Organic Fagonia Cretica Tea - Virgin's Mantle
Cancer in Remission with Medicinal Properties of Leaf and Flower - Dhanvyaas / Dhamasa / Durlabaha (Organic Fagonia cretica)
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Cancer in Remission with Medicinal Properties of Leaf and Flower - Dhanvyaas / Dhamasa / Durlabaha (Organic Fagonia cretica)
Please do share with regards Age and illness details of patient in our email ( AsmiConsultancyHerbals@gmail.com ) so we can confirm the details on Medically recommended intake Dosage of Organic Fagonia cretica Tea. Because in an early case of Cancer, the mixing ratio with regards Organic Fagonia cretica is Leaf 40 : Flower 60 while in Stage 4 / Terminal illness, its Leaf 10 : Flower 90 and similarly as per illness severity / type of carcinoma, the mixing ratio of Leaf : Flower and daily intake dosage also varies.
Below mentioned 5 Medicinal Herbs are recommended for Patients of Cancer to enable a complete and successful remission
Organic Fagonia Cretica Tea Sealed in Humid Proof & Germ Free Pack
Holy Basil decreases tumorigenicity and metastasis of aggressive human cancerous cells. Its a medically proven antioxidant which fights very effectively against Cancer. Holy Basil Tablets are always included in all our medicine parcel for the ease of patients.
Role of Wheatgrass in Cancer : Wheatgrass helps in building a strong immune system, and the key to killing cancer cells is oxygen. To lead an aggressive fight against cancer the body needs to produce more oxygen. Wheatgrass contains Chlorophyll, which is considered the "blood of plants". The molecular structure of chlorophyll is similar to that of hemoglobin. Hemoglobin transports oxygen from the lungs to the rest of the body. Incorporating wheatgrass into the diet will help build and renew blood cells in the body and increase the oxygen available to fight the cancer cells. Chlorophyll and selenium also help build the immunity system. Furthermore, wheatgrass is one of the most alkaline foods known to mankind thus killing "cancer favoring envirnoment".
Role of Giloy in Cancer : Tinospora cordifolia has incredible immune-boosting properties, and its one of the reasons why it is so effective against cancer. A strong immune system is better able to identify any cancerous cells and eliminate them before they have a chance to grown and spread. Tinospora contain a chemical called dichloromethane, which is known to poison and kill cancerous cells. Scientists have also found that Tinospora contain potent cancer-fighting antioxidants such as catalase, glutathione and superoxide dismutase thus enabling in the process of Remission with ease.
With its cell-penetrating ability, Turmeric can cleanse the body at the most vital level to prevent cancers and protect tissues from damage imposed by cancer causing agents. It also prevents cancer cells from damaging DNA and reduces the side effects of chemotherapy.
Using flow cytometric analysis of cells labeled with cyclin A, annexin V and propidium iodide, we describe a time and dose-dependent arrest of the cell cycle in G0/G1 phase of the cell cycle and apoptosis following extract treatment in MCF-7 (WT-p53) and MDA-MB-231 (mutant-p53) human cancer cell lines with a markedly reduced effect on primary human mammary epithelial cells. Analysis of p53 protein expression and of its downstream transcription targets, p21 and BAX, revealed a p53 associated growth arrest within 5 hours of extract treatment and apoptosis within 24 hours. DNA double strand breaks measured as γ-H2AX were detected early in both MCF-7 and MDA-MB-231 cells. However, loss of cell viability was only partly due to a p53-driven response; as MDA-MB-231 and p53-knockdown MCF-7 cells both underwent cell cycle arrest and death following extract treatment. p53-independent growth arrest and cytotoxicity following DNA damage has been previously ascribed to FOXO3a expression. Here, in MCF-7 and MDA-MB-231 cells, FOXO3a expression was increased significantly within 3 hours of extract treatment and FOXO3 siRNA reduced the extract-induced loss of cell viability in both cell lines.
Our results demonstrate for the first time that an aqueous extract of Fagonia (cretica) indica can induce cell cycle arrest and apoptosis via p53-dependent and independent mechanisms, with activation of the DNA damage response. We also show that FOXO3a is required for activity in the absence of p53. Our findings indicate that Fagonia (cretica) indica aqueous extract contains potential anti-cancer agents acting either singly or in combination against cancer cell proliferation via DNA damage-induced FOXO3a and p53 expression.
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Renal cell carcinoma (RCC) is also known as hypernephroma, renal adenocarcinoma, or renal or kidney cancer.
Cancer of the esophagus (also called esophageal cancer) begins when cells in the lining of the esophagus start to grow uncontrol. Cells in nearly every part of the body can develop in cancer, and can travel to other sections of the body.
The various types of primary liver cancer emerge from the various cells that connect up the liver. Primary liver cancer can begin as a single lump rising in the liver, or it can begin in other places inside the liver at the one time
Prostate cancer cells can extend by breaking away from a prostate tumor. They can spread through blood vessels or lymph nodes to impact other parts of the living body.
Stomach cancer mainly starts in the mucus-releasing cells that line the stomach. This type of cancer is known as adenocarcinoma.
Breast cancer is the cancer that evolves in breast cells. Typically, the cancer builds in either the lobules or the ducts of the breast