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!!

On August 31 I had my LAST of four chemo infusions. Besides Paul, I was joined by my friends Melanie and Sarah. Melanie even brought balloons and cupcakes to celebrate the occasion.

After my blood draw I met with Erin, the physician’s assistant, who reviewed my last three weeks, checked me over, and discussed any possible changes for the next three weeks. She did mention that the results of chemo is cumulative and the fourth could hit me a little harder.

My blood work was good, so we all moved to the infusion room. Since it was lunch time by then, I sent everyone off for lunch while I took the Zofran anti-nausea pills and ate my own peanut butter and jelly sandwich along with some things I scrounged from the refrigerators. After the half hour wait for the Zofran to take affect I was hooked up to the Taxotere bag which took an hour to empty.

Sometime during that hour everyone came back from lunch. Paul figured I was in good hands, as Melanie could take me home. Before he left, we got a group picture of my three supporters for the day. (see below)

When it was time to switch to the Cyclophosphamide bag, which only required a half hour to empty, Sarah took a picture of me with my nurses for the day. (see below) They were all excited for me that this was my last visit. I was pleased that my friends cared enough to spend the time with me.

However, I knew this wasn’t the end!!! I still had to endure the three plus weeks of side effects from the final chemo infusion. As I mentioned above, I was told the effects were cumulative, and she was right. They hit harder and faster.

1. Fatigue: Started Day 2 and I noted it was serious until Day 12 when it let up some and came back Day 18 and continues on to Day 21. Hopefully it will not last much longer.
2. Nausea: I took Compazine for nausea on Days 1, 2, 4, 5, and 9, mostly at night. I would take it if my stomach was even a little unsettled so I really never got sick.
3. Tender fingernails: Started Day 5 and lasted until Day 13. My thumbnails are growing out with ridges parallel to the cuticles and all my fingers have vertical ridges. They are very brittle so I keep them fairly short.
4. Feet: About Day 11 I realized my feet felt like I had on very fuzzy socks. When I looked, there were no socks. This has persisted until now, some days more so than others. Sometimes the soles of my feet have spasms, which don’t last long. This was a new side effect.
5. Mouth Sore: Starting Day 4 my tongue became sore, mostly the edges. By Day 6 the texture on the roof of my mouth became rough. This lasted at least a week or so. I rinsed with salt water to help.
6. Taste Changes: The sore mouth coincides with how things taste, including water. Food and water didn’t start tasting normal until after Day 13 and I noticed water tasting normal on Day 18. Finally I can enjoy eating and don’t mind drinking.
7. Atrial Fibrillation: I speculate that because of my extreme fatigue, staying on the sofa, and water not tasting good, I let myself get dehydrated. The night of Day 11 my heart went into AFib, which I noticed after I went to bed. I got up and took my blood pressure, which was low, and my heart rate was 101 bpm. I used my Kardia EKG device that connects to an App on my iPhone and took a 30 second reading, which confirmed my suspicion. I printed it for my records, drank some water and went back to bed. In the morning I started downing Gatorade for the electrolytes, and by noon my heart was back in normal rhythm. This left me even weaker, however. (See below titled “Living With AFib” to learn about this little EKG device and the App.)
8. Imodium: I only needed to use it once, on Day 11.
9. Prunes: I discovered they are my friend and almost daily consumption kept me from needing to use any Dulcolax.

On Day 11, September 10, we had to miss a family wedding because of my extreme fatigue. It was later that night when the AFib started. The next evening I had to miss my Delta Kappa Gamma Chapter meeting because of the fatigue. By Day 15 I made it to my physical therapy session. On Day 16, I enjoyed a long breakfast out with a friend. On Saturday, Day 17 I was feeling strong enough to go to Monmouth for an all-day Delta Kappa Gamma State Leadership Conference. Fortunately, Melanie drove as I was tired by the end of the day. The fatigue came back.

There were two Breast Cancer Support Group sessions during this cycle, Sept. 5 (Day 6) and Sept. 19 (Day 20.) I was able to make it to both sessions, and have been paying particular attention to those who talked about radiation and those who have been taking the anti-estrogen medications, long term. I still have both of these ahead of me.

I meet with my oncologist, Dr. Acheson, on Sept. 28 to discuss the anti-estrogen meds I’ll start after radiation. On October 3 I go in to radiology for the “mapping” appointment where they set up everything so I am positioned exactly the same each time. I will start about a week later. I’m scheduled for twenty-five sessions; every weekday for five weeks. More on that after I get started.

Paul has been such a trooper, doing all the cooking, dishes, watering plants, grocery shopping, etc. and never complaining. What a love!!!

That sums up the last three weeks following my Fourth and Last chemo session. I made it through, like I knew I could. Yippee!!! No Regrets is still my motto.

Living with AFib:
As an aside, you probably noticed that I keep referring to my heart going into AFib. I was asked how I can tell? Usually, the first thing I notice is that my heart is pounding noticeably in my chest. When I sense this, I use test #2 and have my Apple Watch take my pulse, which is an app I have readily available on it. Since my normal resting rate is somewhere in the 60s or low 70s, if it is bouncing around between the 80s and 110 bpm (sometimes as high as 134), I have a pretty good idea I am in AFib. Then there is test #3. This is to use a little EKG recorder a friend told my about. It is made by Kardia and I got it on Amazon for $99. It pairs with an App by the same name that I have on my iPhone. It has two metal plates onto which I place fingers from each hand. They connect over bluetooth and it takes a 30 seconds reading. I then email the results to myself as a PDF and print it out. When I asked my cardiologist, he said that a lot of his patients have them, and he totally approved. I can show a doctor the rhythm printout taken while the event is happening. What I am realizing, however, is that my heart probably goes in and out of AFib more often than I realize, which makes my very happy that I am on Eliquis blood thinner to avoid the clots/stokes that can be generated when your heart functions irregularly. My cardiologists are just trying to get me through all this cancer stuff, then will deal with my other heart issues. I know I’m eventually looking at a pacemaker, but not now. I have two cardiologists watching over me. If you, or any of your friends or relatives have issues with AFib, check this out: ActiveCor and have them consult their cardiologist to see if it is right for them.  https://www.alivecor.com.

On August 9th I had my 3rd chemo infusion. By now I know the routine: show up, pick a chair, get the IV placed and have blood drawn. Melanie was back with us for this visit to act as my scribe. Next I saw Dr. Acheson, my medical oncologist, and we reviewed how everything went during the last session.

Basically, I had the same side effects as the previous sessions.
1. Fatigue: started on Day 4 again and lasted until Day 11.
2.Tender fingernails: started Day 5 and ended Day 8.
3.Mouth sore: started Day 4 and ended about Day 9. No sore tonsil this time.
4.Taste changes: Not significant enough to note, but probably lasted about a week.
5.Didn’t Have: a fever or any AFib episodes.
6.Need for Imodium: Days 7 and 8.
Discovered Prunes: I had forgotten about the prunes I bought before starting chemo. I started eating some daily with breakfast on Day 18 and that eliminated the need for Dulcolax.

On August 10, the day after my infusion, I attended a morning session called “Look Better, Feel Better” put on by the American Cancer Society. They provided a whole packet of beauty and make-up products and the representative went through them all, showing us how to apply each one. It was fun, and I went away all made-up to attend a play at our local Lakewood Theater that night.

The steroid, Dexamethasone, I have to take twice a day the day before, day of, and day after my infusion causes insomnia. By Friday and Saturday I was pretty exhausted. That just leads into my fatigue sequence of days.

I did attend the one Support Group during this time. It was a smaller group, but interesting, and I’ll return next month.

The big event here in our area was the solar eclipse on August 21. We were invited to spend the time at my cousin and husband’s (Linda and Richard) place in Lincoln City on the Oregon coast, and within the area of Totality. To avoid the predicted heavy traffic going to the totality areas we drove there on Friday. We think the weather and traffic predictors scared many people away, as neither dire predictions came about.

Monday morning, Aug. 21, dawned with some fog a short ways inland, but by eclipse time, about 9:00 am, it had pulled back to the beach, giving us a full view of the eclipse. I set up my tripod and camera in a driveway across the street. I used a “White light solar filter” attached to the lens. For those of you interested, I was using my Canon 70-200mm lens with a 1.4X extender attached to my Canon 7D DSLR that has a crop sensor (X 1.6) which gave me a total zoom of 448mm. I got fair shots but missed the diamond effect as I was busy putting the filter back on the lens. Ugh! The picture below is a composite of some of my shots as the eclipse progressed.

Fortunately, the eclipse was on my Day 13 when my energy level was beginning to return. We returned to Portland the next day, managing to avoid some of the heavy traffic.

On Days 15, 17 20 and 22 I felt like going to Curves to exercise. I am still just doing the circuit one, instead of the usual twice, and doing all the stretches. It feels good to be back.

My LAST, #4, infusion was yesterday, August 31. All went well and along with Paul and Melanie another friend, Sarah, joined us to help celebrate the event. I will write about it, and how everything went for the final three weeks sometime around September 20. (See pictures below.)

My Radiation is scheduled to start October 10: every day for five weeks. More on that later.

I am still staying positive and happy with all my decisions. We are both looking forward to celebrating the end to it all by Thanksgiving and Christmas, and looking forward to getting back to Green Valley, Arizona mid January. Remember that my motto is still “No Regrets.”
My favorite aria by Edith Piaf.

Click on each picture to enlarge.

For a quick review, my chemo is scheduled in four sessions or cycles, each three weeks apart. My first was June 28 and the second on July 19. The last two will be on August 9 and 31.

On July 19, I received the second infusion of the two drugs, Taxotere and Cyclophosphamide. Since Melanie was out of town, my friend Jan joined Paul and me to act as our scribe and just be there for moral support.

The routine was the same: IV and blood draw, visit with physicians’ assistant, Erin, to cover the first session, and on to the infusion. All went smoothly.

During this second cycle some of the side effects hit more quickly and lasted a little longer.
1. Fatigue: started on Day 4 and didn’t let up until Day 12.
2. Tender finger nails: started Day 5 and lasted until Day 10.
3. Mouth sore: started Day 4 and lasted until Day 13.
4. Sore tonsil: same as last time, and lasted until Day 13.
5. Fever - new: Day 10 I was cold and my temp went from 100 at 11:00 am to 101.8 at 7:30 pm.
    a. Called the doctor and after eliminating anything viral was prescribed an antibiotic.
    b. Temp returned to normal by Day 12.
6. Taste change - new: part of time between Day 4 and 13 food started tasting different.
    a. Had to force myself to eat.
    b. Added some Gatorade to water so it didn’t taste bad.

As a result of the fever, happening on my low energy days, we had to miss the 50th Anniversary celebration of our good friends Iran and Fran. We also missed the going away picnic for our goddaughter, Molly, who is moving to Honolulu where she will be doing her doctoral residency. We were able to walk three doors down to attend our neighbors’ open house, though, so the whole weekend wasn’t a total wash.

By Day 13 I was feeling pretty good and the rest of the 21 days were good ones. I was able to go to Curves several times and even go shopping a few times. The special day was being able to attend an all-day DKG meeting in Monmouth, and I felt completely normal. I must admit I needed rest the next day.

Another positive outcome of this session 2 was that I did NOT have any more episodes of AFib. None! My cardiologist was very happy to hear that. He also commented that the Kardia EKG printouts I had from all the episodes during session 1 were very helpful (See a couple posts back where I talk about “Living with AFib.)

The Breast Center at St. Vincent Hospital runs a support group which meets twice a month. I was able to attend the first time on August 1st. There were about fourteen who attended, plus the hospital volunteers. The group varied from a young lady who had just been diagnosed to some long term survivors. I was the only one currently in chemo, but several were in radiation and several were going through reconstruction.

When it became my turn, I shared my motto of “No Regrets,” my Kardia EKG machine, and my system of tracking side effects. When it was all over, I was glad I went and will go back. My take-aways were:
1. I was very happy to have decided not to do reconstruction.
2. I was happy with all my decisions.
3. I felt very good about myself and my positive attitude.

The American Cancer Society offers a session called “Look Better, Feel Better” which will be held August 10 at St. Vincent. I have signed up for it. I understand we are given some make-up and shown how to apply it, and other tips for looking good. Sounds like fun.

Today, August 9, I had my third infusion, and all went well. My next post will be after I have completed this third session, sometime around August 31 - when I get my last infusion. In the meantime, I’m staying positive and enjoying life.