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Turmeric could Be The World’s Most Important Herb.600 reasons why.PLEASE SHARE.

Tuesday, November 14th, 2017

This article was supplied by herbs-info.com

We found a simply astonishing page all about Turmeric and had to share! I honestly think it is one of the best pages about a herb I have ever seen (and I’ve seen a fair number!) The link is after our commentary.

There are several things that are amazing about the page we discovered. First – of course – the fact that there is scientific research to support the notion that turmeric may be beneficial for a staggering 600+ conditions. It is one of the world’s most studied items for medicinal potential, with over 4000 scientific studies being recorded overall.

Then there is the fact that the mighty turmeric has been in use for over 6000 years, with an incredible safety record. Note also, the effects of turmeric have been found by scientists to be greatly enhanced when it is taken in combination with black pepper (see our report here – Substance In Black Pepper Increases Bioavailability Of Beneficial Turmeric Compounds by 2000% )

Even more amazing is the way the article weaves a crystal-clear narrative that exposes the farce behind the fact that the modern medical world will perhaps never approve turmeric “officially” for medical use. It explains clearly that “proof” is effectively only purchased by those with very deep pockets (802 million dollars on average is the cost for obtaining a new drug approval). [1] The situation is a complete joke. Turmeric is clearly and obviously one of the most benign and beneficial things in the known universe.

But most amazing of all, to me, was the comment from the man who states calmly that he is one of the world’s longest survivors of the kidney transplant operation (34 years since the op, the world record is 40 years) and he takes capsules of turmeric (and other herbs) daily. Truly inspiring stuff.

The original article is fantastic, electrifying even – and we encourage you to share this article www.newcures.info  far and wide. Here’s the link: http://www.greenmedinfo.com/blog/600-reasons-turmeric-may-be-worlds-most-important-herb

www.foodpassions.net

Henry Sapiecha

HUGE LIST OF HERBS USED FOR DISEASE TREATMENTS CURES & BENEFITS-SHARE

Tuesday, November 14th, 2017

This information has been supplied by herbs-info.com

List Of Herbs

On this page you will find our alphabetical list of 150+ 189 herbs! Every herb in our list has its own dedicated page on this site – with pictures and very detailed info! Follow the links to learn more about each herb. The goal of the individual herbs’ pages is to gather information about the plant in one place, so that anyone researching it can have quick access to information.

Please bookmark this page so that you can use it as a “quick lookup” when you want to learn all about a herb. You can also share our image on Facebook and Pinterest. Each herb page follows a similar format – starting with names for the herb in different languages, then giving background and history, common and traditional uses of the herb, scientific research, esoteric uses and safety notes.

Our method of organization intentionally follows the style of the old herbals, which listed the plants in alphabetical order and often compiled the writings of other herbalists from past times. There is much material to work through and so this list is continuing to expand. Ok, here is the list!

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The Herbs:There are many more to yet come.

Agrimony | Ajwain | Alfalfa | Alkanet | Allspice | Aloe Vera | Althaea Officinalis (Marsh Mallow) | Amla | Angelica | Angostura | Anise | Arabian Jasmine | Arnica | Arrach | Artemisia | Asafoetida | Ashwagandha | Bacopa Monnieri | Bashful Mimosa | Basil | Bay Laurel | Bean | Bears Breech | Belladonna | Benzoin | Bergamot | Betony | Bilberry | Bitter Melon | Black Pepper | Blackberry Bush | Blumea Camphor | Boneset | Borage | Brooklime | Bryony | Bugle | Burdock | Butterbur | Cacao | Cajeput | Calendula | Canella | Capers | Cardamom | Carob Tree | Cascara Sagrada | Cascarilla | Catechu | Catnip | Cat’s Whiskers | Catsfoot | Cayenne | Cedron | Celery | Centory | Chamomile | Cheken | Chervil | Chinese Honeysuckle | Chives | Cilantro | Cinnamon | Clavo Huasca | Clove | Coltsfoot | Comfrey | Contrayerba | Copal | Cordyceps | Cumin | Daffodil | Damiana | Dandelion | Deadly Nightshade | Dill | Dittany Of Crete | Dodder | Dragon’s Blood | Echinacea | Elder | Epazote | Female Peony | Fennel | Fenugreek | Feverfew | Five Leaved Chaste Tree | Flax | Frankincense | Galangal | Garlic | Gentian | Ginger | Gingko Biloba | Ginseng | Goat’s Rue | Goji | Golden Seal | Gotu Kola | Green Tea | Guarana | Guava | Hearts Ease | Heavenly Elixir | Hedge Nettle | Henna | Hibiscus | Hollyhocks | Holy Basil | Holy Basil | Honeysuckle | Hops | Horny Goat Weed | Horseradish | Horsetail | Hyacinth | Indian Laurel | Jew’s Mallow | Juniper | Kava | Ladies Mantle | Lady’s Thistle | Lavender | Lead Tree | Lemon Balm | Lemongrass | Lesser Calamint | Licorice | Lily of the Valley | Male Satyrion | Marjoram | Milk Thistle | Moringa | Mountain Apple | Mugwort | Mullein | Neem | Nelumbo Nucifera | Nutmeg | Nymphaea Caerulea | Onion | Oregano | Orris Root | Paprika | Parsley | Passion Flower | Patchouli | Pepper Elder | Pimiento Pepper | Plantain | Primrose | Queen’s Flower | Red Clover | Reishi | Rhubarb | Ringworm Bush | Rooibos | Rosemary | Rue | Saffron | Sage | Savory | Saw Palmetto | Seaweed | Senna | Slippery Elm | Snake Needle Grass | Snakeweed | Soapnuts | Solomon’s Seal | Spearmint | Spiny Sapindus | St. John’s Wort | St Thomas Bean | Star Anise | Starfruit | Stinging Nettle | Sumac | Sweetsop | Tamarind | Tarragon | Tea | Thyme | Turmeric | Uva-Ursi | Valerian | Vanilla | Vervain | Water Hyssop | Wild Oregano | Wild Tea | Witch Hazel | Yarrow | Yerba Mate |

www.foodpassions.net

Henry Sapiecha

Substance In Ginger Found 10,000x As Effective as Chemo Against Breast Cancer Stem Cells

Tuesday, November 14th, 2017

An intriguing and possibly highly important study [1] has recently been published regarding the action of 6-shogaol (a ginger compound) against cancer cells. This study has been “doing the rounds” on social media but in many cases it has been misreported and highly misrepresented – either through misunderstanding of the (admittedly a little complex) science involved – or through deliberate exaggeration of the facts in order to create “headline sizzle”. Many of the social media articles we saw did not even link to the original research!

We’re going to do our best to clear it all up for you today, “joining the dots” with some of the other amazing research that is being done in this field and attempting to interpret the studies in terms that both make sense to the lay person and won’t offend persons of science.

Short Summary:

The quick takeaway for those in a hurry: 6-shogaol, a compound in ginger, has been found to have amazing activity against breast cancer cells in cell cultures in the lab – including action against simulations of “stem cells” – the “mother ship” of cancer cells that chemo showed no activity against even at 10,000x concentration. The action of 6-Shogaol against the cancer cells happens at concentrations that do very little harm to healthy cells. Other studies have shown that these ginger compounds are bio-absorbed but are converted into other forms in the body, leaving some uncertainty as to whether these new forms are as active, more active or less active against actual cancer. Recent research however has found a strong possibility that ginger may have an actual anti-cancer action in vivo, leading us to conclude that ginger should be considered a prime candidate for inclusion in an “anti-cancer diet” (subject to approval from your physician of course! We have to say this; we do not make actual medicinal recommendations for legal reasons.)

Ginger Compound vs. Chemotherapy (Taxol):

In this in vitro study, 6-Shogaol showed astonishing activity against “spheroids” – stem cell-like simulations – against which taxol (standard chemotherapy treatment derived from yew tree) showed no activity at even 10,000x the concentration. [1] The inability of taxol to kill the stem cells has been a past stumbling block of cancer therapy. 6-shogaol was found “only” 2 to 5 times as active than taxol against the “regular” breast cancer cells (still an impressive result).

What’s really awesome is that 6-shogaol showed high selectivity – and normal (non-cancerous) cells showed strong resistance to it even after 6 days. 6-shogaol was effective in killing both breast cancer monolayer cells and spheroids at doses that were not toxic to noncancerous cells. [1]

This study adds to the impressive list of studies in which ginger compounds have been found highly active against cancer cells in vitro while also showing very high selectivity, not harming normal / healthy cells.

However what remains to be fully understood (this is an essential point) is the bioavailability of 6-shogaol after digestion. In other words, an in vitro study such as this does not indicate whether or not eating ginger will do you any good, because if 6-shogaol is broken down by stomach acids, it is unlikely to reach its intended site anyway. Even if it does make it into the bloodstream – how will it “get inside” the cancer? The “metabolic fate” of compounds which destroy cancer cells in in vitro studies are often overlooked by the casual researcher (and the numerous social media outlets reporting on such matters) – and so the “first step” in your education on this matter should be to understand that an in vitro study such as this cannot be considered as evidence in any way that the nutrient will have an effect on cancer.

That said, it might. We did a little research…

Ginger Phytochemistry:

The chemical constituents of ginger (and ginger supplements) have been known for some years [2][3]. 6-shogaol is one of the 4 main pungent constituents of ginger [4] (the others are 6-gingerol, 8-gingerol and 10-gingerol. Shogaols are chemically similar to gingerols – being the dehydrated form thereof. Interestingly, Shogaols are found in only small quantities in the fresh root and are mainly found in the dried and thermally treated roots; with 6-shogaol becoming the most abundant of these constituents when ginger is dried or cooked. [5] There are smaller amounts of other gingerols, shogaols and many further compounds in ginger; these are largely untested but may contribute significantly to the health benefits of the whole root.

Bioavailability Of 6-Shogaol:

As it happens, a 2010 study has investigated the bioavailability of 6-shogaol. [4] Their notes reported first of all that prior to that study, few studies had examined the bioavailability of 6-Shogaol. They stated: “Despite ginger being investigated in over 30 clinical trials in humans with over 2300 subjects, only a handful of studies in rats and our study in healthy volunteers have examined the absorption, bioavailability, metabolites and elimination of ginger constituents. In rat studies, only two of the pungent

compounds, 6-gingerol and zingerone, have been investigated, and in two of the rat studies 6-gingerol was administered as an intravenous bolus, which is unlikely to be reflective of usual oral dosing. Moreover, until we conducted a study in healthy volunteers no pharmacokinetic studies have been conducted in humans nor had any studies in mammals or in vitro examined the other major pungent constituents, namely 8- and 10-gingerols and 6-shogaols.” [4]

A further study from the same team studied 6-shogoal in a clinical trial to determine whether it is passed to the bloodstream intact. [6] It was found that 6-shogoal is absorbed by the body after oral dosing but is bio-converted (either in the liver or intestinal mucosa, researchers were not sure) to glucuronide conjugates – which can be detected in serum for a few hours after ingestion; before being eliminated by the body’s natural processes.

The researchers summarized succinctly here: “In [previous] study, 6-shogaol [had been] found to induce apoptosis, autophagocytosis and growth inhibition in ovarian cancer cells at 2.21 μg/mL (7.5 μmol/L). All of these in vitro studies required higher concentrations of free ginger constituents than found in the serum in this study – putting the clinical validity of these and similar studies in question. However, gingerols and shogaols may reach higher serum concentrations within target tissue compared to serum, e.g., gut. Ginger conjugates may also be as or more biologically active compared to parent compound. Clearly, further research is needed to answer these questions and determine the cancer prevention relevance of ginger.”

Action Of Ginger Compounds Against Cancer In Vivo:

This research appears to be underway and we are getting closer to a positive result: A further study from the esteemed Oxford University Press, published in Carcinogenesis (2014) [7], has found astonishing synergistic results for the anti-cancer use of whole ginger extract in vivo against human prostate cancer cell lines – demonstrating that ginger extract “showed 2.4-fold higher tumor growth-inhibitory efficacy than” isolated constituents. In addition, gingerol glucuronides were detected in feces upon intravenous administration confirming hepatobiliary elimination. [7]

This important result from a prestigious journal is a “double-win” for herbalism – being not only highly indicative that ginger metabolites may possibly be bioactive against cancer cells in the human body, but also demonstrating the importance of preserving the natural composition of whole extracts.

We await further study with anticipation! In the meantime, ginger is generally recognized as a healthy, safe addition to the diet and one noted by innumerable studies for its health benefits and potential for protection against disease. I believe that those considering an “anti cancer diet” should (with the advice of their physician) hold ginger in high esteem in both raw and dried/cooked form.

The message here is clear: Nature works best when not tampered with – and it makes sense. After all, we did evolve over hundreds of thousands of years in a pure natural environment. Researchers are starting to catch up to what herbalists have known all along – that we are bioattuned to nature and literally “designed by evolution” to thrive on food in the most natural state possible.

Finally – if you happen to chance upon headlines “ginger 10000x as effective as chemo”… now you know the actual facts…

.

Further reading:

Our full “Herbal Report” on ginger.

10 Amazing Health Benefits Of Ginger

Scientists Find Substance In Ginger Kills 91% of Leukemia Cells and Shrinks Tumors in Vivo

References:

[1] 6-Shogaol Inhibits Breast Cancer Cells and Stem Cell-Like Spheroids by Modulation of Notch Signaling Pathway and Induction of Autophagic Cell Death. PLOSone (Sept 2014). http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0137614 (Full Text)

[2] Fresh organically grown ginger (Zingiber officinale): composition and effects on LPS-induced PGE2 production. Phytochemistry (2004). http://www.ncbi.nlm.nih.gov/pubmed/15280001

[3] Identification and Quantification of Gingerols and Related Compounds in Ginger Dietary Supplements Using High Performance Liquid Chromatography-Tandem Mass Spectrometry. J Agric Food Chem (2010). http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2783668/ (Full Text)

[4] Quantitation of 6-, 8- and 10-Gingerols and 6-Shogaol in Human Plasma by High-Performance Liquid Chromatography with Electrochemical Detection. Int J Biomed Sci. (2010). http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2975369/

[5] 6-Shogaol https://en.wikipedia.org/wiki/Shogaol

[6] Pharmacokinetics of 6-, 8-, 10-Gingerols and 6-Shogaol and Conjugate Metabolites in Healthy Human Subjects. Cancer Epidemiol Biomarkers (2009) http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2676573/ (Full Text)

[7] Enterohepatic recirculation of bioactive ginger phytochemicals is associated with enhanced tumor growth-inhibitory activity of ginger extract. Carcinogenesis (2014). http://www.ncbi.nlm.nih.gov/pubmed/24431413

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Henry Sapiecha

Killer cancer we know very little about

Sunday, November 12th, 2017

Kristin Washbourne thought she was doing all the right things to cure what she thought was indigestion. Then she was given a two per cent chance of survival

AT 45, worn out from chasing after two small children and sometimes neglecting to take care of herself, Kristin Washbourne didn’t even think to question her GP when he told her the abdominal pain she had been experiencing was probably indigestion.

She accepted the diagnosis, went to the chemist for some antacids, and promised to take better care of herself.

It wasn’t until loading up on yet more packs of the indigestion tablets, that a very insistent young pharmacist warned her that if she’s been taking the treatment for more than 10 days she had to see her doctor about it.

She’d been popping the over-the-counter pills daily for almost a full year.

“Over that year I had been mentioning the pain to my doctor, but also blowing it off a bit and blaming myself,” she told news.com.au.

“I was a bit overweight, not exercising as much as I should, but I sort of kept downplaying it, but after that I asked him to send me off and get tests for ulcers and bacterins that caused ulcers.”

The tests didn’t eventuate, instead Kristin made another promise to take better care of herself.

But a little while later, after a week of extreme fatigue during the summer holidays – barely being able to move for the pain, and feeling like she could only feel OK if she didn’t eat – Kristin began taking the symptoms a bit more seriously and had her husband rush her to the emergency room.

A lick of fake tan had concealed her yellowing skin, and through her tiredness she didn’t notice her eyes had gone a creamy colour.

This picture was taken a couple of days after Kristin Washbourne was diagnosed with pancreatic cancer and given a two per cent shot at survival. She hadn’t even realised her skin and eyes were turning yellow. Picture: Kristin Washbourne

This extreme jaundice, combined with the stomach pains, the fatigue, and some strange bowel movements, all pointed to one thing: pancreatic cancer.

“It was something that I had never even thought of, and looking back now, even when I got the diagnosis, it makes me realise how much I didn’t know,” she said.

Instead of freezing at the word cancer, Kristin said she felt strangely relieved. She thought: “They cure cancer these days, I guess I’ll be fine.”

But what Kristin didn’t know then, and what most Australians aren’t aware of, is that when it comes to pancreatic cancer, there’s no such thing as an easy fix.

It is one of the most aggressive cancers with one of the lowest survival rates.

Of the nine people diagnosed in Australia every day, only one is likely to survive.

When Kristin was diagnosed, just five years ago, she was give a two per cent chance at survival.

On average, when an Australian is diagnosed with the disease, they’ll only have six months to live.

It was the terrifyingly low instances of survival from pancreatic cancer that make Kristin not only lucky to be alive, but also made her journey so difficult.

Even though she was given such a dark prognosis, her treatment was successful and she never felt as sick as she thought she should.

After a gamut of tests and surgery that left her with a scar from her pubic bone to her sternum that made Kristin look “all zipped up”, she cried for 48 hours, didn’t sleep for days, and stayed in hospital for weeks.

Kristin’s daughter Marla has dyed her hair purple to raise awareness for pancreatic cancer. Picture: Kristin Washbourne

Eight rounds of chemo and radiation left her “knocked out” for months, but every step of the way she was just thinking, it could be a lot worse.

As she went through her recovery, Kristin’s understanding of the seriousness of the disease continued to develop, and she realised how lucky she was.

“The pain (from the surgery) was incredible, the recovery from that was just unbearable, but it eventually was over and I felt pretty much OK,” she said.

“In my recovery, I had a really bad feeling of survivor guilt. I lost 30kg, There were months when I was basically bedridden, completely knocked out by steroids, but every step of the way I knew most other people didn’t make it to that stage.”

When Kristin started to feel better, things began to get even more uncertain.

“The trouble is for me, once I started getting better, it gave me a boost when the oncologist was pretty happy that I was still around so I thought maybe I was here for good,” she said.

“So what I wanted to know was, what happens next? But I couldn’t find any survivors to talk to. No one could tell me what was going to happen, how my life would change, if I would carry on as normal.

“It was a really hard time. I was so desperate to talk to someone to find out what happens next, but the survival rates are even lower than the awareness rates when it comes to this disease.”

Five years on from her diagnosis and fighting fit, Kristin has accepted that she is a survivor, and feels the responsibility to use her experience to help people who have been diagnosed, and those who may be delaying diagnosis like she did for so long.

“The thing about this disease, is there is no reason for it. There’s not like a family history as with breast cancer so you know to get checked, there’s no really obvious or specific symptoms like with bowel cancer or prostate cancer,” she said.

“The only hope now is to know the symptoms, and know if someone’s telling you they’ve got indigestion, if it persists, then go and do something. That’s the only way we’re going to catch it.”

Even when she lost weight and was going through chemo, Kristin’s cancer experience was nothing like what she expected. Picture: Kristin Washbourne

St Vincent’s Hospital pancreatic cancer specialist Dr Lorraine Chantrill says the reason pancreatic cancer doesn’t get the same level of awareness as some others with lower death rates, is the same reason Kristin found it difficult to find answers about her recovery.

“The main reason it doesn’t get that recognition is because people die from it,” she said.

“There are very few people who survive who can go on to campaign for it. The other cancers that have got a lot of visibility are cancers that people survive.”

Dr Chantrill says recognition and awareness around the disease are “getting better”, and it’s rising in line with survival rates.

Having the unenviable badge of one of the worst cancers is getting it noticed as well.

But while recognition is increasing, the symptoms are still vague and hard to pin down.

“It’s a cancer that generally presents in people who are older than 60, it often presents with some vague symptoms like upper abdominal pain, but in people who develop diabetes without being overweight, people who have change in their bowel habits of suddenly lose weight for no reason, we want those people to keep persisting with their doctor and to go and get tests,” she said.

“I think we can start to end the nihilism around pancreas cancer and start actually making a difference and it’s thanks to some really brave people who have participated in research.”

This coming Wednesday is world pancreatic cancer day. The Sydney Opera House will be lit up in purple lights and landmarks across the world will follow.

Kristin’s daughter, Marla, has died her hair purple ahead of the day, and Kristin will wear purple clothing.

Whenever anyone asks them why, they’ll start the conversation Kristin, Dr Chantrill and others affected by pancreatic want Australians to start having.

“If people start talking about it, and people start being aware of it, that’s going to lead to more awareness, more fundraising, more research, and more survivors,” Kristin says.

Leah in hospital after the cancer diagnosis. Picture: 60 Minutes

Mr Debono said the image of Leah in hospital after she had been diagnosed with a brain tumour “haunts me”.

“I never thought I would be thrown into any of this,” he said.

“I was holding onto her till the end.”

He and Leah’s parents are desperately trying to figure out how the medical system could fail the young Aussie, who was told she was cancer-free.

“We watched her take her last breath. You don’t ever want to have to go through something like that, it’s really cruel,” Leah’s father, Lex, told 60 Minutes.

“The GP looked at it, assured her that there was nothing … Some trained professionals may not have done their job properly.”

They are also sharing Leah’s story to spread awareness around melanoma and warn Australians about the risks of this deadly disease.

Henry Sapiecha

ENZYMES FROM PINEAPPLE THAT DESTROY CANCER CELLS

Tuesday, September 19th, 2017

So what is this secret weapon?

Enzymes.

Dr. Wright explains that cancers are smart.

It’s because they’re experts at hiding for long periods of time. Most don’t need oxygen to live. And even when we “kill” cancer with conventional treatments, if just one cell survives…

It’s likely to start the disease process all over again.

As Dr. Wright explains, cancers are “built to survive.”

You see, cancers are able to hide because they have a secret “cloaking device.” It’s called fibrin.

It’s the same stuff scar tissue is made from. And cancer cells are covered in it.

Think of fibrin like a shield of armour.

This armor protects the cancer cells from anything that tries to destroy it.

It doesn’t matter if it’s your body’s natural defenses (like natural killer cells or white blood cells) or chemo drugs…

That fibrin is like a fortress, keeping cancer-killing soldiers out.

Fibrin is a sticky protein that forms a web of scar tissue around injuries. And that’s a good thing if you have an injury.

But here’s the problem: Inflammation causes your body to OVERPRODUCE fibrin in a big way

Check out the research published in the journal Medical Hypotheses:

“The tumor dons a ‘coat’ of the host’s own protein on its cell surface. The coat is composed of fibrin and of a polymeric form of human serum albumin (HSA)… Such a coated tumor appears as ‘self’ to the immune system, and thus is not detected as a tumor by the immune system…

When tumors are prepared for in vitro assays against drugs, they are routinely treated with proteolytic enzymes… which dissolve the protein coat, exposing the tumor cell surface to the drug.”

The reason why some cancer drugs may appear to work in laboratory testing and then fail to work in real people may be due to the cancer shield — it’s broken down with proteolytic enzymes during the lab tests but not in the real world, unless, possibly, the patients happen to be taking proteolytic enzymes.

Enzymes have been used in studies of cancer treatment before.

***In 2007, an animal study published in the journal Planta Medica found that

In 2007, an animal study published in the journal Planta Medica found that bromelain, an enzyme found in pineapple cores, treated cancer better than a chemotherapy drug — without toxic side effects.

Your Best “Weapon” to Fight Inflammation

The “proteolytic enzymes”  are your body’s MOST POTENT WEAPON against chronic inflammation.

And the chronic inflammation that proteolytic enzymes fight are also behind many of today’s most dangerous diseases, including:

> Various forms of cancer

> Heart disease

> Arthritis

> Alzheimer’s

> Chronic fatigue  

> Allergies  

> Fibromyalgia  

> COPD  

> Multiple skin diseases

And many more!

The proteolytic enzymes have even been shown to help heal varicose veins… keloids… other scar tissue… age spots… and much more!

Now this isn’t because it’s some “magical cure-all.”

It’s because proteolytic enzymes are produced naturally in your body and are designed to do the “pain-stopping, disease-fighting heavy-lifting”…

But the older you get, the more DEFICIENT in these proteolytic powerhouses you become.

Henry Sapiecha

Protein converts pancreatic cancer cells back into healthy cells

Wednesday, September 13th, 2017

Scientists working in the area of pancreatic cancer research have uncovered a technique that sees cancerous cells transform back into normal healthy cells. The method relies in the introduction of a protein called E47, which bonds with particular DNA sequences and reverts the cells back to their original state.

The study was a collaboration between researchers at the Sanford-Burnham Medical Research Institute, University of California San Diego and Purdue University. The scientists are hopeful that it could help combat the deadly disease in humans.

“For the first time, we have shown that over-expression of a single gene can reduce the tumor-promoting potential of pancreatic adenocarcinoma cells and reprogram them toward their original cell type,” says Pamela Itkin-Ansari, adjunct professor at Sanford-Burnham and lead author of the study. “Thus, pancreatic cancer cells retain a genetic memory which we hope to exploit.”

For their research, the scientists developed pancreatic cancer cells with heightened levels of the E47 protein. They found that the protein then controlled genes responsible for growth and differentiation. It halted the cancer cells in the growth stage and caused them to revert back to acinar cells, the healthy cells that produce pancreatic juice.

The researchers also conducted in vivo studies where the reprogrammed cells were introduced into mice. They found that the animal’s propensity to form tumors was substantially less than those with regular pancreatic cancer cells.

“Our next step is to test primary patient-derived tumor tissue to determine whether E47 can produce similar results, potentially providing a novel therapeutic approach to combating this highly lethal disease,” says Itkin-Ansari. “Additionally, we are screening for molecules and potential drugs, that can induce over-expression of E47.”

The research was published in the journal Pancreas.

Source: Sanford-Burnham Medical Research Institute

Henry Sapiecha

Potent Plant powder power prevents malaria victims from dying

Monday, May 8th, 2017

So what is this plant?

Weathers has made several high-producing versions of the plant using tissue cultures  (Credit: Worcester Polytechnic Institute)

When 18 malaria patients in the Congo failed to respond to conventional treatments and instead continued to head toward terminal status, doctors knew they had to act fast – and try something different. So instead of turning to more synthetic drugs, they turned instead to nature and found a solution that delivered remarkable results.

The patients were first treated with the regimen described by the World Health Organization (WHO): artemisinin-based combination therapy (ACT). This drug combines an extract from a plant known as Artemisia annua, with other drugs that launch a multi-pronged attack on the malaria parasite. But just as is the case with antibiotic-resistant bacteria, the malaria parasite is evolving to resist the drugs designed to kill it. In fact, according to the WHO, three of the five malarial parasites that infect humans have shown drug resistance.

As the patients continued to decline, with one five-year-old even entering into a coma, the doctors administered a drug called artesunate intravenously, which is the preferred course of action when treating severe malaria. The treatment didn’t work.

Finally, doctors turned to the Artemisia annua plant itself. Also called sweet wormwood or sweet Annie, the plant is the source of the chemical artemisinin, which is used in ACT therapy. The plant has been used since ancient times in Chinese medicine to treat fevers, although this bit of knowledge was lost until 1970 when the Chinese Handbook of Prescriptions for Emergency Treatments (340 AD) was rediscovered. In 1971 it was found that extracts from the plant could fight malaria in primates.

Pamela Weathers, professor of biology and biotechnology at Worcester Polytechnic Institute began researching Artemisia annua over 25 years ago. Along with postdoctoral fellow Melissa Towler, Weathers created a pill made from nothing more than the dried and powdered leaves of the plant. When the pills were given to the 18 dying patients over the course of five days, all of them completely recovered, with no trace of the malaria parasite remaining in their blood.

“These 18 patients were dying,” Weathers said. “So to see 100 percent recover, even the child who had lapsed into a coma, was just amazing. It’s a small study, but the results are powerful.”

Weathers had previously shown that the dried leaves of the Artemisia annua plant (DLA) could deliver 40 times more Artemisia annua to the blood than extracts of the plant alone. In a later experiment, she showed that not only could the leaves beat drug-resistant bacteria in mice, but that after passing the malaria parasite through 49 generations of mice, the parasite still showed no resistance to the plant.

While the exact mechanism through which DLA operates is unclear, Weathers says it’s likely due to the intricate chemical dance that occurs between the phytochemicals in the leaves.

Weathers with the Artemisia plant (Credit: Worcester Polytechnic Institute)

Because the drug is inexpensive and relatively simply to produce, Weathers also says that it could be a source of industry for people living in the areas where malaria is a problem, such as Ghana, Kenya and Malawi where it was recently announced that the first malaria vaccines will be deployed. “This simple technology can be owned, operated, and distributed by Africans for Africans,” said Weathers, who has already established a supply chain on the continent for the leaves using local producers.

Weathers also said that further research into DLA could lead to effective ways to combat other maladies.

“We have done a lot of work to understand the biochemistry of these compounds, which include a number of flavonoids and terpenes, so we can better understand the role they play in the pharmacological activity of the dried leaves,” Weathers said. “The more we learn, the more excited we become about the potential for DLA to be the medication of choice for combatting malaria worldwide. Artemisia annua is known to be efficacious against a range of other diseases, including other tropical maladies and certain cancers, so in our lab we are already at work investigating the effectiveness of DLA with other diseases.”

The results of the case in the Congo have been described in the journal Phytomedicine. You can hear more from Weathers in the video below.

Source: Worcester Polytechnic Institute

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Henry Sapiecha

 

CANSEMA INDIAN BLACK SALVE TREATMENT FOR CANCERS HOW TO USE & A BREAST CANCER SUCCESS STORY

Monday, November 28th, 2016

Amazing: Woman Cures Breast Cancer with Black Salve

 Breast Cancer Tumour-3 image www.newcures.info
You’re entitled to have a giggle at this should you feel inclined to do so …
It’s now just over two weeks ago since I removed my large breast tumour using black salve. The tumour came out in 2 stages, the smaller part after 20 days and the much larger part on day 28. The day after the large part of the tumour came out I hand delivered the breast tumours to the hospital, preserved in a jar of Regan’s best polish vodka (much to his dismay). The surgeon, a very amiable Irish chap, appeared quite dumbfounded and made very little comment. I was accompanied by my mum, Eileen, who with such genuine excitement at the whole event pipes up – ‘Isn’t is marvelous doctor, hasn’t she done well?’ – to which he politely refused to comment. I was keen to have the sample sent for histology in order that it would be documented in my hospital records. He agreed to do so, and he sent a follow up letter to my GP with comments as follows…
‘This lady was seen in breast clinic today. She has a history of left breast cancer, she declined operative therapy and opted for alternative remedies.
She attended clinic today with, what appeared to be, 2 pieces of breast tissue. She had been applying herbal remedies to the area and this appears to have enucleated the tumour from the breast.
She is anxious to have these sent to the lab…I have explained that they may give us limited information as she has preserved it in vodka, but we have agreed to send it and await the outcome.’
I love that word ‘enucleated’ – I even looked it up for the official medical definition:
‘removal of tumour from surrounding tissue without rupturing’.
‘Enucleation is a surgical process during which only the tumor cells are removed.’
‘To remove (a tumor or eye, for example) whole from an enveloping cover or sac.’
I went to the breast clinic yesterday to see the surgeon to get the histology report. It confirmed the obvious, i.e. that the tissue I had removed with the black salve was cancerous breast tissue – it’s just good to have it authenticated for my medical records. I have asked for them to send me the full histology report, they agreed to post it on to me.
My wound is healing up amazingly well – it’s looking great! I am overwhelmed at the body’s capacity to heal. The hole had filled up within 3 days, new skin had covered the wound after a week, and now the wound area is reducing in size on a daily basis. I may yet go topless sunbathing again! (though not in front of my teenage son – he gets far too embarrassed).
I’m still on my strict diet and protocol, and will still be closely monitoring my left breast, especially bearing in mind I’ve still got a small tumour left in there, but I’m very confident that it’s all looking very positive.
Picture 1 – Tumour that came out on  (Day 20)
Breast Cancer Tumour-1 image www.newcures.info
Picture 2 – Tumour that came out on (Day 28)
Breast Cancer Tumour-2 image www.newcures.info
Picture 3 – The wound on  (Day 28)
Breast Cancer Tumour-3 image www.newcures.info
Picture 4 – The amazing healing process –  16 days after tumour came out 
Breast Cancer Tumor 4Breast Cancer Tumour-4 image www.newcures.info

How To Use Black Salve:

**Please Note**much of the info below was received from Alpha Omega Labs, a company that sold black salve under the commercial name “Cansema” which was very successful in treating skin cancers before the FDA shut them down. There are a select few quality black salves that are still on the market today, like those found at:

As Alpha Omega Labs stated, the products found at risingsunhealth.com and bloodrootproducts.com are NOT quality salves and are a waste of money, like many others being marketed as true black salves. As with any ailment, it is important to seek out the advice and treatment of a qualified physician. This site is purely for educational purposes. Information found in this site is not intended to diagnose, treat, cure, or prevent any disease. Many of the comments found on this site have not been evaluated by the FDA, FTC, AMA or any other US government regulatory agency. Please read ALL of the following information for better understanding of the process!

The medical definition of “cure” is the non-reoccurrence of pathology within five years after treatment. By the very definition used by orthodox medicine, black salve is empirically a proven cure for skin cancer for the majority of those who use the product according to our instructions.

Effective black salve ingredients include blood root and zinc chloride at a minimum. Often, black salve will also include other immune boosting herbs such as chaparral, red clover, galangal and graviola.

After Reading ALL of the directions below FIRST, you will want to watch the first video on this page:
 
1. PREPARATION
First, as stated earlier, the user may want to have a biopsy or other diagnostic procedure performed to ascertain whether or not there is, in fact, skin cancer.
Many people, on the observation that they have a “mole” or similar skin marking that is growing and getting darker, have elected to use black salves anyway. After all, black salve is selective in its action and will only “go after” neoplastic (cancerous) tissue. Healthy tissue will only redden and become mildly irritated when black salves is applied. This decision is entirely at the discretion of the user; there is no danger, toxic or otherwise, of applying black salves to healthy tissue, although doing so is simply a waste of the product.
In addition, if you are targeting more than one growth, do one at a time and never apply to a spot larger than a USA quarter.
2. APPLICATION
Black salve comes in a 1/2 oz. container. The product has the consistency of a thick, moist paste. It can easily be self-applied with the fingers and should be spread over the lesion or cancerous tissue in a thin covering, almost lightly “caked.” Wash hands thoroughly before and after applying Black salve.
The applied area will start to tingle shortly afterwards — anywhere between 5 minutes to 6 hours after the initial application. (In fact, if you feel “nothing” after three to six hours, it is most likely that nothing more will happen: Black salve has failed to come into direct contact with the cancer or there is no cancer present. If after 24 hours there is no burning, stinging or pulling sensation, you will want to remove the Black salve, follow the suggestions below in steps 2A, then  reapply, repeating this process, until the Black salve can reach and “grab” the underlying aberrant growth.) If the black salve takes hold and causes a burning, stinging or pulling sensation, then let the rest of the process play out..DO NOT WASH THE SALVE OFF, LET IT BECOME PART OF THE ESCHAR/SCAB THAT FORMS!  In some cases, there is a burning sensation with larger lesions (larger than a USA dime, so it is important to have ibuprofen, or other non-prescription pain killer, available during the process. Note: the moment the eschar falls out, usually within 7-14 days of the initial application, the pain will immediately stop! Areas larger than a square centimeter (or bigger than a U.S. “dime”) may require even stronger analgesics, which, being prescription, will require the services of a cooperative physician.
Otherwise, observing good “pain management” may require that the cancer be “taken out in stages.” This involves applying a small amount to the edge of the growth, waiting for the sensations to die down as the eschar process begins, and then repeating this process on an adjacent area of skin until the entire area has been covered. Observe this same procedure if you are targeting more than one growth.
Do one at a time. In this fashion, any discomfort is minimized because the entire process, which can at that point last several days, has been spread out over time. This bears repeating: never apply Black salve to a large area, unless you are under a physician’s care and advice.
 
It is also a good idea to place a bandage over the area, particularly if the forming eschar is on a place on the body that might be subject to being bumped or bruised in the course of daily activity. Another thing to consider is that Black salve can stain clothing, so for practical, aesthetic, and cleanliness issues, covering the site is a good idea.
” . . . I applied Black salve and no eschar appeared! . . . What do I do now?”
Black salve has to come into contact with the target cancer area in order to work. It has transdermal properties (i.e. skin penetrating ability) However, a couple of simple tricks can also speed up the process and/or reduce the number of applications required to “reach” a skin cancer that is well below the epidermis. Most people don’t need these techniques if the skin cancer is close to the skin surface. We recommend that these “tricks of the trade” only be used if an initial application does not produce results – which turns out to be a minority of cases.
2A. “Deep Loufah Wash” – Many people use a loofah sponge to rigorously wash and prepare the skin before applying Black salve Salve. This serves to remove some of the dead cells in the top layer of the epidermis (the stratum corneum), so that Black salve has less tissue through which to travel to get to the underlying cancer.
  “Needle Points” – This technique is more effective, but more invasive. It involves taking a sterilized needle and carefully making holes in the skin – about a sixteenth to eighth inch deep, very much as an acupuncturist would – except that the needle is removed as soon as the holes usually spaced about a quarter-inch apart. Following the creation of the “skin holes,” Black Salve is then (re)applied. We recommend that this technique be used by practitioners and not end users. We also advise that practitioners prep the area by rubbing peroxide (3-6%) into the freshly “pricked” skin before Black salve is (re)applied.
3. MANAGING THE ESCHAR
After 24 hours remove the bandage. Using hydrogen peroxide (H2O2 – 3%, available in most drug stores) and a Q-Tip, very lightly go over the border of the lesion, removing any organic debris (i.e. puss, serous fluid, etc.) If a full pus formation is not evident or is incomplete, repeat step 2 and leave the new application on for an additional 24 hours before proceeding. Normally one application is sufficient for small tumors (the size of a pencil eraser), but no more than three applications are required for larger tumors. There are instances, however, when repeated applications of Black salve are required because of “accessibility” problems – although this can be limited using the techniques cited in the preceding section. In order to initiate the escharization process, however, and begin killing the cancer, it is vital that Black salve be able to penetrate and reach the subject site. This can take multiple (three or more) applications, though one to two applications is more common.

After the eschar has formed, keep it well protected. Once the scab has formed, you should apply the After Care Cream and continue to use until spot is completely healed.This product will insure the scaring is minimal and keep the scab moist. Normally the bandage can be left on for a period of 10 days: however, in advanced cases there is considerable “drainage,” that is, a steady emission of pus. In the sense that Black salve kills the cancer cells and takes certain leukocytes (defending white blood corpuscles) with it in the process of eliminating the neoplasm, it is a supportive agent: that is, drainage should not be viewed as abnormal. The range of possible response is very little pus and only one bandage ever required, to a regular change of bandages required in the case of advanced melanomas. Your case will be somewhere in-between.

4. REMOVING THE ESCHAR
The eschar itself represents the death of the neoplasm, and this occurs shortly after application. Everything that follows is the body’s own reparative responses. From here on out, the body knows exactly what to do and wastes no time doing it. However, to us the days and weeks that follow may seem lengthy.The next stage is the removal of the eschar, or scab. This usually happens within 10-14 days after initial application, unless the case is advanced and/or cancer(s) cover a large area of the body. As with any scab, let it fall out when it is ready. DO NOT PULL IT OUT prematurely, if you remove the eschar prematurely, you further risk developing scar tissue and the cancer root will be left behind to spread.

5. DECAVITATION & “HEALING OVER”
After the eschar comes out, the pit or “decavitation” can look raw and unsightly. You need to wipe out the healthy pink crater tissue with peroxide, then look for any embedded white spot(s) in the healthy tissue.  If you see any such spot(s), these are cancer roots and you need to immediately cover the white spot(s) only in the crater with more black salve and let the process begin again.  If no white spot(s) is/are present, keep the crater covered and there will be no threat of secondary infection. Continue to apply the After Care Cream twice daily to the area until it is fully healed over and level with the surrounding skin. If you work in an area that is less than clean, however, you might want to have hydrogen peroxide (available in any good drug store) handy and apply it liberally to the site once a day to kill any invasive germs.
Over a period of a few months, or in some cases two years, the entire area will be healed with only some “depigmentation” or scar tissue. The result is rarely more unsightly or unaesthetic than if surgery had been chosen instead.
Only in rare conditions does the cancer “come back” to the area applied, unless there is underlying metastasis. To be sure that the area is clear of cancer, many users elect to initiate a second, or even third, application after they get to the “heal over” stage. We take a dim view to doing this indiscriminately because the risk of scarring is increased with each new re-application. However, with particularly aggressive forms of cancer, such as melanoma, a user may want to weigh the potential advantages of re-application, particularly if the initial cancer is located somewhere on the body that is not usually aesthetically sensitive or viewed in public (i.e. on the back, upper leg, etc.). None of this should be taken as a substitute for using some of the better cancer marker tests that are now available from qualified, licensed physicians. In other words, if you don’t need more than one application, why do it.
In other words, once Black salve has finished its work, there are normally no residual cells from the original neoplasm. This rule finds more exceptions the larger the original cancer growth is, the deeper it is beneath the skin, the more instances of skin cancer the subject has experienced, and/or the more extensive a person’s history of skin cancer is or has been. Remember, you may need to repeat this process if the skin cancer is sufficiently extensive such that residual cancer cells have been left behind after you finish your first “cycle.” (Although, this same admonition would exist if you had your skin cancer surgically removed.) To be on the side of caution, have your health care practitioner check the site to see if there is any remaining cancer. There are excellent antigen marker tests that your physician can utilize to determine if you have a “clean bill of health.”
Update from Ann Devlin
Thank you very much for all the wonderful messages that I have received since posting information on the black salve treatment that I used recently…It is heartwarming to receive such positive messages of support, especially knowing that I may have had a positive impact on others. Since posting the information I have been inundated with comments and questions, and hundreds of friend requests. I am trying to respond but it is difficult to keep up with them, so I am having to prioritize those that appear to be most pressing. I hope you’ll understand If I don’t get chance to reply in a timely manner, I’m not being rude – there’s just not enough hours in the day! I’ve also got to still concentrate on looking after me too  I’m still recovering really well – now 4 weeks today since the main tumour came out, and the wound gets better each day. I’m still on my strict protocol: vegan diet, lots of juicing, good quality filtered water, herbal teas, homeopathy, lots of supplements including high dose Vit C, running, yoga, good quality sleep
wow flashing

What if we told you there exists a blend of herbs so powerful, effective, and safe for treating cancer that no other conventional treatment even comes close? And what if we told you this same herbal formula only targets malignant cells while leaving healthy cells and other tissue alone? The formula in question actually does exist, and it is traditionally known as Indian black salve, a “magical” cancer cure of sorts that also safely treats viruses and many other health conditions without causing harmful side effects.

If you have never heard of Indian black salve, it is probably because the U.S. Food and Drug Administration (FDA) does not recognize it as an official cancer treatment. In fact, most medical authorities who have heard of Indian black salve reject it as any type of medical treatment because it is made from all-natural herbs that are not patented or owned by corporations, which automatically means they “do not work” in the eyes of the medical-industrial complex (even though they actually do work).

The miraculous healing power of bloodroot

But in truth, Indian black salve is one of the most powerful natural cancer treatments known to man. And this is primarily due to the fact that it contains bloodroot, a potent herb native to the United States and Canada that is already recognized amongst many in the natural health community as being effective in the treatment of warts, moles, skin tags, cherry angiomas, and skin cancer. But as it turns out, bloodroot is also effective internallyas a treatment for ovarian, breast, bladder, bone and many other cancers.

There are numerous Indian black salve blends available, and all of them contain bloodroot and several other prominent healing herbs. Lifeline Water, for instance, sells a potent, alcohol-free Indian black salve formula that contains not only bloodroot but yellow dock, licorice, galangal, zinc chloride, and Lifeline Water. You can learn more about this amazing product here:
http://www.lifelinewater.com/herb.html

You may also remember the saga of herbalist Greg Caton, who we previously reported had been illegally kidnapped and extradited from Ecuador for his involvement in producing natural cancer-cure herbal products (http://www.naturalnews.com/Greg_Caton.html). Caton’s Alpha Omega Labs, which still operates out of Ecuador due to medical tyranny here in the U.S., also sells herbal products similar to Indian black salve that contain healing bloodroot: http://www.herbhealers.com/

How does Indian black salve work, and how should you use it?

Since mainstream medicine continues to deny the therapeutic value of Indian black salve, little is known about how it actually works. But many people have successfully used it both externally and internally to treat all types of cancer, viral infections, gastrointestinal problems, and other conditions. Topically, Indian black salve can be applied directly to malignancies for rapid healing. Lifeline Water recommends mixing three grams of Indian black salve with four ounces of natural or bee pollen cream.

Internally, mixing a small amount of Indian salve paste about the size of half of an English pea in water or putting it into a capsule and taking it either once or twice a day, on a full stomach, can help effectively treat and eliminate cancer in as few as 20 days. Though the company is not permitted by law to explain these healing details with customers, many have used Indian black salve successfully to treat their cancers.

Natural News is exercising its free speech rights to share this information with you, and we have absolutely no financial or other connection with Lifeline Water or any other company offering Indian black salve. We are merely informing you about this amazing healing compound for your own benefit, should you or a loved one develop an “incurable” condition like cancer that cannot be treated using conventional methods.

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Henry Sapiecha

THE BLACK SALVE SELF TREATMENT FOR CANCERS TRUE STORY HERE & 22 BLACK SALVE VIDEOS ALSO IN THIS SITE

Monday, November 28th, 2016
This is a story of an individual using the black Salve to treat his cancer with huge success.

black-salve-on-tumour-at-work image www.newcures.info

The following paragraphs and pictures are a personal account of a six and a half year struggle with a pathogen on the surface of my back. The pictures are graphic but I felt it was necessary for people who may have a similar problem to see them, in order to be encouraged that the growth/pathogen, has been destroyed and eliminated from my body once and for all and with a very simple remedy.

About six and a half years ago I was planning a trip to Florida and decided, instead of getting burned down there, I would try a tanning bed to prepare my skin for the powerful rays closer to the equator. If any one tells you that these sun beds are safe they are misleading you! I was in for 10 minutes, that’s all it took to cause the damage. I will say this, I did have a pre-existing condition called tinea-versicolor. The Dermatologic Disease Database defines it as “Tinea versicolor is caused by a yeast type of skin fungus, which is present on normal skin. If the skin is oily enough, warm enough and moist enough, it starts to grow into small “colonies” on the surface of the skin.” Earlier work by the late Dr. Royal Rife showed that cancer is a virus that, when in the right medium/conditions, can mutate into a bacteria or fungus and back to a virus, and that a bacteria and fungus can also mutate into the others and back.

So, my belief is that the radiation from the rays of the tanning bed hit the tinea versicolor (fungus) and mutated it into a new pathogen that started destroying my skin and growing into a mass, not just on the surface, but well below also. On 4/26/05 I put an herbal preparation of Black Salve on, what was at the time a mass about the size of a half dollar. Over the years it looked like cauliflower on the surface of the skin which would bleed quite a bit so I wore band-aids over it for years. Effective Black Salve is next to impossible to find in the US but you can find it if you look hard enough. I felt tingling and then a burning sensation almost immediately after the application. Some people have felt the need to take aspirin or pain killers to help maintain the pain, I believe it will depend upon each individual case, but better to be prepared by having some on hand if the pain gets to be too much. That night the area around the spot swelled all around and out from it until the perimeter of swelling was about the size of a mans fist. The next morning I woke up and took a shower and the excess Black Salve washed off and left behind an indentation of the skin by about 3 millimeters which was covered by a black scab or eschar.

I applied another coating of Black Salve the second night just to make sure, and the pain got even worse than the night before, which led me to believe that the first application may not have been enough. I never did put on a third application as was suggested to me by a friend who has dealt with many cases. Here you can see what the eschar looks like as it begins to pull away from the healthy skin. That is a quarter next to it in the picture

A couple of days before the first application I began taking whole food supplements which helped my immune system greatly! Spanish Black Radish 2 tablets per meal, increasing to 7 tablets per meal after the first application of Black Salve and for the entire month following. The Spanish Black Radish helped dramatically reduce the weeping of pus and debris from the wound, it is an awesome product when taken correctly! Many people have had to change their bandages 4 or more times a day because there is so much leakage of pus, but with the Spanish Black Radish, all the pus was eliminated internally through the lymphatic system and I actually left the same bandage on all day, only changing it the following mornings after getting out of the shower. Here you can see what the wound looked like after the eschar fell out on day six from the first application.

The crater it left behind was pretty deep, but the second the eschar fell out the pain was completely gone! In the next two pictures below you see what the growth looked like from its underside. Pretty nasty! The pic next to it shows how deep it was. That is a quarter laying flat next to it, so as you can see, in certain parts of the growth it was the thickness of 5-6 quarters if they were stacked on top of each other!

Now comes the easy part, healing! I used/use two specific formulas to assist my healing over the area with new tissue. The special body wash and also organic coconut oil from www.bionutz.com . Some areas take as long as a year to completely heal. I do not think mine will take that long because of the aid of these 2 products but I will take them until I am satisfied with the look of the new skin. Below are the last two pictures, one at 2 weeks after the eschar fell out and the second at two months after the eschar fell out. As you can see, the wound is completely healed over and some scar tissue remains, which I will continue to take the special body wash and also organic coconut oil until I feel it is totally finished healing.

 


Hi
I have successfully used black salve on myself and on my mother-in-law. Myself I have photos taken of the various stages of the healing process.


Contact us for more info

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Henry Sapiecha

 

 

 

 

 

 

 

 

 

BLACK SALVE OINTMENT TREATMENT FOR CANCERS [22] VIDEO COLLECTION YOU TUBE

Thursday, November 24th, 2016
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