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Marfan Syndrome

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Dear Marilette,

 

Namaste.

 

Thank you for your constant guidance and assistance to

Pranic Healers

all around the world. Your service is a wonderful

blessing.

 

Can you give me a protocol for Marfan syndrome?

 

Thank you again.

 

With love,

Andrea

=====================================================

 

 

Dear Andrea,

 

Namaste.

 

Thank you for your email.

 

Medical Background:

 

Marfan syndrome is an inherited connective tissue

disorder that can affect the heart, blood vessels,

lungs, eyes, bones and ligaments. Symptoms of Marfan

syndrome may be mild or severe, and may be present at

birth or appear in childhood or in adult life.

 

Marfan syndrome affects about 1 in 5,000 Americans. It

is one of the most common of the more than 100

inherited disorders of connective tissue (material

that holds tissues of the body together). The disorder

affects males and females from all racial and ethnic

groups. It is named for Dr. Antoine Marfan who, in

1896, described a 5-year-old patient with unusually

long, slender fingers and limbs and other skeletal

abnormalities.

 

Affected individuals often are tall, slender and

loose-jointed. Arms and legs may be unusually long in

proportion to the torso. Feet often are flat. The

spine may be curved (scoliosis), and the breastbone

may protrude or look caved in. The face may be long

and narrow, with a high roof of the mouth and crowded

teeth.

 

The most serious problem associated with Marfan

syndrome is weakness of the aorta (the body’s largest

artery), which affects most individuals with Marfan

syndrome to some degree. Blood pumped from the heart

passes forcefully and directly into the aorta, which

branches out to carry oxygen-rich blood to the entire

body. As the walls of the aorta gradually weaken,

(aortic dilation) they can split in places, allowing

blood to leak into the chest, abdomen or wall of the

aorta itself. Sudden, large splits can result in

death.

 

Affected individuals also may have abnormalities

involving the heart’s mitral valves (mitral valve

prolapse). Heart valves are pairs or trios of flaps

that keep the blood flowing in one direction through

the heart. In individuals with Marfan syndrome, these

valves tend to be oversized and floppy. Their motion

during heartbeats may allow brief reverse blood flow

and cause a heart murmur (an abnormal sound heard

through a stethoscope) and, sometimes, irregular or

rapid heartbeat and shortness of breath. In addition,

persons with Marfan syndrome are more prone than

others to sudden collapse of a lung.

 

In some 50 percent of persons with Marfan syndrome,

the lens of an eye is off-center. Nearsightedness and

cataracts are other common problems, whether the lens

is in place or not. Also the retina, the light-sensing

inner lining of the eye, may become detached.

 

The severity of the effects of Marfan syndrome vary,

meaning that some people with the syndrome have more

serious effects than others. This variability can

occur even within one family.

 

Most of the problems associated with Marfan syndrome

can be managed effectively, as long as they are

diagnosed early. The disorder usually is treated by a

team of specialists, overseen by a single doctor who

knows all of its aspects. The greatest danger is death

from a sudden split in the aorta. This may happen from

the normal pumping of blood through a weak aorta or

from extreme physical or emotional activity that sends

the blood rushing at high pressure. Children and

adults with Marfan syndrome are warned to avoid heavy

exercise, contact sports and lifting heavy objects.

However, with their doctors’ guidance, many are able

to participate in less vigorous activities such as

walking, bicycle riding and swimming.

 

Yearly or more frequent echocardiograms are

recommended to see if the aorta is dilating. This and

other heart and aorta examinations (such at CT or MRI

scans) can alert a specialist before problems with the

aorta or other heart structures become severe. High

blood pressure medications called beta blockers often

are prescribed, as these drugs reduce the strength and

frequency of heartbeats and the strain on the aorta.

Studies suggest that beta blockers may slow down the

rate of aortic dilation and help prevent the artery

from splitting.

 

When necessary, other faulty heart valves also can be

surgically repaired or replaced. After any valve

replacement surgery, the patient is given

anti-clotting medication for life, because blood tends

to clot when it comes in contact with artificial

valves.

 

Because of heart valve abnormalities, most people with

Marfan syndrome are prone to infections in those

valves. They must be treated with oral antibiotics to

prevent infection of valves by bacteria in the blood

stream before routine dental work (including cleaning,

filling, extractions), as well as before any kind of

surgery. Those who have had valve replacement surgery

require higher doses of antibiotics, which usually are

given by injection.

 

 

Women with Marfan syndrome who become pregnant are

considered to be high-risk, whether or not they have

symptoms of an enlarged aorta. They face an increased

possibility of aortic splitting during pregnancy.

 

Marfan syndrome is caused by an abnormal gene on

chromosome 15, one of the 23 pairs of human

chromosomes. Normally, this gene enables the body to

produce a protein called fibrillin, an essential

component of connective tissue that appears to

contribute to its strength and elasticity. Fibrillin

normally is especially abundant in the aorta, in the

ligaments that hold the eye’s lens in place, and in

bones. Apparently individuals with Marfan syndrome

have scant or faulty fibrillin in these structures,

which stretch abnormally because of their inability to

withstand normal stress.

 

The abnormal gene usually is inherited from one parent

who has the disorder. The abnormality is a " dominant "

genetic trait, so each child of a parent with the

abnormal gene has a 50-50 chance of inheriting it. In

about 25 percent of cases, a genetic accident (new

mutation) occurs in sperm or egg cells of unaffected

parents and affects their child. In these cases,

recurrence risk for later offspring is unpredictable,

but usually very low.

 

As with other inherited disorders, Marfan syndrome

cannot be " caught " from another person. Although it

may be diagnosed at any age, it doesn’t occur unless

the abnormal gene is present.

 

At present, there is no way to prevent Marfan

syndrome. Early diagnosis may help prevent serious

complications. Genetic counseling allows informed

decisions about childbearing and will provide

information on genetic testing as it becomes available

to more families affected by Marfan syndrome.

 

Research is being done on Marfan syndrome. In 1991,

researchers, funded in part by the March of Dimes,

discovered the gene in which mutations cause Marfan

syndrome and thereby identifed the protein controlled

by this gene. Researchers currently are identifying

the various mutations (changes) in the gene, for

purposes that include developing a more definitive

test for the disorder. Understanding how each mutation

alters connective tissue and causes the symptoms of

Marfan syndrome also may lead to improved treatments.

Scientists also continue to develop improved

treatments for Marfan syndrome, including new surgical

procedures to prevent the life-threatening dilation

and rupture of the aorta wall.

Ref: American Academy of Pediatrics Committee on

Genetics,

 

Pranic Healing:

 

1. Invoke and scan before, during and after

treatment.

 

2. General sweeping twice.

 

3. Localized thorough sweeping on the front and back

heart chakra and on the aorta alternately with LWG and

ordinary LWV.

 

Energize through the back heart chakra with LWG-V then

with Gold.

 

4. Localized thorough sweeping on other affected

organs and their corresponding chakra(s) alternately

with LWG and ordinary LWV.

 

For non-delicate organs: Energize the organ with LWG,

LWO then LWR.

 

For delicate organs: Energize the organ through its

corresponding chakra(s) using LWG-V then gold.

 

5. Localized thorough sweeping on the front and back

solar plexus chakra(s). Energize with LEV.

 

6. Localized thorough sweeping on the navel and the

basic chakra. Energize them with LWR.

 

7. Localized thorough sweeping on the ajna, crown,

forehead, backhead and throat chakra with LEV.

Energize them with LEV.

 

8. Stabilize and release projected energy.

 

9. Repeat treatment 3 times per week for as long as

needed.

 

10. Teach patient proper pranic breathing (6-3-6-3)

to strengthen the energy body and relieve stress.

 

For patient:

 

1. Avoid extreme emotional activity and physical

exertion such as heavy exercise, contact sports and

lifting heavy objects.

 

2. Regular physical exercise under medical doctor's

advice.

 

3. Pranic breathing for 12 cycles several times per

day especially during times when experiencing stress.

 

4. Tithe regularly for healing.

 

Tithing may be made to feeding centers, hospitals or

healing clinics for treatment of indigent patients

with similar ailments. This condition has a genetic

component and affects the body's connective tissues'

ability to withstand stress.

 

Love,

 

Marilette

 

 

 

 

 

Pranic Healing is not intended to replace orthodox medicine, but rather to

complement it. If symptoms persist or the ailment is severe, please consult

immediately a medical doctor and a Certified Pranic Healer . ~ Master Choa Kok

Sui

 

Miracles do not happen in contradiction to nature, but only to that which is

known to us in nature. ~ St. Augustine

 

Ask or read the uptodate pranic healing protocols by joining the group through

http://health./

 

For the latest International Information regarding GMCKS Pranic Healing, visit

http://www.pranichealing.org.

 

 

 

__

Start your day with - make it your home page

http://www./r/hs

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