Breast Cancer: Fancy Gadget and Half A Million Ringgit Failed to Cure Her – What Now?

May (not real name) is a 39-year-old-female. In mid-2008 she delivered her child. Two months before delivery, she noticed the hardening of her left breast. Ultrasonography did not show anything wrong. The doctor suggested it could be due to the breast being engorged with her milk. Although she breast fed her baby the breast remained hard. There was no problem with her right breast. She went to consult order doctors and all of them came to the same conclusion – no problem!

Utrasonograhy of her breasts on 1 December 2008 indicated diffused inflammatory process. The left nipple was retracted. Conclusion: probably diffuse mastitis. A biopsy is advisable. Subsequent needle biopsy done did not show any malignancy. Not satisfied, a tru-cut biopsy was done on 29 January 2009. The result showed atypical proliferation of cells suggestive of an intra ductal carcinoma. An open biopsy of the breast lump confirmed invasive ductal carcinoma with high grade intra-ductal carcinoma.

May sought a second opinion from a doctor in a private hospital in Singapore. The histology slide was restudied. It was concluded that it was a ductal carcinoma in-situ, intermediate grade with comedonecrosis and infiltrative ductal carcinoma.

CT scan done on 31 January 2009 showed: a)  no metastataic deposits in the liver, b) several rounded sclerotic lesions seen in the thoracic and upper lumbar spine suspicious of metastatic lesions, c) a tiny nodule in the upper lobe of the right lung – probably a solitary pulmonary metastatic nodule. A bone scan confirmed bony metastases at the left scapula, left third rib and sites along the spine.

Histopathology report showed carcinoma cells are immunopositive for oestrogen  rerceptors and progesterone receptors.  HER2 oncoprotein is overexpressed.

May was advised to start chemotherapy immediately. The first chemo-treatment started on 2 February 2009. A pump was fitted to continuously deliver 5-FU. May also received two doses of Navelbine for each 5-FU cycle. In addition, May was given Zometa for the bone.  In total May received 13 cycles of chemotherapy from February 2009 to October 2009.

At this point I asked two questions:

  1. What did the oncologist say about the chances of a cure? The answer was: The doctor said there would be no cure. The treatment was only to control the problem.
  2. You must have spent a lot for this treatment? The answer: Yes, approximately RM 500,000. That is half a million ringgit – right? Yes, it is.

A CT scan on 27 April 2009 showed: a) a solitary pulmonary nodule in the right middle lobe. This measures less than 5 mm. It shows no change from previous examination, b) multiple sclerotic bony lesions. These were already noted in the previous CT scan.

May went to China for another opinion in May 2009. A PET /CT scan was done. The doctors in China concluded that May’s condition had stabilised and there was no need for treatment.

A CT scan done on 12 October 2009 showed the cancer had stabilised. However, throughout the whole month of October 2009, May complained of headaches, pains in the neck and shoulder. The oncologist said the pains had nothing to do with her cancer!

In October 2009, May completed her 13th chemo treatment in Singapore.

In November 2009, May went to India for further treatment using the Cytotron (Cytotron is the trade name of the device developed in India. It looks like a MRI machine that uses Rotational Field Quantum Magnetic Resonance Generator).

May received an hour of Cytotron treatment per day. While undergoing the Cytotron treatment, May continued to receive the 5-FU-Navelbine regimen (the 14th cycle). The treatment was scheduled for a total of 28 days but after the 20th tretment, May developed bad coughs and chest pain.  The doctor thought this was due to pneumonia and she was given antibiotics and cough syrup.  An X-ray indicated left pleural effusion (i.e., fluid in the lung). A week later the pains still persisted and the coughs became bad whenever May moved. A CT scan was ordered and revealed pulmonary embolism (blockage of the arteries in the lungs by blood clots that travel to the lungs from other parts of the body).  May was put on Heparin, an anti-blood coagulation medication.

May returned to Malaysia in mid-December 2009. May started to have pains again. Her shortness of breath also persisted. She coughed wherever she moved. The oncologist in Kuala Lumpur mentioned that the cancer appeared stable and there was no hurry to continue with chemotherapy but the pulmonary embolism had to be resolved first.  May was prescribed Warfarin. Her pulmonary embolism cleared off.

A PET CT scan on 23 February 2010 showed stable results. The oncologist said no further chemotherapy was necessary for the time being. But May had to continue receiving Bonefos (for the bone). In addition May was started on Tamoxifen beginning March 2010.

In June 2010, May’s left breast hardened again. The oncologist did not think chemotherapy was necessary but May was asked to continue with her Tamoxifen and Bonefos.

In July 2010 the skin colour of her left breast turned dark. A PET scan on 29 July 2010 indicated increased FDG avid activity and this could represent an inflammatory process of tumour activity. There was also increased FDG uptake in the thymus. At this point, the oncologist suggested a mastectomy.

On 2 September 2010, May had her left breast removed. There were some wound infections after the surgery and it took two months to recover.  The histopathology indicated invasive ductal carcinoma, grade 2 with a few foci of ductal carcinoma in-situ, high grade. Twelve of the 13 lymph nodes were completely infiltrated by malignant cells with infiltration into the surrounding adipose tissue in 4 nodes.

On 20 October 2010, there was a slight swelling in May’s right breast near the nipple. Ultrasonography of the right breast did not show anything wrong. May was prescribed antibiotics. Since there was no improvement, a needle biopsy was done on 27 October 2010. The right breast tissue showed invasive ductal carcinoma.

The doctor suggested mastectomy of the right breast. This would be followed by radiation treatment  for the left breast. There would also be radiation treatment for the right breast after the wound has healed.  Bonefos would be changed to Zometa.

A PET scan done on 10 November 2010 showed cancer activity in the right breast.The bone lesions which were stable before had now become active. In view of this, the oncologist suggested more chemotherapy.

May underwent 3 cycles of chemotherapy  using a combination of 5-FU, epirubicin and cyclophosphamide (FEC) together with Zometa. The 3rd FEC cycle was completed on 14 January 2010.

How CA Care Got Into the Picture

On 3 November 2010, we received this e-mail:

Hi Chris,

I am Don (not real name) and came across your website while searching for some alternative cancer treatments. My wife was diagnosed with breast cancer stage 4 in February 2009. She had undergone chemo and just recently did a mastectomy of her left breast. Unfortunately now her right breast is also affected. Last week the biopsy shows it is an invasive ductal carcinoma. Doctor is suggesting another mastectomy but we are worried as we don’t think it can help.

Can you help us? How good is your treatment? Can I send you the reports for review?

Hope to hear from you soon.

On 14 January 2011 was another e-mail:

Dear Chris,

I would like to come to Penang and meet you to discuss regarding my wife. I have got the latest scan results with me. What are the days and time convenient for you to see patients?

Actually before these e-mails, Don came to our centre to collect some herbs but did not take them due to lack of confidence. Then she started to receive her first chemo treatment and suffered severe side effects. She had headaches, felt nauseous and was dizzy.

Before receiving her 2nd cycle of chemotherapy, May started to take our Chemo-tea. The side effects of this second chemo treatment were reduced by about fifty percent. This built up her confidence in our herbal teas. When May had her 3rd cycle of chemotherapy, she felt even better.

The War Has Not Ended Yet – perhaps a “surge” is just about to begin

May was scheduled to receive three more cycles of chemotherapy. This time the drugs to be used  are Taxotere plus Herceptin. May is supposed to receive Herceptin indefinitely once every 3 weeks (but at least a year). May is also to receive Zometa once every 3 months.

From March 2010 to end of July 2010, May was on Tamoxifen. According to the oncologist since there was a recurrence, Tamoxifen was therefore not effective. He is of the opinion that May should switch to another drug – the newer generation of aromatase inhibitor. But for the aromatase inhibitor to be effective patient must be in her menopause. So to achieve this menopause, the oncologist suggested removal of May’s ovaries.

Don (husband) came  to our centre in Penang and told us the above story on 18 January 2011.

Video 1: The Breast Cancer War – fancy gadget plus half a million ringgit

Most patients (especially those who never had the experience of having a family member undergone medical treatment for cancer) have the misconception that after surgery / chemotherapy, their cancer will go away. Unfortunately, this is far from being true. Read the following two quotations.

Amy Soscia, a cancer patient said: There is no cure for metastatic breast cancer. It never goes away. You just move from treatment to treatment.

A renowned oncologist in Singapore wrote: Oncology is not like other medical specialties where doing well is the norm.  In oncology, even prolonging a patient’s life for three months to a year is considered an achievement. Achieving a cure is like striking a jackpot.

In a review entitled: In the End What Matters Most? A Review of Clinical Endpoints in Advanced Breast Cancer (Oncologist, January 2011; 16:25-35), Sunil Verma et al, wrote:

  • Many agents are being studied for the treatment of metastatic breast cancer (MBC), yet few studies have demonstrated longer overall survival, the primary measure of clinical benefit in MBC.
  • Of the 73 phase III MBC trials reviewed, a strikingly small proportion of trials demonstrated a gain in overall survival duration (12%, n = 9).

From the very beginning May was told the treatments she received were to only control the situation – and in this case, where is the control? Almost half a million ringgit has been spent but May was not getting any better.  In fact her condition became worse. She is starting the second phase of another battle now that the cancer had spread to the other breast, after one had been removed. The war will go on. Based on the review paper published in The Oncologist a week ago, the overall survival advantage due to chemotherapy could just be an illusion.

Can we not learn a lesson from May’s experience?  Albert Einstein said: Insanity is doing the same thing over and over again and expecting different results.

Video 2: Total Commitment – do you really believe in herbs?

Not all patients who come to seek our help believe in what we do. We are firm in saying that It is not for us to “influence” you to follow our ways. This has to be entirely your choice.

We are fully aware that after spending thousands of ringgit on the so-called scientific, high-tech treatments provided by the best brains in medicine, it is hard to believe that some roadside weeds could help your cancer. To the educated mind it seems like a big joke.  So believing in what we do is an important ingredient for success.  Past statistics showed us that only 30% of those who come are really committed or believe in what we do.

Video 3: Chemo-Tea Helped Her – she gained more confidence

I told Don that I would be writing this story.  Otto von Bismarck wrote:  A fool learns from experience. A wise man learns from the experience of others. So the main aim of writing this story is to share May’s experience with others – perhaps those who wish to learn would not have to experience similar bitterness.

Some patients believe even before they experience, but others need to experience before they can believe. It is a choice.

Video 4: Cancer War – In a war, no one ever wins!

Tragic stories about breast cancer war abounds. But all is not lost. There are some patients who have the guts to say: “Chemo? No thank you!”  Many of them survived to tell their sweet stories. You can visit our website: www.cacare.com / Success Story & Hard Truth or www.CancerCareMalaysia.com / Breast Cancer, for stories of both failures and success.

Let me close by quoting Dr. Bernard Jensen (in Empty Harvest): “While the situation is dire, should fear be the correct catalyst for change? I don’t think so. For fear is a disease in itself – a disease of the mind. Therefore, it is not out of fear, but courage, that mankind will be most effective in restoring health and harmony.”

Brain Cancer – Marvelous Technology, Dismal Outcome

As far as cure is concerned, there is no use pretending that brain tumours are truly curable ~ Dr. Jeffrey Tobias and Kay Eaton in Living with Cancer

In the first two weeks of January 2011, we encountered three brain cancer cases at CA Care.

On 1 Janaury 2011, we received this e-mail.

Dear Dr Chris,

We are based in Melbourne and came to know about CA Care through a close family friend in Kuala Lumpur. As we are unable to come there ourselves, the family friend will be visiting the centre with Z ‘s medical reports and scans.

Patient Full Name: Z       Age: 4 years old

Gender: Female              Cancer: Anaplastic Astroblastoma

Medical History:

Z started with headaches and neckaches in early 2010. We only notified the problem when her eyes and mouth cannot move correctly in around March 2010. We had been visiting few doctors, until she started vomiting in the morning, one of the doctor recommended to do a brain CT scan for her. It was done on the 12nd May 2010. Z was referred to Melbourne Royal Children Hospital immediately after the scan. A size of a tennis ball tumor was found in her brain. She had an urgent brain surgery on 15th May 2010. The surgeon and the oncologist suggested radiotherapy and chemotherapy, but we refused to do so. We putted her on Bill Henderson’s cancer free diet since June 2010. Unfortunately her tumor re-grows. Now the surgeon and oncologist recommended the same thing again, surgery and radiotherapy. But we refused to do surgery immediately.

On 13 January 2011, was another e-mail.

Hi Chris,

My name is J. I am contacting you from Adelaide, South Australia. My father has got a brain tumour and has had it since 2004. He has undergone three operations along with radiotherapy and chemotherapy treatments and is now looking for other treatment options. He mentioned to me that he heard that there is other treatment offered in Indonesia and asked me to investigate. What are your thoughts about the treatment you offer and if you think it’ll be beneficial to my father, and what is the process in commencing this treatment.

On 9 January 2011, we received this e-mail.

Hi Dr. Chris Teo,

We are coming to see you from Kuala Lumpur today.  We should reach your office around 7 p.m.

H504, nine-year-old girl came to our centre with her parents as stated in the above e-mail. She had a three-month history of weakness of the right upper limb which progressed to her right hemiparesis (weakness on one side of the body). A MRI scan showed a large solid tumour with cystic areas in the left parieto-temporal lobe extending to the thalamus.

Surgery was done on 15 November 2010. This cost RM 50,000. According to the surgeon only 60 to 70% of the tumour was removed. The histology is that of a sPNET (supra-tentorial primitive neuro-ectodermal tumour). No chemotherapy or radiotherapy was indicated after the surgery.

MRI done on 6 December 2010, i.e. about three weeks after the surgery, still showed a very large residual tumour, 8 x 7 x 6 cm, in the left parieto-temporal lobe extending to the thalamus.

A neurosurgeon in one private hospital was of the opinion that a second surgical resection could safely be done. The parents were reluctant to agree to this.  The treatment plan after the proposed second surgery is craniospinal radiotherapy (CSI) followed by four consecutive courses of high-dose chemotherapy with autologous stem cell rescue (ASCR) each time, i.e. four tandem autologous peripheral blood stem cell transplants over a four to five month period.This procedure would cost about RM 200,000.

The parents were told that there could be a 50 to 70% chance (whatever that means?) if the residual tumour is first removed to about 10% of its size. The procedure carries a risk of causing some degree of handicap.

The parents went to Singapore for a second opinion. They were told by the Singapore surgeon that a second surgery could be done with good chance recovery (whatever that means again!). The operation in Singapore would cost S$60,000.

The Bench Mark: Heroic Acts by an Outstanding Neurosurgeon

Whenever I come across brain cancer cases in CA Care, I cannot help but remember the book, The Scalpel and the Soul written by Dr. Allan Hamilton – a neurosurgeon at the Arizona Health Sciences Centre, USA. Dr. Hamilton wrote a great book and I greatly admire him. Let me highlight some of the brain cancer cases that Dr. Hamilton wrote about. There are many things we can learn from these stories. Let these stories be the bench mark upon which you base your decisions when it comes to brain cancer.

Story 1: Anaplastic Astrocytoma

Taylor was a 18-year-old female and the daughter of Dr. Hamilton’s close friend, Candy. The entire left side of Taylor’s body had gone numb. Dr. Hamilton wrote:

“I was expert at using computer-guidance systems for neurosurgery, so I was not surprised that Candy asked me to do the biopsy procedure.

This kind of biopsy is dangerous – there would be little margin for error.

We would need to enter the brain in a relatively posterior location and then skirt past the motor cortex, where all the muscle coordination for the body lies. Then we’d have to slip seamlessly through millions of motor cell cables and sensory cells to gain access to a structure called the pulvinar. This was where the tumour seemed to have its epicenter. We plotted four different trajectories  … and looked over on the computer.

The team had done hundreds of biopsies together, but this was definitely going to be one of the most challenging cases. There was little doubt we would get the job done, but could we get it done right?

One of the advantages of computer guidance is that you know within a millimeter exactly where you need to drill through the skull. In fact, the incision of this kind of surgery is less than half the width of the nail on your pinky finger. We close it up with a single stitch and cover it with one of those dot Band-Aids, so I could assure Taylor she wouldn’t lose any hair. No one would even be able to see the incision unless she pointed it out.

The news from neuropathology was not good. The tumour was an anaplastic astrocytoma – a high grade malignant brain cancer. And inoperable. We’d to depend on radiation and chemotherapy.”

Chemotherapy-Radiotherapy

“This young woman became bald, bloated and acne-ridden. Taylor was transformed in front of my eyes. It was like being in a horrible fairy tale where a spell is cast upon the beautiful princess.”

Worse news: the tumour did not respond. MRI showed clearly that the tumour was growing ever larger despite all our therapies and best intentions. Taylor died less than two months later.”

Story 2: Malignant Glioma

Alfred was thirteen years old when he felt that his right arm and right leg were not functioning properly. Something must have gone wrong in his brain. A CT scan and MRI showed a large tumour in his brain stem – no doubt a malignant glioma.

Dr. Hamilton wrote:

There are few procedures in neurosurgery more daunting than getting a biopsy of the brain stem – because it’s so full of important neurological functions. We call it “tiger country.” There’s hardly a surgical move that doesn’t hurt the patient. Even a piece of tissue no larger than the tip of a ballpoint pen contains some vital function. There’s no such thing as a safe brain stem biopsy – just a less dangerous one.”

This was what Dr. Hamilton did:

“The patient is affixed to a precisely machined head ring … It’s attached … by four pins directly to the bone of the skull. It must be absolutely unmovable.  The patient then undergoes CT and MR imaging. A sophisticated software program allows the surgeon to pick out the target.

A tiny hole is drilled into the skull at the exact entry point picked up by the computer program. A foot-long probe is slid into postion. It passes down through the substance of the brain stem, almost to the hilt. The patient is awake so that brain stem function can be assessed.

Each time the probe moved into position, Alfred’s speech would become noticeably slurred. From the computer coordinates  … I carefully took a small piece. When I withdrew the biopsy cannula, Alfred’s speech immediately cleared, returning to normal.

Afred was a little groggy when we finally removed the head ring …. treatments in less than eight hours.”

Chemotherapy-Radiotherapy

“Alfred underwent the usual six-week course of radiation treatments. As always, this was followed by a long course of chemotherapy and steroids. His hair fell out. His weight, under the incessant appetite stimulus of steroids, ballooned up to nearly two hundred pounds. He also broke out in a raging case of acne from the steroids. Another brain tumour-induced disfiguration before my eyes.

The tumour resisted everything we threw at it. Alfred lost control of his legs.

Alfred died. He eased into death with a little morphine.”

The only substantive thing I did was to ensure that Alfred’s dog could cuddle next to him in bed. The dog was smuggled into the hospital room in a large shopping bag. When the nurse discovered it, I wrote an order in the chart: “Dog to be at patient’s bedside every nursing shift – no exception.”

Story 3: Glioblastoma multiforme (GBM)

Donald was a twenty-three year old truck driver. He suffered from pounding headache that soon became a daily event. Often the headaches came on with nausea. The sunlight on the road and reflection off the windshield bothered him. CT showed a peach-sized tumour in the back of the brain – in the occipital lobe. The tumour caused a significant amount of swelling and pressure on the brain.

Dr. Hamilton wrote:

“After six hours of surgery, the tumour was removed. He made excellent recovery and was eating breakfast the morning after. He was discharged two days later.

What followed was six weeks of nonstop radiation therapy delivered every single day. I saw Donald lose his hair. I saw the grinding fatigue set it. The circles beneath his eyes.  As soon as the radiation was finished, we launched into an aggressive regimen of chemotherapy for another six weeks. It was a marathon.

One thing I’ve learned over the years is that every tumour is different. Every tumour is nature’s experiment of one.

GBMs are almost never cured. Only five out of five thousand patients with GBM had survived five years or more. The odds of being a long-term survivor were exactly one in a thousand. But the bottom line is that GBMs are usually incurable. You never get to stop the treatments – the only way to hold this tumour at bay was to keep pounding away at it.

Donald was put back on another three rounds of chemotherapy. We also hit the centre of the tumour cavity with the intense single-fraction radiatioin of “radiosurgery.”

For the second year, Donald’s scan appeared reasonably dormant. The tumour seemed to be in remission.

In the third year, however, the tumour did return. With a vengeance. It was like a creature that had been wounded, had gotten up and was now stalking him … the tumour was growing rapidly.

I reviewed the scans. We would need to start a new line of aggressive therapy. We also decided to resect as much of the solid tumour as we could. So once again, I would have to go back into Donald’s brain and attack the tumour surgically.

Following surgery, he threw himself with total concentration into the next round of energy-depleting chemotherapy. Within three months, the tumour’s spread was clogging the flow through the ventricles … we made the decision to take Donald to the operating room and relieve the obstruction.

The operation took an hour and a half. I installed a device called a ventriculoperitoneal shunt (VP-shunt). By the end of the surgery, Donald was wide awake. He was back as bright as a brand-new penny.

Because the tumour was still growing, we turned to more experimental, far-out chemotherapies.

Over the next three months …. the shunt was keeping him out of life-threatening danger. In the spring – on April Fools’ Day – the shunt malfunctioned. It was completely blocked – tumour cells were growing inside it. Donald sank into a coma.

The day after surgery, Donald was already eating and asking to go home. The next morning Donald’s mother called me. She was sobbing. Donald had expired during the night. He was   gone. “

Story 4: Glioblastoma multiforme – A Failure

Sidney (Sy) is Dr. Hamilton’s colleague. He was one of the United State’s outstanding Alzheimer’s disease specialists.  He had a large brain tumour – the dreaded GBM.  Dr. Hamilton described this case was “one of my most public failures in my career as a neurosurgeon.” This is how the story goes.

“The tumour had grown into his speech area. For me, it was paradoxically dreadful. I could end up making things worse. The risk was I might actually destroy his speech capacity in the process of removing the tumour.

Before any big surgery case, I have a ritual. I wake up early. I turn on the shower, steaming hot. I climb in and let the water wash over me for a few minutes. I wash my hair, my body, my face and last my hands. Then I remain under the shower and visualize the whole surgery in my heads. It’s as if I’m already in the OR (operation room). I visualize my OR team there. I watch myself do the operations … the operation seems to roll like a movie behind my closed eyes as I stand there in the shower.”

The Surgery

“It took almost two hours from when we removed the tumour to when we finished reconstructing the skull and closing all the layers of muscle and skin. I wheeled Sydney back to the recovery area.

Sy could process and understand speech perfectly, but he couldn’t utter a single word. My inner state was stark and miserable. I had failed Sy. My skills had failed us both. I didn’t have a choice. I had to sacrifice the small artery along with the tumour wall … I knew that … I might be sealing Sy’s fate. I wondered if we would ever be able to say another word. If not, it would be my doing.

I suppose I could rationalize that I’m not responsible for the patient’s anatomy. But it was my hand.  My agony persisted In silence. Months later, when the tumour reappeared, none of us even mentioned surgery.  Sy lived for another eight months.”

Dr. Hamilton wrote:

“There’s no loneliness like the solitary shadow that comes into a surgeon’s heart when he or she suddenly realize an irreversible error has been committed. You can make a mistake, hurt someone profoundly and not be able to go back and undo your error. The brain simply has no genetic capacity to regrow itself. One mistake and it’s all over. It’s the grace and curse of neurosurgery. “

Two Success Stories

Dr. Hamilton wrote:

“Much of my neurosurgical practice is devoted to brain tumours. I’ve had the honour of taking care of hundreds of patients with astrocytomas, malignant brain cancers. Very few survive for more than a couple of years. As I mentioned, the odds for long-term survival can be a thousand to one. To be cured one needs to be lucky indeed – it’s a real long shot.

Thank goodness every neurosurgeon who deals with astrocytomas has at least some survivors. Without this handful of the lucky few … it would be difficult to keep going. As surgeons, of course we must often resign ourselves to our patients’ unfortunate outcomes.

I have two “home-run” astrocytoma patients.  One’s named Rusty and the other Paul. They are different from each other.”

Story 5: The Story of Rusty

“Rusty was an alcoholic, chain-smoker and a ne’er-do-well  person who attaches himself to women and convince them to live with him. He has brain tumour. Rusty would come into clinic with his latest girlfriend. Usually he reeked of booze and sometimes he was downright obnoxious. When he was drunk, he had a habit of hanging off my shoulder as if he was my best buddy. Or he’d come swaggering down the hall, yelling, “Hey, doc! How ya doin’?

How long do I have? He asked me directly. I can never give a clear answer to that question, because there isn’t one … a surgeon has to be careful not to extinguish the patient’s hope … but the fact was I’d never had a patient survive more than six weeks after an astrocytoma had spread to the opposite hemisphere.”

Rusty was about two years out from the time of his original diagnosis. He had lived with three different girlfriends during that interval.

After thirteen years, in 2003, when I saw Rusty again in clinic, his scan hadn’t changed one bit. He still drank excessively, but he settled down with his mom and became a pretty good cook for the two of them.

His tumour defied all logic. It seemed to have just gone to sleep.”

Story 6: The Story of Paul

Paul was an engineering student who had a malignant astrocytoma.  I resected it a week later. The severity of subsequent radiation and chemotherapy forced him to suspend his studies for an entire semester. The following year, he returned to his master’s degree. On the final scans at the completion of treatment, there was no visibile trace of a tumour. He got married and started working on his Ph.D.

Paul’s scan remained pristinely clean of any recurrent tumour. He’d been able to finish up a very challenging doctoral dissertation. Our whole clinic staff attended his graduation. We threw a small party for him. There were five candles on the “birthday” cake one of the nurses had baked – one for each year he’d survived from his initial diagnosis. He was my first five-year survivor.

In 2003, Paul reached almost fourteen years out from diagnosis. He and his wife had just finished building a little place in the hills. That same year, Paul had a seizure. There was a new spot. It had never been there before.  Paul had to come back and undergo a course of focused radiation, aimed at killing the tumour – now he was haunted by the notion that his tumour was stalking him, lurking among the shadows of his MRIs. Bidding its time. “

On reflection, Dr. Hamilton wrote:

“I have learned that luck, good or bad, can spell the difference between surviving and perishing. It can be the power behind a successful surgery or a frightening complication. We have to just accept it: patient and physician. I still struggle to learn from their examples. But I still experience moments – years after they have passed away – when I cry for some of them. And for myself.  So few home runs.”

Comments

As said earlier, I have great admiration for Dr. Hamilton. I admired his expertise, his humility, his deep sense of connectedness with humanity, his dedication to his noble profession and patient and his compassion towards his patients.  I say this in my heart. If your want to fight and get even with cancer – this would be the man who would help you with the battle of your life. I read again and again the words written by Dr. Hamilton above. I would like to say as loudly as I can: the world needs more surgeons like this great man.

Dr. Hamilton’s book opened my eyes to what modern, high-tech, brain surgery could do.  The techniques and scientific tools are so impressive!

But let us not be caught up with impressive tools and technology.  More importantly, we need a pair of wonder hands who could do things with compassion and love.

Then, ultimately, it is the results that count. At CA Care we too have the privilege to help patients with brain cancer. We do not have those magical tools – ours are primitive by any standard – just drink bitter, smelly herbs.  The tools may be primitive but we too have scored a few home runs!

In our website we have documented the healing of:

Daisy of Indonesia, Sunan of Thailand, CT of Medan,and a twelve-year-old girl from Penang, using only herbs. For details click the appropriate links.

In closing, and when dealing with brain cancer, let us be reminded of what Dr. Hamilton said:

“One of the greatest secrets of surgery, which no mentor can teach, is knowing when to stop a surgical procedure, to call an end to it – when to keep pushing onward and when you’ve gone too far. So often, a surgical outcome depends on where to call a halt.  When to let the patient recover from the intrusion. Because surgery is just that – an intrusion of the body.  Getting out at the right moment is half of a successful surgical outcome.”

Quotation from: The Checklist Manifesto – how to get things right by Atul Gawande

We talk about our great saves but also about our great failures, and we all have them.

The question … to answer was why we fail at what we set out to do in the world.

We have just two reasons.

The first is ignorance – we may err because science has given us only a partial understanding of the world  and how it works.

The second is ineptitude – in these instances the knowledge exists, yet we fail to apply it correctly.

Failure of ignorance we can forgive. If the knowledge of the best thing to do in a given situation does not exist,  we are happy to have people simply make their best effort.

But if the knowledge exists and is not applied correctly, it is difficult not to be infuriated… philosophers gave these failures so unmerciful a name – ineptitude. Those on the receiving end use other words, like negligence or even heartlessness.