Any activity performed or any Stimuli received is reflected in the Brain.
Be it feelings or thoughts.
Love , we know, has a soothing effect and one who is brought up in an Environment of Love,Care and protection grows into a Normal adult, there are exceptions though.
A recent study revealed that the left part of the Brain of the child ,which has been exposed and brought up in an environment of Love and affection grows larger than the one which is deprived of Love.
Age old wisdom never fails.
According to neurologists the sizeable difference between these two brains has one primary cause – the way were treated by their mothers These images are brain scans of a two three-year-old children Brain on the left is considerably larger, has fewer spots and less dark areas, compared to the one on the right
Scroll down for video.
Story:
The chilling images reveal that the left brain, which belongs to a normal 3-year-old, is significantly larger and contains fewer spots and dark “fuzzy” areas than the right brain, which belongs to that of a 3-year-old who has suffered extreme neglect.
Neurologists say that the latest images provide more evidence that the way children are treated in their early years is important not only for the child’s emotional development, but also in determining the size of their brains.
Experts say that the sizeable difference in the two brains is primarily caused by the difference in the way each child was treated by their mothers.
While at first glance, the images might indicate that the child with the right brain might have suffered a serious accident or illness, neurologists said that the truth is that the child with the shrunken brain was neglected and abused by its mother, and the child with the larger and more fully developed brain was raised in a loving, supportive home and was looked after by its mother, according to The Sunday Telegraph.
Researchers told the UK newspaper that the image of the brain scan on the right shows that the child lacks some of the most fundamental areas that are present in the image of the brain scan on the left.
They say that the child on the left with the larger brain will be more intelligent and will be more likely to develop the social ability to empathize with others compared to the child on the right.
Two brain scans: the left one of a normal child, the right one of a neglected child of the same age. The speaker is Dick Swaab, professor of neurobiology at the University of Amsterdam (UvA)
(Broadcast in 2009 on Dutch television)
Members of the public are being asked whether families with a genetic risk of incurable conditions like muscular dystrophy should be allowed to use the DNA of a third party to create healthy children.
Although the resulting babies would inherit a small fraction of their DNA from the donor and not their mother or father, the procedure would spare all future generations from a host of rare and debilitating conditions.
The technique is currently forbidden as a treatment, but a public consultation launched today will help inform a decision by Jeremy Hunt, the health secretary, on whether the clinical benefits outweigh any ethical concerns.
Experts accept the technique, which involves genetically modifying a human egg or embryo, enters “unchartered territory” and raises serious ethical questions.
As well as the moral implications of engineering embryos, there are questions over how the procedure would impact on a child’s sense of identity and whether they should be allowed to contact the donor later in life…..
An estimated one in 200 children born in Britain each year is thought to have some form of mitochondrial disease, with defects in anywhere between a handful and 90 per cent of their mitochondria.
In the vast majority of cases, where the number of defects is low, there are no symptoms and the condition is never even diagnosed.
But in about one in 6,500 people the level of damage causes the development of severe medical conditions including muscular dystrophy and ataxia, a neurological condition affecting balance, coordination and speech.
About 99.8 per cent of our DNA, including all our visible characteristics, is contained in the cell nucleus and is passed down from our father and mother in equal measure.
But a small fraction consisting of 37 genes is located in the mitochondria, the tiny structures which supply power to cells, and is inherited solely from the maternal side.
The new technique, being developed by researchers at Newcastle University, is designed to tackle a range of genetic conditions passed to children by their mothers through mutations in these genes.
The mutations can cause cells to malfunction or fail completely, resulting in complications which are especially severe in parts of the body which use the most energy – the brain, heart and muscles.
By removing the nucleus from a woman’s egg before fertilisation and implanting it into a donor egg which has had the nucleus removed, and then using the egg in traditional IVF, doctors could cut damaged mitochondria out of the family line.
A similar technique could be used on an embryo by removing the nuclear DNA from the mother’s egg and father’s sperm and implanting them into a healthy donor embryo with its nuclear DNA removed.’
..
Researchers have secured £6m in funding to develop the groundbreaking treatment which could prevent genetic conditions affecting the heart, muscle or brain being passed on to children and future generations.
But the method is controversial because it involves transferring the parents’ DNA into a donor egg, meaning the resulting child would inherit a tiny fraction of their genetic coding from a third party.
Regulations currently forbid scientists from implanting such eggs into patients….
As there was no improvement in the patient , we decided to give it a try as we had nothing to lose.
The treatment, as described was given and one dose was taken and there is marked improvement he no longer falls down and becomes unconscious and there is better co-ordination of limbs and he is able to walk on hs own.
It odes not matter how or why, but the treatment has improved his condition.
Why don’t people try this?
Please remember that Indian legends and History records Buddhist and Jain Monks were among the best physicians for treatment of diseases and as an aside, it is one of their methods to proselytize the Hindus.
“Tibetan Medicine Pearl 70 (70 Flavors Pearl Pill, Qishiwei Zhenzhu Wan) is based on the classical prescription of Pearl 25, which initially was recorded in “Four Tandara”, a monumental Tibetan medical text in the 8th Century.
Pearl 70 (or Pearl 25) has significant clinic effects to treat stroke, paralysis (such as facial paralysis), hemiplegia, epilepsy, cardiovascular / heart diseases, hypertension brain concussion, cerebral disorders, such as cerebral arteriosclerosis, cerebral thrombosis, myocardial infarction and other cardiovascular and cerebrovascular diseases, limb numbness, spasm stiffness, opisthotonus and other neurological symptoms.
According to Tibetan medical texts, Pearl 70 can treat “Black Pulse Syndrome” and “White Pulse Syndrome”:
Black Pulse Syndrome: cardiovascular system disorder, including heart diseases, hypertension, stroke, brain concussion.
White Pulse Syndrome: neural system disorder or pathologic damage, including hemiplegia, paralysis, epilepsy etc.
The ingredients of Pearl 70: pearl, saffron, sandalwood, dalbergia, cloves, emblica officinalis, strawberries, codonopsis, licorice, bezoar, musk, and other herbs.
Dosage: For emergency, take one pill immediately. For chronic disorders, soak one pill in water, and consume it the next early morning, one pill every 3-7 days.
Address: Tibetan Medical Centre,
# 295, 5th Main Road, Mahalakshmi Layout,
Near Anjaneya Temple,
Bangalore – 560 086 Phone: 2349 6190 URL: www.mentseekhang.org
Working Hours: 9:00 am to 1:00 PM
3:00 pm to 6:00 pm
Monday Holiday
The CPR Aiyar Foundation
1 Eldams Road, Alwarpet
Chennai 600018
Phone: 044 24341778 / 24346526
Men-Tse-khang
Tibetan Medical & Astro, Institute
Branch Clinic
Middle Bakrota
P.O. Dalhousie
Distt: Chamba Himachal Pradesh-176304
Code:01899
Ph No:40814
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Branch Clinic
Choepheling Tibetan Settlement
P.O. Miao
Distt: Changlang Arunachal Pradesh-792122
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Tibetan Medical & Astro, Institute
Branch Clinic
No.295,5th Main Road,11th Cross
Mahalakshmi Lay-out
(near Anjaneya Temple Bangalore-560086
Code No:080
Ph No:3496190
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Tibetan Medical & Astro, Institute
Branch Clinic
Tibetan Settlement
P.O.Mahendragada
Distt: Gajapati Orissa-761034
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Tibetan Medical & Astro, Institute
Branch Clinic
Tibetan Settlement
P.O. Bhuppur,Paonta Sahib
Distt:sirmour Himachal Pradesh
Code No:01704
Ph No:23547
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Tibetan Medical & Astro, Institute
Branch Clinic
13,Jaipur Estate
East Nizamuddin New Delhi-110013
Code N:011
Ph No:24356503:24351099
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Tibetan Medical & Astro, Institute
Branch Clinic
New Camp,house no:A-32
Majnu-ka-tilla Delhi-110054
Code No:011
Ph No:23816306
:
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Tibetan Medical & Astro, Institute
Branch Clinic
P.O. Tenzingang/via:Bomdila
Distt:West Kameng Arunachal Pradesh-790001
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Branch Clinic
P.O. Gurupura,Hunsur Taluk
Distt: Mysore Karnataka-571188
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Tibetan Medical & Astro, Institute
Branch Clinic
Block No.18/A,No.96/97
Main road,Kusumpti Shimla-171009
Code No:0177
Ph No:224504
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Tibetan Medical & Astro, Institute
Branch Clinic
Tibetan Settlement
P.O. Tindolong/Tezu
Distt: Lohit Arunachal Pradesh-792001
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Tibetan Medical & Astro, Institute
Branch Clinic
Govt,QRS-1/2,Unit-I
Bhubaneshwar Orissa-751009
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Tibetan Medical & Astro, Institute
225,Rajpur Road
P.O.Rajpur
Distt: Dehradun Uttar Pradesh-248009
Code No:0135
Ph No:685383
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Tibetan Medical & Astro, Institute
Branch Clinic
P.O.Bir
Distt:Kangra Himachal Pradesh
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Tibetan Medical & Astro, Institute
Branch Clinic
Tibetan Settlement
P.O. Bylakuppe
Distt: Mysore Karnataka-571104
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Tibetan Medical & Astro, Institute
Branch Clinic
26,H.D Lama Road,Darjeeling West Bengal-734101
Code No:0354
Ph No:54735
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Tibetan Medical & Astro, Institute
Branch Clinic
3/114,Dhobichour
P.O.box no.2823
Chetrapati,Kathmandu Nepal
Code No:009771
Ph No:251994
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Branch Clinic
Dekyiling Tibetan Settlement
P.O. kulhan,Sahastradhara Road
Distt: Dehra Dun Uttar Pradesh-248001
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Tibetan Medical & Astro, Institute
Branch Clinic
Near Gunpa Road
P.O. Manali
Distt: Kullu Himachal Pradesh
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Tibetan Medical & Astro, Institute
Branch Clinic
Tibetan Settlement
P.O. Tibetan colony,Mundgod
Distt: North Kannada Karnataka-581411
Code No:08301
Ph No:45716
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Branch Clinic
Tibetan Settlement
P.O. Tibetan colony/kollegal
Distt: chamarajanagar Karnataka-5711571457
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Branch Clinic
Tibetan Settlement
P.O.Pratapgarh
Distt: bhandara Maharashtra-441702
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Tibetan Medical & Astro, Institute
Branch Clinic
Ragasha Building
Namnang road
Gangtok Sikkim-737101
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Branch Clinic
Tibetan Settlement
Camp No.1
P.O. Kamleshwarpur
Mainpat
Distt: Surguja Madhya Pradesh-497127
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Branch Clinic
P.O.Choglamsar
Distt: leh,ladakh J&k-194101
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Sevoke road(siliguri)
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Distt: Jalpaiguri West bengal-734318
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48/6A,Purna Chandra Mitra Lane
(Swiss Park)tollygunj Calcutta-700033
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Branch Clinic
Kunpheling Tibetan Settlement
P.O. Ravangla
Distt: Namchi South Sikkim-737134
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Branch Clinic
Bhutan Border Road,Deokota toll
P.O.Jaigoan
Distt: Jalpaiguri West Bengal
Kailash Medical
Tibetan Medical & Astro, Institute
7(HA)966/967,Maijubahal
Chabahil,Post box No.2823 Kathmandu,Nepal
Dr.gyurmey Dorjee
Lekshedh Tsal Tibetan Day school
P.O box No.130
Hiletar
Pokhara Nepal
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Tibetan Medical & Astro, Institute
Branch Clinic
rai Bahadur Compound,
P.O. Kalimpong
Distt: Darjeeling West Bengal-734301
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Gangkyi Branch Clinic
P.O. Dharmsala
Distt: Kangra Himachal Pradesh-176215
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Thubten Choeling Gonpa
Junebesi(East No.3)
solokkhumbu Nepal
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Branch Clinic
P.O. Jispa
Distt: Lahaul/spiti Himachal-175132
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Tibestan Medical & Astro, Institute
Branch Clinic
Near NCC Office
Lower Lachumiere
Shillong Meghalaya-793001
Code No:0353
Ph No:227583
Take equal measure Moringaoleifera‘s(from Tamil: Murungai, Malayalam:Mashinga sanga, Konkani: Muringa) Root barks and Garlic,pound them to nicely.
You will get a liquid.
Drop Four Drops of the oil in Right Nostril for left side head ache and the Left Nostril for Right side head ache.
OR
Mix Adhimathuram (Tamil)/liquorice root (English)/ Mulethi (Hindi)/ Madhuka (Sanskrit)/atimadura (kannada)/ bikhe-mahak (Persian)/ Botanical name: Glycyrrhiza glabra L, Fennel and Sugar each 35 gms ,pond them to a paste ;take it with half a teaspoon of Honey thrice a day.
Normally one application is enough.
Migraine (from the Greek wordshemi, meaning half, and kranion, meaning skull is a debilitating condition characterized by moderate to severe headaches, and nausea, about 3 times more common in women than in men.
The typical migraine headache is unilateral pain (affecting one half of the head) and pulsating in nature, lasting from 4 to 72 hours; symptoms include nausea, vomiting, photophobia (increased sensitivity to light), phonophobia (increased sensitivity to sound); the symptoms are generally aggravated by routine activity.[3][4] Approximately one-third of people who suffer from migraine headaches perceive an aura—unusual visual, olfactory, or other sensory experiences that are a sign that the migraine will soon occur.
Signs and symptoms
Migraines typically present with recurrent severe headache associated with autonomic symptoms.[9] An aura only occurs in a small percentage of people.[9] The severity of the pain, duration of the headache, and frequency of attacks is variable.
There are four possible phases to a migraine attack. They are listed below – not all the phases are necessarily experienced. Additionally, the phases experienced and the symptoms experienced during them can vary from one migraine attack to another in the same person:
The prodrome, which occurs hours or days before the headache.
The aura, which immediately precedes the headache.
Prodromal symptoms occur in 40–60% of those with migraines. This phase may consist of altered mood, irritability, depression or euphoria,fatigue, yawning, excessive sleepiness, craving for certain food (e.g. chocolate), stiff muscles (especially in the neck), hot ears, constipation or diarrhea, increased urination, and other visceral symptoms.[10] These symptoms usually precede the headache phase of the migraine attack by several hours or days, and experience teaches the patient or observant family how to detect that a migraine attack is near.
Screenshot of a YouTube video showing a computer simulation of visual field defects during migraine with aura based on a neural network.
For the 20–30%of migraine sufferers who experience migraine with aura, this aura comprises focal neurological phenomena that precede or accompany the attack. They appear gradually over 5 to 20 minutes and generally last fewer than 60 minutes. The headache phase of the migraine attack usually begins within 60 minutes of the end of the aura phase, but it is sometimes delayed up to several hours, and it can be missing entirely (see silent migraine). The pain may also begin before the aura has completely subsided. Symptoms of migraine aura can be sensory or motor in nature.
Visual aura is the most common of the neurological events and can occur without any headache. There is a disturbance of vision consisting often of unformed flashes of white and/or black or rarely of multicolored lights (photopsia) or formations of dazzling zigzag lines (scintillating scotoma; often arranged like the battlements of a castle, hence the alternative terms “fortification spectra” or “teichopsia”[15]). Some patients complain of blurred or shimmering or cloudy vision, as though they were looking through thick or smoked glass, or, in some cases, tunnel vision and hemianopsia. For those suffering from this the prodrome is a small blurred spot that we cannot focus on. This is followed by a growing into a larger object such as a three sided square with the zig-zag line interfering with vision. This grows to a maximum size and then starts moving slowly through the field of vision until it exits the field of view. For all practical purposes the aura phase has then ended even if brain activity could be detected that would indicate an active aura.
The somatosensory aura of migraine may consist of digitolingual or cheiro-oral paresthesias, a feeling of pins-and-needles experienced in the hand and arm as well as in the nose-mouth area on the same side. The paresthesia may migrate up the arm and then extend to involve the face, lips and tongue.
Other symptoms of the aura phase can include auditory, gustatory or olfactory hallucinations, temporary dysphasia, vertigo, tingling or numbness of the face and extremities, and hypersensitivity to touch.
The typical migraine headache is unilateral, throbbing, and moderate to severe and can be aggravated by physical activity.[3] Not all these features are necessary. The pain may be bilateral at the onset or start on one side and become generalized, and may occur primarily on one side or alternate sides from one attack to the next. The onset is usually gradual. The pain peaks and then subsides and usually lasts 4 to 72 hours in adults and 1 to 48 hours in children. The frequency of attacks is extremely variable, from a few in a lifetime to several a week, and the average sufferer experiences one to three headaches a month. The head pain varies greatly in intensity.
The pain of migraine is invariably accompanied by other features. Nausea occurs in almost 90 percent of patients, and vomiting occurs in about one third of patients. Many patients experience sensory hyperexcitability manifested by photophobia, phonophobia, and osmophobiaand seek a dark and quiet room. Blurred vision, delirium, nasal stuffiness, diarrhea, tinnitus, polyuria, pallor, or sweating may be noted during the headache phase. There may be localized edema of the scalp or face, scalp tenderness, prominence of a vein or artery in the temple, or stiffness and tenderness of the neck. Impairment of concentration and mood are common. The extremities tend to feel cold and moist.Vertigo may be experienced; a variation of the typical migraine, called vestibular migraine, has also been described. Lightheadedness, rather than true vertigo,[citation needed] and a feeling of faintness may occur.
The cause of migraines is unknown.
Analgesics
A number of analgesics are effective for treating migraines including:
Non-steroidal anti-inflammatory drugs (NSAIDs): Ibuprofen provides pain effective pain relief in about half of people.]Naproxen can abort about one third of migraine attacks, which was 5% less than the benefit of sumatriptan.[84] A 1000 mg dose of Aspirin (also called ASA) could relieve moderate to severe migraine pain, with similar effectiveness to sumatriptan.
Paracetamol/acetaminophen either alone or in combination with metaclopramide is effective for migraines.
Simple analgesics combined with caffeine may help. Even by itself, caffeine can be useful during an attack,[88][89] despite the fact that in general migraine-sufferers are advised to limit their caffeine intake.
Triptans
Triptans such as sumatriptan are effective for both pain and nausea in up to 75% of people.[9][90] They come in a number of different forms including oral, injection, nasal spray, and oral dissolving tablets. Most side effects are mild such as flushing however rare cases ofmyocardial ischemia have occurred.They are non addictive, but may cause medication overuse headaches if used more than 10 days per month
Ergotamines
Dihydroergotamine is an older medication that some find useful. They were the primary oral drugs available to abort a migraine prior to the triptans. They are much less expensive than triptans and continues to be prescribed for migraines.
Corticosteroids
A single dose of intravenous dexamethasone, when added to standard treatment of a migraine attack, is associated with a 26% decrease in headache recurrence in the following 72 hours.
Migraine can be treated effectively with the help of fresh grape juice. Grind grapes to extract the juice. Consume the juice in the concentrated form, without adding water.
Increase the intake of niacin (vitamin B3), as it has been found to be helpful in alleviating migraine pain. Some of the foods rich in niacin are yeast, whole wheat, green leafy vegetables, tomatoes, nuts, sunflower seeds, liver and fish.
Cabbage leaves are helpful in relieving the pain of a migraine headache. Squash cabbage leaves and place them in a cloth. Place the cloth on your forehead for sometime. Once the cabbage leaves become dry, remove the cloth and make a fresh one.
Lemon peel is helpful in solving migraine headache. Grind lemon peel to form a paste and apply it on the forehead. Let it dry and then rinse off with cool water.
A mixture of carrot juice, either with spinach, beet or cucumber juice, works effectively in curing migraine. Combine 300 ml of carrot juice with 200 ml of any other juice and drink it.
You can also mix 100 ml each of beet and cucumber juices, with 300 ml of carrot juice and drink it on a regular basis.
Massaging the forehead with primrose oil is beneficial in curing migraine. It works as an excellent anti-inflammatory agent, preventing any kind of constriction in the blood vessels.
Include garlic in your diet. Either chew a piece of garlic in the raw form or mix it with other food items.
Another effective method would be to have chamomile tea. This is effective in reducing the occurrence of migraine.
Taking lukewarm water enema is effective. It cleanses the bowels, thereby removing the toxins from the body and helping prevent migraine.
Take some sandalwood powder and add a few drops of water to it, so as to form a paste. Apply this paste on the forehead and let it dry. Once dry, rub it off by hand and wash it.
It is advisable to avoid direct sunlight; smoking and drinking alcohol, as all these can aggravate migraine.
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