Archives for posts with tag: Breast Cancer

As I’ve written about previously, when I was a college student, I worked as a research assistant for an orthopedic surgeon who was completing a research fellowship at the University of Washington working in the Biomechanics Lab at Harborview Medical Center. He was doing a study on the use of an oscilloscope in assessing fracture healing in tibiae. He had a device that made a little thump on the skin over the tibia, thereby making it vibrate. A couple of readings were taken and recorded.

I have long maintained that it is not fair to expect smart people to automatically have professional skills with which they’ve had little or no training. So, I am not putting down the medical profession when I note that an M.D. is not a research degree and it was very clear that this very skilled and compassionate physician, did not always know what he was doing from a research methods standpoint.

One day, he and I were taking readings. There were some he didn’t like. He said, “Those a spurious.” And then he deleted them. I was shocked and said, “You can’t do that!” He repeated his rationale and looked mighty nonplussed for someone who had just DESTROYED DATA. It is true that most things in life are not normally distributed and even when they are, there will be outliers. But outliers count. They can’t just be dismissed. They are still part of the sample, the sample that is designed to represent a larger group.

We spend a lot of time defining what is normal, what is average. An average, or mean, is a measure of central tendency. It measures the middle. But sometimes the mean does not reflect the middle. Take home prices. Have you ever noticed that people talk about median, not mean, home prices? That’s because wealthy people tend to live in much more expensive homes, with prices outlying the general distribution. These outliers, or extreme scores, are described to exert too much leverage on the mean. Extreme scores can count for more than the rest of the group.

Let’s say that all of the houses in your neighborhood are worth $200,000-$300,000 except for one, which is worth $2 million. The mean is going to end up being higher than the price of all but one of the homes and is going to be substantially lower than the highest one. The mean is ghux not very meaningful so a median, the actual middle point of the distribution is used instead. Now the outlier house is not meaningless. There’s some meaning around someone having a lot more than everyone else. That says something. And the majority of the house prices mean something, too. One cannot get a complete picture without looking at both the norm and the exceptions.

If you are still with me on this statistics post, you know that I’m going to apply this to something else. You would be right. There is a lot of discussion in the breast cancer community about what words and experiences best represent us as a group. Sometimes we are talking about educating and changing our culture. We talk about the implications of words for funding, physician/patient relationships, and societal support for individuals with breast cancer. These conversations are very important.

Then there are the times we apply the mean to ourselves as individuals. Sometimes that fits and sometimes it doesn’t. Sometimes we apply our individual experiences to the group. Sometimes that fits and sometimes it doesn’t. Sometimes we want to be the average. Sometimes we want to be the outlier. I had a kind of breast cancer that has a good prognosis based on the type, stage, estimated aggressiveness, and the results of genetic testing. I am hoping very much to be an average breast cancer patient. I don’t want to be an outlier. My friends with metastatic cancer most commonly want to be outliers. They want to live longer and with a higher quality of life than the typical patient.

Some of the more controversial writings and interviews on breast cancer have occurred when an outlier case is treated as the typical case. Melissa Etheridge comes to mind. She is entitled to her own individual opinion about what caused her cancer and what will keep her healthy. She has freedom of speech, even as a famous person, and I have the freedom to think that she is living her life on a foundation of likely erroneous beliefs. But it is her life. Good journalism is supposed to present a story in context. When an individual expresses an outlier belief about the prevention and treatment of a deadly disease, there is a responsibility to present other view points, in particular, to interview an expert in the field. That provides context and a representative story.

Stories about individuals are often more interesting because they are less abstract. They seem so much more real than statistics. But as real as individual anecdotes are they often do not represent the group.

Breast cancer is not always interesting. Some of us are suffering in a way that is not good for print or t.v. Not all of us feel like “survivors” or “warriors” or “fierce”. Some of us do, some of us do not. Some of us believe in the power of prayer, the power of positive thinking, and some do not. For some, mastectomy feels like an amputation, for others not. We all deal with this disease in our own way. We feel losses in our own way.

It is unrealistic to expect all cancer patients to understand the complexities of these diseases, to cope with them, and also to EDUCATE the public. Some people are able to do this, but others are not. Some people argue that public figures have a responsibility to the public to educate because they are influential. I agree that they are influential but this argument is based on the assumption that they also have the skills necessary to educate. It is, however, realistic to expect people whose profession it is to provide health information to do so, and the blur between news and entertainment as well as news and disease commercialization, troubles me greatly.

We may be the mean. We may be outliers.

Every one of us is real.

We are all part of the group.

My husband recently complimented me by noting that in a crisis, I am good at quickly figuring out what needs to be done, assembling resources, and doing it. This is true, in a number of respects, and I am grateful to have the skill and drive to carry it off.

There are some aspects of my life when this is hard and unfortunately, it is related to my physical health. I have a difficult time maintaining a healthy diet and exercise routine. I had coincidentally rejoined Weightwatchers a few weeks before my cancer diagnosis and had already started losing weight. I added walking at least 5 times a week a few months later, and I’ve been walking nearly every day for over two years. Since I started logging my miles on 12/2/12, I’ve walked close to 2000 miles.

I started tracking my miles as a way to help maintain my exercise program. That, combined with my renewed interest in nature photography, has helped me maintain the habit. Admittedly, I am having a little trouble transitioning to the damp part of the year but I’ve gotten out in some rather cold weather and enjoyed the sights and sounds of the outdoors. I know that I am getting my groove back.

My diet is another matter, altogether. I don’t eat a lot of sweets except around the holidays. And my gluten allergy means that I can’t eat most prepared foods anyway. However, I have been eating a lot of fruit, A LOT, and probably too much. I know that sounds silly but it has a lot of sugar in it. Finally, I know that my portion sizes are too big. I have gained nearly 20 pounds over my goal.

This all started when I decided to stop tracking what I ate every day. I stopped following Weight Watchers, basically. I was in a groove. I was ten pounds below my goal weight and walking a lot. I was really fit. I don’t know why I let myself do this. THIS IS HOW I’VE REGAINED WEIGHT EVERY TIME!

I keep restarting Weight Watchers for a couple of days but I have not yet gotten it to stick. Really, I am hoping that by writing this, I will get myself back into the long game, especially since we are in the holiday season.

I usually don’t end my blog posts with questions, but I have some. How do you help keep yourself motivated to maintain a healthy lifestyle?

One of my sister-in-law’s hosts Easter each year. She is a competent cook. She is also able to have people in her kitchen while she cooks. I could say that one reason for this is that she has a large kitchen with places for people to sit at a table, out of the way. I could also note that most of the things she makes are not hot and can be made ahead of time and taken out of the refrigerator. I could also point to the fact that she does not make something that requires the making of gravy. But the fact of the matter is that she is able to concentrate on entertaining people and making food all at the same time.

I am not like this. I can talk to people up until about the last 30 min before Thanksgiving dinner is done. Thanksgiving is the holiday that I host. I have done it for all years except one for the past 10 years. Before the last 30 minutes, I feel relaxed and confident. My apron is typically still clean. I am able to avoid burning myself on the oven’s heating element.

And then half of the food is ready and the other half of the food needs to be finished. The turkey is cooked and needs to be lifted out of the pan to rest on a carving plate. Meanwhile, I place the roasting pan on two burners, pour in alcohol to deglaze it, scraping the fond from the bottom of the pan. I add flour (now a gluten-free blend) and turkey fat and stir constantly. It always gums up immediately and the first worry is that the gravy will turn out clumpy. And it will if I don’t keep my head in the game. I add poultry stock, bit by bit, until I start to see a beautiful brown glistening sauce develop. Then I keep adding stock while I am plating vegetables, side dishes, and heating things up at the last minute. I have to work quickly so that the turkey does not rest too long and become cold. When the time comes, I call my husband to the kitchen to carve the turkey while I finish the last 500 details.

If you are a guest and you ask me what you can do to help, I will ask you to please sit down and enjoy yourself. If you ask me during the last 30 minutes, I insist that you sit down and enjoy yourself. My husband and my mom have both gotten into the habit of running interference for me and helping shoo people out of the kitchen. Even if I am not in the last push of frenzy, my kitchen is small and not a good place for people to hang out to visit with one another. My mother knows this because people congregate in her kitchen when she is cooking, standing in front of the stove or the sink, not realizing that they are setting off her rhythm. My husband shoos people out because he has empathy for me and knows how my brain works.

I love to cook but I am a person who cooks in deep thought. I have a hard time socializing and cooking at the same time. Both socializing and cooking are high interest for me and I have a hard time focusing on anything else when I am deeply engaged in one of these activities. So doing both of them is really really hard. As for those that want to come in to help, unless they know exactly what to do and how to do it, delegating is a chore for me. A chef is a boss of a kitchen and has training to do this. I don’t. I am a home cook with a small kitchen. I have a schedule and a list in my head. I am working at full capacity and the wheels are already in motion. This is also why, if you come to my house with a dish that needs tending to or oven space, I will use my powers of reasoning to tell myself that you have probably not considered that all of the burners and all of the oven space have already been accounted for. I will smile tightly and problem-solve. I may think of the time that friends had a potluck and a mutual friend showed up with a grocery bag full of unwashed vegetables and raw tofu and exclaimed, “Look, I brought stir fry!” That story always makes me smile.

I live my life at a certain pace. I try to live a lifestyle that is not only manageable, but healthy. Sometimes I even think I know what I am doing. I feel relaxed and can coordinate the different spheres of my life. And then there are the times when everything happens at once. I need to be in multiple places to do multiple things, all at once. And the consequences for failure are far worse than lumpy gravy.

I am working my best to be the kind of parent my child needs. So is my husband and so is my child. It seems that we get to the frenzy frequently and often without notice. This is the way our lives have been for the past 4 years. Cancer happened in those years, too. The normal real life bumps and reorganizations have occurred, as well. Last week, I learned that my colleagues and I need to find new professional office space. We’ve been in the same place for 10 years. I don’t like moving. It’s a lot of work. We are working to find the least disruptive and expensive solution to the problem.

During these times when I am racing in my life, I find it harder to talk about the details of my life. Not so much because it is emotionally hard but because my brain is working at capacity. I am finding myself in that mode lately. It is easier for me to organize my thoughts in writing than in conversation but even writing has been hard to organize in the past couple of weeks.

I recently wrote that I was looking forward to this week because I would be able to concentrate on cooking an spending time with my family. And I have done just that. Although I awoke this morning fairly pooped out from entertaining, I think it says something that I am finding writing to be easy again.

Simply live.

I am trying.

Next Monday is my 49th birthday. My husband asked me what I wanted. I told him, “I don’t want anything. I just want to have dinner with you or something.”

I didn’t really have the emotional energy to think about what I wanted. It’s been a stressful few weeks with lots of worries on top of my normal worries. Sometimes, I worry that I think too much. I think about cancer every day. I think about my husband and daughter every day. I think about the obligations I have to my family, my friends, my job, and to myself. When I am really stressed, as I am at this moment, I worry that I am burdening my friends and family by asking for support, even the support of knowing what I am going through so I don’t have to do it by myself. I am worrying about this right now by sharing this with you. But I also know that when I feel most alone and burdened is the time I need to call on my resources and this means friends.

My friend, Nancy, sent me an email with a parenting resource. Actually, the email was to a bunch of people. Nancy is a dear and she always prefaces any email with, “I hope you are well.” I replied just to her. “I am hanging in there. Things are not going well but I hope you and your family are well.”

I’d never done that before. I got a phone call from her within the hour. I felt a great deal better after we talked. I am very lucky to have such wonderful support in my life.

I’ve been wishing very much to go on a vacation. Then I realize that I’ve just had two vacations, which were wonderful. What I really want is to be away from the stress of the current complications of my life.

Yesterday, I thought to myself, “For my birthday, I want a simple life.”

Immediately, I reflected that this was a fantasy. There are people who have simpler lives than mine, but their lives are complicated. More importantly, I can’t be anyone else, anyway. My life is complicated.

I also started thinking about the fact that I am ending another decade of my life, my forties. I thought, “Wow, a lot has gone on during my 40’s.” But then I started thinking about all of the other decades in my life. Just thinking about all of the changes that occurred for me just as a natural part of growing up during the first two decades made my head spin. A lot happens between the time we are born and the time we hit 20 years old. Holy Cow!

But I still want a vacation and I want a simple life.

And then it dawned on me. Although I am working on Monday, my birthday, I will not go into the office for the rest of the week. I host Thanksgiving every year and to do so, I need cooking time. So I’ve made a habit of only seeing patients on the Monday of Thanksgiving week.

My job after Monday will be to cook and spend time with my family. My husband is taking off the entire week.

I think I will get my birthday wish for a few days and this makes me very happy.

As I parked my car at my cancer center last Friday, I thought to myself, ‘This is my last “double-stick Friday”!’ Friday is not a day I see patients so it is the day I typically choose to be a patient. The first stick is a blood draw, which marks the beginning of every medical oncology appointment. Two vials of blood are drawn. Most of the phlebotomists are amazingly adept, which is very important when working with cancer patients, who have veins that are no stranger to the needle. My blood is always drawn on my left arm because I had lymph node removal on my right side. Prior to cancer, I’d had one I.V. placement when giving birth to my daughter 16 years ago and blood draws on a very infrequent basis for some of my annual physicals. Since cancer, my left arm and left hand have been poked and prodded many times a year for blood draws and surgeries. I didn’t even have I.V. chemo and I can tell the difference.

My name was called by an unfamiliar phlebotomist. But they have all been good so I didn’t worry. Then I noticed that it was taking her a very long time to find a vein. I have what they call “difficult” veins. This is why I often get the I.V. line placed in the back of my hand, which by the way, which is kind of ouchie. I could also tell that she was getting nervous. I close my eyes during blood draws because it helps me relax and also because I like to give people privacy to do their job without my staring at their work. I kept feeling the tap tap tapping of her index finger on the inside of my arm and some whispered nervousness. She stuck the needle and then the draw was taking a really long time. Usually, the phlebotomist lets me relax my fist once the needle has been placed. But she didn’t. She kept apologizing and then finally gave up. It wasn’t an adequate blood draw. Then she peered at my arm again, anxiously fretting as she did so. I kept saying, “Don’t worry about it. It’s okay.” She found a vein on the outside of my forearm. This was a new sticking spot.

Again, more time passed than usual. I didn’t mind the extra needle sticking as much as her distress and repeated apologies. Finally, the vials were filled. She fretted over the bruise she knew would be left and in attempt to prevent it, wrapped my arm tightly with medical tape.

I walked upstairs for my oncology appointment with two bandages on my left arm. It would be “triple-stick Friday”. The last stick would be a Lupron shot into my left hip. I have been getting Lupron shots every three months for over two years. Their function is to disrupt the signal from my pituitary gland to my ovaries, which respond by producing progesterone and estrogen. This is a non-surgical way of “shutting down the ovaries” and putting a woman into a near instant and possibly reversible menopause.

And yes, over two years ago, I entered menopause. At the time, Lupron was more commonly used to treat prostate cancer. There was a photo of a smiling middle aged man on the package that held the pre-filled syringe. This struck a few of us in the breast cancer community as funny. The man on the package looked far too happy with his cancer status and the fact that his testes were going to be “shut down” by Lupron.

In three months, the Lupron will wear off and I will wait and see what kind of change ensues. I asked my oncologist what I might expect to happen. It was quickly clear to me as she explained the possible factors (my natural menopause time and the fact that both Lupron and tamoxifen, which I am still taking can cause irreversible menopause) that this was a hard outcome to predict. I said, “Ah, there are many factors involved and they are all DYNAMIC.” Then I covered my eyes and pantomimed throwing a dart. Dr. Rinn replied, “You got it, it’s like throwing a dart at a moving car.”

Like throwing a dart at a moving car.

A great deal of life is like this. My health, parenting a teen.

Mindfulness is like throwing a dart at a moving car with my eyes open.

Wide open.

I remember the beginning of my face to face relationship with my daughter. The nurse put her in my arms. “Welcome to the world,” I said as I placed a tender kiss on her forehead. She was an utterly perfect clean slate full of infinite possibility.

As she grew, she changed and so did our relationship. By the time she was a four year old, she was lively, happy, brilliant, confident, independent but connected, and as sweet as could be. “This little girl is going to change the world someday,” I found myself thinking. She was a slate full of infinite happy and healthy positives.

Many parents of challenging teens rhapsodize about their children when they were younger and perhaps even exaggerate. But I can tell you, I was not alone in being in awe of this child and no, I’m not just talking about her loving father, my husband, John.

A major parenting challenge is when the slate of possibilities changes, for some children earlier than others but for most it certainly changes in adolescence. Teens create consequences, short and long-term than they can’t really fully appreciate as they are putting actions in motion. In other words, a common part of growing up is making foolish decisions that could make adulthood much different.

The slate gets dirty. There are still good possibilities but some scary painful possibilities join them. When we love our children and hold their happiness and dreams in our hearts, it can be all too easy to focus on the dirty parts of the slate. Plus, since adolescence is even harder for the teen than the parent, we get the punched in the gut feeling as we watch them struggle through tumultuous times.

I love my girl. She is still brilliant and lively. She is not always happy. She has highs and lows of confidence. She is still super sweet deep down and it is not rare for it to bubble back up to the surface. But to be honest, it is sometimes anxiety-provoking to introduce her to my friends. There is that worry that she will be obnoxious, provocative, anxious, or lacking in manners. She doesn’t really adjust her behavior much based on whether she is with adults or peers. You could be the Queen of England and there would be a chance that she would greet you with a brain rattling belch.

But the truth is that as unpredictable as she can be, adults actually tend to like her. I know that part of the embarrassment on my part, is the common sense that one’s child is the product of parenting. But that’s not all of it. I think that another piece is that she is different than she used to be and as she moves forward, her fate is less and less subject to my influence and protection.

The slate I see when I view my daughter is no longer clean. It is full of known positives, known negatives, and much gray that has not yet been elucidated by time. I look at her and I just don’t know. She is not like the joyful curious 4 year-old for whom my husband and I were the center of the universe. Time can take her away from her wishes and dreams. It can take her away from her own compass of right and wrong. It can take her away from us. It is very scary.

As a breast cancer patient, I have often felt like an adolescent. I have oft written about how the integration of cancer into my identity calls back to the original phase of my identity development during adolescence and early adulthood.

I have been reflecting a lot about my long time relationships and how breast cancer, and how I have changed in response to it, has impacted them. I am not the same person as I was before. And the slate of possibilities for my life has been dirtied by breast cancer. I realize that some have responded to me like a changeable teen. It is not a constant, but there is strain on some of my relationships and it is palpable. With some people I can feel it in my gut, even over two years past diagnosis. I am engendering fear through my association with cancer.

I have made a number of new friends through my breast cancer blogging. Sometimes these friendships seem like a vacation away. There is ease to them at times that is rare in most of my close relationships. I have been very grateful for this but at the same time, it’s seemed a little odd. And I think given how much writing there is in the breast cancer community about the perceived realness of cyber friendships, I believe I am not alone.

One of the reasons that it feels odd is that I feel small but perceptible twinges of disloyalty to my long time friends. Whee! Cyber-friends all the way!! Mostly, I have tried to appreciate and nurture friendships regardless of their origin and focus my efforts on those that are mutually supportive.

It occurred to me today that one of the reasons that new friendships have been so important to me is that none of them knew me before cancer. None of them have had to incorporate this into a pre-existing concept of me. So even though cancer is on my slate, I started with a dirty slate.

During most of my adult life, I have introduced myself to others with a smile and a handshake. I may talk about the weather or about casual pleasantries. As a blogger, I introduce myself to others with my illness. “Hi, I am a cancer patient. I write about personal and painful things. To relieve my anxiety about this, I sometimes make boob jokes.” Despite the the fact that I lead with my disease in this way, I have become part of an amazing community of people, which has led to other connections outside of the community. What a wonderful gift indeed.

As many of you know, breast surgery often results in a lost of sensation. I had a right side mastectomy. I would make sense that in removing all of that tissue that nerves would also be removed. Now my grasp of physiology is better than the average person, but by no means expert. What I can tell you, though is for nearly two years, I have had no sensation at all in the area where my right breast used to be.

This means feeling no pressure, no heat or cold, and although it is delicate to say, no sexual response. Actually, if I want to be really clear, there is no response at all. No affectionate response. No, ”ow, you just accidentally elbowed me in the boob” response. My husband could hold a hot coal to this breast and I would not feel it. No one warned me of this side effect but I had read about it myself. So prior to my second lumpectomy when my husband asked about whether a bilateral mastectomy was indicated, I responded by spelling out the implications for our love life. I had already completed a literature review on my risk of contra-lateral breast cancer, learned about the Gail Index and so forth. I knew that my estimated risk of cancer in my left breast was at a level low enough that I found personally acceptable.

In the last few months, I’ve noticed something. The numbness in my tissues has subsided to some point. I am starting to regain sensation, at least around the edges of my mastectomy site. But what I am feeling is the occasional itch. Sometimes it is deep down and unreachable. Most times it is on the surface of my skin. I am allergic to wheat and when I do eat it I get a flare of eczema within two days and it takes about two months to clear. If I cook all of my own food, this does not happen. But over vacation last August, I ate out, had a salad, and there must have been some wheat in the dressing because I am still waiting for my skin to clear. At one point, I could see that I had an eczema flare over my breasts. We also had family photos taken at the time. It looked like I had acne. Oh well. In any event, I could feel the itch of the eczema. However, when I scratched it, I felt no relief. As my internist told me when I described it to her, “That’s just not fair!” My rash, however, got worse.

In addition to itch, I have also had the return in a sensation that can only be called, “uncomfortable”. It is the mildest of pain, though still noticeable. And it is, again, felt around the edges of my mastectomy, which was performed in August of 2012. It would not be until March of 2013 that the major part of my breast reconstruction would be completed. I am no surgeon but in my own logic, it seems likely that more digging around and transplanting that occurs, the longer tissues take to heal or as my plastic surgeon describes it, “settle”.

I have numb parts. They are starting to awaken. To what extent they will awaken is unknown. But what I do know is that the awakening is uncomfortable and at times, a bit painful. This has called to mind the numbness that can happen to each of us emotionally and cognitively. I consider myself to be above average in self-awareness. However, I have neglected parts of myself, the parts that are numb. And numb parts get that way through damage, through loss of trust, emotional baggage, past trauma. Our mind protects us from many scary and lonely thoughts and feelings. The problem is, however, that it can do too good of a job.

Sometimes the parts of us that are most important, most in need of attention, are the parts that we just don’t think about or feel. The parts that are tired, afraid, and numb.

As you know, I have been digging deep and trying to feel what I need to feel and process it all through. It is a painful but productive process. In keeping with my mindfulness practices, I have tried to keep with my thoughts and feelings throughout. This has guided my decisions. At times, I move forward, full steam ahead. At other times, I take breaks. At these times, I catch my breath, assimilate new learning, and observe a new way of looking at my life.

There are parts of me that are coming alive. At this point, there is discomfort but I believe that in time there will be continued healing and awakening.

Recently I met with some parents to obtain background information as part of my assessment of their son. They are highly educated people, both with advanced degrees. They have three young sons, all of whom they speak of lovingly. The father charmed me with the fact that he calls his sons, “honey”. There words were measured and they described their concerns about their oldest son, his tendency at time to not to own his own actions, his quickness to anger, and his frequent use of exemplary verbal ability to argue with adults.

Despite their calm and professional demeanor, I could see the mounting fear behind their words. Their fear for their son’s happiness and safety in the world. We had had a chance to establish some rapport and I decided to take a chance on expressing an awareness of an issue that had yet been unsaid. “I can only imagine the stress that you feel in raising a Black son who has these difficulties, in our country.”

Both parents nodded vigorously and the father said with palpable relief, “Finally, someone gets it.”

I am not African American. It was chancy for me as an outsider to make the comment that I did. It was also chancy for me to use the term “Black” instead of African American. The former is more likely to be acceptable when used by African Americans, not by an outsider and further a member of a privileged race, such as myself. But I thought “Black” was a better reflection of their own thoughts and feelings about their son. I also know that due to my personality, I tend to be able to say things like this and they are interpreted in the way I intended. But I am still very careful. I will never know what it is like to be African American.

But I can try to understand the best I can and to be aware of the common challenges that African American families face. And my awareness must be more than an internal event. It needs to be linked to effective action. In this example, my action was communicating my awareness of the rational sources of their fears. These parents have three boys. The number one cause of death for African American males between the ages of 15 and 34 is murder. And one might think that the risk does not apply to these boys because they live in an educated and relatively affluent family. I think realistically, it may buffer this risk to a certain extent. However, even looking at my own life, I know there is a particular danger that cannot be eliminated. I have a lot of friends. A great number of them have advanced degrees. Two of my friends, both Ph.D.’s, have had murder in their immediate families, one attempted and the second resulted in the death by shooting of a friend’s brother, who was waiting in line to get into a night club. Both of these friends are African American women from well educated families. One of them even had an uncle who ran for president of another country.

There are many people who live with the cloud of potential catastrophe. We are often unable to fully appreciate it but we can do our best to understand.

I am awaiting the results of the routine MRI I had yesterday. I am learning to deal with the anxiety of these scans but I am anxious. My husband forgot about the MRI even though I’d told him a couple of times as recently as the day prior and had asked him to accompany me. His alarm went off yesterday morning at 6:30, his normal time to get ready for work. However, he was planning to go to work after my scan and it was not until 9:45. He was getting up too early to have remembered the scan so I reminded him and he came back to bed. My husband is more forgetful than I would like. But I understand that he is not doing it on purpose and further, he would have seen the appointment on his calendar. Plus, he doesn’t live in the perpetual state of Potential Cancer so there are some things he doesn’t quite understand about my experience as a cancer patient. Similarly, a close friend apologized to me yesterday for checking in with me about my MRI. He’d had quite a stressful day of his own and again, he doesn’t live in the state of Potential Cancer. Before I lived there, I didn’t really worry so much about my friends’ scans once they’d had no evidence for disease for a couple of years. The panic subsides. I don’t want my husband or my friends to live in the Potential Cancer state with me. I don’t wish that on anyone just as my friends with metastatic disease wish it for others. But the actions that come from understanding our situation are important.

As a world, we need to find a cure for breast cancers. But as individuals, we also need people in our lives who have an awareness of the unique stresses of being a breast cancer patient who are also able to convert their awareness into emotional support. You,  friends and family, may be helpless to prevent recurrence or to cure a loved one’s active disease, but you can provide emotional support. You can make living in the Potential Cancer state or the state of Perpetual Cancer more bearable and less lonely.

Perhaps it would be helpful to explain to you what scans mean to me. A clear scan means that I can live another six months with “no evidence of disease”. A clear scan to a person with metastatic cancer means that they can live with “no evidence of progression”.  If my scan shows evidence of cancer, I will go into the fast paced chaos of not knowing and having many tests, the perpetual “hurry up and wait”. If it turns out that I’ve had a recurrence, I will likely undergo a more aggressive treatment protocol than I did in the past and to undergo previous treatments for which I now appreciate the full impact having gone through them before. By the way, a lot of cancer treatment sucked. My family will suffer. My patients will suffer. I could go on and on.

I keep telling myself that the results of a scan, assuming accuracy, don’t tell me anything about myself that wasn’t true yesterday. I often tell my patients this about the diagnoses I give them. “You are the same person you were yesterday.” On myself, this is a hard sell. I am a clinical psychologist. Nobody comes to me unless they already know something is wrong. Something is not going well. There is a problem. I didn’t know I had cancer. I felt fine. There was no lump. Right now, due to my mental and physical health practices, I feel healthier than I have in years. But cancer can hide for  a long long time without someone even knowing something is wrong.

For me as a cancer survivor, it is surreal at times to realize that I can’t trust my own sense of my body. I can’t gauge my own health. My body can lie to me.  I try to be a very truthful person with myself and with others. Honesty and clarity are extremely important to me. This is hard.

Offer your loved ones your understanding and support. You don’t need to live with us and we don’t even want you to,  but do connect with us. And when the Pink wave  tells you that awareness is action and pink is helpful, put your money and volunteer time somewhere else. Somewhere that helps.

Gray and black clouds
hide the sky.
The light shines through
There is clarity above.

The clouds will burn off
maybe today
maybe tomorrow
some day, certainly.

I will see the sky
I’ll know if I traveled
during the quiet space
between dreams
to the terrifying place
the familiar chaos,
the Cancer Place.

This morning's sky inspired the poem, my first in nearly 20 years so be kind.

This morning’s sky inspired the poem, my first in nearly 20 years so be kind.

My official title is “Dr. MacKenzie”. This is because I have a doctoral degree, a Ph.D. in psychology. In formal settings, I introduce myself this way. I also introduce myself this way to groups of children, for example, when I used to supervise my daughter’s classroom so that the teacher could have a break for lunch. I didn’t see a reason to introduce myself otherwise and further, I think it is a good example to girls to know that women can get advanced degrees.

My first job after getting my Ph.D. was a post-doctoral fellowship. When my husband was doing our taxes, I felt very diminished when I saw that he had listed my profession as “student”. And then I got really mad at him when he tried to justify it by saying, “What’s the difference?” I am not an unforgiving woman but I will tell you that I get hurt quickly at these times when the response is something other than, “Oops, I’m sorry. I will fix that right away.”

A long time ago, the term “doctor” became the name of a profession rather than reflective of whether one had a doctoral degree or not. The term “doctor” became synonymous with the perfectly excellent and specific name, “physician”. I don’t know when this started but my dissertation chair claimed that the doctorate, the Ph.D., goes back to the Middle Ages and that M.D.’s stole it.

Words matter but I am finding increasingly in my own professional life that it doesn’t matter so much to me. I am older now and established in my profession. I have a good reputation. I no longer live in the very sexist world of academia. In the clinical world, working with children and adolescents, being female is more desirable, generally. Lots of my patients’ parents call me by my first name. It’s not a big deal to me on a personal level. But it is a significant deal when it comes to my profession. People understand that physicians complete many years of training and education. A lot of people think that I have a master’s degree, which is a fine accomplishment, but on average involves five less years of training and education.

Similarly, words matter in the world of breast cancer. Most of us who have it are women and if we are paying attention, we have learned that sexist words matter, too. There are words and phrases in the breast cancer community that have resulted in people feeling diminished such as “survivor” or the war analogy. These words matter because they define us and impact the way others view us.

I don’t want to diminish anybody so I am careful with the words I use. But on a personal level, I don’t mind the terms “survivor” or the war analogy, even if I don’t use the latter in reference to myself.  I understand why they bother people and I empathize with that. And I am a firm believer in each of us having the right to self-define.

But there’s the tricky bit, if we don’t at least a little shared language and identity, having cancer can be even more lonely. And if we have too much shared language that doesn’t resound with us at an individual level, it is that lonely feeling we have even when we are surrounded by people. And when other people who don’t even have breast cancer tell us what our identity is, that’s just hurtful and maddening!

I know I have written about this time and time again but it is no wonder that the balance between connection and distinction is a major task for adolescent identity development.

Whatever we chose to call ourselves, I am so happy to be part of this community and wish all of you the very best of health.

One of the things I like about my camera, is that I don’t have to change lenses. It is a point-and-shoot, not a fancy camera. I find that I take the best photos when I am actually carrying a camera. This sounds silly but my little point-and-shoot fits into my purse as well as into the zippered pocket of my hiking shirt. (Yes, there is such a thing and I wear it over a t-shirt or around my waist.)

My camera has one lens and because of this it is much lighter. But I can’t see as much with it.

In my daily life, I feel that I am constantly changing lenses, the way I see the world. Sometimes, it changes so quickly that I can’t get a good view of anything, just constant changes, blurs of different colors and no definite shapes. These are very difficult days, among the most difficult. It is on these days that I feel frozen for anywhere from a few minutes to a day or two.

I added a cancer lens to my bag a couple of years back. Before the diagnosis, it was a general purpose lens, called, “bad medical stuff that is unlikely to happen but I get it checked out just in case”. And yes, I knew about the one out of eight figure for breast cancer in U.S. women. That’s still the minority and that’s a lifetime incidence, too. The percentage of cancer diagnosed at age 46 is considerably lower.

Then I found myself at age 46, diagnosed with breast cancer and having what would be revealed as four small invasive tumors, of low grade, meaning that tests estimated them to be relatively slow growing.

The cancer lens puts cancer at the center of view when it needs to be there. For me, it was the time of active treatment, which also coincided with continued assessment through scans and pathology reports, the latter occurring after each of my three cancer surgeries.

Now I am considered a “survivor” and  my cancer lens keeps the possibility of cancer in the periphery. I have been told that I have excellent peripheral vision, both literally and figuratively.

My energy continues to return. There are so many legitimate reasons that reduce the energy of a breast cancer patient, chemo, oral medications, repeated surgeries, stress, working to make loved ones feel better, etc.

The cancer lens is also one of those things that can wear us down. Thinking about cancer, every day, even if only for a moment. I see many women worn down by the fatigue of cancer and I believe that this is a very real part of the burden.

The cancer lens can also bring things into finer focus, though. The preciousness of life, the motivation to treasure moments and to appreciate them. This is where people get into this whole, “cancer is a gift” thing. And yes, I agree that it is not a gift. But having a life threatening illness forced my hand to cope with my life and take care of myself better. The way I have dealt with cancer, by and large, has been a gift I have given to myself.

This week, I’ve had a hard time with anxiety, despite the fact that I am on vacation.  I am somewhat disappointed with myself, to be totally truthful, but I am working toward acceptance of the fact that I am a very anxious woman at times and this is one of the times, right before the beginning of a near school year and my daughter’s birthday, when the business of my life can overwhelm me.

My friend, Nancy, also a psychologist and a breast cancer survivor, spent a few hours together earlier this week. We spoke of our friendship. Nancy remarked that even though I have dealt with some heavy problems as a parent and a person, she does not worry about me the way she might worry about her other friends. I actually feel the same way about her. Nancy is very smart, very kind, and very real. She is a very clear thinker. Most of the time, I think I think very clearly, too.

Clarity is a powerful tool.  Clarity means seeing things head on, the possibilities and the certainties. It is at times frightening, at other times just the tool needed to dig through a very deep problem, and at other times, absolutely liberating.

I am real. Sometimes that is hard for people, including me.

Lindbergh High School Reunion '82, '83, '84, '85

Join us this summer for our reunion in Renton, WA!

George Lakoff

George Lakoff has retired as Distinguished Professor of Cognitive Science and Linguistics at the University of California at Berkeley. His newest book "The Neural Mind" is now available.

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