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Watercress plant blocks breast cancer growth

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Health benefits of Watercress

  • Peppery and tangy flavored cress is a storehouse of many natural phytonutrients like isothiocyanates that have health promotional and disease prevention properties.
  • Cress is one of the very low-calorie green leafy vegetables (only 11 calories per 100 g raw leaves) and contains negligible amounts of fats. Being an antioxidant rich, low-calorific and low-fat vegetable, it is often recommended in cholesterol controlling and weight reduction programs.
  • According to the study published in Centers for disease control and prevention (CDC) journal, researchers at William Paterson University at New Jersey, watercress is labeled as the most nutrient dense food, and for the same reason, it tops the list of “powerhouse fruits and vegetables”.
  • Cress leaves and stem contains gluconasturtiin, a glucosinolate compound that gives the peppery flavor. Research studies suggest that the hydrolysis product of gluconasturtiin, 2-phenethyl isothiocyanate (PEITC), is believed to be cancer preventing by inhibition of phase-I enzymes (mono-oxygenases and cytochrome P450s).
  • Fresh cress has higher concentration of ascorbic acid (vitamin C) than some of the fruits and vegetables. 100 g of leaves provide 47 mg or 72% of RDA of vitamin C. As an anti-oxidant, vitamin C helps trap free-oxygen radicals and reactive oxygen species (ROS) through its reduction potential properties. Lab studies suggest that regular consumption of foods rich in vitamin C help maintain normal connective tissue, prevent iron deficiency, and also help the human body develop resistance against infectious agents by boosting immunity.
  • It is one of the excellent vegetable sources for vitamin-K; 100 g provides over 200% of daily recommended intake. Vitamin K has potential role in bone health through promoting osteotrophic (bone formation and strengthening) activity. Adequate vitamin-K levels in the diet help limit neuronal damage in the brain; and thus, it has established role in the treatment of patients suffering from Alzheimer’s disease.
  • Cress is also an excellent source of vitamin-A, and flavonoids anti-oxidants like ß carotene, lutein and zea-xanthin.
  • It is also rich in B-complex group of vitamins such as riboflavin, niacin, vitamin B-6 (pyridoxine), thiamin and pantothenic acid that are essential for optimum cellular metabolic functions.
  • Further, it is also rich source of minerals like copper, calcium, potassium, magnesium, manganese and phosphorus. Potassium is an important component of cell and body fluids that helps controlling heart rate and blood pressure by countering effects of sodium. Manganese is used by the body as a co-factor for the antioxidant enzyme, superoxide dismutase. Calcium is required as bone/teeth mineral and in the regulation of heart and skeletal muscle activity.
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Iron and sweet wormwood herb kill breast cancer cells in 16hrs

sweet wormwood.JPGMao’s project recruited 500 scientists to find a new cure using two chief tactics: synthetic chemistry and ethnobotany based on traditional Chinese medicine. By analyzing ancient medical texts and more than 2,000 herbal remedies, the phytochemist Tu Youyou and her team identified a plant supposedly brimming with antimalarial compounds: sweet wormwood (Artemisia annua), a member of the daisy family that looks a bit like chamomile. Upon initial testing, the plant did not perform well. But a fourth-century handbook of prescriptions provided a vital insight: To extract the plant’s medicinal properties, it should be steeped in relatively cold water, rather than boiled like tea. Subsequent research identified wormwood’s primary active compound, which was eventually developed into artemisinin, one of the most successful treatments for malaria in history. In 2015, Tu received the Nobel Prize in Physiology or Medicine.

According to studies that were published in an issue of Life Sciences, artemesinin – a derivative of the wormwood plant used in Chinese Medicine – can kill 98% of breast cancer cells in less than 16 hours. The herb used alone caused a 28% reduction in breast cancer cells, but when paired with iron, sweet wormwood was able to eradicate cancer almost entirely. What’s more, normal cells were not negatively affected in the experiment by this treatment.

Artemisinin has been used in the past as a powerful anti-malarial herb, but it now has been proven to be a cancer-fighter, too. When subjects in the published study were given an iron supplement, which often accumulates in the breast tissue but especially so in cancerous cells, the artemisinin was able to selectively target ‘bad’ cells and leave ‘good’ cells alone.

“Taken together, our results demonstrate that the artemisinin disruption of E2F1 transcription factor expression mediates the cell cycle arrest of human breast cancer cells and represents a critical transcriptional pathway by which artemisinin controls human reproductive cancer cell growth.”

Read: Watercress Found to Block Breast Cancer Cell Growth

Iron accumulates in cancerous cells due to special receptors that help them in cell division, called transferrin receptors. Normal cells likely have these receptors as well, but cancerous cells have them in greater abundance, and thus can be targeted by the iron-artemisinin combination, like a 1-2 punch.

 

There have been many experiments now that prove this sweet wormwood derivative can effectively eradicate disease in the presence of iron. The extract has been used for thousand of years in China to treat malaria. The malaria parasite cannot live in the presence of artemisinin because they are iron-rich, but the treatment works just as well for cancerous cells, too. Bioengineers Henry Lai and Narendra Singh of the University of Washington, Seattle were the scientists who initially made this discovery. This is yet another example of a natural herb causing cancerous cell apoptosis.

 

While the sweet wormwood extract has been somewhat difficult to obtain for a fair price for countless years, it is now on its way to being mass-produced by biotech. Will the result be positive and promising?

Telemedicine FAQ for doctors

Telemedicine

When can a physician prescribe medications without an in-person meeting with the patient?

As the result of technological advances in “telemedicine” (commonly defined as the use of electronic information and communications technologies to provide and support health care when distance separates participants), physicians are increasingly called upon to prescribe medications without an in-person visit at the time the prescription is issued. This memorandum recaps AMA policy concerning the proper standard of medical care and summarizes selected state requirements incident to such services.

Proper Standard of Medical Care

Under AMA policy guidelines, a patient-physician relationship must generally be established before medication can be prescribed through a telemedicine contact. As part of this relationship, the physician must (i) obtain a reliable medical history and perform a physical examination of the patient, adequate to establish the diagnosis for which the drug is being prescribed and to identify underlying conditions and/or contraindications to the treatment recommended/provided; (ii) have sufficient dialogue with the patient regarding treatment options and the risks and benefits of treatment(s); (iii) as appropriate, follow up with the patient to assess the therapeutic outcome; (iv) maintain a contemporaneous medical record that is readily available to the patient and, subject to the patient’s consent, to his or her other health care professionals; and (v) include the prescription information as part of the patient medical record.

If telemedicine technology is used to establish a physician-patient relationship, a video component is needed to facilitate a face-to-face encounter. Thus, under AMA guidelines, ordinary telephone calls and email communications are insufficient to establish the relationship needed to prescribe medications.

Exceptions to these requirements can arise in on-call or cross-coverage situations, emergency medical treatment, or other circumstances that have become recognized as meeting or improving the standard of care. A further exception can arise if the medication is prescribed in consultation with another physician who has an ongoing professional relationship with the patient and who has agreed to supervise the patient’s treatment, including use of any prescribed medications.

Additional information regarding the proper standard of medical care in prescribing medications without in-person patient meetings can be found in AMA Policy H-120.949, Guidance for Physicians on Internet Prescribing and in AMA Policy H-480.956, Commercialized Medical Screening.

State Requirements

In all instances, physicians must satisfy any state licensure laws applicable to the practice of medicine; this requirement may be of concern if the patient is located in a state other than that in which the physician is located. Beyond this general consideration, specific medical board requirements for prescribing in the absence of an in-person meeting vary from state to state. A review of selected state requirements follows; this should not be deemed exhaustive:

Florida: Telemedicine technology used to prescribe medication must be able to convey the information necessary to meet the standard of care used for in-person encounters, and physicians are responsible for the quality of this technology. Controlled substances may not be prescribed through telemedicine. Patient relationships can be established through telemedicine alone. Fla. Admin. Code R.64B8-9.014.

New Hampshire: A physician-patient relationship can only be established with an in-person examination, history, diagnosis, and treatment plan. Physicians cannot prescribe medication without such a relationship unless it involves: (a) an admission order for a newly hospitalized patient, (b) a patient of another physician for whom the physician is taking call, (c) a patient having been examined by a physician assistant, nurse practitioner, or other licensed practitioner, or (d) a prescription for a new patient who needs medication on a short-term basis prior to the first scheduled appointment. N.H. Rev. Stat. Ann. § 321:1-1-c.

Idaho: Idaho does not have specific telemedicine laws. However, a physician was disciplined for calling in antibiotics over the phone for a patient who described having flu-like symptoms. This was cited as a breach of the standard of care which requires physicians to examine a patient in-person before prescribing medication. Idaho board disapproves of telemedicine (Idaho Press-Tribune, April 28, 2014).

California: Physicians may prescribe medications based on telemedicine encounters. Cal. Bus. & Prof. Code § 2290.5(a)(6). Before beginning any telemedicine procedures, the patient must verbally consent to the use of telemedicine and this consent must be marked in the patient’s file. Cal. Bus. & Prof. Code § 2290.5(b).

Hawaii: Hawaii specifically permits the issuing of prescriptions based on telemedicine encounters. H.R.S. § 453-1.3.

Texas: Texas law allows physicians to issue prescriptions based on telemedicine encounters. 22 TX A.D.C. § 174.8. Texas law draws a distinction between telemedicine services provided to a patient who is at an established medical site and services provided to a patient who is not at an established medical site. 22 TX A.D.C. § 174.2. An established medical site is defined as a location where there is “a patient site presenter and sufficient technology and medical equipment to allow for an adequate physical evaluation, as appropriate for the patient’s presenting complaint” and does not include a private residence. 22 TX A.D.C. § 174.2. If the patient is at an established medical site a distant-site physician may use telemedicine to establish, diagnose, and treat a patient. 22 TX A.D.C. § 174.6. When the patient is not at an established medical site Texas law requires that the physician and patient have had at least one prior face-to-face encounter before providing treatment, including issuing prescriptions, where face-to-face is defined as either in-person or remotely with the patient at an established medical site. 22 TX A.D.C. § 174.7. Texas law also requires that the physician using telemedicine inform the patient of all the risks and benefits of telemedicine before beginning treatment. 22 TX A.D.C. § 174.5.

Disclaimer

The above information is based on general principals and does not constitute clinical or legal advice. It is aimed at the general practice of prescribing medicine and does not contemplate special circumstances such as drugs related to reproductive health or scheduled substances. The reader should consult an appropriate professional advisor for specific clinical or legal guidance.

If I am a doctor, how will I use technology to benefit my patient and have a stable practice?

If I am a doctor, how will I use technology to benefit my patient and have a stable practice? by John Anderson

Answer by John Anderson:

As a physician, educate your patients:

  • Avoid processed foods. There is a statistical correlation in the growth of chronic illness and the western diet with high reliance on refined grains and sugar, grain-fed beef, and processed foods.
  • Keep your body, home, and office free of contagious / infectious germs. Briotech, the world’s most powerful sanitizer, can safely be used on SKIN, in EYES, in the MOUTH and NOSE, on Cuts, Burns, and even inhaled as a mist – – and kills all known viruses, bacteria, and fungi on contact. Briotech, Beyond HOCL

As a medical practitioner,

  • Use a secure messaging system, like those offered with MyCharts, to send your patients references to educational resources / articles / youtube videos, and the like.
  • Leverage advances in pharmacogenomics to ensure that drug selection and dosing is appropriate for patients.
  • As a surgeon, incorporate stem cells to minimize post-operative adhesions and speed wound healing times.
  • As an oncologist, incorporate hyperthermia to make both local and metastasized tumors more responsive to radio- / immune-/ and chemo- therapies.

If I am a doctor, how will I use technology to benefit my patient and have a stable practice?

A platform for health consumers to stop cancer early and collaborate with health care teams

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https://www.indiegogo.com/projects/genetic-health-data-and-health-concierge-cancer/x/3335495#/

Short Summary

  • I am Connie Dello Buono, health author and blogger at www.careme.live ( soon http://www.avatarcare.net )
    Since 2000, I have cared for seniors with cancer, Alzheimer’s and Parkinsons.
    My passion is help reduce chronic care costs, health education and personalize medicine using telemedicine.
  • This campaign will address cancer health issues, identifying root causes early, connecting with doctors real time, access to telemedicine and tele-clinics, matching providers using mobile application and a health application that will hep reduce chronic care costs.
  • As contributors, you will help achieve our goal of reducing chronic care costs thru telemedicine, personalize medicine and a health mobile application serving all population groups.

Motherhealth Inc

Management Team

  • Maddalena Adorno PhD, CTO. She is a professor at Stanford University Institute for Stem Cells and Regenerative Medicine
  • Connie Dello Buono, CEO. She is a health author and completed her B.S in Mathematics with minor in Chemistry at Adamson University, Manila Philippines

What We Need & What You Get

  • $5000 of the funds will go to the mobile application developers and marketers.
  • Your unique perks will be a lifetime discount, 20%, in the many health apps that will come out of this first phase of the product.

The Impact

  • Avatarcare.net or Motherhealth aims to help health consumers navigate in their health issues and collaborations with health care professionals by providing a platform for them to order their genetic and lab tests, join in health care forums, learn about health care issues and prevention, set up appointment with others and health care teams, find and post health care jobs, video chats with doctors and a health concierge provided online and in the future, via a mobile application.
  • Globally, we can now correlate health data and provide valuable insights to all, scientists and the population.
  • Since 2000, I have been educating the public on health, wrote an ebook on women’s health, was pharmacy tech instructor, a senior care administrator and care provider, and quality assurance in many biotech and medical device companies in the USA.

Why New Antidepressant Brintellix May Be a Killer

Why New Antidepressant Brintellix May Be a Killer
 Gaia Health Blog | Heidi Stevenson

Brintellix is being marketed with implications that it’s the best antidepressent yet and that it’s exceptionally safe. What is this based on? 

Close examination shows the usual smoke and mirrors, and an even closer look points out disturbing indications of potentially devastating and deadly effects—with no indication that it’s better than existing SSRIs, which are known killers.

One of the most devastating classes of drugs ever developed is antidepressant SSRIs, selective serotonin receptor inhibitors. Not only can they destroy your own life, but they can also turn you into a murderer. Now, the FDA has approved Brintellix, which may prove to be the worst of them all.

In a press release by pharmaceutical company Lundbeck, the developer of Brintellix[1], it’s admitted that the cause of depression is unknown. Nonetheless, they cavalierly play with brain chemistry about which they know very little. Making this particular drug potentially even worse than any other SSRI is that it doesn’t limit itself to one or two pathways in the brain. It manipulates a total of 6 receptors!

Although Takeda Pharmaceuticals and Lundbeck, the US distributors, are expecting Brintellix to become a blockbuster drug, the hyped studies that appear to demonstrate both efficacy and safety are far from the full story. In fact, some studies have shown no benefit over placebo whatsoever.[2] It’s apparent from their approval announcement that the FDA did not take studies with negative results into account. They referred to only 6 studies, which the agency states, “demonstrated that Brintellix is effective in treating depression”.[3]

SSRIs

SSRIs do not work as claimed. They interfere with normal brain functioning. They don’t stop depression. Instead, they stop the ability to feel emotions. They result in emotional flatness. Some people may find that beneficial, something of a time-out. But it never resolves the problems that lead to depression, and even interferes with resolution. How can anyone resolve a problem when a drug interferes with their ability to even know that it’s there?

All SSRIs do the same thing. They prevent serotonin, also called 5-HT, from being reabsorbed, as their name, selective “serotonin reuptake inhibitors”, indicates. That hasn’t turned out well. These drugs are now known to cause previously nonsuicidal people to take their own lives without warning. They have also made many people violent and are associated with almost all school shootings.

There is little reason to believe that Brintellix will be more effective than other SSRI antidepressants. In fact, the more SSRIs manage to shut down serotonin production, the more harm they do. The brain works to counter the effect. As Dr. Peter Brennan notes, it can result in permanent brain damage.[4]

In fact, the Los Angeles Time reported that Dr. Michael Thase, a Brintellix development consultant, stated:

It is different enough from the welter of SSRIs currently available that it’s not simply a ‘me too’ drug.[5]

That’s likely true, but does that  make it better?

Brintellix May Be Even Worse

Inexplicable violence, turned both inward and outward, is the result of SSRIs causing a single change to brain function. Brintellix will cause several changes! These changes involve the handling of glutamate, which is a critical amino acid that’s required for brain function and cellular metabolism. Glutamate is necessary—at proper levels, in the right places, and at the right times—for learning, remembering, thinking, and emotions. It’s also involved in energy production throughout the body.

Glutamate excites neural function. Too much glutamate can burn nerves out and too little keeps them from functioning properly. Not only does Brintellix manipulate 5-HT (serotonin), like all other SSRIs, it also manipulates glutamate in several neural receptors:

  • 5-HT1A: Agonist
  • 5-HT1B: Partial Agonist
  • 5-HT3: Antagonist
  • 5-HT1D: Antagonist
  • 5-HT7: Antagonist
Note: An agonist triggers a response from a cell. An antagonist does the opposite. It blocks a cell’s response.

Does anyone really know what the effects of this manipulation of neural transmission will be?

No. Here is what the manufacturer’s press release announcing Brintellix’s approval says about it:

The contribution of each of these activities to Brintellix’s antidepressant effect has not been established. It is considered to be the first and only compound with this combination of pharmacodynamic activity. The clinical relevance of this is unknown.

Let’s look at that again:

No one knows what relationship exists between any of these neural receptors and Brintellix’s effect.

No one knows what these manipulations of the brain will do to the body, intelligence, emotional state, sexuality, criminality, empathy, or anything else.

Nearly all the effects of Brintellix are unknown.

How Much Harm?

Like so many drugs, Brintellix is being rolled out as safe. Like others, that safety is based on a very slim thread: short term studies, which evade the risks. The existing studies produced by Lundbeck are short term, and many adverse effects take time to be seen. They’re also based on a small number of subjects. Most severe adverse effects don’t show up in such studies.

At this point, the list of adverse effects is both brief and appears to be fairly minor. Medscape[6]reports the following adverse effects, followed by the percentage who suffered it:

  • Nausea: 21-32%
  • Diarrhea: 7-10%
  • Dizziness: 6-9%
  • Dry mouth: 6-8%
  • Constipation: 3-6%
  • Vomiting: 3-6%
  • Flatulence: 1-3%
  • Pruritus: 1-3%
  • Abnormal Dreams: Less than 1-3%

These adverse effects are not as innocent as they first appear. Notice that as many as a third of the subjects suffered from nausea, and other gastrointestinal effects were not unusual. This is a red flag that there may be a dangerous adverse effect on the digestive tract that doesn’t show up quickly—not something to take lightly.

Dizziness and abnormal dreams are indicative of very serious harmful neurological effects. Pruritus is a neurologically-induced extreme urge to scratch an itch. This symptom is also indicative of neurological damage. Even at this early stage, the adverse effects point to the potential of severe and dangerous, potentially deadly, reactions.

The history of all other SSRIs, which interfere with only one specific function, has been dismal. Is there any reason to expect Brintellix to be different? The studies certainly aren’t more extensive than they’ve been with other SSRIs, so the reality is that, as usual, the people whose doctors prescribe it will be the guinea pigs.
If your doctor tries to prescribe Brintellix, perhaps the correct response should be, “Oink!”

Even Big Pharma’s faithful lapdog called the FDA has acknowledged some risk. They’re requiring a boxed warning that people younger than 24 years are at risk of developing suicidal thoughts. This, of course, is meaningless. All SSRIs carry that warning, and it certainly doesn’t seem to have reduced prescription levels!

SSRI = Killer

As the FDA admits, all SSRI drugs are known to be killers, and worse than most drugs, they can result in the deaths of people who don’t even take them! They are implicated in virtually all the school shootings. That’s a lot of carnage.

Brintellix is an SSRI. Is there any reason to believe that it will produce less harm than other SSRIs? In fact, there is every reason to suspect the opposite.

By its developer’s own admission, no one knows what effects are produced by 5 of the 6 functions Brintellix was designed to cause. But we do know that the 6th function, serotonin/5-HT reuptake inhibition, is a killer. All of the other 5 functions interfere with normal brain activity—and the manufacturer admits that no one knows what those effects will be!

 What more do you need to know?

 Sources:

  1.  Takeda and Lundbeck announce FDA approval of Brintellix™ (vortioxetine) for treatment of adults with major depressive disorder. Lundbeck’s Brintellix press release.
  2. Antidepressant – vortioxetine. Manufacturer’s Chemist’s review of Brintellix.
  3. FDA approves new drug to treat major depressive disorder. FDA’s Brintellix approval announcement.
  4. Psychiatric drug-induced Chronic Brain Impairment (CBI): Implications for longterm treatment with psychiatric medicationInternational Journal of Risk and Safety in Medicine; DOI 10.3233/JRS-2011-0542.
  5. FDA approves a new antidepressant: BrintellixLos Angeles Times.
  6. Vortioxetine Adverse Effects; Medscape Reference.
  7. Vortioxetine (Lu AA21004) hydrobromide.
  8. Glutamate.
  9. Glutamate benefit and side effects, risk and danger.
  10. Vortioxetine: A New Antidepressant Choice in the United States