About Trina Schilling

I am 46 years old, and a three time breast cancer survivor. I have a 16 year old son named Curtis. I began to write my memoir for him while undergoing chemotherapy. This blog contains excerpts from my manuscript as well as my ramblings on breast cancer and life in general. Thanks for stopping by.

The Reluctant Climber

I was asked to give a talk at Dignity Health’s (my employer for the past year) National Sales Meeting. The theme of the meeting was reaching the summit and persevering through a hard climb. Here is the presentation I gave and a long overdue update on my health.

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The Reluctant Climber

This is my true story…

“You have breast cancer” was the name of my mountain.
I was driving between sales calls when the phone rang… Oh heck no I thought; I didn’t sign up to climb this mountain. Besides, I am way too busy for this challenge. I have appointments, meetings, lunches and conferences scheduled. This isn’t a good time for me to climb…

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I went home to my family who had assembled in anticipation of this news. By then, it had sunk in and I knew that I was going to have to climb this mountain in order to save my life. It didn’t matter that I had not trained for such a climb, that I was not equipped, or that I didn’t know anything about this mountain. What mattered was that this climb, this summit, was my only way out.

My friends and family became my Sherpa’s; helping me to carry the load when I was not strong enough to carry it myself. My team of doctors and nurses served as my compass, guiding me through this journey. However like any trek over a mountain, taking those steps; one after the other through harsh terrain, would require a vast amount of determination, as well as physical and mental strength.

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It helped me if I didn’t look too far ahead up the mountain, instead concentrating on the next step immediately in front of me. I could do that; I could take a baby step. And if I could do that, I could take another. And then another…

My legs felt like they weighed a million pounds and tears formed easily in my eyes, but I kept my head down and continued up the mountain. Treatment consisted of a lumpectomy and radiation. I continued to work through most of the treatments, willing myself to continue onward and upward.

After months of radiation, surgeries and healing, the doctors declared that the treatment was a success and they let me off the mountain. I came down feeling like I had dodged a bullet. My cancer was stage zero, and we had caught it early. This was more of a hike than a hard summit climb. I returned to my normal life and tried to put the mountain behind me.

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2 years later I was thrust back onto the mountain when the breast cancer returned. The surgeons and oncologists recommended a mastectomy with a complicated reconstructive plan because of the previous radiation.

This time I was a little better equipped…I had some climbing experience and I even learned how to tie a knot or two in my safety line. But I still didn’t have any choice; I had to summit this mountain or risk death. The surgeries took place in stages, kind of like a high mountain climb with many plateaus and a lot of acclimating that had to take place. It was lengthy and painful.

When I was in the hospital the nurses kept asking me if I wanted graham crackers and juice boxes; I could see zebras painted on the walls. I figured it must be the morphine, because nothing else made sense.
When my pain was under control and I could see straight, the friendly night nurse told me that the hospital was full and I was being cared for in the pediatric wing. I was relieved to know that I wasn’t hallucinating and the sweet demeanor of those nurses got me through some hazy painful days. I never forgot their kindness towards me.

Eventually I healed and the doctors again declared the treatment a success. I was released to return to my life off of that unforgiving peak.

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A year later my hand kept wandering to a pain that I just couldn’t ignore. The pain was in the same exact spot that had been originally biopsied. I figured it must be scar tissue. After all, I had undergone a half- dozen surgeries to that area over the last couple of years.

My surgeon reassured me that it was probably scar tissue but given my history a biopsy was warranted. The call came in around dinnertime. “I’m sorry Trina, but the cancer has come back in an invasive and aggressive form. We will need to do a PET scan right away to see if the cancer has spread to other parts of your body. You will likely require more surgeries, chemotherapy and additional radiation.” I was stunned, silent, scared.

This time the air was much thinner on the mountain, because I could hardly breathe. I felt my knees becoming weak and I wept openly. I cried until I couldn’t cry anymore and then I raised my chin up as high as it would go and said out loud through a long exhale, “Okay.” The word okay would become my personal mantra, as if to say to myself, “You’re okay, you can do this, okay let’s roll, okay you are winning this one.”
It would only take one look into my son’s eyes to know that I would need to summon all of the courage, strength and endurance that I possessed to get up and over this mountain once and for all. There was no way I was going to leave him behind.

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I did inventory. What had I learned from my previous two battles with breast cancer? Who could I rely on to be there for me while I underwent treatments that would feel like a near-death experience? What was I supposed to learn from this experience that I hadn’t learned yet? What could I do differently to prevent this from coming back again? And was this the hill that I was going to die on?

I was on that 3rd mountain for almost 2 years. I had many complications that resulted in many surgeries. My body just couldn’t take that much radiation and chemo without a major revolt. I won some battles and I lost some. But I never gave up. I never felt sorry for myself. I never stopped putting one foot in front of the other. I just kept going until I finally reached the top.

Slowly my body healed and things like hair and fingernails grew back. I grew stronger and more confident after persevering through a challenge as great as this. I was ready to return to work and believe it or not, ready for a new challenge.

I saw a posting for a Market Development Representative position with Dignity Health. My mind went to all of the wonderful nurses, techs, and staff that I had come in contact with throughout my journey. It was always Dignity Health facilities that took care of me. It was that Human Kindness that I wanted to be a part of and it was that value that I wanted to represent. I applied for the job.

RC 2 Curtis Graduation 026 Curtis Graduation 040 Europe 915

Today, I am nearly 3 years cancer free. My son turned 18, graduated from high school, and started college. He and I just returned from a celebratory trip to Europe; we have so much to be grateful for.

Europe 984     Europe 923

Being a patient of Dignity Health has helped me to understand how important all of our work is. It has taught me a deeper level of empathy for our patients and helps me see that the journey in our hospitals is equally as important as the outcome. It has also taught me the importance and healing power of Human-kindness. When I see patients in our hospitals I look them in the eye, greet them and say a silent prayer for their safe climb.

The One Breasted Warrior

One breasted warriorI’m still fighting. It hurts physically and emotionally. I am not getting any closer to complete healing or a body that has all of it’s parts in place. I remain hopeful though, hopeful that the cancer does not return. My foolish, vain self marched into the plastic surgeon’s office recently and  boldly stated that I would like to discuss my options for making another run at reconstruction. I haven’t  stopped worrying or crying since that bold move.

“We need to find the root cause of the chronic pain in your chest.” stated the surgeon. “It is most likely necrosis of the bone from radiation. I can order an MRI and we can see what is going on in there. If it’s nothing than we can start with a scar revision, then blah, blah, blah…” He continued.

MRI? That picks up cancer too I thought. Is he looking for cancer? Why do these doctors want to continuously look for cancer in my body?

I had two MRI’s done the following week on two separate days, double the stress. One was to check the left breast that still remains with it’s small but perfectly proportioned implant. The other MRI was to look at my right chest and ribs where nothing remains but skin tact down onto my bones and pain that never stops. Wearing a bra and a prosthesis is an act of a warrior. It is like my shield as I go out into the world trying to fit in with the normal breasted women. It is incredibly painful to wear this shield as it hits right where all of the pain is concentrated. I  dig for a warriors courage just to get dressed for work in the morning. By the end of the day that bra must come off immediately and I greet my son and his friends with one breast. Most are too polite to stare, but they all hug me sideways, as if they are afraid to hurt me or confirm what they see through touch.

The MRI’s came back inconclusive. “There is something on your ribs but we are not sure if it is injury or metastatic bone cancer.” Said the surgeon. “I am going to have the Tumor Board review your case and make a recommendation. Don’t worry, it’s probably nothing.”

How many times have I heard that? “Don’t worry, it’s probably nothing.” News flash to my team of doctors, it has always been something when you go poking around looking for cancer in me. I cringe when I hear those words.

The “Board” recommended a PET scan. Where in the fuck is my warrior Xanax?!

The last time I had a PET scan was right before I started chemo therapy a couple of years ago. This time, I merely went to the plastic surgeon and inquired about reconstruction and now I am having a contrast dye put into an IV that is hanging out of my arm. The tears rolled freely down my face as I was positioned into the machine. “Are you okay?” Asked the tall, dark, handsome technician as he handed me a tissue and waited patiently for me to stop crying so he could start the test. I dug deep for my warrior strength and fell still and quiet while the machine hummed around me searching for cells that are ruining my life and trying to kill me.

The results were sent to the Tumor Board and they recommended a biopsy of my ribs.

I called my oncologist and pretty much said what the fuck?! “I don’t think there is anything to be worried about,” he said. I couldn’t breath. I walked outside of the hospital where I was at work to continue the conversation but my legs were starting to go numb from panic.

“Let me have another radiologist take a look at the films.” He offered. “I will be in touch, don’t worry Trina.”

One breasted warrior 1

2013 in review

Thank you to everyone who read my blog in 2013. My journey continues; I am starting 2014 cancer free, have a great new job and my son is playing Varsity Basketball and  preparing for college next year, I really could not ask for more. I made it through to the end of the tunnel and the light is shinning on my face. My hope for 2014 is that I will remain cancer free and have a successful reconstruction. I remain hopeful and confident about my future. Love to you for taking this ride with me.

Here’s an excerpt:

The concert hall at the Sydney Opera House holds 2,700 people. This blog was viewed about 14,000 times in 2013. If it were a concert at Sydney Opera House, it would take about 5 sold-out performances for that many people to see it.

Click here to see the complete report.

The SCAR Project – A Look at Breast Amputees

Barbie (1) Courtesy of David Jay Bridgette. Courtesy of David Jay Elisa. Courtesy of David Jay There are many variables that go into a woman’s ability or willingness to have reconstruction following a mastectomy. I have had a successful reconstruction and then I had two failures. I know that adds up to three, but all of that activity was on the same breast. Like I said, a lot of variables…

The pain can be both physical and emotional, just look into some of these women’s eyes. I personally can’t stop thinking about the breast that I lost because the area where it used to be hurts all of the time. There is a possibility that more surgeries could alleviate the pain and maybe even put me back together again. However there is also the possibility that the surgeries could fail and I could end up worse off than I am now.

I began to wonder if there were other women like me out there who were struggling with the aftermath of breast cancer treatments and the realities of what it does to our bodies and our personalities? I also wondered if there was anyone out there who was willing to talk about and expose the shockingly raw realities of breast cancer? Lets cut the crap with the pink ribbons and the movie star smiles and have a game of show and tell.

Courtesy of David JayI came across The SCAR Project by fashion photographer David Jay. Two things impressed me right away; the first being that David is a man. The second is that he started an awareness campaign to shed light on what women really look like following a mastectomy, and encouraged them to feel empowered, instead of  ashamed. It’s somewhat of an oxymoron; a man empowering women to feel beautiful because of her disfigured breasts. Breasts are the quintessential symbol of femininity, and men have made it abundantly clear to us women how much they love perfect breasts. So much so, that we women have spent billions of dollars to augment our breasts to make their appearance desirable to men. And then to top it off, we oblige societies love affair with breasts by parading them around like balloons on Thanksgiving Day . Jolene and Kyle. Courtesy of David Jay

But what happens when the breasts need to be amputated to save your life? What if reconstruction is not wanted, not possible or not available because the woman doesn’t have insurance? For most of us women a part of our sexuality and confidence is lost with those mastectomized breasts. David found that by photographing women for the SCAR Project helped them to reclaim their femininity, their sexuality, and some of the power that they had been robbed of.

Kristen. Courtesy of David JayTo me, these pictures represent a small shift in society’s acceptance of a tribe of scarred, breastless and one breasted women. Since 1 and 8 women will be diagnosed with breast cancer, this tribe that I currently belong to is growing. Exposure will help women like me to accept what we might not be able to change. Perhaps fashion designers will make a bra for women with one breast so we don’t have to wear an external device to appear “normal.” What if not having breasts or having one breast becomes acceptable? What if it is seen as a badge of honor and strength? What if we could tone down our obsession with breasts just a little bit? I appreciate David for helping us to see this through a different lense. Jill. Courtesy of David Jay

Please check out the SCAR Project at http://thescarproject.org/ for more photos and information.

Was Angelina Jolie Being Honest About Her Mastectomy?

Was Angelina Jolie Honest about Her Mastectomy?Every time I hear of a woman being diagnosed with breast cancer or testing positive for the BRCA gene, my heart sinks. I close my eyes and take in a deep breath and hold them in my heart, silently whispering the phrase Namaste (the light in me acknowledges the light in you). I feel all the way to the core of my soul what they are going through or what they are about to go through.

When I woke this morning, I along with the rest of the world heard of Angelina Jolie’s wonderfully easy and glamorous experience with a nipple sparing elective double mastectomy. According to her article in the New York Times, she was back to normal in a few days. Her children have only witnessed tiny scars on her perfectly reconstructed breasts and she wants everyone to know how easy the whole thing was for her. And of course every news anchor is congratulating her for being yet another celebrity who chose to share her courageous decision. Why don’t we ever hear about the dark side of mastectomy? Why don’t we hear that women have a part of their body amputated but the cancer comes anyway. About how surgery can actually increase the risk of the cancer mutating or breaking free and becoming more aggressive? About the emotional toll that this has on women and the suffering that can take place? Why is this information being presented like it is a casual procedure without significant long-term complications?

Can I share the harsh realities with you Angelina? A mastectomy is not the panacea that the surgeons suggest that it is. I tested negative for the BRCA gene, underwent a mastectomy after my second diagnosis with breast cancer and then the cancer returned for a 3rd time in an aggressive invasive form although they had removed my breast and nipple. I have had 16 surgeries on my right breast and my body rejected the implant twice. I am in constant pain, and have not been able to return to work. I cannot even relate to your sugar coated experience and through my blog I have talked to countless women who have had experiences closer to my own. I admire your courage to talk about your decision to significantly decrease your risk; I thought I was doing the same thing when I agreed to be carved up. But were you really being honest? Back to normal in a few days? I’m sad that more women aren’t being totally honest with each other about how difficult a mastectomy is, the risks involved, or the fact that it isn’t the insurance policy that we all hope it will be. I wouldn’t wish my experience on anyone; I wish I had someone who would have shared the other side of the story with me.

It’s Not All About The Pink Bras…Meet Claudia

Meet Claudia

I met Claudia through this blog. I want to thank her for allowing me to share this letter that she wrote to her gynecologist after her doctor missed obvious signs of breast cancer. Claudia is incredibly strong and brave for sharing these pictures of herself in the hope of saving another woman from going through a similar experience. Thank you Claudia for your friendship and for your generosity.

Dear Doctor,

It has been one year since I was diagnosed with Stage 3A breast cancer. I had a tumor measuring 9 centimeters. Ductal and lobular carcinoma, invasive, advanced disease, as you must surely know as a physician. Since then, I have endured a very sad and hard path in my life.

I lost my breasts, lost both of my nipples, lost my hair, and I can’t have estrogen circulating in my body.  As a gynecologist, you know what that does to me physically, and emotionally.

What does breast cancer treatments look like

Claudia sent this picture of herself with this letter to her gynecologist. Her doctor never responded.

I’m not sure if you forgot about it or not but I wanted to remind you of our last conversation.

You were my first line of defense against breast cancer. Here are the facts: one out of eight women will get some kind of breast cancer. Women who have fibrocystic or dense breast tissue have a higher chance of being diagnosed with it. Also, lobular cancer is very hard to detect. Knowing these three things should have made you think twice after reading my last mammogram report and after you personally examined me with your experienced hands.

I had a fat pocket that grew under my armpit and the only reason it grew there was because the tumor had pushed it out. I found out too late because you did nothing about it when I brought it to your attention.

My left nipple was leaking and turning inward, your words were, “It must be because you jog, because of the rubbing on your nipples, your brain thinks you are lactating.”

Burns from radiation treatment

Burns from Radiation Treatment

Well, my nipple was leaking because I had breast cancer. My nipple turned inward because I had breast cancer and that mass under my armpit was due to breast cancer.

You have two girls. Can you imagine if this happened to one of them or to you for that matter? Can you imagine losing your hair, losing your breasts?  How about watching your mom, dad, husband, young kids, and friends see you go through this suffering and not able to do anything about it?

Tamoxifen may save my life but let me tell you something, it numbs me. The side effects take away my quality of life.

I am grieving right now. I don’t know if I will live for two or twenty years. How do you think I feel having to do tests every three months, PET scans every six months and then every day of my life hanging onto the thought that at any time cancer could come back?

Although this is not a blame game, many times my thoughts go to you. I do blame you for your lack of care and attention. Be happy that I am not reaching you through lawyers.

After the mastectomy before reconstruction.

After the mastectomy, before reconstruction.

Pay more attention to your patients, teach them what to look for, educate them on breast cancer, or any other cancer related to your specialty. You made an oath as a doctor, have you forgotten what that really means?

Maybe I couldn’t have avoided the cancer. But you could have helped me avoid it being detected at stage 3.

Claudia Degomme, your ex-patient.

Degomme Family

The Degomme Family

Note: Claudia was smart, she followed her intuition and sought a second opinion when her doctor told her that her symptoms were nothing to worry about. Her best friend who is also a doctor provided the answers she needed to save her life. Here in Claudia’s words are what happened next.

Anaisys came with her family to dinner on a Saturday. Something was telling me that there was something wrong with my left breast because my nipple started to leak a little and it was going inward, even though the mammogram had come back CLEAR. 
I asked Anaisys to take a look and she noticed a dimpling in my breast’s skin and she said that was typical of a tumor. She did not say much more, I guess not to scare me, but she told me afterwards that she feared I had a tumor. So she herself made the call to the breast surgeon and made an appointment for me. Monday I was at the doctor’s office at 9 a.m. with my husband, not knowing that soon I was going to go through the hardest, saddest, craziest ride of my life. 
 Claudia and Anaisys

Claudia and her supportive, loving husband Yvan.

Claudia and her supportive, loving husband Yvan.

Deepak, Oprah…Help!

Oprah and Deepak

An excerpt from my manuscript.

The job-protected portion of my short-term disability was running out, my employer wanted me to come back to work or step aside so they could hire someone else to fill my position. I was in no condition to consider going back to work, and I was devastated when my employer denied my request for an extension of my job protected leave.

I was in the middle of treatment and I had to face walking away from a position that I had held for over 11 years. I negotiated with myself six ways to Sunday trying to figure out a way to maintain my position and continue my life-saving treatments. My doctors, co-workers, family and friends cautioned me to not go back to work, but I struggled really hard and for a long time over this decision. In the end I had to prioritize my health over my wealth. I notified my employer and their insurance company that I would not be able to return to work. They placed me on long-term disability and made arrangements to pick up their company car, computer, printer, etc.

My life was changing before my eyes and there was nothing I could do about it. I was no longer in control, and I didn’t have an exit strategy from my career. I cried a lot over this, it was devastating for me. For over 20 years my career had provided for me and it was the one thing that I could (somewhat) control. As a cancer patient, I felt like I had no control, no power. I had to endure the treatments or risk death. Now two huge aspects of my life; my health and my career were out of my control. I became very depressed. I had trouble sleeping and couldn’t eat. I realized that a huge portion of my identity was tied to my career and my ability to earn. For half of my life my focus had been on my career and now my focus had to be on my health. My ego was in my way and I had to learn to let it go. I turned to the one person I knew who could help me let go of my ego; Oprah.

“We need to subscribe to OWN.” I told Joe. “I need Oprah right now.”

Joe, being the loving, sweet, generous man that he is, picked up the phone and called the cable company. He ordered OWN right on the spot. I set out to see what shows I could find to nourish my soul and get my ego in check. Thankfully Oprah had it covered. Between Super Soul Sunday and her catalog of shows on the topic of spiritual growth, I could learn another way to deal with my ego and my sadness because of it. The ego is a funny thing and it is so powerful. But once you get a handle on your own ego and understand its toxic effects, it is liberating to be able to let it go. I learned that when I am fearful because I have a disease that recurred multiple times or jealous because my friends and family are living normal lives, or perhaps irritated because my fears have been triggered it is always my ego rearing her ugly head and doing so because I am frightened. Being able to recognize it was the first step in being able to corral it.

Ego after Cancer

Our egos and fears get in the way of our true selves and I was embarking on a mission to get-to-know me, the inner me. I was vulnerable, raw and open to learning a new way to cope. What I learned changed my emotional outlook on the aspects of my life that I could not control. By calling out my ego I could control and humble it. I learned that I could recognize fear and deal with it head on. Not dealing with fear head on gave it power and I needed to disarm it so I could simply breathe. I learned that allowing yourself to be vulnerable is the most courageous act there is. And I finally learned how to meditate thanks to Deepak Chopra.

Thank you Oprah, you, your programming and your guests became my spiritual guides, and I plan to thank you in person someday when you invite me to your show to talk about this book. Just putting it out there, creating a new reality for myself, letting my dreams float through the universe, and allowing my ego to quietly sit on the sidelines as this journey unfolds.

Discussion points for readers with cancer: What has cancer taken from you? What tools do you use to cope with these loses?

Responding When Your Relative is Diagnosed with Cancer

Responding When Your Relative is Diagnosed with Cancer_0325_KF_MW (1).docx A special thank you to Kaitlyn Teabo of the Mesothelioma Center for writing this guest blog for my site.

When a family member is diagnosed with cancer, it can be hard to initially handle. It is common and natural for you both to feel overwhelmed, scared, angry, sad and other emotions all at once. This compilation of emotions can make knowing exactly how to react to the diagnosis that much harder.

If you want to help, but you’re not sure how, here are some ways you can make the process easier for your relative and yourself: 

  • Listen. People process issues like a cancer diagnosis by talking about it. Show that you are listening by occasionally paraphrasing what your relative said and asking if that is what they meant. Unless asked, in the early stages of the diagnosis don’t offer advice. Your ears are worth more than anything at this point of the journey. The doctor will help your loved one and yourself through the process, discuss their prognosis, and help find the best treatment centers in your area.
  • Tell Your Relative You Love Them. Even if you think it is implied, hearing that someone loves them can help with feelings of depression and isolation, which are common after a diagnosis. Show affection when you can, this effort can have a huge impact on the coping process.
  • Don’t Compare. Sometimes when someone is going through a similar experience as you or someone you know, it may be easy to bring those experiences into conversation. But not all cancer experiences are the same, which is why you shouldn’t compare your friend’s mom’s cancer to your relative’s cancer.
  • Help Without Being Asked. Some cancer patients don’t like to admit they need help and will neglect to ask when it is necessary. Little gestures can often make the biggest difference. Make your relative’s favorite meal or dessert and stick it in their fridge. Help with the laundry and housework. Drive them to appointments or do daily errands.
  • Provide Comic Relief When Necessary. Yes, this can be a trying time for your relative and other members of the family and close friends, but it is also important to remember to laugh. Be careful not to offend your loved one, and only provide humor when it is appropriate. Remember to stay sensitive when they are grieving and offer a chance to laugh when they could use the reminder. Humor can be a great form of medication and may offer a way of healing.

As each diagnosis and each person affected by cancer is different, the ways to help your relative overcome the disease may also differ. These tips serve as a helpful guide, but you are ultimately the best judge on how to respond and act around your loved one. The most important thing is to just be there for them while providing support.

Author bio: Kaitlyn Teabo is a writer for The Mesothelioma Center. She combines her interests in writing, cancer research and emerging scientific technology to educate the mesothelioma community about asbestos and its related diseases.

1+1=2 Boobs

Breast Reconstruction T-Shirt

I needed to buy a breast, but I haven’t worn a bra in 6 months. I hate wearing a bra in general, they bind my ribs and pinch my still healing tissue. Getting dressed with just one boob is no easy task either. I searched my drawers for a do it yourself solution. I found some removable cups in my bikinis and placed them in my bra-shelf camisole. That didn’t work out too well because they would come loose and end up in the center of my chest or in my armpit. Plus they did not mimic my other breast in size or shape. It was time to get a breast prosthesis. I plan to attempt reconstructive surgery again, but in the meantime, I need some options.

The Certified Mastectomy Fitter was very kind and knowledgeable, and she took her time helping me to find just the right form and bras that I could wear comfortably. It took two visits totaling four hours to get it just right. I had no idea how comprehensive the fitting would be. We were in an exam room, and she had cupboards full of special bras with pockets in them to hold the forms. Once I found a style that was tolerable to me, she fit  the right cup with different size and shaped forms. Some were foam, some were made of soft fabric stuffed with little beads that conform to your body, most were silicone with a nipple built right onto it. When I gravitated towards the weightless foam numbers, she cautioned me that it is important to have some weight in your prosthesis. She explained that the body’s bio-mechanics get all out of whack when you have weight on one side but not on the other. Women, especially large breasted women develop neck and back pains from not having the weight evenly distributed. Makes sense, huh?

Certified Mastectomy Fitter

She pulled out dozens and dozens of these forms and shoved them into the bra one at a time while tugging this way and that way trying to line up my natural nipple with the prosthetic one. I winced in pain every time she came at me with one of this forms; I wasn’t prepared for her hands to be inside my bra the whole time. I left sore and exhausted after the first visit. On the second appointment, I pre-medicated with a pain pill. She had no problem digging around the interior of my bra.  Adjusting both sides this way and that, adjusting and measuring for the perfect alignment, size and shape.

External breast prosthesis after proper fitting

When we got the fit just right, I put my shirt back on to see how it looked under clothes. I was very impressed! She got it just right. I could not see a difference between the implant on the left and the prosthesis on the right, it looked great! I stood a little taller as she was surveying her work; I could feel my confidence rise. This was going to be manageable; I could bridge the gap between reconstruction attempts with this set up. I could also wear more of my clothing, I would no longer be limited to what I could wear with the camisoles and the homemade form that goes awry. She got a kick out of my attempt to make something at home to fill the space until I was healed enough to be fitted. She let me know that my insurance would cover 2 forms and 4 bras so I was able to get the foam one to exercise in and the silicone one for the needed balance of my bio-mechanics.

I was not prepared for my body to reject the implant, twice. This wasn’t supposed to be part of the equation, well, neither was the 2nd or 3rd recurrence of breast cancer for that matter. I have learned a lot about human suffering and about the one thing that I can control when the inevitable suffering comes my way… and that is how I respond to it. We are not meant to be perfect, we are meant to be whole beings; the good, the bad, the beautiful, the ugly, and then most importantly, our response to it all.

For more on this topic, check out part one of this tale: Prosthetic Breast, Seriously?! http://www.trinaschilling.wordpress.com/2013/03/11/prosthetic-breast-seriously/

Prosthetic Breast, Seriously?!

prosthetic breast 1

Part one of my sagas.

The word prosthetic to me sounds old, broken, missing, braced, fake or injured. It gets stuck on my tongue and I don’t like it. I don’t like the way the word sounds, and I don’t like saying it. What is it supposed to mean anyway, a good aesthetic? Does that mean without a prosthesis, I don’t look good, that I am unpleasing to the eye? Crap that is a lot to digest since I have endured 16+ surgeries trying to look “normal.” Still after all of those surgeries, my body rejected the implant, twice.
prosthetic breast

I don’t want a prosthetic breast, although my mom points out that an implant is a prosthesis. Technically she is correct, but for this article I am referring to an external device. I don’t want one because I don’t intend to remain in my current physically unpleasing to the eye state of being. I plan to be fully reconstructed and I have a wonderful and talented plastic surgeon who agrees with that plan. However, in the short-term, until my body can fully heal from the complications of so many surgeries and radiation treatments, I have a missing accessory. One would not be able to stop themselves from staring at my single perfectly augmented breast compared to the empty, hollowness on my right side. I have come up with a temporary solution; gauze (still healing) and cup type inserts that are removable from my bikinis. These breast shaped pads work great, but they sometimes become dislodged from the shelf-bra camisoles that I wear; I’m still too sore for a regular bra. When they become lose they land somewhere in my armpit or in the center of my chest, which is definitely not pro-aesthetic!

After I finished breast-feeding Curtis, my B cup breasts shrank to AA (which really means negative A in the bra sizing world. Why does a DD mean larger than D, but AA mean smaller than A?). I was spending a lot of time on our boat and in bathing suits, and I didn’t want to go out and buy all new smaller cupped bikinis, so I purchased the chicken cutlet looking breast inserts that some women wear to enhance their cup size. They are made of a silicone type gel and they are pretty heavy in weight. They worked fine to fill up my bathing suit tops, until the day I left them in while water skiing. I took a nasty spill that day, and those cutlets flew out of my top and were floating on top of the lake. My friends in the boat had a good hysterical fit of laughter as they were pointing to the fake boobies bobbing up and down in the water while I tried to swim after them to retrieve them. I laughed too, I don’t know why I thought those things would stay in place, and I was slightly embarrassed that my secrets were out and floating on top of the wake for all to see. I hated wearing the cutlets, they were hot and sweaty and obviously prone to fall out because of my active lifestyle. I immediately went out and bought all new bathing suits and sold the cutlets at a garage sale, those suckers were expensive, so I knew someone would buy them. I learned to embrace my small breasts, dress accordingly, and never ever considered augmentation until I was faced with reconstruction post-mastectomy. I quickly warmed up to the idea of insurance paid implants; I think they are the silver lining common denominator for breast cancer survivors or those having a prophylactic mastectomy.

So now I am planning an annual family trip to Puerto Vallarta, and I am wondering how I am going to navigate resort wear with only one breast. I decided it was time to go for a prosthetic fitting. Fitting, the word should be used to describe Kim Kardashian with a flock of stylists pinning her outfits on her in a way that shows off her spectacular curves. That’s the kind of fitting I want, not one for a fake external boob.

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When I lost my hair from chemo, I would only wear wigs if I were going out in public. I wore them mainly to make other people feel comfortable around me. I didn’t want my cancer to be the center of attention and by wearing a wig I could blend in. People around me were more comfortable without ever even knowing that I was making them feel more comfortable. I on the other hand was not physically comfortable; wigs are hot, sweaty, and itchy, just like the cutlets. So mainly I would wear a baseball cap or a beanie type hat more often than wearing wigs for jaunts to the doctors for treatments or to the store or gym. I was able to continue to work out at the gym during my off weeks of chemo and would just throw on a baseball cap. I drew a lot of stares, but eventually people got used to seeing me at the gym with my bald head under a baseball cap, or I simply got used to the stares. However, I’m not prepared for people staring at my chest and trying to put together the pieces of my life in their minds, especially in a bathing suit.
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I called the local cancer resource center and asked them if there was a place in town that sold breast prosthesis. The center gave me three names: a prosthetic business, a pharmacy, and a lingerie store. I called the prosthetic company versus the lingerie store, I already knew what the lingerie store sold; cutlets. I couldn’t imagine that a pharmacy would be a good place to try on fake boobs for size so I didn’t even write that phone number down. The lady who picked up the phone was kind and told me that my insurance would pay for the visit and for the prosthetic, good news, so I set up an appointment for the following Tuesday.

“It’s no big deal,” said my mom who wears a prosthesis after her own mastectomy decades before. She had widespread early stage breast cancer, had a unilateral mastectomy and reconstruction, and fortunately her breast cancer has not returned like mine did. “See look at mine,” she said as she pulled it out of her bra and waved it at me. I laughed as I dodged it. She uses a prosthetic to create symmetry; reconstructive surgeries are far more sophisticated now than they were 25+ years ago. My mom is obviously comfortable with not only saying the word, but showing me the device. “It’s quite comfortable and look here at this area, it absorbs the sweat,” she was saying and pointing. I looked more out of the corner of my eye than dead onto it, I didn’t want to interact too much with my mom’s prosthetic breast. I didn’t want to face my own need.

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We had a good laugh at the whole thing; sitting outside on the deck drinking Chardonnay with the sun on our chests as we shared our battle scars with each other. Anyone could have driven by and seen us, but we didn’t care because we were not alone in our suffering and we could laugh at our circumstance.

Next week,part two, after the fitting, which by the way seems like a very formal process. NOT looking forward to it. Not at all…

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