Archives for posts with tag: Breast Cancer

I had my penultimate Lupron shot. Yes, my second to last jab, on the right hip this time, with a syringe of Lupron stored in a package decorated with a photo of a smiling African American man, whom I am to assume is to represent a prostate cancer patient. Because, you know, both women and men love it when we get our hormones turned off by Lupron. It’s a party!

Lupron made me infertile by disrupting the signal between my pituitary gland and my ovaries. Yeah, I know, I talk a lot in my blog about breasts, a secondary sexual characteristic. However, the ovaries, primary sexual organs, are also commonly involved in breast cancer treatment. That’s because a lot of breast tumors, including the ones that were discovered in what was formerly my right breast, grew in response to progesterone and estrogen, two female hormones.

I could complain about the fact that a big part of my breast cancer treatment has been both a surgical and chemical warfare on my femininity. Remove my breast, then remove my lady chemicals. Go ahead, make me a man!

I’m not going to complain about this. Yes, losing a breast is a big deal. But that happens to many women, regardless of the hormone responsiveness of their tumors. Having had tumors that are progesterone or estrogen responsive is actually a positive prognostic indicator. Reducing hormonal activity is something that can be done to reduce the chance of breast cancer recurrence.

Chemically induced menopause is rough. I can tell you this first hand. Menopause symptoms, on average, are worse. I can tell you this, first hand. At the peak of my menopause symptoms misery, I had about 50 hot flashes EVERY DAY. Does that sound intensely uncomfortable? If yes, I have done an effective job in describing it. IT WAS RELENTLESS.

Currently, I experience almost no menopause symptoms. Also, I do not menstruate. And it is impossible for me to get pregnant. In other words, I am in a state of bliss.

It is likely temporary. Lupron does not permanently shut down my ovaries. In six months, my body will be adapting to the absence of Lupron. I will be 49 years old. At that time, I may become fertile again. My menopause may pause! Thanks a lot, menopause! Let me get used to you for two years and then throw a wrench into the works!

Yes, Virginia, I’m going to have to start thinking about birth control again. Aaaaaaaaaaaaaah!

The last time I took a pregnancy test was at least five years ago. I knew it was unlikely that I was pregnant, but things were not as usual, and I wanted to be sure.

Based on my family history, I am likely to go back to a peri-menopausal state after I discontinue my Lupron shots. In other words, it unlikely that I will be able to conceive, but still possible. My last method of contraception was an I.U.D, which I loved, but then had to have removed, because it secreted female hormones, and I am not allowed to have those.

Yes, I know that I am solely responsible for contraception. And I have talked to my nearly 50 year old husband about perhaps, just perhaps, getting a vasectomy. The first time I raised the issue was when I was 37 years old. I did not raise it again until I was a breast cancer patient, nearly 10 years later. Neither conversation went particularly well. In my husband’s defense, I probably raised it too early the first time, and the second time, he was likely stressed by the prospect of his wife dying.

I may be a two time champion of menopause achievement. It is not a title that I particularly relish but I guess they are far worse things in life to bear, like CANCER!!!!

About five minutes ago, I was trying to remember why this date is important. “Is today someone’s birthday?” I looked at the calendar. August 8th. The memory came to me accompanied by a small visceral twinge. Two years ago today, I had a right side mastectomy. Last year, the date took me by surprise, too. But when I remembered, I sobbed uncontrollably, on and off, for three days.

The sensation in my pectoral muscles has returned somewhat. I can feel pressure beneath my reconstructed breast. My kittens reminded me of this yesterday when they were chasing each other around the house, tearing through the living room. They both used me as part of their race track and kept running across my chest.

My abdomen is still numb, though this continues to dissipate. The plastic surgery nurse, who had the same reconstructive surgery as me, a TRAM, told me that the numbness lasted about three years for her. I also noticed that although my body doesn’t feel the same way it did before, it feels like mine.

I’ve noticed other physical changes. Last night, my husband went out for a late dinner and a walk along Alki Point, a beautiful seaside area. Along the walk, we were able to see the downtown skyline, the water, and two mountain ranges. We walked about two miles to a restaurant on the other side of the point, ate on a balcony overlooking the Puget Sound and the Olympic Mountains, and then we walked back two miles to where our car was parked. John had to pick up our daughter from band practice, so we were in a bit of a hurry walking back.

As usual, I had my camera with me and as usual, there were interesting photo opportunities along the way. We agreed that John would just keep walking, at his normal pace and I would stop to take photos whenever I wanted as long as I could run and catch up with him. That way, he wouldn’t be late. I have a long hate-hate relationship with running. Actually, it is just strong dislike. But I thought I could probably do it.

There was one spot that was particularly photogenic, so I took several shots. Then I needed to run to catch up with my long-legged man. It took me awhile to catch up. When I did, I noted to John, “Hey, I’m not breathing hard.” After complimenting me, he said, “What’s it been, about five years since you’ve run that far?” I laughed. “John, it’s been about twenty years since I ran that far!”

Breast cancer is awful, there’s no doubt. Cancer is powerful and destructive. It is nice, however, that healing and resilience are also powerful.

The "flower houses" at Alki Beach.

The “flower houses” at Alki Beach.

Our view at dinner. Puget Sound and the Olympic Mountains.

Our view at dinner. Puget Sound and the Olympic Mountains.

 

Seattle skyline across Elliot Bay.

Seattle skyline across Elliot Bay.

My husband is out of town this weekend. He left this morning. I came home from driving my daughter around town this evening. The kitties were hungry. I couldn’t find their food. It wasn’t where I had left it earlier today when I last fed them.

They were pestering me for food. I knew that we were not out of kitten food, having bought a large bag of it just last weekend. I spent about ten minutes looking all around my kitchen, in the cupboards, on the counter, and on the small tables that are there. Then I thought, “John must have moved it. John is a very tall person.”

I lifted my head up to the plane of my husband’s vision, where he sees and where he can easily reach in our kitchen. There it was, the kitten food. It was set on a high cupboard above the microwave. I got out a stool to stand on so I could reach it to take it down.

Perspective taking is an important part of marriage. It is not just putting oneself in the life situation of another. Perspective taking requires thinking and feeling like another, as if you were that other person, with that other person’s life view, attitudes, capabilities, likes, wishes, strengths, weaknesses, and feelings.

My husband is a very tall person. I am tall for a woman but much shorter than he. My experience of our kitchen, what I can see and what I can reach, is much different than his, just because of a basic difference between the two of us. It doesn’t matter that the kitchen is the same. We are NOT the same.

That’s just a simple example of a difference in physical stature and how that impacts our perception of the kitchen in our home, as well as what consequences that has on our kitten food storing behaviors.

Intimate relationships can be extremely complex. There are many differences between people in a relationship and mind reading is not yet possible. And honestly, I think that mind-reading abilities would make healthy relationships even less possible. I have some pretty dumb thoughts and feelings on a regular basis. I don’t want people knowing about them! Further, sometimes, my thoughts and feelings are not completely expressed, they are disorganized and incomplete. I don’t want to communicate them until I have time  to process them.

John and I are currently working extra hard to communicate better with each other. We are also trying to understand one another better. This is a time of transition for us. My level of functioning has been in flux for over two years now due to my cancer, it’s treatment, and my physical and emotional recovery. My husband is dealing with his own issues, some of it related to my cancer. We both navigate the shifting tides that are our teen daughter’s unpredictable ups and downs.

The logistics of our lives in the past two weeks have been particularly challenging. We are getting better at working things out. Right now, I no longer feel like I’m jugging water, as I was a few days ago. We are talking and listening. I am working hard to focus on what I can do as a wife and my own responsibilities instead of focusing so much on how I think my husband should be behaving differently.

I am working on thinking tall.

I was quite an awkward 11 and 12 year-old, as many girls are during those ages. I was and I still am very close to my mom and I remember talking to her about that stage of not being a young child but not quite being a teenager. Mom had suitable song lyrics for this and sometimes responded by singing, “Too young for boys, too old for toys, I’m just an in-between.”

“In between” is a phrase that has been popping into my mind frequently. I feel like an “in-between” as a cancer patient.

Actually, when I really think about it, I’ve felt like an “in-between” during this whole process and I see my friends going through the same thing. I remember in the early days of breast cancer I was shuttled back and forth between assessment and treatment. And even some of the treatment, that is surgery, was also used for assessment. There are blurry lines. It is a systematic process but there are many data gathering and decision points.

Other than my tamoxifen and Lupron shots, I am not in active cancer treatment. My oncology appointments are more spread out. I don’t even see my surgeon any more, I just see the nurse practitioner in the surgery office who works with “survivors”, the ultimate “in-between” status. Actually, there’s another in-between because if I am to need to have a breast cancer surgeon again, I need to see someone else. Dr. Wonderful not only “broke up” with me for being too healthy, he also retired from clinical practice, just last week. He is remaining at my cancer center doing research and in a leadership position regarding improving patient care. At least I can still send him a Christmas card later this year. He will not have moved back home yet. (He is Canadian, from Toronto, and I’ve always figured that he and his wife will move back to be with their sons and grandchildren.)

My current “in-between” balancing act is juggling my responsibilities. Okay, this is not a new balancing act as I have done it throughout my entire experience with cancer. However, as my energy is increasing, I have been able to work more. During 2013 my income, after deducting my expenses, was 50% of what it was pre-cancer. 2014 will not be a year like 2011 but it will be a much better year. I can see myself getting out of debt. My husband and I celebrate our 25th wedding anniversaries along with our 50th birthdays in 2015. We would like to take a trip to Turkey along with our daughter, to celebrate. We have a lot of saving to do if we are going to be able to take that trip. I certainly can’t contribute to that kind of expense without getting out of debt.

I am feeling the tug of responsibility to my friends, especially my friends in the breast cancer community. I know that I am not as available for communications as I once was. Some of my friends I know only through online conversations. I don’t like to distinguish them from IRL (in real life) friends because all of my friends are real life friends. Great distances as well as time differences can make communication difficult, though. And further, I confess that I am less likely to ask, “how are you” to friends who are having emotionally and physically difficult times. I don’t like to ask that question unless I am prepared to respond with the kind of time someone needs if the answer is not, “I’m fine, thank you. And you?”  I am frequently pulled away to other responsibilities at home and at work. I don’t want to do a half-assed job of supporting my friends. I’ve had too many times in my life when a friend has asked “How are you?” during a hard spot in my life and my eyes tear up with the anticipation that I will be able to share my burdon with someone only to find out that the friend really does not have the time or mental energy just right then to tend to me.

I am also worried about losing my connection with the breast cancer community. I write frequently, but when I am really busy, I have fewer ideas. I don’t want my ideas to dry up and then the social connections to dry up as well.

Most of all, I am worried about losing my connection to the opportunity (not “gift”, mind you) breast cancer and my emotional recovery have given me to truly cherish life. I want to be connected to and mindful of the full richness of life.

I suspect I will work my way through this. I also suspect that I will not run out of things to communicate, even if not through blogging. And as far as blogging goes, I think I still have much to write here on this page. But I also want to respect and take note of the anxiety and fatigue I’ve been feeling lately. The anxiety is of the “lurking in the shadows” variety and not the spinning top anxiety I get when I go into overdrive.

Maybe the “new normal” that is talked about is actually a radical acceptance that life is always in-between.

My daughter is away at camp this week. John and I decided to go out for a nice dinner last Wednesday. I just happened to have a salon appointment scheduled that day so I knew I was going to have “special occasion” hair. I chose a dress out of my closet that was inappropriate for work but appropriate for a date with my husband. We had a lovely time. I recently bought him a new camera so he was taking photos of me. A LOT of photos. He said it was because, “You look so pretty.” Yes, he is very sweet and he is the only person I would let put a camera two inches from my face in order to take close-ups.

This is one of the best photos.

Photo by Elizabeth's hubby. 2014.

Photo by Elizabeth’s hubby. 2014.

When I first saw it I thought, “That’s a nice photo of me. I look really happy, relaxed, and in love.” And those things are all true.

Then I noticed that I still had hair dye on my forehead near my hairline but I thought, “Who’s going to notice?”

Then I saw my crooked cleavage. I thought, “Oh!” I said to John, “My cleavage is off center!” He said, “Pfff, you look great.”

Now I’ve known about this asymmetry for a long time now. But this was the first time that I’d seen the unevenness in a photo of myself out in public. I had been wearing a low cut dress, displaying décolletage in all its cattywampus splendor.

Then I realized something. I didn’t really care all that much.

I am happy.

My husband loves me.

I’m still in the picture.

There’s nothing wrong with this picture.

Ross McElwee is a documentary film maker originally from North Carolina, the state that is the top grower of tobacco in the U.S. In his 2003 film, Bright Leaves, he explores the industry, especially its impact on his family, who still live in the state. In one scene, he films an examination carried out by his brother, Tom, a physician, on one of his patients, a middle aged woman.

The dropping of her examination gown reveals an enormous black tumor that has replaced where the woman’s breast tissue used to be. It has been there, growing for a VERY long time. This is the first time she has gone to a physician about it. Tom asks her questions with a gentle professional tone that belies his obvious incredulity and alarm. His patient calmly answers the question while the audience feels the horror of, “Oh my God, she has REALLY bad cancer and she’s acting like she has a hangnail!”

After this horrific moment, McElwee zooms in onto just the tumor. No one being filmed is talking. And then he keeps the tumor in view for a very long time; it seemed like several minutes but it probably was not nearly that long.

The disgust and horror abated and I was able to look at the tumor, I mean REALLY look at it. By getting a close up view, it became an abstract and almost sculptural object. I looked at the color, the shape, and the texture. When the scene was over, I thought about it for a great while and obviously, I still think of it today. The horror I felt initially was real. And the tumor, up close, removed from its emotional associations, was also real. And then I integrated both of these experiences into my understanding of this woman, her physician, and her cancer.

There are upsetting aspects of life that keep us noticing our feelings about them. And we can get stuck on the fear. I know this very well being a naturally anxious person. It is easy for me to start fixing a problem that I assume is real because I feel anxious. The real problem may be that I have gotten myself overly stressed and that I need to slow down, think about something else, exercise, talk to someone, write, or something else that calms me.

I started my mindfulness practice two years ago to gain more balance and calm in my life. It has helped me enormously in this respect. I am learning to observe my life in small pieces but much more thoroughly. And in observing little pieces at a time, I find it much more tolerable. It is easier for me to move past the fear, anger, and sadness of the painful aspects of my life. It has helped me understand my experience of cancer, bit by bit, and has contributed dramatically to my emotional recovery.

Since mindfulness is an approach to experiencing life, it can be done at any or all times of the day. Mindfulness meditation is a more discrete practice. I did it several months as a resting meditation, twice per day, using a meditation timer. Then I noticed I was having the experience when walking, especially when I am in the woods, looking at flowers, or at the beach. Although I still do resting meditation, I more frequently do active meditation while on my walks.

When I first started meditating, I could see the benefit but frankly, I thought I was doing it wrong or cheating in some way because my brain was full of jumping monkeys. I was often thinking about other things, in rapid succession. My mind is typically active, but in the stress of cancer and for many months to come, it was kind of ridiculous. I knew that in mindfulness, I was just supposed to notice my distraction and this would typically redirect my thoughts. In other words, I wasn’t doing it “wrong”. Although I still had a little doubt in myself, it was relaxing to meditate and I was committed to my healthier life style so I persisted.
Over time, I have found that mindfulness has gently seeped into the rest of my life. It is not something that I have to schedule though it is a byproduct of other activities that I do on a regular basis such as see my psychologist or more frequently, writing this blog.

I find that mindfulness is more about “what to do” than “what not to do” To a person who has struggled with anxiety, guilt, and depression, I find this to be a very liberating approach. My main goal in practicing mindfulness was to reduce the distress in my life and build my emotional resilience.

It has done just that. It has also increased my experiences of joy, bliss, and contentment. In other words, mindfulness has not only helped me feel “less bad”, it has also helped me feel “more good.”

I have rediscovered myself as a physically active person. Most recently, I have rediscovered my visual talents. I typically think of myself as being very verbal, a talker, a person who thinks in words rather than images. And this is true. I will not deny this. If I were to do so, there would be a line up of friends and family who would remind me of my chatterbox ways.

But I am also a visual person. I excelled at mathematics. I used to be able to read music with a startling array of notes on the page, 32nd notes, 64th notes. I could play really really fast and I needed to be able to visually process that information as well as use the other parts of my brain, which translated the notes into motor movements as I touched the keys of my flute, supported my breath, made the quick changes to my facial muscles needed to produce different sounds.

Most importantly, I love visual arts. I have yet learned how to draw or paint but I am an artistic person. I am good with color. I am good at arranging physical spaces. I have an artistically decorated home and office. I love to make things with my hands. And as I’ve mentioned recently, I have recently resumed taking photos.

I take my camera with me on my walks. I used to take photos with my smartphone. I enjoyed it so much that I bought a “real” camera last April. Little did I realize when I bought that camera that I was adding another layer to my mindfulness practice.

My camera is not expensive but it is surprisingly good. In particular, the macro lens has allowed me to get up close to things and see them in a different way. I started taking photos of leaves and flowers up close. And then I got even closer.

When I get really close, the blooms become abstract and almost sculptural. It is like entering a new visual world. I am not an expert at either mindfulness or photography, but combining these practices has deepened my joy in life. I am noticing patterns, some interesting, some beautiful, everywhere. I am seeing the familiar in a different way.

Kurt Koffka long ago said, “The whole is other than the sum of its parts.” I believe this to be true. But I do find that in looking at parts, lots of them, bit by bit, by examining them in detail, I am not only seeing more of the whole but I am feeling more whole.

DSC01705

Rose

DSC01689 (1)

Poppy

DSC01714

Allium

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Hibiscus

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Passionflower

I took a good number of art history classes while I was a student at the University of Washington. One of the classes, Asian Art, was taught by Glen Webb, a man originally from Kansas, if memory serves. Dr. Webb was an excellent instructor. He was interesting and knowledgeable. He was also daring and adventurous. I remember his describing the amazing Buddha sculptures carved into cliffs in Afghanistan. Even in the 80’s they were already being destroyed by Afghani soldiers. He gently lamented, “I had wonderful slides of them but I dropped them down a crevasse.”

Glen Webb was also the second person I’ve encountered in my life who comported himself with balance, an incredible calm, and peacefulness. (The first was Archbishop Emeritus of Seattle, Raymond Hunthausen.) Glen Webb was also a Zen Buddhist monk. He had followers in Japan.

I could be a ball of anxiety in those days, and for many years to follow. I thought to myself, “I want that. I want what he has.”

So I listened to how he described Buddhism. One of the things he taught us was the axiom, “I am that.” If we are all part of everyone else then there is no self. In other words, “I am that.”

No self? Hmm. “I don’t want that. I am not that. I am me”

Connection threatens identity. Identity threatens connection.

An experience like breast cancer can send us back to adolescence, which is a major period of identity development. “I that this but not that. I am not what you tell me that I am.”

“I am not cancer.” “I am not pink ribbons.” “I am not a survivor.” “I am not a warrior.”

If you ask me who I am, I will tell you, “Elizabeth MacKenzie.” (And if you have a pencil in your hand, I will note that it is “M-a-c” and that the ‘K’ is uppercase.

But if I really think about it, my name says very little about who I am. My name is not my identity. My name merely identifies me.

That doesn’t mean that my name is not important because it is important to me.

I am cancer, it is a part of my life whether it ever returns or not.

I am a cancer survivor if I think of it as a process rather than an end point. I am a cancer survivor until I die, whether I die from cancer or not.

I am a psychologist until I die.

I am a mother until I die.

I am a wife until I die.

I am a friend until I die.

I am that but I am not just that.

I am so many things.

And so are you.

“Mom, do want to see the present I got Dad for Fathers’ Day?”

Seeing that she is headed to the front door of the house, I reply, “Yes, but where is it?”

“I hid it behind the blackberry bush. I want it to be a surprise!”

“You mean the blackberry bushes a couple of blocks from here?”

“No, the blackberry bushes right over here!”

We walked a couple of blocks (I was right about the location) and there it was, a blackberry bush along a neighbor’s retaining wall that spills over onto the side walk. My daughter reached behind it and pulled out my husband’s gift, wrapped in a beach towel. I convinced her to take it home in case it rains in the next few days.

The gift was also not very well hidden. My daughter is not good at hiding, whether it be things, her emotions, or her thoughts. She is not good at being sneaky even when she tries, her emotions are easy to read, and her thoughts if perhaps not shared immediately, come out eventually.

In some ways, this is incredibly refreshing and endearing. For her life to be out in the open to others and to herself. In this way, I think she takes after me. However, I learned the hard way in life that it is important to be able to trust someone before sharing private information. I made a lot of mistakes.

I grew up thinking that not sharing was hiding. Over time, I learned to respect my own need for privacy. I learned to set better limits with people and to better determine who is trustworthy and who has not yet earned my trust. Sometimes setting a limit means something as simple as not answering a question and changing the subject. People I don’t trust with my most vulnerable thoughts and feelings are also ones who are very likely to be offended if I say, “That’s private. I don’t want to talk about it.”

People used to ask, “Why do you have just one child?” Now these folks were close friends or family. They were people I’d JUST MET. As I’ve written in the past, I made evasive jokes or changed the subject. If someone says something rude to me, I don’t respond, “You hurt my feelings” unless I want to maintain or develop a close relationship with that person.

So with all I’ve learned about privacy and trust, how did I end up writing a very self-disclosing blog? One of the main reasons I started this blog was to process a very stressful and traumatic experience in a healthy way. As a psychologist I know that we can get stuck if we don’t integrate painful experiences into the rest of our lives. This is a balancing act. It means that I can neither hide from my cancer nor hide from the rest of my life.

At this present moment, I can’t think of another way I’d rather live. And if I do, you know I’ll probably end up writing about it here.

When I was in graduate school, we had the opportunity to attend colloquia every Monday night as part of the Carolina Consortium on Human Development, held at the Frank Porter Graham Center for Child Development, which is part of the University of North Carolina. The “grown ups” were all developmental psychologists. But child clinical psychology students such as myself, not surprisingly took many child development classes. So, from time to time, we showed up.

The exchanges were lively and fast. The debates were spirited without being disrespectful. It was intoxicating. I remember one psychologist was always asking the main presenter, “But what are the underlying causal mechanisms?” For every presentation, that was one of his questions.

Then it was his turn to present. His talk was brilliant but devoid of any talk of causal factors. So I asked him, “But what are the underlying causal mechanisms?” His response was, “I don’t care about why, there is only how.”

I thought the answer was a bit of a brilliant cheat but it really got me thinking. That exchange occurred over 20 years ago and it still has me thinking!

When I was an older child, I used to ask my mother, “What was I like when I was little?” She’d answer, “You laughed and smiled a lot. You asked A LOT of questions.”

I have long been a question asker. I am a curious person. I like to understand things. “What is it?” “How does it work?” “Why is it?”

I came from a more modest background than most of the people in my Ph.D. program. (Pennie was the exception. She was from Mill Creek, West Virginia and her father worked as a coal miner.) I had many moments of self-consciousness and insecurity as a student. But one of the tools I felt was strong and well honed was my ability to ask questions and to think about the possible answers.

In thinking about my cancer, I believe the question I have explored least of all is, “Why did I get cancer?” I learned about the what and how. But once I realized that I did not have any known genetic risk and set up healthy life habits, I dropped the question for the most part. It certainly could come back, especially the “Why me?” grief question. But for now at least, the question is on the back burner, at least from a personal standpoint. (In other words, I have not backburnered my interest in cancer research.)

In the meantime, I am focusing on how I live rather than why I live.

 

 

 

I remember the thrill of discovery when I was in high school German class. There was a second person plural tense, “You all”.

I was raised in the northwest of the U.S. We are considered to have “no accent”, if that is such a thing. In any event, the closest we have to a plural second person is, “You guys.” As a feminist and inclusive person, that convention leaves much to be desired. But when I was learning tenses from Frau Johnson, my high school German teacher, I learned of the miracle of a second person plural tense. How cool was that?

When I moved to the South, I was inundated with this tense, “Y’all.” Again, how cool was that?. But as a person from Seattle, I really couldn’t pull off, “Y’all.” I just didn’t have the cred for that. Although I did acquire a Southern accent while I lived in North Carolina for six years and northern Florida for one year, I thought saying, “Y’all” was not genuine for me. I did not acquire my accent purposefully and it was not a full Southern accent. Throwing out the term, “Y’all” would classify as being a poser. (Yes, I could write “poseur” but since I do not know French, doing so would make me a “poser” twice over.) It was too different from my native dialect.

But I liked the tense. It appealed to my logic as well as my inclusive sensibilities. Consequently, I settled on, “You all.”

Yes, it is pretty nerdy but so am I. And I am not a real Southerner. But I can say, “you all.”

Time and time again I put my feelings and thoughts out on this blog. Sometimes, and rather recently, I have the fear that I am a big whiner. But I also know that many of us do not disclose our complaints, our fears, our anger, or our sadness because we fear that we are to “get over it” by now.

Yesterday, I posted about my anger and my anxiety. It is not overwhelming but it is unpredictable, bothersome, and sometimes scary. A number of you out there, people whom I’ve never met, responded with a great deal of emotional support.

My first response was regret that I had caused you worry. And then I remembered the many times during which I have been happy to offer another support when he/she was having hard times. I remembered that seeking support in each other is not just a part of life but it is also a beautiful part of life.

I have a lot of gratitude and I would like to say to you all. You all are sweet. Thank you. Thank you very much.

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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