ROOTS AND WINGS

There are two lasting bequests we can give our children. One is roots, the other is wings.
Jonas Salk

Yesterday, my son went off to college. Armed with his bags, his papers and my heart, he eagerly settled into the dormitory building that would be his new home. It is almost laughable because his university is only two hours away from where we live, but for me, it seems like a continent away. I know that he will be coming home most weekends, and yet, somehow, this new chapter in his life seems to be the beginning of his eventual flying away from the nest.

When I was younger, I thought that parenting was all about nurturing, caring, building up. I thought that my primary duty was to shield my children from all emotional and physical discomforts. No one told me that it would actually be a lifetime process of having to let go. I still remember the anxiety when, the first time I held him in the hospital nursery, the nurse came in to tell me that it was time to return him to his crib. From letting him go then, to watching him take those first steps knowing that he is likely to fall, to now sending him off to college, I have learned that parenting after all means letting my kids learn how to maneuver through life on their own.

There were days when his trials and heartaches seemed too big for his little shoulders, but I knew that I had to stand aside so that he will learn. I remember one night a few months ago, when we found out about my cancer, from my room I listened to Kiko cry himself to sleep. I wanted to go to him and comfort him, to promise him what he wanted to hear, but I knew he needed this time alone with God. I knew that I had to simply let go and let him find himself, and God's grace, in this adversity.

Today, he is again full of hopes and dreams, excited for the days ahead.

I would like to think that we taught him the best that we can. We gave him responsibilities at a young age. We complimented him when he did something right and disciplined him when he broke the rules. Now, the time has come to trust that we have done what we can and taught him well enough to make it on his own. I am hoping that his roots were cultivated deeply enough to keep him grounded in God's Word and His purpose. Also, that his wings were strengthened enough by the values and lessons we taught him so that they can take him as far as his dreams will go.

Gone forever are the days when he would rush to me and hug me after an afternoon in preschool. I remember savoring the “doggy” smell he inevitably took home with him everyday. In those days, I was the center of his universe. As the years went by, his world grew bigger and bigger and I knew my importance would become less and less of a need for him. It is a difficult thing to let go of the strings a little more, but it is something which I have to do.

Protecting him is no longer under my control. Forcing him to memorize his multiplication table and to eat his vegetables seem so trivial now. From now on he’ll be making all his own choices and I will continue to support him. But my dreams for him will have to take a back seat to the dreams he has for himself.

I will just have to trust that the world will be kind to him, and if not that he will be strong enough to fight for what should be his.

SOME OF THE HAPPIEST PEOPLE ON EARTH

I entered the room full of strangers, a little uncertain of what to expect but definitely sure that I wanted to be there. After filling in a form and getting my pink ribbon at the registration table, Bong and I found two empty seats on a nearby table. We settled down to observe the people who were clustered in several small groups around the room. They were all animatedly talking and many of the women glanced at me with a smile, as if they have known me for years.

When dinner was served, a tall lady approached me with a smile and took the seat beside mine. She introduced herself as Fely. I am sure she wanted to move around and talk to her friends but it seemed like she had decided to sit with me that night and make me feel welcome. We began talking and I found out that she was first diagnosed with Stage 2 Breast Cancer almost ten years ago. After a radical mastectomy, she underwent chemotherapy for four months. The years that followed saw her have another mastectomy, four surgeries, a metastasis to her bones, and another round of chemotherapy. Today, she is still taking medications and is still uncertain about her health but quite happily working as one of the regional heads of a government office serving indigent people.

After dinner the program began. There were some testimonials, an induction of officers, some speeches, a slideshow. Then, I and three other women were called to the front of the stage to give our pledge as new members of Bosom Friends, a breast cancer survivors’ support group in our city. After the swearing in, the President congratulated us and I couldn’t help but think of what Bong was likely to sardonically say: is that Congratulations for being a new member or for having breast cancer?

As I made my way back to my seat, an old lady of about seventy stood up, grabbed my hand and gave me a long hug. She held me at arms’ length and kept smiling at me for a few moments more, with tears in her eyes. Then she put her hand on my cheek. I was suddenly moved to tears as I totally understood and embraced the compassion, encouragement and affinity I am sure she wanted to express to me. I suddenly had a deep longing for my mother to hug me and all I could do was say to the sweet lady, Thank you.

About to take my seat, Fely called me aside and introduced me to Araceli, who unconsciously fixed her wig as she held out her hand to me. She told me that she just sneaked out from the hospital for a few hours, where she had already checked in for her chemo cycle the next day. She was first diagnosed with Stage 1 Breast Cancer four years ago but a few months ago she found out that the cancer has come back, this time a Stage 3.

At the end of the evening, all the Bosom Friends formed a big circle in the middle of the room, hands held together. Then they started swaying to the music as they sang, If We Hold On Together. I looked at all of them a little self-consciously while imagining Kiko and Angela rolling their eyes as if to dare me to join in the song. I did join the chorus, kids and found myself enjoying it.

After the song, we all posed for a final picture. After numerous hugs and exchanges of cell phone numbers, I started to feel like I was surrounded by some of the happiest people on earth. This bunch of women, ranging from their early forties to their late seventies, came from all walks of life…a bank employee, a dean from U.P., a housewife, a pastor, a doctor, a retired principal. Some were recovering, some were in treatment, some were terminally ill. I could not help but marvel at what they all shared in common: an infectious zest for life, a hopeful optimism, a sincere willingness to share and an attitude of thankfulness and acceptance. Never mind that each one had many more medical issues and physical challenges to surmount, along with the occasional lop-sided breast prostheses and very uncertain outcomes.

Now I am one of them.

CANCER MOVIES TO WATCH

My Life Without Me: This is about a young working mother named Ann with two daughters and a husband. She lives with her family in a tiny trailer in her mother's backyard. After she collapses one day she goes to the doctor who gives her grave news. She tells no one. Ann's emotional journey leads her to unexpected places and gives her life new meaning: the tender moments, the volatile emotions she must keep inside, the recognition that she has the power to understand, examine and fully live her own life.

Sweet November: Each month free-spirited Sara starts a new relationship. Her task is to take a month to make one man become a better person, and then she moves on. While November rolls around and Sara targets a busy Tycoon, she does not plan on falling in love. But they do, and as a result, Nelson learns the painful secret behind the brevity of Sara's romances.

The Family Stone: A comedy with heart. This story is about an annual holiday gathering of an unconventional New England family. Before the holidays are done, relationships will unravel while new ones are formed, secrets will be revealed and the Stone family will come together though its extraordinary capacity for love.

The Doctor: Jack is a doctor who has it all. He is then diagnosed with throat cancer. Now that he has seen medicine, hospitals, and doctors from the patient's perspective, he realizes there is more to being a doctor than surgery and prescriptions.

Fine Things: Bernie Fine, a is a home loving New Yorker. One day, while walking the floors he meets Jane, a little girl who has lost her mother. When they find her mother, Liz, Bernie is enchanted with her and they become involved and eventually marry. Liz becomes pregnant, but their joy is short lived as after their son, Alexander, is born Liz is diagnosed with Leukemia.

Wit: This is a story about a woman who isreceiving treatment for ovarian cancer. She is in the hospital bed showing what life is like for a cancer patient, most likely going to die from her disease, to hold on to her wit.

Stepmom: Jackie and Isabel have nothing in common--one is the ideal mother, the other is struggling to be any kind of mother--until circumstances force them to share a family and put aside their mutual hostility for the sake of the children. They discover how precious life, love and the ties that bind them really are in this tale about the intricate circumstances surrounding what happens when a man's new wife learns from his former wife that she is terminally ill with cancer.

A FEW FLOWERS AND CANCER

Today I walked back through my life again, retracing my steps for the thousandth time since the day I knew I had breast cancer. It has become some sort of a right of passage for me, as I decisively move on to wellness. It is not because I am running out of time, but because now I could appreciate and use time in a new way, and I want to empower myself for personal growth, fulfillment and balance ...whether long or short the future may be.

Ten years ago today, I know exactly what I was doing. I was painting. I had a one-woman-show scheduled for the end of that year, and I was frantically working towards coming up with thirty artworks to display. I was trying to enjoy the process of making paintings that bore my soul while feeling the pressure of the critics’ write ups that would come the day after the show opened.

It seems like a lifetime away now, my days as a painter. In the succeeding years of teaching, ministering, raising my kids, growing our school, it seemed like the most logical thing to do was to give up on painting. After all, being an artist required too much of me. In creating art, I had to be true to myself and yet be brave enough to receive what my audience had to say. It was like setting myself up on a platter for all the world to scrutinize and cut up. And so, because I was not sure of myself, the joy of filling up a canvas with colors, of watching the pigments come together to create magic, slowly faded into a memory.

Thankfully, one of the great blessings of cancer in my life is that all these months of introspection has taught me to love myself in a way that I never did. Instead of letting this illness destroy me, it has taught me that I do have redeemable qualities, skills and wisdom to share.

This morning, I dug up old photos of my “masterpieces”. I no longer feel emptiness nor uncertainty now while looking at them. I reacquaint myself with each artwork, and even if they are no longer mine, I am no longer wary but proud that they will always be an extension of who I am.

I wonder how they are now still touching lives in different offices or homes all over the world, and this makes me more eager to paint again.

DAY 122 A.D.

Today is the 122nd day since my life was so drastically split into two: BC (before cancer) and AD (after diagnosis). It's my 122nd day as a cancer survivor.

I have a new mantra:

My cancer is dead. My cancer is dead. My cancer is dead. My cancer is dead. My cancer is dead. My cancer is dead. My cancer is dead. My cancer is dead. My cancer is dead. My cancer is dead. My cancer is dead. My cancer is dead. My cancer is dead. My cancer is dead.

Long live me!

HEAD OUT OF THE SAND

I had my last shot yesterday to pull up my white blood cell count and so the protocol for my fifth chemo cycle is officially now over. I have one cycle more to go but ironically I am starting to feel scared. Pretty soon, all treatment will be over and then I begin my journey as a cancer survivor on my own. There will no longer be doctors and nurses to check me up every few days. There will no longer be meds to boost my immune system. I will have to deal with the state of counting my days in terms of survival rates and statistics. I will have to deal with the wondering why this ever happened to me and why I did not do what I needed to do way back when I knew something was wrong. I will have to deal with the asymmetrical image I see in the mirror everyday. I will have to be vigilant and fight off the fears on my own.

I need to pull my head out of the sand quick.

POSTING FOR POSTERITY

Since I am almost done with my chemotherapy sessions, I decided to post some sort of a photo journal for posterity...

7:00 a.m.
Getting ready for the hospital for an overnight stay. It's my second to the last cycle so far and I am nearing the finish line...yahoo!

7:15 a.m.
Bong goes to the Admitting Section and I wait in the Waiting Area. I am not allowed in the Admitting Section to avoid any exposure to infection.

7:25 a.m.

I am off to my room. One of the procedures I hate is having to be wheeled in to my room when I can very well walk.

I try to bribe the orderly to let me give him a ride on the wheel chair this time. I have done this over a dozen times since my surgery in January but noone has taken the bite.

7:30 a.m.
All chemo patients here don't go through the normal SOP of passing through ER before admission and so I am in my room now waiting for all the necessary pre-admission procedures. Meanwhile I set up all my "survival equipment" while waiting for the nurse. I brought some homework to kill idle time.

8:20 a.m.

I always request for Ritchie, the nurse from the second floor who is better than the residents in inserting the thick needle into my vein. (I am selfishly glad he didn't make it to the Big Brother auditions!) Today, however seems to be a challenge even for him because practically all the veins on the back of my left hand are weak and blackish from all previous chemo sessions.

Because I had a mastectomy and lymph nodes removed from my right axilla, they are not supposed to do any procedure on my right arm, even for blood pressure monitoring, at least in the next ten years. So its not an option for the I.V.

After the third attempt to insert the needle, the back of my left arm is swollen so they have no choice but to insert just below my open palm. They warn me that it will be painful because the skin there is thin. Let's do it, I say.

9:30 a.m.
Finally, the needle is in. Ouch that hurt!

10:00 a.m.
Talked to my friend Deah. Her husband, Juray and daughter, Iya will be coming over the weekend. She asked me what I want from over there and I started fantasizing about the Donuts and Cinammon Rolls that she sends me. Maybe not this time, Dey. Then she said she was just thinking about Krispy Kremes. Maybe I should venture out of my diet for a day when Juray comes...hmmm...

12:00 p.m.
Doc Jesena arrives and gets down to work. She greets me by saying I am looking better and better everytime she sees me. She first gives me a sedative, but as always it doesn't put me to sleep. Then she proceeds with administering my three medicines for chemo. The last one she gives me is Taxotere, the most toxic of all my meds. She has to monitor it closely, watching the drip constantly because the medicine is quite dense and oily and many of her patients go into cardiac distress while it is being administered.

She seems tensed doing this so I try to draw her out by engaging her in small talk. She tells me about her own cancer scare, about treating depressed and difficult patients, and the health challenges of her two daughters. I tell her about how God has played the greatest role in my postive outlook and how I hope she can let me share this to some of her other patients. I also asked her to look around for children suffering from cancer because I want to give them scholarships in our school.

Finally I am done and the the IV comes off.

5:00 p.m.
Bong goes to the house to check on the kids for a while. In the meantime, I take a few moments to thank God for all his blessings, for all the great friends who I know are praying for me and to visualize the medicines eradicating all remaining cancer cells in my body, if any. Bong arrives after an hour and a half or so.

7:30 p.m.
After a dinner of raw veggies and water, I am off to dream land, as the meds are starting to take effect. Bong goes down to the ICU to visit someone who just had a brain tumor removed. Good night.

The nurses monitor my pulse and blood pressure all night to rule out any cardiac reactions.

Next day...

9:00 a.m.
I am finally discharged from the hospital. I pass by the grocery to grab same parsley and bananas for my green smoothies, and some goodies for the kids.

10:30 a.m.
Since my doctor said that I should relax, what better way to do it than shop for a while. I take a look at some hats ( my new favorite things) and some books (my all time favorite things.)

After lunch I pass by the school to check on the enrollment and grab a few more "homework", and to chit-chat with the teachers and parents there.


3:00 p.m.
I am finally homeward bound.

EMOTIONAL WELLNESS

I just finished reading the book Chinese Cinderella. I bought it as soon as I saw it in the bookstore because my high school friends were just telling me that the girl’s story is not far from my own. Reading through the memoirs of Adeline Yen Mah, I certainly felt her fears and her struggles as if they were mine. I found myself in her loneliness in a family that was emotionally distant, in her struggles with being the unfavored child, her resolve to gain acceptance by achieving in school, her dreams to make it out of her own will and effort. Needless to say, I cried many a tear going through the pages of the book.

Today, I was going through my devotional book, Journeys with the Cancer Conqueror. The chapter I am currently on spoke of how research is providing clear and convincing evidence that cancer can be triggered by charged emotional states. These emotional states are mainly variations of fear, anger and guilt. The presence of these emotional states through a stressful event in the past two years might have contributed to the onset of cancer. The good news: Unburdening often contributes to healing. The devotional book further says that in our society, sickness is a powerful force, one that is rewarded. Patients can manipulate this belief to meet their needs. Some people even cling to cancer as a newfound way to fulfill emotional needs that, otherwise, have gone unmet.

At this point in my treatment, I have done quite my share of introspection and I have come to acknowledge that the stress of the past year must have really compromised my health. When my mother was in the hospital for one hundred days last year, and we struggled to keep her alive, I once again reverted back to my childhood when I would always try to rescue her from trouble. I remember how, as a young girl, I would be overwhelmed with such guilt every time I felt that I could not protect her from my father’s anger. This had gone on and on, when my father left her, when my sister became a problem, when she had to struggle to support my nephews, when she became depressed after my father’s death. Towards the end of her life, when I felt that my tumor had grown too big and I knew for certain that something was wrong, I just could not find it in me to put my health before her welfare. All this time, I could not brush aside the guilt as well as the frustration that I never truly gained her, nor my father’s approval.

Having read that people with cancer tend to use their illness to fulfill emotional needs, I suddenly realized that sometimes it seems like my having cancer has become too much like carrying my medals in childhood, in order to gain admiration and approval. This light bulb moment was a true God-send because I know that in order for me to get past this cancer, I first need to resolve whatever emotional conflicts brought me here.

Slowly but surely, I am changing not only my eating habits, but equally as important, my emotional lifestyle. I have the ability to choose my emotions, everyday in every situation. This is a critical change on my journey to wellness.

A LESSON LEARNED

Yesterday, my son Patrick was interviewed on local tv. He was asked to sing some of the songs he personally composed. I was surprised to find out that one of the songs I really like was actually written with me in mind. Naturally, one of the questions that followed was: What is the greatest lesson you learned from your mom?

During the pause, my mind started running.

Surely, Kiko would have to say courage. He knows how I have risen from the shadows of being an unwanted child to become a person of relative success. I have been quite open with them about my struggle with rejection, poor self-esteem, self-flagellation when I was young, to become a more confident, focused and altruistic adult.

Maybe, he would say creativity because he has watched me paint and write and do creative things. I would like to think he takes after me in that.

At least, he can probably say forgiveness because he has witnessed how I have chosen to forgive people who many would think are unforgivable.

If not, then hopefully he would remember love for reading…compassion...worshipful heart towards God...wisdom...resourcefulness... being hard working. Yes, I'd like to think I have all of these things.

If nothing else, then maybe survivor, for obvious reasons.

After a few moments of grappling for words to say, Kiko finally blurts out:

You know what my mom has taught me? Don’t take crap from anyone.

Oh gosh, what a poetic way to sum up sixteen years of motherhood in five words. I could die laughing.

But having thought about it, I am glad he learned that from me.

LOW FAT DIET AND BREAST CANCER

Having been diagnosed with Invasive Lobular Carcinoma and with Estrogen and Progesterone Receptor Negative Status, it has been an challenge to find anything about treatment beyond chemotherapy and radiation. Because we comprise only 8 to 12 % of all those with Breast Cancer, it seems that studies have not yet conclusively found any treatment after chemotherapy. ER-PR Positive Breast Cancer Survivors, however, have such alternatives as Tamoxifen. Even exercise apparently benefits them more.

But today, I found the article below which is about something that finally benefits those who are ER-PR Negative.

The good news is that there appears to be a relationship between former breast cancer patients eating low fat diets and prevention of the disease's return.

The not-so-good news is that the benefit appears to be confined to women whose breast cancer tumor growth was not hormone (e.g. estrogen) related.

The research was presented this weekend at the San Antonio Breast Cancer Symposium and will be published this coming week in the Journal of the National Cancer Institute.

According to the Associated Press, the U.S. government-sponsored study's results were somewhat surprising. Scientists had expected a low fat diet to have some benefit for most breast cancer survivors. But that wasn't the case.

"Maybe it raises as many issues as it answers," the A.P. quotes John Milner, chief of nutrition science research for the National Cancer Institute, as saying. The research team was led by Dr. Rowan Chlebowski of the University of California at Los Angeles, and it found that there was no significant statistical difference in breast cancer's return among women who were on a low fat diet and whose cancer was hormone-induced.

But that figure changed dramatically when it measured women whose breast cancer wasn't associated with hormones. According to the A.P., just 6 percent of these patients on low-fat diets died compared with 17 percent of the others, a 66 percent lower risk of death.

Now at least, there is something I can work on, to be actively involved in fighting any possible recurrence. I could not imagine myself just sitting back after my treatment ends in July, fearfully waiting for it to come back.

COMPANY I KEEP

I just found out today that reknowned Filipino film director Marilou Diaz Abaya was diagnosed with Breast Cancer at around the same time as I was. I am adding her to the list of women whose company I "keep", those who have been diagnosed and are or working towards being survivors.

• 
  Betty Ford - former US First Lady
  Carly Simon - musician
  Cynthia Nixon - stage and tv actress
  Dede Robertson - wife of evangelist Pat Robertson
  Diahann Carroll - singer
  Elizabeth Anania Edwards - lawyer and wife of Senator John Edwards
  Gloria Steinem - activist
  Greta Garbo - actress
  Jacklyn Smith - actress
  Joan Kennedy - former wife of Senator Edward Kennedy
  Kate Jackson - actress
  Kay Warren - wife of Rick Warren
  Kylie Minogue - pop star
  Lynn Redgrave - actress
  Melissa Etheridge - singer
  Nancy Reagan – former US First Lady
  Olivia Newton John - singer
  Peggy Fleming - muitli-awarded skater
  Sandra Day O’Connor - first female US Supreme Court Justice
  Sheryl Crow- rocker
  Shirley Temple Black - actress
  Bibeth Oteza - Filipina actress and activist
  Marilou Diaz Abaya - Filipina Director
  

RAIN ON A SUMMER DAY

Yesterday it rained for a few minutes. The smell of rain on the hot pavement, the soft patter of the raindrops on the roof, the cool air blowing through the windows. They were all such a delightful respite from the seemingly endless summer heat.

This has been one long and hard summer. To add to the challenges of my chemotherapy, it has been unusually hot and, of all times, the power outages have become more frequent. They were just saying in the month of May, things will even get worse. Hearing that, I felt weighed down with the prospect of having to go through the second half of my treatment and enduring all the discomforts.

Therefore, when Bong came home with a smile from ear to ear, I wasn’t really interested in what he had to say. No amount of cheering up could pull me out of the rut.

Well, he sure proved me wrong.

Apparently, my oncologist had been readjusting my treatment based on my responses to the infusions and medications. Because I was responding quite well, some doses were elevated which means I will have only two more cycles left instead of three! This also means my chemotherapy will end in May instead of June. And the best development of all, I will just have foul taste buds two more times and not three.

Rain on a summer day. Good news on bad days. God’s loving faithfulness in tough times.

Thank You, Lord.

THE CANCER PERSONALITY

I was just reading this article about cancer and though I was skeptical, I was not surprised to see that the writer, W. Douglas Brodie, MD. seemed to be talking about me. Read on...

In dealing with many thousands of cancer patients over the past 28 years, it has been my observation that there are certain personality traits which are rather consistently present in the cancer-susceptible individual. These characteristics are as follows:

• 
  *Being highly conscientious, dutiful, responsible, caring, hard-working, and usually of above average intelligence.
  
  *Exhibiting a strong tendency toward carrying other people's burdens and toward taking on extra obligations, often "worrying for others."
  
  *Having a deep-seated need to make others happy, tending to be ""people pleasers."" Having a great need for approval.
  
  *Often having a history of lack of closeness with one or both parents, sometimes, later in life, resulting in lack of closeness with spouse or others who would normally be close.
  
  *Harboring long-suppressed toxic emotions, such as anger, resentment and/or hostility. Typically the cancer-susceptible individual internalizes such emotions and has great difficulty expressing them.
  
  *Reacting adversely to stress, often becoming unable to cope adequately with such stress. Usually experiencing an especially damaging event about 2 years before the onset of detectable cancer. The patient is unable to cope with this traumatic event or series of events, which comes as a ""last straw"" on top of years of suppressed reactions to stress.
  
  *Showing an inability to resolve deep-seated emotional problems and conflicts, usually arising in childhood, often even being unaware of their presence.

Typical of the cancer-susceptible personality, as noted above, is the long-standing tendency to suppress ""toxic emotions,"" particularly anger. Usually starting in childhood, this individual has held in his/her hostility and other unacceptable emotions. More often than not, this feature of the affected personality has its origins in feelings of rejection by one or both parents. Whether these feelings or rejection are justified or not, it is the perception of rejection that matters, and this results in a lack of closeness with the ""rejecting"" parent or parents, followed later in life by a similar lack of closeness with spouses and others with whom close relationships would normally develop. Those at higher risk for cancer tend to develop feelings of loneliness as a result of their having been deprived of affection and acceptance earlier in life, even if this is merely their own perception. These people have a tremendous need for approval and acceptance, developing a very high sensitivity to the needs of others while suppressing their own emotional needs.

These good folks become the ""caretakers"" of the world, showing great compassion and caring for others, and going out of their way to look after the needs of others. They are very reluctant to accept help from others, fearing that it may jeopardize their role as caretakers or that they might appear to have too much self-concern. Throughout their childhood they have typically been taught ""not to be selfish,"" and they take this to heart as a major lifetime objective. All of this benevolence is highly commendable, of course, in our culture, but must be somehow modified in the case of the cancer patient. A distinction needs to be made here between the ""care-giving"" and the ""care-taking"" personality. There is nothing wrong with care-giving, of course, but the problem arises when the susceptible individual derives his/her entire worth, value and identity from his/her role as ""caretaker."" If this shift cannot be made, the patient is stuck in this role, and the susceptibility to cancer greatly increases.

As noted above, a consistent feature of those who are susceptible to cancer appears to be that they ""suffer in silence,"" and bear their burdens without complaint. Burdens of their own as well as the burdens of others weigh heavily, often subconsciously as well as consciously, upon these people because they, through a lifetime of suppression, internalize their problems, cares and conflicts. The carefree extrovert, on the other hand, seems to be far less vulnerable to cancer than the caring introvert described above.

How one reacts to stress appears to be a major factor in the development of cancer. Most cancer patients have experienced a highly stressful event, usually about 2 years prior to the onset of detectable disease. This traumatic event is often beyond the patient's control, such as the loss of a loved one, loss of a business, job, home, or some other major disaster. The typical cancer victim has lost the ability to cope with these extreme events, because his/her coping mechanism lies in his/her ability to control the environment. When this control is lost, the patient has no other way to cope.

Major stress, as we have seen, causes suppression of the immune system, and does so more overwhelmingly in the cancer-susceptible individual than in others. Thus personal tragedies and excessive levels of stress appear to combine with the underlying personality described above to bring on the immune deficiency which allows cancer to thrive.

BLACK AND BLUE

This is my bruised hand after a hospital staff struggled to find a good vein. It's now difficult to find a good vein to infuse the chemo drugs into. They could not use my right arm because I had my lymph nodes removed from there.

NO WAY BACK

It must have been the long and hot Holy Week and everyone was in a somber mood. Or it could have been the news article I read about John Edward's wife and her incurable condition. It might even be our upcoming 19th wedding anniversary. Or it must also be that I checked on the internet regarding estrogen and progesterone negative breast cancers and I found out that these have a high recurrence rate and survival beyond five years is statistically low.

I don't exactly know what set it off, but the past few days have been my lowest emotionally. It just suddenly dawned on me that this treatment might not work and I will have a recurrence. I kept trying to brush it off but the thought kept coming back. I tried telling some friends about it but one of them said that Satan is just getting a hold of me, and so I have stopped trying to find consolation through them.

I just realized that even when my treatment is over, when my bone scan comes back clear or when my oncologist says I am in remission, there is just no way I can ever go back to those carefree days of old. At some point down the road, the thought will always come back, the fear will always lurk behind the peaceful days, the knowledge will always be there that cancer does come back and that it actually never really goes away.

Now the challenge is trying to live productively through it.

TOGAS, SHOTS AND DREAMS-COME-TRUE

Last Tuesday, the nurse was supposed to come to the house at noon time to give me my shots. The results of my white blood cell count had just come in and it was normal, but my chemotherapy protocol requires that I have follow up shots on the fifth and sixth day of the cycle, to pull up my blood cell counts. By two in the afternoon, I was all dressed to go to Angela's graduation and the nurse had not yet come. Angela had already gone ahead to the Graduation Program and she wasn't expecting me at all. The teacher was already calling us that the parents were becoming restless and were starting to complain about the delay. At this point I was still debating over whether to go or not to go. At the spur of the moment, I decided to leave for the venue and ask the nurse to follow me there.

And so on our school's commencement exercises this year, and my daughter's graduation, I was sitting in a backstage corner hidden from everyone but quite happy to make it. Unknown to most that I was there, I watched the kids sing their farewell songs, receive their medals and pay tribute to their parents. I was in tears most of the time, proud of them all and just a little bit sorry for myself. Although my body was in pain, and my mask was constricting my breathing, I totally enjoyed the wide spectrum of emotions displayed and the bloopers behind the scenes. More than skills and knowledge, I realized that what Bong and I do is that we teach these six hundred or so children how to find their dreams and fulfill it. In the years to come, hopefully the number will become thousands. Isn't that such a privelege?

The nurse finally came in between the farewell speeches and I was able to get my shots in the dressing room. She asked me why I chose to be there when I should for once be selfish and sleep the afternoon off. I told her that of course I wanted Angela to know that discomfort will not keep me from being with her on her special day. And other than that, I wanted to see our graduating students, some hundred of them, and let them know by my presence that I have such strong faith in who they are and what they will be someday.

The shots might have boosted my blood cell count for this cycle, but the happy faces boosted everything else that mattered for my recovery.

When I finally came out of the shadows to pose for some photos, the kids one by one came to give me a wary smile or a quick hug. One little girl asked if I was already well because she prayed for me every night. The parents were teary-eyed and busy taking photos.

I may not have delivered any speech this year but hopefully my being there spoke to everyone as much about how I believe in them and how committed I am to see everyone succeed.

HOME AGAIN

Two cycles down, four more to go. As usual, I am feeling fine physically and the adrenalin is high.

This week though will be tough. The challenge I face this next seven days, however, won't be the after effects of my chemotherapy. Rather, on Friday my niece will be having her grand debut, one I was looking forward to for years. Her dad, my brother and her mom separated years ago and she now lives with her maternal aunt here in Iloilo. I have been the closest kin to her from our side all those years and I have watched this girl blossom into one fine young lady. I was really looking forward to this one. On Tuesday, Angela graduates from elementary. Then a few days after that Kiko graduates from high school at Pisay. Just the thought of missing these three momentous occasions is a hard pill to swallow.

But the way things have been going so well for me, only God knows how He will beautifully see me through.

OVER THE HUMP

The last three days were pretty bad ones. My nails suddenly turned blue and the ones on my thumbs felt like they were about to fall off. My hair started coming off in clumps, my scalp feeling as if I had just been through a week-long catfight. My tongue felt like a bottle of glue that even a glass of water tasted like rubber. It seemed like all the muscles of my body were constantly aching but I was explicitly told to keep away from Ibuprofen. Last but not least, we had to pay off our first hundred thousand installment for my treatment.

My oncologist had to come to the house twice to give me shots to pull up my white blood cell count. Poor Bong had to camp out on a folding bed just outside our bedroom door after running around the whole day and studying the whole night for Sunday’s service.

But today…after using up buckets of ice cubes and a whole bottle of liniment oil, I am up and about, feeling so much better. I just ate scrambled eggs and the taste of the tomatoes was euphoric on my tongue as well as my spirits. Now I begin gearing up for the next chemo cycle which will be in two weeks.

LET THE CHEMO BEGIN

My brother-in-law, Lyndon, texted me a short message today: No fear. It totally inspired me to get a really short haircut and face this chemotherapy head on. I decided that I will not wait in fear that my hair will fall off. Nor wait in fear of any discomfort. I will fight this with all I've got and give the cancer a steep challenge. After the trip to the parlor, we proceded to the hospital for admission.

My oncologist came early and proceeded to give me my first two medicines. She was just telling me how toxic they were and dangerous when handled. After the second medication, she decided to flush out the residue with dextrose and went to another patient. After two hours, she came back to tell me that she cannot proceed to administer the third one because she just got my white blood cell count and it is apparently too high. She told me that she normally never takes a pause and had she gone on to do it, the results would have been catastrophic. I will have to wait another ten days for my treatment to resume.

In the meantime, I continue to contend with so many busybodies who all seem to have an opinion of what I am going through. What I find the most annoying are those people who tend to trivialize the whole thing by saying, that's nothing, or I had a friend who had it worse, or some foolish comment like that. I want to smile sweetly at them and say, I wish cancer on you then and let me hear you say that again.

I was just on the phone with my mother-in-law the other day. She had just gotten into an argument with my husband again, this time about me. Apparently, she just discovered this new alternative medicine that has volcano ash or something of the sort as its product base, and was insisting that I take it in lieu of chemotherapy. I guess Bong laughed at her and she felt insulted. Somebody else was just telling me about coffee enema but I could not for the life of me figure out why I need to shove those beans through down there in order to get healed from cancer.

All I know is that, unlike many of them, I only have one game to play. I have thought about all of these as logically as I could after much research and consultations. I am pretty confident that the chemotherapy, coupled with a positive attitude, a change in lifestyle and faith in God will be get me through.