42: RIP Bert

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At 615 pm Pacific Standard time my 56 year old sister Bert passed away from Stage lV Breast Cancer. My sister and I were diagnosed a little over a month apart. I was Stage lll, she was Stage lV. I chose to fight, she did not. I tried to talk her into changing her mind and to do treatment, ( told her we could be chemo buddies) but she did not want to. The doctors last year told her she would have about 2 months to live without treatment, which meant she would not make it past October 2015. I did Chemo, had surgery, then did Radiation Treatment, one full year of Herceptin Infusions, she chose to be medicated and wait for death. I get angry at times, especially with everything the family has had to endure because of her decision not to seek treatment. Family will do everything for a loved one, but when someone does not want to help themselves that task is challenging . The past couple of months have been especially hard for my family having my sister at home. The day-to-day challenges of keeping my sister from falling, cleaning her up after  uncontrollable incontinence. My sister was not herself anymore, she could not feed herself, she had been falling down, bruises all over her body from the falls. Social Services determined that it was time for a nursing home. She was placed in a nursing home in Yucaipa, ten days later she is gone.

In July when I went to visit my sister I had asked her if she regretted her decision not to do have treatment. With out hesitation she said “No”. She did tell me that she regretted letting them do the mastectomy. I described to her what would have happened to her breast if she refused the mastectomy. She just stared at me, she really didn’t respond. I think my sister had this vision that she would just close her eyes and pass. She did not think she would last a whole year after being told two months. None of us did.

To my sister Bert: I am so sorry that you were so unhappy on this earth that all you wanted to do was depart from it. I am sorry that you always referred to yourself as the black sheep of the family. I am sorry for the years that you alienated yourself from the family, you had your reasons for choosing to be distant. I am sorry that you did not love life enough to want to fight for it. You leave behind a beautiful daughter that is loved by everyone. You are free now, free of pain, free of cancer. I have been praying for you and will continue to. You are now with our other family members that have passed before us, rest in peace, God bless.

This morning here on Maui I did a 3 mile walk for breast cancer. It  was the second annual Spirit of Aloha walk against Breast Cancer. On the walk I ran into a friend that used to work for MDI. Adele and I talked for a little bit on the path, it was really nice running into her, she later then invited me over to a luncheon at a friends house. It just so happened that I did mammograms on three of the ladies at this luncheon. This group of ladies were amazing, I had opened up to them about my story, and the knew about my sister. I was at this luncheon when I got the news about Bert passing away. I am glad that I was not alone when I found out. It was meant for me to run into Adele, so that she would invite me to this luncheon. A couple of hours ago I received a phone call from Brian Burns the founder of this mornings Breast Cancer walk. He called to tell me that I won the “Grand Prize”, REALLY?  What an emotional day!

I won a two night stay at The Wailea Beach Marriott Resort & Spa! I received Brians phone call just hours after Berts passing. I told Brian that perhaps my sisters spirit had something to do with me winning the grand prize!

Mahalo for reading my blog.

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41: Maui to Lana’i and Back !

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When I signed up for this voyage I was a little apprehensive about it…to say the least. But I really wanted to do something significant to celebrate my successful feat in conquering each obstacle this past year. Chemo therapy was no joke, with each treatment I was sicker and sicker, then came surgery . With the help of amazing Physical Therapist, and my personal daughter nurse Mo with me, I recovered seamlessly. Then came Radiation Therapy, again by following doctors instructions on skin care to a tee in addition to  Physical Therapy, the Myofascial release, followed by Lymphatic massage has been a god send. One full year of Herceptin infusion completed……..I am officially done with treatment! How do I say farewell to this past year? I signed up to take part in The Pacific Cancer Foundations “Paddle for Life” “Voyage to Lana’i” fundraiser!

First and foremost, much mahalo to those who contributed to my cause, I am beyond appreciative. Love and support is not just monetary contribution to my cause. The past year I have received many cards (via mail), text messages of support, voicemails left on my cell phone, family coming to Maui, patients that I have imaged inquiring about me. I could go on and on. I truly feel so much love and support from everyone….I am blessed.

The Voyage :

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My day started with a 330am alarm. By 445am I was at our bus pick up location at Maalea Harbor, which took us to the West side of the island. I was not launching off, so therefor I was at the boat ramp. We were taken to our support boat via a zodiac boat. One the first six man exchange I was put in. You transfer in the open ocean from you support boat to the zodiac then to the canoe. I was really out of comfort zone but with the help and encouragement of my team and the boat support team I managed to transfer….no fear! (It’s not like I can say “God, please make the waves stop so I can transfer without the ocean moving”) I did it I am so proud of myself! Kept telling myself “I beat cancer I can do this”. Being in that canoe in the open ocean was intense on the way to Lana’i, the waves were intense, it was beyond exhilarating !!!! After a couple of exchanges I was put in to be part the landing crew. Paddlers in the launch and landing are survivors. Since I didn’t get to launch I got to land. Coming just past that rock that I never thought we would reach was so emotional. Our captain Linda T.A. had us stop just before coming in and said some encouraging words to each one of us, we were the last canoe in. All the other paddlers were lined up at the beach, I could just see and hear the cheer coming from everyone one the beach as we landed. To follow Hawaiian tradition when you land on another island, permission is granted, then you present gifts after Hawaiian chants and prayers. Each paddler presented gifts to the people of Lana’i. We were given Taro plants, and roots to present to them one by one……all 300 plus paddlers!!  It was a beautiful ceremony.

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We were provided lunch, by Hard Rock Cafe. After eating those of us that were camping needed to set up camp before the sunset. We were provided tents to pitch….pink tents!! I don’t remember the last time I camped in a tent! Some paddlers opted to stay at the Four Seasons or the Lana’i Hotel, I believe those were you only options. I opted to camp.img_3700

I pitched my tent and then went a little hike up to “sweetheart rock” with a fellow paddler and friend Flora.

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This is the rock that when paddling into Hulopoe Beach at Manele Bay I thought we would never reach! The view was so beautiful! Dinner was provided by Nalus , I believe they also provided our breakfast Sunday morning as well. A small group of us wanted to ride to visit Lana’i city. We piled into my team captains car and she took us to visit some sites on the island before going into the very small “Lana’i city”. Here is a picture of us by “Jax” which are large concrete barriers in the shape of jax. They create an ocean break where the barges  come in for deliveries of containers. img_3668

Sunday morning come oh so fast, sleeping on the ground was not very comfortable, especially being sore from paddling. By 630am our tents had to be down and packed, our bags with our belongs with our team had to be taken to our specific support boat. We had breakfast, 10 minute yoga stretch , morning prayers and chants in Hawaiian, songs were sang it was truly beautiful. I again did not get to be part of the launching crew, but we did get to see the launch before going to the boat harbor to our designated support boat. img_3698

A total of twenty-four canoes entered the water…and they were off. On the first six man exchange I was put in. Again transferring was a bit intimidating for me but I did it! It was blazing hot, the ocean was calm and our support boat captain turned the motor off and said we could jump in the ocean if we wanted. I jumped!!!! We had a rope to hold onto so we would not drift far, you bet I held onto that rope. It was so refreshing to jump in for that moment. There was going to be a couple of exchanges before I went back in so I grabbed my camera and took some photos. dscn0847

This is a picture of the zodiac coming toward our support boat to pick us up for another exchange. I was put in, and from what I understand the distance was another 3.8 miles away from Maui. Once in the canoe, you are paddling with strength that you did not know you had. No more exchanges, we were taking this canoe in!! Our steersman Buck was very encouraging, telling us that we were survivors and we could do this!! “Stroke, stroke, stroke” he shouted periodically, “timing people”, “stay focused, you can do this”, “stoke, stroke, stroke my matees! Our support zodiac came over to us to make sure that we were all ok to “ironman” in, we were given small water bottles in case there was not any at the beach waiting for us.

To describe the beauty of Maui from the ocean is impossible. We were so far out that you could not even see the beaches of the West side or the high rise resort hotels of Ka anapali. It was blue ocean, the verdant westside of Maui topped off with blue skies and scattered clouds that looked like a halo over an angel. Purely breath taking. As we got closer to Maui, we could see the resorts, with each stroke we got closer, but it seemed to take forever. The end was near as we got closer and closer, we could see that the rest of our team was in the water waiting  to help us bring this canoe in. We landed!!!

This voyage was beyond amazing, never did I imagine that one day I would be part of a team to paddle from one island to another. Doing this was physically and mentally challenging. It was both spiritual and emotional for me sometimes bringing tears to my eyes thinking of the past year….. but that is exactly what it is now…in the past. Time to focus on the the next phase.

Much Mahalo and love to the Pink Paddlers for being so welcoming, you are an exceptional group. I can not believe that this much anticipated event is over, I am so glad I did this.

Much Mahalo and love for taking the time to read my blog.     Pina

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40: Huli Practise

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The photo above was taken at a regatta competition, the canoe flipped over, other wise known as “Huli”.

I have been practicing for The Voyage to Lana’i , which is a major fundraiser here on Maui benefitting The Pacific Cancer Foundation. We will voyage from the island of Maui, to the island of Lana’i. There are over 300 hundred paddlers going across!

Saturday morning was huli practice , all voyagers that have never been in an actual huli were  highly encouraged to attend.  So there I went! I will be the first to admit I was not comfortable with it,  but knew I needed to experience it……..no fear!

Kimokeo, one of the organizers and spiritual leaders was with a canoe just off the shore. I was called over, I was honest and told him I was just a little frightened. (In my head I’m thinking, I am about to embark on a journey across the island….seriously) Kimokeo, (fully aware of my situation) asked my what side my surgery was on? I told him left. At this point he is in the ocean, he instructs me that when the canoe flips, come up next to him and hold on to the canoe with my right hand only. We flipped, I surfaced, I survived. But what happened next was totally unexpected.

I mentioned that Kimokeo is a spiritual leader. He does blessing through out the island. As I was coming out of the water he called me back into the ocean and placed his hands on my head and started praying in Hawaiian over me. He had me repeat the prayer with him, three to five words at a time, all in Hawaiian (pigeon). It was so beautiful and spiritual, I am literally getting chills as I am trying to describe this event. We went under water together three times together. I have been blessed and Baptized by Kimokeo. I truly feel that he sensed a fear in me, I no longer have that fear, I am ready for this voyage.

Mahalo for reading my blog

Pina

 

 

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39: Voyage to Lana’i

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I remember when I first moved to Maui, Jack and I were inside of Safeway grocery store, we saw this lady who was wearing a Mana’olana Pink Paddler t-shirt. Jack started a conversation with her letting her know that we had just moved here and that I was a mammographer . She invited me to paddle, as this is for supporters of Breast Cancer not just for survivors.

It is strange how the universe works. Here we are just over two years later, and I am a survivor!!! Last year I was looking into taking part of this annual voyage, however that ambition was cut short with my diagnosis of Stage 3 Breast Cancer last year in August.

My first chemo therapy was September 25th, exactly one year ago. I did it!!!! I managed to get thru the 6 treatments, recovered. Followed by surgery, recovered. Followed by Radiation Therapy, recovered! On September 2, I had my last of 12 Herceptin  infusions. I am kicking butt!!! All of this would not have possible without the love of my husband, kids, cousins (very special and dear to my heart)! I can’t say enough about all the amazing people I have met here on Maui…..much mahalo for the love and support.

The voyage? I will have to admit I was reluctant to sign up! After all this is traveling from one island to another and back. I have been paddling on Saturdays (cause I work M-F), lots of people here that I paddle with are retired, or have jobs that allow them to paddle out during the week. The more I thought about, the more the challenge excited me! I called the Pacific Cancer Foundation, talked to the director and she encouraged me, telling me that I could do it!

The Voyage to Lana’i  is not a race, I know that it will be physically challenging, but this past year hast been challenging, if I could survive Stage 3 Breast Cancer treatment, then I can do this, I am up for the challenge. And being placed on a team with the Pink Paddlers is just going to make this journey across the ocean extra special . The picture above was taken in 2014, when paddled with them how ironic is that!

I plan on blogging about my experience, I know it will be emotional and bittersweet for me. It will be my way of saying “nice try cancer” “I won”. The following is a link to my page for donations……please only donate if you are able, any amount is appreciated.

http://paddleforlife2016.myevent.com/participant/389253

This week I go see my Radiation Oncologist. A three month follow up appointment. Also I already have my next appointments set for my follow up with my  Medical Oncologist. My next trip to Oahu will be a two night stay.

January 11th: CT scan of the chest and abdomen. And a Bone Scan

January 12th: follow up with Breast Surgeon  Dr. Mari Nakashizuka/ in regards to the prophylactic mastectomy and my first consultation with Plastic Surgeon,  Dr. Vincent Nip (yes Nip!)

January 13th: follow up with Medical Oncologist; he will go over the results of the scans with me. Just need to pray that no new cancer decided to pop anywhere, and that the lung lesion has not grown!!

Mahalo, for reading my blog…have a wonderful work week!….Pina

 

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38: The Hair is Growing!!

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I do not recall ever having short hair! The texture is soft and it is curly in the back and wavy up on top. I had to break down and by a hair product, using Tea Tree Shaping Cream by Paul Mitchell. When some patients  see me and remember me from last year, they say “oh , you cute your hair….that looks really cute” My response : “actually this is new hair growth after Chemotherapy”!  Their jaw drops, patients have teared up, hugged me and have just been so kind with well wishes and prayers.

I do the Bone Densities for MDI, twice a month. One of the x-ray technologists does them on Saturdays. My last Dexa day (as I call it) told me she refused a Saturday appointment because she wanted me to do her exam so she can see how I was doing. Apparently I did her mammogram when I was in the middle of Chemo, she was so sweet.

It is hard to believe that a whole year has passed already. The journey has not been an easy one (especially the chemo part of it) but I did it!!!!!!

TOMORROW IS MY LAST HERCEPTIN INFUSION!!!!!!!!!!!!!!!!  After tomorrow I will officially be finished with my treatment! Except for the Anastrozole that I have to take for the next five years (possibly ten) And of course the ongoing test to make sure the cancer does not decide to pop up somewhere else!!!…..one day at a time!!!

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Well,  besides having a Primary Physician, Oncologist, Radiation Oncologist, Pulmonologist, Breast Surgeon, Plastic Surgeon…..I can now add a Podiatrist to the list! Since Chemo treatment number four and five I have had problems with ingrown toenails. (There has been no coorilation between ingrowns and chemo.) I have experienced and continue to have slight neoropathy of the toes and fingers (not so much on fingers) So the infections seem to creep up on me! I don’t feel them till it’s infected. The past three months have been riddled with frequent trips to the Podiatrist. Literally it seems like I have been to see him every two to three weeks. He has in the past mentioned a procedure to eliminate the growth of the nail going down, causing the ingrown. The procudure is call a Matrixectomy. I had this produre done yesterday, initially went in for the ingrowns, agian. After he (Dr. Lee) numbed both great toes, he offered the procedure. It required more numbing, which was super painful…I mean SUPER painful.  After the side of the nail is removed, acid is placed to kill future growth of the nail. So, once agian I am on ocean restriction…no ocean for two weeks!!! Today was challenging to work, the toes hurt but I managed to work the whole day!!! fyi: the pain was when the injection of lidocaine is administed, after that I didn’t feel a thing… and Dr. Lee continuously kept asking if I felt anything. He wanted to make sure i was completely numbed up.

Hopefully tomorrow mornings flight to Oahu is uneventful. The Hawaiin islands are on huricane watch, so far Maui has been unscathed from this threat (knock on wood), I dont like turbulance on the flights!

It’s getting late and I have to get up early to fly out….good night and much Mahalo for reading…

Pina

oh, one more thing…. I wore mascara the other day for the first time!!! the little things!

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37:Coming up on One Year!

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Since my last blog  a lot has happened, my July infusion of Herceptin was on the 22nd. The day before that on Thursday the 21st I had another Echocardiogram, and a baseline Bone Density. The Echocardiogram (this was my fourth one) I had one before chemo started last year in September, the second was performed in November, the third was done one month after my last chemo and now this one in July. The purpose? The chemo treatment I was given effects cardiac output, also one of the side effects of Herceptin effects the heart. So far so good!!!! The heart is strong!!! I started to take Anastrozole (Arimidex) in February. One of the side effects of Arimidex is bone loss, hence the necessity for a baseline Bone Density. Happy to report I am in the “green”…..fellow technologists will know what the means!!! Normal! As of right now, my bone density is “normal”!….I would like to keep it that way.

I have also been going to Physical Therapy twice a week for Myofascial  Release Massage (covered by insurance) which has been wonderful!!! I have been going to Kihei Physical Therapy with Christine Lachance DPT. MSPT. CLT., she specializes in Cancer patients.

I am back in the ocean! The first week-end in August I paddled out with the Maui Canoe Club, it was beautiful! (With the exception that they were burning cane that Saturday morning and there was a huge brown cloud over the island). None the less, it was beautiful to be out on the water. Once I got back to the condo after the morning paddle out I turned my tv on and started to get sucked into watching the Olympics which were on day 2! I quickly turned the tv off, packed some fruit, grabbed some water, towel, chair, book and to the beach I went!!!! I was at the beach from 10 am till 4pm, so refreshing to be in the water again!

This past Friday, August 8th I was back in Oahu for Herceptin. I had a great visit with my Oncologist Dr. Chong, we talked about the past years treatments and how well I did. He commended me for having that fighting spirit and mentality to fight and stay positive (attitude toward treatment is half the battle) We talked about what is yet to come.

Saturday morning (13th) I had every intention on paddling out, however my stomach said overwise. I have been fortunate that the Herceptin side effects have not been that bad for me, however Saturday morning was plagued with many trips to the bathroom, I didn’t think going paddling was in the cards for me.

My next Herceptin treatment will be my last one!!!!! YES!!!! My last one!!!!!! Can I get an “AMEN” My next trip to Oahu is on September 2nd, after this appointment with Dr. Chong I will see him again in January 2017. It was supposed to be in three months, but that would mean coming in December. So, he pushed the follow-up out to January 2017, also because and that time he would like for me to have an appointment with the breast surgeon Dr. Mari Nakashizuka and the plastic surgeon, Dr. Vincent Nip. So, come January 2017 we will start the ball rolling for the next step……..prophylactic mastectomy and reconstruction!

The picture included with this blog was taken with a feature on my camera called “color selection”. I selected light purple and i pulled that color out with everything else black and white. This next one I selected pink hues!

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Mahalo, thank you for reading and Mahalo for all the patients of MDI that have inquired about me and for all the prayers and well wishes.

 

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36: Happy Birthday Bert

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For those of you that have been following my blog from the beginning, you know that about 5 weeks before my Stage lll Breast Cancer diagnosis last year, that one of my sisters was diagnosed with Stage lV.  My sister did not choose to do treatment, for personal reasons that I personally can not comprehend,  she chose hospice instead. I have and continue to respect her decision. I would also like to mention that I am talking about my sister with her permission to do so.

The doctors told my sister that without treatment she would not have long and we thought she would only live till October 2015. The holidays came and went, and now one year has passed and my sister is still with us. Most recently her condition has declined. Nurse visits from hospice have increased, her pain meds have also increased.

The past year I have had the fight of my life, I started and finished the 6 sounds of the very aggressive Chemotherapy regiment for Stage lll and lV breast cancer. I had my modified mastectomy (skin sparring for delayed reconstruction), I started and finished 29 sessions of radiation treatment. I have faithfully stayed out of direct sunlight and the ocean (really hard to do on Maui). All the while, working through this with exception for medical leave after my surgery. I have been focused and determined…….then I think of my sister. Yes, sometimes it angers me that she did not choose to fight. I run through my head “is there something I could have done to convince my sister to do treatment”? I know  from talking about this at a support group I attend that the answer is no. My sisters decision was made up, nothing we could have done would change her mind.

I flew to California for the 4th of July weekend. My cousins gave one of my aunties a seventies themed birthday party. (can you guess how old she turned) I took the opportunity that I was feeling well enough to travel and surprised the family!

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Visiting with my sister Bert, we talked about our mastectomy surgeries, she shared with me about her condition, details that I will keep private. We talked about hospice, my sister is in pain….we talked about the pain meds that she is given and the need for the meds to be increased to keep her comfortable. I asked her if she regretted her decision not to do treatment, she said no.

I feel for my mom, that she will have to endure the passing of one of her children before her. I feel for my niece, that she is having to care for her dying mother, because her mother wants to die. What do you tell someone who wants to die? Bert cried as she told me she just doesn’t want to wake up, and that it is taking so long to happen. She said, she can’t imagine living in this pain much longer!!! So, what do you say? “I will pray that you pass away soon”? ….my sister shouldn’t be in pain….but I think she is afraid of the stronger pain meds that she is in need of now. I told her that the purpose of hospice is to keep you comfortable.

Tomorrow is my sister’s birthday! Happy Birthday BERT!!! I wish you a Happy Happy Birthday free of pain….and though it pains me to say this I pray that you are at peace with your decision and that soon you will be FREE. God Bless……..Love Pina

 

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35: Twenty-eight of Twenty-nine!!!

Ever since May 11th I have been going to The Pacific Cancer Institute here on Maui. My employer Maui Diagnostic Imaging has been allowing me to work until 2:30 Monday thru Friday so that I can go for my Radiation Treatment at 3:15 everyday. When I arrive, the team of therapist immediately call me back, that blue thing you see on that picture (partially covered with a pillow case) is the mold of my upper body. I place my head, shoulders, arm in there, it positions me in the exact same position daily. Sometimes I close my eyes, other times I watch the beam was it moves around me. My mind wonders at times, I think about the past year and the coming year or just listen to the music that they playing.  The session is really fast, I am usually walking out of there by 3:3ish. I drive home and prepare for the next day…..one day at a time.

The side effect from the Radiation treatment is primarily fatigue. Also, the skin changes of the area being irradiated. Prior to starting my sessions, the Cancer Centers Nurse Practitioner, Anna sat with me and went over skin care. A cream was prescribed to me, for me to gently apply to the area being irradiated after each session. I have only been using dove sensitive skin soap (as recommended). The Cancer Center is also having me see a Physical Therapist for Myofascial Release massage. I go to Kihei Physical Therapy twice a week. My therapist Christine specializes in working with cancer patients. I have appointments scheduled twice weekly till mid July.

I am really grateful that I have been able to work thru radiation, yes I am tired but I am glad that I have been able to work. Last week I called off on Monday, when my alarm went off to get up I was beyond exhausted like nothing I have ever felt before. I knew that I would not be able to drive myself to work, much less keep up with the work flow of the day. I put my phone on airplane mode and slept till 10:30! However I still had to drive myself to my radiation appointment later that day!

Friday the 17th consisted of flying to Oahu in the morning, straight to Queens Medical Center. Dr Chong, again really impressed on how well I am doing. I went to the infusion area for my Herceptin drip. Next month I will be having another Echo Cardiogram and  a baseline Bone Density along with my Herceptin. Purpose of the Echo is because one of the side effects of the chemo I was given was damage to the heart valve. So far so good! I am taking Arimidex, which helps fight breast cancer by lowering the amount of the hormone estrogen in the body. With this med comes a slew of side effects one affecting bone density, hence a baseline Dexa (bone density) scan.

We made it back to the airport for our flight back to Maui. I made a mistake when selecting the flight times. I thought we would be landing back on Maui at 244pm, when actually our flight didn’t leave Oahu till 244pm landing on Maui at 326pm!!!! I immediately called the direct line I was given to the therapist area at the Pacific Cancer Center on Maui. Tim called me with in minutes of me leaving a voicemail and told me not to worry that he would wait for me!!!! When we were done he says “Monday will be you last treatment” I questioned him because I thought that June 29th was my last treatment. Tim reminded me that, that was the date if a “boost” was necessary. Since my mastectomy pathology came back negative for aggressive cancer cells no boost was necessary!  He said “this is Twenty-eight of Twenty-nine,  Monday is your last day my dear”…..made my day!!!!!

Mahalo for reading my blog!

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Whoever thought to do this to the ceiling was genius!!!!

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34: Memorial Day

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While most people here on Maui probably spent the day at the beach, my daughter and I went to a small town in upcountry called Makawao. We stopped at the Veterans Cemetery, where every single plot was adorned with a flag and a floral lei. Thousands of plumeria flowers were scattered throughout, with the slight breeze in the air the fragrant flowers were obvious. Because of my ongoing radiation treatment, a day at the beach was not a good choice for me….and besides, the beaches were really crowded. And it’s not like a can get in the water yet….August can’t come fast enough !!

On May 20th, I had my Herceptin infusion, along with a short term follow-up CT of my lungs for that lesion on my right lower lobe. The day was jam-packed, we flew to Oahu, went straight to Queens Medical Center. The radiology department was right on time with my scheduled appointment, after which we headed to Dr. Chongs for my appointment with him. As soon as the infusion was done we headed back to the airport. I needed to be back on Maui for my 3:15 radiation treatment appointment. The day went smooth, the TSA line had me worried there for a bit but we made it!

I received the results of the CT, “stable right lower lobe pulmonary nodule”…HAPPY DANCE!!!!! So what’s next? The nodule has not grown since the last CT done in February, it remained 7mm in size. Back in August 2015, when it was discovered it was 5mm, now the plan is to repeat with another CT in six months to confirm its stability.

Radiation Treatment: So far I have had 13 treatments. My last scheduled treatment is June 29th. I can do this!!!! After chemo this is a breeze!!! At work I have many patients wishing me well. I had one patient that we were doing a six month follow-up from her November 2015 mammogram. She told me she was hoping that she would get me, as she wanted to see how I was doing. Patients will sometimes ask me if they can hug me, this is the rewarding part of my job….hugs are good. My next infusion is June 17th.

My husband bought me a new camera for our wedding anniversary in April. He said that since I can’t get in the water or paddle out with the canoe club I can take photos, I am having fun with my new camera, it’s a Nikon coolpix900. One of the coolest features of this beauty is that it has its own wi-fi. I have an app on my iPhone , I can transfer the picture from the camera to my phone anywhere! Oh my the possibilities…..83 optical zoom!!

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I took this picture when we were leaving the cemetery today. I was probably a good city block away from this horse!!!!

Mahalo for reading my blog, have an amazing day!!!!……..life is good 🙂

 

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33: Back to Work

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Last week I started my Radiation treatment. As mentioned previously my treatment will consist of  Monday thru Friday for six weeks. If you notice in this picture, the ceiling is made to look like you are looking up at the sky. It is actually quite mesmerizing. Walking into this room the “True Beam” can look really intimidating. The therapist that work under Dr. Baker are truly compassionate and make my feel comfortable. My appointment time slot for this journey is 3:15, when I arrive they are literally ready for me, I am in and out. That mold of my upper body that was made at the simulation appointment is on the table and those two little tattoos enable the therapist to target the area that was configured by the Medical Oncologist.

I have been on medical leave since my surgery March 28th. Tomorrow I go back to work, again,  I am super grateful to Maui Diagnostic Imaging for being flexible with me. My work schedule will permit me to go daily for my radiation treatments. I continue to also get my Herceptin infusions in Oahu. On Tuesday I will get my monthly blood draw to check my blood count levels prior to the infusion. On Friday May 20th, I will have a follow-up Lung CT, followed by my Herceptin infusion, then I need to high tail it to the airport to make my flight to be back for my 3:15 RadTx appointment……yikes……wish me well!!!!

It is going on 10pm, I must somehow try to fall asleep so I can get up early. I have been sleeping in, need to get used to waking up early again. I need to do some physical therapy on my arm before going to work daily, my days will be very structured that’s for sure!!!

 

Mahalo for reading my blog

Aloha, Pina

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