Colon Cancer: My Chemo Experience

Jaya is a 48-year-old Indonesian. He was hospitalised from 18 October 2014 until 3 November 2014. He underwent a laproscopic anterior resection on 22 October 2014 and implantation of venous cathther (installation of chemo-port) on 1 November 2014.

Histopathology confirmed that Jaya had an adenocarcimona – well differentiated, T3N8X. It was a stage 2 colon cancer.

After the surgery, Jaya had 2 cycles of chemotherapy with FLOFOX 6 regimens (Eloxatin (oxaliplatin) + Leucovarin + 5-FU).  The first chemo was on 16 November 2014 and the second on 30 November 2014. Jaya was scheduled for 10 cycles of chemo every 2 weeks. The first chemo treatment cost IDR 45 million. Chemotherapy was done in a hospital in Jakarta.

Unfortunately after the second chemo, Jaya developed serious infection. He was rushed to Singapore and was hospitalised for 17 days for Staphylococcus aureus infection (because of chemo-port infection).  While in the hospital he remained unconcious for 3 days. The doctor had asked the family members to “get ready.” Fortunately, Jaya recovered from this ordeal. The treatment is Singapore cost him SGD31,118.

After being discharged from the hospital, Jaya and his wife flew to Penang to seek our help. Jaya did not want to continue with his chemotherapy anymore although his wife insisted that he follows the doctor’s advice.

Listen to his story.



Colon Cancer: Take Care of Your Diet if You Want to Live

Paul is a 53-year-old from Indonesia. In 2012, he had diarrhoea. An endoscopy indicated rectal cancer. Paul immediately underwent an operation at Pondok Indah Hospital in Jakarta. Histopathology report confirmed a “well differentiated adenocarcinoma of the rectum, suspected that distal margin still contain tumour cells.” The doctor said it was a Stage 2 cancer.

As a follow-up treatment, Paul underwent 30 sessions of radiation at Gatot Subroto Hospital in Jakarta.

A CT scan after the radiation treatment showed rectosigmoid thickening “perhaps caused by inflammation after radiation, residual tumour still present.”

Paul consulted a doctor in Graha Kedoya Hospital and was prescribed an oral drug, Futraful. And a biopsy in March 2013 indicated residual adenocarcinoma.

In April 2013, Paul consulted a doctor in Medistra Hospital. A PET/CT scan was done at MRCCC Hospital. The result indicated “hypermetabolic lesion at anastomosis site suspect of residual malignancy.” There was no spread to the lymph nodes and other organs.

MRI done in May 2013 at Gading Pluit Hospial indicated mucosal wall thickening in the post operative rectal tumour area. The doctor suggested colonscopy and rectal biopsy.

In June 2013, Paul went to Singapore for further consultation. He underwent an immediate surgery at Mt. Alvernia Hospital on 18 June 2013. A diverting ileostomy was created. The histopathology report confirmed a recurrent adenocarcinoma at the rectal stump.

Paul returned to Jakarta and was started on chemotherapy with Oxaliplatin + oral Xeloda. He received a total of 8 cycles of chemo at 3-weekly interval at Medistra Hospital. All treatments were completed in February 2014.

In March 2014, Paul started to use the electrical capacitive cancer treatment apparel (terapi rompi).

In April 2014, Paul was again on Xeloda.

PET / CT scan done at MRCCC Hospital in Jakarta indicated “suspected regional recurrence.” Paul went back to Singapore to consult his previous surgeon at Mt. Alvernia, He was asked to undergo 3 cycles of chemotherapy using Forfiri + Ebitux. The doctor said if the chemo could shrink the tumour, then Paul need not have to undergo any operation. If the treatment did not shrink the tumour the Paul ad to undergo another surgery again.

Paul refused further medical treatment. He returned to Jakarta and consulted a doctor who practised traditional medicine. He was started on herbs and followed a healthy food regimen. Paul also had liver detoxification.

In July 2014, Paul went back to Singapore again and this time consulted with a doctor in NUH. He was given the same advice as the doctor at Mt. Alvernia.

In August 2014, Paul came to seek out help and was started on herbs. He felt better after taking our herbs. His liver function results showed improvements.

4 Aug 2014 27 Oct 2014 15 Jan 2015 26 Jan 2015
ESR 30 45 30
Alk. phosphatase 165 139 98
AST 109 74 50
ALT 149 79 58
GGT 184 150 128
CEA 3.9 2.3 n/a 8.62
CA 19.9 17.6 25.3 n/a
CA 125 3.6 2.8 n/a

In late January 2015, we got this email from Paul.

Dear Dr. Chris,

Today I am very surprise that I got CEA test with 8,62. This is the highest value I have, and even higher than when the first time I got (2,35 before operation in 2012).

I still discipline to eat all capsules and herbal tea until now. I also still have vegetarian diet.

Just for your information, during end of last year I have vacation to Kuala Lumpur and I ate Chinese food but without meat. And last week, 24 Jan, I also ate Yamien noodle. Is that all the reason?

Dr. Chris, please help advise me what to do. From now I will strictly do my vegetarian diet. Do you think that my CEA may down again? Do I need more dosage capsule or herbal tea? Dr Chris, please advice, and thank for your help.

Reply: This man is from Jambi and you are from Jakarta …same problem la… this story carefully. 

8 cm Liver Tumour Shrunk After 8 Months On Herbs. Still Alive and Well After 2 Years 

Again let me repeat what I told this patient that night was very clear, crude and blunt. When patients are “half dead,” they would follow our advice without protest. But when they get well, most of them will “misbehave.” That is normal.  This advice also applies to  all cancer patients.

  • To live or to die is your choice.
  • There is no need to be upset about the patient’s choice. If he wants to die, let him die.
  • My experiences have shown that if a patient eats anything he/she likes, this “good time” would probably last about 2 months. After that the cancer would recur and he/she cannot “enjoy” food anymore.
  • I also told AS, Perhaps it is time you stop taking the herbs. Go home and eat a lot of what you want to eat and “go” faster.
  • AS had lived for almost 2 years. He should be grateful that he is still alive – healthy and without pain. What more do you want? Be grateful for what you are now!

Dear Dr. Chris,
I still want to live, and my choice is back to your way of life. Hopefully it is not too late, and I believe I can do my diet strictly. Thanks for your advice.

Reflect on the following seriously.

9 Disease-enter-through-the-m 10  Nutriton-stop-growth-spread 8-Diet-must-be-integral-par






Surgery & Chemotherapy for Colon Cancer Failed. Go home, no more medicine

KL is a 60-year old female. She felt tired and was told that she was anemic. However, a colonoscopy done on 25 March 2014 indicated tumours in her ascending colon.


KL immediately underwent an operation. The operation cost RM 20,000. Unfortunately on the third day after the operation, KL suffered severe bleeding. The doctor told the family it was a Stage 4 cancer since it had spread to the liver.

About a month after the surgery, KL was started on chemotherapy. Each cycle of chemo cost about RM4,000. After receiving a total of 6 cycles (oxaliplatin + oral Xeloda) the oncologist stopped the treatment because it was not effective.

The oncologist offered KL two options:

  1. Continue with more chemotherapy but using a combination of more expensive drugs – Avastin + Erbitux. This cost more than RM10,000 per cycle.
  2. Go home. There is no more medicine!

Details Of KL’s Medical Records.

CT scan of 27 August 2014: Known case of CA ascending colon, post operation and post chemotherapy.


  1. CA ascending colon with multiple lever metastases. The metastatic lesion in the left lobe of the liver is larger in size associated with progressive dilatation of the left intrahepatic bile duct.
  2. A small stable nodule in the lower lobe of right lung.

Blood Test Results

Date CEA Alk. phosphotase ALT GGT AST
27 Aug 2014 980.2 194 49 437 71
31 Oct 2014 1,914.0 141 21 214 39


KL and her family came to seek our help. She presented with loss of appetite and swelling of the abdomen and both legs. She lacked strength to walk or to stand up. The video below showed her condition that day.



This is what KL’s husband said: “What the doctor said caused us to panic. We followed what the doctor wanted us to do. Money spent but she (the patient) became weak.”

This is a tragic case. Many questions need to be asked:

  1. Why was KL only told that the cancer had spread to her liver after her colon operation? Why not before the operation?
  2. Would it not be prudent or even the norm of medical practice, to check if the cancer has spread to other parts of the body before any surgery is done?
  3. If the cancer has spread extensively, it is sensible to go ahead with the surgery? Chemo?
  4. Why was there severe bleeding 3 days after the surgery?
  5. After 6 cycles of chemo, KL was told that the treatment did not work. With all the experiences (giving chemo to patients over the years), does the oncologist not realize that chemo rarely (if at all) works for patients?

Reflect on the quotations below:

3 Chemo attempt to kill cancer before killing patient JohnLee

8 Chemo-no-benefit-response-n

2 Body-as-human-machine-2



Colon Cancer: Oncologists said,” Try chemo.” But one doctor said, “If he is my relative, I won’t put him through the torture.”

TS (E211) is a 58-yer-old gentleman. On 28 January 2013 he went to see a doctor for abdominal pain, distention and bleeding.  His CEA was normal, at 2.5 but his liver enzymes were elevated: AST = 45, ALT = 29 (normal), Alkaline phosphatase = 137 and GGT = 79. His white blood cell count was at 12.9 (high).

A CT scan indicated an irregular mass at the rectosigmoid region measuring about 6.1 cm in length. It caused narrowing of its lumen. “Features are suggestive with carcinoma rectum with local infiltration and liver metastases.”

Rectum tumour biopsy confirmed infiltrating moderately differentiated adenocarcinoma.

TS underwent surgery on 31 January 2013. Due to the cancer infiltrating the small bowel with perforation and intra-loop abscess, TS was fitted with an temporary ileostomy bag.

TS was referred to an oncologist and was prescribed oral drug, Xeloda plus Leucovorin. TS completed two cycles of these without problem. However, after the third cycle, he started to feel the side effects. He had rashes and dry itchy skin. He became tired, had muscle pains and problems with the taste buds.

By the fourth cycle (i.e., in early July 2013) the muscle pains became worse and he was not able to walk. The doctor advised to take a longer break before going for the next cycle. TS decide to stop the drugs.

On 1 August 2013, TS had shortness of breath during the early morning and was rushed to the hospital. He was said to have a heart attack. He responded well to the emergency treatment in the ICU.

On 2 August 2013, a chest X-ray indicated left lung pneumonia and TS was treated with antibiotics. CT scan of the thorax suggested lung metastases.

From 4 to 7 August 2013, TS’s condition worsened day by day. He was short of breath and needed oxygen all day. His mental alertness was sharply reduced, drifting in and out of sleep most of the time. He had no appetite and felt weak and drowsy. Three doctors attended to him. Two doctors suggested TS undergo chemotherapy but another specialist whispered to TS’s wife, “If he is my relative, I won’t put him through the torture.”  Since the family had bad experience with the Xeloda, they decided to give up chemotherapy.

On 8 to 9 August 2013, TS was still on antibiotics and these were the most critical 2 days. His breathing became very difficult and he was not able to eat. His condition deteriorated drastically and the family were expecting the worse. The pastor came to give the last rites. According to the wife, “He was almost gone”.

From 10  to 12 August 2013, by the grace of God, TS’s condition improved and he was discharged from the hospital since there was not the doctor could do after declining chemotherapy. TS was brought home in an ambulance to “rest” .

At home, TS was under the care of Hospice. The Hospice doctor was told that the family wanted to try herbal therapy. The doctor was understanding enough and said, “It is your choice. You can try but I don’t think it will work.”

20 September 2013. TS his wife and daughter came to CA Care, Penang.

Listen and watch the videos below carefully.




On 29 April 2014, TS wrote:
1. My skin peeled off months ago and new skin have grown at least 6 months ago.
2. I am now experiencing pain when I stand up. When walking my legs feel heavy.
3. I feel numb from stomach area downwards.
4. The Hospice doctor told me my nerves are damaged as a side effect from previous oral chemo Xeloda.

I will plan to visit you asap. God bless.

On 1 May 2014, TS wrote again:

I am now into the 8th month of taking your herbs and capsules. Eat ok, sleep ok, bowel movement now 2-3 times a day. When I came back from the hospital last August my weight was 45kg. Now it is almost 49kg. So there is improvement except for the numbness and pain in my soles when I walk.

Before  undergoing any treatment, patients should always ask yourself or your doctors!

1. What are the side effects of the Xeloda?

The most common side effects are:




sores in the mouth and throat (stomatitis),

stomach area pain (abdominal pain),

upset stomach,


loss of appetite,

and too much water loss from the body (dehydration).

Other common side effects are:

hand-and-foot syndrome (palms of the hands or soles of the feet tingle, become numb, painful, swollen or red);


dry, itchy or discolored skin;

nail problems;

hair loss;






pain (including chest, back, joint and muscle pain);

trouble sleeping;

and taste problems.

Patients could have more side effects related to their heart. The cardiotoxicity observed with Xeloda includes:

myocardial infarction/ischemia,



cardiac arrest,

cardiac failure,

sudden death,

electrocardiographic changes,

and cardiomyopathy.

With the above list of side effects, nobody can tell you what you may end up with if you swallow Xeloda. It’s a matter of your luck – you strike gold or misfortune. So that much about the so-called scientifically proven medicine.

Ask these questions.

1. In August, TS had a “heart attack” after completing 3 cycles of Xeloda a month before that. What triggered that “heart attack”? Cardiotoxicity mentioned above? Was TS warned about this before taking the drug? Or does everyone assume Xeloda is perfectly safe since the doctors prescribe it? This heart episode almost killed TS.

2. When you are told you have cancer, we understand that you are desperate. You don’t know what else to do. You need help – but don’t you think it is wise not to add oil immediately to the burning fire? Don’t you want to hold on for a while so that you can read a bit more rather than blindly follow advice – to be seen to do something immediately?

3. One amusing account is what the “open-minded, understanding” Hospice doctor said. He did not object to herbal therapy, but he weight in and said, “It is your choice. I don’t think it will work, but you can try.” A fair statement. From the view of medical science, herbs are just hocus pocus, unproven snake oil, bla, bla.

But looking at it realistically, for this case and many other cases documented in this website, did TS ever get worse by taking the herbs and NOT doing chemo? If herbs can do what the chemo cannot do, why go for chemo then?

Watch the videos again.

Can you learn something from this case? Or are you still wanting to stick to your biased view that herbs are not effective and unproven? Do you want to still say, “I don’t think it will work”?

Colon-Liver-Lung Cancer: Hunting For The Magic Bullet

A lady school teacher came to see us in early 2012. Her husband is a medical doctor (later, I got to know that her daughter is also a medical doctor).  She did not come with any medical report – she just wanted to tell me her story and based on that prescribe her herbs.

She had colon cancer that had spread to her liver.  She had completed her chemo and had also undergone a RFA treatment (radiofrequency ablation). In spite of that, her CEA was rising.

The first question I asked her, “What do you want me to do? What do you expect to get when you come and see me?”  Her answer, “I want to find a cure.” To that I told her, “No, I am sorry I don’t have anything to cure anybody. My herbs are not magic.”

Then I asked her to read my two books, Cancer – Why They Live and What You Need to Know About Chemos … She would not even look at the books! But she insisted on wanting to try my herbs. My answer was, “No.  For now, I would not prescribe you any herbs. Go home and pray to your god (s) after you have gone through my websites – and

Were we being cruel to send her home without giving her the herbs? Sometimes we need to be “apparently” cruel to be kind and honest. While we fully understand that patients who come to us are helpless, desperate and lost – it is extremely unfair and wrong for us to make them believe that we can offer them a cure for their cancers. Our experience over the past 18 years dealing with cancer patients tells us this fact clearly – No one on earth can cure cancer! You just have to learn to live with your cancer and heal yourself. Saying that the treatment gives you a response does not mean a cure. To achieve a tumour shrinkage after treatment is equally meaningless. Shrinkage generally does not translate into a cure. And saying that if you remain alive for 5 years means your cancer is cured is scientifically baseless.

These are the “truths” that you may have missed out or you have not been told.  Read the medical literature, no one ever talks about cure for cancer. If they do, they generally mean being alive for 5 years. That is not cure! It is only a remission.  We have seen cancer recurring even long after that. My aunty had a recurrence after 13 years. Her cancer spread to her lungs and she died.

So when we sent this lady teacher home to “learn” more we were just being truthful – we cannot cure any cancer. Unfortunately she did not want to learn. She portrayed as a well-informed patient who knew all the medical terms — “after all I am the wife /also mother, of medical doctors.”

Patients who come to us with this kind of “shopping-for-magic-bullet” mentality, are sure to be very disappointed with us. We would send them home without any herbs and ask them to think over.

We understand most patients who come to us are generally medically given up – they have gone though all possible medical treatments and failed. They have nowhere else to turn to for help. I used to jokingly tell patients, “Yes, we are the last one stop.” Given that situation what do patients expect us to do? Cure their cancers? And we, at CA Care, promising them a cure?  Don’t be misled – we cannot cure your cancer. We also do not cure your medical results. At CA Care we want to heal you as a person. Healing is different from cure. Healing happens at all levels – physical, mental and spiritual.

Fast forward, April 2014 – about 2 years later. This same lady teacher came to see us again. I could not recongise her. She was dark (due to too much chemo?). I asked for her medical reports. Again – like before – she did not bring any. And she started to rattle her story below.

P: I was diagnosed with colon cancer in September 2010. I had an operation followed by 8 cycles of chemotherapy. I was okay for about 6 months. After that the tumour marker (CEA) started to go up. The cancer had gone to the liver. I did one time RFA (radiofrequency ablation). After one month, it seemed to be okay but my CEA did not go down. It was still climbing.

I did a PET scan and the result showed 2 tiny lymph nodes (collar bone) was infected, but the liver was okay.

I was started on chemo again – another 8 cycles. The CEA went down. It seemed to be okay. While on chemo, I was also given Avastin. After the chemo was completed, I was still on Avastin as maintenance.

A bit less than 6 months later, I did a PET scan. The doctor said everything was okay. But after the PET scan, the CEA started to go up again.

About a month later, I did a CT scan. There were tiny nodules in my lungs.

The oncologist started me on chemo again. This was the third round and I had 12 cycles. I was also given Erbitux.

After 12 cycles of chemo my CEA went down to 1.7 (normal 5). I continued to receive Erbitux as maintenance.

A scan later showed the nodules in the lung were still there but there were no other additional metastasis.

In October 2013, my CEA started to go up again. It was like 1.9.

My oncologist sent me to see a surgeon, to see if the infected lymph nodes could be removed. But the surgeon asked me to do a PET scan first before considering surgery. I did a PET scan.  The result showed everything was clear except for one nodule in my right lung. This could be an early metastasis. The surgeon was unable to proceed with the surgery because the nodule was too small. So nothing was done.

Today my CEA started to go up again. And all this while I was still on Erbitux.

Just before the Chinese New Year (January 2014) the oncologist started me on 5-FU (chemo again). My CEA was going up and Erbitux was not effective anymore. That was why the doctor added the 5-FU. I received this every week.

Even with the added 5-FU my CEA had gone up to 5 (from 1.7 before October 2013).

I have been going  for the chemo but for a few times now, I started to feel restless 5 or 10 minutes after receiving the drug. I felt restless and did not know where to put my legs, where to put my hands. I could not concentrate. When I talk to you, my eyes cannot focus on you. I am just restless and don’t know what to do. I don’t know whether this is the effects of the drug or it is psychological effect.

Two weeks ago, when they put the drug in, I felt very difficult. They called the doctor in. The doctor wanted to give me steroid (prednisone). But the week before I have asked the oncologist to take off the prednisone because it made me very drowsy. So when they wanted to give this again, I said no!

Last week I went to see my oncologist again. He stopped the Erbitux and said I was already too long on this. So he just gave me only 5-Fu. But I still felt restless even with only 5-FU.

In total I am on chemotherapy  for three and half years. (Note: 3 rounds of chemo with a total of 28 cycles besides the weekly 5-FU, maintenance Avastin and Erbitux).

Chris: To be honest, I am surprised that you are still alive today. I really don’t know what I can do to help you. What do you expect me to do in this situation? Because I don’t believe that by taking the herbs your CEA is going to come down, honestly. Now it is just at 5.

Patient: But I am scared that it will  go up.

C: Why do you worry wanting to get the CEA down – CEA is not going to kill you.

P: But every time the CEA went up, I went for a scan and they found something in there.

C: That is normal. We all know that. Nobody can cure any cancer. That’s my experience. What is more, even when you get cancer, they tell you to eat anything you like.

P: But I did “pantang” (abstain from certain food).

C: But the way you “pantang” is not the way we teach you to “pantang” at CA Care. It is useless if you don’t do it right. Follow what I tell you fully or don’t. No half measure.  Again let me tell you. If you come and see me hoping that your CEA can come down, no, I don’t think that is the correct logic. Honestly, I don’t think it will come down. For three and a half years the doctors could not get it down, and you expect me to do it!

P: It will not come down but I hope it will not go up.

C: I don’t know. You need to know that cancer cells are not the same, they are different. After round and round of chemo, some cancer cells are killed, but some can still remain alive or are not affected by the chemo drugs. Because of that some patients suffer from “more aggressive” cancer after chemo. Researchers have shown that chemo makes cancer more aggressive. That is why chemo does not work.

This is the attitude of patients. When all else have failed they come to us and expect me to do magic. How could I do it? My answer to you is, I am not going to be able to do it – as simple as that.

Other people may say, “Yes take this and take that, your CEA will go down, etc., and etc.” But I am not sure if this is going to be true or not. Why don’t you come back to see us only after you have decided you don’t want to do anymore chemo?

P: I thought of stopping the chemo.

C: It is not a matter of thinking you want to stop chemo. You have to decide – do you still want to continue with your chemo. If you want to continue, go ahead with the medical treatment. You have to be clear about this. I suggest that you go home and continue with your chemo.

Come and see me only after you have decided to give up chemo totally. When you reach that point, and you don’t want to do chemo anymore, and you have nowhere to go, then come and see me. Then we will try the herbs.

For now, don’t take the herbs yet. Go back and when you tell yourself. “I don’t want any more chemo and I have nowhere else to go,” then come and see Chris Teo. Then I’ll give you the herbs.

P: Now, I want to take a break from chemo and I want to take the herbs.

C: Take the herbs for how long?

P: Your wife suggested to try the herbs for one month.

C: You can take the herbs for one month, but I am going to tell you it is not going to give you any significant effects. No way. You have been on medical treatment for three and a half years and it never worked and you can’t expect to take the herbs for a month and it is going to work!

P: Not to go down but to see if it can control it or what.

C: Let me tell you again. When doctors have failed to help you for three and a half years, how can you expect my herbs to help you in a month. No way.

P: But Dr. Teo, I have a friend in Kuala Lumpur. He has lung cancer. The doctor said he only has 3 months to live. He did not go for medical treatment and he took your herbs instead. He is still alive today. It has been one year already.

C: Of course, patients who have not gone for chemo do better with our herbs!

I am obliged to prescribe this patient some herbs. She came back to collect the herbs the next day. She asked my wife:

a) What are the side effects of the herbs?

b) What are these herbs?

c) Some herbs could be dangerous and affect the kidney, etc.

My wife replied: No one has died because of our herbs. And many have been taking these for years. If you are afraid of the side effects or think they are dangerous, please don’t take them!

Comments: For those who have cancer and who know how to read, I strongly suggest that you read my recent book, Cancer – What Now?

Cover Front JPGIn this book I have discussed many topics that are important to you and your survival. Going for whatever treatment for your cancer is about you and your choice. Your life is in your hands.  When you get cancer, it is also about you. YOU, the person. It is not just about the tumour or the rising CEA, etc., etc.

I have written many articles trying to let you all know that shrinkage of tumour and decreasing of CEA are often meaningless. It makes you feel good for a few months and the cancer comes back again. Is this not what happened to the lady teacher above? PET scan said okay, all clear but soon something pop up again somewhere! More chemo again. When do you stop chemo?

In Chapter 3 of the book I talked about the types of patients who come to see us and their attitudes – wanting to find a magic cure when there is NONE. Of course, you can go for chemo, surgery, take this supplements and that supplements – beware of the empty promise! In Chapter 6, I wrote about the virtue of doing nothing!

I am aware that my way of dealing with cancer is rather non-conventional and against the commonly accepted norms. If you are following my writing in the websites, you will know that what we do in CA Care do help many patients. It is just whether you want to believe or not!

Look out for another story after this one. This is about a man with colon cancer who was at the point of death in the hospital and was asked to do chemo! His wife preferred to do nothing and brought him home in an ambulance! Like the Chinese say, if you have to die, die at home! This man remained alive at the point of time when I am writing this article.


by Yeong Sek Yee & KHadijah Shaari

All of us know who Ronald Reagan was but some may not know that he had colon cancer during his presidency. Yet very few would have known that he healed his colon cancer with German alternative therapies (after surgery in the US). Below is a brief story of how Reagan treated his cancer.

A 1984 proctoscopic examination disclosed a small polyp in Reagan’s colon. Biopsy showed it was benign. In March 1985, another polyp was found, as were trace amounts of blood in his stool. A change in Reagan’s diet eliminated the blood. He underwent endoscopic removal of the polyp and colonoscopy on July 12, 1985, at Bethesda Naval Medical Center. The colonoscopy disclosed a second, more dangerous tumor — a villous adenoma — that could only be removed by surgery.

The right-sided portion of Reagan’s colon was removed — about 2 feet of length. Exploration of other abdominal structures found no spread of the cancer. The tumor was ultimately classified as a “Duke’s B,” meaning it had invaded the muscle of the colon, but was confined to the bowel wall. After his surgery, Reagan’s doctors warned him that cancer cells might spread to his liver and other organs.

His wife, Nancy, persuaded him to undergo laetrile treatments. Learning of a reputable alternative provider who worked with laetrile through his close friend, future Oregon Senator Mark O. Hatfield, Reagan received daily IV laetrile treatments in the Oval Office over the next thirteen months.

Later, Ronald Reagan secretly went to Germany and consulted Germany’s leading cancer doctor—Hans Nieper, MD. It would have been front page news if it had not been hushed up at that time. (It is not the scope of this article to discuss how Dr Hans Nieper treated Reagan although it is believed to be Carnivora, an extract of the Venus Fly Trap plant).

The intention of this article then is to let you know that President Reagan, while still in office and with all the best of medical science in the US at his disposal, actually turned his back on America’s cancer treatments—the so called evidenced-based scientifically tested cancer treatments—and lived another 19 years (after surgery) until he died of Alzheimer’s at age 93 in 2004.

We just cannot imagine the enormous amount of cover-ups by the mainstream media and by the various American cancer establishments such as the FDA, AMA, ACS, and the National Cancer Institute. These are the very establishments that have labeled laetrile and other healing modalities as “quackeries.” To them, only surgery, chemotherapy, radiotherapy is evidenced-based and scientifically tested…all others are unproven and unsafe.

Why then did Ronald Reagan choose such an untrodden path? Perhaps the sufferings of the late Senator Hubert Humphrey (the 38th VP of US) were still fresh in his mind. In January 1978, Humphrey died a painful death after a year of chemotherapy treatments for his bladder cancer—he described chemotherapy as “bottled death” just after he started treatments.

However, TONY SNOW, the former Press Secretary to President George Bush may have been too young (born in 1955) to hear about the sufferings of the late Senator Humphrey. Additionally, he would not have heard about how Ronald Reagan healed his colon cancer (because it was all hushed up).

Snow was diagnosed with colon cancer in 2005. He had his colon (the affected part) removed and underwent six months of chemotherapy—the usual “standard of care.” Snow’s colon cancer recurred in March 2007, in the same spot in the abdomen where it had first been found. He had the malignant growth removed from his abdominal area followed by more chemotherapy. The cancer had by then also spread to his liver and elsewhere in his body.

At that time, Snow’s surgeon and oncologist were very upbeat about his condition.

“This is a very treatable condition,” said Dr. Allyson Ocean, a gastrointestinal oncologist at Weill Cornell Medical College. “Many patients, because of the therapies we have, are able to work and live full lives with quality while they’re being treated. Anyone who looks at this as a death sentence is wrong.”

However, Tony Snow died in July 2008 at age 53—just 3 years after surgery and chemotherapy. Would he have opted for the same treatment (or other alternative treatments) after surgery just like Ronald Reagan had he known about Reagan’s secret trip to Germany? We will never know.

So, which path would you choose if you are at the T-junction after being diagnosed with colon cancer? Will it be the so called scientifically tested, evidenced-based medicine path which Tony Snow took or the “unproven” journey which Ronald Reagan took despite all advices and persuasion to the contrary?


There were a lot of criticisms of Reagan regarding the secrecy surrounding his treatment which helped no one but himself. President Reagan was a potential change agent, and he could have advanced healthcare in the US. He was in a position to effect change, to change the course of the “war on cancer” by telling the truth and inspiring others. Anyone in that position has the responsibility to step up and lead others onto the right path. Reagan failed the American people: he failed to lead the Americans down the right path.

But frankly, knowing American style democracy, Reagan was probably under enormous political and medical pressure to keep his mouth shut. Undoubtedly, his hands and legs were tied and the whole world continues to suffer.


1)      Archive for President Ronald Reagan —The Cancer Cash Cycle: Cut, Poison, Burn.


2)      The Illegal Cure Ronald Reagan used for his Cancer


3)      Cancer is curable in Germany but not in America – just ask former President Ronald Reagan


4)      Health and Medical History of President Ronald Reagan


5)      Biography of Dr Hans Alfred Nieper


6)      German Cancer Therapies by Dr Morton Walker

7)      Healing Cancer Inside Out by Mike Anderson

8)      The Cancer Odyssey by Margaret Brennan Bermel

9)      German Cancer Breakthrough by Andrew Scholberg

10)   Tony Snow Dies Following Chemotherapy for Colon Cancer (opinion)


Dissecting Chemotherapy 15: Couldn’t Afford Avastin, Gave Up Xeloda

Leo is a 51-year-old man. He was diagnosed with cancer of the rectum. But his cancer had spread to his liver. He underwent 6 cycles of chemotherapy and 25 sessions of radiotherapy. After the treatment he had a surgery to remove the tumour in his rectum. CT scan showed he was not cured, the tumour in his liver was still there. Leo was asked to undergo more chemotherapy.  He declined. He was prescribed Xeloda instead.  He took Xeloda for 3 cycles and gave it up. He turned to herbs.

Listen to what he said:


Why he declined the second round of chemotherapy – FOLFOX  + Avastin

Leo was asked to undergo chemotherapy using FOLFOX plus Avastin. The treatment is going to cost him RM 5,200 per cycle and he was to receive a total of 9 to 12 cycles. In total, that means spending around RM 50,000 to RM 60,000 for another round of chemo. To some patients, the response to such proposition is plain and simple. They cannot afford it! Period.

I remember Pak Jam who got his wife into a private hospital and had to spend RM 2,000 per day. After 15 days he was reduced to be a bankrupt!  He came to see us appearing like a “mad man.” His wife had leukemia. Perhaps today he still has to keep working to repay the borrowings from friends and relatives.

CPW was diagnosed with GIST and was asked to take Glivec for her condition. One tablet per day would cost RM 293.00. That is to say the family will have to fork out RM 8,790 per month for the medication. How long does she need to go on this medication? No one can tell.

HS from Indonesia came to see me. He was diagnosed with advanced kidney cancer that had spread extensively to his lungs. Since nothing much could be done, he was asked to take Sutent (sunitineb). According to his  wife, a month of Sutent would cost him 100 million rupiahs. I asked the wife, How much does an ordinary man get paid per month doing a normal job. She replied, Average earning per month in her home town (in Indonesia) is one and a half million rupiahs.

I have a lot more to say about the cost of chemo drugs nowadays. But suffice to say that the price of certain chemo drugs have gone crazy!

Why he stopped taking Xeloda after three cycles

Leo was not convinced that Xeloda would do him any good. He had fevers and diarrhea. In addition he vomit and had pains around the colostomy stoma after taking Xeloda.


I wonder what Leo would do if he has the money to pay for his FOLFOX + Avastin treatment – would he go ahead with it?

There are three important issues which patients need to bear in mind when deciding whether to undergo treatment or not.

One, don’t ever believe that money can buy your cure! Leo told us of what he saw. A man had spent more than a million ringgit trying to find a cure for his cancer. He went to Singapore for his treatment but found none. He ended up in a Johor government hospital – bed ridden and debt-ridden. He told his son that he had had enough and told his son not to go around and borrow any more money trying to cure him. One night, this frustrated man jumped out of the window of the 6th floor.  This is not the first time I hear such a story. Some time back, I received a similar e-mail from a lady in Singapore telling me that her father just jumped off the flat after failing to cure his cancer.

Two, ask these question: What is the aim of the treatment? Can this treatment cure me? Or is it just to prolong my life for a while more – if so, is it worth it? You should get these answers straight from your doctor. After getting your doctor’s answers, check them out with other experts as well.

Three, ask your doctor about the side effects of the treatment that he is going to give you. List them down. There is no argument about his – all poisonous drugs have side effects! And you know that chemo-drugs are poisonous. . So ask yourself, are you game with that? Some patients can tolerate the side effects but some patients prefer to die than go through it. Only you can decide. But at the same time, educate yourself about the side effects of these drugs.

Unfortunately some doctors are not forthcoming with such information. They would say, Oh, it is nothing. It is just like ant-bite! I remember one funny episode. A patient from India came to our center for help. She underwent chemotherapy and suffered side effects. She went to her oncologist complaining about a certain problem and was told, That is expected because of your chemo. When another problem cropped up, she was again told, That is expect because you had chemotherapy. This woman was clueless about the possible side effects of chemotherapy. Unfortunately for such patients they have to learn the hard way.

Let me end with one final question. What do you think are the benefits of Avastin?

Do you expect Avastin to cure you – after spending a good sum of your life’s saving? Read what the medical literature has got to say. Be ready for a rude shock!  Are you told of this – or do you ever ask your doctor?

The Phase III study involved 820 patients with metastatic, inoperable colorectal cancer who had been treated with standard first-line chemotherapy and Avastin. The results showed that:

In advanced colorectal cancer, continuing bevacizumab (Avastin) without interruption after tumor progression improves survival modestly.

In another report, it says – patients who received chemotherapy and Avastin did better than patients who received chemotherapy alone.

  • The patients receiving Avastin were likely to have longer tumor control and live longer than patients who did not receive Avastin. On average, they lived about five months longer (Note: this is probably a mistake found in this posting. It is not five months! Five weeks is probably the right number!).

In this article, Avastin prolongs life but drug is too expensive for NHS patients, says Nice,

  • Avastin (bevacizumab) can help patients with advanced bowel cancer which has spread to other organs, usually the liver and lungs.
  • The National Institute for Health and Clinical Excellence (Nice) said it had considered the drug …, but still considered the price too high for the extra benefit it gives patients.
  • Avastin costs almost £21,000 per patient (Note: This is equivalent to RM 102,302.73).
  • Clinical data submitted by Roche to the watchdog shows it can typically offer patients an extra six weeks of life when added to the chemotherapy drugs  capecitabine and oxaliplatin.

The expected benefit (or you call that benefit at all?) is surely miserable compared to the cost that an ordinary patient in Malaysia or Indonesia has got to pay. But that is not all. What about the side effects of Avastin? Click this link,

The most serious side effects (not common, but sometimes fatal) are: gastrointestinal perforation, i.e. developing a HOLE in your stomach or intestine; wound would not heal, serious bleeding including vomiting or coughing up blood; bleeding in the stomach, brain, or spinal cord; and vaginal bleeding, stroke or heart problems, severe high blood pressure, nervous system and vision problems such as high blood pressure, headache, seizure, sluggishness, confusion, and blindness; kidney problems, etc.

The most common side effects are: nosebleeds, headache, high blood pressure, inflammation of the nose and skin, too much protein in the urine, taste change, dry skin, rectal bleeding and back pain.

Worse of all, researchers have  found that tumors treated with Avastin (also Sutent) developed more cancer stem cells, which fuel a cancer’s growth and spread and are often resistant to standard treatment.

Ultimate, you need to make your own decision. Decide wisely!

Colon Cancer Stage 2: Operation but no chemotherapy or medication.

Eight years on and still doing fine

HM (T-337) was 72 years old when she was diagnosed with colon cancer. A colonoscopy done on 21 December 2005 indicated that the lumen of the distal sigmoid colon (30 cm from  the anal verge) was obstructed by circumferential tumour.

HM underwent an operation the next day. The pathology report indicated a well differentiated adenocarcinoma, Duke’s B, T4NoMx.

Perhaps due to her age, no further medical treatments were indicated. HM’s son came to seek our help on 8 January 2006. She was prescribed Capsule A, C-Tea, GI 1 and GI 2 teas.

Initially HM went back to her doctor for routine check up. Nothing was amiss. Her CA 19.9 was at 55.1 on 22 August 2006 and on 24 January 2007 it was down to 45.3. After this no more blood test was done. Also HM did not go back to see her doctor anymore.

The son was very consistent in taking care of his mother. It was not until 28 October 2011 – almost six years later, that I got to talk with his son (video below).

Son: She is my mother. She does not know that she had cancer. I did not tell her about it. That’s the reason why I did not bring her to see you.

She had cancer in December 2005, and she did not undergo chemotherapy?  

Son: No, the doctor said no need to go for chemo. 

Was she alright after the surgery? Can move her bowels? 

Son: No problem at all. 

Then you came to see us on 8 January 2006 – that means more than five years ago – almost six years now. During these five years plus, did she ever encounter any problem at all? 

Son: No, her health was very good. Now she is asking me if she can stop taking the herbs. 

Ha, ha, most people are like that. Hang on, let me ask you some more questions. She did not encounter any problem at all since after the operation? 

Son: No, never had any problem.

Did you return to your doctor for checkup? 

Son: Yes, initially during the first three years. After that we never go and see the doctor anymore. 

What did the doctor say? 

Son: Nothing much, but he started to give her “vitamin” injections. No, we don’t want to go and see him anymore – spending a few hundred of ringgit each time. My mother also did not  want to go and see the doctor anymore. 

Okay, most patients behave like your mother. After taking the herbs for some years, they want to stop taking the herbs. And how old is your mother now? Son: 79 years old.

And she is strong and healthy? 

Son: Yes. In fact I am planning to bring her to Indonesia for a holiday. 

Let me tell you this. We don’t know when the cancer is going to strike back again. There is this lady. She is as old as your mother. And she also had colon cancer and had been taking the herbs for more than three years already. One day she came in and asked to stop taking her herbs. Her cancer came back a few months later and she had to be hospitalized again.  Now she is recovering and taking back the herbs. The situation was made worse because she started to take all the “bad foods” as well, besides stopping the herbs.  I did warn her and her family about this but at the same time said that it is up to her to decide if she wanted to stop or continue with the herbs. So, know that the risk of recurrence is there.  

Son: My mother actually likes to take the herbal teas. It is the capsule A that she does not want to take. 

Capsule A is our “master” herb. What is so difficult about swallowing the capsule?

Son: That is the problem. She did not want to swallow it. But she likes the herbal teas. 

Most patients came to us complaining about the herbal tea – they want us to give them only capsules. They don’t like the teas – too much trouble. Your mother is the other way round.

Okay, over these five years, did she ever complain about the herbal tea – bad taste, bad smell? 

Son: No, the herbal tea makes her move her bowels better. Actually she has not stopped the herbs yet. I shall ask her to go on.

Conversation with her son again on 19 July 2013

Colon Cancer Part 3: Our Privilege to Help This Determined African Lady Who Has So Much Common Sense

You wrote to me sometime in December 2011 asking for help but I hesitated and virtually did not want to take on your case. Why were you persistent in wanting to take our herbs?  Other patients would just have given up and go elsewhere. After all internet / website information are not reliable.

My mind just felt very positive towards trying the herbs. Nobody recommended me, God pointed me in the direction I needed to go.

You have been taking all these supplements before the herbs. These were: a lot of vitamin – B, D, E and K, (mostly chelated), licorice root, milk thistle, wheat grass, raw vegetable protein powder, Poly MVA, Selenium, Chelated iron tablets, broccoli sprouts, colostrums, beta glucans, Co Q10, barley juice, chorella and digestive enzymes. This is besides taking Ibuprofen (for pain) and Xeloda (Oral chemo). Are you still on them now?

I stopped taking some of them. Initially, when I started taking the herbs, I stopped all supplements because I wanted to feel the effects of the herbs. I wanted to know exactly what the herbs will make me feel. I started some of the vitamins after a month on the herbs so that I will be able to identify if need be whichever one causing a feeling/symptom.

How was your health before taking the herbs?

  1. I got intense heartburn that felt like I was having a heart-attack sometimes.
  2. Right now I have a lot of heat! I sweat all time, and I am always hot. I also feel a lot of internal heat. This started after the radiation, I got a test of my hormones and they were elevated and this puts me in pre-menopause.
  3. I don’t get my menstrual period anymore, although I got what I felt like really painful ovulation last month.
  4. I started having psoriasis all over my skin and also a skin outbreak looking like small boils behind my thigh and butt.
  5. The last ultrasound scan showed about 3 uterine fibroids the biggest was about 5cm.
  6. I rarely sleep before 4a.m., although I have gained about 10kg.
  7. I also have a bump on the right inner side of my tongue,
  8. The hospital was planning to remove the whole rectum/vagina and give a permanent colostomy, but I have declined this.  Even the oncologist agrees with me not to do the surgery.  The only thing I am planning to do is close the colostomy after the rectum heals so bowel movements can go the normal route.

Are you in pain? Describe, where, what type and how serious? 

Yes, there is pain, but it has reduced. The pain is in the rectal area, sometimes radiates to the vagina. It aches, sometimes burns. On a scale of 1-10 pain is about 5. 

Can you sleep? 

No can’t sleep. 

Do you feel tired?


How often is your bowel movement? Difficult, constipated, with blood?

Two to three times daily, normal, soft, no blood. 

How is your appetite? 

Appetite is okay, but can be better.

Any swelling?


Do you have any other medical problems such as: gastric?

Multiple uterine fibroids.

Urination: how frequent? Is it painful? Any blood?  

Six to seven  times daily. No pain. 

Do you cough?


Do you have difficulty breathing? Elaborate. 


List and explain any other complaints. 

Very dry skin. Recently I started getting eczema and acne. The bottom of my feet sometimes hurt when I walk. There is a bump on my tongue (pink).

When you started to take the herbs for the first week (r two), did you suffer from any healing crisis? Your conditions got worse and then improved later?

Yes, I had pains all over my body, headache, sore throat, mild temperature and rashes. Some of the symptoms got worse before they got better.

After how long taking the herbs that you felt you were beginning to feel the herbs were helping you?  

From the first week after using the herbs, I felt a difference and I knew that the herbs were helping me.

Why did you say you were getting better after talking the herbs?

  1. In terms of general feelings, I feel great. I am getting stronger physically,
  2.  I don’t sleep at 4 a.m. anymore. I don’t feel tired when I wake up.
  3. Basically, if not for the fistula, I have no symptoms.
  4.  I do more things myself now.
  5. Before I started the herbs, I had slight burning pains from the rectum and sometimes I had to use Ibuprofen (pain killer).  This week, I have not had that pain at all (even when I don’t use the pain tea).
  6. I can sit on a hard surface better now, prior to this moment, it was uncomfortable.
  7. My vagina does not itch anymore. Previously, it was itching so bad that I would scratch it until it bleeds. (Probably this is because you have stopped Xeloda?)  Yes, I was taking Xeloda the month before I started taking the herbs. The psoriasis on my body is also clearing up. They appeared after I started taking Xeloda.
  8. My lower abdomen was very tender upon touch, now I can press it without wincing.
  9. I definitely feel I am making positive progress both mentally and physically. I don’t know what it is but I feel happier!
  10. I tried out my shoulder and neck today. Unbelievable! Zero pain! Just five days ago I was in severe pain.
  11. I walked around for over an hour without getting tired. Before the herbs, I felt tired, and I would always get irritated and my mood changes and I become “snappy.”
  12. I am back to preparing my teas myself without help.
  13. The headache is gone as well as the sore throat and body aches. Yes, I believe it was a healing crisis. It started suddenly, got worse and then disappeared.
  14. I still have some phlegm but, it is clear in color.   It started during the healing crisis, it was milky in colour.
  15. I was able to take a bath without getting fatigued.  I typically spend an hour in the bathroom because of the colostomy. The colostomy is not regulated so, feces  come through it at anytime. Because of the difference in water temperature and body temperature, it stimulates the colon however lightly when water touches it. As I wash, it may come just when I finished washing and before I notice it it’s on my skin, I have to wash again. I could easily take a quick shower to prevent this but, if I go at a normal pace, I would start breathing hard.
  16. I don’t urinate as often as I used to! Previously, I used to urinate about every two hours or four times during the night. Now, maximum is once a night. Lately I don’t urinate throughout the night.
  17. Now, I sleep through the night without the need for urinating. Before the herbs it was difficult getting some sleep. Even if all the lights were off, I still couldn’t sleep till the early hours of the day.  Following the use of herbs, I sleep earlier, even when I try to stay up, I always become sleepy. But most importantly, even if I get six hours of sleep, I still feel very well rested upon waking up.
  18. Now I wake up and I don’t feel tired, I feel well rested.  Previously, I would wake-up, even after sleeping for nine hours and I would be tired.
  19. For me, if I didn’t have the colostomy or if the fistula was fully closed I wouldn’t remember I am healing cancer.
  20. The drainage from the fistula has reduced greatly and the mucus has also reduced. (I remember you saying that one day after the herbs the stools came out a lot into the bag, as never before?) I kept going to the bathroom and frequently too; the stool kept coming and coming like something was pushing them out. But it wasn’t diarrhea, it was soft, very frequent and in copious amount. The second night, the bag would have burst if I didn’t notice it on-time, it was that full.
  21. My nails look better!!! I was looking at them yesterday and I was admiring them because they look pretty, previously they looked terrible. They would bend and contour in odd ways.
  22. I just started sweating and felt the prickly sensation as I was typing this. It happens several times a day, even at night when I am sleeping. 

27 March 2012 

How are you doing over there? What about the fistula wound? Is it closing and improving? Then the heaty feeling inside? Does the C-tea help?

1 April 2012 

Hi Dr. Chris,
I am doing great! I cooked dinner today.  Turned out great! The only thing was, I had to keep my sweat from getting inside the pot.

The fistula is closing, the mucus barely comes out anymore and the exudate has reduced greatly. With the C-tea, I think it transfers the heat from inside the body to outside. I don’t feel the inside heat surge as much as I used to, but the sweating is a lot which is not bad. This is because,  sometimes I don’t feel the heat inside it’s only when I start sweating that I realize my body was hot. I don’t know if what I am saying makes sense? Now I look at the sweating in a positive way. I just tell myself my body is trying to get rid of all the chemo and radiation I bombarded it with. How is Auntie Im? My greetings to her. 

5 April 2012 

Thanks for your email. I am glad that you are living a happier life now —are you going to reconnect the colon? I thought you have done that already since I did not hear from you for a while. 

Okay — you have been on the herbs for more than two months now, going to be three? While on the herbs, did you also take any of the doctor’s medication? 

Compare your life now – after taking the herbs versus those days when you did not take the herbs. A lot of improvements? How do you describe your situation now? Taking the herbs indeed helped you?  Take care, Chris 

Hi Dr. Chris.

I am doing really, really well. I still expelled the dark stuff from my rectum this morning but the horrid smell is reduced.   I am not reconnecting the colon at this time. I prefer not to rush and wait a while for the rectum to heal fully. I may give it another year before deciding.

I am planning to come to Penang soon. But, I will be coming alone.  I will like to have enough money before coming so I can leave with enough herbs.

I have not taken any doctor’s medication since December last year. Now I feel strong /energetic, like I can do anything now. Well, except for my wrist. First it was the left wrist that was hurting. After a while it stopped. Now the right wrist hurts.

The herbs really, really helped the fibroids too! There is no more pressure on my bladder. I gained more weight too. People keep asking me if I am the caregiver to the patient and where the patient is. Of course I say with a huge smile I am the patient.

I thank God for His many mercies. Health is Wealth. 

One last question …

You said you felt well after taking the herbs. What if people put it to you that it is not true and that the “feel good” stuff who wrote about is just your imagination to justify what you are doing for yourself? It is not true!

Fortunately, some of the people who have cancer don’t have pain. However, for those who have pain it can leave you begging for death; even I found myself weighing the benefits of dying rather than continue to suffer the pain. If anyone has been in this kind of extreme pain, I don’t think there is anything in the world that can lead you to imagine “feeling good” when you don’t (well, maybe hypnosis, but I wasn’t hypnotized).

It’s like someone being burned alive, you know your body is healing when the pain reduces even if the scars are yet to fully heal.

When you start losing the muscles in your butt from inactivity, and then you start being active later own, your commonsense should tell you that both experiences are absolute opposites hence they are different and not imagination.

When people around you and even doctors get excited about the changes in you without telling them what you are using, then this is the most definite part proving it’s not being imagined. People are not in my head and they can see me becoming different.

When people can look at you and ask you where the patient is, and even argue with you that you are not the patient; I don’t need anyone to tell me otherwise.

When I can walk for an hour without pain when I could not walk five minutes previously, commonsense tells me things are very different and getting better.

When the pain stopped acting as my alarm clock and I was actually sleeping and waking up on my own terms…oh I knew, I knew without a doubt things were changing for the better.

I could go on, but I’ll hope you get the gist by now. With Stage 4 cancer pain, there is no imagination that can block the pain you are used to experiencing for two years. Unless maybe you are a monk or something (I apologize if that statement is rude). 


I can only say this. This young lady has a lot of common sense. She is not rushing to get herself “cured.” Let the fistula “really” heals first before doing the surgery to reconnect the colon. It is our pleasure to be able to help such an exceptional lady. I am glad that I did recognize my mistake for trying to ignore here request for help. But all the same, this story has a happy ending. May God guide us as we go forward!

Colon Cancer Part 2: Her Treatment in India

India is cheaper with medical treatments and they have similar equipments to advanced countries.

CT scan revealed the tumor was almost obstructing the rectum, the surgeon suggested an emergency surgery to divert the stools so as to prevent blockage. I have had thirty radiation treatments and three cycles of chemotherapy.

You had radiotherapy at the same time took xeloda? Did they tell you radiotherapy is going to cure or shrink your tumour? Why did you agree to do the radiotherapy? Did you suffer any side effects when on radiation?

They told me radiation would shrink the tumor so they could do the surgery because I did not want a permanent colostomy.  Now that I think back, if the tumor was truly about to block the rectum, then I would not be having normal size bowel movements. But my bowel movements were normal in size, I guess they deceived me there again.

I had side effects; my bladder was on fire (burning)! Every time I urinated I cried because it burned as I urinated, I reduced my liquid intake because I did not want to urinate. I was urinating about every 30 minutes.  When I told the radiologist about the pain, he said it was impossible; it was too early to have any symptoms. I started having symptoms after the first week. I lost all my genital hair.  My whole genital area was irritated and which itched and itched and itched! Nothing relieved this itch.  One of the doctors said “you’re young, you should be able tolerate the pain”.  They then gave me Urispass after I complained for 3 weeks, to help with the burn when urinating.

A week after I started radiation was when I started to sweat excessively.  I have bouts of internal heat even when I am in an air-conditioned room. My whole head/face/back and chest would look like I poured water on it.

Also, with the chemo, I had nerve tingles in my hands and feet. I also had prickly sensation all over my body occasionally. I don’t get the tingles anymore, but the prickly sensation still appears once in while.

I was not informed about any side effect of radiation. The only thing they did was to ask if I am married. I said no, and they proceeded. I asked, begged for the doctors to talk to me, all I got was, we are trying to help you, calm down be grateful and take the pain.  But eventually I got tired of them saying they were trying to help me, I quit for three weeks after I had a fight with the clinic.  The doctor actually said “you are going to die if you stop the treatment, the disease is advanced” and I yelled, it’s been advanced for almost two years I AM STILL ALIVE!!!  They then told me, if I do not continue the treatment the only surgery they could do was take out the whole rectum and take out the vagina and if they should try to do that, it would result in death. I cried, my mum cried, nobody cared that I was just another random paying patient!

I asked to know the amount of radiation I was getting, they said they couldn’t tell me, I asked to view my file, they said I couldn’t.  I know every patient has a right to view their file upon request because they paid for it!

I have refused surgery because the surgeon plans to take out the whole rectum and vagina.   I refused Chemo IV after the first, gave me bad burns on both my arms and close up my throat.

When did you complete all these treatment?   

Radiation was completed in October. I stopped taking Xeloda December last year (2011).

What are your plans after treatment?

My plan is to start a fulfilling job in the health industry and enjoy the life I have prevented myself from enjoying for all these years.   Everyone that can afford it wants to eat what Americans are eating.  They need someone to teach them to stick to their own food.

Give us an idea of what it cost to be treated in an Indian hospital.

  1. Visit to oncologist,what is the consulation?  Less than US$20 per visit
  2. Total cost of opeation for colostomy?  About US$6,000
  3. Total cost of 30 radiation?  US$8,000 including tests.
  4. One cycle of Xeloda? Around US$5 per pill. Around $270 for a cycle.
  5. Are the facilities good — clean? The facilities are okay since it’s an international hospital.  About 50percent overall cleanliness, but the toilets were 20 percent clean. I bought my own bleach and cleaning supplies because I am very fussy about clean bathrooms.
  6. Are the doctors and nurses pleasant to deal with, well trained?

For every ten nurses, only two spoke English at a level that can be fairly understood.  I believe they are well trained but the nurses don’t follow procedures like I believe they were trained. I had to remind them to clean the injection site with alcohol/spirit before giving the injection. They rarely wear gloves so there could be cross contamination among patients.

I had to inject myself a few times because they didn’t know how to administer Intramuscular injections in the thigh. My butt was in a sea of pain, because they don’t administer pain medications through the IV unless in the ICU.  However, most of them are pleasant!  The doctors are well trained and spoke good English. The surgeon was trained in France.  I think that is one of their strongest qualities, general surgery, transplant/orthopedics, cosmetic surgery.

What are your experiences with the doctors in indian hospital?

They feel the doctors have the final say and know all, even the nurses dare not question the doctors.  It was surprising that, aside from Indian food, patients were provided junk food like French fries.  The fresh juices were again loaded with sugar.  They didn’t seem to understand that sugar feeds cancer. I declined dextrose IV because it caused pain since it was sugar. They thought it was in my head.  They ignored me until I pulled out the IV myself.

There were flies in the hospital and the food had stones and hair in them.  Most people don’t wear shoes in the hospital with the amount of diseases in the hospital.  In the clinic I went to receive radiation, I was told I would not receive treatment if I do not remove my sandals, meanwhile people walk barefoot on the street, so there really is no difference between those wearing shoes and those walking barefoot. We are all bringing in the same dirt.

I noticed the doctors don’t follow-up with their patients.  If you don’t show up for an appointment, they don’t even bother to ask the nurses to find out the status of the patient.  I stopped seeing my surgeon since October 2011. It wasn’t until I went to the hospital in January 2012 that he saw me walking by and asked “Oh, are you okay?”

The Oncologist

Your article made me remember when I was arguing with the oncologist a few months ago about chemo.  I accused him about the so-called cure and ask for the percentage rate. He said the best is 25%!!! I was flabbergasted! And even when radiation is included the maximum is 30%. Then he proceeded to suggest I have chemo for one whole year. I laughed and said that’s not going to happen, God forbid I stay on chemo for a year. He looked at me as if I didn’t know the severity of the illness. I told him, But you know that chemo and radiation cause secondary cancers.  He told me to stop reading the internet and all those are not true! I smiled and made a mental note not to share anything with him again.


Before radiation, nobody ever bothered to explain the side effects to me, I knew that there would be some effects with my reproductive organs, I asked for a fertility center, so I could at least preserve my eggs. They said there was none in the state and I stupidly believed them.  After twenty bouts of radiation later, I found a clinic, they said they couldn’t help by then.  I cried so much and had a fight with the doctors for acting like they were God and the sole decision maker. I was very upset. I learned that because the cancer was stage 4, they didn’t think I would survive to be able to have children anyway.

Before the treatment you were not told about the side effects of chemo or radiation?

They told me nothing with radiation. But for chemo, they said nausea, hair loss and fatigue but, I didn’t have them.  Instead, I had terrible heart burns that felt like a heart attack.  I still have hair on my head. I’m sure the oncologist will have a heart attack if he sees me without my hat/scarf.

Did the oncologist / radiologist know that you are taking supplements and herbs?

The radiologist said I should not take anything. These might make the side-effects of the radiation worse. The oncologist said not to take anything that may reduce the efficacy of the chemo.  I told them I was only taking one multi-vitamin but continued taking all my supplements.

Did they oppose or support your desire to take herbs and supplements? What did they say?

They opposed as they didn’t think it could have positive effects, only negative. When I informed the oncologist I was going to use herbs to improve my WBC, he said herbs won’t work, that I was better off taking the injection to boost it. When I asked  where I could find alternate treatments, they said only the temple/church.

Then you found cancer care? How do you know us then? Any one told you about us.

God pointed me in the direction of CA Care. Nobody told me. Nobody I know knows CA Care. I prayed during my ordeal and I told God, I don’t want all these chemicals, they are hurting me. I was always sad when taking these treatments. I wanted to be better and not become more sick. A few days later, I started seeing advertisements on TV about Malaysia.  It would show pictures of Malaysia and how beautiful it is, and encouraged tourists to visit.  The commercial always ended with “Malaysia, truly Asia”. I told my mum, I want to visit Malaysia. One of my friends promised me a vacation after I get out of the hospital, and asked where I would like to go. I said Malaysia. I didn’t know anyone or anything about Malaysia but, my spirit wanted to go for some reason. My subconscious knew something I didn’t know.  A few weeks later, I said a prayer and got on the internet just searching. I don’t remember the specific thing I was searching for. I was just searching, knowing God will lead me where I needed to go and I came upon

I don’t believe in coincidences and I know everything happens for a reason. I went through the site and it clicked in my mind, this is why I have been seeing Malaysia on TV.  Since then, I have not seen that commercial on TV. God is indeed wonderful!



Colon Cancer: Oncologist Said Chemotherapy Would Not Cure Her or Make Any Difference –But CEA Declined After Herbs

This is an e-mail we received on 16 October 2010.

Dear Dr. Chris K.H. Teo,

My mom’s oncologist told us her cancer had recurred and if she does chemo it will extend her life by another six months, and if lucky another twelve months.  But the oncologist does not recommend chemo and thought the treatment would make her worse. He suggested waiting until her condition becomes painful or other symptoms appear. He told us chemotherapy does not cure her cancer and it does not make much difference.

I found out about you from the internet. I would like to bring my mom to see you to help treat her.

We are living in Singapore and planning to go to Penang next week to see you. I think we may need to stay in Penang but not sure how many days to stay. Are you able to advise how many days we should stay? I saw the video on healing crisis after taking your herbs. I’m afraid if we just take your herbs and go back, my mom may experience pain, vomiting or has diarrhoea, Then my mom may think the herb is not working and would not like to continue taking the herbs. I think your presence and guidance will give us confidence to face the battle against her cancer.

Here is what I know of my mom’s condition and cancer.

Histology report identified the cancer to be mucinous adenocarcinoma of the iluem which has invaded the muscular wall and peritoneal surface. Conclusion: Pseudmyxoma peritonei, stage 2B.

Surgery was done to remove 10cm of iluem and 7.5 cm of caecum. This was March 2010.

She refused to undergo chemotherapy immediately after surgery.

Subsequently doctor ordered blood tests and PET/CT scan. Her CEA marker has been rising from 5.4 to 6.3, 9.6 and yesterday the oncologist said her CEA was12.9. But the PET/CT did not show any tumour.

My mom easily gets stomach and intestine bloating and discomforts, after she takes cooling food or if it is cold/rainy weather. Even some vegetables make her have loose stools and diarrhoea. Ginger tea helps remove the wind.

Other than that she is losing weight, about 0.5 to 1 kg every 3 to 4 weeks.

She can eat, sleep and has no pain. She has been taking some Chinese medicine to help her but her condition is like above with CEA rising. We do not know what the Chinese medicine contains. Please reply as soon as you can. We pray for God’s help and yours too.

Patient (H-434) and her son came to see us in Penang on 22 October 2010.

e-mail 28 October  2010

Hi Chris,

My mom … is happy and confident about the herbs you prescribed her. She fell asleep Tuesday morning and I didn’t want to disturb her. So we did not come to see you on Tuesday. Please accept my apologies for not turning up Tuesday morning. I’ll keep you updated about her progress via email. Many Thanks and God bless you and Ms Teo.

e-mail 29 October 2010

Thanks for the update —- when she goes home, how is she? Does she feel any better now?


e-mail 1 November 2010

She feels better after taking the herbs you have prescribed. Thanks for your concern and please take care too.

e-mail 18 May 2011

Hello Dr Chris,

After taking your herbs, her cancer marker came down from 12.9 to 8.8 and the doctor advised her to come back in six months for checkup. My mom feels okay now. I made vegetables and apple juice for her once a week. But she finds them ‘cooling’ and gets diarrhea / indigestion or lots of gas after that. Taking ginger soup helps though.

The patient came to see us for the second time on 21 May 2011. Listen to our conversation that day


The doctor conveyed this gloomy prognosis:

  • Since cancer has recurred, patient had only about six months more to live – or at best with luck, a year!

Since human beings are not God, we always tell patients, Believe the diagnosis but don’t believe the prognosis. It is sad that the practitioner of noble profession has come to a point of not realizing what he says is insensitive or   damaging to the patient whom he is supposed to help. Telling patients that they are going to die soon is inflicting a nocebo effect.

The oncologist did not recommend chemo and thought the treatment would make her worse. How many oncologists would admit to the fact that there is no cure for metastatic cancers and that chemotherapy will do more harm than good? In most cases and most of the time, chemotherapy seems to be the standard fare “dished” out to all patients – irrespective of age or stage.

Given that this patient has come to the end of the road, there is no option left other than alternative medicine.  In spite of that, we often have to remind patients that they have to relax and take it easy. Face the fact squarely and fairly. Do not come expecting us to “dish” out an instant or magic cure. One patient wrote that after taking herbs and the change to vegetarian diet and juices for a month, the tumour is still growing in her colon! What do you expect? Cure cancer with herbs and juice within a month?

Another mistake that caregivers often commit is to over-react. After reading about the purported benefits of juices, raw diet, supplements, etc. they would go over-board feeding their loved ones with all these stuff, sometimes resulting in more problems. In this case, the enthusiastic  son thought that juices might perhaps cure his mother. His mother has a yin (cool) body and cannot tolerate raw food and juices. So she ended end up having diarrhea.

Listen carefully to what this patient said if you want to live well with your cancer. She had clearly accepted her lot and has a positive attitude. Relax, be happy and take life easy. Enjoy your days while there is still time to enjoy. You don’t have to give up but at the same time you don’t have to live each day with fear of dying. Go out and smell the flowers.

Update:  27 February 2012

Hello Dr Chris,

My mom is getting better. Just 2 weeks ago she went for medical test and the doctor said he cancer CEA marker has dropped to 5.9. Thank you Dr Chris. And wishing you good health.

Reply:  Wah, your mom is doing well and her CEA  is 5.9 ? What did her doctor say? Did the doctor ask her why? Did he know that she is taking herbs? And is your mom taking the herbs without stopping?

Yes my mom CEA was as high as 12. She continues to take your herbs. We now add ginger into the C-Tea so that she does not get stomach bloatedness.

Doctor did not even ask why the marker reading is low or ask whether she is taking herbs. All they do is blood tests for cancer marker. Also because her doctor got promoted he now passed my mom to one of the doctor in his team. We only found out on the day of the medical appointment. Also I learned from the nurse that the promoted doctor attends to private patients only. What a surprise to us the way they handled patient.

Dissecting Chemotherapy Part 8: Chemo for Colon Cancer – Only Three Percent Benefit

DL is a 47 year-old-male. Sometime in September 2010, he had uncomfortable feelings in his stomach. He went to see a GP who thought it was a food poisoning or gastric problem. He was told not to worry about it as the problem would just go away in a day or two.  Unfortunately it was not to be. The problem persisted and in early February 2011, DL felt there was lots of air/gas in his stomach.  In the early morning of 8 February 2011, DL went to see the same GP again. This time the doctor took his blood sample for analysis. An ultrasound was also done.

The blood test results of 8 February 2011 showed ESR = 40 (high), GGT 67 (high) while the cancer markers were all within normal range; CEA = 0.7, CA19.9 = 7.7, and Total PSA = 0.5.

Ultrasound of the abdomen showed “thickened loop of bowel, suggestive of colorectal malignancy”. He was advised to undergo a colonoscopy and CT scan of the abdomen.  A follow up CT scan confirmed thickening in the colorectal region.

On 10 February 2011, a colonoscopy was performed. There was a caecal polyp, and ulcerated growths in the transverse and sigmoid colon.

Biopsy report confirmed the following:

  1. Caecal polyp:  tubule-villous adenoma with high grade dysplasia, along with suspicious foci of infiltration.
  2. Transverse colon: malignant transformation of a tubule-villous adenomatous polyp with foci of infiltration.
  3. Sigmoid colon: malignant tubule-villous adenoma with foci of infiltration. Grade 2 adenocarcinoma with infiltration.

DL was referred to the government hospital for surgery.  A second colonoscopy was done at the government hospital and on 1 March 2011, DL underwent an operation to remove the cancer. According to the pathology report, the descending colon, part of ileum of appendix, caecum, ascending colon and descending colon and mesocolon were resected.  Histology indicated:

  1. Mycinous adenocarcinoma, well differentiated, pT3NoMx
  2. Tubular adenoma with invasive adenocarcinoma at caecum, well differentiated.
  3. Intramucosal adenocarcinoma (at caecum) forming small polyp.
  4. Inferior mesenteric lymph node: no malignancy.

DL was in the hospital for seven days.  He was told that it was a Stage 2 cancer. DL was subsequently referred to an oncologist in the same government hospital. The oncologist offered chemotherapy and this is what DL was told:

“With chemotherapy, the chance of recurrence would be 17 percent, without chemotherapy the chance of recurrence would be 20 percent.” DL would have to undergo thirty cycles of chemotherapy.

Listen to what DL told us when he came to CA Care on 15 July 2011.


DL was indeed lucky to have met an honest oncologist who told him the “reality” of what chemo is all about.

  • In exchange for thirty cycles of chemotherapy, DL would stand to cut recurrence rate by 3 percent.
  • An equally important   point not said but implied is that even with chemotherapy there is no certainty that DL would remain cancer free. There is a 17 percent chance of recurrence.

So in dealing with cancer, no one will know with certainty its ultimate outcome.  Patients need to be honestly told the odds against them. The cards must be laid out openly on the table. Patients must be the ones to make the decision since this involves their life.

It is most unfair for those in the know to tell only the “good things” about chemo treatment, downplaying the many “bad things.” Patients are sometime “threatened” and “pushed” or “cheered” into taking a path that they are reluctant to take. We salute DL’s oncologist for being honest with DL. Even more so, when he told DL that should DL decids to do chemotherapy in the future, he is welcome to come back to receive the treatment. Many patients tell us, “If we defy our doctors, we will not be able to go back to the hospital again.”  This fear is real and has “cowed” patients into following what their doctors want them to do.

Dissecting Chemotherapy Part 5: Contribution of Chemotherapy to Survival of Colon Cancer Patients

L M Carethers wrote the following in the International Journal of Gastroenterology & Hepatology,  Gut 2006;55:759-761 doi:10.1136/gut.2005.085274:

  • The current gold standard for treating patients with advanced colon cancer is chemotherapy with 5-fluorouracil (5-FU) based regimens. This standard is based on compelling clinical trials utilising 5-FU and levamisole, and demonstrating a survival benefit for patients with stage III (Dukes C) colon cancer.
  • Although there is no set standard for treating stage II patients, some stage II patients do receive 5-FU chemotherapy.
  • Stage I patients with colorectal cancer do not receive 5-FU as their prognosis is excellent with removal of the tumour.
  • Stage IV patients may receive 5-FU for palliation (note: this is not cure).

Dissecting the Gold Standard of Colon Cancer Treatment

In 1975, Dr. Charles Moetel, a renowned oncologist of the famed Mayo Clinic in Minnesota, USA, found that the lives of Duke’s C colon cancer patients could be prolonged when treated with a combination of 5-FU and levamisole (a drug used in sheep, swine and cattle to control stomach and intestinal worms and nematode parasite infections). 

In this study, 971 patients with Duke’s C colon cancer who had undergone surgery were divided into three groups and given one of the three treatments. The actual median follow-up time is 6.5 years.


Number of patients

Number with recurrence

Number died

Surgery only


177   (56.19%)

168  (53.33%)



  172   (55.48%)

158   (50.96%)

Levamisole +  5-FU


   119   (39.14%)

121   (39.80%)

Benefit of Levamisole + 5-FU over  surgery only (no chemotherapy)

Less recurrence by 17.05%

Less death by 13.53%

Source:  Moertel, C. G. et al. Fluorouracil plus levamisole as effective adjuvant therapy after resection of stage III colon carcinoma. Annals of Internal Medicine. March 1995. Vol: 122: 321-326.

The authors concluded that Fluorouracil plus levamisole is tolerable adjuvant therapy to surgery; it has been confirmed to substantially increase cure rates for patients with high risk (stage III) colon cancer. It should be considered standard treatment for all such patients.

The therapy with 5-FU + levamisole: caused nausea, infrequent vomiting, stomatitis, diarrhea, dermatitis, fatigue and mild alopecia. Approximately half of the patients had leucopenia (lowering of the white blood cells).

The unanticipated toxic reaction to 5-FU + levamisole: 40% of the patients had abnormal liver function test results during the course of the therapy. Their toxicity were reflected in elevated alkaline phosphatase levels (which peaked approximately 7 months after onset of therapy), elevated aminotransferase (AST) levels, and elevated serum bilirubin besides causing fatty liver.


  1. Does the result show that if you don’t undergo chemotherapy after surgery, you will die?
  2. Does it not show that without chemotherapy 53.3% of patients were dead but even if you have undergone chemotherapy almost 40% died anyway?
  3. Does it not show too that even with chemotherapy 39% of the patients still suffered recurrence?
  4. Would it not be prudent to weigh this advantage against quality of life issues, taking into account the acknowledged side effects of chemotherapy?

From the above data it is clear that chemotherapy reduced recurrence by 17 % and reduced death by 13.5 % but not without side effects which are often brushed off as insignificant.

Chemotherapy is proven to be beneficial by only a slim margin (13% to 17%). Indeed, from the academic point of view, the result is statistically significant. This would please the statisticians and the scientists, but I am not sure if it pleases cancer patients at all. I believe this is not what patients (especially those in the poor developing country) are looking for. They are seeking for a REAL cure (not a MEDISAL CURE either!). If this is not possible, at least they expect a much greater chance of achieving it. I wonder if anything less than 20% benefit is good enough?

Chemotherapy causes severe side effects in most patients. It is not like an “ant-bite” as one oncologist would tell some patients. With less than 20% benefit, is it worth the gamble?

One question comes to mind: Can this slim margin of benefit of chemotherapy not be achieved by some other non-invasive or non-toxic means? For example, does it ever occur to people that by just a change of diet or taking of herbs, perhaps we can also increase our chances of healing colorectal cancer and the result could be better than chemotherapy? At CA Care we have presented many case studies showing that indeed this hypothesis is valid and has merit — herbs and change of diet and lifestyle can prolong meaningful survival better than chemotherapy!

Gold Standard Plus Targeted Therapy

Today, oncologists have a good number of chemo-drug mixes for patients with advanced stage colon cancer. A new generation of “smart bomb” or targeted-therapy drugs can also be added to the mix to help control (ah, not cure?) the cancer. Examples of these regimens are:

  • FOLFOX (leucovorin [folinic acid], 5-FU, and oxaliplatin)
  • FOLFIRI (leucovorin, 5-FU, and irinotecan)
  • CapeOX (capecitabine and oxaliplatin)
  • Any of the above combinations plus either (not both) Avastin (bevacizumab) or Erbitux (cetuximab)
  • 5-FU and leucovorin, with or without Avastin
  • Capecitabine, with or without Avastin
  • FOLFOXIRI (leucovorin, 5-FU, oxaliplatin, and irinotecan)
  • Irinotecan, with or without Avastin
  • Erbitux alone
  • Vectibix (panitumumab) alone

Avastin and Ertibux are now being commonly offered to cancer patients in Malaysia. Vetibix is still unknown here … but soon it will hit our shore. But what do they say about Avastin and Ertibux? Two things are clear: They are expensive. And they don’t cure colon cancer !

Liver Metastasis: No Chemotherapy – Fourteen Years Still On Herbs

Koh/342, was 75-year-old when she was diagnosed with colon cancer in 1997. She underwent an operation. An ultrasound done on 15 July 1997 indicated ill defined masses in the right lobe of the liver. The left lobe appear spared but slight dilatation of the ducts are seen. Conclusion: liver metastasis.

Due to her age, she did not undergo any further medical treatment. Her daughter came to seek our help   on 25 July 1997. Koh was started on Capsule A & B and Liver Tea. Her conditions improved. Her pains disappeared. She was able to eat and sleep well. She was able to lead a normal life and could even go marketing every morning.

Seven weeks on the herbs, the daughter told us that a medical checkup showed her condition had stablised. Her doctor told the family: Continue taking the herbs!

On 8 October 1997, Koh’s daughter told us that according to the doctor, the liver nodules had shrunk. Their sizes had become smaller.

On 6 June 2003, the daughter came to collect herbs for her mother. Koh was in good health. This means Koh has lived for already six years.

On 25 March 2011, Koh’s daughter came to collect herbs for her mother. We had a rare opportunity to chat with her. Below is the video recording on that day.


According to medical literature, up to 70% of patients with colorectal cancer would eventually end up with metastasis to the liver. Unfortunately, chemotherapy does not cure metastatic liver cancer. In general, the mean survival for patients with minimal disease is 16 months, while those with advanced disease it is 3 months. Generally patients who come to us are often told by their doctors that they have only 6 months to live.

In this case, Koh is still healthy for her age. And she is about to celebrate her 90th birthday. It was 14 years ago that she was diagnosed with metastatic liver cancer. She was only on herbs, no medical treatment at all. Indeed this is an unexpected and unbelievable but true story.

In CA Care we often see miraculous cases like this do happen. In fact is this kind of story that makes us “tick” and encourage us to want to continue our work so that many more can also be equally blessed.

Unfortunately we cannot give you more details about this case. This happened 14 years ago and at that time, we just started CA Care. We made no video recording of patient who came to see us, unlike what we are doing today.

There are many factors that contribute to the success of this case.

One, Koh is indeed very lucky to be at 75 years old when she had cancer. Her doctor had the good sense to think that chemotherapy was not going to help her. The scenario would have been different if she was younger. No one is going to take chances!  And most probably she might or might not survive the treatment.   There is always this rationale – You are young, give yourself a chance and fight your cancer with chemo. In this case, not only the doctor but all family members did not have that will to fight. It turned out to be a blessing for Koh.

Two, there are two kinds of doctors. One kind would take the heroic task of trying to solve problems even if the problem is unsolvable. Fight and fight – change one drug to another, and see what the outcome is. The war only stops when the patient dies.  Another kind of doctor is one who sees the bigger picture.  For this I must admire Dr. Jerome Groopman, professor and oncologist at Harvard School of Medicine. For this wise professor, pressing for a solution when none is apparent can be the worst course of action – “Picking up a scalpel and cutting can be just the wrong thing” when you don’t see the whole picture. Groopman wrote: “Don’t just do something, stand there” as he counsels against the impulse to jump in and do things.

In another story, a son brought his 85-year old mother, who had breast-liver cancer, to an oncologist. After taking the drugs, she became severely breathless and fainted.  She had to be rushed to a hospital for emergency care. Read more here:

Three, a nurse told Koh and her family members about CA Care. They believed what they heard! What could have happened if they had just brushed it off (like many do) as hocus pocus?

A lesson to learn from this story: Don’t ever think that the cancer is going to be “cured”, that is to say, permanently eliminated. Doctors normally  define “cure” as living past 5 years. This is not cure in its true sense. Koh tried not to take the herbs when she became well. The cancer started to come back. In this instance, it was lucky that she came back to us and started to take the herbs again. Things like this happen often. When patients get well they forget all that we taught them! And the cancer came back.

Perhaps you might want to hear a similar story: Liver-Bile Duct Cancer: Herbs Kept Him In Excellent Health:

Vegetable-State Terminal Cancer Brought Back to Life with Herbs

Poh is a 54-year old female. She had a 14 cm tumour in her distal sigmoid colon. She underwent surgery. The cancer was staged as Duke’s C. About two weeks after surgery, Poh underwent twenty-five times of radiation treatment and at the same time took the oral chemo-drug, Xeloda. Within a week after being on Xeloda, Poh became uncomfortable, her heart beat rapidly and she had difficulty breathing. The doctor stopped her Xeloda and replaced it with UFT. Before Poh could even finish a course of UFT, her legs started to weaken and her entire person lost strength. She could not walk and had to be confined to the wheelchair.

MRI of her brain did not show any evidence of metastasis. There were, however, disc bulges at C5/C6, L3/L4, L4/L5 and L5/S1. This was diagnosed as lumbar spondylosis.

Poh’s husband and son came to seek our help on 4 November 2005. Tears welled up in his eyes as he related his wife’s story. He said: “After the surgery, my wife was alright. She was normal – could walk around perfectly, could eat and do the normal chores in the house. It was only after she started radiotherapy and took the oral chemo-drugs that her condition deteriorated. This happened within about two months after the surgery. Everybody I asked told me to do all these.”

Poh was indeed in bad shape. She was put on morphine and had to lie in bed unable to move by herself. If she gets up, she will feel breathless. At one time, she had to be admitted into the Intensive Care Unit (ICU) for twelve days. The family spent about RM 50,000 for her treatment. With anger and frustration her husband said: “I spent money is okay, but how could she end up like this?”

Poh was then a living vegetable.

After one week on the herbs, Poh was able to wake up from her bed and walked ten steps with the help of her husband! Her daughter said she was thrilled when she was able to stand up. Her case was not be hopeless after all. On 3 February 2006, i.e., three months on the herbs, Poh was able to walk into our centre! As of this writing (a year after being on herbs) Poh is doing fine. She leads a normal, pain-free life.