Muscular Dystrophy ( Leg Girdle Type)

[Guest guest]

From Anurdha

January 21, 2010 2:52:45 AM EST (CA)

Leg girdle muscular dystrophy

 

Atma Namaste,

 

Could you please tell me the protocol for Leg girdle muscular dystrophy.

Thank you

Anuradha

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

 

Dear Anuradha,

a Loving Atma Namaste!

 

Thank you for your email.

 

The protocoll for " muscular dystrophy " was given in message #3366. Please find a

copy of the message below.

 

MEDICAL BACKGROUND:

 

Muscular Dystrophy (MD) is the name of a group of

muscle disorders that are characterized by progressive

weakness and wasting of the voluntary muscles that

control body movement. As muscle tissue weakens and

wastes away, it is replaced by fatty and connective

tissue.

 

Anyone can be affected. Contrary to popular belief,

muscular dystrophy is not exclusively a childhood

disorder. While some types of MD are first evident in

infancy or early childhood, other types may not appear

until later in life.

 

Specific disorders within this group vary in many

ways. Which muscles are chiefly involved is different

from disorder to disorder. The severity of the

symptoms, the age at which the symptoms appear, how

fast the symptoms progress and what pattern of

inheritance the disorder follows are all factors which

differ between the various forms of muscular

dystrophy.

 

Muscular dystrophies are genetic diseases. They are

not contagious. Forms of muscular dystrophy can be

passed on from generation to generation, or they can

occur spontaneously in a single individual as the

result of a mutation of a particular gene. In any

case, they are not anyone's fault. Each form of

muscular dystrophy is caused by an error in a specific

gene associated with muscle function.

 

Specific types of muscular dystrophy.

 

1.Becker Muscular Dystrophy:

 

The genetic transmission of the disorder is X-linked

recessive. It is caused by mutations in the same gene

as DMD.

 

The onset of symptoms is generally later in BMD than

in DMD, and can occur anywhere from 5 years of age to

young adulthood. As in DMD, in families where there is

a positive history of muscular dystrophy, BMD can be

detected or ruled out in infants by means of a blood

test.

 

Initial Symptoms: Again, initial symptoms are similar

to Duchenne, only milder in severity.

 

Progression: The rate of progression is slow. Many

people with Becker muscular dystrophy are able to walk

well into their teens and adult years. Life expectancy

is, in many cases, normal.

 

2.Limb-Girdle Muscular Dystrophy

 

Type of Inheritance: This is a group of inherited

forms of muscular dystrophy. Most are autosomal

recessive, but some forms of limb-girdle muscular

dystrophy follow a dominant pattern of inheritance.

 

Clinical Onset: The onset of symptoms is extremely

variable, becoming evident anywhere from early

childhood to adulthood. Usually, affected members of a

family have about the same age of onset and degree of

severity.

 

Initial Symptoms: Some forms of limb-girdle MD affect

the lower extremities initially. Symptoms include

difficulty with gait, running, climbing stairs and

rising from the floor. Other forms affect the shoulder

muscles predominantly with resulting difficulty in

lifting the arms.

 

Progression: Progression of limb-girdle muscular

dystrophy is variable. In some cases, it progresses

very slowly, while in others, progression is rapid.

Life span is often unaffected.

 

3.Facioscapulohumeral Muscular Dystrophy (FSH)

 

Type of Inheritance: FSH is an autosomal dominant type

of muscular dystrophy. The gene for the most common

type of FSH is located on chromosome 4.

 

Clinical Onset: This disorder generally appears when a

person is in early adolescence, but it can also appear

in young adulthood or childhood. It can usually be

detected earlier by clinical examination in a family

where there is a positive family history.

 

Initial Symptoms: Lack of facial mobility (smiling,

whistling), difficulty in raising arms over the head

and forward slope of the shoulders are some of the

common initial symptoms.

 

Progression: The progression of facioscapulohumeral

muscular dystrophy is typically slow, with long

periods of time when the disorder seems to stop

progressing altogether. As the trunk and leg muscles

become involved, persons with this disorder may lose

their ability to walk. Life span is often normal.

 

There are more than 100 forms of muscular dystrophy.

 

The Luque procedure is an example of surgery for scoliosis.

 

 

PRANIC HEALING:

 

1. Invoke and scan before, during and after treatment.

 

2. Apply general sweeping twice.

 

3. Do localized thorough sweeping on the front and back

solar plexus chakra and the liver. Energize the solar

plexus chakra with LWG, LWB then ordinary LWV. Apply

more localized thorough sweeping on the front and back

solar plexus chakra.

 

4. Do localized thorough sweeping on the spine and both

sides of the spine with emphasis on the affected parts

of the spine alternately with LWG and LWO.

 

Do not apply O on the head or above the neck area.

 

Energize the affected parts of the spine with LWR.

 

5. Do localized thorough sweeping on the muscles: from

the neck and below but not on or near the heart or

spleen, sweep alternately with LWG and LWO.

 

For muscles on the head, on or near the heart and on

or near the spleen sweep alternately with LWG and

ordinary LWV.

 

6. Do localized thorough sweeping on the minor chakras

of the arms and legs alternately with LWG and LWO.

Energize them with LWR.

 

7. Do localized thorough sweeping on the basic chakra

alternately with LWG and LWO. Energize the basic

chakra thoroughly with LWR. Simultaneously visualize the

basic chakra becoming brighter.

 

8. Do localized thorough sweeping on the front and back

spleen chakra and the navel chakra. Energize the

navel chakra with LWR.

 

9. Do localized thorough sweeping on the kidneys and the meng mein chakra.

Energize the kidneys with W.

 

10. Do localized thorough sweeping on the front and back

heart chakra. Energize the heart chakra through the

back heart chakra with LEV or EV.

 

11. Do localized thorough sweeping on the ajna chakra,

forehead chakra, crown chakra, backhead minor chakra,

jaw minor chakras and throat chakra. Energize them

with LWG then with more of ordinary LWV.

 

12. Stabilize and release projected pranic energy.

 

13. Repeat treatment 2 to 3 times per week for long as

necessary.

 

14. Play the Meditation on Twin Hearts cd. Encourage the patient to practice

the Meditation on Twin Hearts after each Pranic Healing treatment. This will

facilitate proper assimilation of healing energy.

 

 

With Loving Blessings,

The PHQandA Team

 

 

Source: The books written by MASTER CHOA KOK SUI including:

Miracles Through Pranic Healing

Advanced Pranic Healing

Pranic Psychotherapy

Pranic Crystal Healing

 

NOTICE:

 

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

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

immediately a medical doctor and a Certified Pranic Healer.

 

2. Pranic Healers who are not medical doctors should not prescribe nor interfere

with prescribed medications and/or medical treatments.

~ Master Choa Kok Sui

 

MCKS website: http://www.pranichealing.org

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