week I also see Dr. Gannett. He answers any questions I have and looks at my skin to see how it is fairing. So far, he is very pleased with how everything is going and how good my skin is tolerating the treatment. He is also surprised that I am not yet experiencing any fatigue, but attributes that to my continued exercising. One thing I learned in our discussion is that the side effects (fatigue and skin irritation) should be gone within three weeks of ending the radiation treatments. November 20 is the last one, so that means I should be in good shape by the second week in December, if not before. Also, my hair is growing back, but can still be measured in 1-2 mm. I'm trying to be patient and know it will take a couple more months to be presentable. In the mean time, my warm fleece stocking caps will have to do.

On November 29 I meet again with my medical oncologist, Dr. Acheson, to discuss the anti-estrogen pills I will need to take for at least five years. I expect I’ll be starting them in early December. That can be the next blog post topic.

It has been fifteen years since we have remained in Portland for the fall season, to enjoy all of the gorgeous foliage colors. We have missed that, so we are really enjoying colorful trees and the nice weather we have also had, up until this week. The rain has now hit. That doesn’t stop me from my walks, however, as I have plenty of rain gear.

I finally did put a personal post on Facebook in honor of “Breast Cancer Awareness Month” to encourage everyone to get those annual mammograms. And, if the results come back with a “Too dense to be sure” comment, have a followup ultrasound, at least.

I’ll make another update when the radiation is finished (11 more to go) and the extra three weeks the side effects could last.

Happy Thanksgiving. Paul and I certainly have a lot to be thankful for; especially my getting back to good health!!