Monday, December 31, 2007
I went for a walk this morning with Jubilee and I smelled so much of sulfur that the bugs would not stop swarming me. And then I went to Dr. Lickstein’s office, not knowing if he would take it out or not, since I still have a fair amount of drainage, and he just took it out. Yeah!
Even though I still have some pain and swelling, it seems that my body now is back to its own integrity and has moved into the driver’s seat. I’m now in active HEALING! I no longer have to take the antibiotics, and I’m beginning to think that I have a life again.
Happy New Year!
Sunday, December 30, 2007
I have worn the same clothes for 2 weeks. A woman from the breast cancer support group thought to give me a “mastectomy camisole”. This is the only piece of clothing that I feel secure in. There is a pocket for the drain. It is soft and gently hugs my skin. I wash it about every other day, and then put it right back on. It is like a comfort blanket.
I take a shower every day, but I don’t enjoy it. My drain hangs, precipitously, at my side. If it dangles, the irritation and soreness gets worse. Once the tubing got hung on the doorknob – real pain. And I have to sort of look at the still mangled looking area where my right breast used to be.
I hope the drain will be removed tomorrow. They tell me I have to have 2 days of under 30 cc’s of drainage. Yesterday there was 28 cc’s. But it looks like I’m draining more today – this morning there was 18 already. I’m trying to stay still, do nothing, anything to stop the drainage and get the damn thing out.
I am uncomfortable with the “aggressiveness” with which my cancer has been treated. My cancer sites were small and early stage. But because there were 2 separate sites, mastectomy seemed to be the only option they would give me. My pathology report, as far as I understand now, looks good. The margins were clean. The invasive cancer was only 9 mm at its widest – 1 mm short of warranting the chemotherapy where you lose your hair. I have yet to meet with the oncologist. I’m in no hurry. I expect that she will want to put me on the estrogen-blocking drug, and I’m not keen on the idea. My cancer cells were only 10% responsive to estrogen, which they say is low. I've heard that the estrogen-blocking drug causes weight gain, sleeplessness, and aching bones. Just what I need.
Basically, I want my life back, and I want to have more say in what happens to me. I want the drain out!
At this point, I’m not even sure I want reconstruction – a silicon breast and more surgery. Yet the expander was put in. I didn’t have enough time to consider all of this.
I wish that more women defiantly wore their breast cancer instead of opting for fake “boobs”. I wish that I felt more comfortable walking around with just 1 breast, and not feeling like I have to “cover it up”. I actually like the feel of the no-breast side of me now. There is no need for a bra, it feels a little free-ing.
Saturday, December 29, 2007
Friday, December 28, 2007
Someone has taken my baby – Eric – away. I know that I adopted him, but we had bonded and I was his mother. He would feel abandoned and I wanted him back. I was angry with the women who took him away. But I also knew that I was up against a wall, and that my ranting would get me nowhere. I was not going to get him back, and I had to find a way to live with this pain and loss.
It means, first of all, being quiet and waiting. Finding a new way to experience time: not as an empty transport from what-was-before to what-I-want-to-be, but as a resting place for where I am now. A here place.
Things are not perfect (or what I call hassle-free) here. My drain is still in, and still draining and still hurting. The water balance of my body is “off”, and my ears are quite screw-y.
Despite the discomfort, I have a feeling that this is an important place to be now.
It was Debbie (Taylor’s Mom) who mentioned to me that “patience” was a good thing to know when you are sick. I have learned so much from her. Especially about life not always being what you want or expect it to be.
Thursday, December 27, 2007
The other day Debbie (Taylor’s mother) took my face in her hands, looked at me straight on, and kissed me on the lips. I was a bit embarrassed by such frankness, and looked away. But I appreciated her eye-to-eye and flesh-to-flesh boldness. This is a broad daylight kind of love. Unabashed and unembarrassed intimacy and caring.
Wednesday, December 26, 2007
And, like a toothache, I focus on the pain and discomfort, and can’t seem to get very far beyond it. I feel like I can’t get anywhere else until the drain comes out. I’m hoping by Friday, but I bet it’s going to be Monday.
My dreams last night were permeated by running away from wild boars with these two hooked horns coming up from their noses. They were ravaging my right side. (I was laying on the drain side, but it hurts even when I’m not laying on it.)
The one thing that seems to help some is my simple yoga stretches. Moving through and with the pain.
My life is on hold. I don’t accomplish much. Even though I’m out of sorts, I have a feeling something is changing in me. I want to write more, focus, get organized but I am really out of control and just hanging on. I am not serene or calm.
Some fundamental perceptions seem to be changing. Like about prayer. Like about helplessness. Maybe only in helplessness does prayer make any sense. Some women in NY State sent me a prayer shawl that they had knitted. I don’t know these women and they don’t know me, but they heard about my breast cancer and they “prayed” for me as they knitted the shawl. My gosh. I can’t explain how much this touches me, and I am embarrassed at how arrogantly I’ve pooh-poohed prayer in the past.
My body looks weird, very weird. I think it looks like those wild boars have had their way with me. There is the mastectomy scar, and then there is the swelling under and around it, puffs of ballooning skin, like my body is trying to fill up what was taken away. It all red and black. I want to get on with the healing, but I feel like I can’t get anywhere as long as the drains are in, continually irritating everything.
I don’t mind looking weird anymore, I just don’t want to hurt.
Tuesday, December 25, 2007
Last week was a blur. I was too overwhelmed with just coping to try to write. But it seems clear now that writing is a way that I use to navigate my way through the phenomena of life. Perhaps like art, it is a way that I take what is happening and attempt to form something that I can hold in my hands, or look at, or listen to.
Eric and Jubilee and I took a walk in the rain this morning. As the sky cleared and the sun came out, a clear and complete rainbow appeared. Something magical about that, even on Christmas morning.
Monday, December 24, 2007
“David” is his first name. He looks like a David. At first glance, he seems a bit “nerd-y” to me – scholarly. He looks to be about 45 years old. He also seems dependable, up early taking care of details. He does not seem like the kind of doctor who caters to the rich. But I bet that's what the rich people like about him, his scholarly and medical grounding and his apparent disregard for trendiness. He came to me by way of recommendations from women who had used him.
They have a new office, and boy is it swanky. Actually, I love the décor. Modern, with a lot of glass, but like a forest. The flooring is a mix of pebbles and carpet patterned with a hint of fern. There is a water wall in the lobby, and a large arrangement of green pod-like things. It doesn’t look like a doctor’s office, but more like a high end architect or legal office.
I think it is appropriate that a plastic surgeon’s office be somewhat artsy. When I mentioned to Dr. Lickstein this morning that the office was “swanky”, he seemed a bit embarrassed, saying that he was still finding his way around. This office, though, is more in my neighborhood – I can walk to it if I cut across a construction site. And it is Lickstein’s neighborhood too. In our casual conversation this morning, as he was pulling out a drain, I learned what temple he attends and where he lives – both nearby.
It’s interesting to be going to a “high-end” cosmetic surgeon. It’s obvious that this office is made to appeal to rich women who pay upfront for their services. It doesn’t look so much like a “medical” place. This morning (Christmas Eve) he was only seeing a few patients like me who had a medical urgency (like getting the damn drains out). Still there were a couple of glamour girls in the lobby (how can you call such a sophisticated place a “waiting room”? There is a climate controlled refrigerator with water, china, tea, etc.)
Dr. L’s old office had some modern art on the walls of the waiting room, and when I commented on them to Dr. L he said that they belonged to his partner, Dr. Pinsky. I wonder if Dr. P is the inspiration behind this new décor?
There were too many things going on. My sister was here. There was the hospital, and all the medicine, and the nausea. Seeing the wierd thing that happened to my body – I thought I looked like an alien. The god-awful drains. And the pain, like a toothache, that just stays in my right non-breast. Everyone says that it will go away with time. I hope so. What if it doesn’t?
At first it seemed like I was doing well – walking, healing. Now it seems that I should be feeling better than I do. I am still tired. I still hurt. I still have a drain.
I think I need to start writing again, this time without an audience.
Saturday, December 15, 2007
My sister, FA, is flying in from Buffalo tonight. She was originally scheduled to come in tomorrow, but with the snowstorm expected up there tonight, was afraid that she wouldn’t be able to get out. Boy will she be surprised with the 80-degree weather here. We still have the AC on. She likes to talk and can answer the phone when she gets here.
John and I are going to his company Xmas party tonight. That’s always somewhat of a bore. But I am distracted, and I am ok. I don't feel sad or scared anymore.
Friday, December 14, 2007
I didn’t sleep well last night. I was worrying about the “sentinel node biopsy” part of the surgery, and realized that I didn’t understand too much about that. So I got up and started researching it, only to find out that it involved injecting a radioactive substance into my breast prior to the surgery. Just the idea of a needle going into my breast now makes me a bit nuts. I called Mary Jean Houlihan this morning and she clarified for me that Dr. Rimmer does not use that technique, and that the radioactive dye would not be injected until after I was under anesthesia. Whew! I also called the Dr’s office to reassure myself that I would be able to speak to the Dr before the surgery on Monday morning. I want to remind him to be frugal and not take any more skin than he needs to.
Zangmo sent a Xmas cactus today, and Don & Ann (computer clients) just sent over a rather fancy robe and nightgown. Sometimes I feel like I am witnessing my own funeral! I get cards and phone calls from people I haven’t heard from in years. I am touched by how caring and thoughtful my friends are – and I still feel somewhat unworthy.
The night before we picked up Eric as a baby I remember writing and remarking how I was able to watch my life just before a turning point. I wonder if this writing is like that.
Thursday, December 13, 2007
I don’t like all the papers that have to be signed. I don't like having to read about everything that can go wrong. I don’t like the way I feel reduced to a set of medical numbers.
And I didn’t like the anesthesiologist that I met with. Hopefully he will not be “assigned” to me.
I feel very vulnerable today. On the way back from this pre-op visit I looked at the darkening sky and just started crying.
Wednesday, December 12, 2007
Things can just be as they are.
My sister is coming in from upstate New York on Sunday. This is interesting. Though we are close in age – she is 20 months older than me – we have very different personalities and have never been particularly “close” as sisters. But we were the only surviving children, and there is a strong unspoken bond between us.
She really wanted to come to be with me during the surgery, and I knew I needed to honor that. On the surface, I think I agreed because I wanted John to have someone with him while I was actually in surgery. But there are many layers of complex relatedness going on here and I know that I need to just surrender to it and let myself be amongst family and friends, and let them care for me. I do not need to, and cannot, hyper-manage it.
It’s a little scary to completely put myself into the hands of others. The hands of my surgeons, as well as the hands of my family and my friends. But I do.
Tuesday, December 11, 2007
Early this morning I sat outside in the darkness, watching the stars and the wind blowing in the trees. It occurred to me that all of this is mine/me, that my boundaries are not limited to my particular body.
The message: “know this place(as yours and you)”.
Monday, December 10, 2007
I am feeling a little depressed, a little frazzled and a little sad. Two women from the breast cancer support group called me, and I am grateful for these new friendships. I saw my primary physician’s assistant and waited an hour and a half to get a blood test. They did an EKG and the waves look good though I have an irregular heart beat. I knew I danced to a different drummer. I hassled with trying to get my printer to work. I talked to my sister, who is calling almost every day now (We usually only talk once or twice a month).
I didn’t get to my yoga/sitting until late in the day.
I think I feel the 3rd wave of sadness coming on. It is a more subtle, accepting kind of sadness. A quiet sadness, but sadness nonetheless. My surgery is now less than a week away.
Sunday, December 9, 2007
I am the kind of person who can sit for hours with a cup of tea and watch the sunlight as it plays and makes shadows. Doing nothing relaxes me.
I understand that “worry” can easily creep in if I get too focused on myself. But I do like being quiet and alone.
And I have enough Dr.’s appointments next week to keep me busy. I have to see my primary physician, get blood tests, see the plastic surgeon one more time, have a pre-op consultation at the hospital and meet with the anesthesiologists, meet with an underwear woman for clothing that I can wear immediately after surgery. Each of those appointments will focus on my breast cancer and upcoming surgery, and that’s stressful enough without trying to solve other peoples’ computer problems as well.
I miss not having the extra cash that we have when I work, especially now, but sometimes extra cash is just not worth it.
Saturday, December 8, 2007
I was talking today with my cousin’s husband, who is a doctor in Arizona and an expert on breast disease. It seems that with MRIs, more and more small, previously undetected, breast cancers are discovered. Twenty years ago, the site of my 2nd site of cancer cells would never have been found. I would have had a lumpectomy and then radiation. Would the radiation have killed the 2nd small site? Who knows? Maybe.
So it seems that now with the super-sensitive diagnostic testing, more 2nd cancer sites are discovered. And the protocol, at this point, is that if 2 primary cancers are detected in the same breast, mastectomy is the answer – no matter how small the cancers are.
Because more 2nd cancers are detected, more mastectomies are being done than before. Is this "progress" saving lives, or just generating more surgical business?
It seems like overkill to me. There must be a way to remove small cancers on the same breast without having to remove the whole breast. If we are going to detect earlier and smaller stage cancers, there must be a way to treat them without surgery. However my cousin's husband said that, in this day, I would have a hard time finding a doctor who would risk it.
And then there are the women in my breast cancer support group who elected to remove their healthy breast, and who had mastectomies when only a lumpectomy was required. Perhaps I don't know enough about cancer.
Friday, December 7, 2007
I feel like I may be making a mountain out of a molehill here. My sense now is that breast cancer/mastectomy is a lot more frightening for those who haven’t faced it, than for those who have.
I may even learn from these women how to be more gracious with praying.
Thursday, December 6, 2007
I think that perhaps this safety and reassurance of goodness is what we mean to give each other when we say that we will “pray for” them. As well as the acknowledgement that we are all mysteriously here and in this together.
Yesterday I lost it at the vet’s office. Jubilee had an infection in her paw that needed to be treated. The vet was young and new, and distracted because of an emergency surgery that needed to be done on a dog that had been bitten by a larger dog. She asked me to leave Jubilee for a few hours. When I picked Jubilee up later, a series of blood tests had been done on her (all were normal) and the bill came to $340. In front of everyone in the waiting room, I ranted that I would never bring Jubilee back and that I should have been consulted about the expensive testing before it was done. John told me on the phone that I sounded frazzled and “like my sister”. Jubilee is still limping.
On top of that, people that I barely know are repeatedly sending me “prayer” cards and putting me on their “prayer lists”. This makes me very uncomfortable. For one thing, I have no idea what it means to “pray for” someone. The only thing that I can relate to in my own experience is holding someone in a place of love and concern within myself. The “pray for” wording feels somehow contorted to me, and I do not understand what it means. But I’m trying to let go of that as just a wording peculiarity. What really bothers me is having my name and predicament broadcast on “prayer” billboards and the like. I do not like the attention on me, I feel a need for more privacy, and I don't know how to be gracious about all of this.
I would like to run away somewhere, to another universe, where there is no breast cancer. I would like to disappear.
Wednesday, December 5, 2007
The above is a photo of Darrell Grayson, taken the day before he was executed last July. His grace and his hope – the very call to be – is gift and given to me.
I think of my breast cancer support group (which meets tomorrow night), and how important those women are to me.
Tuesday, December 4, 2007
There is something hanging over these days – an anticipation, a dread, a fear – that is always with me.
I know that it is way out of proportion, but I compare it with how a condemned man must feel when he knows his execution date and time. I watch the calendar, and know that the time is counting down.
I think of the soldiers and civilians who are wounded in war, and then carry and live with their wounds all of their lives.
I wonder about physical woundedness. And yet here I am whole, seemingly healthy, with a body that I mostly love and cherish.
Monday, December 3, 2007
I can acknowledge the worry and fear – and sometimes I have to put all of my fear to word - but I can also choose to let my mind go down another path: a path of quietness. But I have to do certain things to better establish this path. Like little times of yoga. Like reading small parts of my “Book of Hours” through the day. Like taking Jubilee for walk or sweeping the back porch. Like writing to one of my prisoner friends. Like just sitting.
Sunday, December 2, 2007
This must be my 2nd wave of sadness. It is bigger and deeper than the first, welling up inside me and sometimes spilling over in tears. It is about my particular misfortune – my breast cancer – but it is also about all the misfortunes of life, mine as well as others. It is about natural disasters like tsunamis as well as imperfections and break down of body. Things that happen that are out what seems to be ordinary and that bring suffering.
This is my world and this is my life.
It’s nobody’s fault, but the way things are. I suppose I could get mad at God.
Saturday, December 1, 2007
The office was a bit crowded and harried on a Friday afternoon, but Dr. Rimmer was patient and answered all of my questions. Even though I knew the answers, I needed to hear the answers from him. Again I wanted to know why he couldn’t do the 2 lumpectomies with radiation and again he told me that I would end up with a deformed breast that I would never be happy with. He all but implied that he simply would not do it. I wanted to know if he could preserve the nipple area, and yes, he could, but I would have no feeling there and it is possible that the ductal in situ carcinoma could have spread to that area.
He showed me where and how he would cut across my breast and lymph nodes, and told me that he would use the “skin preserving” technique so that when Dr. Lickstein puts in the “expander”, I will start out with a little mound of a breast, rather than being totally flat chested.
He has a nice style for a man who cuts off women’s breasts.
His hands are warm and he unabashedly touches – touches your breasts, your hands, puts his arm around you. Ordinarily I would find this a bit off-putting, but in this situation I find it somewhat reassuring.
I had been a bit confused about the type of reconstruction I would be having – silicon implants rather than the more complicated “trans-flap” surgery where skin and tissue is moved from the abdomen to the breast. They make an effort to not influence your decision and just give you the facts, but I saw Dr. Rimmer wince when I mentioned the abdominal surgery, and the nurse later told me that she felt the expander/implant technique was a good choice.
Dr. Rimmer says that I am going into the surgery with good prospects – the DISC (ductal in situ carcinoma) is a larger area, but has supposedly not reached the invasive stage; the invasive stage cancer is small. It is possible that the lymph nodes will not have been affected.
Finally, the nurse made the final arrangements with the hospital. The mastectomy will be done at 9:30AM with the plastic surgery phase following at 11AM. Hearing these times made it all a bit more real, like this is really going to happen. I’m still scared but am getting better I think.
Next week I go to get the blood tests, chest x-rays etc. that they need before surgery.
Thursday, November 29, 2007
I have been wondering lately about that whole concept of deformity, and why I find it so frightening. I think about carnival freak shows, babies born with extra limbs – and about how these people with abnormalities are ostracized. It is that sense of “not being like everyone else” that is scary – and especially the fear of being shunned.
I think of the lepers of the world, the prisoners, and those who truly have physical deformities.
Here I am, surrounded by supportive and reassuring family and friends as I lose a part of my body that has become diseased, and I talk of deformity. Talk about blowing something way out of proportion.
And yet, that fear of deformity, even having a fake breast, was and is a real and honest part of my feelings surrounding mastectomy.
Wednesday, November 28, 2007
I’ll wake up without a breast though :-( - but I’m ok with that, I think.
The surgery is scheduled for Monday, December 17th.
Dr. Rimmer is the surgeon,
...and Dr. Lickstein is the plastic surgeon.
I feel that they are both very competent and compassionate doctors.
Tuesday, November 27, 2007
Today I saw the plastic surgeon, Dr. Lichstein. He’s a sort of nerdy kind of guy, but very likable. He comes with very good recommendations from my breast cancer support group.
There are lots of options for reconstruction - silicon implant, saline implant, taking fat from the belly (and getting a simultaneous tummy tuck, which I could use) – each with its own advantages and disadvantages.
For now, Dr. L says, the most important thing that I do is treat the cancer, that I can gradually make my reconstruction choices.
Since the idea of a 7-hour surgery (and 4-5 days in the hospital) doesn’t appeal to me, I decided to just go with the mastectomy for now. After Dr. Rimmer removes the breast, Dr. L will put in an “expander” – which will gradually be filled with saline to stretch my skin for an implant (saline or silicon or fat from my tummy). After 3-6 months Dr. L will do the implant surgery, lifting the other breast to match the fake one.
They showed me photos. The final products all looked great. The expander stage looks very weird.
They said that I would have to deal with “drains” for 7-10 days after the surgery because the body tries to fill in empty cavities with fluid. But that it wasn’t going to be as bad as it sounds.
The cancer treatment (chemo, radiation, etc.) will not be determined until after a pathologist examines the removed breast and lymph nodes.
God, I can’t believe I wrote all that. It does sound gruesome. Dr. L's office is now coordinating with Dr. Rimmer’s office for a surgery date, which he says could be next week, but will be no later than 3 weeks from now.
In the women I met at the breast cancer support group I can see, at a certain level, how I will be able to get through the surgery and treatment of breast cancer. They share with me their courage.
These last couple of days I have been watching the Carthusian monks filmed in “Into Great Silence”. They show me the way to quietness. I will never be a Carthusian monk – at least in this lifetime – but there is something in their calling that I also know in myself. I needed to see this calling enacted in their persons in order to know how to tap into it in my own life..
It is in quietness that the fear is abated, and I am sleeping much better. I am learning how to hold the quietness.
And then I realize how much John has taken care of me, all my life, in so many ways. For a while I liked to think that I was an “independent” woman, and could manage myself, by myself. Now I can see how silly that all is, and am beginning to see just how dependant I am, and how much we all need and depend on each other.
Sunday, November 25, 2007
I have wanted to see the film for a while and, in fact, it was next up on my Netflix cue. But now that I have started watching it, I know that it is a film than I need to own, and watch repeatedly – like prayer.
It is a contemplative film that draws me deep into the mystery of life itself, and leaves me resting in the same Silence as that of the monks.
Especially now, I need to keep my focus on this silence.
The experience of breast cancer is breaking down my old walls of control and visions of “how things are”. When I awaken in the night, I immediately know that things are different now. Life itself is different. I am in a strange (and frightening) land. The old rules no longer apply. And it seems as if I need to discover/uncover a whole new way to be and see. But none of this new way of seeing and being is in my hands.
Silence is the only thing that I have to hold on to.
Saturday, November 24, 2007
Today Nancy brought these gifts by. I know that they are books – but the way that she wraps them is so special as well.
I have this sense that I am not worthy of such love as I am shown by others, that I am not nearly so attentive. What did I ever do to deserve this attention and care?
I am not a serious gym-person. I go every now and then and do some of the machines and some of the weights. Sometimes I do an exercise or yoga/pilates class. If I’m not doing a class, I usually am in and out of there in less than an hour, usually around 45 minutes.
Today, while on the elliptical machine, I kind of lost it. As in, I knew that my head was not working right. I was breathing ok, but my thoughts were jumping around. I felt like I was losing it. My short-term memory was gone, and I couldn’t remember any of my doctors’ names. When I came home John took my blood pressure and it was fine. I wasn’t really panicked, but I couldn’t concentrate, and it was a little scary. I had to just keep busy “doing the next thing”.
Actually, I felt like I was having really profound, insightful and imaginative thoughts, but I couldn’t hold on to them, or reflect on them. And they were jumping around a lot. Like I was tripping or something.
Something similar happened the last time I went to the gym, about 10 days ago, only this time the disorientation lasted longer.
I’m a little more focused now, but I think I’ll stick to just riding my bike and doing yoga at home for awhile.
Friday, November 23, 2007
I know that I will lose my breast in a few days, and I have accepted that. I am sad because I am losing something familiar, something that has been with me for a long time, something that I had assumed would be with me forever.
It is like an early good-bye.
I said to Sebastian that I was beginning to understand that this loss/mourning seems to be at the heart of what we call “living”.
Sometimes I cry a little bit, tears that seem to spill over from this place of sadness.
Thursday, November 22, 2007
But the thoughts and feelings continue to emerge in me in the form of a blogpost (of all things), so, for now, I am putting them here.
My friend, Donna, has been in prison for 27 years. She is one of the wisest women that I know. Yesterday I got a letter from her in which she writes:
“… As depressing as this whole ordeal is for you, I hope you realize your situation is not hopeless. And believe it or not, that one small concession can make all the difference in the world. There is a vast sea of possibilities that separates helplessness from hopelessness. Helplessness means, there’s a problem and I cannot fix it. Plus, I realize no one else can fix it either. Hopelessness leads people to suicide and other tragic, irrational actions. Hopelessness causes unbearable grief, and if an individual does not understand the grieving process – and that it is a process – then it is often more than one can deal with. The grieving process, however, ends with acceptance. With acceptance come peace, strength, and courage. People grieve many losses aside from the physical and emotional losses evolving from the death of someone dear. We grieve the loss of a job, a lifestyle, a dream, a belief, ability, and endless other matters that impact our lives through uncontrollable change. There are five stages/steps in the grieving process: denial, anger, bargaining, depression and acceptance.
Beth, I am sorry you must contend with the necessity of losing a breast. I am a lot more optimistic than you are, because I have seen the remarkable difference in the procedure and results, first hands. I also know how fortunate you are to have first-class medical attention and care. Women in here have to wait a year or more, on average, to ever make it to surgery. By then, their chances of survival are greatly reduced to the extent that surgery sometimes becomes impractical. Their situation goes from helpless to hopeless while the powers-that-be haggle over dollars and cents. Ultimately, their health and lives are deemed worthless. I could argue the injustice of this until the cows come home, but it will not improve their outlook, or yours. Life is unfair, and contrary to popular belief, life is not full of promise. There is only one promise life guarantees – and that is hope! Where there is life there is hope! I arrived at that conclusion during my own struggle with hopelessness (after I received my 2033 parole date). That one final conclusion helped me abandon my suicidal quest and risk living again. I now realize there are many things I’d like to do before I die and even if I never get out of prison – there are still many things I can contribute in an effort to better mankind and/or the generations to come …”
I feel sad and scared, but there is something in me that is rising from this bed of sadness and fear. Maybe, like Donna says, this is my struggle for hope, something at the very core of life.
I am almost finished reading William Johnston’s autobiography, “The Mystical Journey”. Besides giving me lots of perspective on Zen and Christian meditation, Fr. Johnston also talks of his lifelong struggle with celibate sexuality – how he repressed his sexuality during the early years of his life, and then how he came to learn to love others within it.
This ability to not repress, not run away, and the ability to hold seemingly opposite and conflicting energies is also part of what I am reaching for.
Wednesday, November 21, 2007
It’s not that I want to boldly assert my feelings and my thoughts – but sometimes it is only in writing that I can even figure out what I am thinking or feeling. And it seems important for me to, in some way, integrate this with how I am with others. My outer face.
So – that’s the long story of why I need to write here (and already I’m imagining the reactions of “what an over-analyst!” – jeez – maybe it’s just an inner-critic that needs to be met and dealt with!)
I had too much wine last night.
For awhile now I’ve been telling myself that if I can’t have just one glass of wine, I should just forego the whole thing.
And then I read in this morning’s paper that there is a study indicating that even small amounts of alcohol have been shown to increase incidents of breast cancer in women.
So maybe that is another reason.
I don’t want to evade the reality of what is going on. Sometimes it seems that a little wine helps me to get more in touch with what I am feeling – loosen up, relax, slow down. But there comes a point where the wine becomes a drug, and I know that I am using it to run away.
And I think that I can find my way through breast cancer without having to drink my way through.
The other night my vegan friend, Sharon, was telling me that if I went on a vegan diet, I could reverse the cancer. I’m not sure that, at this point, I would want to count on it, but it does sound like an interesting change in lifestyle that might prevent new cancers from forming. But I need for Sharon to move in for a week to teach me how to cook and eat vegan!
Tuesday, November 20, 2007
Even though my life has not been outwardly “religious” – I am a rebellious “Catholic” – my inner life has always been preoccupied with prayer. My reading has centered around contemplative writers – Merton, Hammarskjöld, the Cloud of Unknowing, Chuang Tzu …
And now. These days when everything seems a bit dazed, different, distracted – I hear/feel clearly the call the prayer. In some ways, it seems as if this “illness” (can I even call it that? I’m not really sick, it’s more like an alarm or something) is a door leading and helping me toward a more simple and easy and nothing-but-prayer way of living.
I have pretty much let go of all of my computer clients until the end of the year, when I am through the surgery and hopefully recovered. Without the stress of “having to work”, my days open up to me to basically do whatever I want. And what I want to do is what I’ve always wanted to do – pray. So I begin to structure my day more like a monk, with prayer the first thing in the morning, and at least once sometime during the day, and then at bedtime. I use 2 books to help – Merton’s “Book of Hours” and a Benedictine Book of Hours – and I only read one short reading from each book per sitting. More than that and I seem to turn the time into “reading” rather than “praying”.
Then I sit. I am just quiet. I let myself go to the deep place in myself where I know God’s presence. I don’t know how long I do this – sometimes for longer times, sometimes for shorter times. I alternate these times of sitting with some simple yoga stretches.
And then I’m ok. And I know that everything will be ok. All I have to do is be quiet, and remember to pray.
Monday, November 19, 2007
The cells don’t look right, with nuclei that are high grade, and micropapillary architecture showing frequent central necrosis. At the building block level, something is out of whack. Cancer is like an invader, and yet these are my cells that have begun acting differently and turned into something else.
When I first heard that cancer cells had been detected in my body, I thought that I was sort of like a tree with something else growing up the side of it, and eventually it would kill the tree if it were not cut off. Now I feel a little differently. The cancer feels more like it came from within me. Not that my environment – and all the hormone and pesticide laced food – does not play a part. It’s just that I don’t feel myself separate from my environment.
My environment and I are both the same life (if that makes any sense). I cannot hold myself apart from the world I live in, or protect myself from it. We are one.
Sunday, November 18, 2007
I had John take a photo of my breasts today. Outside by the pool. I don’t know why I’m so attached to them. I’m 57 years old, and my breasts do look like old lady breasts. They have fallen. The one on the right is bruised all over and distorted from the biopsies that they have done.
And yet I still find something beautiful in the roundedness, and the balance.
Saturday, November 17, 2007
I visited Donna, my prisoner friend, today in Fort Lauderdale. The prison ambience – mothers with children, fences, guards – though somewhat less harsh than at a men’s prison, is still heavy to hold. Then I missed my turn to the turnpike on the way home and had to weave my way thru Fort Lauderdale until I found I95.
I am somewhat overwhelmed at the love that my friends show me in response to my breast cancer. They call me, offer to accompany me to appointments, send me cards and expressions of love. John is especially attentive to me. I wonder at this – I don’t think that I am as attentive to others as they are to me - and I wonder about the people who have no one to care for them.
Friday, November 16, 2007
“I didn’t think that I looked strange after my mastectomy, I thought I looked like the photo of the Vietnamese girl who was running from the napalm.”
This is what one woman said at the Breast Cancer Support group I went to last night.
The women all were at some stage of Breast Cancer. Some had lost their hair from the chemotherapy. Some were undergoing reconstruction surgery.
I was the only new person. Pre-surgery. I just realized 3 days ago that mastectomy is in my cards. I never in my whole life imagined that I would have breast cancer, or be faced with losing a breast. No one in my family had breast cancer, and it just never occurred to me. It’s like I was unexpectedly dealt the Old Maid from a deck of cards that I didn't know had one.
The women were supportive. They seemed very much like women to me – relational, feeling, nurturing. Like sisters. Like mothers.
Some talked a lot. Some said nothing at all. It was mostly the silent ones that I felt drawn to.
The woman next to me kept leaning toward me with encouraging remarks. Sue, with almost no hair, offered to show me her “Barbie breasts” (no nipples.) I declined. I was too afraid. But they looked good under her clothes. Her plastic surgeon is the same one I will be using.
I feel very grateful to these women, these sisters. I never really knew how to do this “sister-stuff”. Maybe now I will learn.
OK, I’ve said it. I’ve owned it.
It has not even been a month (Oct. 23) since Dr. Mondro (the radiologist) came into the room and said, rather off-handedly, “unfortunately the biopsy came back positive, but the good news is that the cells are still in situ.”
I was a little dazed, but that didn’t seem so bad. This was 2007, and this could probably be taken care of with a simple out-patient surgery. I had had skin cancers like this.
What threw me a little was when she handed me a big Breast Cancer book – somehow it didn’t seem to apply to me.
Then there were the MRIs, and the consultation with the oncologist (Dr. Bertrand) and the surgeon (Dr. Rimmer), and the talk about radiation therapy and hormone therapy. It all seemed so “aggressive”. Wasn’t this supposed to be “beginning stage” breast cancer?
I like my breasts. When I look at them, they look perfect to me. Balanced. And though they are a bit droopy now, they are not too big and not too small. They feel soft to me, comforting. And they are sensitive and like little antennae for me. Sexually, just knowing that they are there makes me feel just a bit turned on. All of this seems connected together to who I am, how I feel, my very passions for life.
I certainly was not ready to give one up, and didn’t even want to go there. I skipped all the chapters of The Breast Book about mastectomy. Just the mention of “drains” and the like scared me.
And then the results of the MRI came back with some “questionable” area in the same breast as the original cancer cells, but in an “opposite quadrant”. Damn MRIs are too sensitive. They pick up anything.
The surgeon, Dr. Rimmer, recommended a sonogram to detect and biopsy this “questionable” area. I wasn’t thrilled with the idea of another needle in my breast, especially when I was still black and blue from the first biopsy. When Dr. Mondro (the radiologist) was not able to see the area with ultrasound, I was relieved. Not only was the needle not going in, but I presumed that this meant nothing was there.
It only meant that now I had to have an MRI- guided biopsy. The day before the MRI-guided biopsy, the MRI doctor - Dr. Mullins - showed me the "questionable" area on a computer screen. It looked like a little silver diamond on the screen, shiny. It certainly didn’t look vague.
I asked what this could be besides cancer. Oh, maybe a fibroid cyst, Dr. Mullins said, a little node of denseness. That felt right. I had little bumps of things all over my body that were not cancer. Maybe this was just one of those.
The day that Dr. Mullins called with the results of the MRI-guided biopsy I was nervous. It seemed like every test I had had lately had come back with something “positive”. I paced the floor, put away the clothes.
I liked Dr. Mullins. I had made sure he knew that I didn’t like the idea of needles going into my breast and wanted to make sure he gave me enough sedative that I wouldn’t feel it. On the morning of the biopsy he came in and said “Oh yes, you’re the woman who doesn’t want any drugs, so I’ve brought a bullet for you to bite “, and we had laughed. He’d done a good job with the biopsy. Clean, he said. We just went in, got the cells, and got out.
Dr. Mullins was sweet the way he told me that the cells were cancerous. Invasive. But the area was small.
Maybe you got it all with the biopsy, I said. Maybe, he said.
I already knew that Dr. Rimmer was going to recommend a mastectomy when he called the next day. Still, I tried to talk him out of it. Why not 2 lumpectomies? I asked. I mean, they are really small.
Dr. Rimmer says that 2 lumpectomies will leave me with a very deformed breast, that I would never be happy with it. He says that they can reconstruct the breast during the same surgery that they remove it.
So this past week I’ve been trying to get my mind around losing my right breast – and having a fake breast. I haven’t even gotten to the part of having cancer cells yet.
Last night I went to a Breast Cancer Support group. One woman suggested keeping a journal, writing about it all. So that is what this blog is all about. Writing down my feelings. Every day as I make my way through breast cancer.
So far it seems like every day has been different. Sometimes I seem ok; sometimes I seem totally whacked out.
Wednesday, October 3, 2007
Copied and pasted from a forwarded mail.
Cancer News from John Hopkins.
AFTER YEARS OF TELLING PEOPLE CHEMOTHERAPY IS THE ONLY WAY TO TRY (TRY THE KEY WORD) AND ELIMINATE CANCER, JOHN HOPKINS IS FINALLY STARTING TO TELL YOU THERE IS AN ALTERNATIVE WAY .
Cancer Update from John Hopkins:
1. Every person has cancer cells in the body. These cancer cells do not show up in the standard tests until they have multiplied to a few billion. When doctors tell cancer patients that there are no more cancer cells in their bodies after treatment, it just means the tests are unable to detect the cancer cells because they have not reached the detectable size.
2. Cancer cells occur between 6 to more than 10 times in a person's lifetime.
3. When the person's immune system is strong the cancer cells will be destroyed and prevented from multiplying and forming tumours.
4. When a person has cancer it indicates the person has multiple nutritional deficiencies. These could be due to genetic, environmental, food and lifestyle factors.
5. To overcome the multiple nutritional deficiencies, changing diet and including supplements will strengthen the immune system.
6. Chemotherapy involves poisoning the rapidly-growing cancer cells and also destroys rapidly-growing healthy cells in the bone marrow, gastro-intestinal tract etc, and can cause organ damage, like liver, kidneys, heart, lungs etc.
7. Radiation while destroying cancer cells also burns, scars and damages healthy cells, tissues and organs.
8. Initial treatment with chemotherapy and radiation will often reduce tumor size. However prolonged use of chemotherapy and radiation do not result in more tumor destruction.
9. When the body has too much toxic burden from chemotherapy and radiation the immune system is either compromised or destroyed, hence the person can succumb to various kinds of infections and complications.
10. Chemotherapy and radiation can cause cancer cells to mutate and become resistant and difficult to destroy. Surgery can also cause cancer cells to spread to other sites.
11. An effective way to battle cancer is to starve the cancer cells by not feeding it with the foods it needs to multiply.
CANCER CELLS FEED ON:
a. Sugar is a cancer-feeder. By cutting off sugar it cuts off one important food supply to the cancer cells. Sugar substitutes like NutraSweet, Equal, Spoonful, etc are made with Aspartame and it is harmful. A better natural substitute would be Manuka honey or molasses but only in very small amounts. Table salt has a chemical added to make it white in colour. Better alternative is Bragg's aminos or sea salt.
b. Milk causes the body to produce mucus, especially in the gastro-intestinal tract. Cancer feeds on mucus. By cutting off milk and substituting with unsweetened soya milk cancer cells are being starved.
c. Cancer cells thrive in an acid environment. A meat-based diet is acidic and it is best to eat fish, and a little chicken rather than beef or pork. Meat also contains livestock antibiotics, growth hormones and parasites, which are all harmful, especially to people with cancer.
d. A diet made of 80% fresh vegetables and juice, whole grains, seeds, nuts and a little fruits help put the body into an alkaline environment. About 20% can be from cooked food including beans. Fresh vegetable juices provide live enzymes that are easily absorbed and reach down to cellular levels within 15 minutes to nourish and enhance growth of healthy cells. To obtain live enzymes for building healthy cells try and drink fresh vegetable juice (most vegetables including bean sprouts) and eat some raw vegetables 2 or 3 times a day. Enzymes are destroyed at temperatures of 104 degrees F (40 degrees C).
e. Avoid coffee, tea, and chocolate, which have high caffeine. Green tea is a better alternative and has cancer-fighting properties. Water- best to drink purified water, or filtered, to avoid known toxins and heavy metals in tap water. Distilled water is acidic, avoid it.
12. Meat protein is difficult to digest and requires a lot of digestive enzymes. Undigested meat remaining in the intestines becomes putrified and leads to more toxic buildup.
13. Cancer cell walls have a tough protein covering. By refraining from or eating less meat it frees more enzymes to attack the protein walls of cancer cells and allows the body's killer cells to destroy the cancer cells.
14. Some supplements build up the immune system (IP6, Florssence, Essiac, anti-oxidants, vitamins, minerals, EFAs etc.) to enable the body's own killer cells to destroy cancer cells. Other supplements like vitamin E are known to cause apoptosis, or programmed cell death, the body's normal method of disposing of damaged, unwanted, or unneeded cells.
15. Cancer is a disease of the mind, body, and spirit. A proactive and positive spirit will help the cancer warrior be a survivor. Anger, un forgiveness and bitterness put the body into a stressful and acidic environment. Learn to have a loving and forgiving spirit. Learn to relax and enjoy life.
16. Cancer cells cannot thrive in an oxygenated environment. Exercising daily, and deep breathing help to get more oxygen down to the cellular level. Oxygen therapy is another means employed to destroy cancer cells.
CANCER UPDATE FROM JOHN HOPKINS HOSPITAL , U. S.
1. No plastic containers in micro.
2. No water bottles in freezer.
3. No plastic wrap in microwave.Johns Hopkins has recently sent this out in its newsletters. This information is being circulated at Walter Reed Army Medical Center as well. Dioxin chemicals causes cancer, especially breast cancer. Dioxins are highly poisonous to the cells of our bodies.
Don't freeze your plastic bottles with water in them as this releases dioxins from the plastic. Recently, Dr. Edward Fujimoto, Wellness Program Manager at Castle Hospital was on a TV program to explain this health hazard. He talked about dioxins and how bad they are for us. He said that we should not be heating our food in the microwave using plastic containers. This especially applies to foods that contain fat. He said that the combination of fat, high heat, and plastics releases dioxin into the food and ultimately into the cells of the body. Instead, he recommends using glass, such as CorningWare, Pyrex or ceramic containers for heating food. You get the same results, only without the dioxin. So such things as TV dinners, instant ramen and soups, etc., should be removed from the container and heated in something else. Paper isn't bad but you don't know what is in the paper.It's just safer to use tempered glass, Corning Ware, etc. He reminded us that a while ago some of the fast food restaurants moved away from the foam containers to paper. The dioxin problem is one of the reasons. Also, he pointed out that plastic wrap, such as Saran, is just as dangerous when placed over foods to be cooked in the microwave. As the food is nuked, the high heat causes poisonous toxins to actually melt out of the plastic wrap and drip into the food. Cover food with a paper towel instead.