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Herbs & Plants

Alpinia galanga

Botanical Name :Alpinia galanga
Family: Zingiberaceae
Subfamily: Alpinioideae
Tribe: Alpinieae
Genus: Alpinia
Species: A. galanga
Kingdom: Plantae
Order: Zingiberales

Common Name : Greater galangal (or simply Thai galangal). The galangals are also called blue ginger or Thai ginger,Galanga Root, Greater Galanga, Siamese Ginger, Siamese Galanga, Java Galangal, El Galangal, El Adkham,hang Dou Kou, Laos, Galgant, Naukyo, Lenkuas, Galanga Maior, Grosser Galgant, Da Liang Jiang, Gran

Habitat :Cultivated in Southeast Asia, India, China and Australia

Description:
It is a perennial herb, between one and two metres in height, depending on variety. The leaves are 25-35 cm long, rather narrow blades. The flowers are borne at the top of the plant and are small, white and streaked with deep-red veining. The rhizome resembles ginger in shape but it is much smaller. Some varieties have a dark reddish-brown skin and the interior is nearly white. The rhizomes are tough and difficult to break. It prefers rich, moist soil in a protected, shady position and is drought and frost tender. Frost will damage the leaves but will rarely kill the clump. In a permaculture system it is a useful understorey plant.

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Alpinia galanga.The plant grows from rhizomes in clumps of stiff stalks up to two meters in height with abundant long leaves which bears red fruit. It is native to South Asia and Indonesia. It is cultivated in Malaysia, Laos, and Thailand. A. galanga is the galangal used most often in cookery. The robust rhizome has a sharp, sweet taste and smells like a blend of black pepper and pine needles. The red fruit is  used in traditional Chinese medicine and has a flavor similar to cardamom. ...CLICK & SEE

Known as Chittarattai in Tamil, this form of ginger is used with another root called Athi-Mathuram (Glycyrrhiza Glabra) as folk cure to cold and sore throat.

Edible Uses: 
The rhizome is a common ingredient in Thai soups and curries, where is used fresh in chunks or thin slices, mashed and mixed into curry paste, or dried and powdered. Indonesian rendang is usually spiced with galangal.

Medicinal Uses:

The rhizome has been shown to have antimalarial activity in mice.

Under the names Chewing John, Little John to Chew, and Court Case Root it is used in African-American folk medicine and hoodoo folk magic.

Alpinia galanga rhizome contains the flavonol galangin

Alpinia Galanga rhizome is used against rheumatism, bronchial catarrh, bad breath and ulcers whooping colds in children, throat infections, to control incontinence and fever. Alpinia species show promise as anti-fungals, hypotensives, enhancers of sperm count and motility. Anti-tumor and anti-dementia effects have been observed in rodents.

Alpinia Galanga is a stimulating aromatic and has been successfully employed to aid the digestive process, preventing fermentation and removing flatus. It is useful in case of dyspepsia, preventing vomiting or sickness of the stomach and facilitating digestion. It may be used in all cases in which a stimulating aromatic is indicated. It tones up the tissues and is sometimes prescribed in fever. Homoeopaths use it as a stimulant. It has some reputation as a remedy for perineal relaxation with hemorrhoids and for a lax and pendulous abdomen. It is used as a snuff to treat cold and flu symptoms. Galangal Root has also been used as a digestive aid, especially in combating dyspepsia and flatulence. It is also seen as a remedy for seasickness and motion sickness. It is used against nausea, flatulence, dyspepsia, rheumatism, catarrh and enteritis. It also possesses tonic and antibacterial qualities and is used for these properties in veterinary and homeopathic medicine. This herb has a constricting or binding effect, for example: one that checks hemorrhages or secretions by coagulation of proteins on a soft surface. It also restores, nourishes, and supports the entire body; it exerts a gently strengthening effect on the body.

An aromatic stimulant.  Has been used as a snuff in catarrh and nervous headache.  It is used for nonulcer dyspepsia with flatulence and inflammations of the gastrointestinal tract and upper respiratory trace.  In traditional medicine it is also used as a tonic for low sexual drive and as an adjuvant for diabetes and hypertension.  Somewhat similar to ginger

In Manipuri, it is known as Kanghu. The rhizome is an abortifacient. It has carminative, anti-tuberculosis and stimulant property. Ground rhizome is also used in the treatment of skin infections like eczema, ringworm, etc.

Disclaimer:
The information presented herein is intended for educational purposes only. Individual results may vary, and before using any supplements, it is always advisable to consult with your own health care provider.

Resources:
http://www.greenharvest.com.au/Plants/galangal_info.html
http://www.indiamart.com/chandraayurved/herbal-medicinal-products.html
http://www.motherherbs.com/alpinia-galanga.html
http://en.wikipedia.org/wiki/Alpinia_galanga
http://www.herbnet.com/Herb%20Uses_C.htm

http://www.gardenworldimages.com/Details.aspx?ID=148569&TypeID=1&searchtype=&contributor=0&licenses=1,2&sort=REL&cdonly=False&mronly=False

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Herbs & Plants

Narrow Leaf Cattail

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Botanical Name : Typha angustifolia
Family: Typhaceae – Cat-tail family
Genus : Typha L. – cattail
Species :Typha angustifolia L. – narrowleaf cattail
Kingdom:Plantae – Plants
Subkingdom: Tracheobionta – Vascular plants
Superdivision : Spermatophyta – Seed plants
Division:  Magnoliophyta – Flowering plants
Class: Liliopsida – Monocotyledons
Subclass: Commelinidae
Order: Typhales

Synonyms:
Typha angustifolia L.
TYANC Typha angustifolia L. var. calumetensis Peattie
TYANE Typha angustifolia L. var. elongata (Dudley) Wiegand

Common Name : Lesser Bulrush or Narrowleaf Cattail or Lesser Reedmace or Cattail

Habitat :This cattail is an “obligate wetland” species that is commonly found in the northern hemisphere in brackish locations.

Description:
Typha angustifolia is a perennial herbaceous plant of genus.
The plant’s leaves are flat, very narrow (¼”-½” wide), and 3′-6′ tall when mature; 12-16 leaves arise from each vegetative shoot. At maturity, they have distinctive stalks that are about as tall as the leaves; the stalks are topped with brown, fluffy, sausage-shaped flowering heads. The plants have sturdy, rhizomatous roots that can extend 27″ and are typically ¾”-1½” in diameter.
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It has been proposed that the species was introduced from Europe to North America.  In North America, it is also thought to have been introduced from coastal to inland locations.

The geographic range of Typha angustifolia overlaps with the very similar species Typha latifolia (broadleaf or common cattail). T. angustifolia can be distinguished from T. latifolia by its narrower leaves and by a clear separation of two different regions (staminate flowers above and pistilate flowers below) on the flowering heads. The species hybridize as Typha x glauca (Typha angustifolia x T. latifolia) (white cattail); Typha x glauca is not a distinct species, but is rather a sterile F1 hybrid.[6] Broadleaf cattail is usually found in shallower water than narrowleaf cattail

Edible Uses:
Several parts of the plant are edible, including during various seasons the dormant sprouts on roots and bases of leaves, the inner core of the stalk, green bloom spikes, ripe pollen, and starchy roots. The edible stem is called bon bon in Vietnam

Medicinal Uses:
In Chinese herbal medicine, the astringent pu huang pollen has been employed chiefly to stop internal or external bleeding.  The dried pollen is said to be anticoagulant, but when roasted with charcoal it becomes hemostatic. The pollen may be mixed with honey and applied to wounds and sores, or taken orally to reduce internal bleeding of almost any kind—for example, nosebleeds, uterine bleeding, or blood in the urine.  The pollen is now also used in the treatment of angina.  Pu huang does not appear to have been used as a medicine in the European herbal tradition.  The dregs remaining after the pollen has been sifted from the stamens and sepals can be browned in an oven or hot skillet and then used as an internal or external astringent in dysentery and other forms of bowel hemorrhage.  It is used internally in the treatment of kidney stones, internal hemorrhage of almost any kind, painful menstruation, abnormal uterine bleeding, post-partum pains, abscesses and cancer of the lymphatic system. It should not be prescribed for pregnant women. Externally, it is used in the treatment of tapeworms, diarrhea and injuries.  An infusion of the root has been used in the treatment of gravel.

Disclaimer:
The information presented herein is intended for educational purposes only. Individual results may vary, and before using any supplements, it is always advisable to consult with your own health care provider.

Resources:
http://en.wikipedia.org/wiki/Typha_angustifolia
http://plants.usda.gov/java/profile?symbol=TYAN&photoID=tyan_004_avp.tif
http://www.rook.org/earl/bwca/nature/aquatics/typhaan.html
http://www.herbnet.com/Herb%20Uses_C.htm
http://www.ct-botanical-society.org/galleries/typhaangu.html

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Ailmemts & Remedies

Restless Legs Syndrome(RLS)

Alternative Name : Wittmaack–Ekbom syndrome

Definitipon:
Restless legs syndrome (RLS)  is a neurological disorder characterized by an irresistible urge to move one’s body to stop uncomfortable or odd sensations.  It most commonly affects the legs, but can affect the arms, torso, and even phantom limbs.  Moving the affected body part modulates the sensations, providing temporary relief.
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RLS sensations can most closely be compared to an itching or tickling in the muscles, like “an itch you can’t scratch” or an unpleasant “tickle that won’t stop.” The sensations typically begin or intensify during quiet wakefulness, such as when relaxing, reading, studying, or trying to sleep.  In addition, most individuals with RLS have limb jerking during sleep, which is an objective physiologic marker of the disorder and is associated with sleep disruption. Some controversy surrounds the marketing of drug treatments for RLS. It is a “spectrum” disease with some people experiencing only a minor annoyance and others experiencing major disruption of sleep and significant impairments in quality of life

Restless legs syndrome can begin at any age and generally worsens as you get older. Women are more likely than men to develop this condition.

A number of simple self-care steps and lifestyle changes may help you. Medications also help many people with restless legs syndrome.

Symptoms:
Commonly described sensations
People typically describe restless legs syndrome (RLS) symptoms as unpleasant sensations in their calves, thighs, feet or arms, often expressed as:

*Crawling

*Tingling

*Cramping

*Creeping

*Pulling

*Painful

*Electric

*Tense

*Uncomfortable

*Itchy

*Tugging

*Gnawing

*Aching

*Burning

Sometimes the sensations seem to defy description. Affected people usually don’t describe the condition as a muscle cramp or numbness. They do, however, consistently describe the desire to move or handle their legs.

It’s common for symptoms to fluctuate in severity, and occasionally symptoms disappear for periods of time.

NIH criteria
In 2003, a National Institutes of Health (NIH) panel modified their criteria to include the following:

1.An urge to move the limbs with or without sensations.

2.Improvement with activity. Many patients find relief when moving and the relief continues while they are moving. In more severe RLS this relief of symptoms may not be complete or the symptoms may reappear when the movement ceases.

3.Worsening at rest. Patients may describe being the most affected when sitting for a long period of time, such as when traveling in a car or airplane, attending a meeting, or watching a performance. An increased level of mental awareness may help reduce these symptoms.

4.Worsening in the evening or night. Patients with mild or moderate RLS show a clear circadian rhythm to their symptoms, with an increase in sensory symptoms and restlessness in the evening and into the night.
RLS is either primary or secondary.

*Primary RLS is considered idiopathic or with no known cause. Primary RLS usually begins slowly, before approximately 40–45 years of age and may disappear for months or even years. It is often progressive and gets worse with age. RLS in children is often misdiagnosed as growing pains.

*Secondary RLS often has a sudden onset after age 40, and may be daily from the beginning. It is most associated with specific medical conditions or the use of certain drugs

Causes:
Disease mechanism
Most research on the disease mechanism of restless legs syndrome has focused on the dopamine and iron system.   These hypotheses are based on the observation that iron and levodopa, a pro-drug of dopamine that can cross the blood-brain barrier and is metabolized in the brain into dopamine (as well as other mono-amine neurotransmitters of the catecholamine class) can be used to treat RLS, levodopa being a medicine for treating hypodopaminergic (low dopamine) conditions such as Parkinson’s disease, and also on findings from functional brain imaging (such as positron emission tomography and functional magnetic resonance imaging), autopsy series and animal experiments.  Differences in dopamine- and iron-related markers have also been demonstrated in the cerebrospinal fluid of individuals with RLS.  A connection between these two systems is demonstrated by the finding of low iron levels in the substantia nigra of RLS patients, although other areas may also be involved.

Heredity
RLS runs in families in up to half the people with RLS, especially if the condition started at an early age. Researchers have identified sites on the chromosomes where genes for RLS may be present.

Pregnancy
Pregnancy or hormonal changes may temporarily worsen RLS signs and symptoms. Some women experience RLS for the first time during pregnancy, especially during their last trimester. However, for most of these women, signs and symptoms usually disappear quickly after delivery.

Related conditions
For the most part, restless legs syndrome isn’t related to a serious underlying medical problem. However, RLS sometimes accompanies other conditions, such as:

*Peripheral neuropathy. This damage to the nerves in your hands and feet is sometimes due to chronic diseases such as diabetes and alcoholism.

*Iron deficiency. Even without anemia, iron deficiency can cause or worsen RLS. If you have a history of bleeding from your stomach or bowels, experience heavy menstrual periods or repeatedly donate blood, you may have iron deficiency.

* Kidney failure. If you have kidney failure, you may also have iron deficiency, often with anemia. When kidneys fail to function properly, iron stores in your blood can decrease. This, along with other changes in body chemistry, may cause or worsen RLS.

Risk Factors:
RLS can develop at any age, even during childhood. Many adults who have RLS can recall being told as a child that they had growing pains or can remember parents rubbing their legs to help them fall asleep. The disorder is more common with increasing age.

Complications:
Although RLS doesn’t lead to other serious conditions, symptoms can range from barely bothersome to incapacitating. Many people with RLS find it difficult to get to sleep or stay asleep. Insomnia may lead to excessive daytime drowsiness, but RLS may prevent you from enjoying a daytime nap.

Diagnosis:
The diagnosis of RLS relies essentially on a good medical history and physical examination. Sleep registration in a laboratory (polysomnography) is not necessary for the diagnosis. Peripheral neuropathy, radiculopathy and leg cramps should be considered in the differential diagnosis; in these conditions, pain is often more pronounced than the urge to move. Akathisia, a side effect of several antipsychotics or antidepressants, is a more constant form of leg restlessness without discomfort. Doppler ultrasound evaluation of the vascular system is essential in all cases to rule out venous disorders which is a common etiology of RLS. A rare syndrome of painful legs and moving toes has been described, with no known cause.

Treatment:
Treatment of restless legs syndrome involves identifying the cause of symptoms when possible. The treatment process is designed to reduce symptoms, including decreasing the number of nights with RLS symptoms, the severity of RLS symptoms and nighttime awakenings. Improving the quality of life is another goal in treatment. This means improving overall quality of life, decreasing daytime somnolence, and improving the quality of sleep. All of these goals are taken care of through nonpharmacologic and pharmacologic therapies. Pharmacotherapy involves dopamine agonists as first line drugs for daily restless legs syndrome; gabapentin (Horizant™) and opioids for treatment of resistant cases.

An algorithm created by Mayo Clinic researchers and endorsed by the RLS Foundation, provides guidance to the treating physician and patient, including non pharmacological and pharmacological treatments. Treatment of primary RLS should not be considered until possible precipitating medical conditions are ruled out, especially venous disorders. RLS Drug therapy is not curative and has side effects such as nausea, dizziness, hallucinations, orthostatic hypotension and daytime sleep attacks. In addition, it can be expensive (about $100–150 per month for life), and needs to be considered with caution.

Secondary RLS may be cured if precipitating medical conditions (anemia, venous disorder) are managed effectively. Secondary conditions causing RLS include iron deficiency, varicose veins, and thyroid problems. Karl-Axel Ekbom in his 1945 doctoral thesis on RLS suspected venous disease in about 12.5% of cases. But due to the unavailability of Doppler ultrasound imaging technology (the diagnostic tool detecting abnormal blood flow in the veins, “Venous Reflux”, the pathological basis for varicose veins) at that time, Ekbom may have underestimated the role of venous disease. In uncontrolled prospective series, improvement of RLS was achieved in a high percentage of patients presenting with a combination of RLS and venous disease and had sclerotherapy or other treatment for the correction of venous insufficiency.   In Nonpharmacologic treatments there are ways patients may be able to reduce the symptoms or decrease the severity of the symptoms. One thing that may worsen the symptoms is fatigue. Therefore using relaxation techniques, soaking in a warm bath or massaging the legs can all help aid in relaxation and relief of symptoms. Another technique is avoiding caffeine, alcohol, and tobacco. Also exercising every day and maintaining a schedule of relaxation and avoiding heavy meals before bed will all help with relief of symptoms. These techniques can be used with medication or just by themselves for those who do not want medication. For symptoms that occur in the evening patients may find that activities that alert the mind like crossword puzzles, and video games may reduce symptoms. Many patients may also benefit from RLS support groups.

Stretching and shaking legs
Stretching the leg muscles can bring relief lasting from seconds to days.   Walking around brings relief also. Tiredness can be a factor and some sufferers may find going to bed usually stops the discomfort. Bouncing or shaking the legs/feet in an up and down motion, with the ball of the foot on the floor when sitting down may bring temporary relief.

Iron supplements
According to some guidelines, all people with RLS should have their serum ferritin level tested. The ferritin level, a measure of the body’s iron stores, should be at least 50 µg for those with RLS. Oral iron supplements, taken under a doctor’s care, can increase ferritin levels. For some people, increasing ferritin will eliminate or reduce RLS symptoms. A ferritin level of 50 µg is not sufficient for some sufferers and increasing the level to 80 µg may further reduce symptoms. However, at least 40% of people will not notice any improvement. Treatment with IV iron is being tested at the US Mayo Clinic and Johns Hopkins Hospital. It is dangerous to take iron supplements without first having ferritin levels tested, as many people with RLS do not have low ferritin and taking iron when it is not called for can cause iron overload disorder, potentially a very dangerous condition

Medication therapy:
Several prescription medications, most of which were developed to treat other diseases, are available to reduce the restlessness in your legs. These include:

*Medications for Parkinson’s disease. These medications reduce the amount of motion in your legs by affecting the level of the chemical messenger dopamine in your brain. Two drugs, ropinirole (Requip) and pramipexole (Mirapex), are approved by the Food and Drug Administration for the treatment of moderate to severe RLS.

Doctors commonly also use other Parkinson’s drugs to treat restless legs syndrome, such as a combination of carbidopa and levodopa (Sinemet). People with RLS are at no greater risk of developing Parkinson’s disease than are those without RLS. Side effects of Parkinson’s medications are usually mild and include nausea, lightheadedness and fatigue.

*Opioids. Narcotic medications can relieve mild to severe symptoms, but they may be addicting if used in too high doses. Some examples include codeine, oxycodone (Roxicodone), the combination medicine oxycodone and acetaminophen (Percocet, Roxicet), and the combination medicine hydrocodone and acetaminophen (Lortab, Vicodin).

*Muscle relaxants and sleep medications. This class of medications, known as benzodiazepines, helps you sleep better at night. But these medications don’t eliminate the leg sensations, and they may cause daytime drowsiness. Commonly used sedatives for RLS include clonazepam (Klonopin), triazolam (Halcion), eszopiclone (Lunesta), ramelteon (Rozerem), temazepam (Restoril), zaleplon (Sonata) and zolpidem (Ambien).

*Medications for epilepsy. Certain epilepsy medications, such as gabapentin (Neurontin), may work for some people with RLS.It may take several trials for you and your doctor to find the right medication and dosage for you. A combination of medications may work best.

Caution about medications:
One thing to remember with drugs to treat RLS is that sometimes a medication that has worked for you for a while becomes ineffective. Or you notice your symptoms returning earlier in the day. For example, if you have been taking your medication at 8 p.m., your symptoms of RLS may start at 6 p.m. This is called augmentation. Your doctor may substitute another medication to combat the problem.

Most of the drugs prescribed to treat RLS aren’t recommended for pregnant women. Instead, your doctor may recommend self-care techniques to relieve symptoms. However, if the sensations are particularly bothersome during your last trimester, your doctor may approve the use of pain relievers.

Some medications may worsen symptoms of RLS. These include most antidepressants and some anti-nausea drugs. Your doctor may recommend that you avoid these medications if possible. However, should you need to take these medications, restless legs can still be controlled by adding drugs that manage the condition.

Lifestyle and home remedies

Making simple lifestyle changes can play an important role in alleviating symptoms of RLS. These steps may help reduce the extra activity in your legs:

*Take pain relievers. For very mild symptoms, taking an over-the-counter pain reliever such as ibuprofen (Advil, Motrin, others) when symptoms begin may relieve the twitching and the sensations.

*Try baths and massages. Soaking in a warm bath and massaging your legs can relax your muscles.

*Apply warm or cool packs. You may find that the use of heat or cold, or alternating use of the two, lessens the sensations in your limbs.

*Try relaxation techniques, such as meditation or yoga. Stress can aggravate RLS. Learn to relax, especially before going to bed at night.Establish good sleep hygiene. Fatigue tends to worsen symptoms of RLS, so it’s important that you practice good sleep hygiene. Ideally, sleep hygiene involves having a cool, quiet and comfortable sleeping environment, going to bed at the same time, rising at the same time, and getting enough sleep to feel well rested. Some people with RLS find that going to bed later and rising later in the day helps in getting enough sleep.

*Exercise. Getting moderate, regular exercise may relieve symptoms of RLS, but overdoing it at the gym or working out too late in the day may intensify symptoms.

*Avoid caffeine. Sometimes cutting back on caffeine may help restless legs. It’s worth trying to avoid caffeine-containing products, including chocolate and caffeinated beverages such as coffee, tea and soft drinks, for a few weeks to see if this helps.

*Cut back on alcohol and tobacco. These substances also may aggravate or trigger symptoms of RLS. Test to see whether avoiding them helps.

*Stay mentally alert in the evening. Boredom and drowsiness before bedtime may worsen RLS. Mentally stimulating activities such as video games or crossword puzzles can help you stay alert and may reduce symptoms of RLS.

Alternative Medication:
Because restless legs syndrome is sometimes due to an underlying nutritional deficiency, taking supplements to correct the deficiency may improve your symptoms. Your doctor can order blood tests to pinpoint nutritional deficiencies and give you a good sense of which supplements may help.

Doctor may also tell you whether certain dietary supplements can interfere with the way your prescription medications work or may pose health risks for you.

If blood tests show that you are deficient in any of the following nutrients, your doctor may recommend taking dietary supplements as part of your treatment plan:

*Iron
*Folic acid
*Vitamin B
*Magnesium

More research is needed to reliably establish the safety and effectiveness of all of these supplements in the treatment of RLS.

Prognosis:
RLS is generally a lifelong condition for which there is no cure. Symptoms may gradually worsen with age, though more slowly for those with the idiopathic form of RLS than for patients who also suffer from an associated medical condition. Nevertheless, current therapies can control the disorder, minimizing symptoms and increasing periods of restful sleep. In addition, some patients have remissions, periods in which symptoms decrease or disappear for days, weeks, or months, although symptoms usually eventually reappear. Being diagnosed with RLS does not indicate or foreshadow another neurological disease.

Prevention:
Other than preventing the  causes, no method of preventing RLS has yet been established or studied.

Disclaimer: This information is not meant to be a substitute for professional medical advise or help. It is always best to consult with a Physician about serious health concerns. This information is in no way intended to diagnose or prescribe remedies.This is purely for educational purpose

Resources:
http://www.mayoclinic.com/health/restless-legs-syndrome/DS00191
http://en.wikipedia.org/wiki/Restless_legs_syndrome
http://www.sleepdisordersguide.com/restless-leg-syndrome-causes.html

Homeopathy for Restless Legs Syndrome

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Ailmemts & Remedies

Progressive Supranuclear Palsy

Definition:
Progressive supranuclear palsy, also called Steele-Richardson-Olszewski syndrome,(after the Canadian physicians who described it in 1963)  is a brain disorder that causes serious problems with walking, balance and eye movements. Progressive supranuclear palsy results from deterioration of cells in areas of your brain that control movement.
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Progressive supranuclear palsy is a rare disorder that slowly worsens over time. Although it’s not life-threatening itself, progressive supranuclear palsy can lead to life-threatening complications, such as pneumonia and swallowing problems.

Because there’s no cure for progressive supranuclear palsy, treatment focuses on managing and improving the related signs and symptoms.

Males and females are affected approximately equally and there is no racial, geographical or occupational predilection. Approximately 6 people per 100,000 population have PSP.

It has been described as a tauopathy

Symptoms:
The initial symptoms in two-thirds of cases are loss of balance, lunging forward when mobilizing, fast walking, bumping into objects or people, and falls.

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Other common early symptoms are changes in personality, general slowing of movement, and visual symptoms.

Later symptoms and signs are dementia (typically including loss of inhibition and ability to organize information), slurring of speech, difficulty swallowing, and difficulty moving the eyes, particularly in the vertical direction. The latter accounts for some of the falls experienced by these patients as they are unable to look up or down.

Some of the other signs are poor eyelid function, contracture of the facial muscles, a backward tilt of the head with stiffening of the neck muscles, sleep disruption, urinary incontinence and constipation.

The visual symptoms are of particular importance in the diagnosis of this disorder. Notably, the ophthalmoparesis experienced by these patients mainly concerns voluntary eye movement. Patients tend to have difficulty looking down (a downgaze palsy) followed by the addition of an upgaze palsy. Involuntary eye movement, as elicited by Bell’s phenomenon, for instance, may be closer to normal. On close inspection, eye movements called “square-wave jerks” may be visible when the patient fixes at distance. These are fine movements, similar to nystagmus, except that they are not rhythmic in nature. Difficulties with convergence (convergence insufficiency), where the eyes come closer together while focusing on something near, like the pages of a book, is typical. Because the eyes have trouble coming together to focus at short distances, the patient may complain of diplopia (double vision) when reading.

Cardinal manifestations:

*Supranuclear ophthalmoplegia

*Neck dystonia

*Parkinsonism

*Pseudobulbar palsy

*Behavioral and Cognitive impairment

*Imbalance and Difficulties walking

*Frequent Falls

*Stiffness

*Awkward movements

*Falling

*Problems with speech and swallowing

*Dizziness

*Loss of interest in pleasurable activities (apathy)

*Depression and anxiety

*Laughing or crying for no reason

*Forgetfulness

True to its name, the signs and symptoms of progressive supranuclear palsy tend to become progressively worse as the disease advances.

Causes:
We know that the symptoms of PSP are caused by a gradual deterioration of brain cells in a few tiny but important places at the base of the brain, in the region called the brainstem. One of these areas, the substantia nigra, is also affected in Parkinson’s disease, and damage to this region of the brain accounts for the motor symptoms that PSP and Parkinson’s have in common.

Scientists do not know what causes these brain cells to degenerate. There is no evidence that PSP is contagious, and genetic factors have not been implicated. No ethnic or racial groups have been affected more often than any others, and PSP is no more likely to occur in some geographic areas than in others.

There are, however, several theories about PSP’s cause. One possibility is that an unconventional virus-like agent infects the body and takes years or decades to start producing visible effects. Creutzfeldt-Jakob disease is one disease known to be caused by such an agent. Another possibility is that random genetic mutations, of the kind that occur in all of us all the time, happen to occur in particular cells or certain genes, in just the right combination to injure these cells. A third possibility is that there is exposure to some unknown chemical in the food, air, or water which slowly damages certain vulnerable areas of the brain. This theory stems from a clue found on the Pacific island of Guam, where a common neurological disease occurring only there and on a few neighboring islands shares some of the characteristics of PSP, Alzheimer’s disease, Parkinson’s disease, and amyotrophic lateral sclerosis (Lou Gehrig’s disease). Its cause is thought to be a dietary factor or toxic substance found only in that area.

Another possible cause of PSP is cellular damage caused by free radicals, unstable molecules produced continuously by all cells during normal metabolism. Although the body has built-in mechanisms for clearing free radicals from the system, scientists suspect that, under certain circumstances, free radicals can react with and damage other molecules. A great deal of research is directed at understanding the role of free radical damage in human diseases.

Genetics and Causal Factors:
Fewer than 1% of those with PSP have a family member with the same disorder. A variant in the gene for tau protein called the H1 haplotype, located on chromosome 17, has been linked to PSP. Nearly all people with PSP received a copy of that variant from each parent, but this is true of about two-thirds of the general population. Therefore, the H1 haplotype appears to be necessary but not sufficient to cause PSP. Other genes, as well as environmental toxins are being investigated as other possible contributors to the cause of PSP.

Risk Factors:
Risk factors for progressive supranuclear palsy include:

*Age. Progressive supranuclear palsy typically affects people around the age of 60.
*Sex. Men are affected somewhat more often.

Complications :
Complications of progressive supranuclear palsy result primarily from hindered muscle movements. These complications may include:

*Frequent falling, which can lead to head injuries, fractures and other injuries.

*Difficulty focusing your eyes, which also can lead to injuries.

*Problems with reading, driving a car, or other tasks requiring hand-eye coordination.

*Difficulty sleeping.

*Difficulty looking at bright lights.

*Problems swallowing, which can lead to choking or inhaling food or liquid into your airway (aspiration). Aspiration can develop into pneumonia — the most common cause of death in people with progressive supranuclear palsy.

*Impulsive behaviors — for example, standing up without waiting for assistance — which can lead to falls.

Complications from progressive supranuclear palsy may eventually necessitate the use of a feeding tube due to choking hazards. To avoid injuries due to falling, a walker or a wheelchair may also be necessary.

Diagnosis:
Initial complaints in PSP are typically vague and an early diagnosis is always difficult. The primary complaints fall into these categories:

*Symptoms of dysequilibrium, such as unsteady walking or abrupt and unexplained falls without loss of consciousness.

*Visual complaints, including blurred vision, difficulties in looking up or down, double vision, light sensitivity, burning eyes, or other eye trouble.

*Slurred speech.

*Various mental complaints such as slowness of thought, impaired memory, personality changes, and changes in mood.

Progressive Supranuclear Palsy is often misdiagnosed because some of its symptoms are very much like those of Parkinson’s disease, Alzheimer’s disease, and more rare neurodegenerative disorders, such as Creutzfeldt-Jakob disease. In fact, PSP is most often misdiagnosed as Parkinson’s disease early in the course of the illness. Memory problems and personality changes may also lead a physician to mistake PSP for depression, or even attribute symptoms to some form of dementia. The key to establishing the diagnosis of PSP is the identification of early gait instability and difficulty moving the eyes, the hallmark of the disease, as well as ruling out other similar disorders, some of which are treatable.

PSP is frequently misdiagnosed as Parkinson’s disease because of the slowed movements and gait difficulty, or as Alzheimer’s disease because of the behavioral changes. It is one of a number of diseases collectively referred to as Parkinson plus syndromes. A poor response to levodopa along with symmetrial onset can help differentiate this disease from PD.

Difference between PSP &  Parkinson’s Disease:
Both PSP and Parkinson’s disease cause stiffness, movement difficulties, and clumsiness. However, patients with PSP usually stand straight or occasionally even tilt their heads backward (and tend to fall backward), while those with Parkinson’s disease usually bend forward. Problems with speech and swallowing are much more common and severe in PSP than in Parkinson’s disease, and tend to show up earlier in the course of the disease. Both diseases share other features: onset in late middle age, bradykinesia (slow movement), and rigidity of muscles. Tremor, almost universal in Parkinson’s patients, is rare in PSP. Although Parkinson’s patients markedly benefit from the drug levodopa, patients with PSP respond poorly and only transiently to this drug.

Treatment :
There is currently no effective treatment for PSP, although scientists are searching for better ways to manage the disease. In some patients the slowness, stiffness, and balance problems of PSP may respond to antiparkinsonian agents such as levodopa, but the effect is usually temporary. The speech, vision, and swallowing difficulties usually do not respond to any drug treatment.

Another group of drugs that has been of some modest success in PSP are antidepressant medications. The most commonly used of these drugs are fluoxetine (Prozac), amitriptyline (Elavil), and imipramine (Tofranil). The anti-PSP benefit of these drugs seems not to be related to their ability to relieve depression.

Non-drug treatment for PSP can take many forms. Patients frequently use weighted walking aids because of their tendency to fall backward. Bifocals or special glasses called prisms are sometimes prescribed for PSP patients to remedy the difficulty of looking down. Formal physical therapy is of no proven benefit in PSP, but certain exercises can be done to keep the joints limber.

A surgical procedure that may be necessary when there are swallowing disturbances is a gastrostomy. A gastrostomy (or a jejunostomy) is a minimally invasive procedure which is performed when the patient has difficulty swallowing or when severe choking is a definite risk. This surgery involves the placement of a tube through the skin of the abdomen into the stomach (intestine) for feeding purposes. Surgical procedures such as fetal brain cell implantation and pallidotomy, which are being tested as treatments for Parkinson’s disease, are not effective in PSP.

Life Style & Home Remedies:
To minimize the effects of progressive supranuclear palsy, you can take certain steps at home. They may include:

*Eyedrops. Eyedrops may help ease dry eyes that can occur as a result of problems blinking. They can also be helpful for persistent tearing.

*Fall-avoidance aids. Installing grab bars in hallways and bathrooms or using a walker that’s weighted can help you avoid falls. Making home modifications, such as removing scatter rugs or other items that are hard to see without looking downward, also can help with balance and vision problems. When possible, avoid climbing stairs.

Prognosis:
As there is currently no effective treatment or cure for PSP, although some of the symptoms can respond to nonspecific measures. The average age at symptoms onset is 63 and survival from onset averages 7 years with a wide variance

Researches:
Studies to improve the diagnosis of PSP have recently been conducted at the National Institute of Neurological Disorders and Stroke (NINDS). Experiments to find the cause or causes of PSP are currently under way. Therapeutic trials with free radical scavengers (agents that can get rid of potentially harmful free radicals) are being planned for the future.

In addition, there is a great deal of ongoing research on Parkinson’s and Alzheimer’s diseases at the National Institutes of Health and at university medical centers throughout the country. Better understanding of those common related disorders will go a long way toward solving the problem of PSP, just as studying PSP may help shed light on Parkinson’s and Alzheimer’s diseases.

Disclaimer: This information is not meant to be a substitute for professional medical advise or help. It is always best to consult with a Physician about serious health concerns. This information is in no way intended to diagnose or prescribe remedies.This is purely for educational purpose

Resources:
http://www.healthtouch.com/bin/EContent_HT/showAllLfts.asp?lftname=NINDS156&cid=HT
http://en.wikipedia.org/wiki/Progressive_supranuclear_palsy
http://www.mayoclinic.com/health/progressive-supranuclear-palsy/DS00909
http://www.nlm.nih.gov/medlineplus/progressivesupranuclearpalsy.html

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Categories
Herbs & Plants

Cat Thyme

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Botanical Name  :Teucrium marum
Family: Lamiaceae
Genus: Teucrium
Species: T. marum
Kingdom: Plantae
Order: Lamiales

Common Name :Cat Thyme

Habitat:Cat thyme, a native of Spain and the Western Mediterranean, will live through the winter in the open, on a dry soil and in a good situation, when the frosts are not severe, though it is frequently killed in hard winters if unprotected by mats or other covering.It grows in  dry hills and bushy places.

Description:
Teucrium marum is an evergreen Shrub growing to 0.3 m (1ft) by 0.3 m (1ft in). It has oval leaves, broader at the base, downy beneath, with uncut margins. It  is not frost tender.  It is in leaf all year. It is in flower from Jul to September, and the seeds ripen from Aug to September. The flowers are hermaphrodite (have both male and female organs) and are pollinated by Bees. The plant is self-fertile.
CLICK & SEE THE PICTURES…..
The flowers,  are in one-sided spikes, the corollas are crimson in color.

The leaves and younger branches when fresh, on being rubbed emit a volatile, pungent, aromatic smell, which excites sneezing, but in taste they are somewhat bitter, accompanied with a sensation of heat.

Some, but not all cats prefer it to catnip and will corkscrew themselves into the plant in ecstasy.

Older plants can shrub 3 or 4 feet high if grown in a mild climate…..click & see

Cultivation :
Succeeds in any moderately good soil, preferring a dry soil and a sunny position. Does well in dry places in the rock garden[1]. Plants are not fully hardy in Britain, they can be killed in severe winters especially if the weather is wet. The bruised leaves release a pungent aroma. Cats are strongly attracted to this plant and may tear it to pieces. Plants in this genus are notably resistant to honey fungus.

Propagation:
Seed – sow spring in a cold frame and only just cover the seed. Prick out the seedlings into individual pots when they are large enough to handle and plant them out in the summer if they are large enough. Otherwise, grow them on in a cold frame for the winter and plant them out in the following spring. Division in early spring. Larger divisions can be planted out direct into their permanent positions. We have found that it is best to pot up smaller divisions and grow them on in light shade in a greenhouse or cold frame until they are growing away well. Plant them out in the summer or the following spring. Cuttings of half-ripe wood, July/August in a frame.

Medicinal Uses:

The whole herb is aromatic, deobstruent, diuretic, nervine, stimulant, stomachic and tonic. The plant is supposed to possess very active powers and has been recommended in the treatment of many diseases, being considered useful in most nervous complaints. It is used in the treatment of gallbladder and stomach problems. The root bark is considerably astringent and has been used for checking haemorrhages. A homeopathic remedy is made from the whole herb. It is said to be effectual against small thread-worms in children.

The leaves in powdered form given in wine. The powdered leaves, either alone, or mixed with other ingredients of a like nature, when taken as snuff, have been recommended as excellent for ‘disorders of the head,’ under the name of compound powder of Assarabacca, but lavender flowers are now generally substituted for Cat Thyme. The root bark is considerably astringent and has been used for checking hemorrhages.

Other Uses:
This herb is nirvana to cats. Its potent fragrance makes cats loll about in ecstasy. Forget about weak yet better known cat mint (Nepeta spp.). But despite its value as a cat pleaser, and its charming beauty, it is very little known.

Disclaimer:
The information presented herein is intended for educational purposes only. Individual results may vary, and before using any supplements, it is always advisable to consult with your own health care provider.

Resources:
http://en.wikipedia.org/wiki/Teucrium_marum
http://species.wikimedia.org/wiki/Teucrium_marum
http://www.herbnet.com/Herb%20Uses_C.htm
http://www.arthurleej.com/p-o-m-July04.html

http://www.pfaf.org/user/Plant.aspx?LatinName=Teucrium+marum

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