The Starfish Project

The combined effort of our whole family.

Posts Tagged ‘lung cancer

Update on Mom (5/19/09)

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Last Friday, Mom’s hand started hurting quite a bit and three of her fingers started getting purple.  After the incident with her thumb, we knew what that meant.  So, Dad and Gretchen loaded Mom up and took her back to the ER.  They saw the same ER doctor we saw last time (which was helpful, as he was already familiar with Mom).  He couldn’t find a clot with the doplar, but felt they were probably small clots that were down in the capillaries of her fingers.  He wrote them a prescription for some nitro glycerine ointment which had to be applied to her hand every few hours and wrapped up.  This ointment is such a strong vasodialater that the person applying it had to wear gloves and be careful not to let their skin come into contact with it.  He said to use this through the weekend and if it didn’t help by Monday, to get Mom in to see a hand doctor.

Dad faithfully applied the ointment all weekend and Mom’s hand was still hurting quite a bit – so much that she needed to take pain pills to take the edge off the pain.  From what I’ve read, the pain from circulation problems caused by blood clots is quite terrible.  Mom and Dad had a pretty rough weekend with it with very little sleep.

On Monday morning, Gretchen started bombarding the primary care doctor’s office with requests for a referral to a hand specialist ASAP.  They were right on the ball and Mom had an appointment for 11:00 AM this morning.

I am still recovering from the flu (the normal one), so I still haven’t seen Mom since the morning of the 15th.  So, Dad and Gretchen took Mom over to the hand doctor this morning.  He did an x-ray and found that the clot was further up her arm, near her armpit.  The doctor was respectful, but still didn’t have any good news either.  He looked at Mom’s three fingers (which were now purple) and said that she would lose them, as well as the index finger and the rest of her hand.  He said all we could do was make her comfortable until all this happened and he could amputate her right hand.  He gave her a prescription for Darvocette and sent her on her way.

Well, this was definitely not the kind of news we wanted to hear.  But, we’ve learned that allopathic doctors generally don’t have good news for us (except for a few who we’ve appreciated so much).

Gretchen called me when they got home from the doctor and she was pretty shook up.  I imagine all three of them were – especially Mom.  I was also pretty shook up too.  I asked Gretchen how long she was going to be at Mom and Dad’s house and she said she was going to be there for a few more hours.

I got on the internet and started looking for anything that looked like it might work.  After only about 30 minutes of searching, I was amazed to find information about a supplement called Nattokinase.  It is an enzyme that aids in breaking up fibrin (a strand-like portion of the blood) that forms blockages in veins.  The Nattokinase is derived from fermented soybeans and has long been used in Japan to deal with and/or prevent blood clots.  It comes in a standardized formula which Gretchen was able to purchase at the health food store for around $30 (but available MUCH cheaper online through VitaCost for less than $7).  But, we needed it today, so Gretchen paid the $30 for it today.

She also picked up some stuff to make a blood thinning soup — it consisted of an organic beef broth base, onions, garlic, and green cabbage.  All of these veggies are good for naturally thinning the blood in both the arteries and the veins.

So, at 4:00 PM tonight, Mom was hurting, a bit scared, but encouraged that we had possibly found a solution that would save her hand.  She took her first 2,000 FU Nattokinase pill.  Gretchen also made the soup and Mom scarfed down a good portion of that too.  And, then we waited…

Gretchen came home (where I was babysitting her kids) at around 9:30 PM, and she said that you could already see a difference in Mom’s fingers.  She said that all day today the three fingers had a very delineated purple line straight across where the circulation was being compromised.  But, only 5 1/2 hours after taking the Nattokinase, the lines were no longer straight and it was now blotchy (with areas of pink) where they had once been only purple.

Gretchen called back at Midnight to remind Dad to give Mom her next dose of the Nattokinase and he said he had just given it to her.  But, then came THE BEST NEWS —- Mom’s hand no longer hurt.  She was sleeping and in absolutely no pain!!!  She hadn’t taken a pain pill since the morning and her hand was no longer hurting.  It had been hurting terribly since last week – but, the pain is now gone.  Gretchen asked if it was still purple, but he said they were in bed and the light was off and he didn’t know.  But, since the pain was gone, that can only mean that the circulation has been restored to her fingers and hand.  Isn’t that just awesome?

The thing that we have come to realize in this journey with cancer is that we, as a family, are alone.  We can’t count on my Mom’s doctors to know what to do anymore because they just simply don’t know what to do anymore.  Perhaps the insurance company doesn’t want to pay for any more treatment for her because they’ve now classified her as “terminal.”  Who knows.  But, perhaps it’s the best thing that could have happened to us.  Because, we’re finding that there are answers out there for many of the things that conventional medicine says are hopeless.

Mom has been taking her Poly-MVA now consistently for a few days and her appetite is returning.  Tonight is the first time in several weeks that she hasn’t had some kind of pain or another.  We’re praising God about that.  He’s been with our family through all of this and showing us that His ways are higher than our ways — His thoughts are higher than our thoughts.

Well, it’s very late and I need to get to bed.  Thank you to everyone (both those we know and those we don’t) who’ve whispered a prayer to heaven on Mom’s behalf.  We know we’re not really alone.  But, sometimes it feels like it.

Until next time (I’ll try to update tomorrow on the status of Mom’s fingers and hand) …

Tracey

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Update on Mom #2 (5/14/09)

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I just got home from Mom and Dad’s house.  My sister, Gretchen, called this morning and said that Dad called her and wanted to have a family meeting this morning.  She said Mom was lucid and sitting on the couch with Dad.  So, Gretchen picked me up and we went over there.

I have a terrible chest cold, so Dad gave me a mask to wear while I was over there.  I really don’t want to give Mom any kind of a respiratory infection.  But, we felt that the need to have a family meeting and discuss everything that was going on was paramount.   So, I wore the mask and tried not to touch anything while I was there.

Mom looked good.  I guess she “woke up” earlier this morning.  She doesn’t remember anything about yesterday.  She doesn’t remember signing a DNR with the hospice nurse.  We didn’t even know she had signed that until the hospice nurse came out of the bedroom holding a signed DNR with Mom’s signature on it.  Well, Mom does not want a DNR and didn’t even know she had signed it.  They had given her a massive dose of liquid morphine before she signed it.  I hardly think a person is capable of making such a decision when so heavily medicated.

Anyway, we explained to her that her body isn’t dying.  She’s just sore from the draining of the pleural effusion and her arm is a little sore where the blood clot is.  But, other than that, she’s not in any pain — certainly not end-of-life pain.

We talked to her about what she wanted to do.  She said she wants to keep fighting and she doesn’t want to be doped up anymore.  So, we were very glad to hear that.  She looked good and was communicating very well with us.  She was nibbling on some ice chips and drinking some water.  It was nice to see her hydrating herself again.  She didn’t have anything to eat or drink yesterday because of the narcotics.

So, we press forward together as a family.  Dad looked absolutely exhausted.  It was a very rough night for him.  He didn’t sleep a wink.  He spent most of the night praying for Mom (as we all did) and keeping a close watch on her like a mother hen.  He is the strongest person I know and I’m so grateful for him.  If it weren’t for him, I think our family would have fallen apart through all of this by now.  He’s definitely the rock for our family.

So, it was a good morning for us.  Gretchen is going to call hospice and talk to them about what we really need.  Mom needs some mild pain management – like prescription Motrin – to manage her arm pain and the pain she’s experiencing from her left lung re-inflating.  It’s sore from that, as well as from all the coughing.  So, we’d like to help her manage that without narcotics.  We’ll see if hospice will honor our boundaries and Mom’s decision to keep fighting.  She’s weak and her fight isn’t very strong – but, she’s fighting nonetheless.  And, for that we’re very, very grateful.

So, like the scripture says … Joy comes in the morning.  While yesterday and last night were very, very dark, this morning is much brighter.  Thank you all so much for your prayers and good thoughts.  We’ve had over 14,000 visitors to the blog and we know there are people all over the world praying for Mom, as well as searching for answers for themselves or their loved ones.  Keep fighting the good fight of faith.  Only the Lord knows the end of the story for each one of us.

I’ll keep you posted on Mom’s progress.

Tracey

Written by Tracey

May 14, 2009 at 10:46 am

Update on Mom (5/14/09)

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Well, we discussed when we started this blog that we would post everything – not just the good stuff.  We wanted people to know the whole truth about how Mom was doing.

Well, we are in our deepest valley so far with this monster called cancer.  He’s trying to devour and rip my Mom apart – but, we’re trying to hold steady as a family and weather this storm.  We would definitely appreciate any prayers you feel led to pray for Mom.

Mom had her second Gamma Knife surgery last month.  That was another tough day for bad news.  We found out when they did the MRI of her brain that she had several other lesions that would need to be treated, as well as a lot of little dots.  We were shocked.  How could this be?  We were so discouraged.  Then, we had another blast of bad news when they had the CT-scan report sent over of Mom’s chest that showed that her primary lung tumor had also grown, and there were some lesions on her liver.  It was a very difficult day.

The doctors at Barrows told us that they could treat the larger lesions with the Gamma Knife, but that the Gamma Knife wasn’t designed to treat small dots.  Mom has about 30 small dots.

So, as you can imagine, we went home feeling very low – even though Mom’s Gamma Knife treatment went very well and was much, much quicker than last time.  There were only two patients getting Gamma Knife that day, so we were in and out by mid-afternoon.

When we got home, I was just puzzled how this could have happened.  How could Mom have been faithfully doing her high dose Vitamin C IV treatments, the Paw Paw supplement, and the low-dose Naltrexone – and nothing had worked to stop the metastases.  In fact, it was like a flood gate had been opened.  Mom had had consistently good reports about her lung tumor getting smaller, as well as the original brain tumor getting smaller too.  So, what caused this setback?  What made things change for her?

After I figured it out, it all made sense to me.  Both the high dose Vitamin C IVs and the Paw Paw supplement are antioxidants.  I discovered that high doses of steriods can diminish the effectiveness of antioxidant treatments.  So, all this time Mom was faithfully doing these antioxidant treatments — the nasty high dosages of Decadron (the demon drug, as we call it in our family) was working behind the scenes making her alternative treatments ineffective.

SO, IF YOU ARE TAKING DECADRON FOR BRAIN METS OR FOR A PRIMARY BRAIN TUMOR — UNDERSTAND THAT ANTIOXIDANT ALTERNATIVE TREATMENTS MAY NOT BE AS EFFECTIVE!!!!

I wish we had learned this sooner, as we would definitely have put Mom on some other types of treatments that weren’t antioxidants – but worked in some other way to fight cancer.

Once we figured this out, Mom started on her Poly-MVA treatment.  In fact, her first shipment of it was waiting for us when we got home from the Gamma Knife treatment.  We were encouraged with that because Poly-MVA seems to work best on brain tumors, lung tumors and one other type (which I can’t remember off the top of my head right now).  So, we weren’t too worried about the little dots.  We felt confident that the Poly-MVA would take care of the dots.

Also, over the course of the last month, Mom developed a pleural effusion – where fluid builds up in the pleural space (around the lung) and caused her a lot of pain and discomfort.  We took her to a pulmonary doctor last Wednesday to make arrangments to have it drained.  His office set her up for an appointment for the procedure for Monday the 11th at the local hospital.

Well, Mom was in so much pain that we took her to the ER so they could drain it.  Little did we know they were going to admit her and keep her for six days.  The next day they did the first drain and were able to pull off 2 liters of fluid from the pleural space.  The next day they pulled off another 750 ml of fluid.  Mom was feeling a lot better.  However, at the hospital, they kept giving Mom pain meds.  First it was Morphine for the pain from the effusion, then it was Dilaudid.  She was pretty doped up, but recovering nicely.

Then, two days ago, she took a downward turn.  Sometime during the night they discovered that she had developed another blood clot in her upper arm.  They moved her IV site to her foot – which meant she could no longer get out of bed to use the restroom.  And, they catheterized her.

From this point, she was very weak and looking like she was going to need some time to get back on her feet again.  It was at this point her internal medicine doctor suggested that we look into hospice.  Of course, we have not given up on Mom.  The doctors all have and they are quite depressing.  These doctors should have a class in how to talk to people.  Some of them are quite abrasive when discussing such sensitive matters.

The social worker for the hospital came in and discussed what hospice was.  She told us that just because someone is working with hospice doesn’t mean that we’ve given up hope.  It just means that the family will get some help  at home and Mom can be made comfortable at home.

Well, we’ve come to find out what that really means is that Mom will be completely doped up into a stuper at home and the hospice people (while very nice) all believe that she’s going to die.  So, tonight, Dad decided to stop with all the crazy drugs the hospice people gave her.  She’s not even in pain.  The only pain she had was from the pleural effusion – and that’s healing up just fine now that it’s been drained.

We’re going to talk about quitting the hospice care tomorrow as a family.  Mom still has a lot of fight left in her and when she’s on the Morphine she just really doesn’t give a crap about anything.  So, that’s not a good drug to take if you’re trying to fight still.  Today she didn’t eat and barely drank.  She was refusing the Poly-MVA in the afternoon and evening.  That’s no good.  So, she’s not going to take them anymore.

So, as you can imagine, it’s been a very emotional couple of days for our family.  However, I talked to Mom on the phone tonight and she sounded better than she did yesterday or even earlier today.  She sounded coherent – even though her voice is still just a whisper from the laryngitis.

Mom had been off of her Poly-MVA while she was in the hospital.  So, now she’s back on that again.  We’re hoping to see her appetite improve and her energy come up once she’s been on it consistently for a week or two.

I was listening to music tonight and the Keith Green song “Your Love Broke Through” came on.  I just broke down crying.  The words to that song are so perfect for where Mom was right then — at that exact moment when the song came on:

“Like waking up from the longest dream, how real it seemed
Until your love broke through
I’ve been lost in a fantasy, that blinded me
Until your love broke through.”

It’s a song about God and how His love can break through our times of absolute hell.  He finds us in the midst of our nightmares and His love is so powerful it breaks through and brings us back to Him.  At least, that’s what this song meant for me tonight when I heard it.  Mom’s been living in a drug-induced, blinding fantasy for a few days and these people had us convinced she’s dying soon.  Well, that’s not true.  It’s just an illusion – a fantasy.  I’m sure they don’t mean any harm.  But, they are very, very wrong.

Like my sister and I always say about the naysayers who doubt natural healing or spiritual intervention:  “We’ll add them to Mom’s Christmas card list.”  🙂

As you can imagine, our family covets your prayers and good thoughts for Mom.  While this is a very tough time, I feel we’ve got some resolve and peace of mind that this is not the end for her.  She has a lot of living yet to do and we still need her to be here with us.

I’ll post when I can…

Tracey

Written by Tracey

May 14, 2009 at 1:42 am

Poly-MVA Testimonial for Lung Cancer

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happydance3kName: John Flint
7300 Bear Ridge Rd.
N. Tonawanda, NY 14120
Date: July 23, 2000
Diagnosis: Lung Cancer
Email:
eileent1@netzero.netUPDATES: April 12, 2001 – December 3, 2003 – July 6, 2004

On September 1997 I started having difficulties with reading comprehension, I could read a sentence but could not understand what it meant. Within a week I also developed strong headaches. My GP made an appointment to see a neurologist which he scheduled for 2 months in the future and suggested I continue to take aspirin.
That same weekend my headaches were so bad that I went to the emergency room of the local hospital.

After a very short examination the doctor concluded that I had a bad set of headaches but “one thing you do not have are brain tumors”. I felt reassured that I did not have anything serious and went home. As the headaches kept getting worse and I became more and more disoriented, I managed to obtain an appointment with a young neurologist. After a ten minute examination, she sent me for a cat-scan and within a few hours she gave us the bad news that I had two large brain tumors. She also suggested that the brain tumors were probably not primary and that they probably had metastasised from somewhere else.

 

 

That day our life changed forever. The quick action of that neurologist might be one reason that I am still alive.
Within a few days they identified the primary as a large lung tumor, non small cell carcinoma, that had spread to the brain. I was rated as stage 4. During the next few weeks I saw 3 different oncologists, they all gave me a prognosis of 3 months to a year at most. All of them suggested I get my affairs in order. They also stated that it would be a waste of time and money to try any alternative methods.

 

 

I started full brain radiation which was followed after several weeks of recovery by chemotherapy. This lasted almost six months until the oncologist refused to give me any more treatments as the chemo was having many negative side effects on my system. At that stage the doctors stated that they had nothing more to offer and that I should enjoy life as much as possible. We felt we were left on our own, like abandoned, with no one to help us.

 

 

During the long months of chemotherapy, my wife had started looking at possible alternative treatments since my doctors did not seem to think that I had much chance. She called survivors to see what they were doing, cancer organizations to see what they could offer, read books, looked at web pages for the latest that kept on recurring among her various contacts. As we spent more time researching these products we got a clearer understanding of why they worked. Some were being tested in various research laboratories and showed definite signs of reducing cancer. Others dealt with helping the immune system and maintaining the body at its peak condition.
The different cancer fighting products we found attack tumors in different ways. Some prevented the tumors from growing the necessary blood vessels required for growth, these are known as angiogenesis inhibitors. Others attacked the protein membrane that the tumors use to shield themselves from the immune system. Others have chemicals that are necessary for some cancers to grow but also contain chemicals that are poisonous to the tumor – Poly MVA.

 

Some prevent the small new tumors from attaching themselves and therefore cannot grow. I take them all. To date, most of the data show that no single chemical is 100% effective and that taking more than one product increases chances of survival. Some are probably more effective than others, none of them are harmful. The cost of many of these products is relatively small.
It has been 3 years since I was first diagnosed. To date I have no sign of any visible tumors in the brain or lung. I even have some hair back. We would be glad to send you a specific list of the products I am taking. Also we are always happy to talk to anyone looking for help. We were not able to get help from the medical profession so we took the initiative to do something ourselves. If we can share this with other people, we are happy to do so. Please feel free to telephone e-mail us at jflint@itcanada.com.

 

John Flint
UPDATE: April 12-2001

 


Hi Tim,
We have written a short paragraph below with the latest on Johns health. As you see, he is still doing very well.

 

 

We receive at least 5 calls or emails a week asking about poly and the other products that John is taking. We are happy to give moral support and provide any information that we have.
Best wishes to you and your father
Judy and John
John is doing great. As of April 2001, recent CAT scans could not detect any sign of his earlier brain or lung tumors. He is still taking all of his supplements, including POLY MVA, although reduced to a maintenance level. He also has maintained a diet of at least 7-8 fruits, vegetables daily balanced with protein.

 

 

 

 
 
UPDATE: December 3, 2003Hi Tim,

We thought we would let you know that John is still doing great and we are into our 3rd year of cruising on our sailboat. This winter we are off to Belize. John is still following his protocol including polymva.

 

 

We wish you and your father the best for the holiday season. Please give him our regards.
Judy and John Flint
 
 

 

 
UPDATE: July 6, 2004Hi TimAnother 6 months has passed and John still enjoys good health. My mother has been receiving at least 2 -3 requests for John’s “protocol” each week. She is happy to forward it to anyone that requests it. John also emails messages to anyone that would like more information. John is still taking Poly MVA

as well as other supplements and continues to eat 7-9 fruits and vegetables per day.
Best Wishes,
John and Judy
 
 

 

Source:  PolyMVA Survivors.com

Update on Mom (4/24/09)

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Well, it’s been a little bit of a rough week for us.  Mom had a follow-up appointment with Dr. Randall Porter, her neurosurgeon, on Monday morning.  The news wasn’t what we were hoping for.  The MRI she had last week has revealed three new lesions on her brain.  The good news is that the large lesion (and the two spots) that were treated in February with Gamma Knife are gone.  So, that’s really great news.  But, the fact that there are new ones is disappointing.

Mom is scheduled for another Gamma Knife treatment next Tuesday (4/28/09) at Barrow Neurological Institute’s Gamma Knife Center.  We believe this treatment will be much easier for Mom for a couple of reasons:

 (1) Her back is much better now and she is able to sit up without pain.  When she had the Gamma Knife treatment back in February she wasn’t able to sit up the whole time and she had to rest her head on the back of the halo (which hurt and caused the back screws to hurt quite a bit);

(2) She was a last-minute addition to the Gamma Knife schedule last time and we were there from 5:00 AM until after 6:00 PM.  They were wonderful to get her added to the Gamma Knife schedule that day and we’re very grateful for it.  But, this time, she’s not a last-minute addition, so we should get out of there quite a bit faster; and, finally,

(3) She’s not going to be admitted to St. Joseph’s Hospital after the procedure (like last time), so we should be home for dinner.  It’s an out-patient procedure and we’re really believing she’s going to have the best possible experience there this time.

Please keep Mom in your prayers as she goes back for another round of Gamma Knife next Tuesday.

On Monday morning, we’re heading over to the local hospital here in Mesa for her to have a chest CT scan to see how her lungs are doing.  We’re believing for good news on that front.  I’ll post when we know anything.

Today I filled out all the paperwork for Mom to be admitted to a study for the Poly-MVA.  There is information here on the blog (it has its own category) if you’re interested in more info on it.  Hopefully, we’ll hear something back pretty soon from them so she can get started on that right away.  The information we’ve read so far is very encouraging when Poly-MVA has been used on cancer patients.

The thing we’re hoping for most is that Mom will get some more energy once she starts taking it.  She’s been feeling pretty drained and it’s difficult to recover when you’re tired all the time.

I’m taking both Mom and Dad to their primary care physician tomorrow for an initial consultation with their new doctor.  We’ve seen one of the other doctors there in the office a couple of times, but we haven’t actually met their official primary care physician yet.  So, we’re looking forward to that.

Mom’s thumb is still pretty jacked up.  She end is still black, but it’s not weepy or weird.  Her Naturopathic Doctor thinks it’s doing well.  We’ll be setting up an appointment for her to see a hand specialist very soon so we can get it checked out.

Well, I think that’s about it for the moment.  As always, we appreciate all your prayers and kind thoughts for Mom.  It’s difficult for her to talk on the phone right now because she’s having some problems with laryngitis – which we’re getting checked out by an ear, nose, and throat specialist ASAP.  So, email works well for her.  We can print them out and read them to her.

I’ll post more info when I have any new info.

Until next time …

Tracey

Written by Tracey

April 24, 2009 at 1:17 am

Laetrile: The True Story Behind B-17 & Cancer Treatment

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Dr. Ernest Krebs

Dr. Ernest Krebs

During 1950 after many years of research, a dedicated biochemist by the name of Dr. Ernest T. Krebs, Jr., isolated a new vitamin that he numbered B-17 and called ‘Laetrile’. As the years rolled by, thousands became convinced that Krebs had finally found the complete control for all cancers, a conviction that even more people share today. Back in 1950 Ernest Krebs could have had little idea of the hornet’s nest he was about to stir up. The pharmaceutical multinationals, unable to patent or claim exclusive rights to the vitamin, launched a propaganda attack of unprecedented viciousness against B-17, despite the fact that hard proof of its efficiency in controlling all forms of cancer surrounds us in overwhelming abundance. Why has orthodox medicine waged war against this non-drug approach?

G. Edward Griffin, author of the book World Without Cancer contends that the answer is to be found not in science, but in politics, and is based upon the hidden economic and power agenda of those who dominate the medical establishment.

Each year, thousands of Americans travel to Mexico to receive vitamin B-17 (Laetrile) therapy. They do this because it has been suppressed in the United States. Most of these patients have been told that their cancer is terminal and that they have but a few months to live. Yet, an incredible percentage of them have recovered and they are living normal lives. However, the FDA, the AMA, the American Cancer Society, and the cancer research centres continue to pronounce that Laetrile is fraud and quackery. The recovered patients, they say, either had “spontaneous remissions” or never had cancer in the first place. If any of these people ultimately die after seeking Laetrile, spokesmen of orthodox medicine are quick to proclaim: “You see? Laetrile doesn’t work!” Meanwhile, hundreds of thousands of patients die each year after undergoing surgery, radiation, or chemotherapy, but those treatments continue to be touted as “safe and effective”.

In the U.S. the FDA has tried to use strict regulations, not law, to ban vitamin B-17 for over 18 years. Vitamin B-17, or Laetrile Therapy is only used by some hospitals in Mexico, which treat cancer with nutrition. These hospitals achieve nearly a 100% recovery rate with virgin cases (localised tumours/cancers that have not yet been burned up with radiation, poisoned with chemotherapy, or cut into with surgery). A majority of Laetrile-treated patients report positive responses, ranging from increase in the feeling of well-being and even brighter outlook of life, to such noticeable reactions as an increase in appetite, weight gain and, frequently, restoration of natural colour, reduction or elimination of cancer-connected pain and cancer-caused fetor. In thousands of cases, total regression of all cancer symptoms has been confirmed.

Vitamin B-17, commonly known as “Amygdalin”, or “Laetrile”, is a natural substance that can be found in a variety of species in the Vegetable kingdom. The greatest concentration is found in the seeds of the rosaceous fruits, such as apricot kernels and other bitter nuts. There are many seeds, cereals and vegetables that contain minimal quantities of vitamin B-17 and form part of our daily diet.

With great satisfaction we are proud to present this vegetable agent whose anti-cancer properties have been known empirically for many years, but in the last twenty years they have been scientifically proven, primarily through the clinical studies directed by Dr. Ernesto Contreras Rodriguez and carried out in the OASIS of Hope Hospital formerly known as the Centro Medico y Hospital Del Mar at Playas de Tijuana, B.C.N. Mexico. More than 100,000 patients have sought Contreras’ care since 1963.

The information on this web site will educate you on the benefits of metabolic therapy and prevention. All the food supplements mentioned in this site can be easily obtained by patients who are not able to go to Mexico because of financial reasons, patients who are too weak to travel, and by patients who have already been to these hospitals and need to remain on metabolic therapy. You will be taught how to benefit from metabolic therapy either in Mexico, or at home at a fraction of the cost. You will find information on where to obtain metabolic products in the “contacts” section of this site.

Throughout this web site you will find valuable information such as documents, research, and studies relevant to vitamin B-17, its monographic summary, clinical studies, the biological and chemical descriptions of the destruction of cancer cells by the components of B-17, testimonials, case histories, biographies, bibliographies, photos, graphs, links, and much more. This guide was created to explain the different elements of metabolic therapy and act as a reference when needed during the course of your therapy. Should you have questions, please refer to the “Frequently Asked Questions” section.

Source:  World Without Cancer

Update on Mom – 1/25/09

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Well, I think we’ve come through the valley and are coming out on the other side.  I just got back from the hospital and Mom is doing just great.

When I go there yesterday morning around 9:15 AM, they had just removed the ventilator tube and she was breathing on her own again.  She was very alert and said she was hungry.  So, the nurses said we could order up some food for her from the hospital kitchen.

Trying to eat a proper “cancer diet” in the hospital has been difficult in the past, but with Barrow Neurological Institute they allow you to order what you want from a menu.  So, Mom has been getting lots of fruits and veggies and some chicken and fish too.  She hadn’t been eating much meat, but since it’s a little too difficult for us to try to make protein shakes for her in the intensive care unit, we decided to just go with a little chicken and fish.

Mom ate a good lunch and dinner last night.  I think that made a world of difference for her.  Plus, Dad had cut up some organic pears and some organic veggies and brought them for her from home.  She gobbled those up while waiting for lunch yesterday.

She was slightly anaemic yesterday afternoon, so the doctor ordered two units of blood and she received those during the afternoon and evening yesterday.  Her color did “pink up” a little bit after that.

Her nurses have been the best we’ve ever had.  They are all so caring and nice to Mom (and to the rest of us too).

Mom had a great night’s sleep last night.  She took little cat naps throughout the day yesterday, and then slept for six hours straight last night.  That might not seem like a big deal – but getting a stretch of sleep that long in the hospital can really be a miracle.

She wasn’t aggitated at all during the night and she slept like a baby until 6:00 AM this morning when one of the doctors came in to do a neurological evaluation of her.  She passed with flying colors.

She’s been in good spirits all day today.  The doctors are a little concerned about the platelets in her blood and are changing her anti-seizure medicine to see if that will correct the problem.

She’s slated to be moved out of the Neuro ICU and into a regular room later today – that is if the doctor feels that the platelet issue is resolved.

At this point, we’re going to believe that Mom is going to be right on schedule for her Gamma Knife treatment next Thursday – so she can be home in time for the Cardinal’s SUPERBOWL game!!  Go Cardinals!

I’m going back to the hospital tomorrow – so, I’ll post a new update when I get home.

Written by Tracey

January 25, 2009 at 5:55 pm